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The Influence of Diet Composition on the

Apparent Digestibility of Crude Protein and


Amino Acids at the Terminal Ileum and
Overall in Pigs
W. C. SAUER,’ A. JUST, H. H. JPIRGENSEN, hlAKONNEN FEKADUZand B. 0. EGGUhl

National Institute of Animal Science, Copenhagen, Denmark

Introduction Sauer, Stothers & Parker, 1977; Low, 19790, 6;


Just, 1980). However, studies in which protein or
The validity of the faecal analysis method for amino acids were infused into the hind gut of
determination of the apparent digestibility of pigs have shown that most of the amino acids are
the amino acids (Kuiken & Lyman, 1948) is degraded to ammonia or amines and absorbed
often questioned partly because of endogenous in the hind gut as the nitrogen is almost fully
protein secretions into the digestive tract and excreted in the urine (Zebrowska, 1975; Sauer,
partly because of the effect of microorganisms 1976; Hodgon, 1977; Just, Jargensen & F e r n h -
in the hind gut (caecum & colon). The micro- dez,’ 1 9 7 9 ~ ) .
organisms may influence protein metabolism and The objective of the present investigation was
thereby confound the determination of crude to study the influence of the chemical composi-
protein and amino acid digestibilities. Bacterial tion of diets on the ileal and faecal digestibilities
enzymes in the large intestine could bring about of crude protein and amino acids and the amounts
hydrolysis of undigested protein through peptides of these nutrients disappearing in the hind gut.
of decreasing length to free amino acids. These
free amino acids may either be absorbed as such
or broken down further to yield ammonia and Material and Methods
carbon skeletons. The latter compounds, in turn,
may be absorbed by the animal or be used for de Nine male castrate Danish Landrace pigs fitted
novo bacterial protein synthesis (Just & Mason, with ileo-caecal re-entrant cannulae were used for
1974; Mason, Just & Bech Andersen, 1976). the digestibility experiments during the growth
The apparent faecal digestibilities of amino period from approximately 50 to 70 kg. Surgery
acids in cereal based diets and in semi purified was performed on the barrows at approximately
diets are generally higher than the corresponding 45 kg live weight, according to the technique
ileal digestibilities (Zebrowska, 19730, 6; Bura- described by Easter & Tanksley (1973). The
czewska, Buraczewski, Horszczaruk, Jones & re-entrant cannulae were made from polyvinyl-
Zebrowska, 1975; Buraczewska, Buraczewski & chloride plastisol, as described by Sauer (1976)
Zebrowska, 1975; CuperloviC, HristiC & Ze- and had an internal diameter of 12 mm.
browska, 1975; Braude, Fulford & Low, 1976; The composition of the diets is given in Tables
Zebrowska, Simon, Munchmeyer & Bergner, 1, 2, 3 and 4. The diets were formulated so
1976; Rerat, Vaissade, Vaugelade, Robin, Robin that they varied considerably in chemical com-
& Jung, 1977; Sauer, Stothers & Phillips, 1977; position but fulfilled the requirements of the
pigs for essential nutrients per feed unit according
Present address: Department of Animal Science, Uni- to the current Danish standard (Andersen &
versity of Alberta, Edmonton, Alberta, Canada. Just, 1979). In experiment 3, however, the factor
* Present address: Faculty of Veterinary hledicine, Insti- in question was protein and therefore the crude
tute of Bacteriology and Epizootology Biomedicurn,
Uppsala, Sweden. protein supply in groups 2 and 3 exceeded the
Acfu Agricrrlturiz Scundiililtacica 30 (1980)
450 W. C. Sailer et al.

requirements. It was difficult to maintain feed analyser. The procedures were described by
intake as planned especially on fibrous diets as Weidner & Eggum (1966), Eggum (1968) and
the appetite of the pigs was poor probably due to Bech-Andersen (1979).
problems with passage of digesta through the Analysis of variance was carried out with aid
re-entrant cannula. In order to diminish problems of the statistical analysis system SAS (Barr,
caused by blockage of digesta, the diets were Goodnight, SalI & Helwig, 1976) taking into
ground through a 1 mm screen. In all experi- account the effects of pig, period, diet and site
ments feed intake was increased gradually from at which digestibilities were determined. Dif-
period 1 to period 3. ferences among treatment means were tested
The background for the composition of the according to Duncan’s multiple range test.
diets is that they should be representative of the
diets used in a number of investigations per-
formed in order to study factors influencing Results
digestibility, utilization of digestible protein
and metabolizable energy (Just, 1970; Just, 1975; Both ileal and faecal digestibility of crude
Just, Rasmussen & Hansen, 1976; Just, 1977; protein and amino acids were decreased with
Just, Jorgensen & Fekadu, 1978; Just, 1979). increasing concentration of dietary crude fibre
The pigs were kept in metabolic cages allowing as shown in Table 1. The source of dietary
separate collection of faeces and urine. Four crude fibre and crude protein, processing etc.
individual experiments were performed according also influence the digestibility of crude protein
to a 3 x 3 Latin square design. Chromic oxide (Just, Jorgensen & Fernindez, 19790) but in
was used as an indicator. Each test period lasted compleiely balanced diets this influence most
seven days and equal amounts of feed were given likely is small. Using a number of different
three times daily at 0700 h, 1500 h and 2300 h. cereal based (different varieties and qualities of
Faeces was collected for 24 hours on day six barley, oat, maize, sorghum) balanced diets
and ileal digesta was collected for eight hours Just (1970) found that dietary crude fibre ac-
on day seven. counted for 50% and dietary protein accounted
Soft plastic tubing was attached to the ileal for 19% of the variation in the digestibility of
cannula during the collection period and led crude protein.
into a container filled with ice. As soon as Most of the amino acids were digested to a
digesta passed through the ileal cannula into the greater extent than crude protein. The explana-
tubing, it was squeezed by hand until the tion most likely is that crude protein contains
digesta was below the ice level in the container. some lower nitrogen compounds, which have
Every 1 or 2 hours, depending on the flow rate, lower digestibilities than the amino acids. Similar
digesta was transferred from the tubing to a results were obtained by Just (1968, 1970, 1971 &
graduated beaker. The volume was made up 1980) and Just, Sauer, Bech-Andersen, Jorgensen
to the nearest 100. ml with distilled water. & Eggum (1980). Just, Andersen & Jorgensen
After vigorous stirring, a 50% aliquot was (1980) similarly found the long chain fatty acids
taken using a 50 cc syringe and frozen im- to be more digestible than crude fat.
mediately. The remainder was made up to the The pattern of the apparent digestibility coeffi-
original volume with distilled water, warmed to cients of the individual amino acids follows that
38°C and gradually infused through the caecal of crude protein, but systematic differences are
cannula. Infusion was usually completed within found among the amino acids and between the
1 hour following the collection of the digesta. individual amino acids and crude protein. In-
After conclusion of the experiments faeces terpretation of these differences is complicated
was mixed before samples were drawn for by the fact that the nitrogenous compounds in
analyses. Faeces and digesta were freeze-dried. ileal digesta and faeces originate from several
Nitrogen and amino acid digestibilities were sources, e.g. diet, endogenous secretions and
calculated based on the levels of chromic oxide microbial synthesis or conversions. Only small
in feed, ileal digesta and faeces. differences were found between the ileal and
Chromic oxide was estimated by the method faecal digestibility of lysine and methionine and
of Schiirch, Lloyd & Crampton (1950), modified the data further indicate a net increase of these
as described for official procedures by Jakobsen amino acids in the hind gut of the pigs fed the
& Weidner (1973). Amino acid analyses were per- most fibrous diet (group 3). Larger differences
formed using a Durrum D500 amino acid between the ileal and faecal digestibility were
Acra Agriculfum Scundinaricu 30 (1980)
Infliierice of diet coripositiori or1 tke apparerit digestibility of criide proteiii 45 1

