Glutamine dipeptide-supplemented parenteral nutrition reverses gut atrophy, disaccharidase enzyme activity, and absorption in rats. 1995

J Schröder, and E Wardelmann, and W Winkler, and F Fändrich, and E Schweizer, and P Schroeder
Department of General and Thoracic Surgery, University of Kiel, Germany.

BACKGROUND Total parenteral nutrition (TPN) is associated with intestinal atrophy and dysfunction possibly attributed to the absence of the nonessential amino acid glutamine from commercially available TPN solutions because of the instability of the monoamino acid during heat sterilization and storage. The use of stable dipeptides may overcome this problem. In this study we tested the hypothesis that glutamine dipeptide supplementation with alanyl-L-glutamine during TPN for 10 days would reverse small bowel atrophy and TPN-induced dysfunction in rats. METHODS A conventional TPN solution (250 kcal/kg bw) was compared with an isocaloric and isonitrogenous TPN supplemented with alanyl-L-glutamine dipeptide. A food-fed control group was included (n = 6 each group). Jejunum mucosal architecture, absorption of water and glucose, and disaccharidase activity of maltase and alkaline phosphatase were evaluated. RESULTS TPN-induced villous atrophy, significantly reduced absorption rate, and decreased activity of villous enzymes, compared with the TPN group, could be reversed by supplementation of glutamine dipeptide alanyl-L-glutamine to parenteral nutrition solutions with no difference to the control group. CONCLUSIONS Glutamine dipeptide-enriched parenteral nutrition preserves mucosal structure and reversed atrophy-associated dysfunction.

UI MeSH Term Description Entries
D007408 Intestinal Absorption Uptake of substances through the lining of the INTESTINES. Absorption, Intestinal
D007410 Intestinal Diseases Pathological processes in any segment of the INTESTINE from DUODENUM to RECTUM. Disease, Intestinal,Diseases, Intestinal,Intestinal Disease
D007422 Intestines The section of the alimentary canal from the STOMACH to the ANAL CANAL. It includes the LARGE INTESTINE and SMALL INTESTINE. Intestine
D008297 Male Males
D010289 Parenteral Nutrition, Total The delivery of nutrients for assimilation and utilization by a patient whose sole source of nutrients is via solutions administered intravenously, subcutaneously, or by some other non-alimentary route. The basic components of TPN solutions are protein hydrolysates or free amino acid mixtures, monosaccharides, and electrolytes. Components are selected for their ability to reverse catabolism, promote anabolism, and build structural proteins. Hyperalimentation, Parenteral,Intravenous Hyperalimentation,Nutrition, Total Parenteral,Parenteral Hyperalimentation,Total Parenteral Nutrition,Hyperalimentation, Intravenous
D004151 Dipeptides Peptides composed of two amino acid units. Dipeptide
D004186 Disaccharidases Enzymes belonging to the class of GLYCOSIDE HYDROLASES which break down DISACCHARIDES into simpler sugars, MONOSACCHARIDES. Disaccharidase
D005973 Glutamine A non-essential amino acid present abundantly throughout the body and is involved in many metabolic processes. It is synthesized from GLUTAMIC ACID and AMMONIA. It is the principal carrier of NITROGEN in the body and is an important energy source for many cells. D-Glutamine,L-Glutamine,D Glutamine,L Glutamine
D000469 Alkaline Phosphatase An enzyme that catalyzes the conversion of an orthophosphoric monoester and water to an alcohol and orthophosphate. EC 3.1.3.1.
D000520 alpha-Glucosidases Enzymes that catalyze the exohydrolysis of 1,4-alpha-glucosidic linkages with release of alpha-glucose. Deficiency of alpha-1,4-glucosidase may cause GLYCOGEN STORAGE DISEASE TYPE II. Acid Maltase,Lysosomal alpha-Glucosidase,Maltase,Maltases,Maltase-Glucoamylase,Neutral Maltase,Neutral alpha-Glucosidase,alpha-Glucosidase,Lysosomal alpha Glucosidase,Maltase Glucoamylase,Neutral alpha Glucosidase,alpha Glucosidase,alpha Glucosidases,alpha-Glucosidase, Lysosomal,alpha-Glucosidase, Neutral

Related Publications

J Schröder, and E Wardelmann, and W Winkler, and F Fändrich, and E Schweizer, and P Schroeder
March 1996, Annals of surgery,
J Schröder, and E Wardelmann, and W Winkler, and F Fändrich, and E Schweizer, and P Schroeder
January 1994, JPEN. Journal of parenteral and enteral nutrition,
J Schröder, and E Wardelmann, and W Winkler, and F Fändrich, and E Schweizer, and P Schroeder
December 1989, Archives of surgery (Chicago, Ill. : 1960),
J Schröder, and E Wardelmann, and W Winkler, and F Fändrich, and E Schweizer, and P Schroeder
December 1994, Gastroenterology,
J Schröder, and E Wardelmann, and W Winkler, and F Fändrich, and E Schweizer, and P Schroeder
September 2004, World journal of gastroenterology,
J Schröder, and E Wardelmann, and W Winkler, and F Fändrich, and E Schweizer, and P Schroeder
January 2005, JPEN. Journal of parenteral and enteral nutrition,
J Schröder, and E Wardelmann, and W Winkler, and F Fändrich, and E Schweizer, and P Schroeder
September 2000, The American journal of clinical nutrition,
J Schröder, and E Wardelmann, and W Winkler, and F Fändrich, and E Schweizer, and P Schroeder
January 1994, Nutrition (Burbank, Los Angeles County, Calif.),
J Schröder, and E Wardelmann, and W Winkler, and F Fändrich, and E Schweizer, and P Schroeder
April 1992, Clinical science (London, England : 1979),
J Schröder, and E Wardelmann, and W Winkler, and F Fändrich, and E Schweizer, and P Schroeder
January 2003, JPEN. Journal of parenteral and enteral nutrition,
Copied contents to your clipboard!