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Papers of
Irvin M. Korr
Presented by the American Academy of Osteopathy
in honor of Dr. Korr's seventieth birthday
Editor for the Academy: Barbara Peterson
American Academy of Osteopathy
2630 Airport Road
Colorado Springs, Colorado 8091 0
Copyright 1979, American Acldemy of Osteopathy
Published for the members of the American Academy
of Osteopathy
Table of Contents
I. Introductory papers
5 Editor' s foreword: Barbara Peterson
6 Acknowledgments
7 Preface: Irvin M. Korr, Ph. D. , Sc.D.
9 Biographical notes and appreciation: Judy Alter, Ph.D.
1 1 Scientific contributions of I. M. Korr: Michael M. Patterson, Ph. D.
1 3 Clinical contributions of I.M. Korr: Edward G. Stiles, D.O. , FAAO
II. Primary research reports: Studies on electromyography, sympathetic ner
vous system, reflexes, and related topics
1 8 Quantitative studies of chronic facilitation in human motoneuron pools
(1 947) (with J .S. Denslow and A. D. Krems)
22 Dermatomal autonomic activity in relation to segmental motor refex
threshold ( 1 948) (with Martin J. Goldstein)
23 Skin resistance patterns associated with visceral disease (1 949)
23 The automatic recording of electrical skin resistance patterns on the human
trunk (1 951 ) (with Price E. Thomas)
29 Relationship between sweat gland activity and electrical resistance of the
skin (1957) (with Price E. Thomas)
33 Patterns of electrical skin resistance in man (1958) (with Price E. Thomas
and Harry M. Wright)
41 A mobile instrument for recording electrical skin resistance patterns of the
human trunk (1958) (with Price E. Thomas and Harry M. Wright)
45 Local and regional variations in cutaneous vasomotor tone of the human
trunk (1 960) (with H. M. Wright and P. E. Thomas)
54 Effects of experimental myofascial insults on cutaneous patterns of sym
pathetic activity in man (1 962) (with H. M. Wright and P.E. Thomas)
66 Cutaneous patterns of sympathetic activity in clinical abnormalities of the
musculoskeletal system (1964) (with Harry M. Wright and John A. Chace)
73 Neural and spinal components of disease: Progress in the application of
"thermography" (1 965) (with H. M. Wright)
75 What is manipulative therapy? (1 978)
77 Sustained sympathicotonia as a factor in disease ( 1 978)
III. Axonal transport, trophic functions of nerves
92 Studies in neurotrophic mechanisms (1 966) (with P. N. Wilkinson and F.W.
Chornock)
93 Axonal delivery of neuroplasmic components to muscle cells (1 967) (with
P. N. Wilkinson and F.W. Chornock)
96 The nature and basis of the trophic function of nerves: Outline of a re
search program (1 967)
99 Studies in trophic mechanisms: Does changing its nerve change a muscle?
(1 967) (with F.W. Chornock, W.V. Cole, and P. N. Wilkinson)
1 00 Continued studies on the axonal transport of nerve proteins to muscle
(1 970) (with G. S. L. Appeltauer)
1 02 The time-course of axonal transport of neuronal proteins to muscle (1 974)
(with Gustavo S. L. Appeltauer)
1 07 Axonal delivery of soluble, insoluble and electrophoretic fractions of
neuronal proteins to muscle (1 975) (with Gustavo S. L. Appeltauer)
1 1 2 Electrophoretic characterization of neuronal basic proteins in skeletal
muscle (1 976) (with G. Appeltauer)
1 1 3 Further electrophoretic studies on proteins of neuronal origins in skeletal
muscle (1 977) (with Gustavo S. L. Appeltauer)
1 1 8 Axonal migration of some particle-bound proteins in the hypoglossal nerve
and their failure to enter the styloglossus muscle (1 978) (with Gustavo
Appletauer)
IV. Interprtation of research findings
120 The neural basis of the osteopathic lesion ( 1947)
128 The emerging concept of the osteopathic lesion ( 1948)
The three fundamental problems in osteopathic research (195 1)
14 The concept of facilitation and its origins ( 1955)
1 Clinical significance of thelacilitated state (1955)
158 Osteopathic research: Why, what. whither? (1957)
169 What "osteopathy" and "the osteopathic concept" mean to me (1962)
170 The sympathetic nervous system as mediator between the somatic and
supportive process (1970)
75 Vulnerability of the segmental nervous system to somatic insults ( 1970)
178 The segmental nervous system as a mediator and organizer of disease
processes ( 1970)
The trophic functions of nerves and their mechanisms ( 1972)
188 The facilitated segment: A factor in injury to the body framework ( 1973)
19 Andrew Taylor Still Memorial Lecture: Research and practice -a century
later (1974)
196 Neurochemical and neurotrophic consequences of nerve deformation:
Clinical implications in relation to spinal manipulation ( 1975)
20 Proprioceptors and somatic dysfunction ( 1975)
0 The spinal cord as organizer of disease processes; Some preliminary
perspectives ( 1976)
214 The spinal cord as organizer of disease processes: The peripheral autonomic
nervous system ( 1979)
V. Osteopathic principles, practice and profession
224 The somatic approach to the disease process ( 1951)
228 The function of the osteopathic profession: A matter for decision ( 1959)
2 An allegory: A forgotten episode in American transportation history
( 1961)
244 Osteopathy and medical evolution ( 1962)
254 Some thoughts on an osteopathic curriculum ( 1975)
Editor's foreword
This is 1 979, and this year Dr. Irvin
M. Korr celebrates his seventieth
birthday. It would have been easy to
find people to contribute their works
to a Festschrit (or Dr. Korr; his
influence and friendships are wide,
both inside and outside the osteo
pathic profession. However, the pub
lications committee of the American
Academy of Osteopathy has done a
wiser thing: It has proposed collecting
Dr. Korr's widely scattered writings
into a single volume, for use and
study by everyone, limiting the birth
day tributes to three short introduc
tory essays.
Even the choice of who shQuld
write the birthday essays could have
been a problem; but again the Acade
my was fortunate. At Texas College
of Osteopathic Medicine, where Dr.
Korr is professor of medical educa
tion, a project was under way to pro
duce a kind of "tribute and inter
pretation" booklet in his honor.
When the TCOM editors heard about
the Academy project, they graciously
agreed to merge their writings with
ours. So, the hard choices were al
ready made.
As it appears, this is a thick book,
but it could have been thicker. Dr.
Korr speaks self-deprecatingly about
how he has "cluttered up the litera
ture," and he calls the task of reading
some of his earlier works "an exercise
in osteopathic archaeology. " Never
theless, when the publications com
mittee discussed what might be left
out, they found themselves praising
the older papers as ofen as the newer
ones. In the end it was Dr. Korr him
self who proposed lopping off the
first 21 items of his bibliography,
representing the work done before he
joined the faculty of Kirksville
College of Osteopathic Medicine in
1 945. Several other items could be
deleted because they duplicated in
some manner material already in
cluded under another heading.
Sections are included from three
published books, all of which are i n
print as of this date; the reader might
be helped in these instances by look
ing at the context in which the essays
originally were set. Everything else
comes either from periodical litera
ture or unpublished sources. The first
two papers in a new series, under the
general title of "The Spinal Cord as
Organizer of Disease Processes,"
appear in this volume, the second
almost at the same time as it is
published in JAOA. It would have
been ideal to have the complete series,
but the two do stand alone -and the
others are not yet written, Dr. Korr's
literary work is very much alive and
well.
One whole aspect of Dr. Korr's
personality had to be omitted for
sheer lack of space. This is repre
sented by writings he calls whimsey,
and they include such sober topics as
nephrotrichosis, fetal suicide, and the
direct conversion of plant protein
into animal protein. The latter topic,
which we are assured is fit only for
the Joural of Irreproducible Results.
evidently has neurotrophic aspects;
there is a subtitle relating to the im
plantation and innervation of an ear
of corn. One suspects, knowing Dr.
Korr, that one should not pursue the
mechanism of this scientifc process
too closely, at least in mixed com
pany.
Let us instead deal with more seri
ous scientific matters. After the
introductory papers, the material
divides neatly into primary research
reports, the interpretation of research
findings, and papers on osteopathic
practice and the osteopathic prQfes
sion. Papers in each section are
arranged chronologically, with the
research reports divided into two
parts. The first contains studies on
electromyography, the sympathetic
nervous system, reflexes, and related
topics. The second includes studies on
axonal transport and the trophic
functions of nerves.
Dr. Korr, from his earliest associa
tion with the profession, ha taken
pains to interpret his studies in a
clinical context, which doubtless is
one of the reasons for his broad and
lasting influence in a patient-oriented
profession. In this connection, Dr.
Korr has provided for this book an
introduction to his own writings,
placing them in context with his
carer. It would be superfuous to say
more about them here.
What should be said. however, i s
that the Academy counts it a privilege
to honor Dr. Korr on the occasion of
his seventieth birthday. The editor is
both professionally and personally
grateful to him for the effort and
cooperation that made this volume
possible.
BA PETERN
5
Acknowledgments
Particular thanks are due Dr. Korr.
for providin materials and com
ments that proved invaluable in the
choice and arragement of materias
for this volume.
Appreciation also is expressed to
Martha I. Drew, Ph.D., director of
the American Academy of Osteop
athy, and to Barbara J. Wood,
assistant to the director, who par
ticipate heavily in the production of
this book.
Members of the publications com
mittee of the American Academy
of Osteopathy who participated
directly in the planning of this
book included: Sara E. Sutton,
D.O., FAAO, chairman; Viola M.
Frymann, D.O., FAAU; John P.
Goodridge, D.O., FAAO; William
L. Johnston, D.O., FAAO; David A.
Patriquin, D.O., FAAO; and Donald
Siehl, D.O., FAAO.
Special thanks go to those who
contributed introductory essays and
whose names appear in connection
with them, and to the co-authors and
publishers of materials included in
this book. Individual references at
the end of each paper identify exact
sources. Following is a list of jour
nals, institutions and organizations
whose materials have been included
herein.
Acta Neurovegetativa
American Association for the Ad
vancement of Science (Science)
American Osteopathic Association
(JAOA, THE D.O . The Forum oj
Osteopathy. Health. Osteopathic
Magazine)
American Physiological Society
(The Americn Joural oj Physi
olog, Joural oj Applied Phys
iolog)
Electroencephalography and Cln
ical Neurophysiolog. Elsevier-North
Holland Biomedical Press
Epermental Neurology
Federation of American Societies
for Exprimental Biology (Federation
Pocedings)
Kirksville College of Osteopathic
Medicine (Journal oj Osteopathy)
Osteopthic Annal, Insight Pub
lishing Company
Plenum Publishing Corporation
The Postgraduate Institute of
Osteopathic Medicine and Surgery
(The Physiological Bai oj Osteo
pathic Medicine)
6 Introductory essays
Preface
My "osteopathic" career began with
my appointment to the Kirksville
faculty in December 1945. At a na
tional convention of the American
Osteopathic Association seven or
eight years later, I was introduced to
a delegate who, on recognizing my
name, said (I think with a smile),
"Oh yes, you're the fellow who keeps
cluttering up our literature." The
litter to which he referred has con
tinued to accumulate in the quarter
century that followed, to the point
that it now seems part of the osteo
pathic landscape. Though blown and
kicked around, it does not seem to get
lost, only more scattered. I am deeply
grateful, therefore, to the American
Academy of Osteopathy for under
taking to tidy up the mess and to tie it
up in one neat, disposable bundle -
and especially for thinking the job
worth doing. Special appreciation is
due Barbara Peterson for wielding
the editorial broom and dustpan so
skillfully.
How did a non-D.O. , a Ph.D. in
physiology, come to fill the pages of
the osteopathic journals with so many
words - quite aside from those he
sent to research journals? (And
perhaps even more perplexing, why
were so many of them read?) In retro
spect, it seems that a pattern became
set with my very first osteopathic
publication. The article was -
pretentiously and naively - entitled,
"The Neural Basis of the Osteopathic
Lesion," as though it were a final
statement I
That paper began as a personal ex
ercise in verbalizing to mysel the
exciting new insights that came out of
my reading of Sted Denslow's earlier
research reports in the Joural oj
Neurophysiology and elsewhere on
segmental motor reflex thresholds,
out of our first joint research effort
(reported in the American Joural oJ
Physiolog in 1947, actually my first
venture into the field of neurophysi
ology) and out of my beginning
studies of segmental variations in
sympathetic activity in humans.
It was, originally, only my intent to
summarize for myself my under
standing of the meaning and possible
implications of the concept of chronic
segmental facilitation. This concept
had already emerged from Sted's ear
lier studies and was reinforced and
further elaborated by our subsequent
investigations. However, on invita
tion from one of the session chair
men, I hesitantly presented my
summary and speculations at the
annual convention of the American
Osteopathic Association in July 1947.
The cordial response of those present
moved me to consider making my
thoughts available to all D.O.'s who
might find something of interest in
them. The paper was prepared for
publication and submitted to Te
Joural oj the American Osteopathic
Association, where it appeared in
December 1947.
The response was amazing, and it
continued for years. Practicing D.O.s
apparently found in it a ratiomiza
tion of their clinical observations
and a plausible explanation of the
ways in which the "osteopathic
lesion" was hazardous to one's
health. It seemed to reinforce their
convictions about the value of osteo
pathic manipulation. As a matter of
fact, I am told that the article is still
required or recommended reading in
at least some colleges of osteopathic
medicine, a practice I am inclined to
view as an exercise in osteopathic
archeology (much as it pleases me).
With this encouragement (I didn't
seem to need much) it became my
practice, from time to time, to report
in publications to the osteopathic
profession on our research, sum
marizing our objectives, our findings,
our views on possible clinical sig
nificance, together with additional
questions for further exploration and
testing in the laboratory or in clinical
practice. These papers are grouped in
Section IV, " Interpretation of re
search findings." They have been
based on research reports previously
or subsequently published in research
journals and presented at scientific
meetings. These, the "Primary re
search reports," are assembled in
Sections II and III.
With my growing grasp of the
meaning of Lhe osteopathic princi
ples, thanks to my colleagues at the
college and the many friends I was
finding in the profession, it began to
become evident to me that physio
logical processes and their distur
bances in the individual human could
be fully understood only in the con
text, not only of human life, but in
the specific context of that person's
total life and his or her total physical
and sociocultural environment, past
and present. The abstract generaliza
tions usually taught in the classroom,
expressed in such terms as the heart.
the renal circulation, the digestive
system. etc.. were indeed abstrac
tions, and they no longer suffced.
As I came to understand more and
more that all physiological processes
were conditioned by the circumstances
of the individual life of which they
were components, the science of
physiology began, for me, to burst
out of its traditional boundaries in all
directions. My studies, outside of the
laboratory. took me into the contigu
ous areas of the behavioral sciences,
social sciences, anthropology. epi
demiology. comparative health care
systems, economics and even the
arts. I began to discern unfortunate
trends and emerging critical needs
and problems in American health
which American medicine (including
osteopathic medicine) was not, gen
erally speaking, recognizing, con
fronting or preparing for. This led me
to try to "teach" the osteopathic
profession its business by presuming
to point out what I regarded as his
toric opportunities for which its f
philosophy and methods uniquely
prepared it. The 1951 paper, "The
somatic approach to the disease
process," was perhaps the first of this
genre. With succeeding papers, the
tone became more urgent, exhortative
and strident, culminating in the
period 1959-62 (the period of the
"California crisis"), in polemic
("The function of the osteopathic
profession" [ 195 1] and "Osteopathy
and medical evolution," [ 1962J) and
even acerbic satire ("An Allegory,"
[ 1961] ).
Following the California debacle, I
withdrew, defeated. from this arena,
and abandoned (for a while) my self
appointed role as pointer of direc
tions and shouter of "Excelsior."
Returning to the ivory tower, I
turned to the completion of reports
on earlier research with my late
colleagues, Price E. Thomas and
Harry M. Wright, and then to new
areas of research on the trophic
functions of nerves with Paul N.
Wilkinson and Gustavo Appeltauer,
both of whom are also deceased.
In 1973 came the invitation to
return to the "arena" through the
annual A.T. Still Memorial Lecture
at the annual convention of the AOA
7
in New Orleans. By this time, how
ever, some maturing had taken place,
and I had beome convinced that a
quiet display of the evidence on a
bed of swet reasoning was in order,
rather than raucous efforts at persua
sion. I think the change of tone is
evident in the lecture (though it
disappointed many who preferred my
fervent evangelism). I had become
convinc, also, that any efforts to
influence diretions of osteopathic
development would best be exerted
through the education of our doctors
to-be. This conviction is reflected in
a short article on curriculum pub
lishe in 1975 (and in my continued
efforts as professor of medical educa
tion at the Texa College of Osteo
pathic Medicine). This heterogeneous
group of articles through which I
sought, to put it briefy, to divert
osteopathic practice, policy and edu
cation from the pursuit of disease to
the putsuit of health, comprises Sec
tion V, "Osteopathic principles,
practice and profession." This sec
tion is related to a personal statement
of what the osteopathic concept
means to me, written in 1962 and pre
viously unpublished, which appears
on page 169. (Incidentally, I continue
to think that the osteopathic profes
sion is still passing up an historic
opportunity to fulfll its role as an
urgently needed reform movement in
American Meicine).
Impossible to include in this col
lection, except for excerpts in Section
II, is the book "The Neurobioiogic
Mechanisms in Manipulative Thera
py" which I edited with the expert
assistance of Mrs. Ethel Huntwork,
published in 1978 by Plenum Pub
lishing Corporation (and available
through the American Academy of
Osteopathy). That volume was the
product of an international work
shop, sponsored by Michigan State
University College of Osteopathic
Medicine, during my tenure there
as professor in the Department of
Biomechanics, and funded by the
National Institute of Neurological
and Communicative Disorders and
Stroke. It was my privilege to chair
the planning committee and the con
ference itself. From the viewpoint of
the osteopathic profession, perhaps
its main achievement has been to
establish manipulative therapy as a
valid and fertile area for fundamental
scientific investigation.
8
The period since 1945 has, for me,
been a great adventure which still
continues. I shall always be grateful
to my friends, J. S. Denslow, then
professor of osteopathic technique
and director of the Still Memorial Re
search Trust, and Morris Thompson,
then executive vice-president (and
soon-ta-be president) of the Kirksville
college, for having attracted me to
that adventure, as I stood, uncertain,
at a post-war fork in the road, and
for the many years of their support
and encouragement as my friends and
colleagues.
There are numerous others to
whom I am indebted for having made
the long adventure so rewarding:
Prince E. Thomas, D.O., and.
Harry M. Wright, D.O., who lef
their practices in 1949 and 1950, re
spectively, to join me in research and
in teaching, and who, through their
academic achievements, eventually
established themselves as profession
ally qualified physiologists. Trag
ically, their careers were cut short by
death due to cancer.
Elliott Lee Hix, Ph.D., who, in
1953, joined the Department of
Pharmacology (then under my ad
ministration), who also soon found
excitement in the new kinds of re
search questions that came out of
osteopathic theory and practice, and
who made fundamental contributions
to the pathophysiology of visceral
organs. He remains a close friend.
The late Paul N. Wilkinson. B.A .
whose skills in radioisotope tech
nology enabled us in 1966-67 to
demonstrate for the first time the
delivery of nerve-cell proteins to
muscle cells via the axons, as a
possible mechanism in the trophic
functions of nerves.
Gustavo S. L. Appeltauer. M.S.,
who came from Uruguay in 1967 to
join me in that research, and whose
skills made possible quantitative
analysis of the dynamics of axonal
delivery of protein to muscle and the
demonstration of four "wlwes" of
delivery, each carrying different
proteins. His promising career also
was interrupted by premature death.
Emil D. Blackorby,who came to
the College in 1951, whose superb
skills and inventiveness in electronics,
metal-working and virtually all
aspects of research-and-teaching
instrumentation were of inestimable
value. Without them, many of our
achievements both in teaching and in
research would not have been pos
sible. There seemed to be nothing
"Blacky" could not fix, and no de
vice he could not design and construct
to solve a technical problem.
Gertrude Krueger, my secretary
and colleague for more than 21 years.
and administrative assistant, librari
an, accountant, grant-manager and
friend to all of us in the conglomerate
known as the Division of Physiologi
cal Sciences, and especially the
Department of Physiology, where she
still continues her skilled and loyal
service.
All the technicians, student assis
tants and Fellows who joined us with
such dedication and skills in our
teaching and research programs.
All the students who responded so
magnificently to the learning oppor
tunities I offered them, and to the
many others who had good reason to
resent my exacting standards, but
who, eventually, found it in their
hearts to forgive me. It is their pro
fessional achievements that have
made my life as a teacher such a
rewarding one.
Especially noteworthy are two
former students, Ralph L. Willard,
D.O., and James R. Stookey, D.O.,
who (among others) achieved the ex
alted state of Deanship, and under
whom I was pleased to serve, frst at
KCOM and currently at TeOM.
All the members of the osteopathic
profession who have read my articles
with interest and who. further, have
taken the time to convey their com
ments and criticisms and to share
their insights and experience. Their
responses to my efforts and their con
tributions to my "osteopathic" edu
cation are deeply appreciated.
The osteopathic physicians who,
through the years, and at three col
leges, have given so generously of
their skills and time to help maintain
my health and vigor through regular
manipulative care: J. S. Denslow, the
late John A. Chace, George A.
Laughlin, William L. Johnston and
Marion E. Coy. I am convinced that
their care has been a critical factor in
my continued good health.
Finally, all the osteopathic editors
and their associates who, through the
pages they provided, so generously
met my need for self-expression.
IRVIN M. KORR, PH. D. , Sc.D.
Introductory essays
Biographical notes and
appreciation
Irvin M. Korr, Ph.D., began his
association with osteopathic medicine
in scientific research, and, through a
long and distinguished career, he has
become known as a major contribu
tor to the modern scientific under
standing of the profession's distinc
tive contribution to the field of
medicine. The impact of his work has
been felt in basic research areas and
in clinical medicine. But the impor
tance of Dr. Korr's career and his
writings goes beyond scientific re
search to embrace both teaching and
philosophy.
Both in the classroom and in areas
such as curriculum planning, he has
become renowned for his knowledge
and insight into the special problems
of osteopathic education. Further, he
has established himself, in writing
and at the lectern, as one of the most
articulate exponents 'of the profes
sion, the philosopher who brings to
the osteopathic concept a blend of
understanding, wisdom and enthusi
asm for his subject.
Dr. Korr was graduated from the
University of Pennsylvania with a
Bachelor of Arts degree in the biolog
ical sciences in 1930. and he was
awarded the Master of Arts degree
from that university in 1931. The win
ner of a fellowship in the biological
sciences at Princeton University. he
spent three years in graduate study
there and was granted the Ph. D. de
gree in 1935. An additional year at
Princeton was devoted to a postdoc
toral fellowship with special re
search in cellular physiology.
In the fall of 1936, Dr. Korr joined
the faculty of the Department of
Physiology at the New York Univer
sity College of Medicine. In addition
to teaching, he continued his investi
gations in the areas of cellular metab
olism and renal physiology and, with
members of the Department of Psy
chiatry, conducted research in the
field of insulin coma. These studies
were supported by the American
Philosophic Society, the Pletz
Foundation, the American Academy
of Arts and Sciences, and Warner
Institute for Therapeutic Research.
From 1942 to 1945, Dr. Korr was
engaged in research under the aus
pices of the War Department and the
Office of Scientific Research and
Development. His investigations in
aviation medicine, wound ballistics
and climatic physiology during this
period were conducted at Columbia
University College of Physicians and
Surgeons and at Princeton Universi
ty. Also during this time, he was ap
pointed senior physiologist at the
Fort Monmouth Signal Corps, where
he directed the Metabolic and Bio
chemical Laboratory of the Climatic
Research Unit.
Dr. Korr joined members of the os
teopathic profession in December
1945 when he accepted an appoint
ment to the faculty of the Kirksville
College of Osteopathic Medicine. The
appointment was for one year, and,
in his own words, Dr. Korr fully ex
pected to return to university teaching
after the year. One year lengthened
into thirty. "One thing led to
another," he has said, "and I just
couldn't leave. I'm glad I stayed. I
wouldn't have missed it for the
world."
During those thirty years, Dr. Korr
served as teacher, departmental and
divisional administrator, research in
vestigator, advisor and counselor to
students, interns, residents, faculty
and staff. In 1945, he was named pro
fessor and chairman of the Depart
ment of Physiology. From 19S2 to
1968, he also served as chairman of
the Division of Physiological Sci
ences, and in 1968 he was named Dis
tinguished Professor of Physiology.
From 1968 to 1975, he served as di
rector of the program in neurobi
ology.
In 1975, Dr. Korr ended his thirty
year association with the Kirksville
college to accept a long-standing invi
tation to join the faculty of Michigan
State University College of Osteo
pathic Medicine as professor of bio
mechanics. For the next two years,
his energies were mainly directed
toward the planning of an intera
tional research workshop on HNeuro
biologic Mechanisms in Manipulative
Therapy," which was held in October
1977. The proceedings of this work
shop, edited and with a preface by
Dr. Korr, were published by Plenum
Publishing Corporation in 1978.
In the fall of 1978, lured by the op
portunity to participate in the devel
opment of a new college, Dr. Korr
left Michigan to join the faculty of
North Texas State University Health
Sciences Center/Texas College of Os
teopathic Medicine. In addition to a
chance to work with a college which
he describes as still experimental and
still willing to make mistakes am
learn from them, the appointment as
professor of medical education at
NTSU/TCOM offered Dr. Korr an
opportunity to be surrounded by
former students. Some forty of his
former students and associates serve
on the faculty and administration of
the Texas college.
Dr. Korr is a member of the Ameri
can Physiological Society, the Society
for Experimental Biology and Medi
cine, the American Association of
University Professors, Sigma Xi, the
American Institute of Biological Sci
ences, the Society of Neurosciences,
and the American Society for Neuro
chemistry. He is a Fellow in the
American Association for the Ad
vancement of Science, a Life Member
in the Harvey Society, an Honorary
Life Member of the American Acad
emy of Osteopathy and an Honor
ary Member of Psi Sigma Alpha and
Sigma Sigma Phi, honorary scholas
tic fraternities. He is listed in Ameri
can Men 0/ Science and World Who's
Who in Scienc, and is the recipient
of an honorary Doctor of Science
degree and a Living Endowment
award from the Kirksville College of
Osteopathic Medicine.
The fact that his most recent ap
pointment is in the feld of medical
eucation rather than basic science
research is signifcant of his reputa
tion as a teacher. Dr. Korr is noted
for his perception of the interaction
between student and teacher and for a
recognition of the burden of responsi
bility on faculty. Former students cite
his commitment to students and his
ability to defne and describe clearly
the holistic osteopathic concept in
terms of modern scientific knowl
edge. In published writings on educa
tion, Dr. Korr emphasizes his com
mitment to maintaining the osteo
pathic principle and idea by stressing
the importance of integrating the
holistic concept into all areas of
teaching.
The same enthusiasm for the osteo
pathic concept that characterizes his
approach to teaching is evident in Dr.
Korr's extensive career as a lecturer.
He has spoken before such scientific
societies as the American Physio
logical Society and the Society for
10
Neuroscience, before a majority of
the osteopathic divisional societies,
and at seminars at various universities
across the country. Lecture invita
tions have taken him twice to En
gland, where he conducted postgrad
uate courses at the British School of
Osteopathy. , and to Australia, where
he spoke at the Lincoln Institute of
Health Sciences in Melbourne, In
1948 and again in 1959, he was the
keynote speaker at the Annual Con
vention and Scientific Seminar of the
American Osteopathic Association.
In 1967 he was asked to give the Scott
Memorial Lecture at the Kirksville
College of Osteopathic Medicine, and
in 1973 he was honored by being ask-.
ed to deliver the Andrew Taylor Still
Memorial Lecture at the Annual Con
vention of the American Osteopathic
Association. In 1975, he presented
the Louisa Burns Memorial Lecture
at the 19th Annual Research Con
ference of the American Osteopathic
Association.
Dr. Korr's published writings in
clude nearly 10 articles in scientifc
journals and abroad. and. they range
from reports of research to essays
on the philosophy of medicine.
Unknown to some, his writing has
branched out to include such philo
sophical pieces as an allegory which
compares osteopathic medicine to a
railroad transportation system. His
short piece, "What 'Osteopathy' and
'The Osteopathic Concept' Mean To
Me" has become a classic.
With the publication of this collec
tion of Dr. Korr's works, not only
will his scientific research be readily
available to the osteopathic profes
sion and the scientific community,
but equally the wit and wisdom of his
educational and philosophical writ
ings on medicine will be easiy accessi
ble to the many who are his friends.
colleagues and former students.
JUY ATER, PH.D.
Introductory essays
Scientific contributions
of I.M. Korr
The evolution of any discipline de
pends upon both the accumulation of
knowledge and the interpretation of
that knowledge within the framework
of the discipline. Without these two
elements providing impetus for both
growth and redefnition of its struc
ture, an area of endeavor soon be
comes obsolete. Medical history is
replete with examples of schools of
thought which have passed from exis
tence due to stagnation of thought,
leading to noncompetitiveness with
more dynamic and growing areas.
The works of I.M. Korr reprinted
in this book represent efforts over the
span of almost 35 years both to accu
mulate knowledge and to interpret it
in the context of osteopathic thought.
In so doing, Korr has also inevitably
altered the very framework of that
thought. The amount and effect of
these alterations can never be
measured accurately, although their
results will be felt for the foreseeable
future.
In this brief overview and introduc
tion, I would like to put Korr's basic
writings into historical context, then
provide some evaluation of the data
and interpretations in light of current
research and theory. This task is at
once humbling and necessarily impos
sible to complete: humbling because
Korr is first a personal mentor and
second a colleague; and impossible to
complete because he is still active in
both gathering data and providing in
terpretations. However, it is hoped
that the perspectives will be helpful.
"Kim" Korr frst joined the faculty
at the Kirksville College of Osteop
athy and Surgery in 1 945, having
already established himself as a well
known scholar in various areas of
physiology. At that time, J.S. Den
slow's work on electromyographic
correlates of palpatory findings and
the "osteopathic lesion" was well
under way. Fascinated by both the os
teopathic theory of structure-func
tion relationships and integration of
function, and by the pioneering work
in Denslow's laboratory, Korr began
an interest which has absorbed much
of his subsequent career: the relation
ships between visceral and skeletal
components of the body.
Collaborating closely with Den
slow, Korr offered interpretations of
the data being accumulated. The re
search group was soon expanded with
the addition of Price E. Thomas,
D.O., in 1 949, Harry M. Wright,
D.O. , in 1 950, and Elliott L. Hix,
Ph.D., in 1 953. This group comprised
the nucleus of research personnel
which remained active for many
years, as the papers reprinted here
show. Others were also essential to
the research, including Emil Black
orby. or "Blackie" as he is still affec
tionately known to hundreds of stu
dents and faculty, whose skill in
equipment design and construction
enabled the research to continpe, as
well as the Chornocks, Eble, Chace
and many others. Important in this
perspective is the fact that Korr was
heavily involved in enticing most of
this innovative and dedicated group
to Kirksville during the formative
stages of modern osteopathic re
search and theory building.
With the passing of years, this
group made many contributions to
current osteopathic thought, and, as
the papers presented here testify,
Korr's leadership was evident and
pervasive. The research thrust of the
group lost momentum in t he
mid-1 960s, and Korr turned t o what
was to be his major research contri
bution to modern neurophysiology:
investigations of the mechanisms
underlying trophic functions of
nerves. Gustavo Appeltauer joined
Korr in 1 967 for this major research
endeavor. In 1 974, Korr lef Kirks
ville for the Michigan State College of
Osteopathic Medicine and at the same
time left active laboratory research.
He has since been involved in redefin
ing some of his earlier interpretations
and in pursuing the implications of
one of his major interests, the role of
the autonomic nervous system in total
physiological function. This activity
has continued with his recent move to
the Texas College of Osteopathic
Medicine.
The direction and weight of Korr's
contributions to osteopathic theory
and research were manifest soon after
his arrival at Kirksville. Two papers
in 1 947, one with Denslow and
Krems, were both germinal contribu
tions setting the stage for the next 1 5
years of work.
The fi r s t paper cont i nued
Denslow's classic research on elec-
tromyographic correlates of palpa
tory findings and extended the results
to provide clear definitions of the
characteristics of abnormal skeletal
muscle activity which was often
found in areas of osteopathic lesion.
There were also speculations about
possible causes and maintaining in
fluences for the objectively observed
abnormal activity.
The second paper, "The neural
basis of the osteopathic lesion," is
one of the most important of Korr's
works in the profession. Here, he put
forth the ideas of the "neurological
lens" and the "facilitated segment."
This major theory of regional excita
tion of the spinal cord serving as an
abnormal area of overactivity. being
driven by both external and interal
sources of stimulation and focusing
this activity into abnormal patterns of
skeletal and visceral activity, was a
conceptual breakthrough. Research
in many areas of central nervous
system activity today is reporting
mechanisms which could serve as
activating and maintaining forces for
t
he effects observed and speculated
on in these early papers. It is now evi
dent that localized hyperactivity in
the spinal cord may be a primitive
form of pattern learning in the spinal
reflex arcs. It is perhaps unfortunate
that the term "facilitated segment"
was used, as it implied a circum
scribed area of abnormal activity
associated with vertebral structure,
an interpretation not strictly intended
in the original formulations.
From these first papers flowed re
search and theories over the next 1 7
years, from 1 948 through 1 96'. The
major impact of this work was the ex
plicit demonstration, through various
means of the existence of abnormal
activity patterns within the auto
nomic nervous system in apparently
normal as well as diseased humans,
and the correlation of some abnormal
autonomic patterns with musculo
skeletal abnormalities. Throughout
this period, Korr wrote on the inter
actions which to him were evident
between the autonomic and skeletal
portions of the nervous system, the
implications of abnormal autonomic
activity for health and disease, and
the long term effects of overactiva
tion of any portion of the nervous
system on innervated structures. Un
fortunately, the concept of close in
teraction between skeletal and auto-
11
nomic nervous systems was not gener
ally accepted in neurophysiology and
certainly not in medicine, and is only
now beginning to be recognized.
Thus, while the concept. of spinal
"facilitation" was evident in the
studies he did and supervised, the
basic neurophysiological data show
ing the actual existence of reflex
pathways subserving Korr's argu
ments was lacking. More recently.
work in various laboratories (see, e.g.
Satol) is demonstrating the neural
paths through which the interactions
seen by Korr clinically and experi
mentally between skeletal and visceral
structures are mediated. It should be
noted that some of Hix's work (e.g.l)
demonstrated in animals very tight
skeletal-autonomic interactions much
earlier. However, while evidence for
the interactions long stressed by Korr
and his colleagues is mounting, it is
still too soon to see a general accep
tance by either the medical or scien
tific community of the widespread
importance of such interactions for
health and disease.
Early in the 1960s, the research ac
tivity of the original group Korr had
recruited began to diminish and Korr
bgan to actively follow his long
standing interest in the question of
special effects of nerves on innervated
organs. Long standing in the field of
neurophysiology was the belief that
the only effect of nerves on their tar
get organs was the release of trans
mitter substance to excite the organ
to activity. However, much evidence,
such as the complete degeneration of
muscle following denervation as op
posed to the atrophy of disuse if only
nerve impulse tramc was interrupted,
argues for some other "trophic" ef
fet, or sustaining infuence, of
nerves upon their target organs.
Using specially developed techniques
ind procedures, Korr found strong
evidence for the delivery of protein
substances trans synaptically from the
hypoglossal nerve to tongue muscle
fbers. This work, published in
Scienc in 1967, was the first evidence
that nerves continuously provide
substances other than transmitters to
the organs they innervate. While
practically heretical, the notion of
transsynaptic protein transfer opened
new vistas of thought about neural
regulation of physiologic process and
of disease mechanisms. In several
papers since, Korr and Appeltauer
12
provi ded other data on the
phenomenon and began characteriza
tion of the proteins involved. Ap
peltauer's recent untimely death left
the research incomplete. However,
there now exists a growing body of
evidence not only for the passage of
proteins from nerve to innervated
organ, but also in the reverse direc
tion (e.g.3). Investigators in other
laboratories are close to characteriz
ing some of the actual proteins which
are passed to muscle by its nerve sup
ply (e.g. 4).
While the studies and theoretical
arguments which led to Korr's find
ing of transsynaptic protein transport
are only now beginning to be ac-. .
cepted, this finding is certainly the
most dramatic and important of his
career. The implications of such slow,
two-way communication between the
nervous system and innervated or
gans are both vast and seem hard to
overestimate, literally opening the
way for a revolution in thought about
neural control and feedback systems
of physiological process. It is still not
known whether the transsynaptic pro
tein delivery is a general phenomenon
in the body, or what all the effects
are, but certainly the pioneering work
done by Korr in the area will be rec
ognized as leading the way to one of
the great advances in our knowl
edge of physiological control. .
Over the past several years since he
has left active laboratory research,
Korr has been formulating concepts
of the function and control of the
autonomic nervous system. His re
cent paper, "Sustained Sympathico
tonia as a Factor in Disease" l which
appeared in 1978, is an attempt to in
tegrate a vast amount of data about
the effects of the autonomic nervous
system on total physiological func
tion. This work, together with the
proprioceptive theories he has re
cently propounded in an attempt to
explain some of the effects of manip
ulative therapy, characterizes Korr's
ongoing interpretation of data within
the framework of osteopathy.
The perspectives and evaluations
given here indicate the breadth of
Korr's efforts. Viewed from the van
tage point of today's science, it is ap
parent that much of his data up to the
mid-l960s has yet to be critically
evaluated and replicated, but stanq as
a guide for future research. The inter
pretations and theories flowing
p
from
that work have markedly infuenced
osteopathic thought and are rich in
material for further work. as well as
ripe for reevaluation in the light of
new findings and interpretations of
physiologic process. The work on
trophic function is only beginning to
be recognized and will stand as classic
in both concept and importance.
Whether the bulk of his earlier work
remains acceptable as theory or ex
planation after reexamination is,
however, not the important point. Of
paramount importance is that Korr
has provided the profession and the
scientific community with a basis for
discussion and a forum for continued
interpretation of the tenets of os
teopathic philosophy. To continue to
reexamine and build upon what he
has provided is the only fitting and
proper method of utilizing this rich
legacy.
References
1. Sato, A., The somatosympathetic refexes: Their
physiologcal and clinical significance. In The
Reserch Statu oj Spinal Manipulative Meicie.
Goldstein, M. (Ed.) National Institutes of Communi
cative Disorders and Stroke Monograph IS, 163-172,
1975.
2. Hix, E.L. Refex communiction between skin
and kidney a infuenced by an active viscera-renal
refex. Federtion Pe ings, 18, 69, 1959.
3. Thonen, H., Schwab, M. and Barde. Y-A.,
Transfer of information from effetor orgns to inner
vating neurons by retrograde aonal transport of
.nacromolecules. In The Neurbiologic Melnims
in Maniulative Thertp). Korr, l.M. (Ed.), Plenum;
New York, 311-332, 1978.
4. Markelonis, G.J. and Oh, T.H. A protein frac
lion from pripheral nerve having neurotrophic ef
fects on skeletal muscle cells in culture. Exrimental
Nerbiolog, 58. 285-289, 1978.
S. Korr, l.M. Sustained sympatheticotonia as a fac
tor in disese. In Tie Neurobiologic Melnim in
Manipulative Tlerpy. Korr, 10M. (Ed.), Plenum;
New York, 229-26, 1978.
MICHAEL M. PATERSN, PH.D.
Introductory essays
Clinical contributions of
I.M. Korr
When one contemplates the impact
I. M. Korr has had on osteopathic
thinking in the clinical realm, one
must be amazed and realize how
many skills and talents were required.
To appreciate his clinical contribu
tion, we must have some appreciation
of the man.
During the early 1 940s, Dr. Korr
was encouraged to join the research
group at Kirksville College of
Osteopathy and Surgery as it de
veloped under the guidance of J. S.
Denslow, D.O. In late 1944, after a
promising career in the aca
d
emic
arena and in military research during
World War I I , Dr. Korr was again
approached by Dr. Denslow and by
Morris Thompson, then president of
the Kirksville college. On the en
couragement of officials of the
Rockefeller Foundation, Dr. Korr
considered the challenge and decided
to join the Kirksville group.
In a manner consistent with his
reputation as a quality scientist with
an uninhibited mind, Dr. Korr dedi
cated himself to a pursuit of neuro
physiology and an all-out effort to
assist the developing research pro
gram at Kirksville.
In 1947, Dr. Korr was asked to
address the teaching group of os
teopathic principles, diagnosis, and
therapeutics at the AOA convention
in Chicago. His topic was the neural
basis of the osteopathic lesion, and
his purpose was to "attempt a char
acterization of the ostopathic lesion
in terms of basic neural mecha
nisms. " Thus he started a process he
continued throughout his career, that
of trying to make clinical applications
for the profession in relation to what
he was learning in his research en
deavors.
As a result of that presentation, the
profession started to contemplate the
concepts of afferent bombardment of
the central nervous system, facili
tation, and the role that the cerebral
cortex, postural equilibrium centers,
bulbar centers, cutaneous receptors,
and others can have on the develop
ment and maintenance of a hyperir
ritable state of the central nervous
system. Dr. Korr speculated, at that
time, about the role the facilitated
state could have not only on seg-
mentally related organs, but also on
the autonomic nervous system. Thus
the concept of the neurological lens
began to be discussed and appreciated
by the profession. The role which the
proprioceptors might play in the
development of the facilitated region
was also postulated at that early stage
of his career.
In that 1 947 lecture Korr also
warned that "the articular derange
ment or the osteopathic lesion cannot
be conceived as the cause of disease;
rather it is one of many factors
simultaneously operating. " He went
on to describe the phenomenon as "a
sensitizing factor, a predisposing
factor, a localizi ng factor, a
channelizing factor. . . . To treat
only the structural source of
bombardment is only to half-treat
and to neglect a most important part
of the lesion mechanism, and to take
the lesion out of context. This does
not mean, of course, that every os
teopathic physician should become a
psychiatrist, but he certainly must
take into consideration the home
factors, environmental factors, fami
ly relations, emotional adjustments,
tensions, etc." Thus at that early date
both the preventive and holistic po
tentials were envisioned.
A year later, Korr expressed to
another group his conviction that
"The attainments of the osteopathic
profession have been possible only
because the profession is founded
upon the solid rock of basic truth."
In that same speech he also said,
"Whether - and how - the pro
fession meets [its] challenge will
determine the future of the os
teopathic profession, but not the
survival of the osteopathic concept;
that seems determined. Good ideas
never die; society eventually makes
places of honor for them."
During the years 1948 to 1 950, the
Kirksville group . investigated the
impact which facilitation has on the
autonomic nervous system and on
organs innervated and affected by the
areas of facilitation. In 195 1 Korr
wrote, "We have come to recognize
that the osteopathic lesion as a
phenomenon of central facilitation is
a most important predisposing, local
izing, and probability-increasing
factor in disease. "
The next year he described oste
opathy as "not merely a form of
therapy but rather a broad philoso-
13
phy, a guide for thinking and acting
in relation to questions of health and
disease." He continued, "From the
diagnostic viewpoint the somatic
component has great strategic sig
nificance because it makes possible
the detection and evaluation of H
disease process far in advance of the
emergence of symptoms."
Thus in a few short years, the pro
fession had gained a dynamic spokes
man who had a deep understanding
and appreciation of osteopathic con
cepts and a vision of the profession's
potential. At this time in his career,
Korr understood that we have the
potential to recognize, by skilled
osteopathic evaluation, the loss of
health which occurs far earlier than
early disease detection.
One must remember that as the po
litical component of the profession
was trying to prove to society that we
were like M.D.s, Korr's was a voice
crying in the wilderness and encour
aging the profession to realize its
potential and not stop at the level of
allopathic acceptance and care.
At the 1956 AOA convention, Korr
called for a serious research effort by
the profession, and said "through the
collaboration of osteopathic physi
cians and scientists, the principles
which guide osteopathic practice
must be transformed into a body of
working hypotheses to guide osteo
pathic research." Thus again we see
a desire to develop a clinically sig
nificant osteopathic research pro
gram.
In one of the years immediately
preceding the M.D.-D.O. merger in
California, Korr was the keynote
speaker at the AOA convention, and
he took the profession to task. He
charged the profession with the
attitude that approval has become an
end in itself, that being is more
important than becoming. The pro
fession's function was envisioned by
Korr a the "continual examination
and reexamination of all the issues
and elements that determine your
obligations to society and the paths to
their fulfillment." He went on to say
in that 1959 address, "[Osteopathic
manipulation] is not just another
form of therapy; it is a whole strate
gy, a whole approach in itself. It is
not merely a treatment of 'lesions'; in
effect, it is the putting of influences
into the whole man through the acces
sible tissues of the body, influences
14
which deflect his life processes to
more favorable paths, and which help
put the man in better command of his
situation, whatever it is, whatever it
may become, whatever his illness,
and whatever its etiology." This non
clinician grasped the role osteopathic
care could play in enabling patients to
realize their health potential.
His depth of understanding of os
teopathic concepts and the profes
sion's political actions set the stage
for Korr to write his masterpiece en
titled "An Allegory." It is a piece of
literature which should be seriously
studied and contemplated by the pro
fession. Its message is as relevant
today as when written in 1961 , in the
midst of the California merger.
4 B
~
B . .
6..
Z3 Z
N N
7 N
N N
N N
N N
N N
3 SEGMENTS INVOLVED
4Z. 6".N
y
3B. 3 z.1-5-N
ZU.
IZ.
17.
Z.
v
4
:
"
4
-
N
~"
I'
34-N
N
N
N
N
N
7
mp. T
4
No.
4 SEGMENTS INVOLVED
3.
ZZ.
28.
3B.
Zb-
3Z.
38.
Fig. 1. All 30 experiments are diagrammed and aranged according to patter. The bold type
numeral under each segment represents the "sel-threshold" (dicused in part I) in kilogram for
that segment, e.g. , the pressure on the spinous proces ofT. required to elicit electricaly detectable
activity in the erector spinae mass at T + The arrows indicate the incidence and direction ofspread
between all possible pairs of segments. The number on each arrow indicates the presure applied to
the spinous process of the segment from which the arrow originates, in order to initiate activity in
the segment to which the arow points. The absence of an arrow in one direction or the other be
tween a given pair of segments indicates that evidence of spread was not obtained within the 7 kgm.
range ofthe pressure meter. Thus, between a given pai ofsegments, dependent upon factors which
are eamined in subsequent sections, there may be no spread, one-way spread, or two-way spread.
I
ties, head, and at times the lower
extremities, or to calm the restless
or apprehensive subject, in order to
eliminate rest activity.
In our series four experiments had
to be terminated because of persistent
rest activity at one or more segments.
Each of the four subjects at another
time served in a successful experiment
in which rest activity was eliminated.
In all cases the persistent rest activity
was found at L or M segments. One
of the subjects, during the unsuc
cessful experiment, was perturbed by
illness of his child; one was much
more apprehensive than the average
subject, and two walked with a limp,
due to poliomyelitis in one and an old
injury in the other.
Occasionally, one or more units in
an L segment fired during inspiration
or expiration. Usually this intermit
tent activity was not long lasting and
could be eliminated by the same
measures which were effective on
ordinary rest activity.
Apparent "rest activity" was only
very rarely encountered at H or N
segments, and was always easily
abolished by correction of some posi
tional stress.
Thus, low threshold segments are
apparently hyper-excitable, not only
to pressure stimuli applied to the cor
responding spinous process, but also,
to impulses reaching them from
higher centers and from propriocep
tors.
Part II.
In part I, observations have been
presented concerning the response of
segments of the erector spinae muscle
to pressure stimuli applied to corre
sponding spinous processes. In this
section observations are reported on
the responses in muscle segments to
stimulation of remote spinous pro
cesses, Le., on observations of ir
radiation or intersegmental spread of
excitation.
Spread Patterns.
Incidence and distribution of spread
among the four segments fell into five
distinct patterns or groups (fg. I).
1. Order oj spread. There is a
definite order to the frequency with
which the different arrows appeared
in the series of 30 experiments. We
consider that these frequencies are an
index of 1 , the probability of spread
in a given direction between a given
T4 T6 T8 TIO
II 0 ( 0 0 NO SPREAD
2) oo 0 0 2 SEGMENTS INVOLVED
3) 0 3 SEGMENTS INVOLVED
4) OO 0
SEGMNTS INVOVED
5)
6) OO
COPETE RECIPROCITY
+
Fig. 2. Progresion ofspread. For explanation
see text. The number on each arrow indicates
the number of times that spread occured in
that direction betwen that pair ofsegments in
the 30 experiments diagrmmed in figure 1.
pair, and 2, the order in which spread
tends to appear in the progression
toward "complete reciprocity"
among the 4 segments. This progres
sion and the frequencies are shown in
figure 2.
2. Segmental level. The upper 2
segments participate in spread with
significantly greater frequency than
the lower two. The number of arrows
(figs. I, 2) to and from each segment
were as follows:
T4-88; T6 92; T,-69; Tlo 47
It will be noted (fig. 1) that when
only 2 segments are involved in
spread they are invariably the upper
two (T4 and T6); when only 3 are in
volved, they are the upper 3.
3. Segmemal threshold. Frequency
of spread to and from a given seg
ment is inversely related to threshold.
No-spread pairs consist predominant
ly of H and N segments; two-way
spread pairs consist predominately of
Land M segments; and the one-way
spread pairs exhibit intermediate
thresholds.
4. Segmental intervals. (Distance
between the members of a pair.) The
incidence of spread dec'ines with in
creasing distance between segments.
Sinc T. and T" are the terminal segments in the ar
bitrarily selected series of segments they are at a
relative disadvantage as regards spread. However,
were the series extended to include T, and T",
segments T. and T .. as well as T. and T". would aso
show increased participation in spread. T. would
probably show the largest increase of all, certainly
larger than .. that of T". The relative superiority of the
upper sewents of the series would remain.
The relation of thresholds and of
segmental intervals to incidence of
spread is shown in figure 3.
5. Direction oj spread. Figure 2
shows that incidence of cephalic
spread far exceeds that of caudal
spread (except for a slight caudal
predominance between Ta and Tlo).
Of 32 cases of one-way spread (fig. 1)
29 are cephalic. Further, where there
is two-way spread, the thresholds for
cephalic spread are predominantly
lower than those for caudal spread.
Our analysis of the data indicates
that preferential cephalic spread is an
intrinsic feature of these reflexes and
that the greater facility for cephalic
spread exists regardless of whether
the threshold of the superior segment
(of a given pair) is lower than, higher
than, or the same as that of the in
ferior segment.
In view of the fact that L' s and M's
are predominantly in the upper seg
ments, this may be related to the in
trinsic directional factor. Neverthe
less, the fact remains that, in our ex
periments, the reflex muscular re
sponses of L and M segments were
relatively easiy evoked by stimula
tion of the spinous processes of re
mote H or N segments; spread in
the reverse direction was uncommon.
Stimulation of the N spinous process
not only failed to elicit responses
from muscles of the same segment,
but also those of (N or H) segments
which intervene between it and the
responding L segment. (Expts. 35, 22,
28, 36, fig. 1 .)
Selective spread of excitation to L
segments was further demonstrated
by the application of slight tactile
stimulation to remote areas of skin
(e. g. , shoulder or scapula) whereupon
activity frequently appeared in L seg
ments, but never in others.
6. Procainization and spread. It is
of interest in this connection, al
though our observations are as yet
few, that while procainization of the
spinous process of an L segment
raised the self-threshold beyond 7
kgm., the reflex responsiveness of
that segment to stimulation of other
spinous processes remained unchang
ed.
Discussion
These experiments confrm, in loca
tion and degree, that significant
subj ect-to-subject and segment-to
segment differences in spinal reflex
EMG, SNS, reflexes, etc.
thresholds occur i n the "normal"
human.
The data indicate that differences
in pressure thresholds reflect differ
ences in central facilitation, and t hat
the facilitation is due to a bombard
ment of the motoneurons by impulses
originating, in part at least, from
points other than the spinous process
which was the site of stimulation. The
evidence may be summarized as
follows:
1 . The L and M segment shows
hyper-excitability to local and distant
stimulation including that from N
segments. Impulses from an N
spinous process may bypass moto
neurons in intervening high threshold
segments to activate motoneurons i n
the ventral horn of a more distant L
or M segment.
2. The effectiveness of pressure at
the spinous process of N segments i n
eliciting activity from remote L or M
segments is not ascribable to mere
facilitation of continuous impulses
from t he spinous processes or supra
spinous tissues of the L and M seg
ments, since at least from our limited
observations, the responsiveness of
an L segment (to distant stimulation)
is unchanged by procainization of the
tissues closely investing its spinous
process.
3. Spread to L segments is much
more frequent than spread frm L
segments.
4. L segments are hyper-excitable
t o i mpul ses ot her t han t hose
originating from external stimula
tion; "rest activity" is common i n
these segments.
5. Right and left sides, at the same
level, may show strikingly different
thresholds to pressure at the same
spinous process.
Lloyd's studies (1 1 , 12), with
facilitating volleys, of the quantita
tive relationship between subliminal
fringe and the discharge zone in the
cat have led to his conclusion that
(1 1 ) "It is unlikely therefore, that any
significant number of motoneurons
are close to or at threshold in the
resting pool, for, if there were, the
first afferent i mpulses t o enter the
pool should secure a post-synaptic
discharge". His work demonstrated
that a motoneuron pool, in the
absence of a facilitating or test volley
or both (to the dorsal root), is resting.
This resting state represents a check
on the far-flung interneuron system
dO
O
V
H
W
u
V
u
9O
C
0
u
0 O
C
7
O
L H!{W
0 Meum
L ...
H0 I woy =. y No 1woy ZM4 No two, 0,
$prH spr.od spnod spt.ad spread sprlad 'O'tod spread sprea
2 SEGMENTS APART R SEGMENTS APART SEGMENTS APART
Fig. 3. Influence ofditance and threhold on sprad ofecitation. Individual segments appar in
the graph a many times as they can be paire, e.c.g., T. and T.o ar pired with level 2, 4, and 6
segments aprt; and T. and T. twic with level 2 segments apart and onc with levels 4 sgment
apart. The croshatching code designate the number ofsgments in L, M, H or N cteore. Thu,
for example. ofthe segments showing no sprd at a 2 segment interval. 4 WMM, 7 WMH, and 69
wreN.
and. in effect, i nsulates the final com
mon path against firing every time an
afferent impulse reaches the pool.
While such a mechanism certainly
exists in man and while Lloyd has
demonstrated it in experimental
preparations where complete control
of facilitating, inhibitory and test
volleys can be maintained, our obser
vations indicate that in "normal", in
tact man it is possible to have quite a
different situation. Not only may dif
ferent pools, in close anatomic prox
imity, show different (and constant)
degrees of closeness to threshold but,
indeed, certain pools may be at, or
above, threshold (rest activity) in the
absence of external stimulation. Since
Lloyd has demonstrated that a con
siderable portion of the cells in a
motoneuron pool must be in a state
of subliminal excitation before
discharge from that pool occurs, it
seems apparent that reflex thresholds
(measured by the pressure meter) are
a measure of the size of the
subliminal fringe or of the degree of
facilitation maintained at a given
spinal segment. Thus a l kgm. seg-
ment has such a large subliminal
fringe that relatively few additional
i mpulses reaching it (from any
source) will extend it into t he
discharge zone.
In addition to the demonstration of
central facilitation, correlation was
found among aJ the reflex threshold;
b, the palpable characteristics of
supraspinous tissues; c, the suscep
tibility of those tissues to lasting
soreness following minor trauma,
and d, the pain threshold (and pain
characteristics); the basis for this cor
relation has not yet been learned.
An attractive possibility which
might account for this relationship i s
that i n a given segment there are
pools of neurons other than anterior
horn cells that are also facilitated and
that their hyper-activity, through
trophic. vasomotor or other in
fluences, produces the observed
changes in the tissue.
The lower resistance to minor
trauma and to painful stimuli may be
secondary to the tissue alterations.
Certain similarities to the nocifensor
tenderness described by Lewis (9) are
II
indicated. The possibility remains,
however, that the lowering of the
pain threshold may also be due, in
part at least, to central facilitation.
The facilitation indicated in the low
threshold pool may explain what
Mackenzie ( 13, 14) referred to as ex
aggerated responses in an area of "ir
ritable focus" and, by direct evi
dence, establishes the latter at either
the interneurons, the motoneurons,
or both. Hinsey and Phillips (6), in
connection with referred pain, have
also translated the "irritable focus"
into terms of facilitation.
The final question to be asked in
connection with the present observa
tions is concerned with the origin or
origins of the impulses which facili
tate the low threshold pools. Several
sources suggest themselves: the higher
centers, viscera, proprioceptors (i. e. ,
j oi nts, tendons, ligaments or
muscles). In these experiments, how
ever, the high degree of constancy
and especially the high degree of
localization - to one or two seg
ments, the frequent differences in
threshold of right and left side of the
same segment, and the absence of
psychoneurotic and visceral symp
toms in our subjects would seem to
rule out the first two as major
sources. We are inclined to believe
that the facilitating impulses arise
from segmentally related structures.
Summar
1. The refex responses of the erector
spinae muscles to measured pressure
applied to the spinous processes at
selected spinal segments were studied.
The existence of constant differences
in reflex thresholds of segments in
different subjects, and from segment
to segment and from side to side in the
same subject, has been confrmed.
2. Low threshol d segments
showed reflex hyper-excitability to
pressure upon the corresponding
spinous processes, to pressure upon
the spinous processes of distant, high
threshold segments, and to impulses
from proprioceptors associated with
This i not to deny that psychogenic or viscerogenic
impulses may significantly afect segmental thresh
olds. Our own experiments demonstrate that appre
hensiveness, anxiety, transient illness, etc., may cause
widespred lowering of thresholds. In our subjects
these influences appear to have been superimposed on
the primarY, and more constant, factors influencing
thresholds.
positioning, from remote areas of
skin and from the higher centers.
3. I t is concluded that low thresh
old segments are those in which a rel
atively large portion of the moto
neurons are maintained in a state of
facilitation due to a chronic bom
bardment by impulses from some
unknown source. Presumptive evi
dence indicates that the facilitating
impulses arise from segmentally re
lated structures.
4. Correlation of motor refex
threshold with a, pain thresholds; b,
susceptibility of supraspinous tissues
to minor trauma, and c, with tissue
texture, has been demonstrated. This
suggests that neurons other than the
motoneurons in the low threshol
d
segments may be simultaneously
facilitated.
References
I. Buchthal, F. and S. Clemmeson. Acta med.
scand. 48:48, 1940.
2. Oenslow, J.S. J. Neurophysiol. 7:207,1944.
3. Denslow, J.S. and G.H. Cl ough. J.
NeurophysioL 4:430, 1941.
4. Denslow, J.S. and C.C. Hassett. 1.
Neurophysiol. 5:393. 192.
S. Gilson, A.S., Jr. and W.B. Mills. This Journal
133:658,1941.
6. Hinsey, J.C. and R.A. Phillips. J. Neurophysiol.
3:175, 1940.
7. Hofer, P.F.A. and T.J. Putnam. Arch. Neurol.
Psychiat. 42:201, 1939.
8. Jacobson, E. Progressive relaxation. Univ. of
Chicago Press, 493 pp., 1938.
9. Lewis, T. Pain. New York, MacMillan, 192 pp.,
1942.
10. Lindsley, D.B. This JournalU4:9, 1935.
II. Lloyd, D.P.C. J. Neurophysiol. 6:111,193.
12. Lloyd, D.P.C. Yale J. BioI. Med. 18:117, 1945.
13. Mackenzie, J. Brain 16:312, 1893.
14. Mackenzie,' J. Symptoms and their interpreta
tion. London, Shaw and Sons. 30 pp., 1912.
IS. Seyffarth, H. Skr. Norske Vidensk Akad. 4: I,
1940.
16. Smith, O.C. This Journal 10:629, 1934.
17. Weddell, G., B. Feinstein and R.E. Pattie.
Brain 67: 1 79, 1944.
Reprinted by permission from American Journal of
Physiology 150:229-238, 197.
Abstract: Dermatomal
autonomic activity in relation
to segmental motor reflex
tttreshold (194)
IRVIN M. KORR and
MARTIN J. GOLDSTEIN (invitation)
Enduring differences in segmental
reflex thresholds involving the spinal
extensor motoneurons have been
demonstrated in man (Denslow, J.
Neurophysiol. 7: 207, 1944). The low
threshold segments appear to be those
in which a relatively large portion of
the motoneurons are maintained in a
state of facilitation due to chronic
bombardment by impulses from seg
mentally related structures (Denslow,
Korr and Krems, Amer. J. Physiol.
105:229, 1947). In the present investi
gation evidence has been obtained
that the facilitation extends to the
cells of the intermediolateral column
in the corresponding segments since
measurements of electrical skin resis
tance indicate segmental differences
in sweat gland activity which are
related to the motor reflex thresholds.
Electrical conductivity of the skin of
the back was measured in our sub
jects by a convenient modification of
the dermohmmeter. Under the condi-.
tions of our experiments most of the
skin of the back has a resistance of
5,(,( ohms or more. However,
portions of dermatomes, and occa
sionally entire dermatomes, related to
segments with reduced thresholds
have markedly reduced electrical
resistance, often as low as 20,(
ohms. The largest, most constant and
most reproducible differences in skin
conductivity, related to segmental
motor reflex thresholds, are found in
the midline, over or near the verte
brae. Areas with reduced resistance
are often hyperesthetic and some may
have the characteristics of trigger
areas. It is concluded that in segments
with chronically reduced motor refex
thresholds, at least some of the pre
ganglionic sympathetic neurons of
the same segments are also main
tained in a state of facilitation.
Reprinted by permission from Federation Proceedings
7:67, 1948.
EMG, SNS, reflexes, etc.
Abstract: Skin resistance
patterns associated with
visceral disease (1949)
This abstract reports the results of a
preliminary investigation of the part
that visceral disease and irritations
may play in determining the electrical
skin resistance patterns previously
described (Federation Proc. 7: 67,
1948, and this issue). Two classes of
patients having visceral disease have
been explored with the dermohm
meter (Jasper) and found to have
low-resistance areas (LRA) which not
only showed segmental relation to the
viscus involved, but were fairly con
sistent for a given disease entity and
were related to the referred pain pat
tern. Patients who had had myocar
dial infarcts had LRA over 2 or more
of the upper 4 thoracic vertebrae,
near the sternum at corresponding rib
levels, and over the medial edges of
one or both scapulae in the cor
responding dermatomes. In one sub
ject, repeatedly examined over a
period of months, such areas were
first observed 3 weeks prior to a cor
onary occlusion. Patients with
duodenal cap ulcer had areas of
markedly lowered resistance over the
spinal muscles, on the right side,
opposite vertebrae T-5 to T-8, over
corresponding ribs on the anterior
chest wall and to the right of the um
bilicus. In both diseases, LRA ap
peared to coincide with or overlie the
most painful or tender parts of the
reference zone.
Reprinted by permission from Federation Proceedings
8: 87. 1949.
Tie automatic recording of electrical skin
resistance patterns on tie human
trunk* (1951)
PRICE E. THOMAS and IRVIN M. KORR
In recent years the study of regional
and segmental differences of sweat
gland activity has found wide applica
tion in the determination of peripher
al nerve fields or dermatomes af
fected by trauma (1, 9, 10, 11, 12, 15,
19), surgical procedures (8, 13, 20,
22, 23, 26), painful syndromes and
visceral disease (6, 7,28), spinal cord
disease (3), and experimental
"
pro
cedures (2, 21). In most of those in
vestigations in which electrical skin
resistance measurement was used, the
operator, applying the methods of
Richter (25) or Jasper (14), or modifi
cations thereof, demarcates, with
hand-held exploring electrode, the
areas of high resistance in a general
background of low resistance induced
by the application of drugs or heat.
The high-resistance areas signify low
sweat gland activity due to impaired
or interrupted sympathetic supply to
the corresponding areas.
Conversely, studies conducted in
our laboratories have demonstrated
the existence of areas of low resis
tance which persist in a background
of high resistance, under conditions
of rest and in the absence of thermo
regulatory sweating. These low-resis
tance areas have been found in all
of the several hundred subjects ex
amined, most of whom are students
in good health. The patterns vary
from subject to subject, but in a given
subject, the patterns of segmental
distribution may remain constant for
many months (16). That is, the low
resistance areas remain concentrated
in the same dermatomes. Correla
tions have been established in many
cases with segmental disturbances of
visceral, myofascial, neurogenic and
experimental origin (17, 18). It has
been proposed that the persistent low
resistance areas represent chronic
segmental facilitation of the sym
pathetic nervous system, similar to
'This Investigation was supported in part by a research
grant from the National Institutes of Health, Public
Health Service and by a grant from the American
Osteopathic Association.
that previously demonstrated for
motoneurons of the paravertebral
muscles (4, 5).
It appears, therefore, that topo
graphical skin resistance studies may
have wider fundamental and clinical
significance and applicability than
has heretofore been recognized. Un
fortunately, the conventional explor
atory techniques have many disad
vantages. The method is very slow, an
exploration of the entire trunk requir
ing to 2 hr., according to the com
plexity of the pattern and the skill of
the operator. To this must be added
the time required for charting. Since,
in addition, the method requires
trained personnel, the number of
studies that can be conducted in a
given period of time is seriously
limited. The slowness of the method
also renders it unadaptable to the ex
perimental study of rapid, transient
alterations in the ESR patterns.
Furthermore, the method h a
number of inherent sources of error:
(a) The time required introduces
variables due to changes in the state
of the subject (fatigue, boredom,
etc.). (b) The patterns found on sub
jects of different body types must be
transferred to standardized body
charts. (c) The establishment of a
boundary may require the repeated
passage of the electrode over a given
area; this procedure may itself alter
the resistance of the area.
These diffculties have been over
come by the method of exploration
developed in this laboratory, which
rapidly and photographically records
the electrical skin resistance patterns
in proper relation to the subject's
trunk. The procedure requires a
minimum of training. A single area is
traversed only once in the course of
the exploration. A series of explora
tions may be completed in the time re
quired for a single exploration "by
hand", thus making possible con
trolled experimental studies. Another
feature of the method is its versatility;
its principle is adaptable to modalities
other than skin resistance.
23
Dl
M
.
&
l
i
t
, 1 '
.
'I
| t+
h
Fig. I A and B
Photographic records of electrical skin
resistance pal/ems obtained with the automatic
dermohmeter. Each l ongitudinal strip
represents the path ofa light source (mounted
over the eploring electrode) whose brightness
varies with the resistance ofthe subjacent skin.
The dark areas represent areas of low
reitance; the darker the area, the lower the
resitance. By means ofappropriate double e
posure the chart appears superimposed on the
subject's body. The white dots in the midline
represent. t he l ips of t he spi nous
processes,marked by a spot of light. The
numbered strip at left of each record is the
calibration, showing, for that exploration, the
variations in light brightness with variations in
current flow through the skin at constant
voltage. The resistance ofa given area ofskin
can therefore be etimated from the current
and the eploration, voltage (6 V. in each of
the above cases). See text for further explana
tion.
I4
Basic principles of lhe mlomalic
dermohmeler
The basic principle of the automatic
dermohmeter is the conversion of dif
ferences in skin resistance, that is,
differences in the current through the
skin at constant voltage, into varia
tions in the brightness of a light
source. If the light source is placed
directly over the exploring electrode,
and the electrode is propelled over the
skin at constant speed, a camera,
properly positioned with respect to
the explored field, with shutter open,
will photograph strips of light which
vary in brightness according to the
electrical resistance differences along
a corresponding strip of skin. To el
plore a large area, a series of con
secutive, parallel strips is recorded.
Figure I illustrates the records ob
tained by this method, on two sub
jects. The areas of relatively low
resistance appear as darkened areas
along the strips; the lower the
resistance, the darker the correspond
ing area on the record. The calibra
tion strip (at left of each record)
makes it possible to estimate the
resistance of any area of skin from
the photographic record (see inter
pretation of photographic records) .