found for threonine, tryptophan, cystine and and faecal digestibility of lysine and methio-
proline. nine, but in most cases. statistically significant
The depressive effect of crude fibre from barley differences were found for the other amino acids.
straw on the ileal and faecal digestibility of crude Increasing concentration of dietary animal
protein and amino acids, shown in Table 2, fat from 4.5 to 26.8y6 of diet dry matter in-
seems to be of the same magnitude as that of creased the apparent ileal and faecal digestibility
crude fibre from cereals and cereal byproducts of crude protein and amino acids by approxi-
given in Table 1. The pattern of the digestibility mately 3 percent units (Table 4), which is in
coefficients given in Table 2 is. also similar to accordance with the results given by Just, Ras-
those in Table 1, but the difference between the mussen & Hansen (1976) and Just (1979). Thus
ileal and faecal digestibility is apparently dietary crude fat has only little influence on the
diminished more by crude fibre from barley digestibility of crude protein and amino acids.
straw than by crude fibre from cereal and cereal The differences between the ileal and faecal
byproducts. The net increase of Iysine and niethio- digestibilities were of the same magnitude as
nine in the hind gut of the pigs fed the diet found in the foregoing experiments and were in
including 15% barley straw was also greater most cases statistically significant. .
than that on the crude fibre-rich diet shown in The apparent ileal and faecal digestibilities of
Table 1. crude protein and amino acids in average of the
The explanation for the diminishing difference 36 individual experiments are given in Table 5
between the ileal and faecal digestibilities with together with the amounts disappearing in the
increasing concentration of dietary crude fibre hind gut. The average difference between the
is most likely an increased microbial activity in apparent ileal and faecal digestibility of crude
the hind gut, which in turn is due to the protein and of amino acids was identical and
transfer of more undigested material to the amounted to 7.6 percent units or approxi-
hind gut as found by Just (1979). Furthermore mately 9 % of the total digested amounts. How-
combined balance-slaughter investigations with ever, there was considerable variation among
growing pigs showed that intake of 1 kg ground amino acids in the ileal-faecal difference. Thus,
barley straw increased the heat production by there was a decrease of 17.8 percent units of
2.0 MJ and increased the faecal excretion of glycine in the hind gut and an increase of 0.8
crude protein by 90-100 g. percent units of methionine.
Increasing concentration of dietary crude pro- Generally, only small amounts of methionine
tein caused a statistical significant increase in and lysine were produced or disappeared in the
the apparent ileal and faecal digestibility of hind gut, whereas tryptophan, threonine, cystine,
crude protein and most of the amino acids as proline, serine and glycine disappeared to a
shown in Table 3. This would be expected as greater extent.
the excretion of endogenous nitrogen into the
digestive tract more or less is proportional with Discussion
dietary dry matter intake and therefore ac-
counts for a greater part of the faecal nitrogen Infusions of crude protein or amino acids into
at lower than at higher dietary crude protein the caecum (Zebrowska, 1975; Sauer, 1976;
concentrations (Just, 1970; Eggum, 1973). In Hodgon, 1977; Just, Jmgensen & Fernindez,
addition to the effect of the concentration of 1 9 7 9 ~ )have shown that amino acids absorbed
crude protein, the digestibility of crude protein (disappearing) from the hind gut have little or no
and amino acids is influenced by numerous protein value as their nitrogen is almost fully
factors such as the dietary concentration and excreted into the urine. The explanation for this
the source of crude fibre and crude protein (Just, is probably that the nitrogen is absorbed in the
1970; Eggum, 1973; Just, Jargensen & Fernindez, form of ammonia and/or amines instead of
1979b), tannins (Eggum & Christensen, 1975; amino acids. This would indicate the ileal
Gohl & Thomke, 1976), the presence of enzyme digestibilities to be the proper ones but in addi-
inhibitors in the diet and the hind gut micro- tion to the former discussed factors influencing
flora (Kidder & Manners, 1978), type of starch the digestibility of crude protein and amino acids
(Mason, Just & Bech-Andersen, 1976), the effect one must be aware of the pitfalls arising in
of processing and age or weight of pigs (Just, experiments with cannulated pigs such as site
1978). As shown in Table 3 no significant dif- and effect of cannulation, particle size of the diet,
ferences were found between the apparent ileal feeding frequency, collection procedures, marker
Arm Agricrhrrre Scondinacica 30 (1 9SO)
452 IV. C. Sailer et al.
Table 1. The irrflierice of dietary crude fibre or1 the apparerit ileal arid faecul digestibility of crude
proteiii arid arnirio acids
Group

