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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 trích dẫn
PubMed DOI
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Study Design

Loại nghiên cứu
Other
Đối tượng nghiên cứu
None
Can thiệp
Low intestinal glutamine level and low glutaminase activity in Crohn's disease: a rational for glutamine supplementation? None
Đối chứng
None
Kết quả chính
Low intestinal glutamine level and low glutaminase activity in Crohn's disease:
Xu hướng hiệu quả
Mixed
Nguy cơ sai lệch
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.

Tóm lược

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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