Studies were carried out to investigate the effect of dietary amino acid level on apparent ileal amino acid digestibility. Six barrows, average initial BW 35 kg, were fitted with a simple T-cannula at the distal ileum and fed six diets according to a 6 x 6 Latin square design. Six cornstarch-based diets containing six levels of CP from SBM (4, 8, 12, 16, 20, and 24% CP, respectively) were formulated. Chronic oxide was included as a digestibility marker. Each experimental period consisted of 8 d. After a 6-d adaptation period, ileal digesta were collected for 24 h during d 7 and 9 at 2-h intervals. The pigs were fed twice daily, equal amounts, at 0800 and 2000. The dietary allowance was 1,600 g/d during the first period and increased by 100 g each following period. There was a quadratic increase (P < .05) in apparent ileal amino acid digestibility as the dietary CP content was increased from 4 to 24%. Initially, the apparent ileal amino acid digestibilities increased sharply then gradually reached their plateaus, after which there were no further increases and the digestibility values became independent of the dietary amino acid levels. The lower end points of 95% confidence intervals of the plateau ileal digestibility values were defined to be the initial plateau digestibilities. The dietary CP and amino acid contents, corresponding to the initial plateau digestibility values, represent the dietary threshold levels.(ABSTRACT TRUNCATED AT 250 WORDS)
Daily outputs of mucin in ileal digesta were estimated in three barrows fed a protein-free diet while administered either saline (SAI) or a complete amino acid mixture (AAI) intravenously. The water soluble-ethanol precipitable fraction of ileal digesta (crude mucin; CM) was used to estimate the composition of mucin in ileal digesta. This fraction exhibited a carbohydrate composition characteristic of mucin and had a high threonine, serine and proline content (40 mol/100 mol). The proportions of soluble gastric and intestinal mucins, approximately 27 and 73%, respectively, were estimated from the N-acetylglucosamine (GlcNAc)/N-acetylgalactosamine (GalNAc) ratio in CM. The daily outputs of soluble mucin, 2.75 and 3.41 g/day from SAI and AAI pigs (p = 0.13), respectively, were determined from the GalNAc outputs in CM, assuming the above contributions of gastric and intestinal mucins. The estimated soluble mucin outputs accounted for more than 99% of the fucose, galactose, GalNAc and GlcNAc in CM. Total mucin outputs in ileal digesta, 5.32 and 5.65 g/day from SAI and AAI Pigs (p = 0.24), respectively, were determined from the total GalNAc output in digesta, assuming soluble and insoluble mucin had similar compositions. Based on these outputs, mucin represented approximately 30, 7 to 22, 15 and 11% of the endogenous threonine, proline, serine and protein, respectively, in ileal digesta. Approximately 74, 76, 100 and 53% of the fucose, galactose GalNAc and GlcNAc, respectively, in ileal digesta from pigs in this study was attributed to mucin. The results from this study demonstrate the importance of mucin as a source of some endogenous amino acids and carbohydrates.
Methodology was developed for measuring the gastrointestinal endogenous phosphorus (P) outputs and true P digestibility values in studies with piglets. Four barrows, average initial body weight 6.8 kg, were fitted with a simple T-cannula at the distal ileum and fed four diets according to a 4 x 4 Latin square design. Four cornstarch-based diets containing four levels of P (1.1, 2.1, 3.2 and 4.3 g/kg diet) on a dry matter (DM) basis were formulated from soybean meal (SBM). Each experimental period comprised 8 d with a 4-d adaptation and 4-d collection of ileal digesta and feces. The apparent ileal and fecal P digestibility values in SBM were affected (P < 0.05) by P levels in the assay diets. The ileal and fecal P digestibility values increased from -24.8 to 37.1% and from 18.8 to 42.5%, respectively, as P contents increased from 1.1 to 4.3 g/kg DM diet. Linear relationships (P < 0.05), expressed as g/kg DM diet intake, between ileal and fecal outputs and dietary inputs of P, suggested that the endogenous P outputs can be determined by linear regression analysis. The endogenous P output was higher (P < 0.05) in ileal digesta than in feces (0.86 +/- 0.09 vs. 0.31 +/- 0.06 g/kg DM diet intake). There was no difference (P > 0.05) between the true ileal (50.7 +/- 7.1%) and fecal (48.5 +/- 5.4%) P digestibility values in SBM. These results suggest that differences in P contents between assay diets are primarily responsible for the large variability in apparent P digestibility values reported within the same ingredient. Apparent digestibility values underestimate the true digestive utilization of P by approximately 25%. True rather than apparent P digestibility values should be determined and used in diet formulation for pigs. In addition, this study shows that the gastrointestinal endogenous P output is important in whole-body P requirement and homeostasis.