1 2 3

Dirt composition, ?La


Maize 24.9 12.5 0.0
Barley 0.0 28.3 56.6
Soyabean meal 31.7 22.1 12.5
bleat & bone meal 2.0 2.0 2.0
hlaize starch 34.3 17.2 0.0
Wheat bran 0.0 5.4 10.7
Oat hulls meal 0.0 7.0 13.9
Animal fat 3.7 2.9 2.0
CJieniicaIcomposition, ?& of D h l
Crude protein 23.9 23.2 18.1
Crude fat 6.9 5.8 4.7
Crude fibre 4.1 5.9 7.8
Nitrogen-free extract 58.6 58.5 63.8
Amino acid composition, g/kg Dhf
Arginine 15.9 13.8 10.1
Histidine 5.4 4.8 3.7
Isoleucine 10.6 9.7 6.9
Leucine 19.4 17.5 12.6
Lysine 13.1 12.1 7.5
hlethionine 3.8 3.9 2.7
Phenylalanine 11.0 10.4 8.5
Threonine 8.5 8.0 5.7
Tryptophan 2.6 2.9 2.2
Valine 9.9 9.7 7.2
Alanine 11.6 11.0 7.5
Aspartic acid 24.4 20.8 13.1
Cystine 3.5 3.4 2.9
Glutamic acid 47.1 49.3 43.9
Glycine 11.2 11.3 8.1
Proline 12.6 15.5 15.5
Serine 10.7 9.7 7.5
Tyrosine 8.3 7.4 5.5
Daily feed intake
kg dry matter 1.14 1.14 1.15
Apparent cligrstibiliiy, 7; Ileum Overall Ileum Overall Ileum Overall
Crude protein 7SbC 89a 75c 87" 74c 82b
Arginine 92ab 95" 87' 9 P 89bC 91abc
Histidine 89b 95" 82' 92ab 87bC 90ab
Isoleucine 81bC 9Ia 78' 8Sab 82C 83bC
Leucine 86bC 92" 81' 90ab 84c 86bc
Lysine 8Sab 91' 84bC 89"b 8Sabc 81'
hlethionine 87" 89' 82"b 87a 85"b SOb
Phenylalanine 84ab 9 la 79b 89" 85ab
Threonine 76ac 89a 67' 87a 73bC S0"b
Tryptophan 77b 90a 75b 90" 82ab 88"
Valine 81bC 89a 77c 87'b 81' 82b'
Alanine 77 b C 89a 71' 86ab 73' 78b'
Aspartic acid 82bC 92" 72d 8gab 76Cd 82bC
Cystine 75b 89" 66' 87" 74bC 85"
Glutamic acid 8Sb 95" 85b 94' 89ab 93"
Glycine 72b 89" 64b 88' 69b 82a
Proline 77c 93a 79bC 93a 86'b 93a
Serine 8IbC 92" 74c 90" 8IbC 86ab
Tyrosine 84abc 92a 78' 90ab 83bC 86ab
Average 82bc 91' 77c 89a 81bC 85"b
a hlinerals and vitamins were added t o the diets according to the Danish Standards (Andersen & Just, 1979).
a * b * c * d * e =Values in the same row with the same letter do not differ significantly (P<O.O5).
Ittflrerice of diet conposition 011 the apparent digestibility of crirde proteiri 453

Table 2. The irillirence of groirrid barley straw on the apparent ileal arid faecal digestibility of crirde
proteiri arid amirio acids
Group

I 2 3

Diet coniposilion, Y',


Barley 75.4 68.6 61.8
Soyabean meal 14.3 14.4 14.5
hfeat & bone meal 2.0 1.9 1.7
Sugar 2.0 1.9 1.7
Barley straw meal 0.0 7.5 15.0
Animal fat 2.8 2.6 2.3

Cltemicul coniposifion, 7; of Dhf


Crude protein 19.1 19.1 17.9
Crude fat 5.4 5.1 4.6
Crude fibre 4.7 7.0 9.4
Nitrogen-free extract 64.8 62.8 62.2

Amino acid contposition, glkg Dhf


Arginine 10.8 10.8 10.2
Histidine 3.8 3.8 3.4
Isoleucine 7.7 6.7 7.2
Leucine 13.5 13.5 12.6
Lysine 8.1 8.4 7.8
hlethionine 2.9 2.9 2.7
Phenylalanine 9.4 9.2 8.6
Threonine 6.1 6.3 5.7
Tryptophan 2.1 2.3 1.9
Valine 8.3 8.3 7.8
Alanine 7.8 8.0 7.5
Aspartic acid 14.4 14.8 13.8
Cystine 2.9 2.8 2.6
Glutamic acid 46.6 44.9 42.3
Glycine 8.3 8.5 7.8
Proline 17.1 16.1 15.1
Serine 8.1 8.2 7.4
Tyrosine 5.8 5.7 5.3

