Total parenteral nutrition supplementation with glutamine improves survival after gut ischemia/reperfusion

JPEN J Parenter Enteral Nutr. 2002 May-Jun;26(3):169-73. doi: 10.1177/0148607102026003169.

Abstract

Background: Total parenteral nutrition (TPN) alters gut cytokines and mucosal immunity and increases intercellular adhesion molecule-1 (ICAM-1) expression, gut neutrophil levels, and mortality after gut ischemia. Supplementation of TPN with glutamine partially supports mucosal immunity by preserving respiratory and intestinal IgA levels, maintaining the proper IgA-stimulating cytokine milieu within the intestine, and reducing intestinal ICAM-1 expression and neutrophil accumulation. This work investigates whether glutamine supplementation of TPN affects mortality in mice after gut ischemic insult.

Methods: Thirty-eight mice were randomized to receive chow, TPN, or 2% glutamine-supplemented TPN (GLN-TPN) for 5 days. After feeding their respective diets, gut ischemia/reperfusion (I/R) was induced with superior mesenteric artery occlusion for 30 minutes followed by resuscitation with 1 mL saline. Survival was recorded until 72 hours after reperfusion.

Results: Survival time was significantly reduced in the TPN-fed mice compared with both chow-fed and GLN-TPN-fed mice (p < .05). Survival at 72 hours after reperfusion was also significantly lower in the TPN-fed mice than in the chow-fed and GLN-TPN-fed mice (p < .05)

Conclusions: Glutamine supplementation of TPN significantly improves survival after gut I/R, suggesting modulation of the inflammatory response or improved gut tolerance to low-flow states.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Cytokines / analysis
  • Glutamine / administration & dosage*
  • Glutamine / pharmacology
  • Immunity, Mucosal / drug effects
  • Immunoglobulin A / immunology
  • Intercellular Adhesion Molecule-1 / drug effects
  • Intercellular Adhesion Molecule-1 / metabolism*
  • Male
  • Mice
  • Mice, Inbred ICR
  • Parenteral Nutrition, Total*
  • Random Allocation
  • Reperfusion Injury / therapy*
  • Survival Analysis

Substances

  • Cytokines
  • Immunoglobulin A
  • Glutamine
  • Intercellular Adhesion Molecule-1