Effect of oral glutamine on intestinal barrier function in young rats with endotoxemia.
- Author:
Xiao CHANG
1
;
Lin-Lin WANG
;
Shu-Jun LIAN
;
Qing TANG
;
Ping CHEN
;
Hua WANG
Author Information
- Publication Type:Journal Article
- MeSH: Administration, Oral; Amine Oxidase (Copper-Containing); metabolism; Animals; Behavior, Animal; Endotoxemia; metabolism; Female; Glutamine; administration & dosage; pharmacology; Intestines; drug effects; metabolism; Lactic Acid; blood; Male; Rats; Rats, Wistar
- From: Chinese Journal of Contemporary Pediatrics 2010;12(10):809-811
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo study the effect of glutamine on intestinal barrier function by examining the changes of plasma D-lactic levels and diamine oxidase (DAO) levels in plasma and intestinal tissue after glutamine intervention in young rats with endotoxemia.
METHODSEighty 18-day-old rats were randomly divided into endotoxemia and glutamine intervention groups (n=40 each). Endotoxemia was induced by lipopolysaccharide (LPS) injection. Plasma and small intestine homogenate were collected 1.5, 6, 24 and 72 hrs and 7 days after LPS injection. The glutamine intervention group was immediately administered with oral glutamine (2 g/kg) after LPS injection. Afterwards, glutamine was administered once daily. Plasma D-lactic and DAO levels and intestinal DAO levels were measured.
RESULTSPlasma DAO activity in the glutamine intervention group was significantly lower than that in the endotoxemia group 6 and 72 hrs after LPS injection (P<0.05). In contrast, the intestinal DAO activity in the glutamine intervention group was significantly higher than that in the endotoxemia group 6, 24 and 72 hrs and 7 days after LPS injection (P<0.05 or 0.01). Plasma D-lactic levels in the glutamine intervention group were significantly lower than those in the endotoxemia group 6, 24 and 72 hrs and 7 days after LPS injection (P<0.01).
CONCLUSIONSGlutamine may reduce the permeability of intestinal mucosa, and thus provides protective effects on intestinal barrier function in rats with endotoxemia.