Daily feed intake


kg dry matter 1.14 1.24 1.33

Apparent digestibility, 7; Ileum Overall Ileum Overall Ileum Overall


Crude protein SOab 85' 76b Slab 75b 75b
Arginine 9oab 93' 8gb 92a 8Sb 8ga
Histidine 8Sb 92' 86bC 91' 85' 87b
Isoleucine 84'bC 88' 79' 8Sab 82bC 82bC
Leucine 85bC 89' 84' 8Sab 83' 84'
Lysine 87' 8Ta 86' 85' 86' 79b
hlethionine 87' 86' 85' 84a 85' 77b
Phenylalanine 86'b 89' 84b 8Sab 84b 84b .
Threonine 76' 86' 75' 84'b 72' 7SbC
Tryptophan 79b 89' SOb 89' 77b 83b
Valine 84abc 87= 8IbC 87ab 80' 81bC
Alanine 7Sabc 83' 76bC Slab 76bc 74'
Aspartic acid 79' 87' 76' 85ab 76' SObc
Cystine 73'b 84' 74'b Slab 6gb 73ab
Glutamic acid 91b' 94' 90' 94'b 90' 92bC
Glycine 73b' 85' 70' 85' 66' 79ab
Proline 90' 95' 87d 94'b 87d 92bC
Serine 83Cd 90' 81cd 8Sab 796 84bC
Tyrosine 83'b 89' 82b 8ga 83'b 84'b
Average 83bC 88' 81' Uab 80' 82'

' Minerals and vitamins were added to the diets according t o the Danish Standards (Andersen & Just. 1979).
'* b* '. dm = Values in the same row with the same letter d o not differ significantly (Px0.05).
454 .'fI C. Sarrer et al.

Table 3. Tjie iitflttteme of dietary protein 011 fhe apparei~tileal a i d faecal dipstibility o j crride proteiti
aud ainitio acids
Group

1 2 3

Diet coiposirion, :Au


Barley 29.0 62.2 42.3
Wheat bran 28.4 5.0 0.3
Soyabean meal 4.5 23.4 47.1
hleat & bone meal 2.0 2.0 2.1
Dried skim milk 0.3 0.7 1.4
hiaize starch 25.9 0.0 0.0
Animal fat 2.0 2.2 2.5
Clieiiiical coinposition, %
' of DAI
Crude protein 16.5 24.1 32.8
Crude fat 5.4 5.4 5.7
Crude fibre 5.7 4.9 5.6
Nitrogen-free extract 66.2 59.0 48.5
Anriiio acid coiqmsition, g/kg DAI
Arginine 10.7 15.1 21.9
Histidine 3.6 5. I 7.3
Isoleucine 6.0 10.0 14.2
Leucine 10.9 17.6 24.2
Lysine 8.8 11.6 17.2
hiethionine 3.2 3.5 4.6
Phenylalanine 7.3 11.9 16.0
Threonine 5.0 8.2 11.5
Tryptophan 2.1 3.1 4.1
Valine 7.9 11.7 15.6
Alanine 7.2 10.0 13.7
Aspartic acid 12.4 21.1 32.6
Cystine 2.8 3.8 4.9
Glutamic acid 35.8 53.9 67.8
GIycine 8.5 10.9 14.6
Proline 12.9 20.5 23.2
Serine 6. I 9.8 14.5
Tyrosine 5.0 8. I 11.5
Daily feed inrake
kg dry matter 1.37 1.38 1.36

Apparent cligestibiliry. % Ileum Overall Ileum Over Ileum Overall


Crude protein 67' 78b 76b 84" 79b 87"
Arginine 81d 90' 86' 92ab 89bC 9 9
Histidine 81d 89b 84' 92a 87b 93a
lsoleucine 77e 80de 83'd 86ab 84b' 88"
Leucine 7SC 83b 83b 88" 84b 89a
Lysine 82b 84b 84b 86"b 84b 90"
hlethionine 85a 83" 86" 82" 86a 86"
Phenylalanine 77' 85b 83b 89" 84b 90"
Threonine 66' 78b 76b 85" 79b 8Sa
Trypiophan 75d 86ab 81' 8Sab 82bC 90"
Valine 74' 8lb 8Ob 86a 82b 88"
Alanine 66' 76b 736 81" 76b 8.4"
Aspartic acid 71' 81b 79b 87" 82b 91"
Cystine 72d 84b 77' 88ab 78' 89"
Glutamic acid 86' 91"b 88b' 94a 86' 94a
Glycine 55' 8 la 63bc 86" 69b 87a
Proline 4Sb 91" 69ab 94" 75ab 94"
Serine 72d 8Sb 78' 89" 83b 92"
Tyrosine soc 82b' 83bC 86ab 85b 89"
Average 74' 84b 80' 8Sa 82bC 90"

hlinerals and vitamins were added to the diets according to the Danish Standards (Andersen & Just, 1979).
"* b* d * = Values in the same row with the same letter d o not differ significantly (P<O.O5).
'p
Iirflrreiice of diet conposition on the apparent digestibility of crirde proteiii 455

Table 4 . The iqflirerice of dietary fat on the apprirriit ileal atid fnecal digestibiliry of crude protein aid
arniiio acids

Group

1 2 3

Diet cottiposilion,';7
Barley 79.6 47.6 18.4
Wheat bran 1.9 16.6 29.0
Soyabean meal 10.3 17.6 24.7
hleat & bone meal 2.0 2.2 2.5
Sugar 2.0 2.2 2.5
Animal fat 0.9 10.7 20.3

