The objectives of this study were to determine the effects of oral Gln supplementation on growth performance, intestinal morphology, and expression of heat shock protein (Hsp) 70 in weaning piglets. A total of 65 piglets after weaning at 21 d of age (d 0) were used in this experiment. Five piglets were randomly selected and euthanized initially at d 0 to determine baseline values for the expression of Hsp70 in the small intestine. The remaining piglets were randomly assigned to 1 of 2 treatments and received 0 or 1 g of oral Gln/kg of BW every 12 h. After piglets were humanely killed at d 3, 7, and 14 postweaning, the duodenum, jejunum, and ileum of piglets were sampled to evaluate intestinal morphology and the expression and localization of Hsp70. The results indicated that oral Gln supplementation increased plasma concentrations of Gln compared with those in control piglets (P < 0.05). Average daily gain and ADFI were greater in piglets orally supplemented with Gln than in control piglets during the whole period (P < 0.05). The incidence of diarrhea in piglets orally supplemented with Gln was 24% less than (P = 0.064) that in control piglets at 8 to 14 d after weaning. The weights of the jejunum and ileum were greater in piglets orally supplemented with Gln compared with those of control piglets relative to BW on d 14 postweaning (P < 0.05). The villus height and the villus height:crypt depth ratio in the jejunum and the ileum were greater in piglets receiving oral Gln on d 14 postweaning (P < 0.05) than in control piglets. These results indicate that Gln supplementation can influence the intestinal morphology of weaned piglets. The expression of hsp70 mRNA and Hsp70 proteins in the duodenum and jejunum was greater in piglets supplemented with Gln than in control piglets (P < 0.05). However, Gln supplementation had no effect on the expression of hsp70 mRNA and Hsp70 proteins in the ileum. Moreover, the localization of Hsp70 in the cytoplasm indicated that Hsp70 has a cytoprotective role in epithelial cell function and structure. These results indicate that Gln supplementation may be beneficial for intestinal health and development and may thus mitigate diarrhea and improve growth performance. The protective mechanisms of Gln in the intestine may be associated with the increase in Hsp70 expression.

The objective of this study was to compare the effect of 2 esters of alpha-tocopherol, all-rac-alpha-tocopherol acetate and RRR-alpha-tocopherol succinate (d-alpha-TOS) on growth and immunity in broiler chicks. Three hundred twenty 1-d-old commercial Arbor Acres broilers were randomly distributed to 4 treatments, each of which had 8 pens of 10 chicks per pen. Birds in the control group were fed with the diets supplemented with 30 mg/kg of all-rac-alpha-tocopherol acetate or the basal diet with d-alpha-TOS supplementation at 10 mg/kg (TOS1 group), 30 mg/kg (TOS2 group), and 50 mg/ kg (TOS3 group), respectively, for 42 d. The results showed that there was no significant difference (P > 0.05) in BW gain, feed intake, or G:F among the treatments. Significant positive correlations existed between dietary supplemental alpha-TOS levels and plasma (R(2) = 0.9831, P < 0.01) or hepatic (R(2) = 0.9336, P < 0.05) alpha-tocopherol concentrations and a negative correlation with plasma (R(2) = 0.9487, P < 0.05) or hepatic (R(2) = -0.9901, P = 0.0518) malondialdehyde levels. The concentrations of serum glutathione (GSH) were highest at 50 mg/kg at 42 d of age (P < 0.05), and hepatic GSH was significantly higher at 30 and 50 mg/kg compared with the other groups. Marked enhancement of splenic T- and B-lymphocyte proliferation occurred in group TOS3 as compared with the other groups. The study suggests that the immunoenhancement effect observed in broilers fed additional d-alpha-TOS between 30 and 50 mg/kg might result from increased retention of alpha-tocopherol and reduction in lipid peroxidation, as evidenced by the decrease in malondialdehyde and the increase in GSH.

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