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Low intestinal glutamine level and low glutaminase activity in Crohn's disease: a rational for glutamine supplementation?

Bernd Sido, Cornelia Seel, Achim Hochlehnert, Raoul Breitkreutz, Wulf Dröge
Other Digestive diseases and sciences 2006 73 citations
PubMed DOI
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Study Design

Type d'étude
Other
Population
None
Intervention
Low intestinal glutamine level and low glutaminase activity in Crohn's disease: a rational for glutamine supplementation? None
Comparateur
None
Critère de jugement principal
Low intestinal glutamine level and low glutaminase activity in Crohn's disease:
Direction de l'effet
Mixed
Risque de biais
Moderate

Abstract

Intestinal glutamine utilization is integral to mucosal regeneration. We analyzed the systemic and intestinal glutamine status in Crohn's disease (CD) and evaluated the therapeutic effect of glutamine supplementation in an animal model of ileitis. In CD, glutamine concentrations were decreased systemically and in noninflamed and inflamed ileal/colonic mucosa. Mucosal glutaminase activities were depressed in the ileum independent of inflammation but were not different from controls in the colon. In experimental ileitis, oral glutamine feeding prevented macroscopic inflammation, enhanced ileal and colonic glutaminase activities above controls, and normalized the intestinal glutathione redox status. However, glutamine supplementation enhanced myeloperoxidase activity along the gastrointestinal tract and potentiated lipid peroxidation in the colon. In conclusion, glutamine metabolism is impaired in CD. In experimental ileitis, glutamine supplementation prevents inflammatory tissue damage. In the colon, however, which does not use glutamine as its principal energy source, immune enhancement of inflammatory cells by glutamine increases oxidative tissue injury.

En bref

Glutamine metabolism is impaired in Crohn’s disease and the therapeutic effect of glutamine supplementation in an animal model of ileitis is evaluated, which indicates immune enhancement of inflammatory cells by glutamine increases oxidative tissue injury.

Used In Evidence Reviews

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