Cfrertriral cotirposilion, % of DAf


Crude protein 20.0 20.1 20.7
Crude fat 4.5 17.0 26.8
Crude fibre 5.5 5.6 5.7
Nitrogen-free extract 64.2 51.0 40.2
Atiriiio acid cotitposition, g/kg DAf
A r g inin e 10.9 12.2 13.6
Histidine 4.3 4.6 4.9
Isoleucine 7.5 7.9 8.3
Leucine 13.5 14.0 14.5
Lysine 7.8 8.4 9.0
hlethionine 3.0 3.2 3. I
Phenylalanine 9.6 9.3 9.3
Threonine 6.2 6.6 7.1
Tryptophan 2.5 2.4 2.6
Valine 8.7 8.9 9.3
Alanine 7.9 8.5 9.1
Aspartic acid 13.9 16.4 18.9
Cyst i ne 3.3 3.2 3.5
Glutamic acid 47.3 43.9 41.3
Glycine 8.5 9.4 10.1
Proline 18.7 16.0 13.6
Serine 7.8 8.4 9.3
Tyrosine 6.4 6.5 6.8
Daily feed itilake
kg dry matter 1.41 1.42 1.42
Apparent cligestibilily, %, Ileum Overall lleum Overall Ileum Overall
Crude protein 74b 82' 73b 81' 76b 85'
Arginine 86d 92b 88Cd 93'b goc 94'
Histidine 84b 93' 84b 93' 85b 9ja
lsoleucine 79' 85'b 80' 87'b 83bC 89'
Leucine 81b 87a 82b 88' 83b 90'
Lysine 83b 83b 84b 84'b 8S'b 87'
hiethionine 83b 83'b 82b 8 84ab 86'
Phenylalanine 82b 8ga 82b- 89' 83b 91a
Threonine 6gb 84a 70b 85' 73b 88'
Tryptophan 77b 89' 79b 8ga 81b 92'
Valine 76b 86' 78b 87' 80b 89'
Alanine 72d 8Ob" 73d 82'b 77' 85'
Aspartic acid 72d 85b 76d 879b soc 90'
Cystine 70b 86' 6gb 85' 73b 87a
Glutamic acid 89b 94' 88b 94' 88b 94'
Glycine 63' 84a 6gbC 85' 73b 87'
Pro1i n e 85b 94' 84b 93a 84b 93'
Serine 74c 88' 77bC 89' 80b 91'
Tyrosine 8IC 8 Ib' 88' 84; 90'
Average 78b 87a 79b 88' 81 90'

a hlinerals and vitamins \vere added to the diets according t o the Danish Standards (Andersen & Just, 1979).
*' b* '* dm = Values in the same row with the same letter d o not differ significantly (P<0.05).
456 IV. C. Sailer et al.

Table 5 . Apparent ileal arid faecal digestibilities arid the disappearatice iri the kirid grit. Acerage of 36
experiments, i.e. Tables 1, 2, 3 and 4

Average apparent Average disappearance


digestibility in the hind gut -

Ileum Overall % of intake g/kg dry matter intake

Crude protein 75.3 82.9 7.6 5.3


Arginine 87.9 92.4 4.5 0.6 I
Histidine 85.1 91.8 6.7 0.3 I
Isoleucine 81.1 86.0 4.9 0.43
Leucine 82.9 88.0 5.1 0.8 1
Lysine 84.7 85.4 0.7 0.15
Methionine 84.8 84.0 + 0.8 +
0.02
Phenylalanine 82.6 88.2 5.6 0.57
Threonine 72.7 84.2 11.5 0.82
Tryptophan 78.7 88.6 9.9 0.25
Valine 79.3 85.8 6.5 0.63
Alanine 74.0 81.5 7.5 0.73
Aspartic acid 76.7 86.4 9.7 1.79
Cystine 72.5 85.0 12.5 0.42
Glutarnic acid 88.2 93.5 5.3 2.54
Glycine 67.1 84.9 17.8 1.76
Proline 79.3 93.2 13.9 2.27
Serine 78.5 88.6 10.1 0.91
Tyrosine 82.3 87.7 5.4 0.38
Average 79.9 87.5 7.6 0.85

recovery, amino acid analyses etc. (Zebrowska, It was attempted that the differently fed pigs
Buraczewska, Buraczewski & Horszczaruk, 1975; should have identical daily intakes of feed units
Zebrowska & Horszczaruk, 1975; Low, 1976; for pigs, which in turn would have resulted in
Sauer, 1976; Livingstone, Atkinson, Baird & identical daily intakes of digestible nutrients as
Crofts, 1977; Low & Zebrowska, 1977; Poppe, the diets were completely balanced on a feed
Meier & Bennke, 1977; Zebrowska, Buraczewska, unit basis. However, the appetite of the pigs was
Pastuszewska, Chamberlain & Buraczewski, generally somewhat poor, and following it was
1977; Bech-Andersen, 1979). not always possible to obtain the planned feed
In the present investigation the pigs were fed intake. This may have a slightly positive effect
the same amount of diet at each of three daily on the digestibility of the fibrous diets shown in
feedings exactly eight hours apart. Under Table 1 as Just, Jmgensen & Fernandez (1980)
such experimental conditions Sauer, Stothers & have found an increase in the digestibility of
Phillips (1977) found the ileal digestibilities crude protein with a decreasing daily feed intake.
based on an eight hours’ collection period to be There was considerable variation among
representative of those based on a twenty-four amino acids in the ileal-faecal difference. It is a
hours’ collection period. question, however, whether these differences are
In order to reduce problems caused by blockage true measures of the availability of these amino
of digesta in the cannulae, the diets were ground acids in the dietary crude protein or an artifact
through a 1 mm screen. Experiments of Sauer, due to endogenous secretions into the alimentary
Stothers & Phillips (1977) showed slightly higher canal (Zebrowska, 1973 a; Buraczewska, Bura-
ileal digestibilities of amino acids in finely ground czewski, Horszczaruk, Jones & Zebrowska, 1975;
than in cracked wheat, but the faecal digesti- Rerat, Vaissade, Vaugelade, Robin, Robin &
bilities were not affected. Just (1978) found a Jung, 1977; Low, 19790, b; Just, 1980) and/or
slight increase in the faecal digestibility by microbial action in the hind gut (Dammers,
fine grinding especially of fibrous diets in young 1964; Eggum, 1972; Salter, 1973; Salter, Coates
pigs. Thus the effect of grinding on the dif- & Hewitt, 1974; Salter & Fulford, 1974; Ze-
ference between the ileal and faecal digestibility browska & Pastuszewska, 1975; Mason, Just &
seems to be small. Bech-Andersen, 1976; Zebrowska, Buraczewska
Acta Agriculture Scandinmica 30 (1980)
Inftireiice of diet composition on the apparelit digestibility of crirde protein 457