Figure 2 shows a view of the instru
ment in use. The electrode-and-light
assembly (A) is propelled in the long
axis of the body while a known
voltage (from component I in figure
2) is applied between earclip and ex
ploring electrode. The light mounted
over the exploring electrode is caused
to vary in brightness with the current
passing between the skin electrodes
by means of the amplifier (also
housed in figure 2I). The camera (J)
mounted over the center of the field
records the light strip and variations
in intensity. Successive strips are
recorded by lateral positioning of the
rails (D) on the frame (H).
1he conslruclion oflhe aulomalic
dermohmeler
A. The drive.
The rigid arm (fig. 28) bearing the
electrode-and-light assembly at one
end, is supported at the other end
from a carriage (fig. 38) which is pro
pelled on ball bearings along a pair of
parallel rails (fig. 3C) by a small syn
chronous motor (fig. 3D). The motor
is itself mounted on the carriage
which it propels through a friction
Fig. 2
The automatic dermohmeter. The electrode
and-light asembly (A) is fied on the arm (B)
which is hinged at one end to the carriage (C).
The carriage is propelled along the rails (D) by
a synchronous motor (E) mounted on the car
riage. The motor is geared for motion in either
direction along the rails. The clutch-arm (F)
which engages the gears in either direction also
actuates an on-offswitch in the light and skin
circuits. This arm acts as a limit switch which
automatically interrupts these circuits at pre-set
etremes (G) on the rail at the same time as it
disengages the motor. The rails can be moved
laterally and precisely positioned on the frame
(H) for the recording ofsuccessive strips. Other
items (described in text): (I) the source of
variable voltage applied across the earclip and
exploring electrode; also houses calibrator cir
cuit and the carrier amplifier which varies light
brightness in accordance with variations in cur
rent through the skin; (J) the camera. Note the
pivot (P) which permits tilting of the entire
frame for explorations in the vertical position.
drive applied to the rails. The drive is
geared to move the carriage at ap
proximately 3.33 cms. /sec. , in either
direction. The clutch arm (3E) which
engages and reverses the gears also
actuates a switch which simultaneous
ly turns on the light source and
voltage through the skin when in
gear-engaging position, and turns
these circuits off in the neutral posi
tion. The clutch arm is automatically
thrown into the neutral position,
thereby interrupting the above cir
cuits, when it strikes the barriers
(figs. 2G, 3F) on the rail . These bar
riers, which determine the length of
the light-strip, are pre-set for in
dividuals of different heights, that is,
at each end of the field of explora
tion.
EMO, SNS, reflexes, etc.
The rails along which the carriage
travels are mounted in a Plexiglas
sleeve at each end. These sleeves are
in turn supported from the short
limbs of a rectangular frame (fi g. 2H)
which, like the rails, is made of one
inch polished pipe. These sleeves are
slid along the frame for lateral posi
tioning of the rails (and therefore of
the electrode) . Precise positioning is
made possible by a slot-and-pin
arrangement, i n which the slots are
spaced on the frame at intervals of 1 5
mm. Since the electrode is 1 2 mm.
wi de there is a space of 3 mm. be
tween strips, an interval large enough
to prevent overlap of strips and still
small enough to permit continuity of
the ESR patterns.
The frame is rigidly supported on
one side by a heavy board ( fi g. 2) af
fixed to the wall. The frame is
mounted on the board by strong
hi nges which rigidly support the
frame in the horizontal position, but
which permit tilting the frame against
the walJ for easy access of the
subject.
B. The electrode-and-Iight
assembly ( fi g. 4) .
The roller electrode (fig. 4A) is a
stainless steel cylinder 23 mm. i n
diameter and 12 mm. wide. The
under-carriage i s supported by a pin
from the arm, permitting free tilting
of the axle as the roller moves over
the ski n. Since, also, the arm is
hinged to the carriage and i s free on
the electrode-bearing end, the elec
trode rests freely on the ski n, and full
contact at constant pressure is as
sured throughout the line of travel.
The light source ( fi g. 4B) is an
evenly etched lucite rod, 5 mm. in
diameter, mounted over the roller,
parallel to the axle, and illuminated
from one end by an enclosed dial
lamp. The exposed part of the lucite
rod is 12 mm. long, corresponding to
the width of the electrode. Since the
light source is cylindrical , rather than
tAlthough fIgUre 2 shows the instrument in posItion
for exploration of the recumbent subject, it can also
be used for exploration in the vertical (or other) posi
tion. The frame may be rotated so that the rails are
vertical (fig. 2P). By means of a pulley and
counterweight, the rate of travel of the carriage in the
upward and downward direction is adjusted to that of
horizontal travel. The camera is placed, of course, in
the horizontal position, aimed at the approximate
center of the exploration field. The entire instrument
may be mounted on a rigid, portable stand rather than
on a wall.
Fig. 3
Close-up of drive mechanism. Arm, bearing
electrode-and-light assembly (not shown) is
hinged to lower end of vertical adjuster (A) on
carriage (8) which is propefed along rails (C)
by synchronous motor (D). Clutch-arm (E)
reverses gears and serves as limit switch for
light and skin circuits; (F) adjustable limit.
Fig. 4
Electrode-and-light assembly. (A) Rofer elec
trode; (8) etched lucite rod illuminated from
one end by dial lamp in (C) housing.
flat, it presents an illuminated surface
of constant area to the camera
throughout its field.
C. The variable voltage source.
Di fferent voltages are applied be
tween the conventional earclip elec
trode and the exploring electrode
(positive) from a series of flashlight
dry cells (size C) which are connected
into the circuit i n 3 V. steps by means
of a gang-switch (fig. 5, S2) . The
range 0-3 V. may be further sub
divided by means of a potential
divider for explorations during active
sweating. (The 0-50 microammeter is
not essential but is included for con
venience in selection of exploration
voltage; see below) . The potential
drop across the variable resistor RIO
shown in the circuit diagram is ap
plied to the grid of the amplifier (fig.
5, V4) which varies the brightness of
the light source i n accordance with
the current passing through the ski n.
D. The calibrator.
For calibration ( fig. 5 , S3) a series of
fixed resistances are switched into the
circuit i n turn (i n place of the ski n
and skin-electrodes) to permit the
flow of known currents, whi l e the
brightness of the light is photographi
cally recorded.
E. Convdsion of variations of
current through the skin to
variations oflight intensity.
Since the current dealt with i n der
mohmetry is of the order of micro
amperes, amplification is required for
the operation of even a small light
bulb.
Figure 5 includes a schematic of the
carrier amplifier currently being used
i n our laboratories, shown i n correct
relation to the variable voltage source
and calibrator circuits. The amplifier
is set to give maximum intensity of
the light source (white on photo
graphic record) at zero ski n current
and minimum intensity (black) at any
pre-sel ected number of mi cro
amperes, according to the desired
range and sensitivity.
The electronic circuit (see block
diagram, fig. 5) consists of a local
osillator, two stages of resistance
coupled amplification, and a control
stage. The oscillator VI (a multi
vibrator) produces a H c/sec.
signal which i s fed through the two
ampl i fier stages V2 and V3, and pro-
I5
1
Fig. 5
Circuit diagram (variable voltage source, clibrator and ampliier)
C1 0. 02 mid papr. 4o volts R9
C2 0.0 md paper, 4o volt RIO
C3 0. 1 md paper, 4o volts Rll
C, C9 0.25 mjd pper, 4o volt R12
C5 1.0 mjd dr electrolytic, 6 volts R13
C6 0.05 mjd paper, 4o volts R14
C7, C8 12.0 mjd. eletrlytic, 6 volts RI5
RI, R, R7 150K, I watt RI6
R2 470 ohm, J watt RI8
R4, R5 2.2 meg, J wtt Sl
R6. R8 lOK, 1 wtt
1.0 meg, 1 watt
5OK, 1 watt
58K, 1 watt
20K, 1 watt
30K, 1 watt
50K, 1 watt
lOK, I watt
3OK, 1 watt
3O0 ohms, I watt
SPST toggle switch
S2, 5 J circuit, 1 J poition, single section, non-shorting rotar switch.
5 DPST toggle switch
TI Power trnsormer, 7o volts ct, 5 and 6.3 voft flament terminal.
T Output trnsormer (Thoraron T-22S90)
F Filter choke, 10. 5 henr
L GE, C-40
VI 6SN7
V2 65
V3
6V6
V4 155
V5 5Y3
Component in block diagram;
OSCILL. multivibrator
AMPL.1 1st ampliier (modulator)
AMPL.2 Power ampliier
LAMP GE, C-40 dial lamp
CONTROL control stage
CALIB. or SIN varible voltage source applied across the skin or the calibration reitors.
16
vides a source of alternating current
sufficient to light the lamp. The
brilliance of the lamp is determined
by the gain of V2, which in turn is
varied by the control tube V 4. The
output of V 4 is determined by the
current flow through the skin circuit
and, consequently, through grid
resistor (RIO). Thus, the carrier signal
is amplitude-modulated by variations
in the resistance of the skin.
The oscillator and amplifer stages
are of conventional design and need
no further description. The control
tube V4 is employed as a poten
tiometer to vary the grid bias of V2.
An independent power supply for the
plate and filament of V 4 makes it
possible to ground the plate. The
voltage drop between the cathode and
plate of V4 is then applied to the grid
of V2.
The direction of current flow
through the skin and grid resistor
causes the grid of V 4 to become more
positive when the current through the
skin (or from the calibrator) is
decreased. More current then flows in
the plate circuit. However, this in
creases the potential drop across the
plate resistor (R9) at the expense of
the voltage drop across the tube.
Under these conditions, the voltage
applied to the grid of V2 becomes less
negative. This increases the amplitude
of the carrier signal with a resulting
increase in b
i
ightness of the light (fig.
5, L). The reverse process occurs
whenever the skin resistance drops
and increases the current through the
grid resistor of V4. For calibration, a
variable source of known current i s
applied in place of the skin circuit by
means of a rotary switch (S 3).
Figure 6 shows a non-electronic
"amplifier" used in an earlier model
of the automatic dermohmeter and
previously described in a preliminary
report (27). Although less convenient
to operate than the carrier amplifier it
is of much simpler construction. The
principle of the device appears, also,
to have a wide range of possible ap
plications.
The indicator needle of a 0-50
microammeter (fig. 6A) actuates the
variable arm of an electrolytic
rheostat in the lamp circuit. This
variable arm is a U-shaped platinum
wire (fg. 6C) which has been at
tached to the indicator needle (fig.
6B) at the center of rotation. The
meter is supported face down on a
EMG, SNS, reflexes, etc.
Plexiglas block in which two semi
circular canals (fig. 6E) have been
cut. Each limb of the U moves in a
canal containing di lute H2S04 Move
ment of the microammeter needle
alters the resistance in the lamp cir
cuit (and therefore the light intensity)
through variation of the length of the
acid column between the limbs of the
U and the fixed electrodes ( fig. 60) .
I n our device, N/6 H2S04 provided a
satisfactory range of resistances.
Froccdurc
To conduct an exploration, the area
to be explored is exposed and the sub
ject reclines on an upholstered tabl e;
one with a face slot comfonably per
mits maintaining the head in the
midline position during exploration
of the dorsal surface. Any desired
topographical features are identified
and marked. The frame is brought
into the horizontal position over the
subject, the rai ls parallel to the long
axis of the area to be explored. The
electrode is placed upon the subject' s
ski n, and the height of the fixed end
of the arm is adjusted ( fi g. 3A) on the
carriage according to the subject ' s
anteroposteri or di mensions . The
l i mits are set on the rai l according to
the length of the field to be explored.
A. Selection ofexploration
voltage.
Before beginning the exploration the
appropri ate vol tage i s sel ected.
Because of di fferences in "basic"
resistance among subjects, some may
require 3 V. or less, others more than
1 8 V. , for demonstration of the
gradations in resistance. We have
found that the voltage which just per
mits a detectable flow of current
(about IpA.) through most of the
ski n, will permit a nice differentiation
and gradation of the areas of relative
ly low resistance by deflections of the
microammeter needle and di mmi ng
of the light source.
B. The calibration strip.
Following the selection of the ex
ploration voltage, the room is dark
ened except for photographic safe
l ight, the camera shutter is opened,
and a calibration strip is recorded,
as follows. The rail is moved to one
side of the exploration field, but still
within the view of the camera, and
the carriage to one end of the rail.
The calibrator is switched i nto the in-
put of the amplifier. The motor is
started, and the clutch engaged, si
multaneously starting the carriage
and turning on the light. As the
electrode-and-light assembly travels
along the rail (electrode not i n contact
with subject) the operator switches
each of the resistances ( fig. 5, S3) into
the circuit i n turn, thus recording i n 6
steps the variations in l ight intensity
throughout the pre-selected range of
current flow. Upon completion of the
strip, the light is turned off by the
automatic limit switch.
C. The exploration .
The rail is then moved to one edge of
the exploration field, and the carriage
brought to one end of the raii. The
electrode is placed on the subject' s
s ki n, the previously selected voltage is
applied to the input of the amplifier
i n place of the calibrator, and the
clutch is engaged. As previously men
tioned, the switch incorporated in the
clutch arm simultaneously turns on
the light source and the voltage to the
ski n electrodes. At the end of the
strip, this arm is automatically thrust
into neutral position as the clutch arm
strikes the limit on the rail, simul
taneously interrupting the circuits.
The rail i s then moved laterally to the
next notch, the clutch is engaged in
the opposite di rection and the next
strip is thus recorded. About 20 sec.
are required for the exploration of a
strip equal to the length of the
average human trunk.
O. Establishment of topographical
relationships.
The positions of the various land
marks (e. g. spi nous processes, scapu
lar edges, il iac crests) are then record
ed by means of a small spot of light.
Figure I shows the spinous process
thus marked as white spots.
The camera shutter is then closed,
the frame bearing the rail, etc. , i s
ti lted back against the wall, and the
slate bearing the data regarding the
exploration is placed within the
camera field but outside the explored
field. A bright bulb, shaded from the
camera but i l l uminating the subject,
is turned on. The explored field is
covered with a black cloth, and, with
out advancing the fi l m, a brief expo
sure is then taken. By this means, as
shown i n figure I , the record appears
in correct montage on a photograph
of the subject's body. The black
Fig. 6
Non-electronic "amplifier". (A) microam
meter; (8) microammeter needle bearing (C)
moving electrode; (D) electrodes fied in (E)
acid trough; (F) U skin electrodes; (G) to light
circuit.
cloth, of course, prevents re-exposure
of that portion of the film on which
the exploration has been recorded.
latcrrctatioa of thc
hotograhic rccords
As the label shows in figure I , both
subjects were explored with 6.0 V.
Since the white areas signify current
of I /A. or less, these represent areas
of ski n whose resistance exceeded 6
million ohms. For the exploration of
figure l a, the ampli fier was set to
cause dim-out at 30 , figure I b, at
25
p
.
t
The black areas, in figure l a,
therefore, indicate currents of 30 /A
or more, that i s, areas of ski n having
resistances of less than 200,00 ohms.
The various shades of gray indicate
i ntermedi ate resi st ances , whose
values can be estimated from the
calibration stri p to the left of the
chart , in which the 30 /A. range has
been divided in 5 /A strips . (The
darkest portion is i'ndistinguishable
from the background. )
tNarrowing t he range, i . e. lowering t he dim-out point.
increases the di fferentiation among the high resistance
areas while sacrificing gradations below the resistance
corresponding to the dim-out current.
2T
Otber applicatons
The principle of the automatic der
mohmeter can, we believe, be applied
to the study of the topographical
variations of features other than elec
trical ski n resistance. I n our
laboratories we have adapted the
device to the demarcation of areas of
cutaneous hyperesthesia by replacing
the eletrode on the arm with an elec
trical or mechanical stimulator. The
light over the stimulator, which is
propelled in the same manner as the
skin electrode, is controlled by the
subject who turns the light off and on
with a thumb-switch to mark the
hyperesthetic zones in each strip. By
incorporating a rheostat in a rubber
bulb grasped by the subject, varia
tions in the intensity of the pain in
duced by the stimulator may also be
recorded.
Another adaptation, in which the
roller electrode is replaced by a ther
mocouple, thermistor or radiometer,
for the study of spatial variations of
skin temperatures on the human
trunk, is in process of construction.
Sources of Error
The automatic dermohmeter, as con
structed by us, has two chief sources
of error, both of which are relatively
unimportant in our application of the
instrument, and both of which can be
gretly reduced or eliminated by cer
tain refinements.
1 . Since the area of contact be
tween electrode and skin (and cor
responding area of illuminated sur
face) are considerable ( 1 2 x 1 2 mm. ),
that area constitutes the limit of error
in the demarcation of a boundary or
in the localization of a small spot.
Thus a small spot of very low
resistance within the area of contact
of the electrode will be recorded as a
rectangle equal in area to the il
luminated surface. In our investiga
tions we appear to be dealing with
segmental phenomena, and therefore
this error is not important since it still
permits the identification of der
matomes. Greater precision of
localization is, of course, attainable
through reduction in size of the ex
ploring electrode and light source, at
the cost of speed of exploration.
2. Since the illuminated lucite rod is
mounted over the roller electrode it is
at some distance above the subjacent
area of skin. At all positions of the
electrode other than those in the axis
2
of the lens, therefore, error due to
parallax is present, and the light will
be recorded by .the film as though
issuing from a rectangle of skin just
beyond the electrode. However, since
the distance between the skin and
light source (3.5 ems.) is small as
compared with the distance to the
camera ( 1 4 ems.) this error is small.
As measured on a subject, with the
electrode assembly at the extremes of
the rail, the maximum error due to
parallax in the instrument described
was 1 8 mm. This error can be
eliminated by maintaining virtual
(optical) alignment of lens, il
luminated rod and un
d
er-surface of
the electrode at all positions in th
camera field.
Summary
1 . A new procedure has been de
scribed for the photographic record
ing of electrical skin resistance pat
terns on the human trunk, or other
areas of the body. The explorations
are accurate, almost automatic and
rapid as compared with exploration
by hand-held electrode.
2. The basic principle of the
method is the conversion of varia
tions in skin resistance into variations
in the brightness of a light source. By
placing the light source directly over
the exploring electrode, and propel
ling the electrode (by synchronous
motor) over the skin at constant
speed, a camera, properly positioned
with respect to the explored feld,
photographs strips of light which
vary in brightness according to the
resistance differences along a cor
responding strip of skin. To explore a
large area, a series of consecutive,
parallel strips is recorded.
3. The adaptation of the procedure
to measure the topographical varia
tions of features other than skin
resistance (e.g. skin temperature,
hyperesthesia) are described or sug-
gested.
.
4. The major sources of error are
describe and shown to be unimpor
tant in our current application of the
instrument . Refi nements which
eliminate or greatly reduce these
errors are suggested.
It is a pleasure to acknowledge the valuable
assistance of Mr. Dwight W. Leighton in the
design of the dermohmeter and the construc
tion of the mechanical parts.
Refernces
l . Blade. B. and Dugan. 0.1. War wounds of the
chest observed at the Thoracic Surgery Center. Walter
Reed General Hospital. J. Thorcic Sur 194, 13:
294-30.
2. Bruesch, S.R. and Richter. C.P. Cutaneous dis
tribution of peripheral nerves in rhesus monkeys as
determined by the electrical skin resistance method.
JahnHapk. Hasp. Bull., 1946, 78:235-26.
3. Craig, C.B. and Hare, C.C. Sweating reaction in
patients with diseases of the spinal cord. Arh.
Neural. Pychit., Chicago, 1935, 33: 478-491 .
4. Denslow. J.S. An analysis of the variability of
spinal refex threholds. J. Neuraphysiol., 194, 7:
20215.
S. Denslow, J. S. , Korr, I. M. and Krems, A.D.
Quantitative studies of chronic facilitation in human
motoneuron pools. Amer. J. Physjal., 1947, lO:
229-238.
6. Guttmann. L. Motorische und vegetative genz
zonenreflexe bei lasionen pripherr und zentraler
abschnitte de nervensystems. Z. gt Neural
Psychit., 1933, 147: 2130.
7. Guttmann, L. Ueber reflektorische beziehunen
zwischen viscera und Schweissdriisen und ihr
Bedeutung bei Erkrankugen inere organe (der
viszerosudorale reflex). Can. Nerl., 1 938. 1:
296-310.
8. Guttman, L. The distribution of disturbances of
sweat secretion after extirpation of certain sym
pathetic cervical ganglia in man. J. Anal .. 19, 74:
537-549.
9. Guttmann. L. Topographic studies of distur
banc of sweat secretion after complete lesions of
pripheral nerves. J. Neurl. Pyhit., 1940. 3:
197-210.
10. Herz. E. and Glaser. G.H . Holdover. 1. and
Hoen, T.1. Electrical skin resistance test in evaluation
of peripheral nerve injuries. Arh. Neural. Pychil
Chicago, 1946, $6: 365-380.
I I . Highet, W.B. Procaine nerve blok in the in
vestigation of peripheral nerve injuries. J. Neurl.
Pychit . 1942, $: 1 10 1 16.
12. Hyman, I. and Beswick, W.F. Mesurement of
skin resistanc in pripheral nerve injuries. WarMe.,
1945, 8: 25826.
13. Hyndman, O.R. and Wolkin, J. The pilocarpine
sweating test: A valid indicator in differentiation of
preganglionic and postganglionic sympathectomy.
Arch. Neurl. Psychiat., Chicago. 1941, 4$: 9210.
14. Japer, H. An improved clinical dermohmeter J.
Neurur .. 195, 2: 25726.
15. Jasper, H. and Robb. P. Studies of electrical
skin resistance in peripheral nerve lesions. J.
Neurosur., 1945. 2: 261 . 268.
16. Korr, I.M. and Goldstein, M.J. Dermatomal
autonomic activity in rlation to segmental motor
reflex threshold. Fe. P., 1948. 7: 67.
1 7. Korr, I.M. Skin resistance patterns assoiate
with visceral disease. Fe. Prc., 1949. 8: 87.
18. KOT. I.M. Experimental alterations in segmen .
tal sympathetic (sweat gland) activity through
myofascial and postural disturbancs. Fe. Pro.,
1949, 8: 88.
19. Minor, L. Uber erhoten electrischen hautwider
stand bei traumatischen affektionen des halssym .
pathicus. Z. G. Neual. Phjal., 1923, 8$:
482 . 507.
2. Palumbo, L.T., Sambrg, H.H., Hohf, J.C.
and Burke. E. T. Postoprative sweating patterns in
thoracolumbar sympathectomy and splanchnicec
tomy. Arh. Neural. Psyh/at., Chicago, 1950, 6:
569-578.
21 . Richter, C.P. and Shaw, M.B. Complete
trtions of the spinal cord at different levels.
Arch. Neurl. Psyh/at.. Chicago. 1930, 2:
107 1 1 16.
EMG, SNS, reflexes, etc.
2. Richter. C.P. and Woodruff. B.O. Change
produced by sympathectomy in the electrical
reistanc of the skin. Surer, 191, 10: 9S7-970.
23. Richte. C.P. and Wooruff, B.O. Lumbar
sympathetic dermatome in man determine by t
electrical skin resistance method. J. Neuropllo.,
I9S, 8: 323-338.
2. Richte. C.P. and Otenasek. F.J. Thoracolum
bar sympathetomies examined with the eletrical skin
resistance metho. J. Neurour., 194. 3: 120-J34.
2S. Richter, C.P. Instructions for usilll the
cutaneous reistance reorder or .. dermohmter", on
peripheral nerve injuries, sympathectomies and
paravertebral bloks. J. Neurour., 1946, 3: 181-191.
2. Richter, C. P. Cutaneous areas deervated by
uppr thoracic and stellate gonetomies deter
mined by the eletrical skin resistance method. J.
Neurour. 197. 4: 221-232.
27. Thomas. P.E. and Korr. I. M. Semi-automatic
recordilll of electrical skin resistanc patterns. Fe.
Pr., 1950, 9: 126.
28. Van Metre. T.E., Jr. Low electrical skin
resistance in the region of pain in painful acute
sinusitis. JohnHopk. Hap. Bull., 1949. 8': 4-41S.
Reprinted by prmission from EEO Clin. Neuro
physiol J: 361-368. 19S I .
Relationship between sweat gland activity
and electrical resistance of the skin (1957)
PRICE E. THOMAS and IRVIN M. KORR
Measurements of the electrical
resistance of the skin (ESR) to the
passage of direct currents are general
ly utilized as an indicator of sym
pathetic activity. In this application,
the techniques used and the informa
tion sought fall into two rather broad
classes: 0) those designed to measure
changes in resistance in a given area
of skin (e.g. psychogalvanic reflex or
galvanic skin response studies) and b)
those used for measuring differences
in resistance among various areas of
skin. For both techniques the basic
electrical method is similar (i.e.
measuring the current flow at a
known voltage and converting to
resistance or conductance according
to Ohm's law). The major difference
in methods is in the type of electrode
used. In the first class (PGR or GSR)
wet, nonpolarizable electrodes are
generally used, while in the latter
class dry, polished-metal exploring
electrodes have been found most
satisfactory and convenient.
With either technique it appears
that activity of the sweat glands
significantly alters the resistance
level. In a study with wet electrodes
Darrow (1 ) found a linear relationship
between the conductance (reciprocal
ohms) and the amount of perspira
tion produced. With dry metal elec
trodes Richter and others (2, 3) have
observed that low skin resistances
were found in normally innervated
areas of heated, visibly sweating,
sympathectomized patients, while
denervated areas showed high
resistance values. These observations
and many others establish visible
sweat gland activity as an important
ESR- I ower i ng fact or whet her
measured by wet or dry electrodes.
In cases of hereditary ectodermal
dysplasia, Wagner (4), using dry elec
trodes, observed consistently high
ESR values at all environmental
temperatures investigated, in skin
areas containing no sweat glands.
'These investigations were supported in part by grants
from the National Institutes of Health (829 and
H1 632) and from the American Osteopathic Associa
tiOIl and by a contract (Nom 243(00 with the Office
of Naval Research.
These skin areas also showed no
resi st ance changes rel ated t o
vasomotor adjustments to heat or
posture. The sweat glands would
seem, therefore, to be the one skin
structure whose physiological activity
produces significant variations in skin
resistance.
Ratcliffe and Jepson (5), using dry
electrodes, showed that significant
differences in ESR between sym
pathectomized and normally inner
vated areas of the skin were still
demons t r abl e even a t cool
temperatures ( l 8QC), in which there
was no visible sweating.
These various observations strong
ly indicate that with dry electrode
techniques any activity of the sweat
glands, even at such low rates as
occur under cool, resting conditions,
lowers ESR below that found in the
complete absence of sweat gland ac
tivity.
The question is now raised as to
whether variations in ESR in a given
area or ESR differences between
areas, in which there is no visible
sweating, such as the patterned dif
ferences described by us (6), are
related to gradations in sympathetic
sudomotor activity.
Affirmative support is suggested by
the observations of Richter and
Woodruff (7) that the size of low
resistance areas around the mouth
and nose was increased during
periods of general sympathetic activi
ty and decreased with lessened sym
pathetic activity though there was no
visible sweating in either case. Low
resistance areas have also been
observed that were regionally or
segmentally related to pathological
states of deep tissues, and which may
diminish or disappear when the
pathological process is alleviated (8).
The participation of sweat glands in
these observations was not apparent,
but cannot be excluded on the basis
that no sweating was visible. Low
rates of sweat gland activity that are
not visible to the naked eye have been
demonstrated by microscopic obser
vation (9, 1 0). To clarify the situation
requires further investigations into
19
Fig. I. Diagram of prism-photo recording
method and appearance of record. The three
components, prism, A. electronic flash light
source, B. and camera, C, are rigidly mounted
in a strong aluminum frame. The camera is
positioned so that light from diffusion screen,
S. is reflected into the lens by the base of the
prism (angle b equals angle c). When these
angles are slightly greater than 45 0 surface
deiails of the skin and presence of sweat drop
lets are clearly observed. Precisely placed
reference marks on prism and skin make it
possible to determine numbers of glands per
unit area of skin regardless of the apparent
angular distortion of the skin field. In this
figure the relati ve size ofthe prism has been ex
aggerated for clarity.
Fig. 2. A. appearance of nonsweating skin; B.
same area of skin shown i n A shortly after
sweating began. An active sweat gland pro
duces a pool ofmoisture that records as a dark
spot in the photograph.
the range of ski n resistance values
than can be related to sweat gl and
activity.
This paper presents an experimen
tal examination of the relationship
between sweat gland activity and ESR
values measured by dry electrodes as
a step toward evaluating the reliabili
ty of such measurements as indicators
of sympathetic sudomotor activity.
Mcthods
The measurements of el ectri cal
resistance were essentially based on
the method of Jasper and Robb ( I I )
i n which a series of dry cells i s tapped
to provide a wide range of voltages in
1 . 5-volt steps. The voltage and di rec
tion of current flow were kept con
stant throughout each experiment.
This necessity was suggested by
Rosendal's ( 1 2, 1 3) identification of
these variables as signi ficantly in
fluencing the measured values of
resistance. The chosen voltage was
J0
applied to an indi fferent electrode
(cathode) fastened to the ear lobe and
making contact with the tissues
through conductive paste, and a dry,
si lver di s k, expl ori ng el ectrode
(anode) . The conductive paste used
was granular, and rubbing sufficed to
abrade the ski n. As demonstrated by
Richter (2) , by Lewis and Zotterman
( 1 4) and by Rosendal ( 1 3) , this
reduces the resistance at the abraded
point to an insignificant level. A
microammeter or galvanometer was
included in the circuit. The resistance
val ues in the data are onl y absol utely
referable to the electrode size stated
since Blank and Finesinger ( 1 5)
observed nonlinear variations in curr
rent density with di fferent el ectrode
sizes.
Each measurement was done by
making brief ( 1 -4 sec. ), firm contact
of the electrode to the ski n and
observing the stable value of current
flow. Resistances or conductances
(reciprocal ohms) were then cal
culated according to Ohm' s law.
Active sweat glands have been re
corded by two methods. In prelimi
nary experiments the iodine-starch
paper method described by Randall
( 1 6) was used. The ski n was painted
with iodine and allowed to dry. A
5-cm2 piece of starch paper was held
lightly against the painted skin area
for a short period ( 1 -2 mi n. ) At the
end of this time the paper was re
moved and a fresh paper pressed
against the area. The number of spots
appearing on each paper represented
the accumulated total of all sweat
glands presenting moisture to the
surface during the test period. ESR
measurements were made on skin im
medi ately adj acent to the gl and
counting areas. Thi s method per
mitted gross observations on ESR
sweat gland relations but had the
disadvantage that the two measure
ments were not made on precisely the
same skin areas.
This disadvantage was overcome
by using the prism technique de
scribed by Netsky ( 1 7) . By uti lizing
the alteration in reflection produced
by contact of moisture against one
face of the prism, active sweat glands
may be observed and photographed
as dark spots through another face of
the prism when evenly di ffused light
is shining through the third face ( figs.
1 and 2) . All photographic records
were taken within 2 seconds of con-
tact of the prism with the ski n. The
prism was wiped clean after each
photograph. By suitabl y adjusting the
light and camera angle the texture of
the skin can also be observed and
phot ographed . I n a seri es of
photographs of the same ski n area,
individual active glands can be iden
tified by their relationship to the
crease pattern and their activity
foll owed through the entire ex
perimental period. Since no chemical
preparation of the skin is necessary,
the ESR of the same area being
photographed can be obtai ned im
mediately before and after each
photograph. This permits a precise
examination of the rel ationship be
tween ESR and the sweat gland activi
ty occuring in the electrode area and
the following of rapid changes in
both.
I n all experiments the subject was
first allowed to rest in a prone posi
t i on at c omfor t a b l e r oom
temperatures until no sweating was
detected by the prism method. The
subject was then heated by an electric
hot pad on the abdomen until
sweating was induced, at which time
heating was discontinued. Recording
of ESR and sweat gland activity was
initiated with heating and continued
through the sweating period until
sweating was no l onger detectable.
LxcrimcataI rcsuIts
An example of the results obtained
using the Randal l iodine-starch-paper
method and an electrode of 2. 54 cm2
is illustrated in figure 3. As seen in
this figure, rising gland count was ac
companied by increasing current flow
(decreased resistance) . However,
when the gland count was falling the
current flow often remained elevated.
This immediate postactivity ' lag' sug
gests some residual effect of sweat
gland activity. The observations of
the ' lag' and of the variations in con
ductance at zero gland count suggest
a ' nonsudorific' i nfluence on conduc
tion. The necessity of using di fferent
ski n areas for ESR and gl and counts
in the Randall technique, however,
precluded any certain identification
of nonsudori fic conductance factors
or assignment of any quantitative
conductance properties to the sweat
glands.
The prism technique made i t possi
ble to measure the current flow and
number of active sweat glands from
EMG, SNS, reflexes, etc.
W
. ,.
"
I "
, l \ l " .
\ ,'
.
E
L
a:
I
0.
1
Q
60
0
i1
|
.
\
Z
~
W
,.
,/
/
,
,
,
,
,
_I
.
.
'.
,,
M
" 4
u
;:
..
4 5 6 1 8 9
MINUTES
Fig. 3. Relation 0/current /Iow to numbers 0/
active glands (Randall method). Active glands
were counted by Randall iodine-storh-paper
method described in text (I-min. periods) and
current flows were measur at end 0/ ech
period. Continuing high current fow during
/alling gland count phase is referrd to as 'lag'
in the text.
>U
o
<
| Q
o
q
w
0
W
..
q
o
a
!
2
Fg . ..
Currl ~
0|or6 Covr!.. _-
4 5 6
MINUTES
8 9 10
Fig. 4. Relation 0/curent flow to numbers 0/
active glands (prism method). Current fow
mesurements and photographic records 0/
number 0/ active gland were initially made
every 30 sec. A t onset 0/ sweating recordings
were made at JS-sec. intervals. Curent was
recorded immediately ater ech photograph.
periments. The smallest differences
are observed in Rg for the same sub
ject. Differences among subjects are
smallest for the values of Ra and
largest for values of Ro
The poorest correlation observed
to date was in subject HW, expo 19.
Although no explanation can be of
fered at this time, environmental
temperature may have been a factor
in that it was lower for that experi
ment than for any other. Further
s t udi es at l ow t emperat ures
(20-24C) may reveal a basis for
such differences in the conductance
sweat gland relationship as observed
in HW, 19.
31
0
.
o
w
C
2
3
I
0
L
2
EB No 17
5-24 - 55
r+
F
Glond Co.n
fncreosin;
Oecreasinq
10 20 30
ACTi Ve SWEAT GLANDS PER 0.44 Cm
Fig. 5. Corrlation graph for exrimental data
shown in fg. 3. Solid line, A. shows the rla
tionhip of currnt fow to swt gland for
both ring and delning pha ofsweat gland
activity. Dhed line, R. shows relationship
during only ring pha and dotted line, F, for
faling phas. The lines wr also obtained by
method of let square.
i
Fig. 6. Simplied schematic ofskin resistance
circuit. Total resitance of the skin i
rpreented as simplied electricl network. A
variable numbr ofswet gland ar pictured as
a variable number of parallel resistances 0.
R .. . . . Rn ... Rn) in the network. A non
sudoric reitance (RJ also appear in paralel
with swt gland ritance and i reprente
a a variable component in accord with surfac
moitur infunc dicusd in the tet.
The equation from which Re was
obtained implies that for A O, R/
should equal R
Q
However, the actual
ly measured value(R
o
) when no active
sweat glands were present (^ 0)
was in every case much larger than
Re. The relation of these observa
tions to the influence of surface
moisture provided by sweat secretion
or other sources is discussed in the
next section.
Ulwuioa
The physiological signifcance of ESR
gradations is i ndicated by the finding
in different subjects of consistently
l inear relationshi ps between the
number of sweat glands propelling
moisture to the surface and the con
ductance through the skin. The data
suggest that each secreting sweat
gland lowers resistance in two ways:
JI
a) by serving as an added parallel high
resistance in the electrical circuit and
b) through the i nfluence of the
moisture produced on the resistances
of nonglandular tissues.
Magni tude of the average
resistance values (R,) calculated for
single glands from the experimental
data presented is similar to actual
resistances of i ndividual active glands
observed in our laboratory, and in
dependently by others (1 8). The con
cept that sweat glands form parallel
resistances is also consistent with
Darrow's observations (1) that the
conductivity in mhos or micromhos
(reciprocal ohms) was linearly related
to the amount of perspiration. That.
the amount of perspi ration was
generally related to the number of ac
tive glands was indicated by investiga
tions of Hertzman et al. (1 9).
The infuence of surface moisture
on ESR has been demonstrated by
Blank and Finesinger (1 5), by Farmer
and Chambers (20) and was shown by
Rosendal (1 2, 1 3) to be a direct
physical i nfluence of moisture on
nonglandular components of the
skin.
Blank and Finesinger showed that
during prolonged wetting of the elec
trode area the resistance decreased to
reach stable values in 304 minutes
of moistening. A similar time course
has been observed for hydration of
the stratum corneum (21), suggesting
this as one factor tending to decrease
the resistance. The resistance lower
ing i nfluence of surface moisture i s
also due i n part t o a change i n effec
tive electrode radius which occurs
when the tangential resistance of the
skin is decreased (1 5).
Since surface moisture i s produced
in our experiments and since the ex
periments have a duration of 1 0-1 5
minuteSt it appears quite evident that
surface moisture is present as a factor
in our data. A measure of its in
fluence i s suggested by the difference
between the values of Ro and Ra, since
Ro is obtained before, and Ra is the
average value obtained during the ad
dition of surface moisture by sweat
secretion. The same influence would
account for the differences between
the values of Ra calculated for the ris
ing sweat gland count portion of the
experiment, and those calculated for
the falling gland count portion. If the
values of Ro and Ra are affected by
hydration of the stratum corneum
TABLE I. Comparison ofeperimental reults.
Subj. 8m
!I / _ I / "'' R. I
Lxp.
`' Hu.
8, 06
'
I
25 , 5,
I
. 90: 1 I3t
EB, 13 25
3 , 9
:
25 . 6 : 9
1
'4. 1 5 S3 , 90:. 04
All resistance values are in megohms, Ra and
R
g
ar reciprocals of calculated values Oa and
Ow repectively, dics e in the tet, R wa
the rsistance meaured at a time when no ac
tive gland were recorde. Column r give the
Pearon product-moment coeffcient of cor
relation btween the data and a lner curv ob
tained by method of least squares.
"Numbr of measurements of corresponding
swt gland counts and current fows during
each experiment.
tStandard error |=
r
2
2
Where n is the
number of measurements.
they should exhibit some dependence
on i nitial hydration as influenced by
environmental humidity. Although
we have not systematically studied
this variable, in repeated expriments
on the same subject (EB) both Ro and
R" were lower when the humidity was
i ncreased.
It appears, therefore, that under
conditions of moderate environmen
tal humidity, with the direction and
magnitude of applied voltage and
electrode size constant, variations in
resistance of an area of skin in a given
individual are related to variations in
the number of active sweat glands
and to the surface moisture produced
by their activity. The relation of con
ductance (reciprocal ohms) to the
number of active sweat glands is very
nearly linear. A given i ncrement in
conduction thus reflects essentially
the same i ncrement in sudomotor ac
tivity r.gardless of the initial level of
activity. The basis for this observa
tion appears to be that each active
sweat gland contributes a conduction
path that is electrically analogous to
adding a resistance in parallel to the
other sweat gland resistances. On this
basis it appears that ESR is a reliable
i ndex to sympathetic sudomotor ac
tivity.
The tentative i dentification of
sudorific and nonsudorific conduc
tive paths provides a basis for future
investigations into the factors in-
EMG, SNS, reflexes, etc.
fluencing each path. This will further
clarify the combination of factors
determining the electrical resistance
of the skin and permit a more precise
interpretation of ESR gradations
among di fferent individuals and
among various skin areas of the same
individual.
References
\. Darrow. C.W. J. Gen. Pychol, II: 451, 1934.
2. Richter, C.P. J. Neurosurg, 3: 181. 1946.
3. Whelan, F. G. and C.P. Richter. Arch. Neurol. &
Psychiat. 49: 454. 1943.
4. Wagner. H. N .. Jr. Arch. Dermot. & Syph. 65:
543, 1952.
5. Ratcliffe. A. Hall and R.P. Jepson. J.
Neurour. 7: 9, 1950.
6. Thomas. P. E. and I . M. Korr. Electro
encehalog. & Cln. Neurophysiol. 3:361, 1951.
7. Richter. C. P. and Bettye G. Woodruff. Bull.
Johns Hopkins Hosp. 70: 4, 1942.
8. Van Metre. T.E . Jr. BUl. Johns Hopkins Hosp.
85: 4. 1949.
9. Jurgensen, E. Dutsche Ztshr. fklin. Me. 144:
2, 192.
10. Jurgensen, E. Deutshe Ztschr. f.klin. Me.
144: 193. 1924.
1 1 . Jasper. H. and P. Robb. J. Neurosurg. 2: 261.
195.
12. Rosendal. T. Acta physiol. scandinav. 8: 183.
1944.
13. Rosendal. T. Acta physiol. scandinav. 5: 130,
1943.
14. Lewis. T. and Y. Zouerman. J. Physiol. 62:
280. 1926-27.
15. Blank. I. H. and J .E. Finesinger. Arch. Neurol.
& Pychit. 56: 544. 1946.
16. Randall. W.C. J. Clin. Invest. 25: 761. 1946.
17. Netsky, M. G. Arch. Neurol. & Psychit. 6:
279. 1948.
18. Suchi. T. Jap. J. Physiol. 5: 75. 1955.
19. Hertzman. A.B . W.C. Randall. C. N. Peiss, H.
E. Ederstrom and R. Seckendorf. Am. J. Phys. Med.
31: 170. 1952.
2. Farmer, E. and E.G. Chambers. Brit. J.
Psychol. 15: 237. 1925.
21. Peiss. C. N . W.e. Randall and A.B. Hertzman.
Fe. P. 12: 108, 1953.
Reprinted by permission from Journal of Applied
Physiology 10: 505510, 1957.
Patterns of electrical skin resistance
in man* (1958)
IRVIN M. KORR, PRICE E. THOMAS and HARRY M. WRIGHT
About 10 years ago we undertook
electrical skin resistance explorations
upon large numbers of subjects as
part of an approach to the study of
regional and segment-to-segment
variations in sympathetic activity.
During this same period there has
been a great growth of interest in this
field, in localized or segmental
autonomic dystonias and in their
functional and clinical implications,
and many of the investigations have
been reported in this journal. While
the ori gi ns , si gni fi cance and
mechanisms of these segmental devia
tions in autonomic function are as yet
poorly understood, there can be little
doubt of their high incidence and of
their importance. This report, based
on skin resistance explorations upon
several hundred subjects and pa
tients, is intended to be a contribution
to this field.
The validity of the electrical skin
resistance method as an index, at least
under certain circumstances. to sym
pathetic activity seemed well estab
lished by evidence such as the follow
ing:
1 . Electrical skin resistance (ESR)
is related to activity of the sweat
glands 5
,
2
8.
3
0.
32-35 . This relationship has
been quantitatively examined by us 5
0
.
2. Interruption or retardation of
the flow of impulses over sympathetic
pathways to a given area of skin
causes marked elevation of resistance
in that area, whether a) by severance
of pre- or post-ganglionic pathways
24
-2,
33. 38.
39. 41 ; b) lesions of the spinal
cord
32
; c) by peripheral nerve lesions
Z, J, Z, J. 7-
36. 37 ; d) or by pharmacologic
blockade', 4.
3. Stimulation of sympathetic
pathways either locally or systemical
ly lowers the resistance
, Z, ZJ, Z, ZY, J, J,
J"- J, J&-34
*
4. Although demarcation of
(anhidrotic, high-resistance) areas to
which the sympathetic supply is inter
rupted is sharpest when done in a
"These investigations were supported in part by
grants from the National Institutes of Health. Public
Health Service (B29 and H1632), and from the
American Osteopathic Association. and by a contract
(Nonr 243(0)) with the Office of Naval Research.
background of sweating (low resis
tance) induced by heat or diaphoretic
agents, the above relations among
ESR. sweat glands and sympathetic
activity hold whether or not there is
the frank appearance of perspira
tion
10.
26.
3
0.
5
0
.
Since our concern was with
topographical gradations in sym
pathetic activity, especially with the
possible incidence and distribution of
areas manifesting exaggerated sym
pathetic activity and their possible
relation to segments of low motor
reflex threshold, we turned to the
study of skin resistance patterns
under cool, resting conditions in
which visible sweating did not occur
and in whi ch resi stance was
predominantly high.
It is shown in this paper that low
resistance areas (LRA) are found in
apparently normal individuals, that
the distribution of these areas varies
from individual to individual and that
the segments of the trunk in which the
LRA predominate may remain con
stant in a given individual for long
periods of time. It is of interest to
note the parallelism (though no direct
relationship is yet established) to the
observations of Dens/ow and his co
workers 7. 8 on intersegmental varia
tions in motor refex thresholds. In
electromyographic studies on refex
responses of the spinal extensor
muscles, they found, in most sub
jects, one or more segments which
were distinguished from the others by
markedly reduced motor reflex
threshold and in which motoneurons
( supplyi ng the paravertebral
musculature) were apparently main
tained in a chronic state of facilita
tion. Patterns of distribution of the
low-threshold segments varied among
subjects but were highly constant for
each.
Although most of the data on
which this report is based have been
available for several years, we have
withheld publication until we could
assure ourselves that the regional skin
resistance differences were related,
not to some random variation in skin
quality or in sweat gland distribution,
33
but to significant functional dif
ferences. Through an extended series
of investigations (to be cited later)
regarding the nature, origin and basis
of LRA, we have become convinced
that they represent neurophysio
logical phenomena of considerable
interest and are worthy of further in
vestigation. Low-resistance areas
seem not to have been systematically
investigated except as reflex
manifestations of painful conditions
or visceral disturbances (see Discus
sion). This and another recent paperso
are the frst full reports of this series
of investigations; they are intended to
introduce the phenomena for further
study.
Methods
Since the explorltions represented in
this paper were done over a period of
several years, a variety of methods
are also represented which were
developed and applied during that
time. These are described in this sec
tion. The conventional principles of
resistance measurement are, however,
common to all three methods de
scribed.
Essentially. each method consists
of measuring or recording, in correct
spatial relationship to the explored
'
area, the momentary current flow
through skin in contact with the con-
standy moving exploring electrode, at
known voltagest. The voltages are
tapped stepwise from a series of dry
cells and applied to an electrode fixed
to an earlobe and an exploring elec
trode. Resistance of the skin of the
earlobe is minimized and stabilized by
means of a needle puncture or by ap
plication of electrode paste. Area-to
area differences in current flow at a
given voltage, therefore, are due to
differences in the "resistance" of the
skin under the exploring electrode.
In view of the multiplicity of
unknown physical factors and "cir
cuitry", such as polarized interfaces
and membranes, capacitances and
critical potentials, which determine
current flow through the skin at
various applied voltages, there seems
to be little advantage in converting
the primary measurements of current
and voltage to an inferred quality
identified as "resistance" and
measured i n ohms. The term "elec-
tIn this way secondary excitatory or polarization
effets of the current are minimized or eliminated
(Rihter").
3
trical skin resistance" (ESR) has
achieved such wide usage, however,
that it would seem unwise to in
troduce new terminology, provided it
is borne in mind that the patterns
presented here are graphic representa
tions of current fows through dif
ferent areas at constant, specified
voltage.
A. The Dermometers. 1 . Explora
tions with Hand-Held Electrode. In
our earlier studies we employed an in
strument basically 'imilar to that
described by Jasperl 4. Current flow is
read from a microammeter as the
electrode is moved over the subject' s
skin.
2. Automatic Explorations. In
order to minimize the sources of
error, the slowness, the inconvenience
and other objections to the above
method of ESR explorations, a nearly
automatic dermometer was developed
which photographically records ESR
patterns on large areas such as the
trunk'.
The automatic dermometer con
verted differences in current flow
through the skin at constant voltage
into variations in the brightness of a
light source. By placing the light
source directly over the exploring
electrode, and by propelling the elec
trode over the skin at constant speed,
a properly positioned camera, with
shutter open, recorded strips of light
which varied in brightness according
to the ESR (i. e. current fow) dif
ferences along corresponding strips
of skin. To explore a large area, a
series of consecutive parallel strips is
recorded.
More recentlySl we have developed
a simplified, more convenient and
mobile adaptation of the automatic
dermometer which eliminates the
need for photographic procedures,
constant speed and optical alignment .
The skin resistance patterns are
recorded directly on paper by a re
cor di ng gal vanomet er whos e
amplitude of oscillations is related,
through an amplifier, to the skin cur
r ent . The pos i t i on of t he
galvanometer writing-point on the
chart is related to t
h
e position of the
exploring electrode on the subject by
means of a pantograph.
Results obtained with all three
methods are presented in this report.
B. Exploration Procedure. 1 . Ex-
ploration Conditions. Explorations
are conducted in a quiet room main
tained between 23 and 25C. The
subject undresses the area to be ex
plored. The studies shown here have
been mainly on the back. Before
beginning the exploration it may be
necessary to permit the general
resistance (see later) to become
stabilized, since it may continue to
rise for a while with cooling or with
rest. Explorations are conducted with
the subject either lying prone on a
padded table with a face slot, or
seated comfortably on a stool with his
forearms resting on a table.
2. Sel ecti on of Expl orati on
Voltage. After marking the tips of the
spinous processes as landmarks on
the skin, the exploration voltage is
selected according to the subject's
general level of resistance. This is
done by applying increasing voltages
(from 1 , 5 to 1 8 volts) while sampling
the different areas of his back with a
touch of the electrode and determin
ing that voltage which keeps max
imum (momentary) current flows well
within the 50-microammeter range of
the meter (20 - 30 "a.) Under these
conditions most of the skin of the
trunk permits barely detectable cur
rent fow or none (1 "a or less).
In this way the low-resistance areas
are sharply distinguished and graded,
according to the method employed,
by large excursions of the microam
meter needle (hand method), dim
ming of the light source on the photo
graphic dermometer, or widened
excursi ons of t he osci l l at i ng
galvanometer of the pantographic
dermometer. By properly selecting
the exploration voltage in such a way
that the maximum range of current
variations is the same in all explora
tions regardless of the general
resistance level, it is possible to com
pare and grade areas in the same sub
ject or in different subjects according
to current fow - or as fractions of
the general resistance.
Regar dl es s of t he met hod
employed therefore, the method con
sists of the mapping (and grading) of
islands of low resistance (high current
fow) in a general background of high
resistance (minimal current flow),
under conditions of rest.
3. Exploring and Recording. Ex
plorations by hand were conducted in
a manner similar to that described by
Richter40 for the mapping of
EMG, SNS, reflexes, etc.
v0 2 1048
:o45uV
20
30
." --
, /
\ * . +
.
7
Figs. 1-3
anhidrotic areas in the sweating
patient. The areas of low resistance
revealed are recorded on standardized
body charts such as that shown i n
Fig. 2a and 3a. The relative resis
tance values are graphically repre
sented on the charts by shading of
the correspondi ng areas . Areas
which permit the flow of no more
than I pa at exploration voltage as the
electrode passes over them are left un
shaded; those which permit a momen
tary flow of 20 pa or more at the ex
ploration voltage are recorded i n
black. The intermediate values are
-lS-4S
*PY
divided among four shades of gray.
I n e x pl or a t i on s by t h e
photographic method, the ESR pat
terns are recorded on fil m and appear
in montage on a photograph of the
subject taken immediately upon com
pleting the exploration. The black
and white areas represent the same
current flows as described above for
the charts, but the intermediate
values may be estimated by com
parison with the calibration strip
which appears i n each photograph,
and which shows 5 pa steps i n shading
from 0 to 22. The current flows can
'
Figs. 4-6
be estimated di rectly from the pan
tographic charts also. In these,
however, the amplifier has been ad
j usted so that the widest oscillations
(producing the darkest area on the
chart) represent 30 p. a. The explored
area is shown, in each chart, in cor
rect spatial relation to a pantographic
tracing of the body outline.
If desired, resistance or conduc
tance (Darrow') values for any areas
in any of the charts may be estimated
from the exploration voltage stated
on each chart and the current flow in
dicated by the recording method.
J5
......
Uy
.o G.
.
|
\
J. G.
"-22-41
| |~ | 0~
1 2 V
Figures 1 -8. Illustrating individuality ofESR pallems and the constancy ofsegmental distribution oflow-resistance areas in 8 subjects. Note the periods
intervening between succeeding explorations for each subject.
As described in text, explorations have been done with 3 different methods:
I. Hand-held electrode: Figs. 2a, 3a, 5a, 7a, 7b, 8a;
2. Photographic recorder: la, Ib, 2b, 3b, 4a, 4b, 5b, 7c, 8b;
3. Pantographic recorder: 6a, 6b, 8c.
In all figures dark areas represent low-resistance areas of skin on back. Darkness of shading in hand-drawn charts and in photographic records is in
proportion to current flow at exploration voltage; the darker the area the lower the resistance. White areas: I} or less; (resistance, in ohms, at least I
million time the number ofvolts); black areas: 20pa or more; i. e., less than 1/20 ofbasic resistance; gray areas: intermediate values. (Reproduction of
these figures has darkened the gray areas and the darker shades have become indistinguishable from the blatk areas.)
In the pantographic records (Figs. 6a, 6b, 8c) amplitude ofoscillations ofthe recording galvanometer are related to current flow through the skin. The
thin vertical fines (no oscillation) represent areas permilling 0 to Ipa a/ exploration voltage; widest oscillations represent current flows of 30pa or more.
In these charts, therefore, the darkest areas represent 1/30 the basic resistance or less.
Tps of spinous processes and the sacral base are marked in photographic and pantographic charts. Also note calibration "strips", showing relation
between current and amplitude of oscif(ations (pantographic method) and between current and shading (photographic method), in step of5Ja.
Resulls
A. Individuality oj ESR patters.
Figs. 1 to 8 represent explorations
conducted on 8 di fferent subjects and
J0
illustrate the diversity of patterns
which are obtained. In our explora
tions of hundreds of subjects we have
not found two identical patterns,
although certain features may occur
i n common, as in certain painful
visceral disturbances and although
low-resistance areas occur wi th
EMG, SNS, reflexes, etc.
significantly higher frequency in
some regions (e. g. , lumbar) than i n
others.
B. Reproducibility of Segmental
Patterns. Explorations conducted
upon the same subject at different
dates are also shown in Figs. I to 8. I n
these subjects, as i n most of those
who were repeatedly explored over
long periods of time, the distribution
of the areas of low resistance showed
a high degree of reproducibility; that
is, the location and arrangement of
the predominant areas, with respect
to segmental levels and left and right
sides, remained remarkably constant
(more than 2Z: years in the case of
L.C. , Fig. 5 and almost 4 years for
J. G. , Fig. 8) .
C. Variations of Individual Pat
terns. "Reproducibility" of patterns
in no sense, however, implies fixity or
constancy of the sizes and shapes of
the low-resistance areas or their
resistance values, nor does it imply in
variable presence of these areas and
the absence of all othersi. As is well
known, ESR is an extremely labile
feature, subject to numerous and sub
tile influences. Nevertheless, despite
this lability, repeated "sampling" of
the patterns of each of many subjects,
during a given day or over periods of
weeks and months, reveals that in
each subject there are certain zones or
segmental levels and sides in which
the probability of finding low
resistance values (that is high current
flows), relative to the general levels, is
far greater than that in all other
areas. Of these, some show a higher
probability than others so that parts
of a given subject's "pattern" may be
absent from time to time while others
are found in virtually every explora
tion.
Furthermore, the recurrent areas of
l ow resistance, that i s, the "high
probability" areas, form a pattern of
distribution which is characteristic
for the subject. Although other areas
of low resistance occur, even under
the conditions of our explorations,
not only are they relatively infrequent
and evanescent, but they are also ap-
tTwo charts of subject J. H. (Fig. 7 a, b) were especial
ly selected to illustrate variations in shape, size, loca
tion and resistance values of LRA while the segmental
levels and sides on which they occur remain essentially
unchanged. Note that in the lumbar area the main di f
ference between the first two charts is in the degree of
spread from the midline .
0
Fig. 9. Apparent dermatomal strips oflow resistance.
parently random, fol l owi ng no
discernible or reproducible pattern.
Toward a better understanding of
the nature of t he patterns and of our
criteria for the determination of
"pattern", it is of interest to review
the range of variations in ESR and in
area-to-area di fferences that may be
seen in the course of a single session
of serial explorations.
D. Transitional Changes in Pat
ter. I n cool weather, in which skin
resistance (of the clothed subject) is
moderately high, the areas of low
ESR are us ual l y i mmedi at el y
distinguishable upon bringing a sub
ject into the laboratory for explora
tion, and many remain so for periods
of hours. In warm weather or follow
ing physical exertion, excitement etc. ,
the resistance of the skin of the trunk
is generally low, even though there
may be no visible perspiration, and
gradually climbs for some time after
tqe subject reclines in the cooled
room. During the period of low
resistance the application of even the
lowest exploration voltages of the
dermometers ( 1 , 5 or 3 volts) produces
large current flows throughout the ex
ploration area, rendering impossible
JT
the differentiation of relatively low
and high-resistance areas. (With the
use of fractions of a volt, however, it
is possible to demonstrate, even
under sweating conditions, large
area-to-area differences in current
flow30.)
As the subject rests, with the ex
plored area exposed, there is a general
progressi ve el evati on i n s ki n
resistance, i n which certain areas lag
far behind others, and a pattern of
relatively persistent low-resistance
areas emerges. That is, most of the
areas of the trunk cease to pass more
than 1 pa at the low exploration
voltages, while certain zones, whose
pattern of distribution is character
istic for the subject, still conduct
large currents at the same voltage.
With continued rest and cooling
there may be further general increase
in resistance so that at low explora
tion voltages there may be no ap
parent current through most of the
skin and only a few microamperes of
current through the low-resistance
areas. An increase in voltage re
establishes the wide differential and
the pattern of low-resistance areas re
emerges. It is of interest to note that,
in general, progressive increase in
resistance during rest and cooling
proceeds from the periphery cen
tralward, so that areas of low
resistance appear to contract toward
the midline.
Eventually there is stabilization of
the basic resistance and no further in
creases in voltage (beyond 6 to 9 volts
for most subjects) are required for the
demonstration of resistance dif
ferences. In this manner, despite the
large changes in absolute values,
areas of relatively low resistance may
remain differentiable over periods of
2 or more hours, although there is
usually a reduction in their size dur
ing this period and some LRA may
vanish entirely. The first areas to
disappear are those which, in
preceding explorations, had shown
only small or moderate current flows
(e.g., 3 to 5 p), that is, those which
would have appeared in gray on
preceing charts.
We have repeatedly observed the contraction and ex
pansion towards the midline under many cir
cumstances. including experimental procedures. rest
and fatigue. cooling and warming of the subject. etc.
These appear similar to observations by Richter and
Wo on changes in facial patterns of low
resistance.
38
With prolonged rest, especially at
lower temperatures, there develops an
almost uniformly high resistance in
most subjects and only small rem
nants of the original pattern may be
distinguishable within the voltage
range of the dermometers. The most
persistent areas are those which
showed large current flows under the
usual ircumstances of our explora
tions. They also show early and large
decreases in resistance upon re
warming the subject.
Of greatest interest in this connec
tion is the fact that those low
resistance areas which are differen
tiable in each subject for the longest
time during a period of rest and cbol
ing, as shown by serial explorations
during such a period, are also the
ones which occur with highest fre
quency in occasional "samplings"
over periods of weeks and which con
stitute the dominant features of the
subject's "pattern".
It should be pointed out that
although most subjects show a basic
stability or reproducibility of pat
terns, conspicuous changes have been
observed to occur spontaneously in a
number of subjects whose patterns
had been followed over periods of
months or years, and others have
been experimentally induced. The
origins and character of these changes
will be examined in a later paper.
E. Possible Segmental Basis jor the
Patters. A segmental basis for at
least some low-resistance areas is sug
gested by the frequent presence of
"strips" of low resistance which ap
pear to have dermatomal distribu
tion. Such strips are apparent in both
explorations of Fig. 2 and in Fig. 7 b.
Fig. 9 illustrates other strips that have
been observed; the strips may extend
from spine to sternum and occa
sionally encircle the trunk. In ex
perimental studies y to be reported
more fully elsewhere, we have also
been able to induce new low
resistance areas which show distinctly
dematomal arrangement .
Discussion
It appears from these studies that the
reproduci bl e patterns of low
resistance areas demonstrable on
human subjects consist of those areas
of skin in which the probability of
finding relatively low resistance
values at any time is much greater
than for skin at other segmental levels
or sides. This high probability is
based on the fact that in these areas
the low resistance is most persistent
under conditions which tend to
elevate skin resistance, and because
their resistance decreases earlier and
to lower levels under conditions
which tend to lower it.
In effect, each occasional explora
tion of a subject over periods of
weeks or months is the "catching" of
a pattern at one stage or another of a
transition from generally low levels of
resistance towards geneally high
levels or vice versa. The high
reproducibility of each subject' s pat
terns of low-resistance areas is related
to the high probability with which the
resistance of those areas will have
dropped in advance of others and
stayed low after the others have risen.
In short, the "low-resistance areas"
are those which are present for the
longest period during each transition
and therefore the most likely to be
found in occasional samplings.
On the basis of the findings
described by Thomas and Korrso and
others cited in the introduction, it
would appear that low-resistance
areas are those in which, at the time
of measurement, a) secreting sweat
glands, serving as parallel high
resistance pathways through the skin,
are present while none are active in
other areas, b) are present in larger
numbers or c) in which larger
amounts of residual moisture (from
past secretory activity) are present.
It would appear that one of the
chief reasons that these regional
variations in the ESR of the trunk
have been previously missed or
disregarded, despite the very large
numbers of subjects that have been
explored in many laboratories and
clinics, is that the 2- to 20- or 30-fold
differences in resistance upon which
our patterns are based, are small in
comparison with the approximately
thousand-fold resistance-variation of
which human skin is capable. Thus,
for example, the resistance of cool,
dry skin is ordinarily treated as
uniformly high (tens of millions of
ohms) and that of sweating skin as
uniformly low (tens of thousands of
ohms), with "negligible" variations
at each level.
In contrast, our procedures and,
therefore, our fndings are based on
the following principles:
EMG, SNS, refexes, etc.
1. We examine the area-to-area
vari ations around the general
resistance l evel found in the par
ticular subject at the time of explora
tion. In this way the differences in
level from subject to subject, and
from time to time and season to
season in the same subject, are "buf
fered" out. This is comparable to the
study of moment-to-moment varia
tions around a general resistance level
in selected areas, as in psychogalvanic
studies.
2. We conduct the explorations
under conditions (the subject resting
in a cool environment) in which the
general resistance level is moderately
high or gradually risi ng, thus
sharpening the differentiation of the
"residual" relatively low-resistance
areas. That is, by avoiding the "level
ing" extremes of very low resistance
(sweating) and very high resistances
(chilled s ubjects) gradations i n
res i s t anc e are most cl ear l y
demonstrated. We were, nevertheless,
able to demonstrate patterns of ESR
variations over a wide range of
resistance levels, i ncluding the low
val ues associ ated wi th acti ve
sweating.
3 . Exploration voltage is adjusted
to the general resistance level in such
a way that the range of current varia
tions is fairly constant and indepen
dent of the general resistance l evel.
When this is done precisely, then
areas showing identical current flows
become equivalent regardless of their
absolute resistance values. That is, a
given current represents the same
fraction of general resistance (or the
same multiple of general conduc
tance) whatever that level may be,
regardless of the subject, the season
or the circumstances.
We have found, however, that, for
purpose of demarcation of patterns
of low-resistance areas, the proper
selection of exploration voltage,
though important, is not critical.
Thus, changes of 3 or more volts only
affect the range of current variations
(and the darkness of shading of the
charts) without signi ficantly affecting
the patterns.
Isolated in this manner from the
I n more recent experiments" to be reponed more
fully elseswhere. we have been able to demarcate the
ESR patterns within a total range of current variation
of 2/1. through the use of low exploration voltageS
and appropriate D.C amplification. (Compare
Levine", Whelan").
gross l evel-to-Ievel changes, these
smaller variations in ESR at any given
level assume a larger quantitative
significance. Though in ordinary
resistance measurements they sum
algebraically with the basic or general
resistance, the smaller ESR variations
show considerable independence of
the basic resistance level. This sug
gests the possibility that the factors
which determine the area-to-area dif
ferences here reported (and perhaps
also those determining psycho
galvanic fluctuations) are different
from those determining the general
level at which those variations take
place - in the same sense that the
coarse and fine adjustments of an in
strument may be separate - and
quite different - mechanisms whose
actions are algebraically additive.
More direct evidence for a duality of
basic factors is reviewed by Thomas
and Korr' O It is interesting to note
that Regelsberger27 also ascribes his
electrodermatograms to a combina
tion of factors.
At any rate, there can be little
doubt of the reality of the ESR pat
terns and of their relation to physio
logic variables. Their very existence
and reproducibility, as well as their
changes with experimental and
clinical variables, raise fundamental
questions regarding their physiologic
basis and significance that demand
answering.
Studies by many investigators,
cited in the i ntroduction to this
paper, appear to have established
quite firmly that ESR is related to
s ympathetic acti vi ty expres s ed
through the sweat glands; i nterrup
tion or retardation of the flow of im
pulses over sympathetic pathways
elevates ESR, while sympathetic
stimulation reduces it. Since the
reproducible, long-term area-to-area
differences in ESR reported here were
in no way related to any apparent
s ti mulation or i nterruption of
selected sympathetic pathways, i n
teresting questions were raised re
garding their origin, basis and func
tional implications.
Although the ESR patterns
themselves permit no firm conclusion
on this point, the observations by
other investigators referred to above
on the relation between sudomotor
(sympathetic) activity and ESR, as
well as our own observations on the
relation between ESR and sweat
gland activity'O, suggested that the
patterned differences in ESR, as
measured by us, were also related to
patterned differences in sympathetic
activity.
A possible reflex origin of LRA (as
well as of other cutaneous manifesta
tions of local sympathetic hyperac
tivityl . ' 9, 46) has been indicated by
several investi gators who demon
strated the segmental or topographi
cal association of areas of hyper
hidrosisl l . of low skin resistance
S
4
or of alterations of other electrical
properties of the skin24 27, 45 with
painful conditions and visceral dis
turbances. (Also see comments by
Richter 41 on low-resistance areas
associated with lung infections and
pleurisy.)
In view, therefore, of the possible
physiologic and clinical implications
of the persistent areas of low resis
tance, such as those described here,
we have undertaken extensive investi
gations i nto their nature, basis and
significance during the past few years,
some of which have been described in
preliminary reports to the American
Physiological Society. In these in
vestigations we have examined the
relation of ESR to measured sweat
gland activity4
8,
7
compared the
functional responses of l ow- and
high-resistance areas to a variety of
stimuli and under a variety of cir
cumstances49, experimentally modi
fied ESR patterns and induced new
LRA
1
9, examined segmental and re
gional correlation of low-resistance
areas with other (vasomotor neuro
muscular and sensory) features
1 7
. 2, S6
and with clinical and experimentally
induced disturbances
1 8, 1
9 .
These s tudi es , which wil l be
reported more fully i n succeeding
papers, have convinced us that the
persistent areas of low skin resistance
do have i mportant functional and
cl i ni cal i mpli cati ons related t o
regional variations i n excitability of
autonomic pathways which merit fur
ther investigation. These changes in
excitability appear to be parallel to
those indicated for motoneurons by
the st udies
7
8 on motor refl ex
thresholds cited i n the introduction to
this paper. However, because of the
uncertainty of relationships between
s ympathetic dermatomes and
paravertebral myotomes, it has not
yet been possible to determine the
relationship of LRA to low-threshold
J
segments, although some common
origins are indicated.
Summar
1 . As an approach to the study of
regional or segmental variation yi n
sympathetic activity, skin resistance
explorations were conducted on the
backs of several hundred subjects
under resting, non-sweating condi
tions.
