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Nitric oxide in inflammatory bowel disease

Authors

  • Raymond K. Cross,

    1. Department of Medicine, Division of Gastroenterology, Baltimore, Maryland
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  • Keith T. Wilson M.D.

    Corresponding author
    1. Department of Medicine, Division of Gastroenterology, Baltimore, Maryland
    2. Greenebaum Cancer Center, University of Maryland School of Medicine, Baltimore, Maryland
    3. Veterans Affairs Maryland Health Care System, Baltimore, Maryland, U.S.A.
    • University of Maryland School of Medicine, 22 South Greene Street, Room N3W62, Baltimore, MD 21201, U.S.A.
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Abstract

Nitric oxide (NO) is a pleiotropic free radical messenger molecule. There is a large body of evidence that the inducible form of the NO synthase enzyme (iNOS) that is responsible for high-output production of NO from l-arginine is up-regulated in various forms of mucosal inflammation. Consistent with this, multiple detection strategies have demonstrated that iNOS expression, enzymatic activity, and NO production are increased in human inflammatory bowel disease tissues. There is also evidence that the level of iNOS-derived NO correlates well with disease activity in ulcerative colitis, while for Crohn's disease, the results are more variable. A substantial number of animal studies have assessed the role of inducible NO production. While the majority of studies have shown improvement in experimental inflammatory bowel disease with iNOS inhibition, there are also a significant number of reports of exacerbation of disease with inhibitors. Similarly, studies using iNOS-deficient mice in colitis models have shown improvement, worsening, or no effect on disease. The authors suggest that additional studies to assess the role of the competing biochemical pathway, namely the conversion of l-arginine to polyamines via the actions of arginase and ornithine decarboxylase, may provide important new insights into understanding the regulation of mucosal inflammation and inflammatory bowel disease.

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