& Horaczyfiski, 1977; Eggum, Fekadu, Wol- considerably. On average a net increase of 0.8
strup, Sauer & Just, 1979; Just, Sauer, Bech- percent units of methionine took place in the hind
Andersen, Jsrgensen & Eggum, 1980). gut, whereas 17.8 percent units of glycine dis-
The amounts of the individual amino acids appeared.
disappearing in the hind gut were very con- The difference between the ileal and faecal
sistent among diets (except the two high in fibre) apparent digestibilities for lysine and methio-
and, agree very well with the data of Just (1968, nine were small, whereas tryptophan, threonine,
1971, 1980), Eggum (1973), Mason, Just & cystine, proline, serine and glycine always
Bech-Andersen (1976), Zebrowska, Buraczew- showed larger differences (10-20%). The amounts
ska & Buraczewski (1977) and Just, Sauer, Bech- disappearing in the hind gut of the individual
Andersen, Jsrgensen & Eggum (1980). The net amino acids were very consistent among diets
formation of methionine and lysine that took except for the fibre-rich diets.
place in the hind gut of the pigs fed the more
fibrous diets was most likely due to an increase
in the amount of undigestible nutrients transferred Acknowledgements
to the hind gut and its effect on the amount of
breakdown and synthesis of bacterial protein The authors wish to express their thanks to Mr
(Mason, Just & Bech-Andersen, 1976; Just, 1979; Tage Olsen and Mr Ole H. Olsen for excellent
Just, Jargensen & Fernindez, 1979a; Just, 1980). animal care and to S. Bech-Andersen, Cand.
It can therefore be concluded that the chemical Pharm., for his valuable technical assistance
composition of diets exerts a great influence on with the amino acid analyses.
the apparent ileal and faecal digestibility of crude
protein and amino acids, but it has apparently
only a limited influence on the amounts dis- References
appearing in the hind gut. However, much more
Andersen, P. & Just, A. 1979. Tabeller ocerfoderiiiidlrrs
work is needed to elucidate, properly, the amount saniniensrtning ni. m. Kcxg-scin. 7. 56 pp. Det kgl.
and amino acid composition of the nitrogen con- danske Landhusholdningsselskab, Copenhagen.
taining substances secreted into the digestive Barr, A. J., Goodnight, J. H., Sall, J. P. & Helwig,
tract, the significance of the microflora in the J. T. 1976. A user’s guide to Statistical Analysis S p i e m .
329 pp. North Carolina State University, Raleigh.
alimentary canal, the influence of type of carbo- Bech-Andersen, S. 1979. Single-column analysis of amino
hydrates, feed processing and the relationship acids in hydrolysates of samples containing chromic
of ileal and faecal digestibility t o BV and NPU oxide (Cr202). J. CJwomatograpliy 179, 227-228.
etc. Braude, R., Fulford, R. J. & Low, A. G. 1976. Studies
on digestion and absorption in the intestines of grow-
ing pigs. hleasurements of the flow of digesta and
Summary pII. Br. J. Nirtr. 36, 497-511.
Buraczewska, L., Buraczewski, S., Horszczaruk. F.,
In order to elucidate the influence of diet com- Jones, A. S. & Zebrowska, T. 1975. An attempt to
estimate the endogenous nitrogen content in the
position on the ileal and faecal apparent digesti- digesta of pigs fed on diets with proteins containing
bility of crude protein and amino acids and the hydroxyproline. Rocz. Nairk Rol. B, 96 (4), 105-1 14.
amounts disappearing in the hind gut, four Buraczewska, L., Buraczewski, S. & Zebrowska, T. 1975.
experiments were performed with ileo-caecal re- Digestion and absorption in the small intestine of
pigs. Part 2. Amino acid content in digesta and their
.entrant cannulated Danish Landrace pigs ac- absorption. Rocz. Nauk Rol. B, 97 (l), 103-115.
cording to a 3 x 3 Latin square design. The diets Cuperlovif, hi., Hristif, V. & Zebrowska, T. 1975.
were formulated to vary in crude fibre (4-8%), Influence of the composition of the dietary protein
ground barley straw (0-15 %), crude protein supplement on the digestion and absorption of pro-
tein in the small intestine of pigs. Acra Vereriimrin,
(1633%) and crude fat (4-2776). (Beograd), 25 (6), 287-300.
Diet composition had a large influence upon Dammers, J. 1964. Verteringsstudies bij het varken.
the apparent ileal and faecal digestibility of Thesis. Leuven. Inst. Veevoedingsonderzoek, “Hoorn”.
crude protein and amino acids, whereas the 152 pp.
Easter, R. A. & Tanksley, T. D., Jr. 1973. A technique
influence of diet composition on the amounts for reentrant ileocecal cannulation of swine. J. Aninr.
disappearing in the hind gut was limited except Sci. 36, 1099-1103.
for the fibre-rich diets. On average 7.6 percent Eggum, B. 0.1968. Determination of tryptophan.’Aeta
units of crude protein or amino acids disappeared Agric. Scand. 18, 127-131.
Eggum, B. 0.1972. Protein utilization by conventional
in the hind gut. The amount of the individual and specific-pathogen-free rats. Z . TicrphpioI. Tierer-
amino acids disappearing in the hind gut differed ncilirirng 11. Fiitternrittelkde 30, 172-175.

