The intestine is not only critical for the absorption of nutrients, but also interacts with a complex external milieu. Most foreign antigens enter the body through the digestive tract. Dietary amino acids are major fuels for the small intestinal mucosa, as well as important substrates for syntheses of intestinal proteins, nitric oxide, polyamines, and other products with enormous biological importance. Recent studies support potential therapeutic roles for specific amino acids (including glutamine, glutamate, arginine, glycine, lysine, threonine, and sulfur-containing amino acids) in gut-related diseases. Results of these new lines of work indicate trophic and cytoprotective effects of amino acids on gut integrity, growth, and health in animals and humans.
Postweaning diarrhea is one of the most common causes of morbidity and mortality in weanling piglets. Feeding sodium butyrate to weanling piglets decreased the incidence of diarrhea, but the mechanism has not been fully elucidated. The present study was to evaluate the effect of sodium butyrate on diarrhea in relation to wound healing of intestinal barrier using IPEC-J2 cell model. Cultured cells were scratched to induce wound and then were treated with 4 mM sodium butyrate. The results showed that supplementation of the cells with sodium butyrate significantly promoted the process of wound healing, indicating the protective effects of butyrate on the intestinal mucosa. Butyrate treatment enhanced mRNA expression of the intestinal mucosal tight junction proteins occludin and zonula occluden protein-1 (P < 0.05), which suggested that the promotion of wound healing by butyrate is related to the maintenance of the function of the intestinal barrier. In addition, in the butyrate-treated group, intestinal total superoxide dismutase and glutathione peroxidase (P < 0.05), two of the main antioxidant enzymes, as well as glutathione (P < 0.05), one of the nonenzymatic antioxidant components, were enhanced whereas the malondialdehyde level, a marker of free radical mediated lipid peroxidation injury, was decreased (P < 0.05) compared with the control group. Collectively, these results indicate that dietary sodium butyrate might, at least partly, play an important role in recovering the intestinal tight junctions having a positive effect on maintaining the gut integrity.
A growth trial and a metabolism trial were conducted as 2 experiments to investigate the effects of dietary enzyme supplementation (primarily xylanase and beta-glucanase) on performance, nutrient digestibility, intestinal morphology, digestive organ size, and volatile fatty acid profiles in the hindgut of broiler chickens fed wheat-based diets. The experimental diets in both trials consisted of a wheat-based control diet supplemented with 0, 200, 400, 600, 800, or 1,000 mg/kg enzyme. Diets were given to the birds from d 7 to 42 of age. In the growth trial, enzyme supplementation improved performance of the broilers; daily gain and feed conversion increased linearly (P < 0.01) with increasing levels of enzyme supplementation. Enzyme inclusion decreased the size of the digestive organs and the gastrointestinal tract to some extent. The relative length of each intestinal segment decreased linearly (P < 0.05). The relative weight of the anterior intestine on d 21 and ileum on d 42 also decreased linearly (P < 0.01). On d 21 and 42, there were negative linear (P < 0.05) relationships between increasing enzyme supplementation and the relative weight of the liver and pancreas, respectively. Furthermore, there was a linear (P < 0.01) increase in total volatile fatty acid content in ileum on d 21 and in the cecum on d 21 and 42. During each period of the metabolism trial, apparent crude protein digestibility increased linearly (P < 0.05), whereas no differences were detected (P > 0.05) in AME.
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