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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
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
' 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
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
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
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
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