Acta Agriculrrrre Scandinarica 30 (1 980)


458 W. C. Salter et at.

Eggum, B. 0. 1973. A study of certain factors influencing utilization of metabolizable energy in growing pigs.
protein utilization in rats and pigs. 406. beretn. forsogs- 291h Ann. hfeet. EAAP, 5 pp. Stockholm.
lab. 173 pp. Copenhagen. Just, A., Jargensen, H. & Fernindez, J. 1979a. Th e
Eggum, B. 0. & Christensen, K. D. 1975. Influence of digcstive capacity of the caecum-colon and the value o f
tannin on protein utilization in feedstuffs with special the nitrogen in the hind gut for protein synthesis in
reference to barley. In Breeding for seed protein im- pigs. 30th Ann. hfeer. EAAP, 5 pp. Harrogate.
procement using nuclear techniques, pp. 135-143.IAEA, Just, A., Jargensen, H. & Fernindez, J. 19796. The
Vienna. digestibility. h l E and N E content of individual feed-
Eggum, B. O., Fekadu, hl., Wolstrup, J., Sauer, W. C. stuffs for pigs. The National Institute of Animal
& Just, A. 1979. The effect of dietary antibiotics o n Science, Rolighedsvej 25, 1958 Copenhagen V. 10 pp.
protein and energy metabolism in rats: Possible Just, A., Sauer, W. C., Bech-Andersen, S., Jorgensen,
significance of the gut microflora. J. Sci. Food and H. H. & Eggum, B. 0. 1980. The influence of the hind
Agric. 30, 177-184. gut microflora on the digstibility of protein and
Gohl, B. & Thomke, S. 1976. Influence of barley tannins amino acids in growing pigs elucidated by addition
o n the digestibility of crude protein. 27th Ann. hfeet. of antibiotics to different fractions of barley. 2.
EAAP, 7 pp. Zurich. Tierpliysiol., Tierernihrung 11. Futterrrrittelkdc. 43,
Hodgon, E. S. 1977. Protein digestion in the large in- 83-91.
testine of the pig. hl.Sci. Thesis, Univ. of Guelph, Just, A., Andersen, J. 0. & Jorgensen, H. 1980. The influ-
Canada. ence of diet composition on the apparent digestibility
Holmes, J. H. G., Bayley, H. S. & Lcadbeater, P. A. of crude fat and fatty acids at the terminal ileum and
1974. Digestion of protein in small and large in- overall in pigs. 2. Tierpliysiol. Tierernifrr. ri. Futter-
testine of the pig. Br. J. Nutr. 32, 479-489. niittelkde. In press.
Jakobsen, P. E. & Weidner, K. 1973. In: Chemistry of Just, A., Jorgensen, H. & Fernindez, J. 1980. Un-
feedstuffs and animals. Comp. 1, Vet. Fac. F A 0 published results.
Fellous, Roy. Vet. Agric. Univ., Copenhagen, pp. Kidder, D. E. & hlanners, hl. J. 1978. Digestion in the
14-55. pig. Scienteclrnica, 201 pp. Bristol.
Just (Nielsen), A. 1968. Digestibility of amino acids in Kuiken, K. A. & Lyman, C. hi. 1948. Availability of
relation t o digestibility of nitrogen in bacon pigs. amino acids in some foods. J. Nutr. 58.359-368.
Kgl. Vet. B Landboliojsk. Arsskr., pp. 79-88. Copen- Livingstone, R. hi., Atkinson, T., Baird, B. & Crofts,
hagen. R. hi. J. 1977. The effect of processing potatoes on
Just (Nielsen), A. 1970. Alsidige foderrationers ener- the apparent digestion by pigs of organic matter and
getiske v m d i ti1 vrckst hos svin belyst ved forskellig nitrogen measured overall and at the terminal ileum.
metodik. 381. beretrr. farsogslab., 212 pp. Copen- Abstracts of Communications 36, 58 A.
hagen. Low, A. G. 1976. Digestion and absorption of nutrients
Just (Nielsen), A. 1971. The digestibility of amino acids in growing pigs. Proc. Nutr. Soc. 35, 57-62.
from different balanced feed rations as related to the Low, A. G. 1979a. Studies on digestion and absorption
digestibility of nitrogen in grouing pigs. Acta Agric. in the intestines of growing pigs. 5. hieasurements of
S c a d . 21, 189-192. the flow of nitrogen. Br. J. Nutr. 41, 137-146.
Just, A. 1975. Feed evaluation in pigs. World Recieiv of Low, A. G. 39796. Studies on digestion and absorption
Animal Production, vol. XI (I), 18-30. in the intestines of growing pigs. 6. hleasurements of
Just, A. 1977. Intake levels of N and energy in relation the flow of amino acids. Br. J. Nutr. 41, 147-156.
with production of animal protein in growing pigs. Low, A. G. & Zebrowska, T. 1977. Dry matter and
2nd Syniposiimi on Protein hfetabolisnr, pp. 100-104. nitrogen in the duodenal contents of growing pigs: a
Lelystad, Holland. discrepancy explained. Br. J. Nutr. 38, 145-147.
Just, A. 1978. The influence of processing on the nutritive hlason. V. C.,Just, A. & Bech-Andersen, S. 1976. Bac-
value of cereals for pigs. 29th Ann. Meet. EAAP, terial activity in the hind-gut of pigs. 2. Its influence
9 pp. Stockholm. o n the apparent digestibility of nitrogen and amino
Just, A. 1979. The influence of diet composition on site acids. Z. Tierpfrysiol.. Tiereriiihrung 11. FulternriitcZkde
of absorption and efficiency of utilization of metabo- 36, 310-324.
lizable energy in growing pigs. Proc. Btlr Syniposirriir Poppe, S., hleier, H. & Bennke, H. J. 1977. Zu einigen
on Energy hfetabolisrii of Farm Animals. Cambridge, methodischen Problemen der Bestimmung der wahren
UK. EAAP publ. Verdaulichkeit von Aminosiuren beim Schwein. Vth
Just, A. 1980. Ileal digestibility of protein: Applied International Synrposiuni O N Antino Acids. 1 1 pp. Buda-
aspects. In Current concepts of digestion and absorption pest.
inpigs (ed. A. G. Low and I. G. Partridge). Nat. Inst. Rerat, A., Vaissade, P., Vaugelade, P., Robin, D.,
for Research in Dairying, Shinfield, Reading. Robin, P. & Jung, J. 1977. Determination of nature
Just (Nielsen), A. & hlason, V. C. 1974.The influence of and quantity of endogenous nitrogen absorbed
the intestinal microflora of growing pigs o n the ap- during the digestion of a protein free meal in the pig.
parent digestibility of fatty acids and energy. Proc. 6th Vlh International Synrposiimi on Amino Acids. 8 pp.
Syntposiirni on Energy hfetabolisnr of Fami Animals. Budapest.
EAAP publ. 14, 193-196. Salter, D. N. 1973. The influence of gut micro-organisms
Just, A., Rasmussen, 0. K. & Hansen, H. L. 1976. Fac- o n utilization of dietary protein. Proc. Nufr. SOP.32,
tors influencing the digestibility and efficiency of utili- 65-71.
zation of metabolizable energy (hiE) in diets for Salter, D. N., Coates, hf. E. & Hewitt, D. 1974. Th e
growing pigs. 716 Syniposiwn on Energy hfetabolisiii, utilization of protein and excretion of uric acid in
Vichy, France. EAAP publ. 19, 289-292. germ-free and conventional chicks. Br. J. Nutr. 31,
Just, A., Jorgensen, H. & Fekadu, hl. 1978. The in- 307-3 18.
fluence of diet composition on digestibility, nutrient Salter, D. N. & Fulford, R. J. 1974. Th e influence of the
absorption from caecum-colon and the efficiency of gut microflora o n the digestion of dietary and en-
Acfa Agricrrlfttre Scandinarica 30 (I 980)
Iilflrrerice of diet cornposition 011 the apporent digestibility of crrrde protein 459