2. The methods used included the
conventional exploration with hand
held electrode and two semi
automatic recording methods.
3 . The following principles
characterize our methods:
a) Momentary current fow is read
or recorded. in correct spatial
relation to the explored area, as
the exploring electrode moves
over the skin, while a constant
voltage is applied.
b) Area-to-area variations in resis
tance upon the general
resistance level found i n the sub
ject at the time of the explora
tion, are determined.
c) The explorations are conducted
under conditions i n which
resistance is generally high or
rising.
d) Exploration voltage is adjuste
according to general resistance
level in such a way that the
range of current variations is
fairly uniform, regardless of the
general resistance level.
4. Areas sharply differentiated by
low resistance (high current) values
were found in all subjets, The pat
terns of distribution varied from sub
ject to subject.
5. Repeate "sampling" of pat
terns revealed that the patterns of
segmental distribution of the relative
ly low-resistance areas were highly
reproducible and characteristic for
each subject, often over periods of
many months, and despite large
changes in the general resistance
level.
6. It is shown that the patterns con
sist. not of skin areas "fixed" in low
resistace, but of areas (segmental
levels and sides) in which the pro/.
ability of finding low resistance
values (high current fow) as com
pared with the general resistance at
any time is high. As compared with
al other areas of skin, these areas
show much larger and earlier
decreses in resistance in transitions
4
from generally high to generally low
levels of resistance; the low resistance
values are much more persistent in
these areas in transitions from
generally low to generally high levels
of resistance.
7. It is suggested that the factors
which determine the area-to-area dif
ferences in resistance may be dif
ferent from those which determine
the much larger variations in general
resistance level.
8. A segmental origin of at least
some of the low-resistance areas was
indicated in the frequent presence of
apparently dermatomal strips.
9. The relation of ESR patterns, as
measured here, to regional variations
in excitability of autonomic pathways
is briefy discussed.
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mobile instrument for recording electrical
skin resistance patterns of the human
trunk* (1958)
PRICE E. THOMAS. IRVIN M. KORR and HARRY M. WRIGHT
Measurements of regional or segmen
tal variations in the electrical resis
tance of the skin are frequently used
to study regional or segmental varia
tions in sweat gland activity and
therefore in activity of sudomotor
fibers of the sympathetic nervous
system. See Richter7 and Korr.
Thomas and. Wright4 for feferences.
Areas of relatively low resistance
found in these investigations appear
to be those in which, at the time of
measurement, a) secreting sweat
glands, serving as parallel high-resis
tance pathways through the skin, are
present while none are present in
other areas, b) are present in larger
numbers, or c) in which larger
amounts of residual moisture (from
past secretory activity) are present
(Thomas and Korr9 10; Thomas,
Wright and Hartl
I
)
_
Information obtained by electrical
skin resistance (ESR) measurements,
therefore, has been found applicable
to investigations on the peripheral
sympathetic alterations accompany
ing trauma, surgical procedures,
painful syndromes, visceral diseases,
spinal cord diseases, and experimen
tal procedures (Korr, Thomas and
Wright',' Katsuki and Wake'; Korf. 3;
Ratclife and Jepson!; Van Metre' 2).
A commonly employed method for
obtaining ESR values is by applying a
voltage and measuring the current
fow between a fixed indifferent elec
trode moistened with conducting
paste and a handheld exploring elec
trode. The "resistance" may then be
calculated according to Ohm's law.
The current is usually kept small
( 1 -30 Ita), and the contact of the
electrode with a local area of skin,
brief, to avoid stimulating or polari
zation effects (Richter6). The topo
graphic distribution (pattern) of ESR
These investigations were supported in part by grants
from the National Institutes of Health, Public Health
Service (B29 and H- 1 632l. and from the American
Osteopathic Association, and by a contract (Nonr
243[0]) with the Office of Naval Research.
variations is recorded on standard
ized body charts by differences in
shading.
Exploration "by hand" is slow,
does not permit following rapid
changes in pattern and requires
considerable practice. We have
previously reported the development
of a faster, more convenient and ob
jective method for mapping ESR pat
terns, involving semi-automatic ex
ploration and photographic recording
of ESR variations on the human
trunk (photorecording dermometer,
Thoma and Korr'). The patterns of
resistance variations were superim
posed, by double exposure technics,
on photograph of the subject's ex
plored area. This apparatus greatly
facilitated investigations of ESR pat
terns and their significance. The need
remained, however, for an instru
ment which fulfilled the following re
quirements.
Us usable in a well-lighted room.
2. Records skin current variations
(ESR) directly on the chart and makes
the pattern immediately available for
study without the need for photo
graphic processing.
3. Requires less time for the entire
procedure (exploration and recording
landmarks) .
4. Is easily moved from room to
room, e. g. , for studies on hospital
ized patients.
5. Operational procedures should
be simple enough that very little train
ing of operators is required.
This paper describes a new instru
ment which meets these requirements.
The type of record obtained is seen in
Fig. 1 . The skin current variations ap
pear as a pattern on an outline of the
subject' s explored area.
Principles of operation
The basic principle is the conversion
of variations in skin current into vari
ations in oscillation amplitude of a
recording galvanometer. By coupling
the galvanometer to the exploring
electrode, through a pantograph arm,
the records inscribed on stationary
41
J B 3-16-55
24" C 18V
I
/, 1 1 1
I
t I
.. '.h.
l : w
'-:<t l
t5P-THEPV0P AMHFER
Fig. 4. Schematic of converter ampliier and associated circuits. The choppr input converts the
dirct currnt /owing through the skin into 60-cycle alterating current. This circuit also include
the calibration and controls for recording from thermocouples. Resistances are given in kilohms and
capcitance in microfarads.
4
"
o
I
u
.
o
&
.
"
o
I
u
42 ! 25
LIcft008 8#aa 0 |B cm,/ #a ,
Fig. 5. Inuence of variations in exploring
speed on recorded current /ow. This compares
records obtained from the same strip ofskin at
the various eletrode speeds indicated. Thee
were obtained by fiing the eploration path of
the electrode and moving the chart paper
laterally ater each pass of the eletrode. The
records were obtained approximately 30
seconds apart. Note that even a thre-fold
variation in electrode speed produces very little
diference in the magnitude ofrecorded current
flow. Even with a 5-fold change in eploration
rate the areas ofrlatively high currnt /ow r
main distinguishable although their recored
value are much smaler.
but with no galvanometer oscilla
tions. The inscription on the chart of
all pertinent data regarding the sub
ject, experimental conditions, etc.
completes the exploration.
Special adaptations
Hinges on the cabinet top permit the
entire pantograph and galvanometer
assembly to be positioned vertically.
With the addition of counterweights
and a special exploring electrode at
tachment (Fig. 3 B) the instrument is
useful for recording patterns of
standing or sitting subjects.
This instrument has wide applica
bility in recording the topographic
distribution of many phenomena,
limited only by the ingenuity required
in devising exploring "pickups" or
transducers. In our laboratories an
exploring thermocouple has been
used to obtain skin temperature pat
terns on the trunk.
Sources of error
Two possible sources of error are evi
dent, both of which are minor and do
not seriously interfere with mapping
ESR patterns. One error results from
the vertical travel of the electrode be
ing an arc rather than a linear motion
at right angles to the plane of the pan
tograph movement. The recorded
topographic relations are, therefore,
slightly distorted. Correct compara
tive relationships can still be main
tained if the exploring electrode is
used as a guide and touches the skin
surface when topographic landmarks
are being recorded. The weight,
constant-pressure, and handling char
acteristics of the electrode assembly
(Fig. 2, B) are satisfactory enough to
make the small error acceptable. The
electrode assembly (Fig. 3, B) devised
for explorat
i
ons of standing or sitting
subjects does eliminate this error and
with some modifcations in weight
would also be satisfactory for ex
plorations of prone subjects.
The other source of error to be con
sidered is due to excessive variations
in exploration speed. This has been
discussed in a previous section (E
ploration). This error is readily
minimized by a little practice in the
exploration procedure.
Summary
1. A mobile instrument for exploring
and recording the topographic distri
bution of ESR on the human trunk
EMG. SNS, reflexes, etc.
has been described. Explorations are
rapid and the record is immediately
available.
2. Topographic relations between
the exploring electrode and a movable
direct recording galvanometer are
established by a pantograph linkage.
3. Variations in current flow at a
fixed voltage ("resistance") along a
strip of skin are recorded on sta
tionary chart paper by variations in
the oscillation amplitude of the mov
ing, recording galvanometer. The
ESR patterns of large areas are re
corded by exploring a series of paral
lel strips of skin.
4. The apparatus is adaptable for
recording the topographic distribu
tion of cutaneous features other than
ESR.
5. Sources of error are identified
and their minimization or corrections
are described.
Rcfcrcncc
I. Katsuki. S o and K. Wake. Clinical studies on the
viscero-cutaneous reflex. Kumamoto Med. J. 6 (1954).
97 - 107.
2. Kor. I. M o Skin resistance patterns associated
with visceral disease. Fed. Proc. 8 (1949). 87.
3. Korr. I. M Experimental alterations in segmental
sympathetic (sweat gland) activity through myofascial
and postural disturbances. Fed. Proc. 8 (1949). 88.
4. Korr. I. M + P.E. Thomas and H.M. Wright. Pat
terns of electrical skin resistance in man. (Submitted
herewith to Acta neuroveget Wien.)
5. Ratclife. A. Hall and R.P. Jepson. Skin
resistance changes in the lower limb after lumbar
ganglionectomy. J. Neurosurg Springfield. 7 (1950).
9 - 105.
6. Richter. c.P o and Bettye G. Woodruff Changes
produced by sumpathectomy in the electrical
resistance of the skin. Surgery 10 (1941). 957-970.
7. Richter. c.P.. Instructions for using the
cutaneous resistance recorder or .. Dermometer" on
peripheral nerve injuries. sympathectomies and
paravertebral blocks. J. Neurosurg.. Spingfield. 3
(1946). 1 81 -191 .
8. Thoma. P.E = and I.M. Korr. The automatic
recording of electrica skin resistance patterns on the
human trunk. EEG Clin. Neurophysiol. 3 (1951).
361-368.
9. Thoma. P. E o and I.M. Korr. Significance of
areas of low ESR. Fed. Proc. II (1952). 162.
10. Thomas. P.E o and I.M. Korr. The relationship
between sweat gland activity and the electrical
resistance of the skin. (In press: J. Appl. Physiol. .
Wash o JO (1951). 305-310.
I I . Thoma. P. E o M. Wright and C. W. Hart. ir o
Relatjon of sweat gland recruitment to ESR. Fed.
Proc. 12 (1953). 143.
12. Van Metr. T. E.. ir. . Low electrical skin
resistance in the region of pain in painful acute
sinusitus. Bull. Johns Hopkins Hosp. 85 ( 1949).
40-4 1 5.
Reprinted by permission from Journal of Neural
Transmission 17: 7. 98-10. 1958.
08 8R0 t6g0R8 V8t80R8 R
u8Rc0u8 V880m00t 0R6 0 h6
hum8R tuRK" (1900)
H. M. WRIGHT, l. M. KORR, and P. E. THOMAS
These studies have been concerned
with regional and segmental varia
tions in sympathetic vasomotor tone
in normal human subjects. Broad re
gional differences in cutaneous vaso
motor tone and in vascular responses,
as shown by differences in the blood
fow, the blood content, the skin col
or and skin temperature, . e. g. , be
tween face, trunk and extremities,
have been recognized for many years.
That regional or segmental differ
ences in cutaneous vascular tone
might normally exist over the topog
raphy of the trunk, related to the
segmental innervation of the skin, ap
pears, however, never to have been
systematically investigated. It appears
to be generally assumed that vascular
ity and vasomotion are uniform
throughout this skin areal
-
3 Several
observations suggest, however, that
there may be consistent topographical
differences in cutaneous vasomotion
and other functions controlled by the
sympathetic nervous system.
a) Cardiovascular adjustments to
the erect posture.
The changes in hemodynamics which
result from a change of body position
from the horizontal to the erect posi
tion evoke adaptive responses of the
peripheral vessels which vary accord
ing to their level in the longitudinal
axis of the body. On assumption of
the erect posture, there is evidence of
a greater vasoconstriction in the
lower part of the trunk and the lower
extremities - structures innervated
by the more caudal segments of the
spinal cord - than in the upper ex
tremities - structures innervated by
the more superior segments of the
spinal cord4-9
b) Segmental differences in the
responses ofthe cutaneous vessels to
stimuli.
Di Palma3 has observed that cutane
ous blood vessels of various regions
of the skin may respond differently to
various types of stimuli according to
their segmental innervation. He has
shown the existence of a positive gra
dient in reactive hyperemia following
local ischemia, from the third cervical
to the fifth sacral dermatome: the
more caudal the segment, the higher
were the thresholds for reactive
hyperemia. Thesholds were measured
by the duration of ischemia just re
quired to elicit a standardized hyper
emic response.
c) Segmental diferences in the skin
temperatures.
A segmental gradient in the skin
temperatures from the cervical to the
ffth sacral segment was also ob
served by Di Palma3: the more caudal
the segment, the lower the skin tem
perature throughout the thoracic and
lumbar segments.
d) Diferences in vasomotor tone be
tween upper and lower etremitie.
The vasomotor tone of the lower
human extremity (lumbar and sacral
innervation) has been found to be
much higher than that of the upper
(cervical and thoracic innervation).
Goetz" and Green9 have shown, for
example, that the vasomotor tone of
the toe vessels is decreased and their
blood flow used for heat elimination
only when the vasodilator capacity of
the hands has been fully exhausted.
e) Regional and segmental variations
in sudomotor activity.
The investigations of Korr, Thomas
and Wright (1 958 ) 1 0 previously
reported in this journal, revealed the
existence of regional and segmental
variations in sudomotor activity in a
study of several hundred subjects.
These studies appeared to have im
portant functional implications re
lated to regional variations in the ex
citability of autonomic pathways
lC
I'
.
In view of the evidence cited above,
it was decided to investigate, in fur-
"These investigations were supported in part by grants
from the National Institutes of Health. Public Health
Service (H-1632). and from the American Osteopathic
Association.
45
Fig. 1. Ski n stroker. With this instrument two
identical stimulators were drawn down the
back by a constant speed electric motor. The
stimulators were independently mounted on
freely pivoting aluminum rods. The intensity of
the stimulus could be varied by changing the
position ofthe 500 gram weight on the lever of
each stimulator. For each individual, that in
tensity ofstimulus was selected which was ade
quate to elicit some degree of erythema (red
response) at all segmental /evels from T, to S, .
ther detai l , the "normal " topo
graphical gradient in cutaneous vas
cular tone along the spinal cord as a
background for studying and inter
preting the local deviations and asym
metries of vascular response which we
have observed i n large numbers of
subjects. The general significance of
these deviations and their neurogenic
origin are suggested by their similari
ty to deviations i n sympathetic sudo
motor activity by Korr et al .
I
{
1
7 . The
possible clinical implications of these
vasomotor deviations are suggested
by the fact that sudomotor variations
were often related to visceral and
musculoskeletal disturbancesl{-
1
4
.
Mcthods
The observations presented i n this
paper were made over a period of
several years, and during that time
several methods were used. Although
a vari ety of di rect and i ndi rect
methods may be used for the investi
gation of the peripheral circulation
(venous drainage recorders, mean
flow recorders, pulsatile flow meters,
perfusi on syst ems , mechani cal
plethysmography etc. ) most of these
methods either cannot be used on the
intact human subject, or at best can
be used only on the extremities. We
40
have, therefore, used three indirect
methods which have commonly been
used in clinical studies: 1 . measure
ment of the ski n temperature, 2.
measurement of the vascular compo
nent of the skin color, and 3. observa
tion of the responses of the skin ves
sels (vasoconstriction and vasodilata
tion) to mechanical stimul i .
These methods enabled us to come
pare the segment-to-segment differ
ences and regional di fferences i n
vasomotor activity in a given indi
vidual as well as in di fferent in
dividuals.
A. Skin Temperature.
Skin temperatures were measured
wi th conventi onal welded i ;on
constantan thermocoupl es made
from 30-gauge thermocouple wire
and read from a sensitive galvanom
eter. A single "exploratory" thermo
couple mounted on a plastic handle,
permitted the investigator to rapidly
ascertai n the ski n temperature on
both sides, at each segmental level , at
poi nt s equi di s t ant from t he
spinal midline.
B. The "Red Response ".
The er yt hema r es ul t i ng from
mechanical stimulation of t he skin
has been called the "red response" by
Lewis' 8 , and is a part of the triple
response described by hi m. Although
Lewis has shown that vascular dilata
tion resulting from mechanical strok
ing of the skin is not dependent on a
nervous mechani sm, the responses to
stroki ng are i nfluenced by nervous
factors, and, other investigators have
used the threshold, intensity, the time
required for the appearance ("laten
cy") or fading ("duration") of the
erythema as a measure of the super
imposed sympathetic vasomotor tone
of the vasculature' 9 .
For our studies, it was necessary to
develop a stimulus which could be
standardized and accurately dupli
cated. To do this, an instrument was
constructed (Fig. 1) which was a
modification of the "ski n stroker"
used by Di Palma ' 9 in his study of the
reactivity of blood vessels.
In conducting a test, the two iden
tical rounded-wire stimulators were
drawn i n straight lines down the back
by a constant-speed electric motor at
the rate of 4. 5 cm. per second from
the level of the first thoracic vertebra
to that of the sacrum. The stimulators
were made of 1 2 gauge copper wire
and were 5/ 1 6 inch (8 mm. ) in
ci rcumference, and i ndependently
mou n t e d on f r eel y pi v ot i ng
aluminum rods 26 cm. long. The
intensity of the stimulus could be
varied i n 25-gram steps from 1 50 to
500 grams by changing the position of
a 500-gram weight on the aluminum
lever of each stimulator.
For any given stimulus, however,
the pressure on the stimulator re
mained constant for the full excur
sion of the instrument , thereby giving
a uniform stimulus to all segmental
levels on the back. The stimulus was
applied 1 Y2 inches ( 3. 8 cm. ) on either
side of the spinal midline.
For each individual, that intensity
of stimulus (the weight applied to the
stimulator) was selected which was
adequate to elicit some degree of
erythema at al l segmental levels from
T, to S, . Observations were made
under daylight fluorescent illumina
tion by two or more persons i n most
cases.
In preliminary efforts to establish
methods for quantifying the red re
sponse, measurement of the thresh
old, latency, intensity and duration
were tried. Measurement of thresh
olds was eliminated when i t became
evident that repeated testing of the
ski n altered its response. The
measurement of latency was also
eliminated because of the rapidity
with which the response developed
throughout the entire test area. Both
intensity and duration, however,
showed wide ranges of gradation. It
was further revealed that these two
factors were proportionately related;
that is, the more intense the ery
thema, the longer its persistence. We
found it convenient, therefore, to
evaluate the red response by deter
mining the time interval between
stimulus and disappearance of the
response.
The duration or "persistence" of
the red response was, therefore,
"graded" as follows:
Grade Persistence ofErythema
1 30 seconds or less
2 30 to 60 seconds
3 60 to 90 seconds
4 More than 90 seconds
(sometimes several minutes)
As the sequence of the disappear
ance of various fragments of the line
of erythema was observed on the sub
ject, each area was appropriately
EMG, SNS, reflexes, etc.
'8
.
ti
11
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6
7
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Fig. 3. Avrage thoraeo-Iumbar ptterns.
Fig. 3 a. A verage skin tempratur at each segmental level. This graph wa derived by ave1ging
together the temperatur of the paravertebral skin at each segmental level in 14 individuals. (Three
obervations were made on each individual.)
Fig. 3 b. A verge rd response grde at each smental level. Tis graph was derived by averaging
together the red reponse of the paravertebral skin at each segmental level in 13 individuals. (Three
observations were made on each individual.) The persistence of the red response was graded as
folows: Grade 1. 30 second or les; Grade 2, 30 to 6 seconds; Grade 3. 60 to 9 second; Grade 4,
mor than 9 second.
Fig. 3 c. A verage light absorption at each segmental level. Thi grph was derived by averaging
together the light absorption of the paravertebral skin at each segmental level in 15 individuals.
(Thre obervation wr made on ech individual.) The diference (10 -R) btwen the refec
tance from a white porelain plate (10) and that ofa tet area ofskin (R) i a measure ofthe
amount oflght absorbe by the skin.
T
I Y Y 1 71 " 1 ' " 11 I 1 1 I t11 1
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Z
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I
5
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,
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f
1
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-AISie
--- LI Site
Fig. 4 Average electrical conductance of the
skin at each segmental level. Thi graph wa
derived by averaging together the electrical
conductance (measurd as currnt J70w at con
tant voltage) ofthe pravertebral skin at each
sgmental level in 25 individuals.
I
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,
5
5
5
f'
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7
4
8 8
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5
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Fig. 5. Individual patterns of skin temperature. In subjet J.B. the temperatures ofthe paravertebral
skin on the right and left sides are relatively symmetrical, except at T, and L, to L" Subject B.M.
shows considerable diferences in the skin temperature between the right and left sides at T, and T,
and throughout the area from T. to L,. In subject W. E., asymmetrie in the paravertebral skin
tempratures are most apparent from T. to T, ,. (Each graph is an average ofthree observations on
each individual.)
1tlu/n$4 dlN 1tISf"nSI dlm ,et,SP"R$#111 1
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8
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11
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13
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6
7
8
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f I J 4 1 f / J 4
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7
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Fig. 6. Individual patterns of the red response. In subject S.S. the persistence ofthe rd response
was generally symmetrical between the right and leftsides except at T. and T" . Subjet J.E. shows
marked asymmetries between the right and left side below the level of T . Subject I.K. shows
marked deviations from the "average" patter at T. to T, on the right side, and, in general, the per
sitence of the red respons was consistently les on the right side than the leftfrom T. to T, . (Each
graph i an averge of3 observations on each Individual.)
asymmetries in light absorption be
tween the right and left sides of the
paravertebral skin at T to T.; the
skin at the level of Lz to LJ on both
sides shows more than average light
absorption.
4. Reproducbity ofsegmental
patters.
The "pattern" or distribution of
local "aberrant" or "asymmetrical"
areas varied from subject to subject,
but the pattern was characteristic for
that individual . Tests conducted on
the same individual on different dates
are shown in Fig. 8. Individual pat
terns of local or segmental deviations
from the average patterns in the skin
temperature (Fig. 8 a), red responses
(Fig. 8 b) and light absorption (Fig. 8
c) of the skin showed a high degree of
reproducibility. The location and ar
rangement of such deviations from
the average patterns with respect to
segmental levels and right and left
sides remained remarkably constant
for days or weeks.
49
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1
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=11:
/-
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11
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Lilt >ISQJjlitQ ('N-I) "''Li1t AbSQljllo (lffI)
-f J/ I SQ 6 7f f Ul J I J 7
7
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, /
Fig. 7. Individual patterns of light absorption. The light absorption ofthe paravertebral skin on the
right and left side is relatively symmetricl in subject I. M. In subject W.B. conspicuous asym
metries appear at Til to Til and in the lumbar area. Subject W. W. shows marked asymmetries be
twen the right and left sides at T. to t,. (Each graph i an average of 3 observations on each in
dividual.)
7
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Fig. 8 a to c. Reproducibility patterns. The ptters ofskin temperature, red response and light absorption of the skin for each individual showed a high
degre ofreproducibility. The location and arrangement of local or segmental deviations (aymmetries) from the average topographical patters re
mained constant for days or weeks.
Fig. 8 a. The paravertebral skin temperaturs of subject WE. on difernt dates.
Fig. 8 b. The red reponse pattern of subject J.E. on different dates.
Fig. 8 c. The light absorption of the paravertebral skin subject J. P. on different date.
J
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J
f
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G
7
8
.
Tt
11
11
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Fig. 9. Correlations of patterns in one individual. For comparion, the patterns ofskin temperature,
red rsponse and light absorption of the paravertebral skin of subject W.E. are shown here.
Marked asymmetrie between the right and let sides are apparent from Ts to T/1 in all 3 patters.
50 EMG, SNS, refexes, etc.
5. Correlations between the skin
temperature. red reponse and light
absorption ojthe skin.
For comparison, the patterns of the
skin temperature, red responses and
light absorption of the skin of subject
W. E. are shown in Fig. 9.
Marked differences between the
right and left sides are apparent from
T6 to T' 2 in all three patterns. In this
area, the skin temperature was consis
tently cooler and the persistence of
the red response less on the right side
than the left side. In the same subject,
however, the light absorption of the
skin was consistently greater on the
right side than the left between T to
T1 2 Similar correlations, among the
three patterns, and directional dis
crepancies between light absorption
and the other two measurements were
seen in other subjects.
Discussion
Signiicance ojindividual and
combined measurements.
The methods employed in these
studies indicate that the cutaneous
circulation over the entire trunk is not
uniform, as appears to be commonly
assumed, but differs with the segmen
tal or topographical level of the trunk
skin. In the normal individua, in
herent topographical patterns in the
skin temperature, vascular responses,
and blood content of the sub papillary
plexus extend throughout the longi
tudinal axis of the thoraco-Iumbar
area. Although the three measure
ments used in these studies refect dif
ferent manifestations and characteris
tics of the cutaneous circulation2
0
21
,
24, 3 5-3 7 , certai n rel ati onshi ps,
similarities, and dissimilarities may
be considered.
The sin temperature indicates the
position of thermal equilibrium be
tween the body and the environment,
and is used only as an indirect
criterion of cutaneous blood flow
2
1 ,
3
5-
45. However, i n a resting subject in
a constant temperature, variations in
the skin temperature may reflect
variations in the cutaneous blood
flow. The segment-to-segment differ
ences in temperature over the topog
raphy of the trunk which we have re
corded, may, therefore, reflect, or be
related to, difference in cutaneous
blood fow.
The red response is due to an active
dilatation of the minute cutaneous
vessels caused either directly by me
chanical stimulation or by the action
of a histamine-like substance which is
released fol l owi ng mechani cal
sti mul ati on
1 8
, Al though the
vasodi latati on observed i n thi s
response is not dependent on a neural
mechanism, its intensity and duration
are infuenced by neural factors. It
has been shown by other investigators
that central and reflex control of the
cutaneous vessels is, apparently,
purely via sympathetic fibers 4
6
-5
1 .
Hence, the intensity and duration of
the response to mechanical stimula
tion will certainly be influenced by ex
isting sympathetic constrictor tone.
The topographical pattern of the
"persistence" of the red response
which we have observed at different
segmental levels on the trunk, may,
therefore, be related to, or reflect,
differences in sympathetic vasocon
strictor tone of the minute cutaneous
vessels.
The vascular component of the
skin color is related to the state of fill
i ng of t he subpapi ll ary venous
plexus20 However, the quantity of
blood i n the skin can be quite dispro
portionate to the rate of blood flow
through the skin
1 21
,
3
5-37. 52. Never-
theless, it has been shown that an in
creased tone of the subpapillary
venous plexus mediated by sympathe
tic pathways diminishes the blood
content (not necessarily the blood
flow) of the skin and contributes to
pallor3
1-3
4
, 53-55. The topographical
differences in the vascular coloration
of the skin which we have observed.
may. therefore, reflect differences in
the sympathetic constrictor tone of
the venules of the skin.
It is obvious, therefore. that be
cause our three types of observations
are related to different kfnds of
manifestations of the cutaneous
ci rcul ati on, preci se correl ati ons
among the three types of data cannot
be expected. Nevertheless, com
parison of the "average" graphs of
the skin temperature and red re
sponses (Fig. 3) shows that, i n
general, hypothermic areas of the
skin also show diminished persistence
of the red response and vice versa.
Thus, the warmest area of trunk skin,
T 4 to T y corresponds to the same
area in which the red responses per
sisted for the longest period of time.
Similarly the coolest area of the
trunk skin, LI to L
4
, showed minimal
persistence of the red response.
Temperature and red response
patterns of individual subjects were
also similar. Variations in red re
sponse and in skin temperature ap
pear, therefore, to be related to varia
tions in a common factor. We believe
the closely correlated regional varia
tions, and local aberrations of red
response and skin temperature are
both manifestations of parallel varia
tions in sympathetic vasomotor tone,
high sympathetic tone producing
hypothermia and brief red responses,
and low tone producing hyperthermia
and prolonged red responses.
That the blood content of the skin
is in some way related to temperature
and red responses is clearly indicated
by the fact that aberrations in all
three have the same distribution in a
given subject. Since, however, the
direction of the aberrations in blood
content is not consistently related to
direction of the aberrations of tem
perature and red response, the nature
of the relationship is not clear. For
example, as shown in Fig. 9, the ap
parent blood content of the right side
is greater than the left, whereas the
skin temperature and red responses
indicate vasoconstriction on the right
side relative to the left. It is possible
that skin color, on the one hand, and
temperature and the red response. on
the other, refect variations in dif
ferent parts of the cutaneous vascula
ture, thus accounting for this incon
sistency. As HertzmanS2 has pointed
out, the quantity of blood in the skin
and the changes in the blood content
of the skin can be quite dispropor
tionate to the level of blood flow and
to changes in blood flow. For exam
ple. in certain pathological states an
increase in cutaneous blood fow and
pallor may develop simultaneously,
The pallor must represent an increase
in venous tone, while the increase in
cutaneous blood flow is associated
with arteriolar dilatation.
Moreover, the configuration of the
"average" pattern of the light ab
sorption also differs from those for
temperature and red response. The
reason for the difference, limited ap
parently to upper thoracic segments,
is not clear, but may have part of its
basis in pigmentation, skin thickness
or vascularity of this part of the trunk
as compared to lower segments23 26
, 28
.
51
Normal regional diference.
All three methods clearly reveal the
existence in the normal individual of
regional differences in vasomotor
function of the skin of the trunk. The
basis and functional implications of
the patterns are not clear. but may
represent adaptations to postural and
thermoregulatory demands.
The investigations of others, as
well as our own, suggest that these
variations have a functional rather
than an anatomic basis. Hertzmanl in
his studies of regional differences in
cutaneous blood fows, concluded
that the vascular anatomy of most of
the body's skin (trunk, legs and arms)
is uniform with respect to the number
and size of the vessels. Wetzel and
ZottermanZo also found that the num
ber of capillaries in the cheek, ear
lobe, forearms and hand does not dif
fer signifcatly. Di Palma3 also con
cluded that it seemed reasonable to
assume that segmental threshold dif
ferences in the responses of the small
cutaneous vessels were the result of
functional alterations, rather than
anatomic ones. The existence of simi
lar patterns in sudomotor activity
(Fig. 4) strongly suggests that the
vasomotor, Uke the sudomotor varia
tions, refect normal variations in
sympathetic tone.
A segmental pattern in the motor
reflex thresholds of the paravertebral
muscles, reflecting activity of the ven
tral hor cells of the cord, has been
shown by Denslow' 6 It is of interest,
that while these measurements are
concerned with a different kind of
nervous activity, and while there is
variable topographical displacement
between corresponding dermatomes
and myotomes, an essentially similar
pattern was evident. This suggests
that the normal segmental and re
gional variations of vasomotor (and
sudomotor) activity reported here are
functionally related to similar varia
tions in activity of the ventral horn
cells. That is, together they reflect
patterne variations in spinal integra
tion of somatic and autonomic motor
activity.
Local abrrations.
The local al terati ons i n the
temperature, red response, and blood
content of the skin which we found
"superimposed" on the average pat
ters of these measurements, may
also have a functional basis; that is,
52
they may represent local refex altera
tions in sympathetic vasomotor tone.
These individual patterns of local
deviations in vasomotor functions ap
pear to b similar to the distinctive
ESR patterns which Korr et al.
10-
1
3
found in many individuals with
visceral and musculoskeletal distur
bances.
Other investigators have also ob
served local vasomotor disturbances
associated with visceral distur
bancesS7-6
1
Almost 40 years ago
Weroe62-6 observed pale areas of
skin segmentally related to diseased
viscera in numerous patients. Adams
Ray31 , 33 has described pallor of the
skin in the fourth cervical segment in
patients with cardiac pain, and in pa
tients with gall bladder disease in seg
mentally related dermatomes. Doret67
found the skin temperature lower in
the area of pain in the majority of pa
tients with myocardial infarction.
That reflex cutaneous vasoconstric
tion can be experimentally induced on
the trunk has been shown by Adams
Ray31 who was able to demonstrate
pallor of the skin in the eleventh and
twelfth thoracic segments when the
bladder was di stended, and by
Stirup61 who was able to induce
ischemia of the skin over the sternum
by distending the esophagus.
In view of the parallelism in vaso
motor responses, under many circum
stances, between skin and viscera,
regions of pallor, hypothermia or
other signs of cutaneous vasocon
striction may be related to ischemia
of reflexly related visceral tissues.
The reflex origin of local vaso
motor aberrations is indicated not on
ly by their relation to visceral distur
bances, but, as we have repeatedly
observed, by their relation to muscu
loskeletal stresses, of both pathologi
cal and experimental origins. These
relations will be subsequently
reported.
Summar
1 . These studies have been con
cered with regional or segmental
variations in vasomotor activity in
"normal" individuals.
2. The methods used included the
segment-to-segment measurement of
the temperature, red responses, and
light absorption of the paravertebral
skin.
3. The observations show that the
cutaneous vasomotor activity on the
trunk is not uniform, as appears to be
commonly assumed. Topographical
patterns of temperature, red re
sponses and light absorption of the
skin were found.
4. Local or segmental deviations
from these average or "normal" to
pographical patterns were found in
most individuals.
5, Local deviations in all three
types of observations were usually
found at the same segmental levels in
a given individual.
6. The topographical patterns of
vascular activity appear to be func
tional rather than anatomic and are
analogous to similar patterns in su
domotor activity.
7. The topographical patterns of
cutaneous vasomotor manifestations
appear, therefore, to reflect normal
regional variations in sympathetic ac
tivity.
8. The local deviations of vaso
motor activity from the "normal"
patterns appear to be related to local
deviations in sympathetic activity.
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We gratefully acknowledge the valuable assistance
of Mr. E. Blackorby in the design and construction of
instruments and of Mrs. Tova Brooks in the prepara
tion of the illustrations.
Reprinted by permission from 10urnal of Neural
Trasmission 22: 3,34-52, 19.
5J
Effects of experimental myofascial
insults on cutaneous patterns of sympathetic
activity in man* (1962)
I.M. KORR, H.M. WRIGHT, ad P.E. THOMAS
In recent years our laboratories have
been engaged in the study of regional
and segmental variations in sym
pathetic activity, as revealed by
cutaneous sudomotor and vasomotor
manifestations. Studies of electrical
skin resistance (ESR) , reported in this
Journal in 19581, revealed persistent
areas of low electrical skin resistance
in most individuals. The topographi
cal distribution or "pattern" of these
low resistance areas varied from in
dividual to individual; but in a given
individual, the distribution, with
respect to right and left sides and
segmental levels, remained constant
for weeks, months and sometimes for
as long a three or four years. Studies
of regional and segmental variations
in cutaneous vasomotor activity also
revealed topographical "patterns"
2
that remained similarly characteristic
and constant for each subject.
That these measurements and pat
terns of ESR as recorded by our
methods reflect variations in sym
pathetic activity was shown by the
studies of Thomas and Korr 3, 4. 5 and
Kawahata and Th
o
mas 6. Although
these studies did not reveal the physi
ologic ongms or functional
significance of the sympathetic
hyperactivity manifested in the low
resistance areas, their distribution,
that is, the patterned differences in
sympathetic activity, were in some
individuals apparently related to vis
ceral or myofascial disturbances.
Reports of areas of hyperhidrosis7 8
or low skin resistance9-13, lowered
skin temperaturel4
IS
and cutaneous
pallorl6--19 reflexly related to painful
myofascial and visceral conditions
also suggest such a possibility.
In view of the possible physiologic
and clinical implications of the topo
graphical variations, asymmetries
and local aberrations in sympathetic
activity, we have attempted to explore
factors that might contribute to them.
*T_ investigations were supported in part by grants
from the National Institutes of Health, Public Helth
Service (H 1632). and from the American Osteopathic
Association.
54
This report deals with the effects of
experimentally induced irritations
and stresses in musculoskeletal tissues
on the patterns of cutaneous
sudomotor activity.
Methods
Since the methods we have used for
the study of sudomotor activity-have
been previously describedl,
2,
2
1
, they
are only briefly characterized here.
ESR Explorations.
The experiments reported in this
paper were done over a period of
several years. During this time three
methods for recording ESR were
used, each yielding a different type of
record. However, all three methods
are based on conventional principles
of skin resistance measurement.
Essentially, each method consists
of measuring or recording, in correct
spatial relationship to the explored
area, the momentary current fow
through the skin in contact with a
constantly moving exploring elec
trode, at known voltages. The volt
ages were tapped stepwise from a
series of dry cells and applied to an
electrode fixed to an earlobe and an
exploring electrode. Resistance of the
skin of the earlobe was minimized by
means of electrode paste. Area-to
area differences in current flow at a
given voltage, therefore, were due to
differences in the "resistance" of the
skin under the exploring electrode.
1. Explorations with hand-held
electrode.
In our earlier studies we used an in
strument similar to that described by
Jasperll. Current flow was read from
a microammeter as the electrode was
moved over the subject's skin.
Figures 1 to 6 and 16 to 18 show
charts obtained with this method.
2. Automatic Explorations.
In later studies a mobile automatic
dermometer was developed 21. With
this instrument skin resistance pat
terns on large areas of the dorsal
trunk were recorded directly on paper
by recording galvanometer whose
amplitude of oscillations is related,
through an amplifier, to the skin cur
rent. The position of the galvano
meter writing-point on the chart was
related to the position of the explor
ing electrode on the subject by means
of a pantograph. Records obtained
with this instrument appear in Figures
8,9, 11, 12, 14, 15. Records obtained
with an earlier automatic dermometer
(Thomas and Korr20) are not included
in this report.
Exploration Conditions.
The explorations were conducted in a
quiet room maintained between 230
and 250 C. The body was unclothed
above the level of the sacrum. The
tips of the spinous processes were
located by palpation and marked on
the skin. In these studies, "segmen
tal" level refers to the topographical
level on the trunk as identified by the
corresponding spinous process,
rather than the dermatomes. There is,
however, close correspondence be
tween topographical and segmental
levels for paravertebral skin, except
at the uppermost thoracic segments.
The experimental irritations used in
these studies were produced by the in
jection of hypertonic NaCl solution
into paravertebral structures. The
postural stresses included the artifi
cial lengthening or shortening of one
lower extrcmity by the insertion or re
moval of heel lifts, and the inclina
tion ot the pelvis by seating subjects
in tilt-chairs. In some of the tilt-chair
experiments the changes in skeletal
configuration were monitored with
roentgenograms.
Results
Myojascial Irritations.
For the purpose of studying
sudomotor responses to local myo
fascial irritation we adopted the
method described by Kellgren in con
nection with investigations of refer
red pain of somatic origin
2
3-26 As
Lewi and Kellgren26 reported, when
small volumes (0.1 to 0. 3 ml) of
hypertonic saline (61o NaCl) were in
jected into superficial tissues (e.g.,
skin, periosteum of the tibia, sheath
of the achilles tendon) only a sharp,
localized pain was produced. When,
however, the irritant was injected into
deeper tissues, especially those on the
trunk and most particularly around
EMG, SNS, refexes, etc.
the spinal column (e. g. , interspinous
ligaments, paravertebral muscles),
the local transient pain was soon
followed by a crescendo of deep pain
felt in areas often quite remote from
the site of injection, but apparently
innervated from the same segment
and side of the spinal cord. The pain
was usually accompanied by deep and
cutaneous tenderness and muscular
rigidity in the corresponding der
matomes and myotomes. The mani
festations subsided within a few min
utes after a peak often of great inten
sity. It was our purpose to determine
what changes in ESR were associated
with these phenomena.
In our experience with a total of 1 5
subjects, some of whom received two
or more injections, a significant
change in the ESR pattern was ob
tained only when we were succesful in
producing referred pain. Injection of
superficial structures, such as the inter
spinous ligaments or periosteum of
spinous processes or injection of a
deeper structure, which for some
reason, produced only local pain, if
any, was followed either by local
decreases in ESR in the immediate
vicinity of the injection site or by no
evident change. Some subjects, how
ever, showed a transient, generalized
drop in resistance, with quick return
to pre-existing patterns. Such
responses might, i n apprehensive sub
jects, even precede the insertion of
the hypodermic needle. The injection
of the periosteum of spinous pro
cesses was, in some cases, immediate
ly followed by considerable distress to
the subject, with diffuse and poorly
localized pain, nausea and faintness,
and pallor, coldness and clamminess
of the skin. Two subjects (injected in
mid-thoracic spinous processes) suf
fered with vomiting and diarrhea
several hours after the experiment.
The appearance of ESR changes in
the reference areas was especially
clear following injection of the hyper
tonic saline into the erector spinae
and intercostal muscles. Figures 1, 2
and 3 illustrate the results of four
such injections.
F
igure 1 represents
the results of two injections, 35
minutes apart, in two sites, in the
same subject. The areas of low resis
tance which appeared following the
injections are represented by the two
rows of encircled black spots. The
other areas, mainly in the midline,
were present before the injection and
In all figures dark areas rprsent low-resistance areas (LRA) of skin. Darknes of shading In hand
drawn charts (Fig. 1 to 6, 16 to 18) is in proportion to currentfow at exploration voltage; the darker
the area the lower the resistance. White areas: / pa or less; (rsistance. in ohms, at least 1 million
times the number oj volts),' black areas: 20 p or more; i. e., less than 1120 oj basic resistance , ' gray
areas: intermediate values. (Reproduction oj the hand-drawn charts ha darkened the gray areas and
the darker shade have become inditinguishable Jrom the black aras.)
Fig. 1. Subject D.H. 12 20 48: Area of low skin reistance (circled black dots) elicited by the inec
tion oj 0.3 mi. of 600 NaCI into the erector spinae mass to the left of the spinous proces oj T. and
into the eighth intercostal space in the right axillary, midline (both sites marked by x).
FilS.
Fig. 2. Subject L.L. 12 21 48: Areas of low skin resistance (circled black dots) elcited by the injec
tion oj 0.3 mi. oj 6% NaC1 into the erector spinae mas to the leJt oj the spinou process of T,.
Fig. 3. Subject L.L. 12 649: Area oj low skin resistance
(Ts_I
I
'
right) present 24 hours ater the in
jection of 0.3 mi. oJ 6% NaCl into the erector spinae mass to the right of the spinous proces oj T,.
55
Fig. 4
I
Fig. 6
.
f
I
1
. \,
I
' J
Fig. 4. ESR patterns of Subject L.L. I2 22 49: a) seated horizontally,' b) 6 minute 4ter pelvi was
tited to the left.
Fig. 5. ESR patterns of Subjet J.R. 12 2349: a) seated horizontally; b) 6 minutes after pelvis was
tilted to the let; c) 30 minute following retur to the horizontal position.
Fig. 6. ESR ptterns of Subject J.D. 1 3 50: a) seated horizontaly,' b) 120 minutes after pelvi wa
tilted to the left. Ti subject showed very little change in hi ESR patter in contrst to the subjects
shown in Figs. 4 and 5.
5
were representative of the ESR "pat
tern" (Korr, Thomas and Wright!)
repeatedly observed in previous ex
olorations of this subject.
Immediately following the comple
tion of the control exploration, 0.3
ml of 611 0 NaCl was injected 2.5 cm.
deep into the erector spinae mass to
the left of the spinous process of the
8th thoracic vertebra. The subject
almost immediately reported pain in
the anterior chest wall in the region
below the left nipple. In approximate
ly 30 seconds severe pain had also
developed in the back. over the
transverse processes and rib-heads of
the region T, to Tlo on the left side.
The new areas of low resistance began
to appear during the second minute
after injection and, after 5 minutes,
appeared as shown in Figure 1, by the
encircled spots on the left side, at
which time the pain had vanished.
Thirty-five minutes after the frst
injection a second injection of hyper
tonic saline was made, this time into
the 8th intercostal space in the right
mid-axillary line. The pain which
developed was realtively mild and was
felt mainly in the anterior chest wall,
in the mammary region. Neverthe
less, new areas of low resistance ap
peared, as shown on the right side in
Figure 1. more conspicuously on the
dorsal than ventral surface.
When the subject was re-explored
six hours after the second injection.
the low-resistance areas were still evi
dent in the same distribution, but
they had become less punctate and
nearly continuous. The exploration
of the chest was conducted at a volt
age which permitted no more than
lJ of current through most of the
skin. Nevertheless. the current flow
through the areas shown was suff
cient to cause the two strips of low
resistance skin to become sharply
delineated as two erythematous bands
in the course of the exploration. Re
sistance had returned to control levels
before the next exploration 18 hours
later.
The encircled black spots shown in
Figure 2 represent the new areas of
low resistance which appeared, and re
mained, over a period of 5 minutes
following the injection of 0.3 ml of
600 NaCl into the erector spinae at
the level of the fifth thoracic spinous
process in another subject. Numerous
spots, not shown, also appeared on
the ventral aspect of the correspond-
EMG, SNS, refexes, etc.
"
F ig. 7. Roentgenogram tracings ofthe spine of
Subject S.P .: H) seated hori z ontally; L) seated
with pelvis tilted to the left; R) seated with
pelvis tilted to the right.
In the pantographi c records (F igs. 8, 9, 1 1, 12 ,
}4, 1 5), amplitude ofoscil l ations ofthe record
ing galvanom eter is related to current flow
through the skin. Th e thin vertical lines (no
oscillation) represent areas perm itting 0-1 p a
at exploration voltage; widest oscillations
represent current f ows of 30
p
a or m ore. In
these charts, therefore, the darkest areas repre
sent / /30 the basic resistance or less. Note the
calibration "stris" showing relation between
current and ampli tude of osci ll ations in steps
of5
p
a.
L
."
'''_J
r,
'
"'
m
>
/
J
, ,
. .
=
=
j
-.
/
"
:
'-.
;1r
$L
-'_l
.. " !
H
F ig. /0. Roentgenogram tracings of the spine
of Subj ect H.K. H) seated hori z ontally; L)
seated with pelvis tilted to the left; R) seated
with pelvis tilted to the right.
I
'
" .
|l.
\ '
'I
"
F ig. 8 ESR patters ofSubj ect S. P. 6 17 55: a) seated hori z ontally; b) 4 m inutes after pelvis was
tilted to the left; c) 14 m inutes following retur to the hori z ontal position.
I
F ig. 9. ESR patterns ofSubj ect S.P. 616 55: a) seated hori z ontall y; b) 9 m inutes after pelvi S was
tilted to the right; c) 8 m inutes following return to the hori z ontal position.
F ig. II. ESR patterns ofSubj ect H.K. 7 19 55: a) seated horiz onlally; b) /8 m inutes after pelvis was
tilled to the left; c) / / m inutes fol lowing return to I he horiz ontal position.
57
c
m
i
.
F ig. 12. ESR po l/ ems of Subj ect H.K. 7 25 55: a) seated hori z ontall y; b) 18 m inutes after pelvis was
tilted to the right; c) I I m inutes following retur to the hori z ontal position.
f'
58
F ig. /3. Roentgenogram tracings of the spine
of Subj ect C.B.: H) seated hori z ontall y; L)
seated with pelvis tilted to the left; R) seated
with pelvis tilted to the right.
F ig. 14. ESR po l/ ems of S ubj ect C.B. 62 455: a) seated hori z ontall y; b) 15 m inutes after p elvis was
,t illed to the left; c) 14 m inutes following return to the hori z ontal position.
F ig. 15 . ESR patters of Subj ect C. B. 62 855: a) seated hori z ontall y; b) 1 7 m inutes after pelvis was
tilted to the right; c) 14 m inutes following retur to the hori z ontal position.
EMG, SNS, refexes, etc.
t,
d
Fig. 1 ESR patterns of Subject A.M. 12 27 48 - 122848: a) without heel-lift; b) afer wearing !
inch heel-lit in right shoe for 5 hours; c) patter immediately upon arising the fol/owing moring;
d) "! hours later, heel-lit still in place.
5
.,
Fig. 18. E/ects 0/ removal 0/ heel-lits on ESR patterns 0/ subject R. H. who had wor ! inch lit
under his right heel/or more than a yer to compensate/or shortness 0/ that extrmity. oj 12124149:
Control ESR pattern (subject wearing hel-lift) in the moring (a 1, 9:00 A.M.) and afteroon (a 2,
4:15 P.M.). Moring and ateroon explorations were also done on three other days with similar
reults. b) 12128149: Following the ESR eploration at 9:30 A.M., (bl) the lit was removed. The
fgure at 4:05 P.M. (b 2) shows the altered ESR patter which developed during this interval.
the chosen direction while the subject
remained seated. He was then re
explored at various intervals after
tilting. In some experiments explora
tions were also conducted after res
toration of the seat to the horizontal
position.. In all experiments to be
shown the angle of tilt with respect to
the horizontal was 1 5. In explora
tions done with hand-held electrodes
(Fig. 4 to 6) the charts representing
the experimental exploration indicate
the patterns that had developed by
the time the exploration was com
plete.
Comparison of Figures 4 a and 4 b
indicates the change in pattern which
6
developed in subject L.L. in the
course of one hour of sitting with the
left hip tilted downward. New areas
of low resistance were especially
marked in the lower cervical, lower
thoracic and lumbar areas. Pain
developed at the base of the neck on
the left side within 1 5 to 20 minutes
after tilting.
Fig. 5 shows an experiment on
another subject (J.R.). A comparison
of charts a and b reveals the new
areas of low resistance which ap
peared while the subject was seated
for one hour with the pelvis tilted
1 5, left hip down. The new areas in
the thoracic and lumbar regions, es-
pecially on the left (convex side of the
spinal curve) and the exaggeration of
the low resistance areas at the cer
vicodorsal junction are particularly to
be noted. These changes were almost
entirely reversed within 30 minutes
after restoration to the horizontal
position (Fig. 5 c).
In contrast to the above subjects,
subject J.D. (Fig. 6) showed very
little change in ESR pattern after 1 20
minutes of sitting in the tilted posi
tion. This subject was a tall, slender
individual who felt remarkably little
discomfort. He reported only a slight
sensation of "strain" in areas over
the upper borders of both scapulae.
The topographically related areas of
slightly lowered resistance which ap
peared after about one hour are to be
noted, although they were probably
extensions of the small areas evident
above the scapulae in the control ex
ploration.
In more recent experiments, it has
been possible, with the automatic der
mometer ( Thomas. Korr and
Wright21), to record the progressive
development of new patterns after the
assumption of the tilted posture and
their regression following return to
the normal seated posture. Antero
posterior roentgenograms of each
subject were taken in the level and
tilted postures in order to visualize
the configuration of the vertebral col
umns. Tracings showing the spinal
confguration in each subject in nor
mal and tilted sitting, were made
from these films and accompany the
ESR patterns in the following figures.
Subject S.P. had abnormalities of
the vertebral column evident in Fig. 7
H (seated level) as conspicuous lateral
curves in the thoracic spine, with
sharp reversals of direction at upper
and mid-thoracic levels. Figures 7 L
and R reveal the poor adaptation of
the subject to the tilted posture and
the marked lack of symmetry of the
spinal confguration in the right and
left tilt. The imposition of these
postures on the subject provoked in
tense and diffuse sudomotor re
sponses as revealed by comparison of
chart b with a, pre-tilt, and c, post-tilt
control in both Fig. 8 (left tilt) and
Fig. 9 (right tilt).
Differences in response to left and
right tilt are also revealed. The sharp
upper boundaries of low-resistance
areas at the mid-thoracic level in Fig.
8 b and the elevation of the boundary
EMG. SNS, reflexes, etc.
to upper thoracic levels in the reverse
tilt (Fig. 9 b) are especially to be
noted.
Subject H.K. had no gross postural
or spinal abnormality evident in the
roentgenograms taken in the level
seated position (Fig. 10 H). Never
theless, those taken in the tilted posi
tions (Fig. 10 L, R) revealed various
restrictions and asymmetries in spinal
moti on. Accordi ngl y, marked
changes in ESR patterns occurred
during tilt-seating in both directions,
the patterns of the left and right tilts
being quite different. Low-resistance
areas at lumbar levels on the right
side were the first to appear in tilting
both to the left and to the right.
Following the appearance of these
areas of low resistance, however, the
patterns during right and left tilts
developed quite differently (compare
Fig. 1 1 b and 1 2 b), the additional
areas being in each case on the convex
side of the induced spinal curve.
Thus, while the low resistance areas
developed during the tilt to the left
(Fig. 1 1 b) were quite extensive, there
were only scattered small spots of low
resistace in the upper right quad
rant. It is thi area, however, in which
resistance was diffusely lowered when
the tilt was in the reverse direction
(Fig. 1 2) , the left side being relatively
free of low resistance areas.
In contrast with the above subjects,
C. B. showed, on X-ray examinati
o
n,
both excellent vertebral alignment in
the level-seat posture and smoothly
rounded, symmetrical spinal adapta
tion to the tilt of the pelvis in both
directions (Fig. 1 3). The new areas of
low resistance that developed were
small and limited mainly to the upper
thoracic levels (Figs. 14, 1 5).
Hel Lits.
The experiments reported under this
heading illustrate the regional sym
pathetic responses to artifcial change
in length of one leg, either by insert
ing a heel lift (hard-rubber wedge in
serted in one of the shoes) under one
heel, or removing one to which some
adaptation has been made.
In this series of experiments the
postural stress was not so gross as
that imposed by tilting the seat 1 50,
but, on the other hand, the stress was
permitted to act for much longer
periods of time, and under conditions
of locomotion. Consequently, the
discomfort and the changes in ESR
patterns have often been more severe.
All the subjects used in this series had
shown stable ESR patterns over
periods of at least several weeks. The
stress was applied after a control ex
ploration, and the subject was re
explored at various intervals there
after.
The series of charts comprising Fig.
1 6 shows, on subject M.O., the effect
on ESR pattern of wearing a lift one
day and the subsequent effect of
removing it. Fig. 1 6 a represents the
pattern repeatedly found on this sub
ject with only minor modifications
from day to day. This exploration
was begun 30 minutes afer the sub
ject had completed a 1 Y' mile walk
from his home to the laboratory. His
only complaint was a continuous ache
in the lumbosacral area on the right
side, in which general region was also
found an area of moderately lowered
resistance. X-ray flms taken in the
standing position indicated that the
right leg of this subject was approx
imately 7t inch shorter than the left.
Upon completion of the exploration a
3/8 inch lift was placed in his right
shoe and he was instructed to wear it
throughout the day and the following
morning to return for an exploration
the next morning, also after walking
(with heel-lift in place) from his
home.
Fig. 16 b shows the pattern ob
tained the next day. Both ache and
low-resistance areas in the lower right
quadrant had vanished, but the sub
ject now complained of discomfort in
the midthoracic region in which there
was especially marked extension of
low-resistance areas. The lift was
removed at 2:30 P. M. , after a "spot
check" revealed that there had been
further lowering of resistance and
some extension of the areas shown in
Fig. 16 b.
Fig. 1 6 c shows the pattern found
the next morning, again after the
walk from the subject's home. The
ache (and the low-resistance area) in
the lower right quadrant had returned
and the midthoracic ache had been
exacerbated. Areas of markedly
lowered resi stance had spread
throughout the midline of the back.
A totally new strip of low resistance
appeared on the right side in the mid
thoracic region, extending peripheral
ly from the level of vertebra T 8 on the
right side (Fig. 16 c; possibly a lateral
extension of the paravertebral area
evident in Fig. 1 6 b). It had not pre
viously been observed on this subject
but it continued to be observed on
every subsequent exploration until
the final exploration on this subject
almost 16 months after the experi
ment.
Another subject's response to ar
tificial increase in length of one leg is
shown in Fig. 1 7. This subject's ESR
pattern, repeatedly recorded over a
period of three weeks, was remark
ably undistinguished by any conspic
uous and persistent areas of low
resistance, and the control pattern
(Fig. 1 7 a) was typical. At 1 1 :0
A. M., following this exploration, a
one-half inch heel lift was inserted in
the subject's right shoe. He was in
structed to go about his usual activi
ties and to return later the same after
noon for exploration. Fig. 1 7 b shows
the pattern obtained in an exploration
begun at 4:0 P. M. , at which time the
subject complained of discomfort in
the region of the lumbosacral junc
tion. The extensive development of
low-resistance areas below the
thoracolumbar junction and in the
vicinity of the cervicodorsal j unction
is especially to be noted. Fig. 1 7 c
represents the pattern obtained on
this subject the following morning
shortly after rising. In general, a
recession of the low-resistance areas
of the previous afternoon is evident.
However, by early afternoon the sub
ject's discomfort, generalized in the
low back, was sufficiently severe that
he came to the laboratory to request
discontinuation of the experiment,
and the heel lift was removed. Ex
ploration done at that time disclosed
the pattern shown in Fig. 1 7 d. In
general, this seems an exaggeration
of the pattern of the previous after
noon (Fig. 1 7 b). Unfortunately, the
subject was not able to return until
two days later ( 1 2/30), at which time
low-resistance areas were still present
at the cervicodorsal junction, the en
tire midline below T s and to the right
of the dorsolumbar j unction.
The experiment shown in Fig. 1 8
was also conducted t o examine the
response to alteration of relative leg
length. In this case, however, the
stress was that of removing a lift
worn for therapeutic purposes. Sub
ject R.H. had been wearing a one
fourth inch lift in his right shoe, for
approximately one year, to compen
sate for relative shortness of the right
0I
leg and as part of the treatment for
low-back pain previously suffered by
this subject. At the time of the experi
ment he had been symptom-free for
at least 10 months.
Control explorations in this experi
ment consisted of a series of morning
and afternoon explorations on four
successive days. Of these, one pair is
shown (Figs. 1 8 a, b), representing
the extremes of variation. The subject
was engaged in physical labor and the
two charts on each day indicated the
changes in pattern which took place
in an interval of 6 to 7 hours. Follow
ing the morning exploration on the
ffth day of the experiment (Fig. 1 8 c)
the lift was removed and the subject
continued with his work as usual,
returning for exploration at 4:0
P.M. Fig. 18 d shows the great expan
sion of low-resistance areas in the
lower part of the back which had
taken place in the interval. The sub
ject also volunteered the information
the the "old pain", especially in the
vicinity of the lumbosacral junction,
had returned, in his recollection, for
the first time in many months.
Discussion
These studies reveal some of the
autonomic changes as refected in
sweat gland activity, provoked by
myofascial irritations and postural
stresses in human subjects. Related
changes in vasomotor activity, to be
reported separately, also occur. In
general these changes recorded in the
skin, were regionally, laterally and
often segmentally related to the site
of trauma, postural stress or discom
fort. Although the responses of the
sweat glands (and cutaneous blood
vessels) may be viewed as incidental
reflex responses of sympathetic path
ways to noxious myofascial stimula
tion, we believe they are better inter
preted as modifications of normally
existing patterns. Visceral, circula
tory and thermoregulatory functions,
controlled by the autonomic nervous
system, are continually coupled, in
highly organized patterns, to muscu
loskeletal activity and changes in
posture. That is, efferent activity in
neuromuscular and autonomic path
ways is, as is well known, functional
ly coordinated by the central nervous
system.
For example, augmentation of the
blood flow to muscles that are active
or about to become active is achieved
62
by differential adjustments of vascu
lar resistance in active and inactive
tissues and by increased cardiac out
put; and heat loss is adjusted, accor
ding to changed thermoregulatory de
mand accompanying the muscular ac
tivity, by changes in cutaneous blood
flow and sweat secretion. While, in
considerable part, local adjustments
are effected by direct action of
chemi cal agent s (e. g. , C02t
metabolites) and physical factors
(e.g., temperature), the local ad
justments are integrated in complex,
highly organized reflex patterns by
the central nervous system. Indeed,
the alteration of vegetative function
during and preparatory to muSular
activity and according to environ
mental demands appears to be the
special province of the sympathetic
nervous system, which for these
reasons, has been designated
"ergotropic" by Hes21,
As adaptive patterns they are con
tinually subject to modification and
to "turning on and off" according to
changing circumstances. They also
have a considerable degree of "local
sign", subject as they are to modifi
cation according to local or regional
circumstances and activities. That is,
although the efferent components of
these patterns (motoneurons and pre
ganglionic autonomic neurons largely
spinal in origin) are multisegmental
'and under the control of bulbar,
diencephalic and cortical centers,
their activity is continually influenced
by afferent impulses that arise in ther
mal receptors, pressure receptors,
proprioceptors, pain endings, etc.,
and that are conducted to the spinal
cord by sensory fibers entering via the
dorsal roots.
We believe that the local, more or
less segmental responses of the sym
pathetic nervous system reported in
this paper (and the chronic segmental
facilitation of motor pathways pre
viously reported28 are exaggerated
versions of these local components.
In these stressful and, in some cases,
painful experimental situations af
fecting small parts of the musculo
skeletal system, the afferent volleys
of impulses entering through in
dividual dorsal roots appear to have
become so prepotent as to dominate
that part (i.e., corresponding and
neighboring segments) of the sym
pathetic nervous system, and to take
precedence over vertically organized
patterns they ordinarily serve, and
even to disrupt them. They do not,
therefore, meet any particular func
tional demand, they are not adaptive
and, in many cases, they persist after
the provoking insult has ended.
The autonomic concomitants of
local myofascial irritation, injury,
stress or pathology have not received
widespread recognition in clinical
practice. They have received even less
experimental investigation, other
than in such studies as on cardiovas
cular or respiratory responses to pain
ful stimulation of various tissues. On
ly two experimental studies on human
subjects can be cited. In a study on
the patterns of referred pain produc
ed by injections of hypertonic saline
into paravertebral muscles of the
neck and back at various levels,
Feinstein, Langton, Jameson and
Schitler29 made some incidental
observations on "autonomic con
comitants". Usually produced by in
jections in the thoracic region
(seldom by injections in cervical and
sacral regions), the manifestations
were pallor, sweating, bradycardia,
fall in blood pressure and subjective
faintness and nausea. Sweating was
usually generalized, seldom even be
ing confned to the side of the pain.
As previously stated, we have made
similar observations, especially
following injections into periosteum,
following injections in apprehensive
subjects or when, for unknown
reasons, paravertebral injections were
unusually painful or distressing.
However, the methods used in our
study also revealed the regional and
segmental responses sometimes
superimposed on generalized changes
in electrical skin resistance.
Steinbrocker et al30 also studied
pain patterns associated with local in
jections of hypertonic NaCI solution
into myofascial structures, but made
only occasional observations of color
changes (pallor or erythema), temper
ature change and sweating in areas of
skin in the vicinity of the referred
pain. The patterns of both pain and
autonomic changes, were not
referable, however, to any known
nerve pathways, nor was there any
evidence of segmental relationships.
Unlike the above experimental
studies, clinical studies, such as those
by Travel and by Dittrich. yield
distinct and reproducible patterns,
sometimes showing segmental rela-
EMG, SNS, reflexes, etc.
tionships and sometimes not.
Travel!' 1 described the piloerection,
the frank perspiration and cooling of
the skin that may, individually and in
combination, be induced in reference
zones (in which deep pain is also felt)
on irritation of sensitive myofascial
trigger areas, and the reddening and
warming of the skin that may be
observed following infiltration of the
trigger area with procaine. Travel,
Berry and BigelowJ2 also recorded
changes in pulsations of the temporal
arteries associated with irritation and
anesthetization of triggers in the
trapezius muscle.
Dittrich 33 , in a paper on the
autonomic concomitants of somatic
pain, described in several patients the
referred pain, skin-color change (in
tense redness or cyanosis) and edema
associated with intensely tender spots
or triggers in paras pinal tissues of the
lower back and the {esponses to in
filtration of the triggers with pro
caine. The autonomic changes were
often quite remote from the triggers,
as was also true in Travell's studies.
Thus, for example, autonomic
changes in the upper trunk, shoulder
and upper extremity were demon
strably associated with irritation of
the latissimus dorsi muscle at lumbar
and sacral levels of the back. The
location of these
a
pparently segmen
tally remote reflex phenomena is
ascribable, of course, to the fact that
the latissimus dorsi receives its inner
vation from segments C6-8 of the
spinal cord. Anesthetization of the
triggers in the tendinous attach
ments of this muscle in the low back
produced relief of the referred pain
and of reflex autonomic changes.
Travel/H, on the other hand,
points out that segmental relations or
organized nerve pathways between
locus of the trigger and the reference
zone are seldom clear, though the
reflex nature of the relationship is
undeniable. The intervention of other
refex phenomena such as spasm of
vasa nervorum and resulting neural
Ischemia (Robertsl4) has been im
plicated.
Also to be included among the ob
servations on autonomic repercus
sions of somatic irritation are the in
creasing number of reports on vari
ous forms of "reflex sympathetic
dystrophy" associated with musculo
skeletal disorders or trauma to
myofascial tissues which are effec-
tively treated by silencing of the myo
fascial source of impulses or by
blockade of the appropriate sympa
thetic ganglia (e.g., Bonica 35 ).
It is important to point out that
reflex vegetative changes in the skin
and other superficial structures are by
no means peculiarly associated with
afferent stimulation of myofascial
origin. Similar patterns of autonomic
changes (as well as pain, tenderness
and muscle spasm) often accompany
visceral distrubances. In these cases,
the impulses dominating the segmen
tal pathways originate in injured,
ischemic, distended or irritated inter
nal organs, but the sensory fibers,
usually accompanying smpathetic
pathways also enter the spinal cord,
via the dorsal roots, along with those
innervating the somatic tissues. The
mechanisms involved and the pat
ters of manifestations of visceral
and of somatic stimulation may
therefore be quite similar, as strongly
suggested by the experiments of
Lewis and Kellgrenl6 The patterns
associated with visceral disturbances
will be discussed more fully in
another paper on that subject. A
preliminary report by KorrlO sum
marizes our early findings on patients
with visceral disease. We have men
tioned them here only to show that
our concept of exaggerated local or
segmental influences on normally
nonsegmental patterns applies to vis
ceral as well as to somatic structures.
We believe that the studies reported
in this paper on the changing patterns
of electrical resistance of the skin, in
conjunction with such observations
as discussed above, suggest at least
one possible origin - or category of
origins -of the patterns found in ap
parently normal, resting subjects.
Our observations strongly indicate
that the aberrant areas ot low resis
tance (Korr, Thomas and Wrightl)
and of vasoconstriction or -dilatation
(Wright, Kor and Thomas2) may
begin as parts of reflex responses to
centripetal streams of impulses
originating in somatic (or visceral)
structures or, possibly, in nerve fibers
irritated by them.
Whether such a reflex mechanism
could continue to be the sustaining
mechanism for periods of weeks,
months or years is not known. Unfor
tunately, most experimental studies
on reflexes are based on brief periods
of stimulation - fractions of a sec-
ond to a few minutes - and little is
known of the changes that take place
during greatly protracted stimulation.
The available evidence, mainly of
clinical origin, indicates that it is
unlikely that circumstances (such as
severe tension on a muscle) which
would profoundly modify the pat
terns of afferent impulses from a
given tissue or organ could, if con
tinued, sustain such afferent bom
bardment for long periods without
also initiating some adaptive or
secondary pathological change in the
affected tissue that abolishes, silences
or otherwise alters the original source
of irritation. Fibrosis of chronically
stretched, irritated or ischemic muscle
is a familiar example of such a
change.
It seems equally unlikely that
neuronal structure, chemistry and ir
ritability of the affected part of the
central nervous system would remain
unchanged in the face of prolonged,
intense afferent bombardment.
It is possible, therefore, that pat
terns of very long standing, even if
reflexly initiated, may be maintained
by mechanisms other than the mere
prolongation of that same reflex ac
tivity. The experiments of Kawahata
and Thomas6 indicate, however, that
the increased sweat secretion of low
resistance areas is maintained by
tonic hyperactivity of efferent
neurons supplying such areas. But the
possibility must be left open that the
sustained hyperactivity of the efferent
(sympathetic) neurons, and therefore
of the sweat glands, may, in the
chronic phase, be due not so much to
chronically modified afferent bom
bardment as to chronically aug
mented irritability of central neurons.