Sauln, W. C., JoncENseN A method for measuring protein digestibility of small feed samples was developed with growing pigs fitted with a single cannula in the duodenum. Feed was ground through a 0.8-mm mesh screen and 1-g samples were enclosed in 25 x 40-mm monofilament nylon bags (50-pm mesh). Following pre-digestion in vitro to simulate gastric digestion (0.01 N HCI; pepsin I glL 2.5 h), the bags were inserted into the small intestine vra the duodenal cannula. recovered in feces within 48 h. frozen, lyophilized and analyzed for protein. Apparent
Nine barrows with an average initial weight of 60 kg were fitted with simple Tcannulas at the distal ileum. The animals were fed four different protein-free diets according to an incomplete latin square design. Diet 1 (control diet) consisted of 79.7% cornstarch, 10% sucrose, 3% Alphafloc (a source of cellulose), 3% canola oil and a vitamin-mineral premix. Diets 2, 3 and 4 contained, respectively, 4% pectin, an additional 7% cellulose and an additional 10% canola oil, each included at the expense of cornstarch. Feces were collected during 3 d following a 7-d adaptation period. Thereafter, digesta were collected during two 24-h periods with a 24-interval between periods. The pigs were fed 800 g of feed twice at 0800 and 2000. Added pectin increased (P < .05) the recovery of endogenous protein in ileal digesta from 19.8 diet (diet 1) to 24.0 g per kg dry matter intake. This increment was largely due to increases (P < .05) in glycine and proline from 1.9 to 2.4 and from 6.2 to 8.4 g per kg dry matter intake, respectively. In feces, only added cellulose increased (P < .05) excretion of endogenous protein (8.4 vs 11.1 g/kg DM intake) and of most amino acids. Including additional fat did not affect the quantity of endogenous protein and amino acids recovered in ileal digesta or feces. Small but significant differences (P < .05) were observed in the amino acid composition of endogenous protein recovered in ileal digesta when the different protein-free diets were fed. The amino acid composition of endogenous protein in feces was relatively constant (P > .05).
Three methods were evaluated for the determination of apparent ileal digestibility values of amino acids in feedstuffs with a low protein (barley, 10.2% CP) and a high protein content (canola meal, 38.2% CP). Five barrows, average initial BW 40 kg, were fitted with a simple T-cannula at the distal ileum and fed five diets according to a 5 x 5 Latin square design. Diet 1 contained 42.7% canola meal providing the sole source of dietary amino acids. Diets 2, 3, and 4 contained three graded levels of barley (22.5, 45.0, and 67.5%, respectively) and three graded levels of canola meal (36.6, 30.5, and 24.4%, respectively). Diet 5 contained 90.0% barley, which provided the sole source of dietary amino acids. With the exception of diet 5, the diets were formulated to contain 16% CP. Chromic oxide (.4%) was included as the digestibility marker. The pigs were fed twice daily, equal amounts, at 0800 and 2000. The dietary allowance was 1,800 g/d. Each experimental period comprised 8 d. Ileal digesta were collected for a total of 24 h during d 7 and 8 at 2-h intervals. Apparent ileal digestibility values of amino acids in barley were determined with the direct method from diet 5, with the difference method from diets 2, 3, and 4, and with the regression method from diets 1, 2, 3, and 4. Digestibility values of amino acids in canola meal were determined with the direct method from diet 1, with the difference method from diets 2, 3, and 4, and with the regression method from diets 1, 2, 3, and 4. There were no differences (P < .05) in the digestibility values in barley between the difference method when barley was included at 67.5% in the diet and the regression method. However, the digestibility values were lower (P < .05 or < .10) when these were determined with the direct method. There were no differences (P > .05) in the digestibility values of canola meal when these were determined with the direct method, the difference method, when canola meal was included at 36.6% in the diet, and the regression method. In conclusion, amino acid digestibility values in feedstuffs with a low protein content should be determined with the difference or regression methods rather than with the direct method. Amino acid digestibility values in feedstuffs with a high protein content can be determined with either method.
The objective of this study was to determine the effect of supplementing a wheat-based diet with xylanase and phospholipase either alone or in combination on the ileal and fecal digestibilities of nutrients and energy in early-weaned pigs. In addition, the concentrations of ammonia, lactate, and VFA were measured in ileal digesta and feces. The experiment was carried out with 16 barrows weaned at the age of 11 d with an average initial BW of 4.1 kg. On d 4 and 5 postweaning, the piglets were fitted with a simple T-cannula at the distal ileum. The experiment was designed as a balanced incomplete block design with three periods. The piglets received the basal diet with or without supplementation of either xylanase or phospholipase or a combination of these. There was a positive (P = 0.005 to 0.018) effect on the digestibility values of GE, OM, CP, crude fiber (CF), and NDF with xylanase supplementation. Apart from lysine, threonine, cysteine, glycine, and proline, the digestibility values of all AA were improved (P = 0.001 to 0.024). Phospholipase supplementation had a positive effect on CP (P = 0.047) and CF (P = 0.002) digestibilities, but no effect on ether extract (EE) digestibility. Supplementation of both enzymes showed the largest response in nutrient digestibilities, except that EE digestibility was not affected. No differences were found in D-/L- lactate, and ammonia concentrations among treatments. Acetate and propionate concentrations tended to increase when xylanase was supplemented and were highest for the combination of both enzymes. Despite the positive effects on ileal nutrient and energy digestibilities, there was no effect of xylanase or the combined enzyme supplementation on the fecal digestibilities of OM, CP, EE, CF, NDF, ADF, or GE, and on fecal concentrations of VFA. Phospholipase alone slightly decreased the total-tract nutrient and energy digestibilities (P < 0.05). In conclusion, the combination of both enzymes generally led to the highest increases in ileal digestibilities, which were of small numerical magnitude (approximately 2%). However, on a relative basis, this increase of 2% represents approximately 13% of the remaining diet that was available for digestion based on the fact that approximately 15% of the diet was not digested in the control pigs. Thus, the potential benefits in the nutrition of weanling pigs from combinations of enzymes should be validated under practical conditions.
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