dogenous proteins: studies of the amino acid com- tion of amino acids in faeces by pigs fed on horsebean
position of the excreta 'of germ-free and conventional diet. 26111 Ann. hfccl.,EAAP. 7 pp. Warsaw.
chicks. Br. J. Nrrtr. 32, 625-637. Zebrowska, T. & Horszczaruk, F. 1975. Effect of feeding
Sauer, W. C. 1976. Factors influencing amino acid frequency on the amount and composition of digesta
availabilities for cereal grains and their components in the small intestine of pigs. Rocz. Nark Rol. B, 96
f or growing monogastric animals. Ph.D. Thesis, Univ. (3), 91-96.
of hlanitoba. 180 pp. Zebronska, T., Buraczewska, L.. Buraczewski, S. &
Sauer, W. C., Stothers, S. C. & Phillips, G. D. 1977. Horszczaruk, F. 1975. Digestion and absorption in
Apparent availabilities of amino acids in corn, the small intestine of pigs. Part 1. Digestion and
wheat and barley for growing pigs. Can. J. Anini. Sci. absorption of dry matter and nitrogen. Rocz. Narrk
57, 585-597. RoI. 8 , 96, 79-30.
Sauer, W. C., Stothers, S. C. & Parker, R. J. 1977. Zebrowska, T., Simon, O., hliinchmeyer, R. & Bergner,
Apparent and true availabilities in wheat and milling H. 1976. Untersuchungen zur Sezernierung endo-
by-products for growing pigs. Con. J. Anini. Sci. 57, gener Aminosauren in den Verdauungstrakt und zur
775-784. Aminosi?urenresorption beim Schwein. Arch. Ticrcr-
Schiirch, A. F., Lloyd, L. E. & Crampton, E. W. 1950. ndhrrrng 26, 69-82.
The use of chromic oxide as an index for determining Zebrowska, T., Buraczewska, L. & Buraczewski, S. 1977.
the digestibility of a diet. J. Nurr. 41, 629-636. Comparison of apparent digestibility of amino acids
Weidner, K. & Eggum, B. 0. 1966. Proteinhydrolysis: in the small intestine and in the whole digestive
A description of the method used at the Department tract of pigs. Vrlt Ititernarionul Synposirtni on Aniino
of Animal Physiology in Copenhagen. Acra Agric. Acids. 3 pp. Budapest.
Scanrl. 16, 115-1 19. Zebrowska, T., Buraczewska, L. & Horaczyriski, H.
Zebrowska, T. 1 9 7 3 ~ . Influence of dietary protein 1977. Apparent digestibility of nitrogen and amino
source on the rate of digestion in the small intestine of acids and utilization of protein given per 0 s or t o the
pigs. Part I. Amount and composition of digesta. caecum in pigs. Vrh Inrcrnatioiial Syniposirrni on Amino
Rocz. h'arn? Rol. B, 95 (I), 115-133. Acids. 4 pp. Budapest.
Zebrowska, T. 19736. Influence of dietary protein Zebrowska, T., Buraczewska, L., Pastuszewska, B.,
source o n the rate of digestion in the small intestine Chamberlain, A. G. & Buraczewski, S. 1977. Effect of
of pigs. Part 11. The rate of protein digcstion and diet and method of collection on amino acid composi-
amino acid absorption. Rocr. Nark Rol. B, 95 (I), tion of digesta and on digestibility of nitrogen and
135-151. amino acids in pigs. Vth International S~niposirrmon
Zebrowska, T. 1975. The apparent digestibility of nitrogen Amino Acids. 6 pp. Budaptst.
and individual amino acids in the large intestine of
pigs. Rocz. Narik Rol. B, 97 (I), 117-123.
h ls received February 4, 1980
Zebrowska, T. & Pastuszewska, B. 1975. Effect of caecal
infusion of neomycin on nitrogen balance and excre- Printed November 28, 1980

Acta Agriculturm Scandinarica 30 (1 980)

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