We must also leave open the
possibility that some of this efferent
hyperactivity may not even be cen
trally ordered. This is suggested by
some of the areas of low resistance
that we have recorded. We have in
mind particularly those areas of low
resistance which seem to occupy parts
of a single dermatome (e.g., Fig. 9 in
Korr, Thomas and Wright'. and Fig.
1 and 1 6 c in this paper). It is diffcult
to accept a reflex basis for an auto
nomic response which is limited to a
single segment when one keeps in
mind the divergence of afferent
neurons as they enter the cord and
synapse on secondary neurons, the
further divergence of the inter-
63
neurons with which they synapse and,
finally the divergence of the
preganglionic sympathetic neurons.
Axons in a given white ramus com
municans are known to send branches
above and below their level of entry
into the sympathetic chain and to
synapse in several ganglia.
While the highly selective chan
nelization of a reflex response or of
preganglionic discharge to postgan
glionic neurons of an individual
ganglion cannot be entirely ruled out,
it would'seem that, in these cases, the
pathways are more directly selected.
We believe it more likely that irrita
tion may have been directly affecting
paricular ganglia, gray rami com
municantes, ventral roots, spinal
nerves, primary divisions or inter
costal nerves. Certainly, dermatomal
bands of sweat gland activity or
vasoconstriction would be produced
by direct stimulation of any of these
structures (Randall and coil. 36). It is
possible that at least in some of the
experiments direct mechanical (com
pression, friction, stretch) or
chemical (hypoxia, accumulated
metabolites, pH shift) irritation of
one or more of these neural structures
may have taken place, in addition to
refex phenomena. (Some of the
associated vascular changes in the
skin may even be due to the initiation
of antidromic impulses in dorsal root
fibers (Folkow37).
Whether reflexlY or directly pro
voked, the hyperactivity of isolated
portions of the sympathetic outflow
serves no obvious adaptive function.
Yet one may expect functional im
plications of such hyperactivity of
isolated portions of the sympathetic
outfow and, if sustained, clinical im
plications. Certainly, the affected
segments, which our previous studies
indicated are in a state of facilitation,
cannot participate in a well coor
dinated manner in the organized pat
ters of motor and autonomic activi
ty associated with changes in en
vironmental temperature, posture or
muscular work2
-s.
38. Since the parts
of the sympathetic outtow related to
the persistent low resistance areas
have low reflex thresholds and, in
general, make exaggerated responses,
some degree of disruption of these
patterns and some imposition of
compensatory burdens on the other
participating elements in each pattern
are to be expected.
Although the autonomic con
comitants of myofascial stimulation
reported in this paper have been
measured only in the skin, there is no
reason to assume that they are limited
t o the skin. Numerous clinical
studies, a few of which have been
cited above, strongly suggest that the
sympathetic neurons regulating secre
tory, contractile and vasomotor ac
tivity in viscera may also be in-.
volved. Experimental studies by
Kuntz 39, Kuntz and Haelwood4 and
Richins and Brizzee41, on the
simultaneous vascular responses in
skin and viscera to the cooling and
warming of the skin, clearly reveal
the rich access of somatic afferefts to
visceromotor pathways and the paral
lelism between the vascular responses
of skin and viscera. Studies on renal
circulation by Nedz
(
l42. 43, and by
H' in our laboratories, confirm
and extend these observations. An in
genious study on human subjects by
Ralston and Kerr' reveals the pro
found reflex vascular changes in the
mucous membranes of the upper re
spiratory tract in response to thermal
stimulation of the skin in the upper
part of the body. Conversely
numerous studies on reflex somatic
concomitants of visceral stimulation
or pathology, show the reciprocity of
reflex relationships between visceral
and somatic tissues.
. We believe that these studies,
revealing some sympathetic manifes
tations of myofascial irritation, con
tribute to a clearer understanding of
the mechanisms involved in the wide
variety of syndromes encompassed in
the category, "reflex sympathetic
dystrophies". In the context of the
foregoing discussion, they also help
to explain the exacerbation of many
pain syndromes (e.g., reflex sym
pathetic dystrophies, referred pains
associated with myofascial triggers,
joint pains of many origins, referred
pain of visceral origin, etc.) by ex
posure of the patient, or even a small
part of the body, to cold, by provoca
tion of emotional responses, or by an
environmental change which in
creases sympathetic activity.
Some of these implications and the
autonomic changes occurring in
association with musculoskeletal
disturbances of clinical origin and in
association with visceral disease will
be explored further in succeeding
reports now in preparation.
Summar
1. The purpose of these studies was to
examine the changes in sudomotor
patterns in the skin of the human
trunk produced by experimentally in
duced irritation and stresses in the
musculoskeletal tissues, as a step
toward understanding the origins of
the patterns found in apparently nor
mal individuals.
2. Irritation of the musculoskeletal
tissues was produced by the injection
of hypertonic saline into paraverte
bral tissues. Postural stresses were
produced by the insertion and
removal of heel lifts and by the lateral
inclination of the pelvis by the use of
tilt-chairs.
3. Sudomotor patterns were re
vealed by recording electrical skin
resistance on the dorsal skin of the
thoracic and lumbar regions in rela
tion to segmental level.
4. New areas of low electrical
resistance appeared when the saline
injection produced referred pain; the
areas were distributed in the reference
zone, in dermatomes related to the in
jection site.
S. Postural changes produced
changes in patterns which included a)
exaggeration of existing patterns and
b) the appearance of new areas of low
resistance (increased sweat gland
secretion), according to the applied
stress, the individual's vertebral
adaption to the stress and the areas of
discomfort.
6. We believe the findings support
the following hypotheses:
a) That the manifestations of
altered sympathetic activity observed
in these studies represent distortions
of normally existing patterns of ef
ferent activity.
b) That the distortions begin as
responses to exaggerations of seg
mental or local afferent influences
which ordinarily have only local ad
justive infuences on the patterns, and
that these impulses may be visceral or
somatic in origin.
c) That although the aberrant areas
of low resistance described in normal
subjects, may reflect chronically
altered or intensified patterns of af
ferent bombardment from foci in vis
ceral or somatic tissues, other factors,
such as adaptive or pathological
changes in those tissues and altered
central excitability, may eventually
become involved.
7. Since, however, the affected
EMG, SNS, refexes, etc.
areas may be limited in extent to
single dermatomes, it appears that in
dividual ganglia, gray rami communi
cantes, ventral roots, spinal nerves or
their branches may in some cases be
dirctly, rather than reflexly, ir
ritated.
8. Some of the functional implica
tions of chronically altered activity in
localized portions of the sympathetic
outflow are identified.
9. The relation of these findings to
mechanisms involved in such clinical
phenomena as reflex ympathetic dys
trophy, myofascial triggers, referred
pain, etc. , is briefy examined.
The valuable assistance of Mr. Emi D.
Bl ackorby wi t h i nstrumentati on and
illustrations is gratefully acknowledged.
We are grateful to Dr. Joh n A. Chace, U. S.
Public Health Service Special Research Fellow,
in the Biomechanics Laboratory of this
College. for taking these roentgenograms and
for his valuable guidance in analyses of the ver
tebral mehanics involve in each experiment.
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Reprinted by permiSSion from Journal of Neural
Transmission 23: 22, 330355, 192.
05
Cutaneous patterns of sympathetic activity
in clinical abllornlalities of the
musculoskeletal system (1964)
IRVIN M. KORR, HARRY M. WRIGHT and JOHN A. CHACE
In previous investigations we have
reported on regional and segmental
variations in sympathetic activity as
revealed by cutaneous sudomotor and
vasomotor manifestationsl 2. I n
studies of topographical variations i n
electrical skin resistance (ESR) , we
have observed persistent areas of low
electrical skin resistance in most
"normal" resting individuals ' . The
topographical distribution, or "pat
tern", of these low resistance areas
(LR) was found to be characteristic
for a given individual and remained
relatively constant for weeks or
months. Studies by Thomas and
others in our laboratories3-s have
shown that these measurements and
patterns of ESR, as recorded by our
methods, refect variations in activity
in the sympathetic fibers. Studies of
regional and segmental variations in
cutaneous vasomotor activity also
showed topographical "patterns" in
the skin temperature, < fred response"
and apparent blood content of the
skin; and, like the ESR patterns, the
vasomotor patterns showed a high
degree of constancy and reproduci
bility in any given individual2
These studies, on apparently well
and resting subjects, however, did not
reveal the physiologic origins and
functional si gni ficance of these
cutaneous manifestations of sym
pathetic activity. Preliminary evi
dence obtained in our laboratories6 7
and reports of areas of sudomotor
and vasomotor dysfunction reflexly
related to painful myofascial and
visceral conditions (cited in detail in
our previous paper S), suggested that
these patterned differences in sudo
motor and vasomotor activity were
related in some individuals to visceral
and myofascial disturbances . We
undertook investigation, therefore,
of factors which might contribute to
these local asymmetries and vari
ations in sympathetic activity .
A detailed report on the changes in
sudomotor patterns in the skin of the
human trunk produced by experi-
mentally induced irritation and
stresses in the musculoskeletal tissues
has already appeared in this journals.
New areas of low electrical skin resis
tance appeared in areas of re
ferred pain and in segmentally related
dermatomes when the paravertebral
tissues were injected with small-uan
tities of hypertonic saline. Postural
stresses produced exaggeration of ex
isting LR patterns or elicited new
areas of LRA according to the stress,
the individual's vertebral adaptation
to the stress ad his discomfort.
In this paper we report our obser
vations of sudomotor patterns in
clinical subjects with known musculo
skeletal disturbances, myofascial
stresses and pain syndromes.
Methods
1. Methods /or evaluation 0/
musculoskeletal abnormalities.
Methods of examination utilized in
this study included radiographic
. studies of posture and skeletal abnor
malities, electromyographic assess
ment of the activity of postural
muscles, and palpatory testing for
areas of cutaneous and deep tender
ness. Postural radiographic studies of
the spine and pelvis, taken with the
patient in the standing position ac
cording to methods which have
previously been described
1
2, were
made on some of the patients. Our
electromyographic procedures are
described in the legend of Fig. 8 c.
The palpatory methods were those
conventionally utilized in clinical
practice.
2. ESR Explorations.
Since the methods used for the study
of cutaneous sudomotor activity
which have been used in these studies
have been previously described
1
9, 10
,
they will be only briefy characterized
here.
The experiments reported in this
paper were done over a period of
several years. During this time three
methods for recording ESR were
used, each yielding a different type of
record. However. all three methods
are based on conventional principles
of skin resistance measurement.
Essentially, each method consists
of measuring or recording, in correct
spatial relationship to the explored
area, the momentary current flow
through the skin in contact with a
constantly moving exploring elec
trode, at known voltages. The volt
ages were tapped stepwise from a
series of dry cells and applied to an
electrode fixed to an earlobe and an
exploring electrode. Resistance of the
skin of the earlobe was minimized by
means of electrode paste. Area-to
area differences in current flow at a
given voltage. therefore. were due to
differences in the "resistance" of the
skin under the exploring electrode.
a) Explorations with hand-held
electrode.
In our earlier studies we used an in
strument similar to that described by
Japer
1 1
. Current flow was read from
a microammeter as the electrode was
moved over the subject's skin.
b) Automatic explorations.
In later studies two types of auto
matic dermometers were developed9,
10,
With the frst 9, differences in cur
rent flow through the skin were con
verted into variations in the bright
ness of a light over the exploring elec
trode which was propelled over the
skin at a constant speed. A camera re
corded strips of light which varied in
brightness according to the ESR (in
versely as current flow) along strips
of skin.
To eliminate the disadvantages of
photographic recording, however, we
developed a dermometer with which
skin resistance patterns on large areas
of the trunk were recorded directly on
paper by a recording galvanometer
whose amplitude of oscillations is re
lated. through an amplifer, to the
skin current '0. The position of the
galvanometer writing-point on the
chart was related to the position of
the exploring electrode on the subject
by means of a pantograph.
The explorations were conducted in
a quiet room maintained between 23
and 25 C. The body was unclothed
above the level of the sacrum. The
tips of the spinous processes were
identified by palpation and num
bered. In these studies, "segmental"
EMG, SNS, reflexes, etc.
level refers to the topographical level
on the trunk as identified by the cor
responding spinous process, rather
than the dermatomes. There is, how
$ver, close correspondence between
topographical and segmental levels
for paravertebral skin, except at the
uppermost thoracic segments.
c) Interpretation of ESR charts.
In the figures showing ESR patterns
the dark areas represent areas of low
electrical skin resistance. The dark
ness of shading in the hand-drawn
charts (Fig. 4, 5, 8 bi) and in photo
graphic records (Figs. 1 -3, S bii) is in
proportion to current flow at explora
tion voltage; the darker the area the
lower the resistance. White areas: I
or less (resistance, in ohms, at least
I million times the number of volts);
black areas: 20 pa or more; i. e. less
than I 20 of basic resistance; gray
areas: intermediate values. (Repro
duction of these figures has darkened
the gray areas and the darker shades
have become indistinguishable from
the black areas.)
In the pantographic records (Figs.
6 b, 7 b, 8 biii) amplitude of oscilla
tions of the recording galvanometer is
related to current flow through the
skin. The thin vertical lines (no oscil
lation) represent areas permitting 0 to
I pa at exploration voltage; widest
oscillations represent current flows of
30 pa or more, i n these charts ,
therefore, the darkest areas represent
I 30 the basic resistance or less.
Tips of spinous processes and the
sacral base are marked in photo
graphic (light points and lines) and
pantographic charts (short horizontal
lines). In the figures both the photo
graphic and pantographic charts are
spatially related, by superimposition,
to the subject's body.
Rcu|l
ESR explorations were conducted on
more than 1 30 persons presenting
complaints referable to postural and
musculoskeletal disturbances, such as
pain, tenderness, severe and per
sistent backache and limitations in
motion, or in whom anomalies or
other potentially stressful musculo
skeletal problems were discovered.
Such problems and complaints as
gross inequality in leg-length, verte
bral anomalies, injuries to the spine,
pelvis or shoulder, abnormal spinal
curvatures, herniations of interverte-
Fig. I a. Radiograph ofpatient D. C. R., stand
ing (see text, Case I). The white vertical line
appearing in this and succeeding radiographs is
the upward projection ofthe subject 's mid-heel
line". All radiographs, as well as other figures
in this paper, are to be viewed as though the pa
tient were being seen from the back; i.e., left
side is on the reader's left hand side.
Fig. I b. The ESR pattern of patient D. C.R.
shows low resistance areas in the region of the
lumbosacral junction. Recorded with the
photographic method ofESR exploration.
bral discs, spondylolistheses, etc. ,
were included.
Eight are presented to illustrate the
type of information revealed in our
studies.
Case I. Patient D. C. R. , Male, 49
years (Fig. IJ.
Complaint: Severe ache i n low
back, of long standing, beginning in
childhood; often incapacitating. Pa
ti ent compl ai ns of di ffi cul ty i n
"straightening up" after being seated
for prolonged periods and after
stooping over.
Radiographic and physical ex
amination. Antero-posterior X-ray
films of the pelvis and lower lumbar
spine, taken with the patiert. standing
(Fig. 1 a) revealed a) an inequality of
leg length (heights of femur heads),
the right being 5/8 inch (approxi
mately 1 6 mm. ) shorter than the left;
b) a considerable displacement of the
pelvis to the right of the mid-heel line;
c) ti lting of the sacral base-plane
toward the right; d) scoliosis of the
lumbar spine, convex to the right,
with considerable rotation of the
vertebral bodies toward the con
vexity; and e) congenital, unilateral
anomalies of the first sacral segment.
Electrical skin resistance (Fig. 1 b) .
The ESR pattern, obtained with the
photographic method, reveals the
predominance of low-resistance areas
in the region of the lumbosacral j unc
tion.
Case 2. Patient H. M. , Male, 34 years
(Fig. 2J
Complaint: This man also com
plained of backache and "stiffness"
beginning in childhood and reported
several incidents of painful back in
j ury and strain, due to lifting and
pushing in the course of his work as a
farmer. Although palpatory examina
tion revealed generalized tenderness
over the back, pai n, tenderness and
muscular rigidity were most severe in
the vicinity of the lower lumbar spine
and lumbosacral j unction, particular
ly on the left side.
Radiographic examination (Fig. 2
a) of the spine revealed failure of fu
sion of the neural arch of the fifth
lumbar vertebra and anomalous, ru
dimentary or asymmetrical articula
tions in the lower lumbar spine and
lumbosacral junction. The discrepan
cy in leg length, the right leg being 3 8
inch (approximately I cm. ) shorter
than the left, seems not to have pro
duced significant tilt of the sacral
base or lumbar scoliosis.
Electrical skin resistance (Fig. 2 b) .
Low-resistance areas were mainly in
the lumbosacral region, predominat
ing on the left side, where symptoms
were most marked.
Case 3 Patient W. P. , Male, 46 years
(Fig. 3).
Complaint: This subject had his
07
F ig. 2 a. Radiograph ofpatient H.M., standing
(see text, Case 2).
F ig. 2 b. The ESR pattern of patient H.M.
shows m ost conspicuous low-resistance areas in
the lum bosacral region, particularly on the left
s
i
de, where symptoms were m ost m arked.
Recorded with photographic m ethod.
left leg amputated more than 30 years
prior to this study, because of osteo
myelitis. He had no complaint (other
than occasional , mild gastrointestinal
distress), but was selected for study
because of our interest in his muscu
loskeletal adaptations to the amputa
tion.
Radiographic and physical ex
amination. Accordi ng to relative
heights of his femur heads measured
radiographically in the standing posi
tion, his aFtificial leg (attached to the
mid-thigh stump) was almost one
i nch (approximately 2. 5 cm. ) too
08
short. He had a long mild scoliotic
curve, convex to the left, extending
from the tilted sacrum to a sharp
"breakover" point between the sixth
and seventh thoracic vertebrae. Para
spinal musculature was thickened and
tense on the left side throughout the
length of the scoliosis and one or two
segments above, as compared with
the right side. Deep tenderness was
especially marked on the left side in
the lumbar region and in the mid
thoracic region.
Electrical skin resistance (Fig. 3).
The exploration revealed a virtually
continuous area of low resistance on
the left side, extending from the level
corresponding to the top o the
sacrum to the mid thoracic region.
Case 1. Patient A. W. , Female,
30 years (Fig. 1J.
Complaint: About two weeks prior
to this study the patient had sli pped
on an icy sidewalk and fallen heavily,
the impact being mainly on the left
buttock. In addition to painful bruise
of the coccyx, she complained of per
sistent pain and muscular spasm
along the l umbar spine on the left
side. She had also observed areas of .
exquisite hyperesthesia of the low
back, groin and thigh.
Radiographic examination revealed
nothing significantly related to the
complaint.
Electrical skin resistance. Fig. 4
shows areas of low resistance found
on this patient. They corresponded
very closely with the areas of hyper
esthesia, even light movement of the
exploring electrode over them causing
considerable discomfort. Compari
son of this chart with maps of the
sympathetic dermatomes based on
the boundaries between high and low
resistance areas found on patients
following ganglionectomies at vari
ous segmental levels (Richter and
Woodruffl 3 ) , indicate an irritative in
j ury of spinal roots L- l and L-2 on
the left side, as a consequence of the
fall.
Case J. Patient M. S. , Male, 12years
(Fig. J/.
Complaint: This man, a farmer,
was brought to the hospital unable to
bear his weight on the right leg be
cause of severe lumbosacral pain on
the right side, with sciatic radiation.
Onset followed a series of severe
"bumps" while driving a tractor on
F ig. 3. The ESR patter ofpatient W P. shows
a large area of low resistance on the left side,
from the m idthoracic region to the base of the
sacrum . Photographic m ethod (see text, Case
3).
F ig. 4. The ESR pattern of A. W. shows low
resistance areas which correspond closely to the
areas ofhyperesthesia in this patient. Explora
tion with handheld electrode (see text, Case 4).
his farm. Similar attacks, though less
severe, had occurred in previous
months, especially following vigorous
physi
'
cal work and operation of mo
torized farm equipment on which he
was seated. On the basis of symptoms
and physical findings a diagnosis of
EMG, SNS, reflexes, etc.
Fig. 5. The ESR paller ojpalienl M.S. The
areas oj low resislance are shown as black
SpOIS: Ihe areas oj lendernes are indicaled by
X marks. Exploralion wilh hand-held eleclrode
(see lexl. Case 5).
rupture of the intervertebral disc be
tween L-5 and the sacrum, with her
niation on the right side was made.
This diagnosis was confirmed at
surgery.
Electrical skin resistance. The
lower part of the trunk of this patient
was explored with hand-held elec
trode about one hour following
admission to the hospital. The areas
of markedly lowered resistance are
shown as black spots of various sizes
in Fig. 5 . According to the system
described in a previous paper' the
resistance in the areas marked in
black is ' 20 or less that of the back
ground resistance, 10 this case
1 50, 000 ohms or less as
'
compared
with a general resistance of at least
3, 000,000 ohms ( 1 /a of current flow
or less at 3 volts) . The area shown
over the left ilium was intermediate
(about 750,000 ohms) and was shown
in gray on the original chart: the dif-
Fig. 6 a. Radiographs ojpatient I.M., standing (see tet, Case 6).
Fig. 6 b. The ESR palter ojpatient I. M. The areas oj low resitance in the lumbosacral region
developed aJter applying heat to the ventral surJace oj the patient. Recorded with pantographic
method (see text, Case 6).
Fig. 7 a. Radiograph ojpatient G. c, standing (see tet, Case 7).
Fig. 7 b. The ESR palter ojpatient G. c. shows areas ojlow resistance in the lumbosacral and cer
vicodorsal regions which were related to the areas ojmusculoskeletal stres. Pantographic method.
ference in density from the other
areas was, however, lost in photo
graphic reproduction of the chart.
A reas oj tenderness. At our re
quest, the attending physician in
dependently conducted a palpatory
examination of the patient in which
he elicited areas of most severe deep
tenderness by digital pressure and
recorded them on a chart similar to
that used for the ESR patterns. His
chart was then superimposed on ours
and, in the composite chart shown in
Fig. 5, the areas of tenderness are in
dicated by X marks. Vigorous digital
pressure to the areas caused not only
local pain but, in most of the areas,
also radiation and even remote refer
ence of pain similar to that described
by Travell1 4 and others.
Case 6. Patient I. M. , Male, 2years
(Fig. 6).
Complaint: Severe pain over the
lumbosacral area.
Radiographic examination (Fig.
6 a) revealed bone change in the ar
ticulation of L-4 and L-5, including
erosion of the lamina of L-5 on right
side, probably due to pressure of in
ferior articular process of L-4. The
inferior facets of L-4 and L-5 are
frontal, rather than sagittal, in orien
tation.
Electrical skin resistance. The pa
tient' s ESR pattern, obtained with the
pantographic method, is shown in
Fig. 6 b. The apparently facilitated
area shown in the lumbosacral area
was elicited in this subject by apply
ing heat to the body. Though ex
plored in mid-spring (April 30) at
room temperature 25. 6C, the skin of
his back had a uniformly high resis
tance. Electric heating pads were ap
plied to the ventral surface and the
area shown in the figure had ap
peared after 30 minutes. An addition
al 20-minute period of heating pro
duced only slight upward spread of
this area .
Case /. Patient G.C., Male, 2Iyears
(Fig. /).
Complaint: Lumbosacral pai n;
discomfort and restricted motion at
the cervicodorsal junction and occa
sional torticollis.
Radiographic and physical eami
nation. Stress at the lumbrosacral
j unction is evident in the apparent
loss of cartilage and the thickening of
the articular plates between L-5 and
0
J. G.
Fig. 8 a. Radiographs of patient J. G. , standing (see text, Case 8).
L
j'
__ I
..... I
'
Fig. 8 b. The ESR patters of patient J. G. taken over a period of 4 years consistently shqwed areas of low resistance at the lumbosacral, the dorso
lumbar and the cervico-dorsal junctions and in the midthoracic region. The relation of the patterns to clinical findings is discussed in the text. - 8 bi.
November 1949; patter recorded with hand-held electrode. - 8 bii. March 1951; photographic method. - 8 biii. November 1953; pantographic
method.
Fig. 8 c. Electromyographic record of the posterior vertebral muscles during quiet standing, in patient J.G. - The cardiac artifact is evident on each
record, but is easily distinguished from electromyographic activity which was consistently most marked. in this subject. at the upper thoracic levels
(especially on the right side) and at lumbar levels on the left side. Slight or moderate activify, as shown here, was also usually evident at lower thoracic
levels.
Activity of the paravertebral muscles at various segmental levels during standing was sampled in the following manner. Silver surface electrodes were
tightly affixed to the skin at selected sites (resistance lowered with electrode paste) over the spinal extensors. Electrodes were placed at levels
corresponding to the tips of spinous processes of alterate vertebrae T I, T 3, T 5 . . . L 5, on left and right sides. Electrodes were led through a switchbox
to four differential amplifiers (Offner) for recording with pen writers (and for monitoring with cathode ray oscilloscope and loudspeaker).
Two consecutive electrodes on each side T - T3, T3 - T5 . . . L3 - L5) served as electrode pairs, thus sampling activity in the intervening
musculature. Four such areas (electrode pairs) were sampled simultaneously, the switchbox making possible a survey of the entire length of thoracic and
lumbar spine (16 electrode pairs) within 30 seconds. Subjects were asked to stand at rest and relaxed, serial records being taken until activity had subsided
to a minimum.
S- 1 on the left side (Fig. 7 a). Asym
metry with respect to planes of the
articular surfaces (sagittal on the left,
more nearly frontal on the right) be
tween L-4 and L-S and between L-S
and S- 1 may have contributed to the
stress. A lateral ti l t of the cervical
spine to the right is also evident i n the
fil m.
Examination of the patient dis-
closed considerable muscular splint-
ing in the l umbar area, particularly
on the left side, and fixity of the
thoracic spine with some loss of the
normal posterior convexity. The pa
tient' s head was carried in a forward
position. This was associated with
considerable thickening of tissue over .
the cervicodorsal junction and much
muscular tension i n this area.
Electrical skin resistance (Fig. 7 b) .
Pantographic exploration showed
that the areas of low resistance
predominated i n areas of ski n which
are regionally related to areas of
musculoskeletal stress.
t i on; occi pi tal and subocci pi tal
headaches.
Radiographic examination. Mul ti
pl e lateral curves of the spinal column
are evident in Fig. 8 a, possibly
' related to the discrepancy in leg
length, the l eft femur head being ap
proximately one inch ( 2. S em. ) lower
than the right. One scoliotic curve,
convex to the left, involves the entire
lumbar spine. The planes of the ar
ti cular surfaces between L-3 and L-4,
L-4 and L-S , L-S and S- I appear to be
factors in the l umbosacral stresses
contributing to the symptoms in this
area. Another lateral curve, also con-
vex to the left, involves the lower half
of the thoracic spine, wi th relatively
sharp angulations at the extremes of
the curve, T- 1 2-L- l and T-S-T-6.
The cervical spine (not shown) leaned
considerably to the l eft, there also be
ing a lateral curvature, convex to the
right, and a sharp i nflection at the
cervicodorsal j unction. This patient
carried his head well over the l eft
Case d. Patient J.G. , Male, 2J years
(Fig. dJ.
shoulder, with considerable tension in
the posterior cervical musculature on
the right side.
Complaint: Pain in low back; pain
and sti ffness at cervicodorsal j unc-
70
Electrical skin resistance. The ma
jor areas of l ow resistance (Fig. 8 b)
L H
Fig. 8 c
.....
1 00".
J G 3 IS SI
!' ."d, ,
EMG, SNS, reflexes, etc.
appeared over a period of several
years (November, 1 949 -November,
1 953) to be consistently associated
with the regions of sharpest angula
tion of the vertebral column: the
vicinity of the lumbosacral j unction,
the dorsolumbar junction, the mid
thoracic region and at the cervicodor
sal junction.
Electromyographic observations .
An electromyographic sampling of
the activity of the posterior vertebral
muscles during quiet standing (Fig.
8 c) indicated that considerable ac
tivity of the spinal extensors, much
stronger on one side than the other,
was required in these same regions for
the maintenance of the erect posture
in this patient. Thus, there was con
spicuous activity of the lumbar mus
culature, extending somewhat to the
lower thoracic levels, on the convex
(left) side of the scoliosis, and of the
upper thoracic segments, especially
on the right side, possibly because of
the lateral displacement of the head
and neck. (Activity of the cervical
musculature was not sampled.)
This electromyographic study was
part of a series done on a large
number of subjects, many of them
observed repeatedly over long periods
of time (Kor and Thomas
I
S. Wright
- unpublished observationsI 6). As
has been shown by Floyd and Silveri
1
,
Portnoy and Morin 1 8, Joseph and Mc
Coli, 19. 2 and others, we too found
that some subjects were able to
achieve a standing posture in which
there was very little activity of the
posterior vertebral muscles. How
ever, in our experience, some degree
of localized, often asymmetrical ,
activity was found in every subject.
The patterns of such activity -
location, extent, relative amount,
etc. , varied from subject to subject,
according to body build, posture,
weight distribution, spinl and pelvic
configuration and other, unidentified
factors. As we have found to be
true for sudomotor and vasomotor
activity I. 2 the patterns are remark
ably constant and characteristic for
each subject.
Ucuon
In the preceding report from this
series of investigations!, we showed
that we were able to modify the ESR
patterns of human subjects by experi
mentally induced i rritations and
stresses in the musculoskeletal tissues.
I ntramuscular inj ection of small
quantities of hypertonic saline, for
example, caused the appearance of
new areas of low ESR in those indivi
duals in whom referred pain was in
duced, the new areas of low resistance
appearing in the reference zone. Pos
tural stresses caused exaggeration of
existing patterns of low-resistance
areas (further lowering of resistance
and spreading of areas) and the ap
pearance of new areas of low resis
tance according to the nature and lo
cation of the applied stress, the in
dividual ' s vertebral adaptation to the
stress and the areas of discomfort. On
the basis of studies by Tlomas and
others in our laboratories previously
cited3-, the induced changes in ESR
(and accompanying vasomotor
changes) would seem to represent
sympathetic responses to the ex
perimental musculoskeletal insults.
In discussing our findings in the
foregoing paper, we proposed that
the sympathetic changes were not
anomalous reflexes, invoked de novo
by the noxious myofascial stimula
tion, but that they were modifications
of normally operating patterns of
somato-autonomic coordination. Ex
amples of these patterns are those of
centrally ordered adjustment of vis
ceral, cardiovascular and thermoreg
ulatory functions which continually
take place according to changing
muscular activity, heat production of
muscular work and posture. Al
though the efferent components of
these reflex patterns (motoneurons
and preganglionic neurons, largely
spinal in origin) are multisegmental ,
and under control of higher centers,
their activity is also under the contin
ual influence of afferent impulses
arising in peripheral receptors and
nerve endings, conveyed over dorsal
root fibers. Indeed, the local and
segmental sensory inputs are essential
to the proper execution of the pat
terns with appropriate adjustment to
local circumstances and demand. It
was our conclusion that the sym
pathetic responses (indicated by
altered ESR patterns) to the experi
mental myofascial insults reported in
the preceding paper were exaggerated
versions of the local components.
The studies reported in this paper
on subjects with musculoskeletal
stresses and irritations of traumatic,
congenital, postural or pathological
origin revealed similar regional exag-
gerations of sympathetic activity. Al
though the changes produced in the
affected musculoskeletal tissues in a
few minutes or even a few hours, by
saline injection or by experimental
postural stresses, may be expected to
bear only superficial resemblances to
those associated with clinical condi
tions of much longer duration such as
are reported in this paper, it is likely
that the neural and refex mechanisms
are fundamentally the same. As we
stated in the previous paper' , we
believe that the altered patterns of
sympathetic activity (as well as associ
ated alterations in muscular activity)
are either refex manifestations of
changes in sensory input arising in
nerve endings and receptors in the
musculoskeletal tissues or the effects
of direct insults to nerve fibers (or
ganglion cells) or a combination of
both.
Nevertheless, the question arises as
to how the processes that are involved
are modified with time. Our experi
mental studies certainly indicate that
the altered sudomotor and vasomotor
activities in the aberrant areas at least
begin as parts of reflex responses to
centripetal streams of impulses orig
inating in somatic structures or,
possibly, as the effects of direct
mechanical or chemical irritation of
nerve fibers. But one wonders
whether the same mechanisms would
continue to operate in essentially the
same way for periods of weeks to
years. Clinical and pathological evi
dence indicates that in the face of
chronic stress or irriation and of sus
tained reflex activity, adaptive
changes would take place either in the
stressed or irritated tissue (e.g. ,
fibrosis of muscle), in the participat
ing neurons (e.g. , altered excitability),
in the responding organs or tissues
(e.g., altered contractility of blood
vessels, altered secretory activity of
sweat glands) or in combinations
thereof.
In studies to be reported more fully
in a subsequent publication3,2I.22 we
investigated the functional alterations
in the apparently aberrant segments
by comparing the simultaneous re
sponses of these areas with those of
apparently normal adjacent or corre
sponding contralateral areas to such
generalized stimuli as ateration in en
vironmental temperature, change in
posture from recumbent to standing,
pain, threat of pain, startling, etc. We
7I
found that the segments represented
by aberrant dermatomes (with respect
to sudomotor and vasomotor activi
ty) are profoundly altered functional
ly. The responses of these segments to
thermoregulatory, postural or emo
tional demand were, relative to the
adjacent or contralateral control
segments, so altered quantitatively, in
terms of threshold, latency, magni
tude and duration of response, as to
be inappropriate to the demand. The
direction of the alteration in the
segments represented by low-resis
tance areas have been consistently in
such a direction as to indicate facilita
tion of the sympathetic pathways to
the skin. Whether this reflects an
alteration i n those neurons
themselves or sustained afferent (or
pre-ganglionic) bombardment has not
been determined. The recent studies
of Thoma and Kawahata' clearly in
dicate that in our subjects the altered
sudomotor responses in the low
resistance areas were due to changes
in impulse traffc in the sudomotor
pathways rather than in the sweat
glands themselves. Whether changes
in the sweat glands would eventually
occur in such situations has not yet
been determined, although the occa
sional finding of extremely high
resistance, nearly anhidrotic, areas,
similar in size, shape and distribution
to low-resistance areas reported in
these studies, suggests that such
changes may occur.
The reader is referred to our pre
ceding paper' on experimental insults
and stresses for a more detailed dis
cussion of the theoretical and clinical
implications of the segmentally and
regionally pattered autonomic con
comitants of myofascial stresses and
abnormalities, and of the relevant
work of other investigators. The pres
ent study confrms that local changes
in sympathetic function may be not
only acutely and temporarily induced
by relatively brief experimental re
sults, but that enduring changes in
patterns of sympathetic activity may
become associated with musculoskel
etal disturbances of clinical origin.
This study also strengthens our sug
gestion that the patterns of aberrant
areas of sudomotor and vasomotor
activity previously described in ap
parently healthy subj ectst 2 may
refect subclinical and asymptomatic
disturbances of afferent bombard
ment, over selected dorsal roots, or of
72
direct irritation of nerve fibers or
ganglion cells. The patterns associ
ated with visceral disturbances as
such sources of afferent bombard
ment and neural irritation will be
presented in the succeeding paper.
Summar
1 . These studies on 1 30 patients
have been concerned with topograph
ical patterns of sudomotor activity
associated with known musculoskel
etal disturbances, myofascial stresses
and pain syndromes.
2. The method employed for
measuring sudomotor activity, as an
indicator of regional variations in
sympathetic activity, was tnat of
recording the electrical resistance of
the skin (ESR). Radiographic, elec
tromyographic and palpatory ex
aminations, as well as other conven
tional clinical methods, were used in
the evaluation of the musculoskeletal
disturbances.
3. The observations frequently
showed the presence of regional and
segmental patterns of low electrical
skin resistance (LRA) in areas of re
ferred pain and dermatomes segmen
tally related to the musculoskeletal
disturbances or myofascial stresses.
4. These paterns of altered electri
cal skin resistance appear to reflect
enduring changes in the patterns of
sympathetic activity associated with
. musculoskeletal disturbances of
clinical origin.
5. These studies suggest that the
patterns of aberrant areas of sudo
motor and vasomotor activity, which
we have previously described in ap
parently normal subjects, may refect
subclinical and asymptomatic sources
of afferent bombardment, over
selected dorsal roots, or of direct ir
ritation of nerve fibers or ganglion
cells. That is, the altered patterns of
sympathetic activity appear to be
either reflex manifestations of
changes in sensory input arising in
nerve endings and receptors in the
musculoskeletal tissues or the effects
of direct insults to nervt fibers (or
ganglion cells) or a combination of
both.
References
I . Korr, I. M., P.E. Thomas and H.M. Wright, Pat
terns of electrical skin resistance in man. Acta
neuroveget .. Wien. 17 ( 1 958). 77-96.
2. Wright. H.M., I.M. Korr and P.E. Thoma,
Local and regional variations in cutaneous vasomotor
tone of the human trunk. Acta neuroveget . , Wein. 22
(1 9). 33-52.
3. Thoma, P. E .. and I.M. Korr, The relationship
between sweat gland activity and electrical resistance
of the skin. J. Appl. Physiol. , Wash. , /0 ( 1 957,
505-510.
4. Kawahata. A . and P.E. Thomas. Further studies
on the neural basis for regional differences in ESR.
Fed. Proc. /8 ( 1959). 80.
S. Thomas. P.E . and A. Kawhata. Neural factors
underlying variations in electrical skin resistance of
apparently non-sweating skin. J. Appl. Physiol..
Wash. , 19. 1 7.
6. Korr. I. M . Experimental alterations in segmental
sympathetic (sweat gland) activity through myofascial
and postural disturbances. Fed. Proc. 8 (1949), 88.
7. KOI, I. M., Skin resistance patlerns associated
with visceral disease. Fed. Proc. 8 ( 1 949). 87.
8. Korr. IM., H.M. Wright and P.E. Thoma Ef
fects of experimental myofascial insults on cutaneous
patlerns of sympathetic activity i n man. Acta
neuroveget . Wien, 23 ( 1 926). 329-355.
9. Thomas, P.E., and I.M. KOI, The automatic
recording of electrical skin resistance patterns on the
human trunk. Electroencephalogr. 3 ( l 951 ) ,
361-368.
10. Thomas. P. E., I. M. Korr and H.M. Wright. A
mobile instrument for recording electrical skin
resistance patterns of the human trunk. Acta
neuroveget . Wein. 17 ( 1 958). 97-10.
I I . Jasper, H., An improved clinical dermometer.
J. Neurosurg . Springfield. 2 ( 1 945), 257-26.
12. Denslow. J.S., J.A. Chace, O.R. Gutensohn
and M. G. Kumm, Methods in taking and interpreting
weight-baring X-ray films. J. Amer. Osteopath. Ass.
54 ( 1 955), 63-670.
1 3. Richter, C. P., and B. O. Woodruff Lumbar
sympathetic dermatomes in man determined by the
electrical skin resistance method. J. Neurophysio!..
Springfield. 8 (1945), 323-338.
14. Travel/, J., Pain mechanisms in connetive
tissues in C. Ragan. Ed. Second Conference on Con
nective Tissues. Josiah Macy Jr. Foundation ( 1 952),
86-125.
15. Korr, I. M., and P.E. Thoma. Segmental pat
terns in man. Fed. Proc. 10 ( 1 951 ), 75.
16. Wright, H. M . Unpublished observations.
17. Floy, W.F, and P. H.S. Silver, The functions
of the erectores spinae muscles in certain movements
and postures in man. J. Physiol. 129 ( 1955). 1 84-203.
1 8. Portnoy. H., and F. Morin. Electromyographic
study of postural muscles in various positions and
movements. Amer. J. Physio!. 186 ( 1 956), 122-126.
19. Joseph. J., Man's posture; electromyographic
studies. p. 1-88, Thomas, Springfield. 196.
2. Joeph J., and I. McColl, Electromyography of
muscles of posture: posterior vertebral muscles in
males. J. Physio!. 157 ( 1 961 ), 33-37.
21. Thoma, P.E., H.M. Wriht and C. W. Hart,
jr.. Relation of sweat gland reruitment to ESR. Fe.
Proc. 12 ( I 953), 143.
22. Korr, I.M., P.E. Thoma and H.M. Wriht.
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265-282.
Reprinted by permission from 10urnal of Neural
Transmission 25: 589-6, 196.
EMG, SNS, reflexes, etc.
P0ul0l 0nd Sln0l Comon0nlS o dlS00S0
Vrogl0SS ln lh0 0pllC0llon o
' lh0lmogl0hy` (195)
H. M. WRI GHT and I . M. KORR
The participation of the peripheral
nerves and the spinal cord in various
clinical syndromes has been recog
nized in clinical practice for many
years. Among the most familiar ob
servations of the neural and reflex
components of disease are those on
referred pai n, but many observers
have also described the other patho
physiologic changes that often occur
i n the tissues of the "reference
zones. " These changes include ten
derness, changes in the blood flow
and/or blood content of the ski n,
sweating, muscle contraction, various
trophic changes, and others. Similar
patterns of manifestations, often
simulating those of visceral origi n,
may be associated with painful mus
culoskeletal disturbances or myo
fascial irritations.
Last September, a 5-year study was
i ni tiated at KeOS, of measurements
of physiologic activities and re
sponses in intact human subjects that
reflect segmental and regional varia
tions in activity of peripheral senory,
motor, and sympathetic neurons of
the spinal cord. I n this project, both
normal (preclinical) subjects and
clinical patients with various somatic
and visceral disturbances are being in
vestigated.
The observations, most of which
are being made on the dorsal trunk,
incl ude t he manifestations mentioned
previously, that is, pai n, changes in
vasomotion and sweating, and muscle
activity. Structural , palpatory, and
radiographic examinations are used
in the identification and evaluation of
vertebral anomalies, areas of stress or
lesion, abnormal curvatures, and
various musculoskeletal disturbances.
In individuals wi th visceral disease,
the usual diagnostic tests are done.
Finally, the relations between the
findings on the trunk and the clinical
signs, symptoms, and pathologic
Supported by lhe A. T. Slill OSleopal hic Foundalion
and Research Inslilule; Bureau of Research of lhe
American OSleopalhic Associalion (T-ZO); and
General Research SUppOrl Gram ( I SOI FR 054390)
of lhe Nal ional Inslilules of Heahh.
findings, i n both somatic and visceral
syndromes, will be examined i n each
individual . Some of our patients, as
well as most of our "normal" sub
jects, are drawn from the Student
Health Service of the college. Dr.
Ira Rumney, director of the Student
Health Program, and members of his
division, are responsible for the
cli nical aspects of this project.
This preliminary report deals wi th
only one phase of this project:
cutaneous vasomotor acti vity. We are
using the new technique of "ther
mography" as one method of study
ing the skin temperature as it is
related to cutaneous vasomotor ac
tivity. I n princi pl e, this recently
developed instrument (Fig. I) called a
"thermograph" * generates thermal
photographic images of the body by
measuring the i nfrared energy emit
ted by the ski n.
Briefly stated, the i nfrared energy
emitted by the ski n falls on a scanning
mirror and is then focused on a sen
sitive thermistor heat detector. After
the i nfrared radiation has been con
verted by the thermistor to an elec
trical signal, and the signal has been
amplified and processed, the propor
tional output is used to control the i n
tensity of a glow modul ator tube
which emits visi ble light, and this
light is focused on the film of a
Polaroid camera. The maximum scan
ti me is 4 minutes and, depending on
the size of the area to be scanned,
may be only 1 minute or less. Thus, a
perfectl y regi stered , quant i tati ve
record of the i nfrared emission from
the object is obtained directly from
the density of the photographic fi l m;
that i s, t he hotter t he object, the
whiter its image.
A hand-held i nfrared thermometer
(not visible in Figure 1) is used to
determine the temperature range or
delta T ( 6T) of the area to be ther
mographed. Knowing the 6T of the
area, the sensitivity of the ther
mograph can be set . For example, to
' Barnes Engineering Company, Slamford, Connee
lieu!.
Fig. I . The thermograph instrument and scan
ning mirror. Not shown in this picture is a
hand-held infrared thermometer which is used
in determining the temperature range of the
area to be studied by thermography. or the
photo comparator which is used to measure the
optical density of the thermograms.
change the film from white to black
at a 6T of 1 0 requires a lower sensi
tivity than if the 6T is 2 . The greater
the sensitivity setti ng, the greater the
contrast in the picture. A "bright
ness" control on the instrument sets
the low temperature point in the
temperature di fferential selected by
the sensitivity.
I n the first phase of this program,
two or more thermograms on the
back have been recorded on each of
the 1 02 members of the first-year
class at KeOS. Figures 2 to 5 show
the thermograms recorded on four of
these students. In each case, the in
dividual is lying face down on a heat
pad (which gives a white background
for the picture. The temperature of
the heat pad is approximately 1 00
F. ) . In the thermograms, the warm
areas appear whi te and the cool areas
black, with i ntermediate tempera
tures in varying shades of gray. The
"thermal gray scal e, " seen to the left
of the subjects, is a calibration device
whereby one can compare the optical
density of any point on the ther
mogram with the optical density pro
duced by known temperatures. Thus,
the various shades of gray of the ther
mogram can be converted to
temperature if that is desired.
The thermograms of the four in
dividuals shown in Figures 2 to 5
show that the topographic distribu
tion of warm and cool areas on the
back varies with di fferent individuals,
and at di fferent levels on the trunk in
a given individual. Of the 1 02 individ
uals in the first-year class of KeOS,
7J
74
Fig. 2 (far left). Thermogram of subject B. B. Observe the large warm (while) area that covers most of the thoracic region and the
warm "band" in the lumbar area and also below the sacrum. The black dots are markers placed on the spines ofT. T6. and T2; the
top of the sacrum is also marked. The sides of the body are cool (black). The individual is lying on a heat pad which appears white at
the sides ofthe body. The thermal gray scale is seen at the left ofthe subject. Fig. 3 (left to center). Thermogram ofsubject R. B. The
temperature patter ofthis individual is quite different from the individual in Figure I. Note the long "cold" streak down the midline
ofthe back. etending from T to 7. and the asymmetrical lumbar area. Fig. 4 (right ofcenter). Thermogram ofsubject K H The
distribution of warm and cool areas in this individual is diferent from that of the subjects in Figures 1 and 2. The asymmetrical
lumbar area is also ofinterest. Fig. 5. (right). Thermogram ofsubject S.B. Note the large cold area in the neck and the large warm
triangular lumbar area of this individual.
Fig. 6. Two thermograms on subject J. G. The one on the left was
taken on Nov. 5. 1964. and the one 01 the right 01 Jail. 22. 1965.
The two thermograms appear almost identical.
Fig. 7 (left). Two thermograms ofsubject S. B. The one 01 the left was taken Sept. 23. 1964. and the one on the right. Jan. 27. 1965.
The warm triangular lumbar area appears smaller in the later thermogram. Fig. 8 (right). Two thermograms ofsubject B. B. The one
on the left was taken on September 30. 1964. and the one on the right. on Jan. 5. 1965. Note the change in the lumbar area in the later
picture.
EMG, SNS, refexes, etc.
no two individuals had thermograms
exactly alike, although most in
dividuals had certain features in com
mon.
We have also frequently observed
that in some individuals the temper
ature patterns were "asymmetrical"
or differed between the right and left
sides at certain levels on the trunk. To
ascertain if these temperature pat
terns - and especially the asym
metrical or "aberrant" areas - re
main stable or vary from day to day
or month to month, we took more
thermograms of selected individuals
again after several weeks or months.
Figures 6, 7, and 8 show twe ther
mograms on each of three different
individuals taken on different dates.
In each case an interval of several
weeks intervened between the two
thermograms. It may be observed
that most features of the temperature
patterns remained remarkably cons
tant, although certain "features" in
the thermogram may change with
time, therapy, or other factors.
As previously mentioned, we found
that most thermograms had certain
temperature "features" in common.
For example, in most individuals the
sides of the body are cool, the lumbar
area - especially over the spinous
processes - is very warm, the neck is
warm, and so forth. In order that we
might better interpret the thermo
grams, and particularly the temper
ature patterns over the paravertebral
areas, we did a quantitative analysis
of the thermograms of 30 subjects at
each segmental level from the neck to
the sacrum. This was done with a
photocomparator especially made for
this purpose which measures the op
tical density of any point on the ther
mogram. The optical density - or
percentage of opacity - can be con
verted to temperature, i f that is
desired, by comparing the optical
density to actual temperatures on the
cal i brati on or "gray scal e . "
Measurements were made over the
spinous processes (except at Tl , T6,
Tl 2, and Sl ) and at distances of 2 and
4 mm. lateral to the midline on the
thermograms - which corresponds
roughly to 2 and 4 inches lateral to
the midline on the back.
We found that in the "average" in
dividual, the neck is quite warm both
in the midline and laterally; the
temperatures throughout the thoracic
area show only small differences but
with a slight tendency to be warmer in
the midthoracic area than at the
cervico-dorsal area and thoracolum
bar junction. Temperatures are very
warm in the lumbar area over the
midline, but decline as one passes
laterally from the midline.
Questions immediately arise con
cerning the mechanisms of the warm
and cold areas and their physiologic
significance. Are the warm areas
related to greater cutaneous blood
flow? less evaporation from the skin?
the activity of underlying muscles?
Are the cold areas related to vasocon
striction? to areas of sweating? or
other factors?
In an attempt to ascertain the
answers to some of these questions,
we are now engaged in the second
phase of this program: that is, to
determine the functional differences
between the warm and cold areas, to
ascertain how these areas are related
to differences in cutaneous blood
flow, blood content, vascular reac
tivity, sweat gland activity, muscle ac
tivity, and so forth. Also, we wish to
ascertain how these areas function
under stress and participate in reflex
responses. Other methods previously
descri\ed in our early work are being
used for this purpose. Finally, we
wish to know what relationship the
asymmetrical or aberrant temper
ature patterns bear to somatic or
visceral lesions. The structural and
palpatory examinations, structural
x-rays, and other diagnostic data on
the members of our first-year class
are now in the process of being
analyzed, with the assistance of Dr.
Rumney, for this purpose.
Reprinted by permission from JAOA 6: 918-921 .
1965.
Introductory note:
What is manipulative
therapy? (1978)
One of the unusual features of the
Workshop was that few of the neuro
scientists who convened to contribute
their knowledge had had any prior
contact with the area of medicine to
which they were to make their con
tributions. Most of them arrived still
uncertain of the relevance of their
research, done for quite different
purposes, to the subject of the
Workshop. Because the Workshop
setting was that of a forum rather
than a clinic, they departed with a
better perception of relevance, yet
without a clear image of how manip
ulative therapy is performed or of its
clinical value.
It seems likely that many readers,
more interested in the nervous system
than in manual medicine, will find
themselves with similar uncertainties
about the latter. To them, we recom
mend, as we did to the participants,
the proceedings of an earlier work
shop sponsored by the National In
stitute of Neurological and Com
municative Disorders and Stroke,
and offer the following paragraphs.
Manipulative therapy involves the
application of accurately determined
and specifically directed manual
forces to the body. Its objective is to
improve mobility in areas that are
restricted, whether the restrictions are
within joints, in connective tissues or
in skeletal muscles. The consequences
may be the improvement of posture
and locomotion, the relief of pain
and discomfort, the improvement of
function elsewhere in the body and
enhancement of the sense of well
being.
Diagnosis, leading to the selection
of body sites for manipulation and
the mode of manipulation, is based
on analysis of the patient's history
and complaints and on the evaluation
of signs provided by palpation (tissue
texture, muscular and fascial tension,
joint motion and compliance, skin
temperature and moisture), by visual
observation (body contour, posture,
locomotion, skin color), and by
*NINCDS Monograph No. IS. The Researh Status
of Spinal Manipulative Therapy, edited by M. Gold
stein, Bethesda, Maryland, 1 976.
75
radiographic and other instrumental
means.
Manipulative procedures, even in
the hands of the same practitioner,
vary according to the findings and
their changes in each visit; they vary
from practitioner to practitioner,
from patient to patient, and, for the
same patient, from visit to visit.
Manipulative therapy is no more a
uniform therapeutic entity than is
surgery, psychiatry or pharmaco
therapeutics. Clinical effects are
thought to be achieved through im
provement in musculoskeletal bio
mechanics, in dynamics of the body
fuilds (including blood circulation
and lymphatic drainage) and in ner
vous function. It is on the last that
this Workshop was focused. Its con
cern, therefore, was with neither the
clinical efficacy of manipulation nor
its evaluation, but with its neural and
neuronal mediation.
What are the neurobiologic
mechanisms?
It has been clear for many decades
that the nervous system is a major
mediator of the clinical effects of
manipulative therapy, yet the precise
mechanisms are still, for the most
part, obscure. In view of the burgeon
ing of the neurosciencs in recent
years, it seemed timely to convene a
research workshop to examine to
what extent that great mass of new
knowledge might illuminate the
neurobiologic mechanisms at work in
manipulative therapy, while at the
same time to discern new and funda
mental areas in the neurosciences for
exploration.
The objectives of the Workshop on
which this volume is based were:
1 . To identify new fundamental
questions in neurobiology which
emerge from clinical observa
tions in the practice of manip
ulative therapy. .
2. To seek answers in research al
ready accomplished.
3. To identify and project needed
lines of research.
The design of the Workshop was
based on the following assumptions
and hypotheses. It seemed to the
planners of the Workshop that the
musculoskeletal problems to which
manipulative therapy is addressed
initiate their impairment of normal
physiological processes in two
primary ways:
7
1 . Alterations in sensory input
from the muscles, tendons,
bones, joints, ligaments and
other tissues which are involved
in the musculoskeletal aberra
tion.
2. Direct insult to neurons, nerves
and roots, and associated glial,
connective-tissue and vascular
structures.
According to our hypotheses, both
the changes in afferent input and the
trauma-induced changes in excitation
and conduction of neural elements
produce. in turn, changes in the cen
tral nervous system and in the
periphery, refected in aberrant sen
sory, motor and autonomic' func
tions. We chose to give emphasis to
the impact on autonomic function
and, therefore, to somato-autonomic
interrelations.
The changes in afferent input (and
the resultant changes in efferent out
put) and the nerve-trauma both af
fect, also, neuronal functions which
are not based on excitation and con
duction of impulses, much as they
may be affected by impulses. These
functions are subsumed under such
rubriCs as axonal transport, trans
synaptic influences, trophic function,
neurotrophic relations, neuron
target-cell interactions, etc. Hence,
the Workshop was organized around
two maj or themes, impulse-based and
nonimpulse-based mechanisms, in
troduced by the Fragestellung implicit
in reports by clinicians skilled in
manipulative therapy as taught and
practiced in three different profes
sions.
It became clear in the course of
discussions, not only between clini
cians and scientists but between two
groups of neuroscientists, that there
is no clean separation between
impulse-based and nonimpulse-based
mechanisms. Each is involved in and
infuenced by the other, and distur
bances in each potentially contribute
to dysfunction elsewhere and are sub
ject to manipulative amelioration. If
barriers existed, they were i n minds
and methods, and not in the biolog
ical system; proving again that con
ceptual barriers, until identifed and
assulted, are often much less perme
able than cellular barriers. Perhaps
one byproduct of the Workshop,
therefore, was a somewhat more
coherent and unifed view of nervous
function and plasticity, incorporating
both reflexes and neurotrophicity,
both the instantaneous and the long
term phenomena.
An important feature in the design
of the Workshop was the dialogue
between clinician and scientist. The
clinicians were chosen not only for
their clinical proficiency in the ap
plication of manipulative therapy,
but for their concern, expressed in
publications, about mechanism. The
neuroscientists were selected not only
for the quality and importance of
their research, but for the relevance
of their work, as perceived by the
planners, to manipulative therapy
and to the problems with which it
deals. While no maj or answers have
as yet emerged, the way has been
opened for the formulation of new,
approachable questions and testable
hypotheses.
Reprinted by permission from I. M. Korr, Editor,
Neurobiologic Mechanisms in Manipulative Therapy.
Plenum Publishing Corpration, New York. 1 978. Pp.
IS-17.
EMG, SNS, reflexes, etc.
Sustained sympathicotonia as a factor
in disease (1978) .
There is a large though scattered body
of clinical and experimental literature
that gives the distinct impression of a
significant, often critical sympathetic
component as a common feature in a
large variety of syndromes. Chronic
hyperactivity of the innervating sym
pathetic pathways seems to be a
prevailing theme in many clinical con
ditions, involving many organs and
tissues. Whatever the etiological or
therapeutic implications, it appears
that this widely shared feature of
local, regional or segmental sym
pathetic hyperactivity is overlooked
or dismissed because of the barriers
erected by specialization. Thus, the
ophthalmologist is not ordinarily ex
posed to the gastroenterological
literature, the gastroenterologist to
the cardiological, the cardiologist to
t he gynecol ogi cal , et c. Each
discoverer of a sympathetic compo
nent seems, therefore, to regard it as
peculiar to this or that disease within
his or her area of specialization,
rather than as part of a general
theme.
My l ong- t i me expos ur e t o
osteopathic theory and practice and
my research experience in related
fields have led me to the following
hypotheses:
( 1 ) Long-term hyperactivity of
par t i cul ar s ympat het i c
pathways i s deleterious t o the
target tissues and may indeed
have a rather general clinical
significance.
.
(2) Clinical manifestations are
determined by the organs or
tissues which are innervated by
the hyperactive sympathetic
neurons, each responding in its
own way, even to the sympa
thetically induced vasocon
striction that may be a com
mon factor.
(3) The ',bih impulse traffic in
selected sympathetic pathways
may be related to musculo
skeletal dysfunction, especially
in the spinal and paraspinai
area.
It is the purpose of this paper to
review the support for these
hypotheses in available knowledge of
the autonomic nervous system, in ex
perimental findings, including our
own, and in clinical literature.
The sympathetic role in musculo
skeletal activity
One of the most important roles of
the sympathetic nervous system
(SNS), not always emphasized or
recognized in textbooks, is part of its
"ergotropic" function (Hess, 1 954),
that of adjusting circulatory, meta
bolic and visceral activity accord
ing to postural and musculoskeletal
demand. These adjustments include
changes in cardiac output, in distribu
tion of blood flow by regulation of
peripheral resistance, in heat dissipa
tion through the skin, and release of
stored metabolit es. These ad
j ustments are of systemic nature, yet
they have a high degree of localiza
tion according to the site and the
amount of muscular activity. (It i s
understood of course that autoregula
tion is also important and often the
dominant factor in these ad
justments.)
In order for the SNS to perform
this role, it must receive, directly
( t hr ough s egment al affer ent
pathways) and indirectly (through the
higher centers), sensory input from
the musculoskeletal system. Coote
has given us an excellent review of
this aspect. It seems safe to assume
that the SNS would be similarly in
formed about strain. injury or
malfunction of some part of the
musculoskeletal system (e. g. , of a
joint), and that there would be a ma
jor impact locally or segmentally if a
segment of the vertebral column was
involved.
On this assumption, in the late
1 940's, my colleagues and I at the
Kirksville College of Osteopathic
Medicine undertook studies on
human subjects to see if any altera
tion in sympathetic activity was
associated with the vertebral and
paravertebral dysfunctions to which
osteopathic physicians give attention
in diagnosis and therapy.
In a series of studies in which we
used sudomotor and cutaneous
vasomotor activity as physiological
indicators of topographical variations
in sympathetic activity, we showed
the following:
(1) In most individuals, even under
cool, resting conditions, there are
areas of hydrated skin associated with
persistent, low-grade sweat-gland ac
tivity (reflected in low electrical skin
resistance, hence "low-resistance
areas, " LR) and of high vasomotor
tone (Wright, Korr & Thomas, 1 953;
Thomas & Korr, 1 957; Thomas, Korr
& Wr i ght , 1 95 8 ; Thomas &
Kawahata, 1962).
(2) The segmental patterns of
distribution of these aberrant areas
varied from subject to subjet, but
were highly constant and reproduc
ible for each subject over periods of
months. This is not to say that the ac
tual shapes and sizes of the aberrant
areas were invariable; they were areas
in which, at any given time, the prob
ability was very high, as compared
with all other areas, that we would
find high sudomotor and vasomotor
activity. They were areas, for exam
ple, in which in the course of cooling
the warm, lightly perspiring subject,
the sweat-gland activity persisted long
after it had subsided in other ares,
and were the first to respond with in
creased activity as the subject was
warmed (Korr, Thomas & Wright,
1958; Wright, Korr & Thomas, 1 960).
(3) These areas of sympathetic
hyperactivity correlated well, in
segmental distribution, with existing
musculoskeletal strain. trauma, deep
and superficial tenderness, elec
tromyographic activity of paraspinal
muscles, etc. New areas could be in
duced experimentally with postural
and myofascial insult which were
related regionally or segmentally to
the site of insult (Korr, Wright &
Thomas, 1 962; Korr, Wright &
Chace, 1 964).
(4) Similar signs of sympathetic
hyperactivity were found to be
associated with visceral pathology,
apparently in areas of referred pain
and tenderness, segmentally related
to the visceral pathology. In a few
subjects studied over long periods of
time, the aberrant areas appeared in
advance of the frst symptoms of
visceral disease (Korr, 1 949).
(5) The sympathetically hyperactive
areas of skin functioned differently
from the normal areas. Thus, the
sudomotor responses of the low
resistance areas to a variety of factors
77
were grossly exaggerated. This was
demonstrated in a group of subjects
who had asymmetrical patterns, that
is, in whom we had found low elec
trical skin resistance on one side at a
given segmental level, while the con
tralateral area was normal.
As previously shown (Thomas &
Korr, 1 957; Thomas & Kawahata,
1 962), we found that in a low
resistance area, there was con
spicuous sweat-gland activity under
cool, resting conditions when, as
shown by most areas of the trunk (in
cluding the contralateral area), there
was no evidence of thermoregulatory
demand for sweat secretion. That
same low-resistance area also made
exaggerated sudomotor responses
(earlier and more rapid recruitment
of sweat glands and more copious
secretion) to generalized stimuli (e.g. ,
heating other parts of the body),
painful stimuli, threat of pain and
other emotional stimuli. These areas
seemed to be continually in, or verg
ing on, a "cold sweat" (Korr,
Thomas & Wright, 1 955).
On the basis of these fndings and
other considerations, we concluded
that peripheral sympathetic pathways
at segmental levels corresponding to
somatic dysfunction in and around
the spinal column are jn a state of
chronic facilitation similar to that
shown by Denslow and his co
workers for neuromuscular activity
(Denslow & Hassett, 1 942; Denslow.
1 944; Denslow, Korr & Krems, 1 947).
Persistent local, regional or der
matomal elevation in sympathetic ac
tivity and predisposition to high ac
tivity appear to be related to spinal
and paras pinal motor dysfunction as
disclosed by osteopathic palpatory
diagnosis. In general, the concept of
chronic segmental facilitation has
been found to be consistent with
observations in osteopathic practice,
and helpful in their rationalization.
The concept has recently been re
viewed in a broader context (Korr,
1 976) and re-examined in terms of
conditioning, habituation and sen
sitization in spinal reflex pathways
(Patterson, 1 976).
1hc nflucncc8 of8)mpalhclc
nncralon
What is the clinical significance of
chronic facilitation and hyperactivity
of sympathetic innervation on
various tissues and organs? Let us
T8
review first the physiological in
fluence of sympathetic innervation.
This is a great deal more varied than
can be ascribed to the regulation
merely of exocrine secretion and of
contraction in smooth and cardiac
muscle and the metabolic energizing
of these activities, as is widely taught.
The literature, some of it quite old
and long ignored, indicates a much
larger repertoire, as illustrated by the
following examples.
1. Skeletal muscle.
The sympathetic innervation of
skeletal muscle appears to have a
direct augmentor effect on the
energetics of skeletal muscle, pssibly
similar to the inotropic effect on car
diac muscle ("Orbeli phenomenon";
see Bach, 1 953; Kelly & Bach, 1 959).
It al so appears to faci l itate
neuromuscular transmission (Hutter
& Loewenstein, 1 955; Naseldov,
1 960) . Sympathetic innervation is
also involved in the development of
contractures following trauma to the
spinal cord (Galitaskaya, 1 965).
2. Peripheral sensory mechanisms.
Several types of receptors and sense
organs have been shown to be in
fluenced by sympathetic impulses. In
general, the effect of repetitive sym
pathetic stimulation is facilitatory,
that of increasing the frequency of af
ferent discharge and lowering the
threshold. In some cases, threshold
may be reduced to zero, causing af
ferent discharge without direct
stimulation of the receptor. In short,
the effect of increased impulse traffic
in the sympathetic fibers innervating
receptors is that of exaggerating their
discharge, causing them to report a
greater intensity of stimulation than
is actually occurring. The sensory
mechanisms in which sympathetic in
fluence has been demonstrated in
clude: (a) muscle spindle (Hunt, 1960;
Eldred, Schnitzlein & Buchwald,
1 960); (b) tactile receptors (Chernet
ski , 1 964a); (c) taste receptors
(Chernetski, 1 964a); (d) olfactory ap
paratus (Tucker & Beidler, 1 955); (3)
carotid sinus chemo- and barorecep
tors (Koizumi & Sato, 1 969; Mills &
Sampson, 1 969; Sampson & Mills,
1 970; McCloskey, 1 975); (f Pacinian
cor pus cl es ( Loewens t ei n &
Altamirano-Orrego, 1 956); (g) retina
(Mascetti, Marzi & Berlucchi, 1 969);
and (h) cochlea (Vasil'ev, 1 962).
J. Central nervous system.
Following the demonstration by Bon
vallet, Dell and Heibel (1 954) of
adrenergic elements in the reticular
formation and of the effect of the
SNS thereon and on the reticulospinal
system, a series of studies appeared in
the Soviet literature, indicating strong
influence of the superior cervical
ganglion on cortical and subcortical
activity. Thus, Karamian (1 958) and
his co-worker, Sollertinskaya (1957),
found that unilateral removal of the
superior cervical ganglion in rabbits
resulted in behavioral changes, in
cluding lowered intensity and even
total disappearnce of established
positive . food-conditioned motor
refexes. These effects were accom
panied by profound changes in spon
taneous cortical electrical activity and
in responses to peripheral stimula
tion. The effects were more marked
in the ipsilateral hemisphere. After
removal of both lef and right ganglia
followed by adrenal demedullization,
the EEG voltage became very unsta
ble and changes in behavior and
response to peripheral stimulation
also took place. Subcutaneous injec
tion of adrenalin produced a transient
return to normal activity.
Tay-An ( 1960) demonstrated that
ganglionectomy also affected elec
trical activity of the hypothalamus. In
a later study, Tay-An and Gelehkova
(1961) studied the effects on the
recruitment reaction in the ipsilateral
hemisphere of stimulating one cer
vical sympathetic nerve in cats. (The
recruitment reaction is the increase in
cortical electrical activity produced
by stimulation of non-specifi c
thalamic nuclei. ) In most cases, sym
pathetic stimulation reduced the
amplitude of the reaction in the ip
silateral hemisphere. Occasionally,
usually on repeated stimulation, there
was an i ncrease. Intravenous
adrenalin more consistently weak
ened the recruitment reaction. In con
trast, there seemed to be little sym
pathetic influence on the primary
responses of the auditory cortex to
stimulation of the specic nucleus,
the medial geniculate body.
Changes in electrical activity of the
visual regions of the cerebral cortex
following unilateral extirpation of the
superior cervical ganglion in rabbits
support Zagorul ' ko' s conclusion
( 1965) that the sympathetic innerva
t i on pri mari l y i nfluences the
EMG, SNS, reflexes, etc.
mechanisms responsible for the
generation of the background elec
trical activity, the "rhythm assimila
tion reaction" (reproduction of
various frequencies of fashing light)
and the secondary components of the
induced responses to light.
Aleksanyan and Arutunian (1 959)
observed diffuse electrical activation
on stimulation of the cervical sym
pathetic nerve, and concluded that
the sympathetic effect is on the total
brain, including the reticular forma
tion, and that the cortical effect is not
necessarily mediated by the reticular
formation. Ganglionectomy also pro
duced electrical changes in both cor
tical and subcortical structures, of
such a nature as to indicate diffuse in
hibition. Observations of Vesel kin
(1 959) on the pigeon indicate that the
cerebellum is similarly under direct
influence of the sympathetic innerva
tion.
