Literature DB >> 20593496

Heme oxygenase-1 as a therapeutic target in inflammatory disorders of the gastrointestinal tract.

Vijith Vijayan1, Sebastian Mueller, Eveline Baumgart-Vogt, Stephan Immenschuh.   

Abstract

Heme oxygenase (HO)-1 is the inducible isoform of the first and rate-limiting enzyme of heme degradation. HO-1 not only protects against oxidative stress and apoptosis, but has received a great deal of attention in recent years because of its potent anti-inflammatory functions. Studies with HO-1 knockout animal models have led to major advances in the understanding of how HO-1 might regulate inflammatory immune responses, although little is known on the underlying mechanisms. Due to its beneficial effects the targeted induction of this enzyme is considered to have major therapeutic potential for the treatment of inflammatory disorders. This review discusses current knowledge on the mechanisms that mediate anti-inflammatory protection by HO-1. More specifically, the article deals with the role of HO-1 in the pathophysiology of viral hepatitis, inflammatory bowel disease, and pancreatitis. The effects of specific HO-1 modulation as a potential therapeutic strategy in experimental cell culture and animal models of these gastrointestinal disorders are summarized. In conclusion, targeted regulation of HO-1 holds major promise for future clinical interventions in inflammatory diseases of the gastrointestinal tract.

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Year:  2010        PMID: 20593496      PMCID: PMC2896748          DOI: 10.3748/wjg.v16.i25.3112

Source DB:  PubMed          Journal:  World J Gastroenterol        ISSN: 1007-9327            Impact factor:   5.742


  104 in total

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Review 3.  Cell biology of heme.

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6.  Unconjugated bilirubin inhibits VCAM-1-mediated transendothelial leukocyte migration.

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7.  Oxidative stress causes enhanced endothelial cell injury in human heme oxygenase-1 deficiency.

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10.  Nitric oxide mediates the lipopolysaccharide dependent upregulation of the heme oxygenase-1 gene expression in cultured rat Kupffer cells.

Authors:  S Immenschuh; M Tan; G Ramadori
Journal:  J Hepatol       Date:  1999-01       Impact factor: 25.083

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