The work of Skoglund ( 1 961) and
of Chernetski ( 1964b) indicates that
the facilitatory influence of the SNS
may also extend to the spinal cord. In
the cat, Skoglund showed that
threshold doses of noradrenalin con
verted single-spike responses (to
single afferent volleys) to repetitive
discharges, set up discharges in ini
tially silent cells and increased the
frequency of prevailing activity. In
the frog, Chernetski showed that
sympathectomy markedly reduced in
tersensory facilitation of the leg flex
ion refex. He attributed the depres
sion to reduced central nervous
responsiveness in the absence of the
sympathetic influence.
To what extent these SNS-related
changes are based on vasomotor
changes is difficult to determine,
especially in view of conflicting
reports regarding the role of SNS in
nervation on circulation through the
CNS. Whether the observed changes
are of indirect vasomotor origin or
are the more direct effects on
neuronal excitation or metabolism,
such as that described by Hunter and
Stefanik (1975), the influence of the
sympathetic innervation on CNS
function seems an important and
neglected area of neurophysiology,
despite the obvious importance of the
catecholamines in brain function and
dysfunction.
4. Colateral circulation.
Bardina (1 956) showed that, follow-
ing experimental occlusion of the
lingual artery, interruption of the
sympathetic innervation of the
tongue greatly accelerated the
development of collateral circulation.
Similarly, Dansker (1957), using the
Clark-Chamber rabbit-ear technique,
found that unilateral sympathectomy
i ncreased the devel opment of
arteriovenous anastamoses, both in
number and diameter.
5. Bone growth.
Sympathetic innervation has been
found to exert an important influence
on longitudinal bone growth (Kottke,
Gullickson & Olson, 1958). Other in
fuences, e. g. , on the . response of
bone to estrogens (Rosenfeld et aI . ,
1959), and on the activity of bone
cells, possibly in collagen elaboration
and matrix formation (Chiego &
Singh, 1 974) , have also been
reported.
6. Adipose tissue.
It is now well established that adipose
tissue may also be regarded as a true
effector organ making its own
specific responses to stimulation of its
sympathetic innervation. The sympa
thetic innervation is requisite for the
rapid lipolysis (release of free fatty
acids and glycerol) that takes place in
cold exposure and for the slower
lipolysis in starvation. Sympathetic
blockade or sympathectomy (the lat
ter usually done unilaterally, the con
tralateral fat pad serving as control)
prevents the adaptive response
(Paoletti & Vertua, 1 964; Hull &
Segall, 1 965). Sympathectomized
adipose tissue increases in fat con
tent, suggesting a tonic influence on
the balance between release and
mobilization.
Electrical stimulation of the nerve
supply to adipose tissue causes the
release of free fatty acids and
glycerol. Obviously, sympathetic ex
citation, either experimentally or as
part of an adaptive response such as
that to cold. involves the rapid activa
tion of several enzyme systems. The
noradrenalin content and metabolism
in adipose tissue is the same as in
other organs with adrenergic innerva
tion (Fredholm, 1970).
The lipolytic effect of sympathetic
stimulation with accompanying
glycogenolysis and increase in O
2
con
sumption are not dependent on the
concurrent vasomotor responses to
nerve stimulation. I ndeed. the
metabolic response is delayed by the
accompanying vasoconstriction. The
independence is further substantiated
by the fact that the adipocyte
responses to sympathetic stimulation
are blocked by adrenergic p-receptor
antagonists, whereas the vasomotor
responses i nvol ve a- recept ors
(Fredholm, 1 970; Fredholm et al .
1 975; Rosell & Belfrage, 1 975).
7. Reticuloendothelial system.
I n 1 953 Kuntz summarized the
evidence then available that sym
pathetic innervation has important
i nfluences not only on blood fow
through the blood-forming tissues,
but also on such specific functions
and factors as the phagocytic activity
of the reticuloendothelial cells of
bone marrow, on erythropoiesis and
on the release and distribution of
leucocytes and on endothelial
permeability. Linke ( 1 953) showed
t hat prol onged, l ow- frequency
stimulation of the splanchnic nerves,
lumbar sympathetic trunks and sym
pathetic nerves to the liver (but not to
the spleen) caused large increases in
circulating reticulocytes and nor
moblasts. The increases lasted for
periods of 80 min to 30 h. depending
on the nerves stimulated. Responses
to stimulation of the sympathetic
nerves were unchanged by clampin
of the adrenal blood vessels .
I n a more recent study on the mar
row of the rat femur, DePace and
Webber ( 1 975), using electrostimula
don and morphological methods,
have extended these older observa
t i ons . They found abundant
adrenergic fibers terminating on
arteries and fibers coursing through
parenchyma close to many marrow
cells. but no evidence of terminations
on these cells. Stimulation of lumbar
sympathetic trunks triggered the
rel ease of l arge numbers of
reticulocytes and neutrophils into the
circulating blood. The changes affect
ing other cells were somewhat
variable. The mechanism governing
the release of blood cells from the
bone marrow following sympathetic
stimulation seems to be a selective
one apparentl y i nvol vi ng the
sinusoidal wall. On the basis of cited
electron micrographic evidence and
the studies of numerous other in
vestigators, the authors conclude that
the transmitter released at sym-
79
pathetic terminals increases the (ap
parently active) passage of seleted
white blood cells through cells of the
sinusoidal wall, in a manner similar
to that described for erythrocytes .
8. Endocrine systems.
One of the most interesting examples
of sympathetic control is that on the
pineal body and, through the pineal,
on other endocrine systems, par
ticularly those related to sexual
development and reproduction. (For
reviews, see Wurtman, Axelrod &
Kelly, 1 968; Wolstenholme & Knight,
1971 . ) The pineal controls the release
of releasing factors for luteinizing
hormone, follicle stimulating hor
mone and prolactin inhibiting and
releasing factors. This pineal control
of releasing factors is mediated by the
el aborati on and secreti on of
melatonin and other polypeptide hor
mones which exert antigonadal ac
tion.
The synthesis of melatonin is under
the control of the sympathetic inner
vation of the pineal, from the
superior cervical ganglion. Synthesis
is augmented in the dark and reduced
in the light, the optic pathways
somehow being involved in the
regulation of impulse traffic in the
sympathetic branch to, the pineal
(Brooks, Ishikawa & Koizumi, 1 975).
This accounts for the impaired
growth and sexual development of
rats raised in the dark and for diurnal
behavioral phenomena related to
photoperiodicity. These behavioral
phenomena also refect the influence
of the pineal on functions of the
higher centers on the brain. Section
of the sympathetic innervation of the
pineal obliterates the diurnal fluctua
tion of melatonin synthesis and
related diurnal changes, and blocks
the anti gonadal and growth
inhibiting infuence of the pineal in
the dark.
Other. more direct, infuences of
the sympathetic innervation on secre
tion of hormones by endocrine have
long been known, e.g . on the thyroid
(Friedgood & Cannon, 1 940; Comsa,
1963; Lowe, Ivy & Brock, 1 949;
Melander et aI. , 1974), on the adrenal
cortex (Jung & Comsa, 1 958), on the
secretion of insulin by the pancreas
(Porte, 1971 ; Shevchuk, Sandulyak &
Rybachuk, 1 970) and the testicle
(Khodorovski, 1 964). Koizumi and
Brooks (1 972) have summarized re-
8
cent confirmation and extension of
these older observations on the sym
pathetic control of endocrine func
tion.
9. Others.
There are many other examples of
sympathetic influence on various
functions and processes, e.g. , on en
zyme activity (Nordenfelt, Ohlin &
Stromblad, 1960), on mitosis and
RNA and DNA synthesis (Schneyer,
1 973) and on growth and develop
ment of the salivary glands (Wells,
Handelman & Milgram, 1961 ) and of
the kidney (Hix, 1 966). Additional
examples will be found in the review
by Koizumi and Brooks ( l 97. Still
others, including the sympathetic
conditioning of tissue responses to
other factors, e.g. , to parasym
pathetic stimulation, hormones, etc. ,
are evident in connection with clinical
and pathological manifestations of
sympathetic hyperactivity discussed
in the next section. The examples
discussed above, however, will serve
to illustrate the diversity of sym
pathetic influences which cannot be
explained merely on the basis of
regulation of secretion and contrac
tion (including that of blood vessels).
The diversity of the effects of
stimulating various peripheral sym
pathetic pathways is not in the in
fluences of the sympathetic neurons,
but in the reponses of the innervated
tissues and organs. The responses are
as varied as the tissues and organs
which are innervated - virtually
every tissue in the body. Sympathetic
stimulation i ntroduces no new
qualities, but modifies (increases or
decreases, accelerates or retards,
stimulates or inhibits) the inherent
functional properties of the target
tissue, each, therefore, responding in
its own manner.
Clinical impact of sympathetic
hyperactivity
It should not be surprising, in view of
these diverse organ and tissue
responses, that sympathetic hyperac
tivity, sustained over long periods of
t i me, may t end t o produce
pathological changes i n the target
tissues, the clinical impact varying
with the tissue and its role in the
body. Evidence for sympathetic com
ponents in a variety of clinical distur
bances is reviewed in this section. The
evidence is in four categories: (a) the
manifestations, that is, signs, symp
toms and pathophysiology; (b) the ef
fects of chronic experimental stimula
tion; (c) the effects of therapeutic or
experimental interruption or reduc
tion of sympathetic activity; and (d)
morphological changes in sym
pathetic components.
Since sympathetic vasomotor fbers
are contrictor in most areas, ischemia
of various degrees is often a common
consequence of sympathetic hyperac
tivity. The reduced blood flow would,
in turn, alter the functional properties
of the tissues and their responses to
other factors, e.g. , parasympathetic
or endocrine influence. It may also
render them vulnerable to various
agents (such as normal digestive
secretions, infectious agents and
toxins) and less able to recover from
insult. In some of the following ex
amples of the pathogenic influences
of sympathetic hyperactivity, the
vasomotor component is clearly evi
dent; in others it is of minor impor
tance or is obscured by other
sympathetic effects.
1. Neurogenic pulmonary edema.
A dramati c exampl e of t he
pathogenic influence of intense sym
pathetic discharge is neurogenic
pulmonary edema. Severe pulmonary
edema, with marked vascular conges
ti on, atelectasi s, i ntra-alveolar
hemorrhage and protein-rich edema
fuid, appears very rapidly after
severe, often fatal blows to the head
and other severe injuries to the cen
tral nervous system (CNS). It occurs
quite independently of underlying
pulmonary or cardiac disease. It has
been produced experimentally in
various species by blunt head trauma,
electrolytic lesions in various parts of
the brain, sudden large increases in
cerebrospinal fluid pressure (see
Theodore & Robin, 1 976, for
references), hyperbari c oxygen
(Johnson & Bean, 1957), injection of
chloramine (Rudin, 1 963) and local
ized pulmonary infarction (Kabins et
aI. , 1 962). Of great interest is the fact
that pulmonary eder with its
associated changes, i s also produced
by stimulation of the stellate ganglia.
Conversely, treatment of animals
with various adrenergic blocking
agents or extirpation of stellate or
other sympathetic ganglia prior to ad
ministration of any of the above
forms of trauma and stimuli com-
EMG, SNS, reflexes, etc.
"
pletely prevents the appearance of
pulmonary edema.
It seems to be assumed by most
workers in this feld that the SNS
induced pulmonary edema is due to
vascular responses and hemodynamic
changes in the pulmonary circulation,
perhaps including constriction of
pulmonary veins (Kadowitz, 1 975);
other factors such as changes in
capillary permeability have also been
postulated (Theodore & Robin,
1 976). In the course of their extensive
studies on pulmonary edema pro
duced by head trauma, high oxygen
pressure and stellate ganglion
stimulation, Beckman and his col
laborators (Beckman & Houlihan,
1 973; Droste & Beckman, 1 974;
Beckman, Bean & Blaslock, 1 974;
Sexton & Beckman, 1 975) have im
plicated another, non-vascula, fac
tor. They have demonstrated, under
these circumstances, a large, abrupt
decrease in lung compliance, accom
panied by a large increase of
minimum surface tension and of
cholesterol content of the wash fluid.
The changes in compliance and sur
face tension are tentatively ascribed
t o inc reas ed ( i nt r a- al veol ar)
cholesterol. I n monkeys and cats
these changes in lung compliance oc
curred independerly of, or in ad
vance of, any signs of lung injury
such as congestion or edema.
Whatever the mechanisms even
tually disclosed, it is well established
that severe lung damage may be pro
duced by intense sympathetic bom
bardment of the lungs, triggered in
various ways.
2. Peptic ulcer and pancreatiti.
Sympathetic components have been
identified in peptic ulcer (e.g. ,
DeSousa-Pereira, 1 959) and i n pan
creatitis. Gage and Gillespie (l95 1)
and Walker and Pembleton ( 1 955)
showed the therapeutic effects of con
duction block i n pancreati ti s.
Gilsdorf et al. (1 965), on the other
hand, demonstrated that sympathetic
stimulation converted mild, non
lethal, bile-induced pancreatitis to the
hemorrhagic, necrotizing and lethal
form. That this sympathetic effect
may be ascribable to vasoconstriction
is indicated by an earlier study by
Block, Wakim and Baggenstoss
(1 954). In their experimental study,
obstruction of the flow of pancreatic
j uice, even when permitted to mix
with bile, produced only non-necrotic
changes in the parenchyma of the
pancreas. When, however I brief
i schemia was superimposed on
obstruction of the pancreatic duct,
parenchymal necrosis developed
which varied in severity with the
degree of arterial obstruction. Le
sions comparable to acute hemor
rhagic pancreatitis in man were occa
sionally produced by ischemia alone.
J. Arteriopathy.
Gutstein, LaTaillade and Lewis
( 1962) produced the histological
features of arteriosclerosis in the aor
ta by sustained stimulation of the
splanchnic nerve in unanesthetized
rats. Sympathetic stimulation ap
parently produced some change in the
arterial wall that favored the develop
ment of arteriosclerotic lesions. A
tendency toward thrombosis seems to
have been a factor. It is interesting in
this connection that in studies on ex
perimental thrombosis in the rabbit
ear, denervation of the ear markedly
accelerated thrombolysis (Fowler.
1 949; Cho, 1 967).
4. Cardiovascular-renal syndromes.
Hypertension. It has long been
s us pect ed , o n t he bas i s o f
physiological, pharmacotherapeutic
and behavioral considerations, that
high activity of the peripheral SNS is
an important contributing factor in at
least some forms of arterial hyperten
sion. This has been difficult to
establish, by direct means, in pa
tients. Recent studies of Wallin,
Delius & Habgarth ( 1 973), in which
they recorded multiunit sympathetic
activity in skin and muscle nerves,
have yielded preliminary support for
this hypothesis. In a more quan
titative study on spontaneously
hypertensi ve rats, Iri uchij i ma' s
studies (1973) indicated a much
higher efferent impulse traffic in the
splanchnic nerves of hypertensive
than of normotensive rats.
Heart Disease. Among the most
threatening and often fatal complica
tions following myocardial infarction
are ventricular fibrillation and other
arrhythmias. The recent work of
several investigators indicates that
heightened discharge through the
sympathetic innervation of the heart
may be a most important factor. In
an experimental study on transient
coronary occlusion in cats, with the
use of direct recording techniques,
Malliani, Schwartz and Zanchetti
( 1969) showed an increase discharge
in most of the fibers tested (in the
third thoracic ramus communicans).
The reflex, which the authors
characterized as a sympathetic
cardio-cardiac reflex, occurred also in
the spinal animal, did not depend on
the baroreceptors, on vagal refexes
or on direct anoxic stimulation of
preganglionic neurons.
Others have found that experimen
tal coronary occlusion lowers the
ventricular fibrillation threshold
(determined by repetitive electrical
stimulation of the ventricle) and in
creases the incidence of ectopic
di s c harges and ar r hyt hmi as .
Adrenergic blockade and ablation of
the stellate ganglia protected the heart
against these manifestations and even
prevented them, especially during the
first few hours of occlusion (Harris,
Bocage &Otero. 1975; Kliks, Burgess
& Abildskov, 1 975). Conversely,
stimulation of the stellate ganglia,
even in the absence of coronary oc
clusion, markedly lowered the
fi br i l l at i on t hr es hol d. When
ganglionic stimulation was superim
posed on occlusion, the threshold was
depressed far below that following
occlusion alone. The conclusion that
postinfarction sympathicotonia is a
critical factor in the triggering of ec
topic activity and fbrillation is fur
ther supported by the demonstration
that cardiac sympathectomy prior to
occlusion protects against these com
plications and lowers the mortality
rate (Fowlis et al. , 1 974).
A study with unilateral stellectomy
or reversible cold block of individual
stellate ganglia revealed significantly
different infuences of the right and
left ganglia on cardiac excitability,
perhaps comparable to the well
established differences with respect in
inotropic and chronotropic infuences
(Schwartz, Snebold & Brown, 1 976).
Thus, left sympathetic denervation of
the heart raised the ventricular
fibrillation threshold 72 3S percent
above control values, whereas right
sided denervation lowered the
threshold 48 1 4 percent. The
authors believe that these observa
tions help explain the pathogenesis of
ventricular arrhythmias and fibrilla
tion (e. g. , in the so-called long Q-T
syndrome) associated with increased
sympathetic activity. They recom-
8I
mend left stellectomy as a logical
measure in patients at high risk from
such arrhythmias, when medical
therapy has not been effective.
Schwartz (1 976) has further pro
posed, on the basis of these observa
tions and studies on infants, that the
Sudden Infant Death Syndrome is
due to the long Q-T syndrome
brought on by an abrupt sympathetic
discharge taking place through asym
metrical cardiac sympathetic innerva
tion in which the right side is, for
some reason (congenital?), subnor
mal in activity.
At any rate, it seems clear that the
increased sympathetic discharge to
the heart which accompanies myocar
dial infarction (Malliani et ai. , 1 969)
greatly imperils the effective function
of the heart and the survival of the
patient. There is not only the hazard
of ectopic activity and fibrillation,
but also cardio-acceleration and in
creased oxygen demand. Also to be
considered is the probability that the
increased sympathetic discharge to
the heart includes that of the
a-receptor sympathetic coronary con
strictors (Szentivany & Juhasz-Nagy,
1 963a, 1963b; Feigl, 1975) which
would contribute to intensification
and spread of the myocardial
ischemia. Indeed, it is. possible that
hyperactivity of these neurons would
contribute to coronary arteriospasm
implicated in acute myocardial
ischemia and angina pectoris. The ap
parent inhibitory influence of the
sympathetic innervation on the
development of collateral circulation,
previously discussed, may also have
important implications for the patient
with coronary artery disease.
Other examples of sympathetic
components in cardiovascular disease
are the following:
(a) Dietzman et aI. (1 973) found
heightened SNS activity during car
diogenic shock in dogs. Renal and in
testinal vascular beds were most af
fected. Reduction of SNS influences
lengthened the survival period. These
studies support the concept that the
SNS plays a lethal role in cardiogenic
shock in dogs.
(b) Raab ( 1 963) and Kaye,
McDonald and Randall ( 1 961 ) have
shown that hyperactivity of cardiac
sympathetic pathways may produce
severe cardiac lesions.
(c) Barger ( 1 960) found that reten
tion of Na and water in congestive
82
heart failure is ascribable to increase
in sympathetic activity in the kidney.
As a matter of fact, the renal sym
pathicotonia is evident before the
development of heart failure. Block
ing the adrenergic nerves produced
diuresis and natriuresis. In patients
with ureteral calculi and during ex
perimental stimulation of the ureter
in humans and dogs (by ureteral
catheterization), Hix (1 970) found the
renal sympathetic pathways markedly
facilitated on the affected side. In
these subjects superimposed emo
tional stimuli caused unilateral,
abrupt reduction i n glomerular fltra
tion and renal blood flow. In dogs,
Kottke, Kubicek and Visscher ( 1 945)
produced arterial hypertension by
chronic renal artery-nerve stimula
tion.
It is of interest in this connection
that Anselmino (1 950) found that
novocaine blockade of the renal in
nervation reduced arterial blood pres
sure in most eclamptic patients, im
proved diuresis and, in some, stopped
coma and convulsions. Blockade of
the stellate ganglia in these patients
improved diuresis, stopped coma and
convulsions in some and improved
subjective manifestations including
headache, ocular disturbances and
nausea.
5. Posttraumatic pain syndromes.
"The expected response to trauma in
an extremity after proper treatment is
orderly and predictable healing of the
wound, return of function, return of
'
circulatory dynamics, and gradual
cessation of pain. Occasionally this
predictable response reacts in a
bizarre fashion despite adequate
treatment and the absence of any ob
vious factors detrimental to prompt
healing. Pain may become severe and
unrelenting, with a marked disparity
between severity of pain and the ap
parent injury. Sympathetic dysfunc
tion, usually over-activity, becomes
evident. Trophic changes usually en
sue to varying degrees, and if the pro
cess is left unattended for any length
of time they become irreversible."
This is the way that the surgeon
authors of a contribution to the
management of posttraumatic syn
dromes i ntroduce thei r paper
(Thompson, Patman & Persson,
1975). The paragraph is a synopsis of
an assortment of causalgia-like syn
dromes affecting the extremities, in
which, at least from the therapeutic
viewpoint, hyperactivity of the sym
pathetic innervation is a critical
feature.
The manifestations (and the in
citing factors) of these syndromes
occur in such great variety, with
respect to intensity and quality of the
pain, motor dysfunction, sympathetic
dysfunction and trophic distur
bances, that many different terms
have been invented reflecting not only
these variations but also the special
interests, emphases and viewpoints of
the observers. Among the terms for
these "entities" are the following:
minor causalgia, reflex sympathetic
dystrophy, Sudek's atrophy, painful
osteoporosis, acute atrophy of bone,
shoulder-hand syndrome (following
myocardial infarction or stroke),
chronic traumatic edema, post
traumatic pain syndromes, sym
pathetic neurovascular dystrophy,
t r aumat i c angi os pas m, pos t
traumatic spreading neuralgia, sym
pathalgia, peripheral trophoneurosis,
and others. The most favored in
current literature seem to be refex
(or posttraumatic) sympathetic dys
trophy and posttraumatic pain syn
dromes (Patman et al. , 1 973; Thomp
son et aI. , 1 975; Genant et ai. , 1 975;
Kozin et aI. , 1 976; Kleinert et aI. ,
1 973; Omer & Thomas, 1 974). The
terms "mimocausalgia" (proposed
by Thompson et al.) and "minor
causalgia", however, would seem to
be most useful, especially for those
familiar with causalgia through
clinical experience or through the
classical descriptions of causalgia by
S. Weir Mitchell and associates, in
reports of their experience with gun
shot wounds in the American Civil
War, and in more recent reviews
(Richards, 1 967).
The pain may vary from the ex
tremely severe, burning, unrelenting,
personality-destroying type of full
causalgia to the equally chronic but
more tolerable pain of the "minor"
causalgias. Hyperesthesia may be so
exquisite that the patient cannot
tolerate the weight of clothing on the
extremity, the gentlest touch or the
slightest air current. Paroxysms of
even more intense pain are often trig
gered by any of the above and by such
minor disturbances as noise, change
in ambient temperature or movement
of the limb. The limb is held as im
mobile as possible. The patient is,
EMG, SNS, reflexes, etc.
therefore, extremely resistant to
therapy.
The manifestations of sympathetic
dysfunction include vasospasm and
hyperhidrosis, cold and wet skin,
cyanosis and chronic edema. In some
cases, however, or temporarily in an
early stage, the skin may be hot and
dry as well as edematous, possibly
due to the release of vasoactive agents
and irritants from sensory endings by
antidromic impulses (discussed later).
The most bizarre manifestations
are those in the "trophic" category.
They include change in the thickness,
texture and other qualities of the
skin, changes in the nails and hair
growth, shortening of tendons,
atrophy of musculature, osteoporo
sis and other degenerative changes in
bones, joints (which become stiff and
even frozen) and juxta-articular
tissues. The arthropathies and other
skeletal changes have recently re
ceived thorough study by Genant et
al. ( 1 975) and Kozin et al. ( 1 976) with
fine-detail radiography, radionuclide
techniques and mineral analyses.
The degenerative changes in bone,
"frozen" joints, muscle atrophy,
etc.; have been ascribed by some to
immobilization of the affected limb
by the patient, and this is almost cer
tainly a factor. Wowever, the distri
bution of pathological changes be
speaks a central neural mechanism.
Whether the trophic manifestations
are due to circulatory changes, some
other infuences of sympathetic im
pulse activity or the non-impulse
mechanisms discussed by others in
the Workshop remains to be investi
gated.
Another feature difficult to explain
is the gross disparity between the re
sponse, on the one hand (the' severity,
persistence and progressive nature of
the pain and other manifestations),
and the injury, on the other. In some
cases the injury may not only be non
penetrating but so slight that it would
ordinarily be dismissed as a superfi
cial bump or a bruise; in other cases it
may be a small fracture, a minor sur
gical procedure, a laceration, a tool
dropped on the foot.
One of the most remarkable com
mon features of these syndromes and
their variants is their responsiveness
to interruption of impulse traffic in
the sympathetic innervation of the
affeted extremity. In many cases, the
pain and autonomic manifestations
may be immediately relieved by
blockade of the appropriate ganglia
(ipsilateral stellate or lumbar). The
relief may outlast by several hours or
days the usua anesthetic action of
the agent injected around the ganglia.
The relief may even be permanent
following a single block or a series of
blocks. When, as is more usual, and
if the ganglionic blockade has given
temporary relief outlasting anesthetic
action, then permanent relief and
"cure" may be obtained with surgical
interruption of the sympathetic path
way to the extremity.
Ganglionic blockade and sympa
thectomy are much less likely to be
effective if diagnosis
'
and effective
treatment have been too long de
layed. Most authors urge early recog
nition and treatment of the syndrome
not only because delayed interruption
of the local sympathicotonia is less
likely to be effective (which, in turn,
often prevents examination of the
extremity and application of sup
portive measures such as physical
therapy), but because the trophic and
degenerative changes may become so
advanced as to be irreversible. Under
such circumstances, even were the
pain and vasomotor changes even
tually relieved, the patient would be
left with a disfigured and disabled
extremity and often with severe
emotional disturbances.
No hypothesis has yet been offered
that satisfactorily explains refex sym
pathetic dystrophy. In general, three
mechanisms (Sternschein et aI. , 1 975)
seem to have won adherents:
(l ) Increased excitability (facilita
tion) of internuncial neuronal pools
at the involved cord levels, presum
ably incited by aberrant sensory input
from the injured site. Sensory, motor
and sympathetic pathways are
thought to be affected by the en
hanced central excitatory state. The
increased sympathetic discharges pro
duce changes in the periphery which
incite secondary afferent discharges,
thus initiating and sustaining vicious,
autogenic cycles of impulses.
(2) Excitation of ectopic impulses
in pain fbers by impulses passing in
neigh boring sympathetic post
ganglionic fibers (interaxonal "cross
talk", lateral or ephaptic transmis
sion, "artificial synapse"). The anti
dromic (as well as orthodromic,
afferent) impulses triggered in this
manner are thought by some to re-
lease vasoactive agents and irritants
at the endings.
(3) Various adaptations of the gate
control theory of pain.
While hypotheses (2) and (3) may
possibly contribute to understanding
of the pain components of the syn
dromes, they offer none regarding the
signs of sympathicotonia (which the
first hypothesis does) or of the
trophic manifestations (which are re
ferable, at least in part, to the sym
pathicotonia). This seems a worthy
area for investigation, perhaps in an
animal model which simulates the
causalgia- l i ke syndromes . The
preparation described by Kennard
( 1 950) may be a promising one with
which to begin.
6. Other skeletal disorders.
In 1 957 Herfort first reported ex
cellent results following lumbar sym
pathectomy in patients bedridden by
arthritic pain in weight-bearing
joints. The extirpation of the lumbar
ganglionic chain affected the rheuma
toid activity only in the denervated
extremities, and equally good results
were obtained in rheumatoid and
osteoarthritic dsiease. Neurons and
neuroglial supporting cells in sym
pathetic ganglia surgically removed
from patients with chronic poly
arthritis showed morphological signs
of prolonged preganglionic stimula
tion (Kuntz, 1 958).
Coujard ( 1 96) reported a variety
of osteodystrophies produced in the
guinea pig by irritation of the sym
pathetic fibers in the sciatic nerve
(and by diencephalic lesions). The
bony manifestations included various
arthropathies mimicking those of
tabes and syringomyelia, alteration of
calcium fixation, and heterotopic
osteogenesis, such as spicules on the
periosteum and tumor-like out
growths of bone.
Kottke et al. (l 958) studied longitu
dinal bone growth in children who
had paresis of one leg and nearly nor
mal strength in the other after acute
anterior poliomyelitis. The average
rate of growth of the bones of paretic
legs was substantially less than that of
normal legs; total extremity length
was 82.9 percent of normal. Treat
ment with a sympatholytic drug re
stored growth to the rate of the nor
mal leg. Th authors attributed the
retarded bone growth to reflex hyper
activity of SNS in response to cold,
83
which results in vasoconstriction in
the extremity and inhibits epiphyseal
bone growth. They cite an earlier
study in which chronic unilateral
stimulation of the lumbar sym
pathetic chain in puppies substantial
ly reduced growth of the hipd limb on
the stimulated side. Coujard ( 1 957),
however, reported evidence that the
sympathetic innervation influenced
the sensitivity of bone and other
tissues to morphogenetic hormones.
We may also include in this
category many clinical reports on the
painful joint syndrome known as
shoulder-hand syndrome, occasional
ly a distressing sequel to myocardial
infarction and stroke, which is often
dramatically responsive to stellate
block. Some of these studies are cited
in the references of the foregoing sec
tion on reflex sympathetic dystrophy.
7. Shock.
Pre-treatment of experi mental
animals to be subjected to traumatic
shock (Levy, North & Wells, 1 954;
Ross & Herczeg, 1 956) or hemor
rhagic shock (Berger, 1 965) with
adrenergic blocking agents at certain
critical dose ranges or with sym
pathectomy protects them against the
lethal effects. Apparently, as is true
in other clinical situations, " . . . . the
sympathetic discharge is a protective
mechanism, but initiates processes
which are detrimental to survivial"
(Levy et ai. , 1 954).
8. Hepatotoxcity.
This principle i s again illustrated in
liver pathology produced by ad
ministration of carbon tetrachloride.
According to the evidence of Calvert
and Brody (196), the characteristic
hepatic changes are the result of
massive discharge of the peripheral
SNS. This leads to hepatic ischemia,
hypoxia and necrosis around the cen
tral vein of the hepatic lobule and cer
tain changes in enzyme activities. As
discussed in an earlier section of this
paper, the sympathetic discharge also
releases fatty acids from the periph
eral fat pads and the consequent
deposition of lipids in the liver.
9. The Uteru.
On the basis of their own experimen
tal work with animals and review of
clinical and research literature,
Shabanah, Toth and Maughan ( 1 964)
concluded that many unexplained
8
obstetrical and gynecological condi
tions involving disturbances i n
uterine contractility may be ". . . .
related to abnormal neurohumoral
causative factors reflected in a fnal
picture of autonomic imbalance -
sympathetic hyperactivity."
A study by Miller and Marshall
( 1 965) on rabbits lends support to this
conclusion. They found that stimula
tion of the hypogastric nerve in
hibited spontaneous uterine contrac
tions in rabbits treated with estrogen
+ progesterone. This effect was
abolished by adrenergic blocking
agents, but was unchanged by
atropine or hexamethonium.
10. The eye (as a model il ustrating
sympathetic inuences on tissue
reponses to other factors).
The role of the innervation of the eye
in such disorders as glaucoma has
long been under study, but no clear
picture has emerged despite evidence
for an important sympathetic in
fluence on intraocular pressure,
through infuences on formation or
drainage of aqueous humor or both.
Sympathetic influence on the per
meability of the blood-aqueous bar
rier to protein, and therefore outfow
resistance, may also be a major factor
(Langham, 1 958).
The detrimental influence of the
sympathetic innervation on the
responses of the eye to other factors is
much clearer. For example, when the
trigeminal nerve was interrupted, cor
neal ulcerations developed in all of
the animals (cats). Prior stellectomy
prevented the lesion in almost all of
the animals, and permitted healing if
the lesion did appear (Baker & Oot
tlieb, 1 959).
Howes and McKay ( 1 972) dem
onstrated the protective effect of
sympathectomy in quite a different
kind of situation. Systemic bacterial
endotoxin in rabbits produces a
marked increase in ocular vascular
permeability, primarily in the iridial
portion of the ciliary process. The in
itial consequence is edema. followed
by hemorrhages and thrombi. Post
ganglionic sympathectomy (extirpa
tion of the superior cervical ganglion)
reduced the severity of the ocular re
sponse to systemic endotoxin. This
effect required several hours to ap
pear, and at 4 h after administration
of the toxin to the unilaterally sym
pathectomized rabbit there was a
decrease in the altered vascular per
meability as measured by
1 25
I-serum
albumin, in stromal hemorrhages and
in small-vessel thrombi in the sym
pathectomized eye as compared to the
contralateral or sham-operated eye.
The apparent exacerbating in
fluence of the sympathetic innerva
tion in conjunction with systemic en
dotoxin i s by no means peculiar to the
eye. As is evident, for example, from
the reports of other investigators
cited by Howes and McKay, sympa
thetic denervation and a-adrenergic
blocking agents are known to sup
press or prevent other reactions to en
dotoxins (local and generalized
Schwartzman reaction). As far as the
eye alone i s concerned, it would cer
tainly seem important to investigate,
from the etiological and therapeutic,
as well as pathophysiological, view
points, the role of the sympathetic in
nervation in such common and
damaging disorders as uveitis or iritis.
11. Other example.
Other clinical situations may be cited
in which a contributing, exacerbating
and often critical role of the sympa
thetic innervation has been im
plicated, but which are only men
tioned here without documentation in
the interest of space. These include
col i t i s, megacolon, peri pheral
vascular disease, ulcers of the legs,
dermatitis, postsurgical paralytic il
eus, various diseases of the kidney,
Dupuytren's contracture and "pelvic
congestion" in women.
A mass of clinical evidence, beyond
the scope of this paper. much of it
empirical, indicates an important role
of the peripheral autonomic nervous
system, and particularly the SNS, in
determining reactivity, resistance and
responses of individual tissues - and
therefore the defenses of the entire
organism - to infectious, toxic, an
tigenic and irritative agents. These in
fluences apparently extend to such
processes as inflammation, immune
reacti ons, anaphylaxi s, allergic
mani fest at i ons and "phys i cal
allergies". There i s even evidence for
sympathetic i nfluences on the
response of tissues to carcinogenic
agents and on immunobiologic
mechanisms that determine tumor
"take" in experimental implants.
(See, for example, Stein-Werblow
sky, 1 974.) These interfaces between
neuroscience and immunology and
EMO, SNS, reflexes, etc.
microbiology would be worthy areas
of investigation, from scientific and
clinical viewpoints.
The "normal" influences of sym
pathetic innervation on various end
organs, discussed in an earlier
section, may also be-expected to be
deleterious when the impulse activity
is intensifed and sustained. For ex
ample, falsely exaggerated reports
from sympathetically bombarded re
ceptors, especially baro- and che
moreceptors, would certainly have
a disturbing effect on reflex
regulatory mechanisms. This would
be true also of SNS influences on
CNS functions. The effects of sym
patheti c hyperacti vi ty on the
reti culoendotheli al system, fat
metabolism, enzyme activity, en
docrine systems and others may also
be expected to be harmful over long
periods of time.
Finally, it is important to mention
again that any clinical disturbance or
augmented tissue vulnerability in
which ischemia is a contributing fac
tor often may be related to sym
pathetic hyperactivity in view of the
strong constrictor influence of sym
pathetic vasomotor fibers.
12. Other kinds of evidence for a
general SNS role in d iease proceses.
(a) Neuropathological. Profound
morphological alterations are ex
hibited by ganglion cells in ganglia
removed surgically in the treatment
of patients with various diseases and
at autopsy. There is also marked pro
liferation of neuroglial supporting
cells. The changes are such as to in
dicate overstimulation of the gan
glion cells, and indeed many alter
ations sen in surgically removed
ganglia and their cellular components
have been induced experimentally by
prolonged preganglionic stimulation
(Kuntz, 1 958; Schilew, 1 965).
(b) Irritative Lesions. Prolonged ir
ritation, with various agents and in
juries, of peripheral sympathetic
structures ( e . g. , col l ateral or
paravertebral ganglia, splanchnic
nerve) or of sensory fbers in spinal
nerves produces many types of lesion
and dysfunction of visceral and
somatic structures, often lethal,
which simulate naturally occurring
pathology (Mosinger, 1957; Reilly et
at, 1955).
Mehanisms
In considering the participation of the
SNS in disease processes, we are con
fronted with an apparent paradox.
On the one hand, thanks especially to
the pioneering studies of W. B. Can
non, we have reason to be impressed
with the important role of the SNS in
organizing adaptive, moment-to
moment responses of the total
organism to changes in environment,
posture and physcial activity, and to
injury and emergencies. As adaptive
responses, they are protective and ap
propriate to the situation (or to what
is perceived to be the situation). On
the other hand, we have many ex
amples of harmful and even life
endangering effects of sympathetic
activity which is focused too intensely
and for too long on individual tissues
and organs.
The roles of the higher centers,
including the cerebral cortex, in
initiating and organizing somato
autonomic response patterns are now
fairly well understood. However, in a
prevailing emphasis on these whole
body patterns, which are based on the
capacity of the SNS to discharge as a
whole and to broadcast its infuences
throughout the body, there is a ten
dency to overlook the high degree of
local and regional control that is
essential to proper execution of the
responses, as they change from mo
ment to moment. Much of the capaci
ty for localization resides of course in
some of the higher centers, which can
direct descending impulses (e. g. , via
corticospinal fibers) to appropriate
neuron pool s. But the precise
modulation of the local and regional
components of the total pattern is
based on sensory signals from par
ticipating and affected tissues and
organs and on specificity and selec
tivity of connections, through
segmental pathways, between af
ferents and sympathetic neurons.
These two moieties of the total pat
terns seem to correspond to what
neurophysiologists, recording from
sympathetic efferents at various
spinal levels, as they stimulate
selected somatic afferents, have
designated as "late" (supraspinal)
and "early" (spinal) somatosympa
thetic refexes (Koizumi & Brooks,
1972). All or nearly all of the total
SNS neuron pool can be activated
in this way via the supraspinal path
ways. Only a fraction of the pool,
however, is activated by the same
afferent stimulation via the spinal
pathways; and some somatic affer
ents (Group I) seem to have no ac
cess, normally, to sympathetic neu
rons via segmental pathways. The
fraction of the efferent (pregangli
onic) neuron pool that i activated via
spinal pathways by stimulation of
selected somatic afferents is concen
trated at the corresponding spinal
level, the number of responding
neurons declining sharply with in
creasing segmental interval (reviewed
by Koizumi & Brooks, 1 972, and by
various authors in Sato, 1975). In
other words, the "early" and most
direct impact of impulses entering via
a given dorsal root (and hence coming
from a given dermatome, myotome
or viscerotome) is mainly focused on
the neurons whose axons emerge
through the corresponding ventral
roots (conveying motor and sym
pathetic impulses to organs and
tissues in the same body "seg
ments").
I suggest that the clinical distur
bances which are apparently based on
hyperactivity in related sympathetic
pathways, described in the previous
section, are aberrations of these local
and regional feedback mechanisms.
They appear to be triggered by
unusual patterns of afferent impulses
originating in part in i nj ured,
strained, impaired or chemically
altered tissues or at sites of injury in
nerves or roots. The aberration ap
pears to be sustained (and intensified)
by either (I) secondary afferent
discharges from tissues bombarded
by the sympathetic impulses, (2)
facilitatory changes in the spinal
cord, or both. While the initial
trauma need not be painful to launch
the vicious cycle, pain may be
brought on by the sympathetic dis
charge (e. g. , in ischemia) and by
lateral (ephaptic) transmission at sites
of nerve deformation, from sym
pathetic postganglionic axons to
neighboring unmyelinated sensory
fibers.
The aberration may also begin as a
component of a total response pat
tern. The patterns are adaptive and
protective when initiated by cir
cumstances likely to occur in daily
animal life, such as environmental ex
tremes, exertion (" fight or fight"),
injury by external forces, threat of in
jury and death, hypoxia, etc. When
85
confronted wi th ci rcumstances
unlikely to have been encountered i n
the course of evolution of these adap
tive sympatheti c patterns, the
responses may not only be inap
propriate, but even harmful and
detrimental to survival. Thus, while
refex vasoconstriction (and accom
panying cardiovascular and other
systemic changes) may be appropriate
for, let us say, a painful laceration of
an extremity, sympathetic hyperac
tivity with resultant ischemia is totally
inappropriate and definitely "con
traindicated" for a joint which is
painfully irritated or infamed. The
ischemia itself causes pain which fur
ther intensifies the sympathetic
discharge. The vicious cycle set up in
t hat manner aggravat es t he
pathological state (Kuntz, 1958). For
similar reasons , heightened sym
pathetic discharge to a heart already
laboring under i mpairment by
myocardial ischemia can only, as we
have seen, further impair and burden
the heart and decrease the. probability
of survival. Bodily responses to anox
ia, a common hazard in terrestrial
life, are the adaptive product of
evolution, which become destructive
and lethal when evoked by a cir
cumstance as unlikely as high O2 ten
sion (Ramey & Goldstein, 1 957).
Similar, spinally organized reflexes
seem to operate in the therapeutic ap
plication of hot packs, cold packs and
counterirritants (e.g. , rubefacients) to
the skin in the region of inflamed,
congested, ischemic, edematous or in
jured viscera and joints. When,
however, the skin over apparently
healthy organs is chilled, the
responses may be such as to
predispose to infection or other ill
ness, as, for example, in the upper
respiratory tract (Ralston & Kerr,
1 945), gastrointestinal tract (Richins
& Brizzee, 1 949) or kidney (Nedzel,
1956).
One of the most interesting and
clinically significant features of these
aberrant, spinally organized so
matosympathetic reflexes is the
making of synaptic connections that
are not ordinarily in use. This is
similar to the experimental situation
in which Group I afferents, which do
not have access to sympathetic
neurons via the "early" , spinal
pathways, are able, through the open
ing of "potential" pathways, to ac
tivate these neurons when the spinal
86
cord is moderately cooled (Koizumi &
Brooks, 1 972). The result in the
clinical situation is to link, refexly,
somatic and visceral structures which
are not functionally coupled in any
normal bodily activity or adaptive
response pattern. In the clinical situa
tion, they become linked only by vir
tue of the segmental proximity of
their innervating neurons. Not only is
this reflex "entanglement" nonadap
tive and harmful to each of the struc
tures involved in this aberrant reflex
coupling, but it is disruptive of the
adaptive refex patterns in which
these organs and tissues are called on
to participate.
Dysfunctional, segmental coupling
is clearly illustrated in patterns of
referred pai n and associated
phenomena, of both visceral and
somatic origin. Not only is the
distribution of referred pain (e.g. ,
from ischemic myocardium to chest
wall, upper back, left shoulder and
arm) unrelated to any normal func
tional pattern, but the same is true of
the reflex motor and sympathetic
( s udomot or and vas omot or )
responses i n the reference zones. The
reflex responses to the initiating insult
are not only useless, but secondary
pathology may be instigated in the
reference zones (as in postinfarction
shoulder-hand syndrome). The af
fected tissues may in turn become
secondary sources of abnormal af
ferent bombardment that helps sus
tain, intensify and spread the sym
pathetic hyperactivity. Although
referred pain and refex patterns of
visceral origin have been more
thoroughly investigated and de
scribed, it is important to point out
that similar and even indistinguish
able patterns may be initiated from
deep somatic structures (Lewis &
Kellgren, 1 939; Kellgren, 1 940;
Travell & Rinzler, 1 949). Reflex
activity through sympathetic path
ways seems to be elicited with equal
facility by painful somatic or visceral
afferent stimulation (Tunt', 1958),
and with no fundamental difference
in the manifestations.
Relation to manipulative therapy
In accordance with the objectives of
the Workshop, I venture to offer for
exploration hypotheses which pur
port to link the clinical and ex
perimental materia j ust reviewed and
their apparent mechanisms to those at
work in manipulative therapy. In
view of the rich access of somatic af
ferents, via spinal and supraspinal
pathways, to sympathetic neurons, it
would be truly amazing if even rela
tively minor disturbances in motion
of intervertebral or other joints,
which are amenable to manipulative
therapy, did not have autonomic and,
therefore, circulatory, metabolic and
visceral repercussions of some degree.
It would be equally surprising if the
cost did not increase with time and
with the superimposition of other
detrimental factors in the patient's
life.
On the basis of available data and
my observations of the skillful prac
tice of manual medicine over a third
of a century as a physiologist, I sug
gest that:
1 . Local musculoskeletal dysfunc
tions, especially in and around the ax
ial and weight-bearing parts of the
skeleton, are clinically significant not
only because of the motor impair
ment and the pain that are sometimes
present, but also because they in
stigate or contribute to the sustained
sympathicotonia which is a common
feature in so many syndromes. Like
those syndromes, they also appear to
be aberrant versions of the spinal
("early") somatosympathetic reflexes
discussed above.
2. The disturbance in the cord is
due to distorted patterns of afferent
impulses from (a) the affected
musculoskeletal tissues and/or (b)
irritative lesions of nerves, roots and
ganglia, such that adaptive, appropri
ate responses are not possible. (In
view of the sharply delineated der
matomal bands showing sympathetic
hyperactivity. often encountered in
our studies. i t is likely that part of the
segmental sympathicotonia may be
due to irritation of sympathetic
ganglia.)
3. Effective manipulation is that
which results in the reestablishment
of coherent patterns of afferent input
such that local adjustive reflexes are
once more appropriate and har
moniously integrated in the total,
supraspinally directed patterns of ac
tivity and adaptive response. The
most critical effect, clinically, is the
subsidence of sympathetic hyperac
tivity and its pathogenic, pain
producing influences.
4. Improvement in the afferent in
put is accomplished by appropriate
EMG, SNS, reflexes, etc.
adjustment of articular, interosseus
relationships, muscle lengths and
muscular, fascial and ligamentous
tensions that enable these tissues once
more to report in coherent pro
prioceptive patterns; and, in the same
process, by relieving mechanical
deformation or irritation of neural
structures.
5 . The mechanisms are the same
when the primary perturbation of the
cord is of visceral origin, and the
musculokeletal involvement is of
secondary, reflex origin, as occurs in
association with referred pain. The
therapeutic effect (among others) of
manipulation is still to slow the
vicious cycle and reduce the sym
pathetic discharge to the visceral and
somatic structures whi ch have
become reflexly coupled to their
mutual detriment.
6. The impaIrIng effects of
biomechanical insult to nerve on the
transfer of information (and materi
al), explored in a later section of the
Workshop, are also part of the pro
posed mechanisms in manipulative
therapy, as reflected in our earlier
publications (Appeltauer & Korr,
1 975, 1 977; Korr, 1972; Korr & Ap
peltauer, 1 974; Korr, Wilkinson &
Chornock, 1 967).
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8
hypoglossal nucleus labeled with P-phosphate. Left hypoglossal nucleus unlabeled. The animal
was killed on the 8th day. (c) Left; (d) right.
consistent feature, whether the label
was PH- phosphate of C4-amino
aci ds. Labeling of cells other than
muscle cells (and, in some sections,
branches or axons) was, as in Fig. 1, b
and c, negligible or absent.
When neural delivery of labeled
substances was l imited to one side,
there was unilateral labeling of
tongue muscle cells (Fig. 2). Sections
shown in Fig. 2, a and b, were taken
from the tongue of a rabbit in which
the left hypoglossal nerve had been
cut i mmediately before the hypoglos
sal nuclei were labeled with glycine-I
e14 The left side (Fig. 2a) showed
early signs of degeneration and no
radioactivity. In the normal, inner
vated section (Fig. 2b) the muscle
cells were strongly labeled. (Figure 2b
i l lustrates a frequent finding in some
of our preparations, the transverse
al i gnment of radioactive substances
in the muscle fibers. Precise localiza
tion awaits autoradiographs of higher
resol ution. ) The results were the same
in other experiments in which a small
segment of nerve was crushed and ax
oplasmic continuity thereby inter
rupted while the gross continuity of
the trunk and, presumably, of en
doneural fluid spaces was preserved.
No labeling of cells other than muscle
was found on either side. In two
experi ments we were able to label the
hypoglossal (and vagus) nerve only
on one side, while leaving intact the
nerves to both sides, thereby eliminat
ing any question of altered physio
logical state on the denervated side.
In one animal (Fig. 2, c and d) only
the right hypoglossal nucleus had
Axonal transport and trophic studies
M
d
K
M 9 Z d , M MMM l Z l Z
NL N LH W W
l l
L
Fig. I.Expriment showing reults I8days ater sham opration and in
trperitoneal injection of'H-leucine. Ordinate-dpm/mg freh weight of
the various specimens. Black-TCA-insoluble frction; Oray-TCA
soluble-fraction; Cros-hatched-(M-medulla and P-plama) total
radioactivity. NL, NR-hypoglossal nerve, let and right; segments 1-
in proximodistaf sequence; SL, SR-stylohyoid muscle, let and right,'
MHL, MHR-mylohyoid muscle, left and right; OL, OR-genioglosus
muscle, left and right; SOL, SOR-styloglossus muscle. let and right.
w r M
--
`
" 0 f " 0
0 0
0
c 0 8 4
Fig. 2. Incorporation ofblood-bore 'H-leucine into protein by tongue
and control muscles. Ordinate-dpm/mg freh wight; abscisa-days
after sham opertion and intraperitoneal inection. -average ofJpor
tion of styloglos us mucle (SOL) O-average of4 control muscle (SL,
SR, ML, MR; see Fig. I).
9UUU
ZUUU
M | Z 9 | Z 0 4
DPM/mg
` ` `
NL NH H
Fig. J. Eperiment showing results II. /5days after intraventricular ad
minitration of 'H-Ieucine. Symbol same as in Fig. 1. Note ZOfold di
ference in radioactivity scales for nerve and muscle.
I0J
30
I .
I
,
,
,
,
UU
W~. .
c
, ,
g ,
.
. g
,
Z
. ,
9
, ,
DPN
K
_
.
" ,
. . . ' .
,
. . ' - " .
. . . :
.
. .
.
:
.
.
.
_
.
.
, .
. .
' . "
`
g
.
"
1
'
,
.
.
.
| f-
, .
g
P
O
I
9 "
., : . :. r
.
,_( ).: u" tgfg
. .
8
".
.
lU Z N %
Fig. 4. Summary ofeperiments with intraventricular adminitration of
'H-Ieucine. Ordinatedpm/mg fresh weight; abscisa-days ater ad
ministration . -average of3 portions of left styloglossus muscle (SOL).
O-average of4 control muscles (SL, SR, ML. MR) showing portions of
protein incorporating blood-bore precuror.
o o
o
K
o o
&
o
0Y AP ADI5TAT|0N
Fig. 5. Tratment ofdata from Fig. 4 presenting 2, 3 and 4-day means and
standard deviations. "Corrected" for apparent dosage . -SOL muscle;
O-control.
length. Radioactivity (undifferenti
ated into protein and acid-soluble
fractions) of medulla and blood
plasma were routinely determined in
all of the experimental animals, pri
marily to monitor our techniques,
and do not enter into analysis of the
data. In all specimens in this experi
ment, maximum protein radioactivity
was below 4 dpm/mg.
Figure 2 shows the results of 1 8
such experiments, the specimens of
styloglossus and control muscle hav
ing been taken at various intervals be
tween 1 and 76 days after the intra
peritoneal injection. Evidently, the
control muscles that we selected give
a reliable index of radioactive protein
incorporating blood-borne lH-leucine
in the styloglossus muscle of the
tongue.
meach of the experiments described
in the next section, we therefore
used the stylohyoid and mylohyoid
muscles to indicate the blood-derived
portion of protein radioactivity in the
tongue muscles, the remainder being
10
ascribable to delivery via the hypo
glossal nerve.
Intraventricular labeling ojhypoglos
sal neurons. Figure 3 shows one ex
periment in which the 3H-Ieucine had
been applied directly to the left hypo
glossal nucleus, as described. The
rabbit was killed and the specimens
taken 1 1 . 7 5 days after surgery.
Unlike Fig. 1 , the scales for nerve
radioactivity and for muscle radio
activity differ by 20-fold, that in the
nerves being much higher than in the
muscles. The protein radioactivity of
the left nerve was much higher than
that of the right nerve. (Nevertheless,
the radioactivity in the right nerve
was substantial, and indicates, as did
the other experiments, that some dif
fusion of the precursor across the me
dian sulcus and perhaps to other parts
of the ventricle floor was unavoid
able, and a variable in our experi
ments.) Correspondingly, the left
styloglossus muscle had much higher
protein radioactivity than the right,
which was only slightly higher than
the control levels. As previously men
tioned, and typically of the other
experiments, the left genioglossus
muscle received much less radioactive
protein than the left styloglossus.
Apparently no measurable amount
of radioactive material unincor
porated in protein reached the axon
(Fig. 1 , NL, NR). Correspondingly,
almost all of the radioactivity ex
tracted from the left styloglossus
muscle (SOL) was in the protein
(TCA-insoluble) phase. This is to be
contrasted with the much larger por
tion of supernatant radioactivity
(probably largely unincorporated pre
cursor) when the precursor was ab
sorbed by the muscles from the blood
stream (control muscles in Fig. 3, and
all of the muscles in Fig. I ) .
Figure 4 graphically presents the
data from the left styloglossus and
the control muscles in 1 48 such ex
periments. Three experiments were
done for each of the first 42 days in
the interval between application of
precursor to the hypoglossal nucleus
and the killing of the rabbit. After 42
days, experiments were at longer in
tervals . Each experiment is repre
sented by two points. The open cir
cles, each representing the average of
four control muscles, show that
throughout the entire period of 76
days there was a small and progres
sively declining portion of radioactive
protein ascribable to incorporation of
blood-borne 3H-Ieucine.
The solid circles, each representing
the average of three portions of left
styloglossus muscle, show that unlike
experiments with intraperitoneal in
jections, the protein radioactivity of
the left styloglossus muscle was well
above control-muscle levels through
out most of the 76 days, and that
waxing and waning of protein radio
activity was evident during the frst
4 days. The frst peak of activity
occurred within the first 24 hours,
above-control activity being evident
after 6 hours, followed by several
other waves, and then a gradual de
cline over the next month or so.
In such a study as this, many fac
tors, some intrinsic to the animals,
others experimental, enter into the
spread of data for each post-labeling
interval. In analyzing the data we
have tried to compensate for varia
tions in some of the factors. One im
portant animal-to-animal variable is
Axonal transport and trophic studies
in the length of the nerve, contribut
ing to proportional variations in
transport time; the slower the migra
tion, the wider the variations.
Accordingly, we divided the entire
experimental period into three arbi
trary subperiods, using two-day
means for the first 10 days, three-day
means for the following period to day
33, and four-day means to day 42.
Another important variable is in
the actual amount of precursor pene
trating the hypoglossal nucleus and
remaining available for incorporation
into protein. Lajtha and Toth ( 14, 1 5)
showed that maximum penetration of
leucine into brain tissue after sub
arachnoid administration is achieved
in the first 5 min, and that 1 hr later
only 800 of the amount which had
penetrated had been incorporated in
to protein, 1 0% was still in the TCA
soluble fraction and 82% had left the
brain. That is, the major reason for
decrease in free amino acid was effux
rather than incorporation into pro
tein.
Hence, in seeking to compensate
for variations in effective dose of
3H-leucine, we adopted the premise
that effux from the brain, apparently
by active transport ( 1 4), into the
plasma, (from which it was then ab
sorbed and incorporated by the
muscles in our study), was directly re
lated to the amount that had pene
trated into the medullary tissue. We
therefore applied to the data for the
left styloglossus muscle from each
animal in this series a correction fac
tor that transformed the average
value of the control muscles for that
animal into the mean for that 2, 3 or
4-day period.
The data treated as described above
have been plotted in Fig. 5, and in
dicate four periods of arrival of
nerve-borne protein incorporating
labeled leucine. The first wave begins
to appear within a few hours, peaking
n the frst and second days, and de
clining to almost control levels by
day 3 . The second wave, which corre
sponds to that in our previous radio
autographic study ( 1 2) , peaks be
tween days 9 and 14. A third wave
peaks between days 22 and 27. A
fourth is evident in the 30-40 day
interval, after which protein radioac
tivity declines gradually. The troughs
seem to represent overlap of the de
clining phase of one wave and the ris
ing phase of the succeeding one. That
is, during at least a part of each wave
other than the first, protein radioac
tivity may represent the algebraic sum
of overlapping waves and possibly in
clude residues of preceding waves.
Correspondi ng fluctuations of
proximodistal transport along the
hypoglossal nerves were also evident,
but since the radioassay of the nerve
extracts represented protein in transit
through relatively long portions of
nerve, a precise definition of waves
was not possible.
Discussion
These findings indicate that at any
given time a mixture of proteins car
ried in the hypoglossal axons is reach
ing the tongue muscle. Some of these
proteins have been synthesized by the
perikaryon a few hours earlier, some
a month earlier, and the remainder at
two intermediate periods. These
waves may be ascribed in part to dif
ferent rates of axonal transport of
protein, which have been shown to
vary in mammalian nerves from a
slow rate of 1-2. 5 mm/day up to
several hundred mm/day, with an
intermediate rate between these two
extremes evident in some axons (2, 4,
1 6). In the rabbit, Karlsson and
Sjostrand ( 1 1 ) found four rates of
intra-axonal transport in the retinal
ganglion cells ( 150, 40, 6- 1 2 and 2
mm/day), but Sjostrand (23) found
only two rates in the hypoglossal
nerve (300 mm/ day and 5 mm/ day,
as well as two somewhat higher rates
in the vagus nerve). We have no ex
planation for the apparent discrep
ancy between their findings and
ours.
Our experimental design does not
permit accurate measurement of rates
of axonal transport corresponding to
the four waves, but rough estimates
can be made on the basis of the extra
cranial, extramuscular lengths of the
hypoglossal nerves in our rabbits (an
average of about 4mm) and the time
of arrival in the muscle. Since nerve
delivered radioactive protein was
already present in the shortest of our
experimental periods, 6 hr, the rate of
transport would have been no less
than 1 60 mm/day. The fourth wave
seems to correspond to the mam
malian "slow" rate of 1-2. 5 mm/day.
The waves may be related not only
to transport rates but also to differ
ences in departure time after leucine
uptake. Droz has shown that some
sedentary protein may remain in the
cell body for periods up to two weeks
before being dispatched into the axon
(3). It is conceivable that a "late
starter" may overtake an earlier
"starter" but slower "runner. " We
propose that the multiple waves of
neuronal protein arriving at the mus
cle are the product of these two fac
tors: rate of transport and interval
between precursor incorporation and
entrance into the axon hillock.
We cannot ascertain from the data
of this part of the study what portion,
if any, of each wave of protein actual
ly enters the muscle cells, and how
much has remained in the intramus
cular nerve endings, and we must
await completion of our analysis of
the radioautographic specimens taken
from the same animals. Our previous
radioautographic study ( 1 2) certainly
supports transjunctional transfer
during what is now identified as the
second wave. There is no reason to
believe that such transfer would be
limited to only one of the four waves.
Moreover, since the publication of
that report and the completion of the
present study ( 1 3) , reports have ap
peared which strongly suggest trans
synaptic transfer of proteins within
the central nervous system (5, 10, 20).
These observations are consonant
with the ample and growing evidence
that proteins do normally move in
and out of cells (e. g. , 22).
Our hypothesis ( 1 2) that the proxi
modistal conveyance of proteins from
nerve cells may underlie their trophic
influences is supported by recent
studies. Lentz (1 7, 1 8) demonstrated
that such influences can be repro
duced in vitro, and that they are
mediated by diffusible, thermolabile
substances released by nerve cells. Al
buquerque et al. ( 1 ) showed that
blocking axonal transport, without
impairing the ability of the nerve to
maintain muscle activity, caused the
appearance of trophic signs of dener
vation.
In the present study it was possible
to distinguish four peaks of delivery,
which probably correspond to several
rates of axoplasmic transport. The
radioactive material seems to be deliv
ered rather continuously to the nerve
terminals and possibly thereafter to
the muscle. In a pulse experiment
such as this, the presence of several
overlapping waves makes it difficult
to determine whether material trans-
16
ported at a discrete rate within the
nerve can be found in the muscle at a
similarly discrete time interval. Con
sequently, in another study now ap
proaching completion, : we have
chosen to differentiate the labeled
proteins on the basis of the specific
macromolecules comprising each of
the waves. This study indicates that
soluble proteins carried in three of the
four waves are electrophoretically
distinct and that electrophoreticaUy
identical proteins are, in correspond
ing intervals, subsequently found i n
the muscle. The consistent observa
tion that only certain of the radioac
tive axonal proteins appear in the
muscle extracts suggests selective
axon-to-muscle transport. Of course,
, in addition to radioautographic
studies. analyses will ultimately have
to be made on portions of muscle de
void of nerve terminals, to ascertain
whether transsynaptic transport of
these protein species has actually oc
curred.
References
I. Albuquerque, E.X., J. E. Warnick, J. R. Tasse,
and F.M. Sansone 1 972. Effets of vinblastine and
colchicine on neural regulation of the fast and slow
skeletal muscle of the rat. Exp. Neurl. 37: '67-634.
2. Barondes. S.H. (Ed.) 1 967. Axoplasmic
transport. Neurosci. Re. PagIm Bull. 5: 3 1 1-419.
3. Draz, B. and H.L. Koenig. 1 970. Localization of
protein metabolism in neuron, pp. 93-108. In "Pro
tein Metabolism of the Nervous System." Abel Lajtha
[Ed.). Plenum. New York.
4. Grafstein, B. 199. Axonal transport: Com
munication between soma and synapse, pp. 1 1 25. In
Advances in Biohemical Psychopharmacology." E.
Costa and P. Greengard (Eds.). Raven. New York.
5. Grafstein, B. 1 97 1 . Transneuronal transfer of
radioactivity in the central nervous system. Science
172: 1 771 79.
6. Guth, L. 198. "Trophic" infuences of nerve on
muscle. Physiol. Rev. 48: 65-687.
7. Guth. L. (Ed.). 1 969. "Trophic" effects of
vertebrate neurons. Neuroi. Res. Program Bull. 7:
1-73.
8. Guth. L., F. J. Samaha, and R.W. Albers. 1 970.
The neural regulation of some phenotypic differences
between the fiber types of mammalian skeletal muscle.
E. Neurol. 26: 1 261 35.
9. Guth. L. . P. J. Dempsey. and T. Cooper. 1 97 1 .
Maintenance of neurotrophically regulated proteins in
denervated skeletal and cardiac muscle. Exp. Neurol.
32: 478-488.
10. Ingoglia. N.A = B. Grafste!n. B.S. McEwen,
and I.G. McQuarrie. 1973. Axonal transport of
radioactivity in the goldfsh optic system following in
traocular injection of labelle RNA precursors. J.
Neurchem. 2: 165-1 61 5.
I I . Karlsson, J.O. and J. SjOstrand. 1971 . Syn
thesis. migration and turnover of protein in retinal
ganglion cells. J. Neurochem. 1 8: 749-767.
1 2. Korr. I. M P. N. Wilkinson. and F.W. Chor
nock. 197. Axonal delivery of neuroplasmic com
ponents to muscle cells. Science 1 55: 342-345.
tPreliminary report in pres (Fed. Pro., March 1974).
10
1 3. Karr. I . M = and G.S.L. Appeltauer. 1 971 . Ax
onal transport of nerve-cell proteins to muscle. Fed.
Proc. 30: 65.
14. Lajtha. A oand J. Toth. 1961 . The brain barrier
system - II Uptake and transport of amino acids by
the brain. J. Neurochem. 8: 21 6-225.
IS. Lajtha. A + and J. Tath. 1962. The brain barrier
system III The efflux of intracerebrally ad
ministered amino acids from the brain. J. Neurochem.
9: 1 9-212.
1 6. Lasek. R.J. 1 970. Protein transport in neurons.
Interal. Rev. Neurobio/. 1 3: 289-324.
17. Lentz. T.L. 1971 . Nerve trophic function: In
vitro assay of effects of nerve tissue on muscle
cholinesterase activity. Scienc 1 71 : 1 87189.
1 8. Lentz. T. L. 1972. Development of the
neuromuscular junction. Part I l l . Degeneration of
motor end plates after denervation and maintenance
in vitro by nerve explants. J. Cell. Bioi. 55: 93-103.
19. Miani. N. 1 963. Anaysis of the somato-axonal
movement of phospholipids in the vagus and
bypoglossal nerves. J. Neurochem. 10: 859874.
20. Neale. J. H E.A. Neale and B.W. Agranoff.
1 972. Radio-autography of the optic tectum of the
goldfish afer intraocular injection of ('H) Proline.
Sience 176: 40741 0.
21 . Patterson. M. S. and R.C. Greene. 195.
Measurement of low energy betaemitlers in aqueous
solution by liquid scintillation counting of emulsions.
Anal. Chem. 37: 854-857.
22. Ryser, H.J.P. 1 968. Uptake of protein by mam
malian cells: An underdeveloped area. Science 159:
39-39.
23. SjOstrand. J. 1 970. Fat and slow components
of axoplasmic transport in the hypoglossal and vagus
nerves of the rabbit. Brain Res. 18: 461 -467.
Reprinted by permission from Experimental
Neurology 43: 452-463. 1 974.
Axonal transport and trophic studies
Axonal delivery of soluble, insoluble and
electrophoretic fractions of neuronal
proteins to muscle* (1975)
GUSTAVO S. L. APPELTAUER and IRVIN M. KORR
For more than a century, the role of
peripheral nerves in the differentia
tion and maintenance of skeletal mus
cles has been a major area of research
and debate (4, 7, 8). Many tentative
explanations for the trophic relation
ship between nerve and muscle have
been based on those nerve-controlled
functions which are well known to in
fluence the muscle properties, such as
the release of acetylocholine, the
transmission of impulses, and the
initiation of muscular contraction.
These activities, however, cannot
alone account for all the changes that
may occur in the muscle after its in
nervation is disturbed.
The nerve may also influence the
muscle by the release of substances
which participate in muscle differen
tiation and which are essential for the
maintenance of structural and func
tional integrity. Research done at this
laboratory has shown that, after the
administration of 32P-phosphate and
14C-Iabeled amino-acids to hypo
glossal neurons of rabbits, some
radioactive macromolecules that are
transported along the axons cross the
neuromuscular j unction and are
incorporated into the muscle cells
( 1 3) . A later study showed that label
ed nerve proteins reach the muscle at
four different time periods, with
peaks at approximately 1 , 12, 22 and
34 days after incorporation of
3H-Ieucine by the neurons (1 2) . The
experiments reported here were de
signed to determine whether different
proteins are axonally conveyed in
each time period and whether there is
selectivity in the nerve-to-muscle
transfer. The radioactive proteins
transported in the four periods were
compared with respect to relative spe
cific activities of soluble and insol
uble proteins and relative specific ac-
'Supported by NIH Grant No. NS-07919 from the
National Institutes of Neurological Diseases and,
Stroke and by a grant from the American Osteopathic
Assoiation. We are grateful to Mr. Robert N. May
for preparation of the figures.
tivities of soluble fractions separated
by acrylamide gel electrophoresis.
Methods
Surgical procedures. Twenty-three
New Zealand white rabbits of either
sex, weighing 1 . 8-2. 4 kg were used.
For the intraventricular labeling of
hypoglossal neurons, 250 JCi of
4-5- 3H-L-Ieucine (Amersham-Searle,
specific activity 38-58 CilmM) were
deposited on two small pieces of filter
paper. The fourth ventricle was then
exposed, and each paper placed on
the area over the left hypoglossal
nucleus for 20 min. The surgical tech
niques were those previously de
scribed ( 1 2) , except that posterior
choroidectomy was omitted.
Tissue specimens. The rabbits were
killed at each of the four peak periods
following the administration of tri
tiated leucine: 1 , 12, 22 and 34 days (5
rabbits each) , and also at 43 days (3
rabbits). The following specimens
were taken: (a) medulla (left half of
the floor of ventricle IV); (b) left
hypoglossal nerve (extracranial por
tion, divided into a proximal and a
distal segment); (c) left styloglossus
muscle (which is innervated by the
hypoglossal nerve) ; and (d) control
muscles (pooled stylohyoid and mylo
hyoid muscles, which are innervated
by the facial and trigeminal nerves,
respectively, and which were used to
determine the incorporation of
blood-borne tritiated leucine by the
styloglossus muscle ( 1 2) . Because of
their small size, nerve and medulla
specimens were supplemented with
sciatic nerve and medulla from unop
erated animals (see later) .
Extraction procedures. All tissues
and solutions were kept at 0-2 C.
Each specimen was first homogenized
in saline solution (6.25 11 per mg
fresh tissue) and centrifuged at 1 3, 800
g for 1 hr. Each precipitate was then
twice rehomogenized and washed
with 5 ml saline containing 2. 5 mg
serum albumin and 2. 5 mg leucine as
carriers. After an extraction with
organic solvents, done as previously
described ( 1 2) , it was prepared for
liquid scintillation counting. The pre
cipitated material will be referred to
as the insoluble protein fraction.
The supernatant from the first
centrifugation was separated into two
measured portions. One part was
pooled with aliquots representing the
same fractional volumes of the sec
ond and third supernatants. After
the addition of 2. 5 mg serum albu
min, it was extracted with 1000 tri
chloroacetic acid and organic solvents
( 1 2) . The precipitate, identified as the
soluble protein fraction, was also
prepared for radioassay.
Electrophoretic separation ofsolu
ble proteins. From the remaining part
of the first supernatant, two to four
0. 1 25 ml aliquots were fractionated
by acrylamide gel disc electrophoresis
at pH 8. 3 and 7. 51o concentration in
1 5 cm long tubes (Canalco, Inc. ).
Each gel was stained with Coomassie
blue, washed with distilled water and
cut into 34-40 segments, as shown in
Fig. 2, with loops of human hair. The
equivalent segments from the two to
four gels obtained for each tissue
specimen were pooled, weighed and
prepared for liquid scintillation
counting as described in the next
section.
Experience showed that cutting the
gels according to the band patterns,
rather than in slices of uniform thick
ness, gave a much more accurate and
reproducible approach to the study of
radioactivity distribution among the
various fractions. In different batches
of gels, the position of the bands
relative to the tracking-dye band and
to the cathode end of the gel varied
slightly, whereas all well-defined
radioactivity peaks appeared at pre
cisely the same stained bands in all
animals. It is possible that a given
stained segment may include several
proteins differing in concentration,
staining properties and incorporation
of radioactivity. Nevertheless, the
sites of concentration of protein
incorporated radioactivity were more
than sufficiently discrete, reproduc
ible and referable to stained bands to
make possible reliable comparisons
of radioactivity distribution from
animal to animal and period to
period.
I0T
<00,UUU
l
200,000
VLDULLA
.
40,00
|
NER
2UD00
(PXIMAL)
U
m
o
40,00
`
.
NERVE
[ 30,00
(DISTAL)
l
200_
|00
t
^
|d 2d Zd d 4$
Fig. I. Average specific activity (disintegra
tions per minute per milligram fresh tissue) of
the insoluble (dark bars) and soluble proteins
(clear bars). Data were averaged from five
(days 1-34) or three animals (day 43). The or
dinate scales are much lower for muscle than
for medulla and nerve because the activity has
been diluted in the relatively large muscle mas.
NE
N
NU
6 6 H J 8
'
Fig. 2. Electrophoretic pallers of medulla
(ME), nerve (N) and muscles (MU). The
brackets and numbers indicate the way the gels
were sliced. The lengths of the segments were
obtained from the weights of the gel slices and
averaged for all 23 animals. The segments were
numbered from the buffer front toward the
cathode. Equivalent numbers do not represent
equivalent protein bands in the different
tissues. The letter designations, A-K, are ex
plained in the legend for Fig. 3.
108
Radioassay. For al l speci mens,
radioactivity was determined in a
Packard 3375 Liquid Scintillation
Spectrometer for 50 mi n at 7000 gai n
and 50- 1 000 wi ndow settings. The
soluble and insoluble protein frac
tions were digested in 0. 1 5 ml water
and 1 . 5 ml NCS (Amersham-Searle)
first for 1 6 hr at room temperature,
then for 90 mi n at 50 C. Before the
final 30 min of digestion, 0. 1 ml 30%
hydrogen peroxide was added to each
vial to prevent color quenching. After
3 hr at room temperature, the digests
were dissolved in 1 5 ml toluene-based
scintil lator (Spectra fluor , Amersham
Searle) contai ni ng 0.2 ml Triton
X- 1 00. After 3 additional hr the vials
were placed in the scintillation spec
trometer and counted after tempera
ture equilibration.
The equivalent gel slices from each
tissue were placed in scintil lation vials
and dried at 90 C for 2 hr. After the
addition of 0. 1 mg serum albumin to
each vial, the samples were digested
in 0. 4 ml 30% hydrogen peroxide first
at 60 C for 1 6 hr and, after the addi
tion of 1 . 5 ml NCS, at 50 C for 90
mi n. Since the hydrogen peroxide and
NCS treatments yield volatile radio
active materials, all incubations were
carried out in hermetically sealed
vials. Digests were also cooled to
-1 5 C before opening the vials for ad
di tion of the scintillator. The digests
were then left at room temperature
for 3 hr and, after cooling to -1 5 C,
dissolved i n 10 ml scintillation
cocktail and 0. 4 ml Triton-X- 1 00.
Before counting, the vials containing
the digests were briefly opened three
times under a fume hood, at i ntervals
of 3 hr, in order to eliminate some
volatile quenching agent (probably
oxygen).
The recovery of radioactivity was
determined by processing nonradio
active specimens to which a known
amount of l H-leucine had been
added. Recovery was 99% for the
soluble and insoluble protei ns, and
96% for the gel s. The counting effi
ciency, as determined by i nternal
standardization, was 43% for aU
specimens. The specific activities of
total protein extracted from stylo
glossus muscles, in this study as i n the
previous one ( 1 2) , were relatively low
as compared with those of nerve and
medul l a. Nevertheless, the threefold
larger dose of l H-leucine used in this
study raised the levels substantially,
and good reliability was obtained in
those animals ki lled between 1 2 and
34 days after l H-leucine admi nistra
tion. The lowest counts obtained in
an animal for an identifiable radio
activity peak (peak G at day 34,
Fig. 3D see results) were 69. 7
counts/min above a background of
29. 0 ( 1 . 40) .
Calculation of specific activities of
gel segments. I n each animal, the
specific activity (disintegrations per
min per mg fresh tissue) of each gel
segment was cal culated by the
formula:
dpo
Z.4 7 (o| ioia|supe:aa|aa:, (couats/m|a,
. l ml (o,|resa t .ssae) (aamoetote|spoo|eo)
where 2. 42 is a correction factor for
the counting efficiency and for the
activity lost while processing the sam
ple; 0. 1 25 ml is the volume of tissue
extract used for each gel ; and the
total volume of supernatant was ob
tained by adding the ml of saline i n
which the sample was homogenized
and the calculated water content of
the specimen ( I ) .
For plotting, each gel was divided
i nto 40 arbitrary length units. (See
Figs. 2 and 3. ) The average length of
the correspondingly numbered gel
segments of each tissue obtained
from the five animals (three at 43
days) ki l led at a given postsurgical
i nterval was calculated as follows:
+l h
average | cngth o| scgneut "
L
K is the weight of the pooled
equivalent gel segments in each
scintillation vial, from each animal,
divided by the number of gels pooled;
m is the number of animals killed at
the selected postsurgical time, and n
is the total number of segments into
which the gel was divided (muscle 38,
nerve 34, medulla 40) . (See Fig. 2. )
Although the electrophoretic pro
cedure used concentrated certain pro
teins i nto well defined bands, it did
not provide for a complete separation
of all the radioactive proteins. Some
times a distinctly high level of radio
activity located at a given band was
accompanied by lower, but si gni fi
cant, levels of activity in the neigh
boring gel segments; or, radioactivity
was spread over extended lightly
Axonal transport and trophic studies
k
j
, "
K
vw
` @
! p (p
Wm
*
m
34dg
0'
-
1 ? < >
K
M
41
1 Y ZD O M
M
MX
'
9!|M
tmvQ
T ^
. 11 u
1 B
omo;
. ,. . . .
1 T d W
43dg
k,
I
K
v1
'21
_ v rw
WW
1 < H
urw
% N
fiirjpM
1 ' d'
Nw
- ~
t=A
! 1 <
4 *
L
w|m
1 1 #
Fig. 3. Spifc activity distribution along the electrophoretic gels ofmedulla and nerve specimens. The values indicated a styloglossus-control rpresent
the amount ofnerve-delivered radioactivity in the styloglossus muscle. The abscissae represent the segments into which the gels were cut. The height o/
the bars represents the speciic activity (disintegrations per minute per milfigramsfresh tis ue) per length ofthe gel segment (see text). Data were averaged
from fve (days 1-34) or thre animals (day 43). Letters A-K represent equivalent fractions with high speic activities in the diferent tis ues.
o
.
' i
0-
43 DAYS
`7 f I |X
' !
B 5
Fig. 4. Speciic activity ditribution along the
electrophoretic gels of the control muscles.
Abscissae and ordinates are the same as in
Fig. 3.
stained gel portions. The radioac
tivity not concentrated into bands
appeared as a sort of "background, "
over which the discrete peaks pro
jected, that made the radioactivity of
each gel segment dependent on its
length. Thus, for a better visualiza
tion of the radioactivity distribution
in the gels, the results were plotted as
histograms (see Figs. 3 and 4). The
abscissae represent the gel segments
(intervals between numbered lines);
the height of each bar represents the
average radioactivity concentration in
each gel segment; and the area in
dicates the average radioactivity con
tained in the segment per milligram of
tissue. The height of each bar was
calculated with the formula:
v-:.,-c,/,
8Vct8gf lfnglh ul--,--:
c,J,
E E W W
W
m
jW # c,],
,
||
H
| |
!
NERVE
|5OLUBLE)
MU5CLE
|5OLUBLE)
NERVE
| TR| TONX)
MU5CLE
| TR| TONX)
Fig. I. Electrophoretic patterns of the soluble and Triton Aextracts from nerve and muscle. The
brackets and numbers indicate the way the gels were sliced. The lengths of the segments are the
averages from the three nerve specimens and from the styloglossus and control muscle specimens of
the 30 animals. The segments are numbered from the anode toward the cathode; equivalent numbers
do not represent' equivalent protein bands in the different electrophoretic patterns. The letters A
through H show the position ofnerve-delivered proteins to the styloglossus muscle.
A
.
J
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neighboring segments.
I n the hypoglossal nerve gels,
several radioactivity peaks appeared
at Day I , and some remained visible
at Day 70, two of them, A and D,
quite prominently. By Day 12 radio
activity was slightly higher in the dis
tal than in the proxi mal nerve seg
ment. This di fference increased at
longer i ntervals, but became conspic
uous only by Day 34, when the activ
ities had decreased to about one-sixth
of their Day- 1 2 values.
Most peaks found in the nerve gels
were also identifiable by Day 1 2 in the
styloglossus muscle gels. As in the
nerve, peaks A and D were the most
prominent i n the muscle. The course
of appearance of radioactivity varied
for di fferent muscle proteins. Peak H
was visible only at Day I , and the re
maining peaks were identifiable be
tween Days 1 2 and 70. In contrast to
the styloglossus muscle, the specific
activities of the control muscles (not
shown) were very low and only two
significant peaks, at the positions of
A and H, were found.
To examine the axonal flow and in
corporation of individual proteins in
to the styloglossus muscle, the specif
ic activities of the gel segments con
taining the most prominent peaks (A
and D through G) were averaged and
plotted against time, making the
average Day- 1 2 values of the three
nerve segments equal to 1 00 to enable
comparisons between fractions with
di fferent activities (Fig. 3). In al l
three nerve segments, the radioactivi
ty of most of the soluble proteins in
creased sharpl y from Days I to 1 2,
decreased t o 2500 by Day 22, and
then decreased very slowly thereafter
(exceptions were H and protein at
segment 36) . In the muscle, proteins
A and D through L reached their
Fig. 2. Bar graphs depicting specific activity
distribution along the electrophoretic gels of
soluble proteins extracted from nerve and from
muscle at various intervals after injection of
L f' Hl lysine. The values indicated as
styloglossus - control (difference between
styloglossus and control represent the amount
of nerve-delivered radioactivity in the
styloglossus muscle; their peak values and the
equivalent peaks in the nerve are indicated as A
through H. The abscissae represent the
segments into which the gels were cut. The
height of the bars represents the specific activi
ty (dpmlminlmg fresh tissue) per length ofthe
gel (see text). Data were averaged from five
(Days I, 22, and 34), four (Days 12, 45, and
56), or three animals (Day 70).
Axonal transport and trophic studies
highest activity at Day 34. Fraction F
behaved similarly, although i ts
Day-22 and Day-34 values did not
differ at the 0.05 level of significance.
The activity of fraction G, however,
was already near maximum by Day
12. When plotting the ratios between
the specifc activity of G and the
other proteins as obtained from each
animal (Fig. 3), there was a sharp and
significant decrease in values between
Days 1 2 and 34, indicating an earlier
appearance and possibly a shorter
lifetime of radioactivity in muscle for
G than for A through F.
Radioactivity in Triton A Extracts.
The results obtained for the Triton X
extracts are illustrated in Fig. 4. The
specific activities were lower than
those in the soluble extracts. Two dif
ferent groups of radioactive proteins
were found in the hypoglossal nerve .
One of them was present at the distal
part of the nerve at Day 12 and con
sisted of fve activity peaks, four of
them equivalent to D through G. The
other group contained seven peaks
(one with the electrophoretic mobility
of D) which appeared in the proximal
nerve segment at Day 12 and moved
slowly in the distal direction reaching
the end of the nerve by Day 45. The
amount of nerve-transported radioac
tivity in the Triton X-soluble fraction
of the styloglossus muscle was at all
times low, and no clear peaks could
be discerned in the gels.
Discussion
Axonal fow ofproteins. Somatoax
onal transfer and axonal flow can oc
cur at various rates. Both processes
can take place rapidly, giving the
classic picture of the "fast ax
oplasmic fow" ( 1 6), which is prob
ably responsible for the radioactivity
peaks A and H in the styloglossus
muscle at Day 1 . Other soluble pro
teins (peaks A through G) followed a
pattern described previously (2): slow
penetration into the nerve, as re
vealed by their highest activity at Day
12, followed by a fast proximodistal
fow, as revealed by their pattern of
increased and then decreased radioac
tivity which took place simultaneous
ly in the three nerve segments. Most
proteins in the Triton X extract
moved proximodistally at 1 to 1 . 5
mm per day, according to what has
been called "slow axoplasmic flow"
( 1 6) . It is not possible to tell whether
1
the other radioactive proteins in the
Triton X extract, found in the distal
nerve segment at Day 12, migrated as
insoluble complexes or were bound to
particles locally.
Nerve-Io-muscle delivery. The prox
imodistal flow of proteins was either
interrupted or interfered with to
various degrees between the distal
nerve segment and the styloglossus
muscle. The anode-migrating "acid"
proteins studied previously (2) either
did not enter the muscle or reached
their highest activity in muscle at Day
22, whereas most of the cathode-mi
grating "basic" proteins examined in
this study did penetrate the muscle,
but followed heterogeneous patterns,
with at least three fractions reaching a
peak at Day 34. These results confirm
previous findings that two different
groups of neuronal proteins penetrate
the styloglossus muscle by Days 22
and 34 after their synthesis (2, 1 4) .
Because soluble proteins (other than
fraction H in this study) showed only
minor differences in their patterns of
appearance and disappearance in the
nerve, these distinct periods probably
represent different rates of nerve-to
muscle transfer and different life
times in the muscle.
There was little or no nerve-to
muscle transfer of proteins in the
Triton X fraction. After the arrival of
most radioactive proteins at the distal
nerve segment between Days 34 and
1 15
|0
_
100
EL SECNENTS
FRACON NERVE
P I - 4
| - |
L -
-
| ~
Nerve l
Nerve 3
M>0If 5YWL
| O
| ~ ^
-
| ~ O
~ *~
10 20 30 40 50 60 70
Doys
Styloglossus - Control
(Fraction and )
_ i 1 l
0 10 20 30 40 50 60 7
Styloglossus- Control
( Fraction 0l
Doys
Fig. J. Graphs ofaverge specic activitie at peks A and D through G plotte against time. Nerves
I, 2, and ! are the proximal, medial, and dital nere segments; styloglos us - control is the di
ferenc between the styloglos us and contrl value. The average Day-I2 values ofthe three nerve
segments were made equal to I0. The inet lits the nerve and muscle gel segments containing each
pk. Turover of nerve-delivered radioactivity to styloglosu muscle was diferent for A through
F and for G. Thi i indicated by the rtios between the activity ofG and the activity of the other
segments in ech animal (setet) shown in the lower right.
45, the muscle activities decreased
and remained at trace levels, indicat
ing exclusion of these proteins from
the muscle. The very low activities
found in the muscle between Days 1
and 34 could be the effect of con
tamination or binding of soluble pro
teins to particles.
Trans-synaptic transfer of proteins.
Numerous studies have revealed a
trans-synaptic transfer of protein
bound radioactivity ( 1 , 3, 4, 6-8, 1 2,
1 3, 1 5, 1 7, 1 9-24). However, it has
been recognized that products result
ing from proteolysis at nerve termi
nals are utilized by surrounding cells
(5, 1 2) and the findings may reflect a
transcellular transfer of small mole
cules and not of protein. This is not
the case in at least some trans
neuronal ( 1 9, 20) and nerve-to-muscle
transfers (2) . In the present study, if
the radioactive proteins in the stylo
glossus muscle were synthesized local
ly, the electrophoretic distribution of
nerve-delivered radioactivity should
result in the labeling of mainly pro
teins A and H, as found after the
II
systematic injection and in the con
trol muscles. Thus, reutilization of
nerve breakdown products may ac
count for the results found at Day 1 ,
but not at Day 1 2 or later.
The main problem involved in
these electrophoretic studies is con
tamination of the muscle specimens
by nerve terminals, which was small,
as indicated by the few end plates
found in styloglossus muscles dis
sected like the specimens used in the
experiments and by the fact that
radioactive proteins that penetrated
the entire length of nerve examined
were not found in significant
amounts in the styloglossus muscle.
The possibility that the neuronally
synthesized proteins in the muscle
were confined to and extremely
highly concentrated in the few re
maining nerve terminals is improb
able in view of the autoradiographic
studies ( 1 5) which located radioactivi
ty inside the muscle cells. Because
nerve-to-muscle delivery is an impor
tant subject in view of its possible role
in trophic interactions, experiments
will be continued toward finding the
location of these proteins in the mus
cle cells, isolation of the proteins, and
determination of their function.
References
I. Alvarez, j., and M. PlIschel, 1972. Transfer of
material from efferent axons to sensory epithelium in
the goldfish vestibular system. Brain Res. 37: 265278.
2. Appeltauer, G., and I.M. Korr, 1975. Axonal
delivery of soluble. insoluble and electrophoretic frac
tions of neural proteins to muscle. Ep. Neural. :
1 321 46.
3. Casagrande, V.A and J.K. Harting. 1975.
Transneuronal transfer of tritiated proline in the
visual pathways of the tre shrew. Tupaiglis. Brin
Re. %: 367-372.
4. DrAger, U.C. 1974. Autoradiography of tritiated
proline and fucose transported transneuronally from
eye to the visual cortex in pigmented and albino mice.
Brain Re. M: 284-292.
S. Droz, B., H.L. Koenig, and L. DiGiambera
dino, 1973. Axonal migration of protein and
g1ycoprolein to neve endings. l. Radioautographk
analysis of tile renewal of protein in nerve endings of
chicken ciliary ganglion after intracerebral injection of
'H lysine. Brin Res. W. 93-127.
6. Globus, A., H.D. Lux. P. Schubert, and P.
Kaups. 1 971 . Labelling of nearby neurons following
the intracellular iontophoresis of 'H glycine. Anat.
Ree. 16:325.
7. Grafslein, B. 1971 . Transneuronal transfer of
radioactivity in the central nervous system. Science
172: /77-179.
8. Grafstein, B., and R. Laureno. 1 973. Transport
of radioactivity from eye to visual cortex in tile mouse.
Exp. Neuro/. 39: 44-57.
9. Guth. L., 1 968. "Trophic" influences of nerve
on muscle. Physial. Rev. M. 65-687.
10. Gutmann. E. 1 976. Neurotrophic relations. An
nu, Rev. Physial. M: 1 77-216.
I I . Harris. A.J. 1 974. Inductive functions of the
nervous system. Annu. Rev. Physiol. :251 -305.
12. Heacock. A.M and B.W. Agranoff. 1977.
Reutilization of precursor following axonal transport
of 'H proline labelled protein. Brain Res. 22:
243254.
1 3. Hendrickson, A. 1972. Electron microscopic
distribution of axoplasmic transport. J. Camp.
Neural. 14: 381397.
14. Korr, I.M., and G.S.L. Appeltauer. 1 974. The
time course of axonal transport of neuronal proteins
to muscle. Exp. Neural. 4t 452-463.
1 5. Korr, l.M., P. Wilkinson, and F.W. Chorok.
197. Axonal delivery of neuroplasmic components to
muscle cells. Scince 155: 342-345.
16. Lubinska, L. 1975. On axoplasmic flow. In/.
Rev. Neurbial. 17: 241-296.
17. Neale. J.H E.A. Neale, and B.W. Agranoff.
1 972. Radioautography of the optic tectum of the
goldfISh after intraocular injection of ('H) proline.
Science 176: 407-410.
18. Reisfeld, R.A., V.J. Lewis. and D.W. Williams.
1962. Disc electrophoresis of basic proteins and pep
tides on polyacrylamide gels. Natur (Lond.) 195:
281-283.
19. Schwab, M.E + and H. Thoenen. 1976. Electron
microscopic evidence for a transsynaptic migration of
tetanus toxin in spinal cord motoneurons: An
autoradiographic and morphometric study. BrainRes.
10: 213-227.
2. Schwab. M and H. Thoenen. 1977. Selective
trans-synaptic migration of tetanus loxin after
retrograde axonal transport in peripheral sympathetic
nerves: A comparison with nerve growth factor. Brain
Res. 122: 459-474.
Axonal transport and trophic studies
IL
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Fig. 4. Bar graphs ofspecific activity distribution along the electrophortic gel ofthe Trton 7
tracts. Abscissae and ordinates same U in Fig. 2.
IIT
Abstract: Axonal migration of
some partcle-bound proteins
in the hypoglossal nene and
their failure to enter the
styloglossus muscle
GUSTAVO APPELTAUER and
IRVIN M. KORR
In 1 967 Korr, Wilkinson. and Chor
nock' found that. afer labelling the
fourth ventricle of rabbits with 32-P
phosphate or 14-C amino acids. mac
romolecules migrated along the hypo
glossal axons and appeared in the
tongue muscles. Studies were then
undertaken with the purpose of char
acterizing nerve-to-muscle t rans
ported proteins and determining their
patterns of axonal flow and entry into
the muscle. A first series of studies
was conducted on the axonal soluble
proteins.23 It was found that elec
trophoretically separated fractions
had their highest radioactivity in
the nerve at day 1 2 after labelling
of the hypoglossal neurons. Also. the
activity appeared and decreased si-
multaneously in the proximal and
distal portions of the nerve. Finally,
after variable time intervals, some of
the radioactive proteins entered the
styloglossus muscle in the tongue.
The present study revealed a com
pletely different dynamics for a group
of proteins that were detached from
the particulate elements of the medul
la, nerve, and muscle with Triton
X- tO, and then analyzed by disc
electrophoresis (pH 4.2 and 1 5 per
cent gel concentration) . After label
ling the ventricle with 3-H lysine,
radioactive proteins appeared in the
most proximal portion of the nerve at
day 1 2. Subsequently they migrated
proximodistally at a rate of approxi
mately 1 .5 mm. per day, and ap
peared in the most distal portion of
the nerve by day 45. Up to day 70, no
significant levels of radioactivity were
found in equivalent electrophoretic
fractions of the styloglossus muscle.
Bcfcrcacc
1 . Korr, I. M. , Wilkinson, P.N., and Chornock.
F.W.: Axonal delivery of neuroplasmic components
to muscle cells. Science 155: 34245, Jan 67.
2. Appeltauer, G.S.L .. and Korr. l . M. : Axonal
deliver of soluble, insoluble and electrophoretic frac
tions of neuronal proteins to muscle. Exp Neurol
461 ): 132-46, Jan 75.
3. Appeltauer. G.S.L., and Korr. I. M. : Elec-
II8
trophoretic Characterization of nerve-to-muscle
delivered basic protein. JAOA 76:294. Dec 76.
Supported by AOA Research Grant #75-122. "The
Isolation of Some Neuronal Proteins Delivered to
Muscles and the Determination of Their Function."
through the AOA Bureu of Research, and through
NIH Grant #NS-07919.
Reprinted by permission from JAOA 77: 479. 1978.
Axonal transport and trophic studies
Interpretation of research findings
II9
The neural basis of the osteopathic
lesion*t (1947)
Four of the main principles in
osteopathy appear to be:
1 . Joints and their supports are
subject to anatomic and functional
derangements.
2. These derangements have distant
as well as local effects.
3. They are related, directly or in
directly, to other pathologic in
fluences.
4. They may be recognized, and
their local and distant effects in
fuenced favorably by manipulation.
Accepting the existence of joint de
rangements (osteopathic lesions), it is
our purpose in this paper to examine
not the mechanical and etiological
factors involved, but rather the fun
damental basis for principles 2 and 3
and to a small extent principle 4, and
to report progress in our understand
ing thereof.
The osteopathic lesion has many
aspects which are partly revealed in
the local and distant effects referred
to as principle 2. Included among
these are:
1 . Hyperesthesia, especially of the
muscles and vertebrae.
2. Hyperirritability, reflected in
altered muscular activity and in
altered states of muscular contrac
tion.
3. Changes in tissue texture of mus
cle, connective tissue, and skin.
4. Charges in local circulation and
in the exchange between blood and
tissues.
. Altered visceral and other auto
nomic functions.
How are these effects produced?
What are the central factors responsi
ble for these manifestations of struc
tural and postural abnormalities?
What in the intrinsic nature of the
osteopathic lesion is the basis for the
peripheral, palpable, and clinical ef
fects? What fundamental changes
take place as a result of effective
manipulative therapy?
Presented before the Teaching Group on Osteopathic
Principles, Diagnosis and Therapeutics at the Fifty
First Annual Convention of the American Osteopathic
Association, Chicago, July 21 , 1947.
tThe research on which this paper is based was made
possible by grants from the Research Committee of
the American Osteopathic Association.
II0
The detailed answers to these ques
tions are, of course, not yet available,
but reliably indicated are the general
nature of the final answer and the
direction in which we must proceed in
order to obtain it. The research pro
gram of the Kirksville laboratories is
designed to procure some of these
answers through exploration of the
intimate mechanisms involved in the
osteopathic lesion. We believe that
the answers are obtainable only
through fundamental, experimental
research and that the emerging con
cept of the lesion and its implications
will have considerable impact on the
practice of osteopathy.
In this paper will be presented some
of our current views, some of the
practical implications, and some
speculations. The details of the ex
perimental methods and the raw data,
available in earlier publications,
l,J
will not be presented, but rather the
general experimental approach and
the immediate conclusions therefrom.
From these, in turn, will be drawn
some generalizations.
The neural basis of the osteopathic
lesion
Within the nervous system, in the
phenomena of excitation and inhibi
tion of nerve cells, and in synaptic
and myoneural transmission, lie the
answers to some of the most impor
tant theoretical and practical osteo
pathic problems. The existence of a
neural basis for the lesion has been
known, of course, for a long time.
The segmental relation of the osteo
pathic lesion to its somatic and vis
ceral effects is explainable in no other
way.
The activity and condition of the
tissues and organs are directly in
fuenced, through excitation and in
hibition, by the efferent nerves whIch
emerge from the central nervous sys
tem and which conduct impulses to
these tissues and organs (Fig. !). For
example:
Mucle.
A. Anteri or horn cel l s ( Moto
neurons) - muscular contraction
B. Lateral horn cells (Sympathetic
preganglionic neurons through
postganglionic neurons) - vaso
motor activity
Skin.
C. Lateral horn cells - vasomotor
activity
D. Lateral horn cells - sweat gland
secretion
E. Lateral horn cells - piloerection
Viscera.
F. Lateral horn cells - smooth mus
cle contraction
L. Lateral horn cells - glandular
secretion
H. Lateral horn cells - vasomotor
activity
The activity of these organs and
cells is directly determined by the ac
tivity of their motor nerves. This
nerve activity is measured in terms of:
(a) The number of impulses con
ducted by each efferent nerve fiber
and (b) the number of fibers in
volved. Thus, in the absence of im
pulses in the corresponding motor
nerve, a muscle is completely at rest.
The amount of contraction (tension
produced or degree of shortening) at
any moment is in proportion to the
number of motoneurons which are
conducting impulses at that moment
and the average number of impulses
per second which each is conducting
to the muscle. With certain modifica
tions this principle also applies to
organs other than muscle. Abnor
malities in these 'rgans are produced
by overactivity or underactivity of the
efferent nerves.
Secondary effects of neural
imbalance
It is important to emphasize, how
ever, that not all the effects of over
activity or underactivity of the effer
ent neurons are direct and immediate.
Secondary effects often assume pre
dominate importance. Thus, a mus
cle's overactivity, over a long period
of time, may result in fibrosis and
major chemical and metabolic
changes; underactivity, in atrophy.
Overactivity of sympathetic fbers
which control arterioles may result in
local anoxemia, inflammation, al
tered capillary permeability, edema,
etc. Imbalance in the efferent neurons
controlling the smooth musculature
of the gastrointestinal tract may
result in faccidity or spasm with
serious effects on digestion and ab-
Interpretation of research
sorption and, therefore, on the entire
body economy. Overactivity or
underactivity of the neurons control
ling glands may result in disastrous
shifts in acid-base, fluid, and electro
lyte balance and in such conditions as
peptic ulcers. If the gland happens to
be one of the endocrines, the effects
may be especially serious and exten
sive. We may for the present purpose
include the spinothalamic fibers
among the "efferent" neurons. These
convey pain sensations to the brain
and, when overactive, produce not
only physical but also important
psychological changes with potential
ly serious and extensive changes in
motor and visceral activity. With the
crucial importance of the efferent
neurons in mind, more precise for
mulation of the problem is possible.
There are three main questions:
1 . What factors control the activi
ty, i . e. , the number of impulses, in
the efferent nerve fbers?
2. How does structural abnor
mality, i . e. , the osteopathic lesion,
play upon these factors to produce
overactivity or underactivity of these
fibers and, therefore, of the organs
which they innervate?
3. How does manipulative therapy
play upon these factors to restore
balance and cause regression of signs
and symptoms?
Factors controlling efferent activity
Let us proceed to the first question.
What factors has physiological re
search demonstrated to be primary in
the control of activity of the efferent
neurons? Two main principles have
special pertinence here.
A. The principle of reciprocity
states that through the network of in
terneurons (also known as internun
cial neurons, intercalated neurons,
and connector neurons), which is
situated within the central nervous
system, every neuron potentially in
fluences, and is influenced by, almost
every other neuron in the body.
B. The principle of convergence
states that many nerve fibers con
verge upon, and synapse with, each
motoneuron. These presynaptic
fibers convey impulses from a large
variety of sources to the efferent
neuron which, therefore, represents a
final common path. 4
Let us examine how these prin
ciples operate with respect to the
anterior horn cells, keeping in mind
e
-
.
*
.
A
`
t
I
' :
*
:
"*ee
W
"T
l V
Fig. I. -Diagrammatic representation oj segmental refepathways among somatic and viceral
ajJerents and eJJerents.
Afferents (Dorsal root neurons):
A-From spinous process, joints; B-From stretch and tension receptors (proprioceptors) in
musdes and tendons; C-From touch, presure and pain endings in skin; DFrom vicera;
ABC-Somatic ajJerents.
Efferents: b-motoneurons to skeletal musde; c-sympathetic postganglionic neurons to blood
vessels oj skin and musde; to sweat glands and pilomotor muscles oj skin; d-sympathetic
postganglionic neurons to visceral smooth musde, blood vessels and glands; S-Spinothalamic
fbers; I ~ Intereurons; L - Lateral hor cells (sympathetic preganglionic neurons); V. G. -
Vertebral ganglion; C. G. - Colateral ganglion.
that they probably operate in a
similar fashion upon the other ef
ferent neurons (Fig. 1 ) .
1 . Each anterior horn cell receives
impulses from a large number of
sources through the presynaptic
fibers which converge upon and
synapse with it. All the descending
tracts in the spinal cord, conveying
impulses from such sources as the
cerebral cortex, red nucleus, medulla
oblongata, the vestibular nuclei, cere
bellum, the pons, superior colliculi ,
and other hi,her centers, establish
synaptic connections wi th the
anterior horn cell for the mediation
of voluntary motion, equilibrium,
post ural r efl exes, vis uospi nal
reflexes, and others. The propriocep
tors, stretch and tension receptors sit
uated in the tendons and in the
muscles themselves, are a steady and
continuous source of impulses. They
exert their influence directly through
the dorsal root fibers into which they
discharge their impulses or, indirect
Iy, through the higher postural and
equilibrium centers. Afferent fibers
from the viscera may also play an im
portant role. In fact, every afferent
nerve fiber, whether it mediates
touch, pain, pressure, temperature,
sight, or any other sense modality, ex
erts infuence upon the final common
path represented by the motor nerves.
2. Some of the converging fibers
exert an excitatory influence, others
an inhibitory influence on the same
motoneurons.
3 . The activity of the motoneuron
at any moment, that is, the frequency
with which it delivers impulses to the
muscle fibers, represents a dynamic
balance among all the excitatory and
inhibitory infuences being exerted by
the many neurons which converge
upon it. The proprioceptors and some
of the higher centers, through their
steady, tonic control, act as gover
nors or buffers. The balance, how
ever, is shifted from moment to mo
ment in accordance with changes in
the internal and external environment
and in response to volition. As pre
viously stated, pathology results
when the balance is shifted too far in
one direction or the other (excitation
or inhibition) for too long.
4. The collective action of the pre
synaptic nerve fibers upon the fnal
common path is further reflected in
the phenomena known to physiolo
gists as reinforcement and facilita
tion. Before the anterior horn cell can
discharge impulses into the muscle
fibers, it must itself receive excitatory
impulses simultaneously from a
number of presynaptic fibers. Stated
1Z1
another way: Before a given stimulus
(e.g. , to the skin) c produce a reflex
muscular response, the anterior horn
cell must frst be "warmed up" or
"put on edge" (facilitated) by im
pulses from other (excitatory) fibers
which synapse with it. The efferent
neuron must already be in a state of
subthreshold or subliminal excita
tion. In other words, the various
fibers converging upon a given group
of motoneurons must cooperate
(reinforce each other) in order to
open the final common path leading
to the muscle. In a whole nerve it has
been demonstrated that a con
siderable portion of the nerve fbers
must be in a state of subliminal ex
citation before any of them fire and
cause muscular contraction.
. This requirement serves as a
margin of safety or an insulaton,
preventing muscles from responding
to every impulse which reaches the
anterior horn cell.
6. When a signifcant percentage of
the anterior horn cells in a given seg
ment of the spinal cord is maintained
in a state of subliminal excitation,
they require little additional stimulus
to produce a reflex response. This is
reflected in our frequent use of the
terms . "on edge, " "jumpy, "
"tense," which imply motor aspects
of psychic imbalance. In individuals
thus characterized the anterior horn
cells are maintained close to, or at,
threshold, even during rest.
The osteopathic leion and the
factors controlling effernt
activity
The second question in our series of
thre was "What is the relation of the
osteopathic lesion to the above
factors?" How do anatomic and
functional derangements of the joints
and their supports operate on these
factors to produce seriously altered
activity of the efferent neurons? Con
siderable light is being thrown upon
this problem by the research in
progress at Kirksville College of
Ostepathy and Surgery under the
directorship of Dr. J. S. Denslow.
The research has revealed close
relations between lesion mechanisms
and certain well-established physio
logical principles. The general ex
primental approaches and the major
conclusions from each are presented
in the following section.
12
Experimental
Refex threhold.
Denslow, ' proceeding from the ob
servation made by all osteopathic
physicians that pressure to the spi
nous processes of lesioned segments
produces much more contraction in
the spinal extensor muscles, and with
less pressure, than is true at non
lesioned segments, set out to
determine i n a precise, objective
manner how much pressure is re
quired at each spinous process to
elicit reflex contraction of the spinal
extensor at the same level. In other
words, his object was to determine
whether, and to what degree, lesioned
segments were distinguished from the
normal by differences in reflex
threshold.
Muscular activity was determined
electromyographically, that is, by
recording the electrical signs of
muscular activity. Measured pressure
stimuli were applied to the spinous
processes by means of a calibrated
pressure meter which simulated the
action of the osteopathic thumb. At
each segment gradually increasing
pressure stimuli were applied to the
spinous process until just detectable
activity in the erector spinae mass was
obtained; this represented the reflex
threshold for that segment. The reflex
arc under investigation might be said
to consist of these parts: spinous
process. dorsal root fiber, inter
neuron, anterior horn cell, and
muscle fibers. (See Fig. 2, dis
regarding segmental designations and
intersegmental connections.)
This pioneer study upon a large
number of human subjects resulted in
the demonstration that the refex
thresholds in lesioned segments were
much lower than in normal segments.
The more severe the lesion, as
determined by palpation, the lower
the threshold. The thresholds may be
constant over periods of months.
What is the basis for the lowered
reflex threshold of the lesioned
segment? There were two obvious
alternatives. (1 ) The sore spine. It
was reasonable to suppose that the
pressure receptors and nerve endings
in the tender spinous process were
hypersensitive and that, per gram of
pressure, they fired more impulses at
the anterior horn cells than did the
corresponding endings in the normal
spinous process. (2) Hyperirritable
motoneurons. It appeared equally
reasonable to suppose that for some
reason or other the anterior horn
cells of the spinal extensor muscle
in the lesioned segments were main
tained at a higher level of excitability.
In order to decide which was the more
likely alternative. the following
experimental approaches were under
taken. l
Intersegmental spread 0/
ecitation.
A lead to the answer was given in
experiments in which spread of
excitation from segment to segment
was examined in relation to their
respective thresholds, to the distance
between them, and to other factors.
The experiments were conducted as
follows (Fig. 2). The four thoracic
segments, designated as T4, T6, T8.
and Tl O, were selected for this series
of experiments on 30 subjects. Needle
electrodes were inserted into the
spinae erector mass 5 cm. to the left
of the spinous process in each of the
four segments, for the detection and
recording of muscular activity. Pres
sure stimuli were applied to the
spinous processes with the pressure
meter.
The minimum pressure stimuli
(threshold) required at each of the
four spinous processes to elicit
activity from each of the four muscle
segments was then determined in
turn. Thus, the pressure required
upon the spine at 1to elicit activity
in the muscle at T4, in the muscle at
T6, in the muscle at T8 and in the
muscle at Tl O was determined. This
was then repeated at the other
spinous processes, giving four
thresholds at each spinous process,
sixteen in all, in each experiment. The
results will be summarized by
illustrating with one hypothetical
subject, eliminating some qualifica
tions for the sake of brevity.
It was found that there was much
more spread to lesioned segments
than/rom lesioned segments. Thus, if
T6 were a severely lesioned segment
(very low threshold) while T8 and TIO
(neglecting T4 for the moment) were
normal or high threshold segments,
the following obtained. It required
very little pressure to the spinous
process of T6 to elicit activity of the
muscle in the same segment; but even
very strong pressure stimuli to the
same spinous process failed to pro-
Interpretation of research
duce any signs of activity in the
muscles at T8 or TID. Conversely,
although even very high pressures to
the spinous processes of the latter two
segments produced no activity in
either of these segments, relatively
slight pressures upon the spinous
processes of each of them did
stimulate reflex contraction at T6.
Thus, excitatory impulses entering
the cord at TID "by-passed" the
motoneurons of the same segment
and those of a neighboring high
threshold segment, to emerge or
produce effect at a more remote
lesioned segment.
If T4 were moderately lesioned (as
was often the case if there was a
leison at T6), it participated in
exchange of excitation with T6, but
usually only received excitation from
T8 and TID.
Our conclusion from this series of
experiments can be simply stated in
an analogy. The anterior horn cell of
the lesioned segment represents a bell
easily rung from a number of push
buttons, while the spinous process or
push button of the lesioned segment
does not easily ring bells other than
its own. The hyperexcitability of the
lesioned segment (that is, the rela
tively low reflex threshold) i s
demonstrable without applying pres
sure to the corresponding spinous
process.
Procaine studies.
It was of interest in this connection to
determine whether and how the ex
citability of the lesioned segment was
affected by desensitization of the
spinous process with procaine. Infil
tration of the periosteum around the
spinous process raised the local
threshold to that of a normal seg
ment, that is, it was no longer
possible to produce reflex response of
the muscle of that segment with
slight, moderate, or even heavy
pressure stimuli to the spinous
process of that segment.
In contrast, however, spread of ex
citation to that segment from other
segments remained unimpaired; al
though pressure to the procainized
spinous process of T6 no longer elicit
ed reflex contraction at T6, it was still
possible to elicit contraction at T6 by
pressure upon spines T8 and TID.
Thus, the hyperexcitability of the
lesioned segment was again demon
strated independently of the spinous
d 9
Fig. 2 -Diagram ofrefexpathways involved
in experimental measurement of segmental
refethreshold and of intersegmental spread
of ecitation. (See text.)
sp-sensory endings in spinous process; a, d -
ascending and descending intersegmental
neurons; m - erector spinae mass; e -
recording electrodes.
process; it exists even when the
spinous process is desensitized.
Bilateral diferences.
On a few subjects the reflex responses
on both sides of the same segment
were simultaneously observed (Fig. 2,
T6) . It was found that the spinal
extensors on one side of the segment
may respond reflexly to very slight
pressure upon the spinous process
while the other side requires much
higher pressure to the same spinous
process. In other words, low or high
thresholds are not determined by the
spinous process. The neurons in the
left and right horns of the same
segment may be maintained in differ
ent degrees of excitability. The left
and right "bells" are rung with dif
ferent degrees of facility from the
same "push button. "
Rest activity.
The differential excitability of
anterior horns in lesioned and
nonlesioned segments was further
and clearly shown in experiments in
which the anterior horn cells were
exposed, not to impulses from
spinous processes but to generalized
stimuli coming from within and
without the body.
When a patient is prone and com
pletely relaxed there is usually no
activity in the spinal muscles; there is
not even tone, as indicated by the
absence of action potentials in those
muscles. This is true, usually, even of
segments in lesion.
Occasionally, however, it was
found that muscular activity persisted
in the absence of external stimula
tion. The subjects had to be carefully
positioned and repositioned to elimi
nate as far as possible the afferent
bombardment from the propriocep
tors. It was found that when rest
activity did occur, it was almost
invariably in the lesioned, low
threshold segments. Thus, the seg
ment in lesion is the most sensitive to
positional stress, conveyed by the
proprioceptors in the muscles and
tendons.
Mental factors may also be re
sponsible for test activity. Subjects
who are apprehensive, anxious, or
emotionally upset often show per
sistent rest activity. Such activity was
always most marked in the lesioned
segment; often it occurred only in the
lesioned segments. The lesioned
segment is thus hyper-responsive to
impulses descending from the
cerebrum.
Tactile stimuli also demonstrated
the hyperexcitability of the anterior
horn cells in the segment of lesion. If
the back was slightly scratched or
tickled with a pin, as over the
shoulder or scapular area, continuing
activity in the spinal extensors at the
lesioned segment was often precipi
tated, but very rarely in the non
lesioned segment of the same subject.
Thus impulses from touch and light
pressure receptors in skin also find
the most responsive anterior horn
cells in the segments of lesion.
Occasionally we found a motor
unit which fired in synchrony with
inspiration or expiration; such a unit
was invariably situated in the lesioned
segments. Apparently such segments
are hyper-responsive also to impulses
from bulbar and pontine centers.
Interpretation ofexperiments.
The following general conclusions
1ZJ
may be drawn from these experiments
as regards to motor activity in
lesioned segments.
1 . An osteopathic lesion is associ
ated with a segment of the
spinal cord which has a low
motor reflex threshold, i. e. , it
represents a hyper-excitable seg
ment of the cord. At least in the
lesioned segments studied by us
it may be said that the balance
has been shifted too far for too
long toward the excitatory
side.
2. The lowered reflex thresholds
are demonstrable independently
of the related spinous process.
Even though changes in the pal
pable characteristics and in pain
sensitivity of the spines are
important diagnostic features,
they are apparently secondary
to other, more fundamental
alterations in the cord. This
aspect will be discussed later.
3 . The lesion represents an anteri
or root at least some of whose
motoneurons are maintained in
a state in which they are rela
tively hyperexcitable to all
impulses which reach them. I n a
severe lesion many of the moto
neurons are so close to thresh
old, even when the subject is at
rest and reclining comfortably,
that it requires very few addi
ti onal i mpul ses from the
neurons which synapse with
them to trigger those moto
neurons into overt activity.
Those additional impulses may
come apparently from almost
any source; the spinous process
is but one such source.
4. The lesion, therefore, is to be
conceived, not as a radiating
center of irritation, spreading
excitation to other segments,
but rather as a segment upon
which irritation is focused. It
represents a place in the cord
where barriers to motoneuron
excitation have been lowered
and which, therefore, chan
nelizes impulses into muscles
receiving motor i nnervation
from that segment.
Basis for segmental hyperecitability.
What is the basis for this segmental
hyperexcitability? What keeps the
motoneurons of the lesioned segment
"on edge, " that is, at a high level of
12
subliminal excitation? These anterior
horn cells can be maintained in this
facilitated state by continuous and
excessive bombardment from some
untiring source or sources.
The source ofimpulses.
What are the untiring sources of
impulses with which the anterior horn
cells in the lesioned segments are
continuously and excessively bom
barded? First, their excessive activity
is apparently associated with pos
tural, mechanical, and articular
derangements. Second, it must be
recognized that they are apparently a
highly stabilized and chronic source.
Reflex thresholds in segments of
lesion have been found to be very
constant over periods of months and
even years. Third, it must be rec
ognized that they are probably highly
localized, often restricting their
facilitating effect to only one or two
segments.
The sources which, in our opinion,
most closely fulfill these qualifica
tions are the proprioceptors, Le. , the
stretch, tension, and pressure recep
tors in the muscles and connective
tissues.
First, postural, mechanical, and
articular derangements unquestion
ably cause increased fiber-length or
tension in the muscles and tendons on
at least one side of the articulation in
question. The proprioceptors are
highly sensitive to changes in fiber
length or tension.
Second, they are the nonadapting
type of receptor. They keep firing
impulses into the cord via the dorsal
root fibers as long as they are under
tension and at frequencies which are
proportional to the tension. The
higher the tension, the higher the
afferent bombardment for as long as
the tension is maintained.
Third, the afferents from pro
prioceptors not only have segmental
distribution, but they specifically
influence the activity of the muscles
to which they are most closely related
or in which they are situated. This
specificity extends not only to the
muscles themselves, but to specific
muscle heads. It is thought that the
muscle spindle cells reflexly influence
only the muscle fibers in their im
mediate vicinity. In this way, highly
localized, vicious cycles of irritation
may be set up.
We, therefore, believe that these
receptors play a prominent role in
maintaining segmental hyperexcit
ability in areas of lesion. As a result
of the continuous barrage of im
pulses which they fre into the cord
at their level, the anterior horn cells
of the corresponding segment are
maintained in a state of chronic
facilitation - at a high level of
subliminal excitation, even during
rest.
Efects ofchronic faciltation.
In these segments, therefore, it
may be said that the normal "insula
tion" which keeps the efferent
neurons from firing in response to
every impinging impulse has become
worn. Since under normal conditions
of life, requiring constant adjustment
to the external and internal environ
ments, requiring motion and the
maintenance of the erect posture, so
many impulses from so many sources
are constantly impinging on the
motoneurons, in all segments of the
cord, that those which are already
facilitated, as in the lesioned segment,
will inevitably be more active than the
other. The muscle fibers to which
they are connected will then be
excessively high in tone. If main
tained for sufficient periods of time
this hypertonus would lead to
textural, morphologicll, chemical,
and metabolic changes which may, in
turn, become secondary and chronic
sources of irritation.
Other neurons.
We have thus far discussed only the
motoneurons and alterations in
motor refex activity in areas of
lesion. What of the other efferent
nerve fibers and the organs and
tissues which they innervate?
Our experimental studies have
demonstrated that closely and quan
titatively correlated with lowered
motor reflex thresholds are three
other features of the lesion: (1) Alter
ation in the texture of the tissue over
lying the spinous process, (2) lowered
pain threshold, and (3) increased
susceptibility to trauma.
1 . Tissue texture: As is well known
to osteopathic physicians, there are
striking changes in the texture of the
tissues over the spines of lesioned
segments. It was found that the
degree of change in tissue texture
was so closely related to the degree
of lowering of motor reflex thresh-
I nterpretation of research
old from th
e
normal that Denslow,
through palpation of subjects prior to
each electromyographic determina
tion of reflex threshold, was able to
predict with remarkable accuracy the
reflex threshold of each segment.
It is probable that these changes in
texture are due to local changes in
vasomotor activity, fluid balance,
capi llary permeabi l i ty, trophi c
factors, and other features which are
directly or indirectly under the in
fluence of the lateral horn cells of the
sympathetic nervous system.
2. Pain threshold: A direct correla
tion was found between motor reflex
threshold and segmental sensitivity to
pain. As is well known, the spines in
lesioned segments are much more
tender than those in normal seg
ments. In other words, it is easier to
reach the "consciousness" of the
patient, i . e. , the cerebral cortex,
through the lesioned segment than
through the nonlesioned. This, we
interpret as signifying a facilitation of
the spinothalamic fibers.
3. Susceptibility to trauma: It was
found that if one applies equal
mechanical irritation (measured
impacts) to the spinous processes of
lesioned and nonlesioned segments,
the former may remain painful for
several days, whereas the subject
soon forgets which of his normal
spines received the pounding.
We may conclude from these cor
relations with motor reflex threshold
that neurons other than the anterior
horn cells may also be facilitated and
maintained in a state of hyper
excitability in the lesioned segment.
This appears to be true, at any rate,
of certain of the preganglionic fibers
of the sympathetic nervous system
and of the spinothalamic fibers
conveying pain sensation to the
higher centers.
Experiments are now in progress to
establish the degree of involvement 'of
neurons of the sympathetic nervous
system. Dermatomal alterations in
sweat gland activity are being
determined by measuring the elec
trical conductivity of the skin in
lesioned and nonlesioned segments.
We are measuring alteration in the
activity of sympathetic fibers con
trolling vasomotor activity by
electrical measurements of skin and
deep muscle temperature. Although
these studies are still in a preliminary
stage, it has become evident that
sympathetic activity in the skin is
altered in lesioned areas and that
instruments used for the measure
ment of these peripheral changes, and
others which are contemplated, will
in one form or another become
valuable diagnostic aids. They are
much more sensitive than fingertips
and certainly easier to standardize.
There is no reason to doubt that
lateral horn cells which influence
specifi c vi sceral functi ons are
fundamentally similar to those
controlling the sweat glands. A
project, in collaboration with Dr.
D. E. Drucker of the Department of
Physiology, is under way for the
objective and precise determination
of alterations in various visceral
functions resulting from acute experi
mental spinal lesions in animals. The
effects on visceral function, in
normal unanesthetized dogs, of
lesions in segments related to the
viscus under examination will be
compared with the effects of similar
lesions elsewhere. At present, these
investigations are limited to a study
of renal blood flow, glomerular fil
tration, and tubular secretion. The
kidney was selected for the first such
investigation because methods for
quantitative study in normal animals
and humans are highly developed and
because of the clinical significance of
renal blood flow and renal metab
olism in connection with such entities
as hypertension. Similar studies upon
other visceral organs are projected
for the near future. It is hoped that
from these studies will emerge a
clearer understanding of the relations
of the osteopathic lesion to visceral
disease.
Characterization of the lesion
On the basis of the experimental
studies so far, I believe we are ready
to attempt a characterization of the
osteopathic lesion in terms of basic
neural mechanisms. Let us first
summarize our general conclusions.
1 . Normally, efferent neurons are
kept from firing in response to every
impulse that reaches them by the fact
that a relatively high level of sub
liminal excitation - or facilitation -
must be established, by other im
pulses converging upon them, before
the firing point is reached. This
requirement serves as a sort of
insulation.
2. In the lesioned segment this
insulation has been weakened. A
large portion of the efferent neurons
are kept near the firing point (fa-
cilitated), even under conditions of
rest, by chronic afferent bombard
ment from segmentally related
structures.
3. Proprioceptors are undoubtedly
an important source of this bom
bardment, but any segmentally
related structure may be such a
source. A pathological viscus, or a
cutaneous trigger spot, or any other
inflamed or irritated structure which
concentrates its afferents in one or a
few dorsal roots may be responsible
for more or less tonic facilitation.
(The close relation of the osteopathic
lesion to referred pain mechanisms is
clear, but space does not permit a
discussion of this most important
aspect.)
4. The firing process in the fa
cilitated efferent neurons may be
completed by any impulses impinging
on those neurons, whether the source
of those impulses be the cerebral
cortex, postural and equilibrium
centers, bulbar centers, cutaneous
receptors, or others. Should this
superimposed bombardment be suf
ficient and enduring, the facilitated
neurons (and the organs they inner
vate) may be maintained in a continu
ous state of excessive activity.
5. The state of facilitation may ex
tend to all neurons having their cell
bodies in the segment of the cord
related to the lesion, including the
anterior horn cells, preganglionic
fibers of the sympathetic nervous
system, and apparently the spino
thalamic fibers.
6. Because a structural defect, an
osteopathic lesion, sensitizes a seg
ment to impulses from all sources,
and for reasons previously given, the
lesioned segment is to be considered
not a radiating center of irritation,
but rather a neurological lens which
focuses irritation upon that segment.
Because of the lowered barriers in the
lesioned segment, excitation is chan
nelized into the nervous outflow from
that segment.
7. It is a truism in neurophysiology
that when something is excited, some
thing functionally related is simul
taneously inhibited. Although in our
studies we have not yet directed atten
tion to this aspect, it cannot be
doubted that facilitation in the
segment of lesion also extends to
1Z5
neurons exerting inhibitory infuences
upon other neurons or organs.
It may then be concluded that:
An oteopathic leion represents a
faciltated segment ofthe spinal cord
maintained in that state by impulse
of endogenou origin entering the
coresponding dorsal root. Al struc
tur, receiving eferent nerve fiber
from that segment are, therefore,
potentialy expoed to eces ive ex
citation or inhibition.
Manipulative Therapy
We come now to the last question:
What, basically, does manipUlative
therapy do? Here, we can only guess,
but at least our guesses are based on
sound, experimentally established
hypothesis.
Manipulative procedures applied
by osteopathic physicians induce
relaxation of muscle which has been
maintained in a continuously con
tracted state and which, as a matter
of fact, may not be able to relax
spontaneously, even when excitation
is removed (contracture). The in
crease in muscle-fiber length eases the
tension on the proprioceptors in the
muscles and tendons, bringing about
at least a temporary diminution in
afferent bombardment of that
segment of the cord.
Since the excessive tendinous and
muscular tension produced around a
joint, let us say, by some bony dis
placement tends refexly to produce
more tension, the manipulative easing
of tension breaks a vicious cycle.
Still another type of vicious cycle
may be in operation and be broken
by manipulative therapy (Fig. 1 ).
Through overexcitation of sympa
thetic fbers in the segment of lesion,
visceral pathology may be estab
lished. The anterior horn cells may
then be subjected to additional
bombardment with impulses con
veyed by visceral afferents, thus
causing exaggeration of the somatic
lesion which, in turn, further irritates
the viscus. Maipulative relaxation of
the muscles may break this cycle, too,
through diminution of proprioceptor
discharge into the cord. Even a brief
respite from this irritation allows
better opportunity for the natural
healing processes to operate.
By manipulative rearrangement of
the skeleton and through postural
adjustments, the original cause of the
strain, that is the excessive tension on
126
muscles, tendons, and ligaments, may
be eliminated and the beneficial
results made more lasting.
This is unquestionably an over
simplified version of the basic effects
of manipulation, but it certainly will
serve as a working hypothesis, as a
guide to further experimental investi
gation.
Speculations
Assuming the importance of the pro
prioceptors in the lesion mechanism,
it must be kept in mind that any
segmentally related structure which
sends afferents to the spinal cord may
be an important participant in the
establishment or maintenance of the
lesion In fact, through the network
of interneurons, practically any
afferent, segmentally related or not,
may exert some influence.
To all these sources of impulses
must be added the suprasegmental
sources - all the higher centers, from
medulla to cerebral cortex - which
contribute to the descending spinal
tracts. Many of these are continuous
and highly variable sources of im
pulses. They exert their influence -
excitatory or infibitory - upon
efferent neurons at every level of the
spinal cord.
It is, inded, most important to
keep in mind that the efferent
neurons do represent final common
paths shared by a host of impulse
sources, in addition to those associ
ated with joint and supporting tis
sues. I n this light, it is apparent that
the articular derangement or the
osteopathic lesion cannot be con
ceived as the cause of disease; rather
it is one of many factors simul
taneously operating.; The lesion is a
most important factor - it is a
sensitizing factor, a predisposing
factor, a localizing factor, a chan
nelizing factor. The lesion sensitizes a
segment of the cord, lowers the
barri er, faci litates - without
necessarily producing symptoms,
although signs of its presence may be
demonstrated by the osteopathic
physician. Sufficient additional
+In fact. it is doubtful whether there is ever a single
cause of any effect. whether there is ever an isolated
etiological factor in any clinical entity, Each factor
operate in the context of many factors and produces
certain effects only in a certain combination of
factors.
excitation has to be superimposed
upon that from articular and peri
articular origins. This is not to
minimize the importance of the
osteopathic lesion. On the contrary it
is to widen the concept. For one
thing, it certainly points Up " the
t remendous cont ri but i on that
osteopathic diagnosis and therapy
can make to preventive medicine.
To osteopathic physicians there is,
of course, nothing unfamiliar in the
practical aspects of this concept. One
patient has relatively severe lesions,
yet is sympton-free, pain-free, and not
readily subject to fatigue, etc; an
other patient with very similar lesions,
on the other hand, may be subject to
serious disturbances directly related
to those lesions. Further, the lesions
of the first patient may "act up"
under certain circumstances, and
then subside into "quiescence"
again. Why? What accounts for the
difference between such patients,
and between the "acting-up" and
"quiescent" periods in the same
patient? In our opinion and, I
believe, implicit in the osteopathic
concept, one important basis for the
difference lies in differences in the
amount of nervous excitation con
tinuously impinging on the efferent
neurons of the lesioned segments,
over and above that from the muscles
and joints. The lesion operates in
different contexts with different
effects.
Given an articular disturbance
which, through the mechanisms
discussed above, determines the
location of the low threshold
segments, then the severity of the
lesion, the associated pathology, and
the response to treatment will be to a
great extent, often to a decisive
extent, determined by how much
additional neuron pressure from
other sources is chronically present.
Such pressure may be present upon
all the segments, but because of
lowered synaptic barriers, the effects
will be exaggerated at the lesioned
segent. The lesion not only focuses;
it magnifies.
This superimposed excitation may
come from any of the sources pre
viously enumerated, and others,
which converge upon the anterior
horn cells and the other efferent
neurons: the cortex, the basal
gangl i a, cerebel l um, vestibular
nuclei, bulbar center, the eyes (via the
Interpretation of research
tectospinal tracts), or any steady, ton
ic source of impulses.
Since all these sources may directly
affect, favorably or unfavorably, the
lesion and its associated phenomena,
they are all properly within the
province of the osteopathic phy
sician. All of them may contribute to
the lesion and to its effects on total
body economy. Important as is the
structural factor, treatment of it
alone is not to treat the patient as a
whole and would be, i f I interpret it
correctly, a corruption of the
osteopathic concept.
I shall try to illustrate with one
source of bombardment which is of
very general signifcance, namely, the
cerebral cortex. As previously indi
cated, the words "tense," "high
strung, " "jumpy, " "keyed-up,"
"on edge" are more than figures of
speech. They bespeak the well-rec
ognized fact that psychic stress,
emotional imbalance, environmental
strains, etc. , influence and are
reflected in motor activity - an
increased muscular tone and hyper
responsiveness, in generally lowered
refex thresholds. A familiar illustra
tion is the exaggerated knee jerk of a
tense individual. (Other types of
imbalance may, of course, have de
pressing or i nhibit ory effect s,
resulting in fatigue, hyperrefexia,
inertia and other symptoms.)
These are obviously due to
impulses passing down the descend
ing spinal tracts and impinging,
directly or through interneurons, on
the anterior horn cells and increasing
their excitability and activity.
In a segment already sensitized by
an osteopathic lesion the effects will
be especially severe. Just as important
is the fact that descending impulses
may exacerbate the lesion and pro
duce increased effects on segmentally
related organs, may cause or intensify
pain, and make the lesion less respon
sive to manipulative therapy. To treat
only the structural source of bom
bardment is only to half-treat and
to neglect a most important part of
the lesion mechanism, and to take the
lesion out of context. This does not
mean, of course, that every osteo
pathic physician should become a
psychiatrist, but he certainly must
take into consideration the home
factors, environmental factors ,
family relations, emotional adjust
ments, tensions, etc.
In this light the as yet unexplored
relations of osteopathy to psychoso
matic medicine become obvious. It
is now well established that many
organic ills, including angina pec
toris, gastric and duodenal ulcer,
gallbladder disease, mucous colitis,
asthma and others, may be directly
related to psychoneuroses, emotional
imbalances, and anxieties. What
factors determine the organic
manifestation of the neuroses? The
autonomic nervous system, of course,
has regional representation in the
cerebral cortex and the hypothalamus
is under cortical influence. It has been
thought that the unconscious may
select the organ or organs to be
affected. Without prejudging these
and other theories, it would seem
most profitable, clinically and
experimentally, to explore the
probability that the incidence and
location of osteopathic lesions may
be an important factor in determining
the incidence and nature of psychoso
matic ills. Certain aspects of this
hypothesis are under experimental
investigation in the Ki rksvi l l e
laboratories.
Summar
1 . Some of the neural mechanisms
involved in the osteopathic lesion, in
its local and distant effects, and in
manipulative therapy are examined.
2. The results of experimental
investigations are presented which
indicate that the lesion is associated
with a segment of the spinal cord
which is hyper-excitable to all
impulses which reach it, and that the
hyperexcitability may extend to any
neurons having their cell bodies in
that segment.
3. It is concluded that osteopathic
lesion represents a facilitated segment
of the spinal cord maintained in that
state by impulses of endogenous
origin entering the corresponding
dorsal root. All structures receiving
efferent nerve fibers from that seg
ment are, therefore, potentially
exposed to excessive excitation or
inhibition.
4. Evidence is presented that the
stretch and tensi9n end-organs
(proprioceptors) in the muscles and
tendons are the most important
source of afferent impulses which
produce the changes in the cord that
are associated with the osteopathic
lesion.
5. The effect of the lesion as a
predisposing and localizing factor is
emphasized and discussed in relation
to certain aspects of osteopathic
practice.
References
I . Denslow. J. S. : An analysis of the variability of
spinal refex thresholds. J. Neurophysiol. 7:207-215.
July 1 94.
2. Denslow, J. S.; Korr, I. M., and Krems, A.D.:
Quantitative studies of chronic facilitation in human
motoneuron pools. Am. J. Physiol, 105:229-238,
Aug. 1 947.
3. Lloyd, D. P. C. : Intercellular transmission, in
Howell's Textbook of physiology. edited by J. F.
Fulton. Ed. IS. w. B. Saunders Co Philadelphia,
1 946, p. 134.
4. Sherrington, C. S. : Correlation of refexes and
the principle of the common path. Brit. As. Rep.
74:728-741 , Aug. 18, 19; abstr., Brit. M. J. 2:43,
Aug. 27. 19.
5. Lorente de N6, R. : Synaptic stimulation of
motoneurons W a local proces. J. Neurophysiol.
1 : 1952, May 1938.
6. Lloyd, D. P. c.: Reflex action in relation to the
pattern and peripheral source of afferent stimulation.
J. Neurophysiol. 6: 1 1 1-1 19, March 1943.
Reprinted by permission from JAOA 47: 1911
98,
1947.
117
The emerging concept of the osteopathic
lesion* (1948)
The survival, growth, achievements,
and increasing effectiveness of
osteopathy are eloquent testimony to
the soundness of the principles upon
which it was founded. The attain
ments of the osteopathic profession
have been possible only because the
profession is founded upon the solid
rock of basic truth. Its continued
growth and prestige indicate that
those truths continue to be correctly
applied and soundly developed.
The time has come, however, when
increasing attention must be given to
the theoretical reserves upon which
continued technical advance is
predicated. For many reasons these
reserves have been consumed far
more rapidly than they have been
replenished. In osteopathy, as in all
technological aspects of modern life,
large backlogs of fundamental in
formation must be maintained and
enlarged if continued practical ad
vances are to be assured. They are,
indeed, the springs from which the
advances fow.
In osteopathy these reserves consist
of our understanding of the basic
biological processes and mechanisms
associated with the phenomenon des
ignated as the osteopathic lesion.
Today this understanding is not, or at
least until a very few years ago was
not, a great deal larger than in Still ' s
day. Although knowledge of the
mechaical aspects of the lesion (the
"cause") and of its clinical mani
festations (the "effect") has greatly
advanced, there has been no parallel
advance in our knowledge of the
processes intervening between these
two aspects of the probleP.
These processes are the problems
before us today. Given a lesion - so
well known to osteopathic physicians
through their trained fingers and
through x-rays - how does it
produce its effects? Through what
mechanisms and channels does it
impair the defensive, reparative, and
homeostatic functions of the body?
How does H predispose to disease
?
'Based on an address of the same title read before the
General Sessions of the Fifty-Second Annual Conven
tion of the American Osteopathic Association.
Boston, July 19, 1948.
II8
How does it upset physiological
equilibria? What processes does it
initiate? The very future of osteop
athy, 8 a distinct and advanced
system of practice, is directly related
to the accuracy and thoroughness
with which these questions can be
answered in the next few years.
It is my purpose in this paper to
present our current theories regarding
these central aspects of the osteopath
ic lesion. Then I wish to draw some of
the practical implications of these
emerging concepts. Paradoxically, I
shall present our current theories by
dealing to a large extent with other
matters. It is possible to do this
because those other matters are so
intimately, and sometimes insep
arably, related to the osteopathic
lesion. The discovery of these
relations is as important as the
discovery of the new facts about the
lesion itself because, with the estab
lishment of each such relation, a
whole body of knowledge, ready
made and usually still growing; is
automatically incorporated into the
osteopathic concept. With every such
incorporation our concepts, in which
clinical and professional advances
have their origin, are deepened and
widened.
The history of science - physical,
biological, or medical - records
again and again the collapse of fences
separating scientific and technical
fields. As a result of certain funda
mental discoveries entire fields of
scientific pursuit, whole schools of
thought, and major concepts begin to
develop and attract disciples. These
felds may develop independently and
remain separate one from the other,
and apparently unrelated, for many
years. However, as the knowledge
and understanding within each field
accumulates, through experience and
research, it becomes apparent in
many cases that the walls which
separate these fields have very little
substance; in fact , they exist only in
the minds of men, and not in nature
itself. Each field begins to draw from,
and give to the other, new and
additional meaning. Finally they
merge.
Nowhere is this better illustrated
than in the fields of immediate
interest to the osteopathic profession.
I have selected for discussion only
three major fields which, from our
perspective, appear to have much
basic and distinctive substance in
common. Each has yielded a major
body of concepts, a school of thought
or a school of practice. Each origi
nated independently, at different
periods and in t hree di fferent
countries, separated by thousands of
miles, and under very different
circumstances. Today they are ad
joining fields and the fences between
them are crumbling. They have in
common the following general
concepts:
1 . The body is a unit; all parts
function in the context of the entire
organism.
2. Disease is a reaction of the
organism as a whole. Abnormal struc
ture or function in one part exerts ab
normal influence on other parts and,
therefore, on the total body economy.
3. The organism has the inherent
capacity to defend itself, to repair
itself, and to resist serious upsets in
equilibria.
4. The nervous system plays a
dominant organizing role in the
disease processes.
5 . There is a somatic component to
every disease which is not only a
manifestation of the disease, but an
important contributing factor.
6. Appropriate treatment of the
somatic component has important
therapeutic value in that it leads to
i mpr ovement i n t he ot her
components.
The concepts I refer to are: ( 1 ) the
osteopathic, (2) the concept of re
ferred pain and associated phenome
na, and (3) the concept of disease
developed by A. D. Speransky and
his colleagues in Leningrad. These
concepts have not only had very
different origins, but very different
courses of development.
The osteopathic concept soon led
to the development of a most effec
tive therapeutic weapon which
became, and for more than 60 years
has been the basis for a new and
expanding school of practice. From
the beginning, this weapon - osteo
pathic manipUlative therapy - was
so revolutionary and so effective that
the major concern of its designers,
developers, and practitioners was
with: ( 1 ) Learning how to use it most
Interpretation of research
effectively, (2) winning the right to
use it, (3) determining its effects on
the various ills to which man is heir,
and (4) reproducing the weapon, win
ning recruits, putting the weapon in
their hands and teaching them how
best to use it.
Possessed of such a weapon, but
with few other material resources,
and preoccupied with those struggles
in the face of opposition, it is un
derstandable that the founders, the
disciples, and the earlier practitioners
of this school found it impossible to
engage in the more leisurely pursuits
of investigating experimentally the
fundamental basis for the effective
ness of their therapeutic weapon.
The founders of the other two
schools did not, however, strike upon
new therapeutic measures in the early
development of the concepts. They
and their disciples, therefore, devoted
themselves to seeking the mechanisms
whereby pathological processes are
initiated, and the channels whereby
pathology of one part affects others.
These investigations have led to
extensive research programs which
are now conducted throughout the
world and which have won much
support and many recruits.
These research programs have
made available a great wealth of
information, which has led to some
sound theory. This, in turn, like all
good theory, is today leading to good
practice. New and promising forms
of therapy are emerging from the
work of these schools. It is to be
expected that these forms of therapy,
experimental though they may be to
day, but based as they are on rapidly
expanding bodies of fundamental
knowledge, will rapidly develop and
i ncrease i n appl i cabi l i t y and
effectiveness . As I hope to dem
onstrate, both of these felds of
investigation are actually concerned
with certain fundamental aspects of
the osteopathic lesion, though they
may not be recognized as such.
In preparing this lecture, I have
found it convenient to review the .
work of these two fields - referred
pain and the work of the Speransky
school - before summarizing the
emerging concept of the osteopathic
lesion, si
n
ce that concept is emerging,
not only from osteopathic research
and experience, but from their in
tegration with contributions of these
two schools in particular.
Referred pain and associated
phenomena
This field of investigation had its
most important beginnings in En
gland in the work of Sturge, 2 Ross, 3
Head,4 Mackenzie, and others i n the
early 80's and 90' s. More recently
important contributions have been
made by Sir Thomas Lewis and his
co-workers, 6 also in Britain, and by a
number of laboratories and medical
institutions in this country. These
workers were primarily concerned
with the somatic manifestations of
vi sceral disease, especially the
somatic pain, and with related
phenomena.
Even very superficial study in the
field of referred pain reveals the close
resemblance of this syndrome to the
osteopathic lesion. Mackenzie,' for
instance, many years ago spoke of the
triad of somatic manifestations of
visceral pathology: ( 1 ) referred pain,
(2) hyperalgesia, and (3) motor phe
nomena.
1 . Referred Pain. * In many
cases, the pain of visceral disease is
felt not in the organ itself, but is
referred to the soma, that is, skin,
muscles, etc. Very often these somatic
structures do not overlie the area of
disease and may be remote from it.
It was soon demonstrated, however,
that the zone of reference bears a
segmental relationship to the area of
origin; both are innervated from the
same segments of the spinal cord. The
pain is said to be referred to the
corresponding dermatome and myo
tome. Many examples are familiar
to the physician: The pain of
angina pectoris, originating in the
myocardium and referred to the chest
wall, the back, shoulder, and medial
surface of the arm; renal colic, which
produces intense pain in the lower
back and groin; irritation of the
diaphragm which is referred to the
base of the neck and shoulder tip.
2. Hyperalgesia. * Tenderness is
also found in somatic structures seg
mentally related to the pathological
viscus:
a. Cutaneous tenderness - the
over-sensitivity to pinching and to
friction in the dermatomes related to
the sick viscus;
b. Muscular tenderness and exag
gerated sensitivity of the muscles to
deep pressure; and
c. Tender spinous processes. In
terestingly enough to osteopathic
physicians, Mackenzie' placed great
diagnostic significance on the tender
spinous processes. He demonstrated,
for instance, that diseases of the heart
were commonly associated with
tender spines Tl to T4; stomach, with
T4 to T8; liver, with T8 to TI l ;
rectum and uterus, L5 to S2.
3. Motor Phenomena. - Mac
kenzie described the spasm, ustained
contraction, and rigidity in muscles
segmentally related to the pathologi
cal organ. He included under motor
phenomena the autonomic changes in
the zone of reference although they
properly belong in a fourth category.
What is the basis for the "referred
pain complex"? Much of the final
answer is certain to be found in the
spinal cord. (Fig. I [same as Fig. 1 in
preceding article. There is obvious
interchange of excitation among all
the types of neurons which meet or
have their origin in a given segment of
the spinal cord: The dorsal root (af
ferent) fbers conveying centripetal
impulses from all the tissues, somatic
and
v
isceral; the various efferent or
motor neurons, including those which
have their cell bodies in the anterior
horn and which regulate activity of
the skeletal musculature, and those
originating in the intermediolateral
column which tegulate visceral ac
tivity (motor and secretory) , sweat
gland activity, vasomotion, etc. The
spinothalamic fibers which convey
sensation of pain to the higher centers
are also obviously involved in the
complex. Although the spinothalamic
fibers can be excited by impulses
transmitted by the afferent fibers
from the viscera, nevertheless the
cerebral cortex projects or "refers"
these sensations to somatic structures
whose afferent fibers enter the same
dorsal root. (See the paper by
Drucker' for a review of the
mechanisms.)
On the basis of these observations
Mackenzie developed the hypothesis
of the "irritable focus. " This hy
pothesis stated, in essence, that
irritation from the viscera, conveyed
by the afferent fibers, renders many
of the nerve cells in the same segment
hyperirritable. As a result, tissues and
organs innervated from that segment
are affected by the visceral pathol
ogy. The "irritable focus" hypothesis
IZ9
has since been modified and restated
in accordance with more modern con
cepts of facilitation. 9
More recently Lewis and his col
league, J. H. Kellgren, 1O showed that
the phenomenon of pain reference
was not peculiar to visceral irritation,
since similar and even identical pat
terns ("triads") could be evoked
by irritation of deep-lying somatic
structures. They found that injection
of 0. 1 to 0. 3 cc. of 6 per cent sodium
chloride solution into certain liga
ments, tendons, and muscles, could
produce intense pain in relatively
large and often remote areas of
the corresponding dermatome and
myotome. The pain reference was
accompanied by the other com
ponents of the classical triad, namely
cutaneous and muscular hyperalgesia
and muscular rigidity.
Even more striking was the demon
stration that such localized irritation
of the interspinous ligaments or
spinal extensor muscles in certain
segments, reproduced with remark
able precision the pain patterns and
other somatic phenomena which are
associated with visceral pathology.
l l
This was true to such an extent that
patients who had experienced the real
disease could not distinguish between
the experimentally induced and the
naturally occurring syndromes. For
instance, the injection of the eighth
cervical interspinous ligament with
the hypertonic saline solution pro
duced a perfect facsimile of an an
ginal attack, not only with respect to
pain distribution (including the
substernal pain and the radiation
down the ulnar surface of the arm),
but also the hyperalgesic areas, the
muscular rigidity, and the sense of
compression of the chest. Injection of
the first lumbar interspinous ligament
produced the typical pain distribution
of renal colic (lower back, lower ab
domen, groin, and scrotum), rigidity
of abdominal and spinal muscles,
hyperalgesia, and often a marked cre
masteric reflex on the corresponding
side. (In our own laboratory, we have
not only confirmed these observa
tions, but have demonstrated certain
associated autonomic changes. )
Furthermore, these workers l o and
others demonstrated that experi
mental trauma to certain visceral
organs produced recordable contrac
tions of skeletal muscles in cor
responding segments. These con-
I
tractions could be almost perfectly
reproduced (with respect to location,
amplitude, and time characteristics)
by irritation of certain somatic
strutures in the same segment.
(Studies on the converse, namely the
influence of somatic irritations on
visceral function, are in progress in
our laboratories. )
It may be concluded from these
observations that not only does
irritation or pathology in one tissue
or organ stir up abnormal activity of
other tissues in the corresponding
segments, but that the complex -the
patter of the overall response to the
primary pathology - is organized by
the spinal cord. The character of the
pattern is determined by the segment
or segments which are involved, and
not by the tissue which is first
irritated (somatic or visceral) nor by
the nature of the irritation.
It was early recognized by workers
in this field that the secondarily
irritated structures, that is, those
tissues in the zone of reference, may
themselves, as a result of this patho
logical influence, become secondary
sources of irritation - leading to the
establishment of a vicious cycle. This
recognition has formed the basis for
certain important therapeutic mea
sures which have begun to emerge
from this work. Given such a pattern,
including visceral pathology and the
reference phenomena, then why not
eliminate the irritation contributed by
the most accessible part of the
complex - the somatic component?
The potentialities of this approach
were indicated 20 years ago by Weiss
and Davis who showed that at least
the pain, due to visceral pathology,
could be relieved by local anestheti
zation of the skin areas to which the
pain is referred. It is of special
interest that the relief from pain often
outlasted the expected duration of
the local anesthesia by considerable
periods of time.
Other work (reviewed by Wolff
and Hardyl4 and Wolff and Wolfl S)
has demonstrated that the sustained
muscular contractions or spasms
which are part of the referred pain
patterns, may themselves comprise
sources of irritation. Local infiltra
tion of the rigid muscles, identified by
palpation, relaxed those muscles,
relieved the pain, and often produced
improvement in the associated auto
nomic disturbances.
This general approach has been
receiving especially significant de
velopment in the hands of Travell and
her colleagues at Cornell University
Medical College. They were able to
produce complete and immediate
relief from cardiac pain due .to
myocardial infarct by infiltrating
appropriate trigger areas with dilute
procaine hydrochloride.
1
6
, 1
7 These
were intensely hyperesthetic areas
located in the myofascial structures
of the reference zone (usually in the
pectoralis major, petoralis minor, or
serratus anterior) . When sufficiently
near the surface the trigger areas
could also be effectively blocked by
spraying the overlying skin with ethyl
chloride. Relief from pain was not
only immediate, but lasting. Relief
was obtained for periods of months
and even years. It is of interest that
when similar trigger areas, in patients
with skeletal muscle disorders with
out organic disease, are irritated, as
by needling, referred pain occurs
"which is indistinguishable in
distribution and quality from the
substernal and radiating pain of
coronary insufficiency. "
1
7
Of interest to those familiar with
the osteopathic concept and the
current theories of the osteopathic
lesion are the explanations of these
observations proposed by these
workers. Thus Travell and Rinzlerl
6
say, "The most reasonable explana
tion is that the initial insult, whether
to visceral or somatic structures, sets
in motion a chain of events perpetu
ated by a vicious cycle of nerve
impulses which have no further
dependence on afferent impulses
from the heart and which are prob
ably transmitted to and from the
soma by virtue of sustained facilita
tion of the noxious impulses by the
closed self-reexciting chains of
internuncial neurons in the central
nervous system. " Apparently, even
brief interruption of this self
sustaining cycle of nerve impulses at
any point in the chain may be effec
tive in permanently abolishing it.
` In explanation of the lasting effect
of this brief interruption by local
somatic block therapy they offer the
possibility that the "somatic trigger
mechanisms contribute to the per
petuation of the primary source
of pain," that is, the coronary
insufficiency. In support of this
hypothesis they refer to the evidence
Interpretation of research
99
W
M
u+v
m
Fig. 20
J. H Z
Fig. 2b Fig. 3
Fig. 2. /llustration ofconstancy ofsegmental distribution oflow resistance areas (shaded). Explorations 2 months apart, on same subject, by different
methods and diferent examiners are recorded in 20 and 2b. This case was selected to show extreme variations in size, shape, and intensity of low
resistance areas while segments involved remained essentially unchanged. (Other explanations in text.) Fig. 3. Bilateral dermatomal strips oflow skin
resistance found in case ofacute gastritis.
Fig. 40 Fig. 4b Fig. 50 Fig. 5b
Figs. 40 and 4b. Effects ofintramuscular injection ofhypertonic saline. Injections of0.3 cc. of6 per cent sodium chloride into sites marked by (left
erector spinae mass at eighth thoracic segment and right intercostal, ninth thoracic) cause appearance of new low resistance areas in corresponding
dermalOmes. (New areas encircled U distinguish from pre-existing areas.) Figs. 50 and 5b. Distribution ofthe new areas several hours after experiment of
Figs. 40 and 4b.
that most of those that come to mi nd
are peripheral and will fall into line as
i nformation accumulates on the
central ones.
Methods of the Department of
Physiology
In the space that remains I wish to
review a few of the methods that are
being adapted and developed in the
Department of Physiology for the
investigation of the problems dis
cussed above and for incorporation
into this continui ng survey.
It must be emphasized that these
14I
procedures have been developed for
investigative purposes only and are by
no means to be considered ready for
inclusion in the diagnostic arma
mentari um. Although i t is probable
that at least some of these procedures
will eventually be of cli nical value,
since they do evaluate segmental
features associ ated wi th cl i ni cal
disturbances, a great deal more
i nformation remains to be ac
cumulated and analyzed before it can
be known what cli nical significance to
assign to these measurements.
Denslow and his coworkers578 have
shown that the spi nal lesion has
associated with i t a low motor reflex
threshold, that is, it takes less of a
stimulus to induce reflex muscular
ativity i n the lesioned than i n the
nonlesioned segment. This means
that in the lesioned segments, the
anterior horn cel ls, at least of t he
paravertebral muscles, are in a state
of hyperirritability. The segment is
said to be, faci litated with respect to
motor activity. We are now correlat
ing measurements to other segmental
features with motor reflex theshold.
I t was of i nterest to determine
I nterpretation of research
llB
tHng .9
. .
P
W
.
0 l -
.:.
Fig. . Changes in skin resistance pal/ern with postllre and activity. (See text.) (a)Afternoon, seated; (b) morning, standing; (c) late afteroon, standing.
M6m Hl J. . 66
t Z l Z
Z'90
&B
d lnf,
fP
9 M
W~
.
W"
/
Fig. 7. Efects oftilting sacral base plane. "acllte scoliosis. " (See text. (a) Level seat. (b) right side elevated I hour, (c) retur oflevel seat.
whether the facil itation extended to
other neurons in the lesioned seg
ments. We turned to the sympathetic
outflow and, as Thomas stated in the
preceding paper of this Symposium,
have used the electrical ski n resistance
method for this purpose.9. I O. 1 1 In this
method, the sweat glands are the
physi ol ogi cal i ndi cat or s of t he
relative activity of the lateral horn
cells in the various segments.
Figure shows a ski n resistance
expl orat i on in progres s . Known
voltages are applied through t he ski n
in such a way that t he current which
flows, measured in mi llionths of an
a
mpere, indicates the resistance of the
ski n underlying the exploring elec
trode at a given time. By adj usting
the voltage so that little or no current
flows through most of the ski n, areas
of low resi stance are sharply di f
ferent i ated by excursi ons of t he
microammeter needle. These findings
are then recorded on body charts.
The low resistance areas represent
sympathetic hyperactivity.
Repeated explorations over long
periods on many subjects have shown
that low resistance areas are present
in all subjects; that the distribution
of low resistance areas, that is, of
sympat hetic hyperact i vi t y, vari es
from individual to individual, but
t hat i n a gi ven i nd i vi dual , t he
segmental distribution may remain
constant for many months. In these
segments, therefore, the sympathetic
outflow appears to remain i n a state
of activity while elsewhere i t is at rest.
Thi s hyperactivity, or state of alarm,
presumably extends not only to the
sweat glands, but to structures in
nervated by the sympatheti cs -
blood vessels and viscera.
Figure 2 compares two explora
tions done i ndepe
'
ndently by two
examiners 2 months apart on the
same subject and i ll ustrates the
stability of the patterns. Note that
although the size, shape and intensity
14J
144
Fig. 8a Fig. 8b Fig. 8c
8. Heel-lift eXperiment (See text.) (a) Control, (b) 24 hours ajter lift inserted in right shoe, (c) 24 hours ajter removal oj lift.
L 6 vo|u
6 | 3 5O | | O 8M.
Fig. 10
Fig. 9. Device jor semiautomatic photographic
recording oj skin resistance patterns. The
recording camera is mounted above the
subject. Fig. 10. Record made by device shown
in Fig. 9. Dark areas, as in "hand
explorations, " represent areas oj lowered
resistance. Record is photographically
superimposed on subject 's body. Numbered
white dots indicate tips oj spinous processes.
Note calibration strip on lejt, jrom which
actual resistance oj any area can be accurately
determined.
of the areas are variable, since they
may change with posture, previous
activity, temperature, et cetera, the
low resistance areas remain concen
trated in t he same segments.
The segmental nature of these
patterns is further reflected in the
frequentl y observed dermatomal
stri ps of l ow resi stance, often
extending from spi ne to sternum.
Figure 3 illustrates an extreme case of
dermatomal i nvolvement in a young
man during an attack of acute gas
tritis. Over several preceding months
he had consistently showed sym
pathetic hyperactivity i n the sixth to
ninth thoracic segments.
Fai r l y s peci fi c and const ant
patterns have been shown t o be
associ ated wi th certai n vi sceral
syndromes, the l ow resistance areas
occurring in those segments from
which the involved viscus derives its
i nnervati on.
l 0
I n several cases we
have observed the appearance of
these patterns long in advance of the
fi rst symptoms. Since our primary
concern in this symposium is with
myofascial and postural stress, the
patterns associated with visceral
disease wil l not be reviewed i n this
paper.
Time does not permit review of the
various patterns we have found asso
ciated with acute lesion pathology,
severe back disorders, trauma, and
the effects of treatment. " The next
five figures illustrate the effects on
ski n resistance patterns of experi
mentally induced myofascial i rri ta
tions and postural stressses.
Figure 4 shows the effect of inject
ing 0.3 cc. of 6 per cent sodium
ch
i
oride solution into skel etal muscle.
The ringed areas on the left appeared
within a few minutes following the
injection of the hypertonic salt solu
tion one inch deep into the spinae
erector mass at the eighth thoracic
segment (site marked by X). The
areas (ri nged) on the right followed
injection into the i ntercostal at the
ninth interspace (X) . Note the in
volvement of entire dermatomes.
Several hours later the newly i nduced
area appeared as shown in Figure 5.
I n the course of exploration, these
dermatomes became vivid hyperemic
strips due to the repeated passage of
current although all other areas, ex
plored at the same voltage, remained
unchanged i n appearance.
Figure 6 shows a series of explora
tions of a subject who i s the victim of
frequent backaches in the lumbar
regi on. The first chart (6a) shows his
pattern in the afternoon while seated.
The middle chart (6b) shows his
pattern i n the morning while in the
I nterpretation of research
standing position. The third chart
(6c), an exploration done i n the
standing position late in the after
noon of the same day after a full
day' s work, shows the greatly ex
aggerated effect of continued activity
and fatigue on the sympathetic
nervous system i n the facilitated
segments.
Figure 7 illustrates some of the
effects of postural stress. In the first
exploration, the control (7a), the
subject was seated on a treating stool
with his elbows resting on the desk
before him. Following the completion
of this exploration, the right end of
the stool was raised 1 1/2 inches, while
he otherwise maintained his position.
The middle exploration (7b) was
made at the end of an hour. The new
areas thus induced are quite con
spicuous, especially the one in the
lower thoracic regi on, on the left side,
located on the convex side of the
induced spinal curve. The third chart
(7c) shows the effect of return to a
level seat.
Figure 8 i l lustrates one of the
experiments in which postural stresses
are induced or modi fied by means of
heel li fts. The first chart (8a) shows
the pattern which had been character
istic of this subject over a period of
several months. His right femur head
was approximately 7 i nch lower than
his left. He was occasionally troubled
with pain in the lower l umbar area,
on the right side, corresponding to
the low resistance area in that regi on,
especi al l y after exert i on. Thi s
exploration was done i n the morning
following a 1 12 mile wal k. A 1/2 inch
heel l i ft was inserted in the right shoe
immediately after - this exploration.
The subject wore the lift throughout
the day and the fol lowing morning
while engaged in his usual activities
and during the 1 Y mi le walk to the
laboratory. The second chart (8b)
shows the expl orati on of that
morning. The extensive low resistance
i n the lower right side has been
eliminated, but there is a flare-up and
expansion of the areas in the thoracic
segments, indicating, we believe,
severe insults to these segments. The
lift was removed after this explora
tion. The third chart (8c) shows the
skin resistance pattern on this subject
. the following morning, again after a
1 12 mile wal k. The area over the
ileum returned, and there was further
increase in sympathetic hyperactivity
Fig. II. Comparison of "hand" and "automatic" explorations. (See text.)
Fig. 12. Colorimetric visualization of regional
diferences in sweat gland activity. The method
Ulilizes the color change of cobalt chloride
from blue O red when moistened. In our
preparation the coball sail is mixed with
hygroscopic calcium salts to increase the
contrast. Photographed through an appropri
ate red filter, blue areas (dry) appear dark; red
(moist) appear faded. The photographs, taken
at short intervals (note time on each picture),
show the regional differences in the rate of
thermoregulatory sweating response in this
subject. The experiment may be repeated by
permitting the subject to cool, whereupon the
blue color returns. Mild thermoregulatory
response is induced by applying heat to
extremities or ventral surface.
Fig. J. Part of equipment for measurement of
cutaneous and deep muscle temperatures with
galvanometer and thermocouples incorporated
in fine hypodermic needles. Skin lhermocouple
and constant temperature bath for "reference"
thermocouples are not shown.
145
Fig. 16a
Fig. 14. The measurement ofmuscle hardness
and resiliency, by contact time and rebound of
dropped weighl.
Fig. 15. Measuremenl of segmenlal pain
thresholds (cutaneous). Adaption of Hardy
WolffGoodell thermal stimulus method.
Fig. 16b
Fig. 16. Renal clearance experiment. (See text.) Trained dog, unanesthetized, has received large
volumes of water through stomach tube to establish diuresis; intravenous infusion was administered
through vein in paw. (a) Urine specimen being taken through catheter. (b) Blood specimen being
taken from external jugular vein. The dog is "Ma, " happy veteran ofJyears ofexperimental work
and respected matron of the kennels.
140
in the thoracic segments, presumably
induced by a second acute postural
adj ustment .
The ski n resistance explorations by
means of the hand-held electrode are
slow and tedious, requiring from 30
to 90 mi nutes for each exploration.
They, therefore, make impossible the
study of rapid changes. They require
a considerable amount of training on
the part of the observer and patience
on the part of the subject. Figure 9
shows an instrument designed in our
laboratory and constructed in the
laboratory machine shop, ' 2 which
photographical l y records the elec
trical ski n resistance patterns almost
automatically, in about 10 minutes. I t
can be operated in the vertical
position, for t he study of acute
postural stress, as well as in the
horizontal . Space does not permit a
description of the instrument, except
to say that the trunk is explored
automatically i n longitudinal strips,
and that a light mounted over the
exploring electrode is caused, by a
simple amplifier, to vary in brightness
in accordance with the resistance of
the skin over which i t passes. A
camera mounted above records these
strips of light of varying intensity, as
though they were coming from the
corresponding strip of ski n itself.
By means of a controlled double
exposure, the record is accurately
superi mposed on a photograph of the
subj ect ' s body, with the body promi
nences marked. (Fig. 1 0) .
Figure I I shows a comparison of
one of our earl i est automati c
explorations with a hand exploration
done i mmediately afterward. Note
the high degree of correspondence
between the two; the mid thoracic
dermatomal strip on the right side is
especially clear i n the photographic
record. It is of i nterest to point out
that the subject used for these ex
plorations was the one used in
maki ng Figure 8. However, the
explorations recorded in Figure I I
were done 1 6 months later by another
experimenter. The charts in Figure 8,
especially the third (8c) are almost
superimposable on the later ones,
again stressing the stability and
chronicity of the segmental patterns
of sympathetic hyperactivity.
The photographic dermometer has
already made possible a considerable
expansion of our program. It will
make possible a rapid evaluation of
I nterpretation of research
the diagnostic or prognostic value of
skin resistance, through the correla
tion of patterns with many kinds of
clinical entities in large numbers of
patients.
Figure 12 shows one procedure
under development in our labora
tories for the visualization of regional
or segmental differences in sweat
gland activity, by colorimetric means.
Other visual and photographic tech
nics , involving fluorescence or
regional color differences under
ultraviolet and infra-red light, related
to differences in blood supply and
tissue fluids, are also under investiga
tion.
Figure 1 3 shows some of the equip
ment utilized in the measurement of
cutaneous and deep muscle tempera
ture as a guide to vasomotor activity
or inflammation at various depths,
in relation to lesion pathology.
Thermocouples have been con
structed in No. 26 gauge hypodermic
needles which can be inserted into
muscle, tendon, or ligament at
various depths and at different
segments. Another type of thermo
c
o
uple, not shown, is used for the
recording of skin temperatures. A
high degree of stability of the patterns
of segmental distribution of relatively
warm and relatively cool skin has
been demonstrated in each of a large
number of subjects, while the pat
terns vary from subject to subject.
Large differences in intramuscular
temperature have also been found
between neighboring segments. The
significance of these differences is
expected to emerge from correlation
with other segmental features.
In Figure 1 4 is shown another
device being developed in our
laboratm:ies, for the precise and
objective measurement of muscle
hardness and resiliency, with which
we hope to be able to quantitate
abnormalities in tissue texture
associated with postural and other
disturbances. In addition, Shirley A.
Johnson, Ph. D. , also of the Depart
ment of Physiology, is conducting a
study on the chemical and metabolic
changes in contractured muscle, so
frequently associated with lesion
pathology.
Figure IS shows one approach we
are taking to the sensory or
suprasegmental components of the
lesion complex. This method permits
the precise measurement of cutaneous
pain thresholds at various segments
for correlation with other segmental
measurements. Another procedure is
being designed for the measurement
of hyperalgesia in deeper tissues.
The methods which have been
briefly reviewed here, and others in
process of development, are charac
terized by a high degree of precision
and objectivity in that they are
relatively i ndependent , of the
subjective senses and judgment of the
observer; they are therefore more
easily subject to confirmation. They
are characterized, also, by the fact
that they are applicable to the study
of the osteopathic lesion complex in
its natural habitat, so to speak -as it
occurs in the human body. Through
analyses of the patterns in which
these various segmental features, and
others to be added, appear, we shall
acquire a deeper insight into the
processes which organize those pat
terns. It can be said that, through
these procedures, a true physiological
mosaic of the osteopathic lesion has
begun to be laid.
More direct approaches require, of
course, the use of experimental ani
mals. In one investigation, conducted
by Dr. Johnson and the writer, we are
attempting to evaluate the effect of
myofascial irritations applied to vari
ous segments of the back on renal
function, especially renal hemo
dynamics. We selected the kidney
because methods are now available
for the precise measurement of the
amount of blood flowing through the
kidney per minute, the rate of glo
merular fltration and tubular activity
in the intact unanesthetized animal or
human, and the acute and chronic ef
fects thereon of various experimental
lesions. Its potential importance to
cardiovascular-renal disease is clear.
Figure 1 6 shows an experiment in
progress on one of our six dogs which
have been trained to lie still and at ease
for several hours while they receive
water through stomach tubes (to in
duce diuresis) and intravenous infu
sions and while numerous blood and
urine specimens are taken at precise
intervals.
Other visceral studies, utilizing
roentgenologic and other technics,
are in prospect. In another series
of experiments to be begun in the
near future, we shall undertake a
direct analysis, by electrophysio
logical methods, of the exchange of
excitation between the somatic and
autonomic nervous systems.
Conclusion
In conclusion, we wish to affirm our
belief that from such studies and
from the continuation and expansion
of such surveys as reported in this
Symposium, there will emerge new
and unforeseen approaches to urgent
and universal health problems whose
solutions are inherent in the osteo
pathic concept.
References
I . Korr. I . M. : Emerging concept of osteopathic
lesion. J. Am. Osteop. A. 48:127-138. Nov. 198.
2. Korr, I. M. : Neural basis of the osteopathic
lesion. J. Am. Osteop. A. 47: 1 91 1 98, Dec. 1 947.
3. Swift. R. J. : Small-nerve motor system in
relation to osteopathic lesion. J. Am. OSleop. A.
49:378-380, Mich 1950.
4. Drucker, D. E. : Referred pain and the osteo
pathic lesion. J. Am. Osteop. A. 47:623629, Aug.
198.
5. Denslow. J. S. , Korr, I. M. , and Krems, A. D. :
Quantitative studies of chronic facilitation i n human
motoneuron pools. Am J. Physio!. 150:229238, Aug.
1 947.
6. Burns, L. : Pathogenesis of visceral disease
foHowing vertebral lesions. American Osteopathic
Association. Chicago, 1948.
7. Denslow, J. S., and Hassett, C. C. : Central
excitatory state associated with postural abo
normalities. J. NeuTophysiol. 5:393402. Sept. 1942.
8. Denslow. J. S.: Analysis of variability of spinal
reOex thresholds. J. Neurophysiol, 7: 20721 5. July
1944.
9. Korr. I. M. , and Goldstein, M. J. : Der
matomal autonomic activity in relation to segmental
motor reOex threshold. Federation Proc. 7:67, March
1 948.
10. Korr, L M. : Skin resistance patterns associated
with visceral disease. Federation Proe. 8: 8788, March
1949.
I I . Korr, L M. : Experimental alterations i n
segmental sympathetic (sweat gland) activity through
myofascial and postural disturbances. Federation
Proc. 8:88, March 1949.
12. Thomas. P. E., and Korr, L M. : Semiauto
matic recording of electrical skin resistance patterns.
Federation Proc. 9: 126. March 1950.
Reprinted by permission from JAOA 50:407416.
195 1 .
147
The concept of facilitation and its
origins* (1955)
This symposium is a report on a ma
jor aspect of one of the research pro
grams being conducted in osteopathic
institutions. It has enjoyed the gener
ous support of the osteopathic pro
fessi on t hrough t he American
Osteopathic Association, that of the
National Institutes of Health, and of
the Offce of Naval Research.
In selecting a problem for investi
gation the researcher must identify
the broad general area in which he
wishes to work, the areas which ad
j oin it, the specific portion which he
wishes to explore in the area, the rela
tion of that portion to the others, and
the kinds of information he wishes to
seek. The audience to whom he
reports should have the benefit of
that preliminary perspective. The first
part of this paper is, therefore,
devoted to orientation.
Because the recognition of the
osteopathic lesion and of its impor
tance to the health of man is a distinc
tive feature of osteopathic theory and
practice, it has, in our opinion,
become the unfortunate custom to
characterize researches under osteo
pathic auspices, as researchers on
"the osteopathic lesion, " on "the ef
fects of the osteopathic lesion on"
this or that function or structure, or
some other variation of the same
theme.
We believe that far more than this
is required to identify the area and
objective of each investigation. In ac
cepting such a designation for a
research project one accepts either the
reduction of the scope, meaning, and
complexity of the lesion to the limits
set by the project or one accepts a
most unrealistic estimate of what can
be accomplished by a human being or
group of human beings in a single
endeavor - or even in an entire
lifetime. Even worse, unless the in
vestigator puts his question to nature
explicitly and unequivocably he may
receive answers to questions other
than those he thinks he is asking.
Since a physician must first locate
"Based in part on papers read at the General Sessions,
Fifty-Eighth Annual Convention of the American
Osteopathic Association, Toronto, Canada, July 14,
1954.
148
and diagnose an osteopathic lesion
before he can treat it, the term
"osteopathic lesion" has, through
usage, come to designate, in the
minds of many, a rather simple, dis
crete entity, a thing or structure to
which one can point and on which
one can place his hand. As so often
happens, the designation becomes the
thing itself. I t seems that the osteo
pathic lesion is becoming implicitly
equated with the palpable concomit
ants of the constellation of complex
biologic processes which the lesion
truly represents. In our opinion this is
scientifically as wrong, misleading,
and unproductive as equating gly
cosuria with diabetes mellitus. It i s
as dangerous as assuming that the
visible part of the iceberg i s the
iceberg.
The osteopathic profession is earn
ing its place in the world of the
healing arts through demonstrating
that the above-surface manifestation
is a sign of, and a participant in, a
large, massive, dangerous process go
ing on below, and that forces prop
erly applied to that accessible part
may move the entire iceberg into
warm waters.
Too much research, in our opinion,
has been devoted to "proving" the
existence of the iceberg. l What is
required in order that osteopathy may
now earn its place in the scientifc
world is the disclosure of the nature
of the processes going on below the
surface, their origins, the factors that
influence them and their relation to
the above-surface manifestations.
Further clinical advance in this area
awaits such disclosure by funda
mental research.
The osteopathic lesion - even i f
through usage i t has come to repre
sent only the palpable pathology of
the somatic or musculoskeletal tissues
- must therefore be viewed a rep
resenting the local, somatic factors,
concomitants, and manifestations of
a highly organized response of the
man a a whole to the demands,
stresses, and insults which are part
of his life and to which he is not
quite adequate. These include most
especially the stresses of gravitational
origin to which man' s musculoskele-
tal system is especially subject. This
response involves the interaction of
many processes going on in many
tissues, mediated through the nervous
and circulatory systems and being
continually changed with time, cir
cumstances, activity, and all the
factors operating in the individual' s
life. This i s t he part of the iceberg
lying below the surface. There is no
doubt of its immense complexity.
Here, unlike the nonliving iceberg,
there is not the rigid fixity of
relationship between the conspicuous
and inconspicuous components -
with respect to quantity, importance,
origins, history, or even location.
Faced with such a vast and deep
problem the investigator must care
fully select and equally carefully
define an aspect of the total and the
kinds of information he seeks within
that aspect. He must avoid the danger
of identifying the aspect which oc
cupies him as the osteopathic lesion.
The study, for example, of vertebral
strain or other somatic components i s
not synonymous with the study of the
osteopathic lesion. To assume so is to
destroy its very meaning and to pre
determine a blind-alley investigation.
From the very moment that the verte
bral strain begins, the entire body
is already organizing its responses,
and from that moment on the insult
and the response have no separate
existence.
The area of investigation
The laboratory investigations at
Kirksville have been directed at an
understanding of the role of the
nervous sytem in organizing that
response at the segmental level. The
program of the Department of Phy
siology has been concerned especially
with the mechanisms, patterns and
pathways of interchange between the
somatic and autonomic divisions of
the nervous system.
While not specifically on "the
osteopathic lesion, " these are studies
of factors and mechanisms intrinsic
to it. Furthermore, as will be shown,
"physiologic lesions" have been
demonstrated in these studies which
are closely related, by nature and
location, to the phenomena clinically
identified as osteopathic lesions by
the osteopathic physician.
These investigations are still very
youn, and they have but scratched
the surface. Perhaps their main con-
Interpretation of research
tribution has been not so much the
new information which has been
yielded, but that through that in
formation and through relating it to
other previously explored areas. it
has become possible to restate some
old basic osteopathic problems in
such a way that for the first time
they become approachable by experi
mental methods. In the time that is
available for this research report we
cannot possibly summarize 8 years of
research but we can show our general
strategy. the direction in which we
are probing, a few of the kinds of
information we have found, a few
tentative generalizations, and finally
our interpretation of the clinical
significance of these findings as we
see them now.
The strategy of our approach to
this aspect of the general problem
took its origin in the clinical
observations of thousands of osteo
pathic physicians, over a period of
several decades. Two main general
izations established the point of
departure and direction of our in
vestigation.
1 . The signs and symptoms associ
ated with the osteopathic lesion
include (a) the presence of tenderness,
spontaneous pain or both; (b) altered
functions and activities of the
associated muscles; (c) vasomotor,
sudomotor, and. frequently, visceral
changes. In short, they include dis
turbances in a basic triad of nervous
functions - sensory, motor, and
autonomic. t Our studies are con
cerned with alterations of these
functions, their interrelations, and
their association with other features
at the segmental level.
2. Every osteopathic lesion had its
origin and development in the context
of the life and activities of the in
dividual in whom it is found. The
lesion. therefore. with its associated
sensory, motor, and autonomic dis
turbances, has meaning and is
interpretable only in that context. We
t A virtually unexplored field exists in a fourth
category of nervous function - the so-called trophic
functions. Exploration i n this field awaits the
development and application of satisfactory methods
for the study of the slow. long-term innuences of
peripheral nerve Fibers upon the tissues which they
innervate. in contrast to the faster. recordable.
impulse-transmitted innuences. The trophic functions
of nerve unquestionably have a very important
bearing on the phenomena with which osteopathic
physicians deal. They are a rich field for exploration
by physiologists. biochemists. pathologists and others.
have studied these disturbances (and
their experimental modification) in
their natural "habitat" - in the
voluntary subjects and patients
in whom they are found. (Although
certain aspects and features of the
osteopathic l esi on and related
phenomena may be experimentally
simulated in animals, conclusions
drawn from such studies are applica
ble to the naturally occurring lesion in
man only to the extent that their basic
similarity to the naturally occurring
phenomena can be demonstrated. )
I n order to study the triad of
nervous functions in man it has been
necessary to develop. adapt, and
apply methods which would yield
reliable information regarding activi
ties in regional or segmental sensory,
motor, and autonomic pathways,
which would do so without altering
those activities and without dis
turbance of the human subject him
self, and which would make possible
a comparison of the activities in
disturbed areas with those in the
normal.
With these methods and with
others in continual process of
development i t became possible t o
begin the uncovering of what we have
called a physiologic mosaic - the
related patterns of variations in
sensory, motor, and autonomic ac
tivity in the various segments. From
the patterns in each of these three.
from their relations to each other,
and from their responses to experi
mentally induced or spontaneously
occurring variables it is becoming
possible to deduce the nature of
the processes which organize those
patterns. The details of those
processes and the precise mech
anisms, the patterns, and pathways of
interchange between the somatic and
autonomic divisions of the nervous
system can be studied, of course. only
in experimental animals, in which the
involved parts of the nervous system
can be exposed and directly explored
by electrophysiologic recording of
impulses and by other methods. Such
experiments are now in progress.
Previous studies in this area
Investigations conducted at the Kirks
ville College have indicated that the
musculoskeletal stress initiates, or is
associated with, unbalanced streams
ot Impulses entering the central ner
vous system. and that these have
the effect of upsetting the delicate
balance of that part of the nervous
system with which the lesioned part is
most directly connected. This was
first demonstrated for the muscular
or motor component by Denslow and
his colleagues in the early 1 94's. 46
He demonstrated that the segments
which are in lesion, as determined by
subjective clinical criteria commonly
utilized by him and many other osteo
pathic physicians ( ti ssue-texture
abnormality and deep hyperalgesia),
were objectively distinguishable by
physiologic criteria of motor activity.
Segmental motor refex thresholds
were determined by measuring, in
kilograms, the amount of pressure
applied to the spinous process of each
segment which just evokes contrac
tion of the paravertebral muscles at
that segmental level. Muscular con
tractions were detected and evaluated
by electro myographic recording.
Lesioned segments invariably re
quired weaker stimuli than did non
lesioned segment s. The lesioned
segment was therefore said to be
characterized by lower motor reflex
thresholds - the more severe the
lesion the lower the threshold.
In a later study, Denslow, Korr,
and Krems demonstrated that
diffuse and remote stimuli, including
those from the higher centers, and
stimuli that occur in normal life,
preferentially excited the pathways
to paravertebral muscles of the
l esi oned segment s. Responses
occurred i n these segment s, to
impulses from many sources, while at
the same time nonlesioned segments
remained quiescent . Under condi
tions in which there was generalized
muscular contraction the activity in
the lesioned segments was relatively
exaggerated. The easier opening of
the motor pathways in lesi oned
segments suggested that this was a
sustained form of the phenomenon of
facilitation under study in numerous
neurophysiologic laboratories and
that, like the experimentally induced
form, it too had its origin in a
sustained afferent bombardment by
impulses from some segmentally
located source.
In the next few years the Depart
ment of Physiology adduced a large
body of experimental evidence that
segmental pathways mediating the
other two members of the triad of
nervous functions, namely the
149
Fig. 1 Fig. 2 Fig. 3
Figs. 1-4. A Comparison ofSegmental Pal/ems in the Same Subject.
L
I
Fig. 4
Fig. 1. Lesion Pathology. Diagrammatic representation of the distribution and relative severity of osteopathic lesion pathology as determined by
palpatory examination. Fig. 2. Electrical Ski n Resistance (ESR). Skin resistance oblained with Ihe photographic recording dermohmeter. Dark areas
orrespond to areas of low skin resistance on the subjeci 's back. The resistance of these areas is less than 5 per cent of the high-resistance (white) areas.
The /ighl spots in the mid-line mark the tips of the spinous processes. Fig. 3. Cutaneous Vascular Responses. -Diagram showing the relative intensity
and persistence ofthe red response to standardized mechanical stimulation in different regions on left and right sides ofthe back. The thin lines represent
feeble and short-duration responses in corresponding strips ofskin. Evidence discussed later indicates high vascular tone in these areas. Fig. 4. Activity
of the Spinal Extensor Muscles. Simullaneous electromyographic activity ofthe spinal extensor muscles al the segmental levels recorded while the
subject is standing quietly.
sensory and the autonomic, might
also be maintai ned i n a state of
hyperirritability and hyperactivity.
8 1 1
The sensory component s were
evaluated through measurement of
cutaneous pain thresholds i n various
derma tomes and through mapping
areas of cutaneous and deep hyper
esthesia. The autonomic component,
l i mi ted in t hese s t udi es to t he
sympathetic division because of i
t
s
segmental di st ri but i on, has been
e
v
aluated through measurement of
the activities of the sweat glands and
blood vessels of the ski n. That i s,
these cutaneous structures served as
physiologic i ndicators of the activity
of the sympathetic outflow to the cor
responding areas or segments.
EVidence for hyperirritability of
sensory pathways was found i n the
presence , i n most s ubj ect s , of
persistent areas of l owered pai n
threshold and of tenderness. For the
testing of sweat gland activity we
turned at first to the measurement of
the electrical resistance of the ski n. 8
Ski n resistance had been shown by
others to be lowered by sweat secre
tion and elevated in its absence. (See
Reference 1 2 for references.) The
possi bi l i ty of l ocal or segmental
hyperirritable sympathetic pathways
was first suggested by the finding of
areas with consistently l ow electrical
skin resistance i n most subjects, even
150
under cool resting conditions, when
sweat gland activity was generally
absent. It was also suggested by the
related and persistent areas of rela
tively cool skin and other signs of
high vascular tone.
l l
An ill ustrative case
The ki nds of patterns with which we
are concerned, and their interrela
tionships, wi l l be i l l ustrated on a
si ngle subject. This patient, whose
cl i ni cal status i s not relevant to
this purpose, was explored with the
various methods over a period of
many months during which time the
patterns remained remarkably con
stant . A sample of each of the kinds
of patterns is shown i n Figures 1 -4.
Figure is a diagrammatic repre
sentation of the distri bution and
relative severity of osteopathic lesion
pathology as determined i n a palpa
tory examination by Dr. Denslow.
Especialy conspicuous are the severe
lesions in the lumbrosacral bilateral
ly; the l umbar area, especially on the
right side; and the midthoracic levels
on the right side. The cervical lesions
will be disregarded for this purpose
because the physiologic tests were
l i mited to the thoracic, lumbar, and
upper sacral segments.
The presence of a sensory com
ponent i n relation to this lesion
pathology was manifest in the deep
hyperesthesia present in the same
areas. Measurements by the thermal
radiation method i n our labora
tories showed lowered cutaneous pain
thresholds i n essentially the same
areas.
Figure 2 shows the electrical skin
resistance (ESR) pattern of this
subject as photographically recorded
with an early model of the automatic
dermohmeter developed in our lab
oratories.
1
4 The darkened areas on
the photograph represent the location
on the subject of low-resistance areas
of ski n, whose resistance is less
than 1 120 that of the normal, high
resistance areas, which are unshaded
in this photograph. As an indication
of the sensitivity of the method the
white areas i n this chart indicate
resistances of 20,000,000 ohms or
more, the black areas, 1 00, 000 or
less. The si mi l ari ty i n regional
distribution between the l ow-re
sistance areas and the clinically
determined are
a
s of lesion pathology
is to be noted.
Evidence for segmental l y related
di fferences in vasomotor tone is
shown in Figure 3. This is a diagram
matic representation of the red
responses of the paraspinal skin on
both sides to standardized mechanical
stroking to be discussed later. The
thin lines represent strips of skin
i n which the red, vasodilatation
I nterpretation of research
1
7
illustrate our
investigations of these questions and
some of the answers obtained. As so
often happens in basic research, in
the course of further testing the
hypothesis of facilitation, we also
learned a great deal more about it
and its meaning to the living man.
The studies on the sweat glands are
discussed in the next paper.
Reprinted by permission from "Symposium on the
Functional Implications of Segmental Facilitation".
from JAOA54: 265268, 1955.
151
Clinical significance of the facilitated
state (1955)
It appears from studies such as those
that have been presented, in which
certain sensory. motor, and auto
nomic characteristics are measured
on or near the surface of the body,
that:
1 . Aberrant segments of the spinal
cord occur in most individuals, in
cluding apparently healthy persons.
2. These segments are abnormal in
their tonic activity and in their
responses to various stimuli.
3. In these segments at least some
of the neurons mediating sensory,
motor, and autonomic function are
maintained in a state of hyperex
citability, which they manifest in their
easier, augmented, and prolonged
responses to impulses reaching them
from many sources.
4. They are therefore susceptible to
sustained and exaggerated activity
under conditions of daily life.
5. The infuence normally exerted
by these neurons on the tissues which
they innervate may thereby be exag
gerated.
6. These segmental disturbances
appear to be physiologic lesions
related, by nature and location, to the
clinical phenomena designated as
osteopathic lesions.
Since our experiments showed that
the pathways through these segments,
including those of the sympathetic
outfow, were more easily "opened"
and sustained in activity, these obser
vations further strengthen and enrich
the hypothesis of chronic segmental
facilitation thought to be associated
with the osteopathic lesion.
8
,7s,76 What
does facilitation mean, functionally
and clinically? In general, it means
that the tissues innervated from the
lesioned segment, and therefore the
individual as a whole, are sensitized
to all the infuences operating within
and without the individual.
Facilitation of the sensory path
ways in the disturbed or lesioned
segments means that there is easier
access to the nervous system - in
cluding the higher centers - through
these segments. The lesioned segment
is one through which environmental
changes - especially noxious or
painful stimuli - have exaggerated
impact upon the man.
152
Facilitation of motor pathways
leads to sustained muscular tensions,
exaggerated responses, postural
asymmetries, and limited and painful
motion. Since the muscles have rich
sensory as well as motor innervation,
under these conditions they and re
lated tendons, ligaments, joint cap
sules, et cetera may become sources
of relatively intense and unbalanced
afferent streams of impulses.
The physiopathologic effects of
facilitation of local sympathetic
pathways depend, of course, on the
structures which are innervated by
those pathways; that is, which
viscera, which blood vessels. which
glands. Our studies showed the ex
istence of facilitated sympathetic
pathways to the sweat glands and
blood vessels in the skin innervated
from the disturbed segments and illus
trated the effects of such facilitation
on their functions and on their re
sponses to impulses arising in various
receptors and in the higher integrative
and cerebral centers. It is important
to determine whether these cutaneous
signs are indicative also of facilitation
ofthe sympathetic pathways to other
organs, tissues, and blood vessels in
nervated from the same or related
segments.
Significance of cutaneous signs of
local sympatheticotonia
Experimental studies designed to
clarify this question are now in prog
ress in relation to the kidney. As yet,
the evidence. mainly clinical and pre
sumptive, is strong ( 1 ) that local sym
pathetic hyperactivity refected in the
skin may be associated with sym
pathetic hyperactivity in the viscera,
(2) that the cutaneous manifestations
are associated with disturbances
elsewhere in the segment, and (3) that
local sympathetic hyperactivity is an
important factor in disease. This evi
dence will be briefy summarized.
1 . As stated in the introductory
paper of this symposium, prominent
areas of low ESR are often found in
dermatomes segmentally related to
pathologic viscera. Hyperhidrosis in
dermatomes related to pathologic
viscera has also been demonstrated by
others.77,7
8
2. In a significant percentage of ap
parently healthy subjects, prominent
areas of low ESR marked segments in
which overt disease later appeared or
which were especially susceptible to
disturbances under stressful condi
tions.
3 . Clinical reports are rapidly ac
cumulating in the literature that many
serious clinical entities are associated
with local autonomic imbalance i n
t he direction of sympatheticotonia
(even when the manifestations of the
disease are those which would be
simulated in experimental animals by
parasympathetic stimulation). Symp
tomatic relief, lasting improvement,
and even "cures" have been achieved
through surgical, pharmacologic, or
other blockades of the sympathetic
pathways to the involved organs .7
9
-88
4. A number of visceral and other
chronic diseases
appear to begin as
ischemic states of the involved tissues
due to local neurogenic vasospasm.
This vasospasm seems to be of sym
pathetic origin and is also associated
with vasospasm (pallor, hypother
mi a) in related segments of
skin.
33,34,
6
8-
7
0,8
9
-
9
1
5 . It appears well established
through clinical and experimental in
vestigations that the vasomotor
responses in skin and in viscera are
quite parallel. Stimuli which elicit
vasoconstriction in one, commonly
do so in the other also.
8
9
9
2-
9
6 (This is
the pattern, of course, associated
with diffuse sympathetic activation,
for example, in muscular efforts and
in certain responses to intense envir
onmental or emotional stimulation,
when blood is shunted from viscera
and skin to the skeletal muscles. )
I t appears certain, therefore, that
the facilitation of local sympathetic
pathways to the skin, such as that
demonstrated in our sweat gland and
vascular studies, is commonly part of
a generalized sympathetic hyperir
ritability affecting other tissues inner
vated from related parts of the ner
vous system. It appears equally cer
tain that the resultat sustained loca
sympathetic hyperactivity has con
siderable clinical significance, many
diseases, especially of the chronic
degenerative type, being associated
with, and perhaps ascribable to,
hyperactivity of the sympathetic in
nervation of the affected organs and
of somatic structures refexly related
to them.
Interpretation of research
Why is the exaggeration of sym
pathetic infuence so dangerous and
so frequently an etiologic and con
tributory factor in disease? Normally,
the sympathetic nervous system plays
a most important role in organizing
the adaptive and protective adjust
ment of the body's resources to en
vironmental variations and extremes,
to muscular work, to emotional stress,
to alarm, et cetera. It suppresses the
activity of internal organs not im
mediately involved in the emergency
action and shunts the blood supply
from these organs and from the skin
to the skeletal muscles. But high
levels of sympathetic activity normal
ly occur only intermittently or for
relatively brief periods. When,
however, such sympatheticotonia -
whether local or general - becomes
sustained, then the associated reduc
tion in visceral blood flow, inhibition
of seretory and smooth-muscle activ
ity, spasm or sphincters, et cetera,
eventually result in some damage and
dysfunction of the affected organs
and in disturbance of the entire body
economy.
Nature, origins, and significance of
segmental sympatheticotonia
Our laboratory observations and the
many years of clinical observations in
osteopathic practice appear not only
to have established that the osteo
pathic lesion represents such a state
of local sympatheticotonia, but they
also extend our understanding of its
nat ure, OrI gms , and cl i ni cal
significance.
In the background of the available
knowledge, our studies indicate that
under conditions of daily life there
may be steady streams of impulses
flowing o
u
t of the facilitated seg
ments through the sympathetic path
ways to the structures which they in
nervate, beyond - or in confict with
- demands made by the homeostatic
mechanisms. Under circumstances in
which sympathetic activation or
dinarily occurs, the "drive" through
the facilitated segments is initiated
earlier, reaches higher intensities
sooner, and is sustained longer than
in others. Under conditions of
chronic
'
environmental or emotional
stress, for example, the deleterious in
fluences will be preferentially focused
upon and channelized through the
facilitated segments.
The lesioned segment, therefore, is
Interpretation 0/reults.
How does one translate these pulse
labeling experiments into what is go
ing on normally? What has been
found for the tongue and hypoglossal
nerve of the rabbit may be assumed to
be true, with various modifications,
of other nerves and end organs in
other species. But with regard to the
normal rabbit, our data seemed to in
dicate that at any given time a mix
ture of proteins carried in the hypo
glossal axons is continually reaching
the tongue muscle. Some of it had
been synthesized by the perikaryon a
few hours before, some about a
month before, and the rest at two in
termediate periods. These waves may
be ascribed in part to different rates
of axonal transport of protein and in
part to differences in departure time.
(It is known that some proteins may
remain in the cell body for long as
2 weeks before being dispatched into
the axon.)
It is not certain from these data
alone what portion of each wave of
protein actually enters the muscle
cells, and how much has remained in
the intramuscular nerve endings. This
knowledge must await completion of
our study of the autoradiographs pre
pared from these experiments. Our
previous auto radiographic study cer
tainly gave convincing evidence of
crossing during the second wave.
Although the dogma still persists
among many authors of textbooks
and monographs that cell membranes
are impermeable to proteins, the
penetration of cell membranes by
proteins and even larger particles
seems no longer to be the problem it
used to be. Considerable evidence has
accumulated that large protein
molecules do traverse cell membranes
and intercellular junctions, by active
transport, pinocytosis, discharge of
vesicular contents, or moment-to
moment changes in permeability. At
any rate, there is reason to believe
that cellular barriers are not so im
penetrable as conceptual barriers
often are.
Curent and projected studies.
In order to test the hypothesis that
different neuronal proteins (or mix
tures of proteins) are transported and
delivered to the muscle during the
four different waves of radioactive
protein, Mr. Appletauer and I are
labeling the hypoglossal neurons in
many rabbits, in the manner previ
ously described, and sacrificing them
for the tissue specimens at the peak
periods identified by the previous ex
periments. We are separating soluble
from insoluble proteins by centrifu
gation and measuring the shifts in
distribution of radioactivity between
the two fractions. In addition, we are
fractionating the soluble proteins in
each wave by disc gel electrophoresis
to determine the changing patterns of
distribution of radioactivity among
the many fractions, and to determine
which proteins are found in both the
muscle and its nerve. Although we are
finding many exciting things (in
cluding apparent selectivity as to
which of the nerve proteins reach the
muscle), it is much too early to re
port on these or to draw any conclu
sions.
We hope eventually to be able to
fractionate the insoluble (structural)
proteins also, by gradient ultracen
trifugation and by the use of electron
microscopy to identify the subcellular
components in each of the fractions,
and then to measure the radioactivity
of each.
Clinical implcations.
This work strongly supports the con
cept that peripheral nerves, supplying
various tissues and organs, not only
conduct impulses to or from those
structures, but supply them with pro
teins (and other substances) that are
essential for their maintenance and
self-repair, that i nfluence their
various characteristics and their func
tional capacity, and that condition
their responses to other factors, in
cluding nerve impulses, circulating
substances. hormones, microbes, and
toxic substances. This concept has
many exciting clinical implications.
Some of
'
these have been briefly ex
plored and need not be repeated
here. Suffice it to say that any factor
which for a protracted period alters
the activity (and therefore the energy
exchange), metabolism, or protein
synthesis of the neuron or which im
pedes axonal transport could cause
the neural infuences on the inner
vated structures to become adverse
and detrimental, thereby contributing
to disease. Such factors could include
disturbances (for example, emotional
stress) in descending impulse traffic
from higher centers, impulse traffic
in sensory pathways from various
parts of the body, nutritional factors,
drugs, and toxicologic agents, viral
insults. changes in the chemical en
vironment of the neurons and their
axons, and, of course, the mechanical
stresses and large forces exerted on
and generated by the myofascioskel
etal tissues through which the nerves
pass, and the accompanying chemical
changes in these tissues. It seems like
ly that the efficacy of manipulative
therapy may occur in part through
alleviation of some of these detrimen
tal factors.
References
I. Korr. I. M .. Wilkinson, P. N = and Chornock.
F.W.: Axonal delivery of neuroplasmic components
to muscle cells. Science 1 55:3425. 20 Jan 67
(Reprinted. JAOA 66: 1057-61 . May 67).
2. Korr, I . M .. and Appeltauer. G.S. L. : Studies on
the transfer of neuronal protein to muscle celis,
Preliminary report. JAOA 68: 1 03-5. Jun 69.
3. Korr. I . M . . and Appeltauer. G. S. L. : Continued
studies on the axonal transport of nerve proteins to
muscle. JAOA 69: 1028-30, Jun 70.
4. Korr. I. M . . and Appeltauer. G. S. L. : p onal
transport of nerve-cell proteins to muscle. Abstract.
Fed. Proc. 30:65, Mar-Apr 71 .
5. Korr, I. M. : The nature and basis of the trophic
function of nerves. Outline of a research program.
JAOA 66:984-8, May 67.
6. Gutmann. E + ed.: The denervated muscle.
Publishing House of the Czechoslovak Academy of
Sciences. Prague. 1 962.
7. Gutmann. E and Hnlk, P eds. : The effect of
use and disuse on neuromuscular functions, Pro
ceedings of a symposium held at Liblice near Prague,
September 1823. 1 962. Elsevier Publishing Co
Amsterdam. 1963.
8, Guth. L.: "Trophic" infuences of nerve on
muscle. Physiol. Rev. 48:65-87. Oct M.
9. Guth, L. : "Trophic" effects of vertebrate
neurons. A report based on an NRP work session.
Neurosci Res Prog Bull 7: 1 70. Apr 69.
10. Gutmann. E.: Metabolic reactibility of the
denervated muscle. In Guttman '.
I I . Hix. E. L. : The trophic function of visceral
nerves. In Symposium: The physiological basis of
osteopathic medicine. Postgraduate I nstitute of
Osteopathic Medicine and Surgery. New York. 1 970.
12. Singer. M. : Nervous control of the regrowth of
body parts in vertebrates, In Gutmann and Hnik.' pp.
83-94.
1 3, Mizell. M. : Limb regeneration. Induction in the
newborn opossum. Science 161 :2836. 19 Jul 68.
14. Barondes. S.H and Samson. F.E . . Jr.: Ax
oplasmic transport. A report of an NRP work session
held April 2-4, 1967. Neurosci Res Prog Bull
5: 307-41 5. IS D67.
1 5. Grafslein, B.: Axonal transport. Communica
tion between soma and synapse. Adv Biochem
Psychopharmacol I: 1 1 25. m.
16. Lasek, R. J. : Protein transport in neurons. Int
Rev Neurobiol. 1 3:289324. 70.
17. Weiss, P e and Hiscoe. H, B, : Experiments on
the mechanism of nerve growth, J Exp Zool
107: 31 595, Apr 48,
This study was supported by PHS Research Grant No.
NS-0791 9 from the National Institute of Neurological
Diseases and Stroke. and by a grant from the
American Osteopathic Association.
Reprinted by permission from JAOA 72: 1 63 1 71 ,
1972.
I8T
The facilitated segment: A factor in injury
to the body framework (1973)
Osteopathic physicians have always
relied for their diagnostic evaluation
of stresses and strains of the musculo
skeletal system upon the subjective
sensations and perceptions that
emerge from their palpatory and kin
esthetic examinations. They are con
cerned with such things as very subtle
changes in tissue texture, tissue defor
mability, elasticity, resilience, joint
motion, and other such characteris
tics. These are purely subjective judg
ments that are made from moment to
moment, and guide the physician's
diagnosis and therapy.
These procedures introduce tre
mendous difficulties in communi
cation, because a sensation is entirely
private - something that simply can
not be shared. This is true of all sen
sation, but there is a special
d
ifficulty
with respect to palpation, because
while any two or more persons can si
multaneously look at the same view
or listen to the same sounds, or taste
the same concoctions, no two people
can put their fngers upon the same
spot precisely at the same moment.
They can do it only in sequence, and
this introduces real problems of com
munication between professions, be
tween people, from teacher to stu
dent. It is something we are still
studying.
In the late 1 930's and the early
1 940' s, 1. S. Denslow, D. O. , a distin
guished faculty member at Kirksville
College of Osteopathic Medicine
began a series of studies to see if he
could objectify the procedures that all
osteopathic physicians do, each in his
own way, each one paying particular
attention to skin or muscle or deeper
structures. Denslow paid much atten
tion to the textur.e of the tissues over
the spinous processes, and he was in
terested in the responsiveness of the
paravertebral musculature, to the dig
ital pressure that he applied to the
spinous processes. But he recognized
that this type of observation was the
same as that made by other osteo
pathic physicians who noted related
tissue changes in the area that for
many years we have called the osteo
pathi lesion.
So Denslow started to measure the
pressure that is applied at each spinous
18
process, each segment, and electro
myographically to determine what
pressure is required to elicit the first
signs of refex response of the muscles
at the corresponding segments. In
other words, he did what the physiol
ogist knows as the measurement of
motor reflex thresholds, except that
instead of electrical stimulus to this or
that nerve, Denslow applied mechan
ical pressure measured from 1 to 7 kg
of pressure to the tip of the spinous
process, and recorded that pressure
which brought about a reflex re
sponse as indicated on the elec
tromyogram
. 1
,
2
Denslow was the first osteopathic
physician to be elected to membership
in the American Physiological Society
on the basis of these investigations
and those that followed.
Out of these early observations
emerged the conclusion, that the so
called area of osteopathic lesion was
related to a segment of a spinal cord
in which the reflex motor thresholds
had been lowered. It took less pres
sure to elicit the first reflex response
of the paravertebral and paras pinal
muscles.
Denslow studied large numbers of
subjects and emerged with the rather
important generalization that this
segmental lesion was one with a low
motor reflex threshold.
As he studied subject after subject,
he found that the patterns of distribu
tion of the low thresholds were rather
enduring. A given individual could be
picked up week after week, month
afer month, and essentially the same
pattern of distribution of low thresh
olds would be found, and the patterns
were somewhat characteristic of the
individual.
Nevertheless, there were certain
areas that were found to be more vul
nerable than others: in the neck,
especially at the atlanto-occipital area
at the junction of the cranium and
cervical spine; at the junction of the
cervical spine and the relatively rigid
thoracic spine; and in the lumbosacral
area. These were the areas of high
est frequency of low thresholds or
"osteopathic lesion.
t t
Having j ust joined the Kirksville
faculty, I developed a great preoccu-
pation with the osteopathic lesion. I
worked with Denslow in the labora
tory where volunteer students were
the subjects, recording readings from
the application of the pressure meter
he had devised. I determined that low
reflex motor thresholds were found in
the area of the osteopathic lesion and
that high refex motor threshold areas
of the spinal tissues indicated normal
,segments. This led us into the in
vestigations of the physiological
mechanisms underlying the lowering
of refex motor thresholds in seg
mental spinal areas. ' From this
work emerged the concept of
"'hronic segmental facilitat ion, "
reflecting the hypersensitivity and
hyperresponsiveness of the affected
segments of the spinal cord to im
pulses from virtually any source in
l
the body.
Details of this work and other
related studies have been brought
together in a publication from the
Postgraduate Institute of Osteopathic
Medicine and Surgery. Some very
practical ideas and procedures have
merged from our studies.6
1
2
The literature on the sympathetic
i system, which has become a specialty
:
for me, indicates that in almost any
kind of trauma to the musculoskeletal
system or, for that matter, to any
visceral system, the sympathetic ner
vous system is almost invariably
brought into play. And very often it
rticipates in a most inappropriate
( manner, which not only does not con-
tribute to recovery from the injury,
but actually produces trouble that
_ prolongs it. It exaggerates and exacer
b
l
tes the disturbance, and tends
toward positive feedback. toward the
perpetuation of vicious cycles. The
syndrome - the injury - becomes
more and more disabling the more
overactive the sympathetic nervous
system becomes.
Conversely, therapy directed to
normalizing or quieting the involved
segments of the sympathetic nervous
system is very often quite beneficial,
and sometimes almost miraculous, as
shown in the classic studies of S. Weir
Mitchell on causalgia and causalgia
like syndromes during the Civil War.
We know that the sympathetics are
the main vasomotor controlling
system of the body; they control the
caliber of most of the vessels of the
body. Therefore, when the sympa
thetics are hyperirritable in a given
Interpretation of research
area, in a given segment, in a given
peripheral distribution, there is in that
area a tendency for either exaggerated
vasoconstriction or exaggerated vaso
dilation, or a mixture of the two,
which contributes to chaos and the
perpetuation of pathology. When you
control the blood supply to a given
area, you control its life; you control
its capacity for recovery, its capacity
to resist infection, its capacity to sur-
vive and maintain its integrity as a
tissue.
f - -
-
- - - - - - - -
-
-
g = = = = = = = = = = = = = =
g = = = = = = = = = = = = = =
g = = = = = = = = = = = = =
g= =e- - - -.. - . =
g = = = = = = = = = = = = = = =
g= = = - = = = = = = = = = =
g = = = = = = = = = = = = = =
g = = = = = = = = = = = = = =
g = = = = = = = = = = = = =
g = = = = = = = = = = = = = &
g = = = = = = = = = = = ==
g = = = = = = = = = = = = = =
g = = = = = = = e = = = = =
gee e e eeeeeee
g = = = = = = = = = = = = = =
gm= = = = = e
Fig. 5. Somatic structur, including the musculoskeletal system (and the nervous system itsel are
repreented on the left side of the diagram. Note that somatic strcturs receive their autonomic
supply excusivelyfrom the sympathetic diviion (via the spinal nerve).
features are immediately evident:
1 . Unlike the parasympathetic divi
sion, whose sphere is almost entirely
visceral, the sympathetic division pro
vides autonomic innervation to every
part of the body, including the ner
vous system itself.
2. Unlike the parasympathetic,
which is really a collection of highly
"private" lines to individual organs
and tissues, divergence is a conspicu
ous feature of the SNS. Note, first of
all, the rather extensive origin in the
spinal cord, then the "fanning-out"
of the preganglionic axons to ganglia
along the entire length of the verte
bral column and to the collateral gan
glia and, from these, the spread of the
postganglionic axons throughout the
body.
3. To be emphasized again is the
general vasomotor role of the SNS,
which is part of its capacity for
mobilizing resources throughout the
body.
4. Finally. a is symbolized in
Figure 6, the SNS is, in effect,
strategically situated between the
visceral and somatic tissues, whereby
218
it can adjust function of the viscera
(right side of the diagram) to the
demands and requirements of the in
tegumentary and neuromusculoskel
etal systems (left side) .
Obviously, unlike the parasympa
thetic division, the organization of
the SNS provides for coordinated,
body-wide broadcasting of sym
pathetic influences, reinforced and
sustained by circulating epinephrine ,
and norepinephrine from the adrenal
medulla. Yet, like the parasympathet
ic, the SNS is also capable of selec
tive, localized activity. Central activa
tion of the entire sympathetic divi
sion, as in exertion, emergency (real
or perceived), or environmental ex
tremes, results in well-orchestrated,
adaptive changes in visceral, circula
tory, and metabolic activity through
out the body. The SNS, therefore,
can be appropriately described as a
system. I n contrast, the unlikely event
(fortunately) of central activation of
the entire parasympathetic outflow,
that is, simultaneous, intense activity
of all four pairs of cranial nuclei and
the sacral nuclei or the circulation of
a (nonexistent) parasympathomimetic
hormone corresponding to the
adrenomedullary hormones, would
result in utter physiologic chaos.
Relation ofperipheral ANS to
somatic innervation .
In accordance with functional rela
tions of the SNS to the musculoskele
tal system, and its responsiveness to
environmental changes (for example,
in thermoregulation), the SNS is also
intimately related anatomically to
musculoskeletal innervation, both
sensory and motor. As Figure 7
shows, SNS outflow and the motor
supply to the skeletal muscles begin
close together in the cord, where they
are subject to many of the same pre
synaptic influences. The axons of the
preganglionic cells and of the moto
neurons then leave the cord together
via the ventral roots, the motor axons
proceeding to termination in skeletal
muscles, the preganglionic axons
proceeding to synapses in the ganglia.
However, the motor axons are again
rejoined by sympathetic fibers, name
ly the postganglionic axons entering
the spinal nerves (via the rami com
municantes) , on their way to tissues
of the neck, trunk, and extremities.
Because motoneurons and sympa
thetic preganglionic neurons are sub
ject to similar presynaptic sensory,
intraspinal, and supraspinal (that is,
higher-center) inputs, they are also
both vulnerable to disturbances via
these inputs. Similarly, since their ax
ons course together in the spinal roots
and in the spinal nerves, which also
include somatosensory fibers, soma
tic and sympathetic fibers are to
gether vulnerable to deformation and
other trauma of bi omechanical
origin. The clinical implications of
these somatosympathetic distur
bances were discussed in the previous
paper, and their mechanisms and
manifestations will be the primary
subject of the next. It is neverthe
less important to emphasize that
every human action involves the si
multaneous, coordinated activity of
the somatic and autonomic nervous
systems, and that dysfunction of one
inevitably leads to dysfunction of the
other.
Like the SNS, the sacral outfow of
the parasympathetic division also has
close functional relations with the
musculoskeletal system, as in elimina
tion, sexual intercourse, and parturi-
Interpretation of research
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4- - ~ - - - - - ~- ~~ ~
0 * - - ~ ~ ~ ~ ~ - ~ -
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4
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4~ - - - - - - - - -
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- - - - ~ - - - - - - - - -
4 - . - - _ _ - - _ - _ - - -
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4
~ ~ ~ ~ ~ ~ ~ ~ _ . . . . .
~ - * * - * * - * *
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~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~
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9~ ~ * ~ =
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Fig. 6. Schema ofthe peripheral autonomic nervous system, completed. (Reprinted with permision.),
tion, in which coordination of vis
ceral and motor activity is essential.
Accordingly, this part of the para
sympathetic outfow has its origin
and course in close relation to the
motoneurons . In contrast, the entire
cranial outflow has little if any re
lation to motor function, in accor
dance with its remoteness from in
nervation of skeletal muscle.
Afferent pathways in relation to ANS.
The sensory inputs to which they reo
spond also reflect the respective roles
of the two divisions of the ANS. The
responses of the SNS to sensory input
from receptors in skin, muscle,
j oints, et cetera, via segmental and
suprasegmental pathways, in what
have come to be called somatosympa
thetic reflexes, are highly organized
and adaptive. Feedback from pro
prioceptors is important in local and
regional adjustments according to site
and kind of activity. These reflexes
have been the subject of intensive
study and excellent reviews in recent
years .6-8 Disturbances in these reflexes
and their clinical manifestations have
been previously reviewed, 9 and will
be examined in Part I I I of this
series. l I need only emphasize now
that since this continual sensory feed
back from the soma to the SNS is es
sential for normal function, somatic
dysfunction will also be communi
cated to the SNS, with adverse effects
on other sympathetically innervated
structures.
Although both divisions are assem
blages of efferent pathways, numer
ous sensory fibers run in "sympathet
ie" nerves such as the majority of the
splanchnic and in parasympathetic
nerves such as the vagi and pelvic
splanchnic. Those in the sympathetic
trunks are excited by noxious, painful
states in the viscera, such as severe
di stenti on, chemi cal i rri tati on,
spasm, and ischemia. It is of interest
that these "pain" fibers, through
interneurons, not only sti mulate
sympathetic preganglionic neurons in
the cord, thus producing changes in
target organs (for example, viscera,
blood vessels, sweat glands), but they
also excite neighboring motoneurons,
producing the sustained muscular
contractions so often associated with
referred pain of visceral origin.
In contrast, the sensory fibers run
ning within parasympathetic nerves
bring feedback from various report
ing stations in the viscera. In vagal af-
ferent pathways, for example, these
signals serve mainly regulatory roles
in respiration, circulation, digestion
and other visceral functions. In the
sacral circuits, t hey signal such
circumstances as fullness, that i s,
readiness for evacuation, of uri
n
ary
bladder and rectum. In these sacral
examples, muscular activity is in
voked to assist and help to execute
primarily visceral activity. The con
verse is true of the SNS, which ad
justs visceral function to support
muscular activity.
Repertoire ofSNS.
In view of the divergence of the sym
pathetic outflow to virtually every tis
sue in the body, it is important to ask
what effects impulse activity in these
efferent pathways has on all these di
verse tissues and organs. This is a key
question to explore in preparation for
a survey of the clinical effects of sym
pathetic hyper-activity, which is the
subject of the third article in this
series. `
As has already been mentioned,
there seems to be a prevalent miscon
ception in this regard, too. The tradi
tional view is that whatever the ef
fects of sympathetic activity (and,
119
Fig. 7. Cros-section of the spinal cord at thoracic or upper lumbar levels. Sensory (dorsal root
ganglion) neurn and their fibers (black), convey impulse from receptors and endings in somatic
and visceral tis ue. Motoneuron (ventral hor cel/s, lighter) and their aons supply motor
innervation to skeletal musculatur. Sympathetic neurons (lghtet), the preganglionic neurons in
the intermediolateral cll column, whose fbers (sold lines) synapse in ganglia with postganglionic
neurns the aons of which (interrpted lnes) innervate vicera and certain components of somatic
tisue. A sondarysensory neuron (spinothalamic) conves impulses to higher centers and mediate
sensations of pain and temperature. (Reprinted with permis ion.) 2
presumably, hyperactivity), they are
mediated by regulation of contraction
of smooth or cardiac muscle (the
smooth muscle including that of
blood vessels) and of secretion by
exocrine glands, such as sweat glands
and glands of the digestive tracts.
The truth is, however, that the
sympathetic repertoire is a great deal
more diverse than that, as the follow
ing few examples will indicate. (The
experimental and clinical evidence for
the following statements, and the cor
responding bibliographic references,
can be found in an earlier paper.)9
1 . Mucle. Stimulation of the sym
pathetic innervation of skeletal mus
cle increases the force of contraction,
diminishes the fatigue of repetitively
stimulated muscle or delays its onset,
and facilitates neuromuscular trans
mission.
2. Peripheral sensory mechanims.
Sympathetic activity influences the
function of various sensory organs, in
most cases in the direction of in
creased excitability, that is, lowered
thresholds and exaggerated frequency
of discharge. Receptors and sensory
organs in which this effect has been
demonstrated include muscle spin
dles, tactile receptors, taste receptors,
ol factory apparatus, chemo- and
baroreceptors of the carotid sinus,
pacini an corpuscles, retina, and
cochlea.
ZZ0
J. Central nervous system (CNS).
Sympathetic influences, demon
strated by stimulation, ablation, in
terruption, ganglionic blockade, et
cetera, have been shown on various
parts of the eNS, including the cere
bral cortex and subcortical structures,
reticulospinal system, hypothalamus,
cerebellum, and spinal cord. Effects
have been shown on behavior (for ex
ample, alteration of established con
ditioned motor reflexes), electro
encephalographic patterns, responses
to various kinds of stimuli, motor
reflexes, and many others, signifying
a direct influence on neuronal ex
citability and activity.
4. Development ofcolateral circu
lation, following arterial occlusion, is
impeded by sympathetic activity and
is accelerated by sympathectomy.
S . Sympathetic activity exerts an
important influence on activity of
bone cels and on longitudinal bone
growth.
6. Stimulation of the sympathetic
innervation of adipose tissue favors
lipolysis (release of free fatty acids
and glycerol), whereas interruption of
impulse traffic increases fat content,
a result that suggests a tonic influence
on fat metabolism. Indeed, the rapid
lipolysis that takes place during cold
exposure and the slow lipolysis during
starvation do not occur in sympathec
tomized fat pads. These sympathetic
influences on lipid metabolism have
been shown to be quite independent
of sympathetic influences on blood
fow.
7. Reticuloendothelial system.
Since bone marrow has a rich sym
pathetic innervation, it is not surpris
ing to find effects of sympathetic
activity not only on blood flow, but
on erythropoiesis, phagocytic activity
of reticuloendothelial cells, release
and distribution of leukocytes, and
endothelial permeability.
8. Sympathetic influences have
been demonstrated on various en
docrine organs, including thyroid,
adrenal cortex, pancreas, testicle, and
pineal body. The pineal body is of
special interest in this connection. Its
elaboration of melatonin, which in
fluences growth, gonadal develop
ment, and sexual activity, is con
trolled by sympathetic innervation
from the superior cervical ganglion.
The secretion of melatonin follows a
diurnal cycle in that synthesis is in
creased in the dark (inhibiting growth
and sexual development) and de
creased in the light. When the sym
pathetic fibers to the pineal body are
sectioned, the diurnal fluctuation of
melatonin synthesis and the as
sociated diurnal changes in behavior
cease. Under these conditions, the
animal kept in the dark is no longer
subject to the antigonadal and
growth-inhibiting influence of the
pineal body.
9. Many other examples could be
given of sympathetic influences on
enzyme activity, mitosis, synthesis of
nucleoproteins, growth and develop
ment, and on responses of various tis
sues to other factors (for example,
hormones, parasympathetic stimula
tion, toxins).
The variety of the effects of stimu
lating peripheral sympathetic path
ways does not lie in the sympathetic
neurons or their influences, but in
the responses of the organs that are
innervated. These responses are as
diverse as the target tissues and
organs - virtually every tissue in
the body. Sympathetic stimulation,
rather than introducing new qualities,
modifies the inherent physiology and
molecular processes of the compo
nent cells, so that each tissue re
sponds in its own way.
This provides the basis for under
standing the diversity of clinical con
sequences (discussed in a succeeding
Interpretation of research
paper)' of chronically exaggerated
sympathetic influences associated
with somatic dysfunction. IO'ls
Appreciation is expressed to Mr. Robert N.
May, Director, Audiovisual Department,
Kirksville College of Osteopathic Medicine. for
the illustrations in this paper and for teaching
the author the principle of "progressive
disclosure .
.
.
References
I . Korr. I . M. : The spinal cord as organizer of
disease processes: Some preliminary perspectives.
JAOA 76:3545, Sep 76.
2. Korr, I . M. : The sympathetic nervous system as
mediator between the somatic and supportive pro
cesses. I n The physiological basis of osteopathic
medicine. by The Postgraduate I nstitute of Os
teopathic Medicine and Surgery The Institute, New
York, 1970.
3. Hess, W. R. : The diencephalon -autonomic and
extrapyramidal functions. Grune & Stratton, New
York, 1954.
4. Netter, F. H. : The Ciba collection of medical i1.
lustrations. The nervous system. eiba, New York,
192. Vol. I, plate 54, p. 81 .
5 . Korr, I. M. : The spinal cord as organizer of
disease processes: Hyperactivity of sympathetic
innervation as a common factor i n disease. JAOA,
Dec 79, in press.
6. Kolzum!, K. , and Brooks, CM. : The integration
of autonomic system reactions: A discussion of auto
nomic reflexes, their control and their association with
somatic reactions. Ergeb PhysioI 67: 1-68, 1972.
7. Sato, A., Ed.: Central organization of the auto
nomic nervous system (Symposium). Brain Res
(Spcial issue, No. 213) 87: 137448, I I Apr 75.
8. Coote, J. H. : Somatic sources of afferent input as
factors in aberrant autonomic, sensory and motor
function. In The neurobiologic mechanisms in manip
ulative therapy, edited by I.M. Korr. Plenum Press,
New York, 1978.
9. Korr, LM. Sustained sympathicotonia as a factor
in disease. In op. cit, ref. 8.
1 0. Korr, I . M. , Thomas, P. E. , and Wright, H. M. :
Patterns of electrical skin resistance in man. Acta
Neuroveg 1 7:77.96, 1958.
I I . Wright, H. M. , Korr, I . M. , and Thomas, P. E. :
Local and regional variations i n cutaneous vasomotor
tone of the human trunk. Acta Neuroveg 22:3352,
196.
12. Korr, I . M. , Wright, H. M. , and Thomas, P. E. :
Effects of experimental myofascial insults on cutane
ous patterns of sympathetic activity in man. Acta
Neuroveg 23:32955, 1962 .
13. Wright, H. M. : Progress in osteopathic research:
A review of investigations in the Division of Physio
logical Sciences, Kirksville College of Osteopathy and
Surgery. IAOA 61 :34752, Jan 62.
14. Korr, I . M. , Wright, H. M. , and Chace, I. A. :
Cutaneous patterns of sympathetic activity in clinical
abnormalities of the musculoskeletal system. Acta
Neuroveg 25: 5896, 19.
15. Wright, H. M. : Perspectives in osteopathic
medicine. Kirksville College of Osteopathic Medicine,
Kirksville, Mo., 1976.
Reprinted by permission from JAOA 79:82-9, Oct
1979
The third paper in this series, "The spinal cord as
organizer of disease processes: Hyperactivity of
sympathetic innervation as a common factor in disease
process," appeared in JAOA in December 1 979. This
paper is a less technical version of a longer paper in
this collection, "Sustained Sympathicotonia as a
Factor in Disease," which begins on page 77.
111
IIZ
l
"
'
Osteopathic principles,
practice and profession
223
'
l
These
factors have "contributed more to
the control of infection than did all
drugs and medical practices. "
2. P
:
//
"The toll of human lives exacted by
i nfection had begun t o decrease
several decades before control
measures inspired by the germ theory
were put into effect and almost a cen
tury before the introduction of an
ti mi crobi al drugs . "
~:
6
3
The
"monster of infection" had become a
mere shadow of itself before medicine
could provide rational and scientific
methods for its control. The effect of
the antibacterial drugs has been but a
"ripple" on the long-established
decline in mortality, a decline largely
attributable to widespread improve
ment in human factors.
This is not to deny, of course, the
great effectiveness of drugs and
medical practices in interrupting and
preventing many infectious processes,
even many which would be fatal, but
it is to put them in proper - and
urgently needed - perspective.
Moreover, this is not merely a matter
of historical perspective, for it has
critical bearing on our present prob
lem.
Etiologic-curative medicine, so
preoccupied with disease and death
and with their, microbial "causes, "
finds little of interest in the human
factors which permit them to become
causes. Overlooked is the simple but
vital everyday observation that while,
certainly by defnition, microbes are
essential elements in the production
of infectious diseases, the fact re
mains that infection usually occurs,
and even exists for whole lifetimes,
without production of disease.
Disease i s the exception. It is the con
sequence, not of infection, but of a '
breakdown of the mechanisms of ad
aptation and resistance . . . In man the
provocative cause of microbial dis
ease may be a disturbance in any of
the factors of his external or internal
environment. . . ."
/
'
P
:
7
9
As Pasteur
himself said, unrestricted multiplica
tion of germs is no less a consequence
of illness than its cause. For this
reason, "drugs cannot be effective in
the long run until steps have been
taken to correct the physiological and
social conditions originally responsi
ble for the disease . . . . "
2
.
J7
Thus, constructive a force as the
doctrine of specific etiology has been
in medical research, it cannot provide
a satisfactory account of the causa
tion of even the microbial diseases, in
which specific etiologic factors are
known. A system of medicine which
bases itself on such a doctrine, which
directs its skills so much against infec
tious agents and so little for the man;
which relies so much on bullets and
Osteopathic principles
shotguns aimed at the infinite variety
of infectious agents, while neglecting
to identify and influence the factors
which determine man' s vulnerability
and resistance to all of them; a system
which disregards and upsets the
natural processes of mutual adapta
tion between man and microbe -
such a system can only continue to
fail to meet even the problems of in
fectious disease, which it proclaims as
its area of greatest success. Even
worse, it creates new problems, some
times worse in the long run than those
that are "sol ved. " The current
"staph problem" which is plaguing
American hospitals is but one exam
ple.
Great as has been this general fail
ure with respect to the infectious
diseases, how much greater is the
failure - etiologically, therapeutical
ly, and preventively -with respect to
those diseases which cannot even
remotely be ascribed to invading
agents and which today are even a far
greater burden than the infectious
diseases. They, the chronic killers and
cripplers - the heart and cardiovas
cular diseases, the metabolic diseases,
the collagen diseases, cancer, peptic
ulcer, and many other long-term
diseases - are, even more than the
infectious diseases, the products of
whole constellations of human fac
tors. These now present a burden of
incalculably immense proportions,
already overwhelming even the
palliative resources of medicine and
growing at an increasingly rapid
rate.417 A system which continues in a
hopeless quest for the causes of each
and the cures for each, while neglect
ing the human factors from which
they do arise, can only be regarded,
basically, as a fai l ure, however
brilliant, effective, and welcome the
expedient measures with which it tem
porizes.
Unlike the i nfectious diseases,
which man shares with other animals,
the degenerative diseases are almost
peculiar to man. It is a challenge to
the experimenter to produce even
thei r most palli d facsi mi l es i n
ani mal s. The natural , bui l t-i n
defenses, w
h
ich man shares with
other animals, ag
a
inst the microbial
pathogens - fever, inflammation,
immune reactions, phagocytosis, and
so forth - are the adaptive products
of evolut i on. The degenerati ve
diseases are quite another problem.
As t he expression of pecul i arl y
human frailties, "natural" and self
inflicted, they, and not the defenses,
are the products of human evolution.
Indeed, there can be few if any adap
tive biologic defenses against the
rapidly changing stresses peculiar to
human l i fe, many of them man
created, and certainly not against
man's own inadequate or misdirected
responses to those stresses. In most
circumstances the biologic responses
and "adaptations" are worse than
the provoking factors and are in
themselves disease. Not only are they
not self-limiting, but they become
sustaining and exacerbating factors,
initiating and propelling vicious cir
cular processes which continually ex
act larger and larger tolls of the in
dividual as he ages, and as the dis
parity widens between his biologic
resources and the demands upon
them. In effect, the patient writes
larger and larger checks on a shrink
ing account.
For the most part, the chronic
degenerative diseases are not the "ef
fects" of specifc "causes" which can
be identifed, exorcised, combated,
and abolished with magic bullets.
They are the products of whole lives.
Their origins and their basic manage
ment (in contradistinction to their
palliation) are to be found in the
unique nature of man, of his life and
of his environment, in the differences
among men that cause them to em
bark on separate and divergent physi
ologic paths, in the fact that man is
required to live a human life with
biologic apparatus which he inherited
from lower animals. Hopes lies in the
creation of those circumstances which
will permit each individual to stay on
hi s most favorable physiologic paths
and defect him from unfavorable
paths. To speak of causes, cures, and
reversal is to reveal ignorance of the
basic character of chronic degenera
tive disease.
A study recently completed at Cor
nell University Medical College by
Hinkle and W 0lffl 8 magnificently
epitomizes the primacy of human fac
tors in all disease. The illness pat
terns, during 20-year periods in
young adulthood, of approximately
3, 50 people drawn from the ambula
tory populati on, revealed t hat
episodes of illness were most uneven
ly distributed. One fourth of the in
dividuals experienced a majority of
all the episodes of illness that had oc
curred among all of the people, while
another fourth had only 5 to 1 0 per
cent of the illnesses.
Even more startling than the wide
differences in susceptibility was the
comprehensiveness, the non-selectiv
ity, of the susceptibility. The authors
state:
These differences in susceptibility to illness
were not simply the result of differences in
susceptibility to one or another specific syn
drome. In every group the members displayed a
difference in their susceptibility to illnes in
general, regardless 0/its type, or 0/the causal
agents involved. Thus, as the number of
episodes of illness experienced by an individual
increased, the number of different types of
disease syndromes that he exhibited increased
also. Although a great many of these syn
dromes might involve one or two organ sys
tems, episodes of illness were not limited to a
few systems; instead, as the number of episodes
of illness experienced by an individual in
creased, the number of his organ systems
involved in disease increased also. Likewise, as
the number of episodes he experienced in
creased, he exhibited illness of an increasing
variety of etiologies. He was likely to have
more 'major' , irreversible and life-endangering
illnesses, as well as more 'minor', reversible
and transient illnesses. [Italics supplied.]
In the opinion of the authors, these
findings are most reasonably ex
plained by assuming that they are
dependent upon "factors operating
within the individual, " influencing
his responses to the "great variety of
other factors known to be capable of
causing disease. " Consistently high
illness rates in susceptible individuals
refect continuing inability of th
e
in
dividual to make adequate adapta
tions to his total milieu.
One of the most significant results
of the study was the remarkable con
stancy of individual illness patterns.
for it indicates "that the illnes pat
terns of these people were relatively
little infuenced by the therapeutic ef
forts of the physicians who treated
them. (Italics supplied.) It may be
assumed that these "therapeutic ef
forts" were reasonably representative
of specifistic-etiologic medicine and
included a representative sampling of
the several hundred new pharmaceu
tical products and miracle drugs pro
duced each year, I 9 selected for their
effectiveness in each illness. Perhaps
nothing more clearly dramatizes the
basic inadequacy of a system of
medicine which, in the name of
sc
i
ence. concentrates so hard on in
dividual diseases, their "causes" and
their "cures, " while, in its contempt
for what it regards as armchair
IJT
philosophy, it so tragically disregards
the man and the factors in him which
determine his vulnerability to illness
in general. As Hinkle and W olffl 8
conclude:
Ultimately medicine will have to take account
of this in treatment of illness. It is very prob
able that an increasing proportion of the
therapeutic effort will have to be directed at the
patient's relation to his environment i we wih
to make any signicant improvement in hi
health . . . . The problem stands before us as a
stern challenge to medicine, and not as an easy
opportunity. [Italics supplied.]
Obviously, it is becoming more
widely recognized that disease, and
most particularly the rapidly rising
tide of degenerative disease, can be
stemmed only through identification
and control -especially prophylactic
identification and control - of the
variables in the human organism and
in his life situations which determine
the physiologic path he travels.28
This recognition, however, has had
little impact on medical practice. The
basic strategy remains essentially un
changed, though a transformation in
medical knowledge and technic has
taken place. Society' s urgent need for
the holistic-ecologic-physiologic ap
proach is now far greater than ever.
That approach now offers the only
hope. But, unfortunately, this move
ment still awaits organized, dedicated
leadership and implementation. This
is the movement, the great improve
ment in the design of health care, that
this profession, as its only organized
voice set out to lead 67 years ago. 1 6
Seldom i n history has an organized
group of men and women perceived,
grasped, and then seemingly relin
quished, a greater opportunity.
Presented, by its history and now by
society, with an immense opportuni
ty, your professi on still debates
whether it has a function of its own
and a reason for existence, and
wonders where the resources would
come from if it had.
Fortunately, there is still time - a
little time - for a second chance.
Were this profession to proclaim to
the world, again and again, factually,
clearly, courageously, that this is the
movement it seeks to propel, and
why; and were it to demonstrate that,
given the means, it is qualified to do
so, it woule be given the means.
There is no doubt that the frst
criterion, "Is there need for a change
of system?" is amply satisfied.
Is thi function appropriate to, and
238
within the power of the osteopathic
profession?
Not only was thi s movement
toward holistic medicine your found
ing purpose; it is a rich part of your
total experience as a profession. It is
more deeply a part of your insights
than of any other profession, more
than you apparently recognize and
certainly more than now finds expres
sion in your function as a profession.
Your profession is still the greatest
reservoir of physicians oriented in its
principles and skilled in their applica
tion. You are now stronger, better
organized, better armed, more ac
cepted than ever before. Though you
are now preoccupied with numbers,
some of your greatest assets are those
provided by your small size: mobility,
maneuverability, flexibility. You
have the independence that imparts
power to every minority movement.
You lack only the commitment, the
conviction, the objectives to put that
power into motion and to give it
direction.
Does it offer comprehensive design
for your total effort and for the
mobilization and utilization ofyour
resources?
The answer to this question also is
a resounding affirmative, as you
would discover. Long absorbed in
catching up and keeping up with all
the advances in modern medicine and
with meeting standards in all the in
strumentalities and technics of
medicine, you would now be able to
give leadership and to set new stan
dards in the integration of those in
strumentalities and of the available
knowledge on behalf of human
health. It would become possible for
every segment of the profession,
every specialty, every physician, and
every organization to define their
own best roles and for the profession
as a whole to achieve balance among
all of its many, often conflicting,
areas of endeavor. It would offer
design for new and needed forms of
professional organization and of
clinical practice.
Similarly, the profession has long
operated on the apparent premise
that osteopathic education consists of
a more or less conventional medical
curriculum to which simply another
element has been added, like the
cherry on an ice cream sundae. The
profession would recognize that an
improved system of medicine de-
mands an improved system for the
education of physicians. A truly
osteopathic curriculum still awaits
development. The profession and its
educators would discover that the
horizon that is proposed for your un
folding provides the basis for total
design of the curriculum, of its com
ponents, and of its faculties. De
manding, as the system does, new
forms of medical practice, it would
also prescribe the new forms and in
strumentalities of medical education.
Does it define your tasks and your
obligations?
Let me identify but two, which are
of such vast significance that they
alone would demand the existence of
your profession.
The first is the continued develop
ment of one of your most important
and certainly your most conspicuous
ly distinctive contribution to medi
cine. Were you fully to commit your
self to the function which has been
proposed, you would discover that
osteopathic manipulative therapy,
with its ancillary diagnostic methods,
is not merely another form of therapy
in your total arsenal. It is not one
which may be arbitrarily withheld
from the patient just because its
mechanisms are not understood, be
cause the physician has not taken the
trouble to develop the necessary
skills, because he fnds it incon
venient, or because it is politically
inexpedient. You would discover that
you have no greater moral right to
withhold manipulative therapy than
any other therapy.
But it is not just another form of
therapy; it is a whole strategy, a
whole approach in itself. It is not
merely a treatment of "lesions"; in
effect, it is the putting of influences
into the whole man through the acces
sible tissues of the body, influences
which deflect his life processes to
more favorable paths, and which help
put the man in better command of his
situation, whatever it is, whatever
it may become, whatever his illness,
whatever its etiology. To speak and to
think of manipUlative therapy as
though it were a discrete, uniform
entity independent of the unique
understanding and skills of the in
dividual physician, one which can be
designed for a mythical "average
man," as something which can, in
wholesale manner, be declared "indi
cated" or "contraindicated" for this
Osteopathic principles
or that "condition, " or to regard it as
an aspect of physical medicine, is to
miss the strategic significance of
osteopathic manipulative therapy and
to limit its great potential.
As a physiologist who has studied
deeply in this area I am firmly con
vinced that this is an area of medicine
of such vastness, of such depth, of
such endless ramifications and inter
connections, and of such import to
human health that it is as demanding,
as exacting, as honorable a life work
as any other. Its potential has hardly
been explored. Commitment to the
proposed horizon will help you recog
nize your obligation to give manipu
lative therapy and its cognate arts and
sciences their appropriate status and
full expression in your educational
system and, through that, in practice.
Above all, it will guide you in the
recognition and the fulfillment of
your obligations in the development
of this contribution.
I mconvinced that commitment
to the total design of which I have
spoken will in itself give great impetus
to that development, not only within
your profession and its institutions
but throughout the world. For ex
ample, there can be no doubt that the
unfavorable influences of musculo
skeletal stress and the favorable
influences of osteopathic manipula
tive therapy are mediated to a large
extent by the peripheral and seg
mental nervous system.
2
0,
2
1
In the past
quarter-century there has been an
immense increase in laboratory and
clinical investigation in every civilized
country demonstrating (l ) the deci
sive influence of the innervation of
tissues, not only on their moment-to
moment activities, but on their total
condition and on their responses to
all other factors; (2) the subversive
"organizer" role of the spinal cord,
brain stem, and peripheral nerves in
virtually every disease process; and
(3) the common origins of the unfa
vorable influences in the musculo
skeletal and other somatic tissues of
the body. The literature is now so
vast, extending into every function,
every organ, every disease, every area
of health and disease, as to constitute
a massive new movement in medicine.
This is a movement to which the
osteopathic profession should long
ago have given leadership. Not only
has it not given that leadership, but it
seems not even aware that the move-
ment is under way. Unfortunately,
because there has been no conceptual
framework to unite them, t hese
countl ess contri buti ons remai n
scattered fragments which fnd no
place in prevailing frameworks. The
erecting of the needed framework by
this profession would have tremen
dous impact on this and many other
areas of investigation and would give
needed direction to its own investiga
tions. 2 2
The second obligation with which I
would illustrate may be designated as
medical statesmanship. The function
of physicians, and particularly of
their professions, is far more than the
practice and advancement of their
art. They must be deeply concerned
with all factors in society which
have a significant bearing on human
health. They must seek, with the
cooperation of all social agencies,
the best possible environments for
human life. Among the factors that
deeply affect the public health and
the effectiveness of medical service
are the forms and structure of medi
cal service itself and the social,
economic, and political framework in
which medicine is practiced.
There is much that is good, of
course, in the present framework of
medical practice. But there is also
much that is inimical to the health
needs of society; much that prevents
the best use of clinical talent; much
that needlessly and severely limits its
availability and exaggerates its cost;
much that prevents the most effective
utilization of available knowledge
and technic; much that degralies the
physician and the profession of medi
cine; much that is evil. And much,
therefore, that the public finds in
creasingly intolerable. It is not a
coincidence that these same features
are completely inimical to the great
contributions the osteopathic pro
fession set out to make. Indeed, they
are incompatible with - and indefi
nitely postpone - the practice of any
system of comprehensive, construc
tive, prophylactic, ecologic medicine.
Such a system of medicine not only
demands a change in the structure of
medical service, but provides the
design.
The strong voice of this profession
has yet to be heard on these issues.
It has been remarkably willing to
acquiesce to the present framework
and to demonstrate its ability to
adapt to it. Its silence on these
issues contrasts sharply with the vigor
with which this same profession bat
tles for rights and privileges for itself.
To give support, even by silence, to
those parts of the framework and
those forms and aspects of medical
practice which, for society's sake,
need changing is to lend your strength
to the prevention of the unfolding of
your own brightest horizons.
Now is the time for medical criti
cism2l and medical statesmanship of
the highest order. Now is the time to
utilize your organized strength fear
lessly, creatively, imaginatively, and
unselfishly in the promotion of the
needed changes. This is not only your
obligation as a profession. It is the
only way, along with development
and dissemination of your own clini
cal, scientific, and humanistic con
tributions, to win the strength and
the support from society that you so
desperately need.
Conclusions
You have before you, then, a mo
mentous decision: the function you
propose to perform for society. I do
not know whether you will make a
decision or what decision you would
make. I do know that to make the
wrong decision or to delay much
longer (which is the same thing) is to
miss your second and last chance, to
abdicate the right to existence as a
profession and to make of your illus
trious history a shameful fiasco. Far,
far worse, it would delay for many
decades a great forward step in hu
man health and therefore contribute
to untold waste of human life in
needless suffering. In effect, the
decision is between becoming, as you
set out to be, the head of a new move
ment in medicine or the withering
appendage of a declining one. Ac
cording to its decision, the os
teopathic profession either will
always loom bright in the mind of
man or be recorded as a passing
footnote in the history of medicine.
What horizon, then, do you pro
pose to unfold? What contribution to
society do you wish to make? That is
the decision before the osteopathic
profession. It will either merit so
ciety' s nurturing or it will not. Society
will be the judge of that. Society' s
judgment awaits your decision.
IJ
References
I. Thompson, M. ; Continuing growth of pro
fession keyed to continuing college growth. J.
Osteopathy 6: 15-20, April, 1959.
2. Dubos, R.; Mirage of health; utopias, progress,
and biological change. Harper &Brothers, New York,
1959.
3. Marti-Ibafez, F. ; Disease as biography. M. D.
2: 1 1 , Oct. 1958.
4. Scheele, L. A.; Medcal research - unfinished
business. J. Am. Osteop. A. 58:653-655, June 1959.
5. Stieglitz, E. J.; Future for preventive medicine.
Harvard University Press, Cambridge, 1945.
6. Gregg, A.; Challenges to contemporary medi
cine. Columbia University Press, New York, 1956.
7. Dunn, J. H.; Points of attack for raising level of
wellness. J. Nat . " M.A. 49:225-235, July 1957;
reprinted Forum of Osteopathy. 32:32-38, March
1958.
8. Galdston, I.; Psychosomatic medicine; past,
present, and future. A.M.A. Arch. Neurol. &
Psychiat. 74:41-450, Oct. 1955.
9. Sigerist, H. E. ; Civilization and disease. Cornell
University Press, Ithaca, 1943.
10. Dubos, R.; Biochemical determinants of
microbial diseases. Harvard University Press,
Cambridge, 1954.
I I . Galdston, I . ; Meaning of social medicine.
Harvard University Press, Cambridge, 1954.
12. Galdston, I.; Homines ad deos: or Clinical bull
in ecological china shop. Bull. Hist. Med. 28:51 5-524,
Nov.-Dec. 1954.
1 3. Selye, H. ; Stress and disease. Science
122:625-631 , Oct. 7, 1955.
14. Wolff, H. G.; Stress and disease. Charles C.
Thomas, Springfield, Ill., 1953.
IS. Jensen, J.; Modern concepts in medicine. C. V.
Mosby Co., St. Louis, 1953.
16. Ogilvie, C. D., et al. : Symposium: Degenerative
disease: engima? challenge. opportunity! J. Am.
Osteop. A. 58: 151-157, Nov. 1958.
17. Commission on Chronic Illness: Prevention of
chronic illness. Chronic illness in United States, vol. I .
Harvard University Press, Cambridge, 1957.
18. Hinkle, L. E., Jr., and Wolff, H. G.; Ecologic
investigations of relationship between illness, life
experiences and social environment. Ann. Int. Med.
49: 1 373-1388, Dec. 1958.
19. Kramer, L. M.; Drugs and medicines. Pub.
Health Rep. 73: 929-939, Oct. 1958; reprinted J. Am.
Osteop. A. 58: 155-A-I6, Feb. 1959.
20. Korr, I. M., Thomas, P. E., and Wright, H. M. ;
Symposium on functional implications of segmental
facilitation; research report. J. Am. Osteop. A.
54:265-282, Jan. 1955.
21. Korr, I. M.; Monograph in preparation.
22. Korr, I. M. ; Osteopathic research: why, what,
whither? examination of its content, direction, and
relation to function of osteopathic medicine. J. Am.
Osteop. A. 56:275-285, Jan. 1957.
23. Bean, W. B.; Critique of criticism in medicine
and biological sciences in 1958. Perspectives in BioI. &
Med. 1 : 224-232, Winter, 1958.
Reprinted by permission from JAOA 59: 77-9, 1959.
An allegory: A forgotten episode in
American transportation history
From Breeder's Digest, April 20
This story came to light a few years
ago while foundations were being dug
for a new fission power plant in Kan
souri. The cornerstone of what had
apparently been a school or a library
was uncovered and found to contain
several books, in which were recorded
the facts from which this summary
has been drawn.
More than 20 years ago, in the late
1 850s, when mechanized transporta
tion in this country was still very
young and
q
uite primitive, there was
a young railroader named Taylor An
drews, who worked on the only ex
isting line of the time. Young Taylor
was the sort of person who was in
clined to doubt that the way things
were being done was necessarily the
best way, and who was always look
ing for better ways of doing things.
He began to become convinced, as he
rode up and down the railroad line,
loading and unloading freight at one
depot after another, and continually
firing the engine as it went back and
fort h bet ween s t at i ons , t hat
something was wrong with the basic
principles.
How foolish it is, he thought, to
make the same stops at the same com
munities to deliver the many little
things they needed and used up day
after day. Why not, he mused,
deliver, instead, the raw materials,
tools, and machinery with which they
could manufacture and raise the
things they needed? By delivering
means-of-production instead of con
sumer goods, the railroad could help
each community develop its own
economy, allowing it to become more
self-sufficient and less dependent on
frequent deliveries. He recognized, of
course, that such a system would re
quire different kinds of equipment
than were then in existence or even on
the drawing boards.
Equipment would be needed, he
reasoned, which could make occa
sional mass deliveries - rather than
many small ones -to each communi
ty of machinery, tools and raw pro
ducts. The cars would have to be
lower and wider to carry the massive
freight and the engines would have to
be a great deal more powerful. How
wasteful, he though, that engines
must use so much of their power just
to move their own weight and to carry
such immense stocks of their own fuel
over hundreds and thousands of
miles. There must be some way of
reducing engine and fuel mass, or
perhaps even of designing an engine
which somehow draws its fuel as it
runs.
Taylor studied these problems over
a period of years and by the early
1 870s, he had become convinced that
such an engine was possible and,
therefore, that the kind of economy
building railroad system he en
visioned was feasible. By 1 874 he had
drawn his preliminary plans and
specifications for the engines, the
strong, capacious cars, and the wide
gauge tracks and a sketch of the
system as a whole, and proudly began
showing them to other railroad men.
He tried to show them to fellow
workers on the line - engineers,
firemen, brakemen, section hands,
foremen, district managers, station
masters, the vice president in charge
o(promotion, development, advertis
ing, design, etc. , and even to the
president and the chairman of the
board.
Meets Opposition. Everywhere the
response was essentially the same.
"Nonsense. Humbug. We don't need
a new system. This is the way
railroading has a/ways been done.
Our present system is the only possi
ble system. If a better way were possi
ble, we' s have found it ourselves -
long ago. " The leaders in the railroad
said, "We don't know what crazy
thing you've drawn up there, but it's
wrong and it's un-Railroad and
subversive, and we wouldn't touch it
with a t o-foot camshaft. And who
are you, anyway, to tell the experts
how to run their business?" Hardly
anybody in the railroading world
would even look at his sketches.
But Taylor Andrews was not one to
be easily discouraged. So sure was he
that his general plans were sound,
that for 18 more years he continued
to refine and develop them and to
take them from railroader to
Osteopathic principles
railroader, from shop to shop, and
station to station, asking only that his
plans at least be tested, that at least a
little pilot model be set up; at least
think about it. But more and more
doors were shut in his face until it
became evident even to him that there
was no hope in bucking the existing
system, and that there were only two
alternatives: either forget the whole
thing or get started on it himself.
Transecon is Bor. By 1 892 his
mind was made up. "The only thing
to do, " he said, "is to set up my
own model railroad system and
show that it works -and better than
the one we now have. " With a few
nonrailroaders and one or two
refugee railroaders from other coun
tries, he organized and incorporated a
small company with the express pur
pose of establishing "an improved
system of railroading. " They named
t hei r company " Transec on , "
representing "transportation for
stronger economies. " They managed
to interest some investors, set up a
little shop, secured some right of way,
and began accumulating parts and
scrap metal with which to start con
struction. The first thing they did was
to lay a mile or two of broad track in
the direction they wanted their system
eventually to go, and began assem
bling their locomotive right on the
tracks.
As their work progressed, others
joined them; still others brought
scrap or old tools and even money;
some came just to help or to run er
rands. In the course of a few years,
Andrews and his little band had
become quite a large and determined
group. They completed their first
engine and one or two flatcars and
ran them back and forth on their
short length of tracks, endlessly
testing, improving, refining, revising,
replacing, and "ironing out the
bugs. " (We presume this quaint
phrase refers to some sort of metal
grill for excluding the many insects
which would have been drawn in
from the atmosphere together with
the fuel. How this was accomplished
and precisely how the engine
operated, we shall never know, since
the technical language used to
describe the working of the engine
and other equipment is now utterly
unintelligible.)
Some time after the turn of the
twentieth century, they and many
others who had ridden back and forth
on the short tracks were convinced
that the time had come to complete
their pilot system. All that remained
was to complete the laying of their
first line of tracks and open up for
business - to demonstrate to the en
tire railroad industry and the world in
general that, with the right kind of
equipment, there could be a better
system of railroading, which would
liberate communities from their
growi ng dependence on dai l y
deliveries of consumer goods.
Presents Plan. Ard so a few of the
more presentable and articulate
members of the group doffed their
overalls, put on their Sunday suits,
and set out for the state capitol to
seek permission to extend their tracks
to a few communities in the chosen
direction and to license Transecon for
carryi ng means - of- product i on.
(Taylor Andrews, now aging, stayed
home to keep the engine wiped and in
functioning order.)
"Very well, " said the Railroad
Commission and other official Guard
ians of the Public Welfare, "we
can't see any need for all this tom
foolery, but there's no law against it.
So, we'll approve you for a license to
operate your two-bit spur - pro
viding you can prove to our satisfac
tion that you know how to operate a
locomotive and a freight line and can
give the kind of service people have
come to expect of railroads. "
"But, " the delegates objected,
"our proposed system is not j ust
another railroad; it's Transecon. It
should be judged by its own stan
dards, and not by those we're trying
to improve. "
"Poppycock, " the Official Guard
ians responded, "it may be a Fan
cycon or whatever-you-call-it to you,
but sure sounds like a railroad line to
us. We'll have to inspect you. "
Gets Once-Over. Several hundred
application forms and a thousand let
ters later, the Commission made a
visitation to Kansouri to inspect the
engine and other equipment. They
were accompanied, of course, by ex
pert advisers from Big Railroad. One
look was enough.
"This will never do, " they ex
claimed. "No train has ever run on
such ridiculously wide tracks . Con-
trary to all established standards.
And what's the matter with your
locomotive? That is a locomotive,
isn't it? Looks like nothing we've ever
seen - and we've seen them all. Ob
viously too small to be powerful
enough. And where's the tender?
What? Nonsense! Every engine must
carry a certain minimum of fuel at all
times. Also, we don't see any fender
skirts or hubcaps. Absolutely essen
tial. And only one cowcatcher! You
know the law requires one in front
and in back, in case you have to
reverse. And no smokestac k!
Hogwash; smoke or no, no engine is
complete without a smokestack. And
you're going to have to put on some
chrome trim, all around - lots of
it. "
After the inspection, the crestfallen
Transeconners sat around debating
and shaking their heads for many
days. Quite a few were in favor of
chucking the whole thing and return
ing to their farms and shops. And
some of them did. But the stalwarts
said, "No, we must go on. This is
bigger than all of us. Sure, the nar
rower gauge defeats some of our pur
pose. Sure, the unnecessary fuel car,
and all the chrome, the hubcaps,
fender skirts, extra cowcatcher, and
dummy smokestack will waste half of
our power, but at least we can make a
start. And when we've proved how
good our system can be, even under
all those handicaps, then we . can
gradually widen the tracks again and
take off the superfluous load. " As a
matter of fact, some of them even
thought the engine would look pretty
with the trim and extra attachments.
Conforms, Then Accepted. It was
decided to make the required
changes. The men worked hard and
long, narrowing the track and
wheelbases on the engine and cars,
putting on outriggers to keep them
from toppling over, and putting on
tons of trim and other paraphernalia.
And the Commission was invited for
another inspection.
"Strangest looking equipment
we've ever seen, " they said, "but it
seems to meet minimum railroad
standards. In fact, we rather like
those outriggers. Equipment ap
proved. Now - what are you going
to carry?"
-When they were told. they said
"No, that won't do. Oh, all right, go
1
ahead and carry that means-of
production stuff if you insist, but
you're also going to have to carry the
things that people need and want and
have come to expect railroads to
bring them - bread, milk, eggs,
ketchup, cravats , stereopticons,
zithers and mandolin picks. gum
drops, curtains, hair oil, antima
cassars, footstools, rocking chairs,
and the like. And Sears Roebuck
catalogs - so they can order more. "
After much debate, the Transecon
ners reluctantly agreed to carry an
assortment of consumer goods in ad
dition to such means-of-prOduction
as they could also carry. And they
proceeded to finish laying the tracks
to a few of the many communities
they hoped eventually to serve.
Everyone Prospers. Transecon
began to prosper in its small way and
the communities it served also pros
pered - especially those they could
persuade to accept deliveries of
means-of-production for the develop
ment of their own industry and agri
culture. Oradually, Transecon was
able to add a few more engines -all
well-trimmed with chrome and
equipped with tenders, fenders,
smokestacks, and cowcatchers. Many
more people came to work for the
line, and new communities grew up
along the right of way, demanding its
services.
As the years went on, Transecon
grew in equipment, staff, and
resources, and won approval after ap
proval and recognition after recogni
tion. However, it found itself more
and more absorbed in doing the
things which had to be done to win
and keep approval and recognition,
and less and less in the building of an
" improved system of railroading. "
Life, for Transecon, had become a
continual race to keep up with the
changing standards prescribed by
Big Railroad. It became so involved
in continually changing the width
of the tracks to meet "advancing
standards" and adding new im
provements such as tailfins, power
stering, and even calliopes to replace
outmoded whistles and bells that
there was little opportunity to lay new
track.
Equal Rights. To be sure, these
problems were diffcult enough. But,
in its quest for "equal rights, " which
141
gradual l y became i t s sl ogan,
Transecon' s greatest problem was the
freight it was required to carry. To
prove the full diversity of its
qualifications, Transecon had con
tinually to demonstrate its willingness
and its ability to carry the countless
new consumer goods which endlessly
rolled off the assembly . lines and
floOded the market in response to ad
vancing standards and to meet the
demands of the populace for "the
very latest. "
Among the items for which
Transecon sought and proudly won
approval were automobiles, washing
machines, hair curlers, pens for
writing under water, refrigerators,
electric guitars, devices for shaving
peaches, mix-masters, cameras, lip
sticks, phonographs, radios, movie
films, comic books, hula hoops, and
many others totally unfamiliar to us
now. It even won the right to carry
products that were known to dull the
senses, cripple the intellect, and
destroy the will to work: television
(apparently a primitive form of
telesense), tobacco (a noxious weed
which was somehow burned in the
mouth and its fumes inhaled) , and
liquor (as far as we can tell, a kind of
beverage containing high concentra
tions of an alkyl hydroxide known as
ethyl alcohol).
Inevitably, it became more and
more of a problem to find space for
the means-of-production freight.
More and more it was left until last
on the loading platform, until it
became the practice " i there was
enough power and i the space was
not required for consumer goods -
to load it in the caboose. Transecon
ners became very proud of their abili
ty to meet the advancing Big Railroad
standards and to carry the things that
were in demand, in fashion, and ex
pected of them.
A Loaded Caboose. "See," they
boasted, "we may be small and we
may be poor, but we can carry the
same kinds of things Big Railroad
carries, but in addition, please note,
we also have a loaded caboose."
Gradually, the previous deliveries of
means-of-production deteriorated
faster than it was replaced, and the
communities served by Transecon
became more and more dependent on
daily deliveries of consumer goods.
This troubled the few old members
of the Board who still remembered
Taylor Andrews, now deceased, and
said, when they were given permis
sion to speak, "Oentlemen, aren't we
forgetting that our basic concept was
to help our communities to develop
independent economies? Haven' t
things gotten kind of turned around?
Isn't it the consumer goods that
should be in the caboose?"
.
The young progressive leaders tried
to be very patient with the aging
veterans and said, "Now, grandpop,
we're not forgetting. Just putting first
things first. Railroading has come a
long way since Transecon Railroad
began and we have to meet advancing
standards. As a complete railroad
we're going to have to prove our com
petence in every possible area of
railroading. You do agree, don't you,
that we have to be complete? Now,
you go back to your checkers. Don't
worry, when we're fully recognized,
that will be time enough to give some
thought to means-of-production and,
like you say, to ' developing econ
omies. ' We might even put on some
more cabooses. "
As more and more cars had to be
added to carry the growing variety
and volume of consumer goods -
and since there wasn't time or money
to develop more powerful engines -
the caboose was, with increasing
frequency, left standing on a siding.
"Pick it up the next trip," the
engineers said, "or maybe the one
after . " Duri ng vi si tati ons of
di sti ngui shed Rai l roaders and
Commissioners the idle cabooses
were occasionally pointed to as the
" Transeconic Contribution to Com
prehensive Full-Scope Railroading. "
When, however, they eventually
failed even to elicit polite curiosity,
the cabooses were painted to look like
private cars for the president and
board of directors.
Fully Approved. Finally, one day
(no precise date was given, but it
seems to have been in the late 1950
or early 1 96s), the great news burst
upon the land: "Transecon is fully
and unreservedly approved as a fully
qualified and complete railroad,
equal in rights and privileges to Big
Railroad. " (The Big Railroaders, of
course, still crossed their arms and
said, "They're still nothing but un
Railroad cultists; it is unethical for us
to work with them." )
Osteopathic principles
After due celebration of their vic
tory, the Transeconners turned to ex
panding their line, saying, Now
we'll show them what a railroad
system can be like. But the old men
who remembered had died off.
Nobody could recall in what direction
they had set out to lay the tracks, how
to build self-fueling engines, and the
purpose of all the heavy freight
rusting in the camouflaged cabooses
on the sidings.
For a year or so, therefore,
Transecon laid track beside the track
of Big Railroad and made deliveries
at the same stations. It soon became
obvious to everyone that it was
foolish to lay duplicate track and give
duplicate service. Besides, Transecon
was rapidly running out of money for
expansion and for replacement of
deteriorating equipment. Besides, the
Commissioners kept saying, "We
don't need two of you. One of you
must go. "
We'll Join You. Finally, the Great
Decision was made. Again, as many
years earlier, the more presentable
and articulate of the Transeconners
(none of whom, of course, now
owned overalls and all of whom wore
Sunday suits every day) went to call
upon the Big Railroaders, saying,
"We've always been very nice to you
and lately you've been real nice to us,
and besides, as everybody knows, we
both want what's best for Humanity.
So, why don't we become one big
happy company? We'd be willing to
run our equipment on your tracks,
and we won't charge you for the
equipment if you won't charge us for
the use of the tracks. "
After a brief caucus, the Big
Railroaders said, "Well, all right; we
could use a few more engines and
cars. But yours are in pretty poor
shape, so if you want to come in with
us, you'll have to fx them up our way
and we'll run them together -
according to our policies. "
After suitable objections, the
Transeconners agreed, holding frm
ly, however, to one stipulation: that
their joining with the Big Railroad be
publicized, not as an absorption,
which some ignoramuses called it, but
as the amalgamation of two equal,
complete systems. and that a name
be agreed on which would appropri
ately memorialize for posterity the
Transeconic part of the amalgama-
tion. Accordingly, they proposed the
name 'Transeconic Railroad' . This,
of course, was rejected and after a
short debate and a series of com
promises, a name was agreed on
which properly recognized the
Transeconic Contribution to More
Comprehensive Fuller-Scope Rail
roading: 'Big Railroad' was changed
to ' Bigger Railroad' .
And that is how Transecon came to
pass. The yellow pages from which
this story was obtained, record that
after the amalgamation there was
great celebration in the homes and
shops of the former Transeconners
who were now Big Railroaders, and
the last page concludes with the
words, "Mission accomplished. "
* * *
Postscript. One century after the
close of the Transeconic episode, it is
diffcult - even for professional
historians - to understand what it
was they were celebrating and what
mission they considered accom
plished. From present perspectives it
would seem that if their objectives
had been to wOfk for Big Railroad,
they could have done so at the very
outset and avoided an exhausting
7S-year struggle. If, on the other
hand, their objective had been to
launch, as they said, an "improved
system of railroading, " one wonders
how they could have celebrated, as
the crowning triumph of their 7S-year
struggle, the placing of their equip
ment at the service of the old system.
Certainly, the opportunity to develop
the improved system remained before
them until that time. One wonders
how acceptance by Big Railroad
became for them the higher goal and
how abject surrender was interpreted
as victory.
These questions are all the more
perplexing in the middle of the
twenty-first century, when we
remember that that old system has
long been replaced and that our entire
transportation system and the
economies it supports, though now
technically more advanced, are based
on the same principle as those of the
original Transecon movement. As
far as we can now tell, however,
Transecon's only surviving contribu
tions to civilization are the yellow
pages from which this story has been
taken.
Reprinted by prmision from THE 0 I (8): 162.
April l9L
Osteopathy and medical evolution (1962)
Organized medicine has consistently
opposed the existence of the osteo
pathic profession and vigorously
resisted its growth. That the profes
sion has survived such powerful op
position, and prospered and grown in
spite of it, is testimony to its vitality.
However, while the osteopathic pro
fession was prospering and growing,
the opposition of political medicine
was also growing in intensity and
vigor, and the contest is now at the
decisive stage. For the frst time
organized medicine has succeeded in
gaining substantial organized support
for these efforts from within the
osteopathi c professi on i t sel f.
Encouraged by its triumph i n
Cal i fornia, organi zed political
medicine has declared its intention*
of carrying this strategy to its logical
"conclusion" - the piecemeal elimi
nation of the ostopathic profession.
The survival of the osteopathic pro
fession is now more gravely threat
ened than ever before, for while its
defenses against external attack are
strong, they provide no immunity
against interal collapse.
Organized osteopathyt responded
to these new threats to survival by
strongly reaffirming its intention to
maintain its separate and independent
existence, and demonstrated its de
termination by creating a sizable war
chest through dues increases and
assessments, "to promote the public
health by preserving and extending
the availability of osteopathic health
care in all states.
t t
Essential as is the will to survive
and to resist absorption and destruc
tion, survival of the profession de
mands that its function a a profes
sion have survival value. It demands,
also, that its members understand
Base on an address by the same title given at the
annual meeing of the Michign Association of
Osteopathic Physicians and Surgeons, Grand Rapids,
October 3, 191 . Dr. Korr is chairman of the Division
of Physiological Sciences. Kirksville College of
Ostepathy and Surgery.
In a statement unanimously adopted by the House of
Delegates, American Medical Association, June 28,
1 91 .
tAt the Annual Convention of the American Osteo
pahic Association, July 191.
24
that function and its value to society
in order that, individually and in
organized aggregate, they may dedi
cate themselves to its performance
and improvement. That function,
motivated by clear understanding of
its value, and well performed, is the
source of the profession's strength;
and it would seem to be the primary
responsibility of the profession's
organizations to ensure and promote
the exercise and development of that
strength.
Nowhere is this more lucidly illus
trated than in the very catastrophe
to which the profession's organiza
tions are now making their response.
Can we really regard it only as a
coincidence that California was the
osteopathic profession's largest,
"most powerful, " and "strongest"
segment? Can we really avoid the
conclusion that, having been the first
to succumb to the blandishments of
organized medicine, it was, in fact,
the weakest? Do we not have com
pelling reason to question the validity
of the criteria by which the profession
has measured strength and power? I s
i t not a possibility that the pursuit
of what passes for strength and power
may be the very source of weakness,
and that it has been bought, and may
again be bought, at suicidal prices?
Can we avoid the conclusion that pre
serving and extending the availability
of "osteopathic health care, " osten
sibly most amply available in Cali
fornia, does not necessarily "pre
serve" the profession and may even
hasten its demise? Can we not be con
cered that in its preoccupation with
quantity as a measure of strength,
the profession may have forgotten
that its true strength is in the quality
-perhaps the special quality -of its
function? Can we, in short, disregard
the paradox that truly osteopathic
health care was, in fact, feeblest
where the profession was "stron
gest"?
I f it asks questions which are
sufficiently incisive and searching,
the osteopathic profession can learn
some extremely valuable lessons from
its experience in California, and its
course henceforth will be decisively
determined by the lessons it does
learn. Although the California pro
fession was the largest blossom on
the osteopathic vine, it was, in fact,
and had long been, a dying part of the
vine, because it chose to "emanci
pate" itself from its roots. At this
point, in my opinion, the remainder
of the profession would do well to
look to its roots, and to turn all
possible resources to nourishing
them; else its other ministrations,
whatever they may be and however
well done, will, as in California, be
to a hollow, dying structure. The pro
fession now more than ever needs to
return to and develop the sources of
its vitality.
The Calforna profession had
obviously decided there was not
sufficient reason, if any, for the
continued existence of the osteopathic
profession. The remainder of the pro
fession has. in response, reaffirmed
its conviction that there are good
reasons for its continued independent
existence. It is now challenged, there
fore, to make clear what those reasons
are. What, other than survival, are its
purposes and objectives? What is its
function in society? What is, should
be, or could be. its value to society?
What is the profession for? These
same questions have been asked be
fore! but now they must receive
answers, lest the answer from Cali
fornia stand, with finality, as the
right one.
The myth of monolithic medicine, or,
Why not two schools of medicine?
It might be well, in the quest for clari
ty on these issues, to begin with a sim
ple question: Why should there be
more than one profession of medi
cine? As so often happens, a question
begins to answer itself when it is in
verted: "Why shouldn't there? Why
should there not be two. three, or
even more professions of medicine?"
In asking the question that way we
begin, immediately, to destroy a myth
with which most people of this coun
try have lived so long that they have
forgotten its origins in human conceit
and human design, and have accepted
it as though it were as inherent a part
of our environment as the atmo
sphere and as natural as the wetness
of the water. Even those -
osteopathic physicians, for example
- who might be expected to recog
nize it as artifact are often its chief
victims. In fact, the osteopathic pro-
Osteopathic principles
fession does appear entrapped in the
myth, and by its acquiescence, as well
as by act and word, the profession
helps perpetuate the myth and
deepens its own entrapment.
This is the myth: That there can be
but one true profession of medicine
-the one, of course, that dominates,
and has long dominated, the scene;
that only its members, holders of
a certain degree from certain "ap
proved" institutions, are the bona
fide, rightful, and exclusive inher
itors, custodians, proprietors, practi
tioners, and judges of medicine; that
only they are, and only they can be,
physicians; that they, and they alone,
have the divine right to control all
aspects of medical practice; indeed,
that this is so inexorably a fact of life
that they and their organizations and
institutions are medicine.
This myth has so much conditioned
our thinking that any other profes
sion, would-be profession, or group
of men and women that presumes to
speak and practice in the name of
medicine is, by its very separateness,
automatically suspect, and must, for
the protection of science and society,
submit to judgment - the judgment,
of course, of the medical profession,
the only "valid" profession, the ony
acceptable standard, and, by self
appointment, the only arbiter of stan
dard.
Because, however, any other pro
fession, would-be profession, or
group of practitioners is outside the
only "valid" profession and departs
from the only acceptable standard, it
is, ipso Jacto, unacceptable; it is a
cult of impostors, charlatans, or
upstarts whose practice and principles
- even without benefit of scrutiny -
are inherently wrong and even dan
gerous. Its adherents must be denied
the title of physician and the right to
practice "medicine. "
We have accepted this myth so long
that any new profession, regardless of
the soundness of its principles and the
efficacy of its practice, has, at best,
only the most tentative, the most pro
bationary right to existence, which it
must continually defend, by justify
ing and explaining why, and in what
way, it presumes to be "different
from medicine. " Osteopathic physi
cians and their spokesmen give
substance and credence to this myth
every time they accept as reasonable,
and set out to answer, the question,
"How does osteopathy differ from
medicine?" - or one of its many
variants. The question is as absurd as
"How do robins differ from birds?"
or "How does sculpture differ from
art?" Even worse, both the questioner
and the answerer have, by implica
tion, accepted the premise that the
dominant profession is the standard
against which all others must be
measured.
We have lived with this myth so
long that we no longer see the
ludicrous paradox of a system by
which a new profession of medicine
can win the right to existence only by
qualifying for acceptance by the
dominant school of medicine, thereby
ending its existence! We shruggingly
accept a system in which the only
possible seal of approval is the kiss of
death.
This is the great myth with which
the American public has lived, and by
which it has been victimized, for
many decades. This is the great myth
to which the osteopathic profession
has tried to adapt (California having,
thus far, been the most successful) in
stead of ruthlessly searching out and
exposing its basic falseness for all to
see.
To whom, then, does medicine
belong, if not to the medical profes
sion? Who are its judges, custodians,
guardians, proprietors, standard
bearers? Medicine is certainly not the
exclusive province or private property
of any particular profession, organi
zation, or association of institutions,
any more than education belongs to
the teachers, or religion to the clergy,
music to performing artists, and the
theater to stagehands and actors.
Medi ci ne i s a vast body of
knowledge, skills, understandings,
experience, facilities, services, agen
cies, and institutions related to health
and belonging to all of society.
Medicine has evolved through the
cumulative experience of the entire
history of the entire human race. In
modern society it is the product of the
activities of dozens of professions,
vocations, industries, arts, and
sciences. Physicians, regardless of
academic degree or particular profes
sion, are those charged with the
responsibility of delivering medical
service, with wielding some of the in
struments and applying some of the
methods of clinical medicine. They
practice it, they "perform" it, they
apply instruments and methods i n
health care. They do not own medi
cine; they are not its personifcation.
They do not design it, create it, or,
with relatively few exceptions, even
nurture it or plot the course of its
progress. The practice of medicine is
a great enough calling in itself,
without the arrogation of others.
The evolution of medicine
Medicine, therefore, is a pervasive
part and product of human culture.
Like all other major endeavors and
sociocultural phenomena - indeed,
like human culture itself - medicine
always has been and, for as long as
the human race survives, always will
be, in a continual process of evolu
tion. This evolution is not merely the
accumulation and turnover of bio
logic and clinical facts and the
multiplication and refinement of
methods and instruments. It is also
the evolution of ways of looking at
the facts, ways of arranging them and
interpreting their confgurations, and
of understanding them - and facts
accumulate much more rapidly than
understanding.
It is the evolution of scales ojvalue
and oj emphasis, the evolution of
strategies and systems for utilizing the
facts and applying the methods and
instruments. It is also the unfolding
of perspectives about human health
and disease. It is the evolution of the
objectives of medicine and medical
practice and of the concepts regard
ing the obligations and qualiications
ojphysicians. It includes the evolu
tion of concepts regarding the social
contexts of medical practice. In short,
the evolution of medicine is as much
the evolution of ideas behind
medicine and its practice as it is of the
knowledge and technique that nur
ture, and are nurtured by, those
ideas. Indeed, it is primarily these
ideas, comprising the philosophy of
medicine, that determine the direc
tions of the quest for new medical
knowledge and technique. It is these
ideas that determine the discoveries
for which the mind is prepared and
for which it goes seeking, and the
meanings it ascribes to them. Per
ceived or not, the prevailing philos
ophy of medicine is 'the little leaven
[that] leaveneth the whole lump" of
medical practice and research.
Because technique is easy to see
and experience, easy to describe and
document, and because its change is
dramatically rapid, we overlook the
pervasive presence of the perspec
tives, strategies, motivations, and
ideas that underlie the use of the
technique and their design and that
guide the quest for new ones. We also
overlook, therefore, their slower, less
dramatic change. Nevertheless,
throughout the recorded history of
medicine, the numerous "schools,"
cults, professions, and systems of
medicine that have had a place in that
history have been formed not only
around methods and instruments, but
around the much subtler, yet power
fully motivating concepts and
strategies.
Some of the schools, cults, sys
tems, and professions of medicine
have been soundly based, others not.
Some have had very brief lives, either
because they did not have significant
answers to human health needs and
better ways of interpreting and utiliz
ing available knowledge, or because
they could not convince enough peo
ple that they had. Others survived for
long periods either because they did
offer better ways of utilizing available
knowlege in the struggle against
disease or because of the persuasive
nes of their proponents and the will to
believe of the human species. Each has
had some impact on human health and
some impact on the course of medical
history - some favorable, some un
favorable. Some have speeded
progress, and some have retarded it.
The coexistence of two or more
schools, systems, or professions i n
the same era has been the rule. Their
lifetimes were usually overlapping,
rather than coextensive. A dominant,
enduring school was often flanked or
surrounded by others coming in or
going out, striving for ascendancy or
resisting decline. All learned from the
past, some better or more willingly
than others; each learned from the
others and each selected, rejected,
and adapted the available methods
and knowledge to its own perspec
tives, some with good success, others
with less success. But for each,
however brief or prolonged its life
and however simple or elaborate its
biography, rise and decline was the
inevitable theme. The rise and decline
of various schools or systems of
meicine, especially of those which
held sway for long periods and had
many followers, may be regarded as
landmarks or stages in the evolution
of medicine.
The history of medicine in this
country, though relatively brief, also
reflects -perhaps even with unusual
clarity - the evolution of medicine
and the struggle for survival and
dominance among schools of medi
cine. A rather large series of schools
and cults is to be found in our
history: thomsonianism, naturop
athy, chiropractic, homeopathy,
allopathy, eclecticism, osteopathy.
Most powerful, most enduring, and
most "successful" of all, of course,
has been allopathic medicine.
The allopathic era of medical
evolution
Since the passing of homeopathy, the
terms "allopathy" and "allopathic
medicine" have fallen into disuse.
Allopathy has worn many guises
. designated by many euphemisms.
Most medical leaders and educators
disown this identity and call for other
approaches. Nevertheless, the over
whelming bulk of medical practice is
still guided by allopathic concepts.
They are now so deeply ingrained, so
much a part of our environment and
pattern of thinking, that we are no
longer aware of their existence. As a
matter of fact, as a demonstration of
freedom from dogma and fixed prin
ciple, it has become fashionable to
deny adherence to any medical
philosophy.
The origins of the allpathic ap
proach are lost in antiquity. It is
perhaps the most direct, the most ob
vious, and the simplest approach:
Undo or reverse the affliction and its
manifestations, counteract the action
of the agents or factors presumed to
cause it; the mor specific the attack
on the disease and its cause, the bet
ter. Allopathy received its greatest
impetus from the epoch-making
scientifc advances that came in the
latter part of the nineteenth and the
early part of the twentieth century.
when the discoveries of Pasteur,
Koch, Virchow, Ehrlich, and others
gave good reason to hope that medi
cine was now well on the way to
characterizing and differentiating
man's diseases, identifying their
causes, and developing the means to
combat them, and that in time, man's
diseases would be conquered one by
one until health had been won for
humanity.
Although the experience and sci
ence of succeeding years have dis
pelled the basis for that hope, it has
nevertheless persisted as a kind of in
sidious faith which guides much of
our research and which provides the
framework for the organization and
financing of research, for medical '
education and practice, and for the
forms of practice. That faith, often
piously expressed by such admoni
tions as "treat the disease by
eliminating the cause" is renewed
from time to time by a discovery or
development that permits some tri
umph over one or another of our dis
eases, one that can be ascribed to a
specific "cause" - usually one of
many contributing or essential fac
tors.
The decline and fall of allopathic
medicine
While the great mass of clinical prac
tice in the existing schools of practice,
including the osteopathic, is largely
allopathic in orientation, and while
the dominant medical profession,
more purely allopathic than any, is
magnificently organized and speaks
with such a loud voice that it is
regarded, not as a particular school
of medicine, but as medicine itself,
the fact remains that it is not
medicine. Allopathy is but another
stage in the evolution of medicine,
and, like the others, it too will pass.
Why will it pass? It will pass for the
same reasons that other traditions, in
stitutions, institutional forms, agen
cies, and governments pass. It will
pass because it does not adequately
meet the needs of society, because the
defects in its basic strategy preclude
the full use of available resources and
knowledge in the war against disease
and for health. What is more, the
failure becomes deeper and deeper as
time goes on. This is true in spite of
the great advances that the allopathic
approach has fostered and the vast
research that it has inspired. A
basically unsound or archaic strategy
cannot possibly make sound use even
of the best of the improvements in
tactics and technique that it may itself
inspire, and it leaves idle or
undeveloped others that are no less,
and often more, effcacious. The
basic fact of strategic failure has for a
long time, however, been concealed
by dazzling displays of tactical
bravura and technical virtuosity, by
Osteopathic principles
Osteopathic principles