Protective role of hemeoxygenase-1 in gastrointestinal diseases

Cell Mol Life Sci. 2015 Mar;72(6):1161-73. doi: 10.1007/s00018-014-1790-1. Epub 2014 Nov 27.

Abstract

Disorders and diseases of the gastrointestinal system encompass a wide array of pathogenic mechanisms as a result of genetic, infectious, neoplastic, and inflammatory conditions. Inflammatory diseases in general are rising in incidence and are emerging clinical problems in gastroenterology and hepatology. Hemeoxygenase-1 (HO-1) is a stress-inducible enzyme that has been shown to confer protection in various organ-system models. Its downstream effectors, carbon monoxide and biliverdin have also been shown to offer these beneficial effects. Many studies suggest that induction of HO-1 expression in gastrointestinal tissues and cells plays a critical role in cytoprotection and resolving inflammation as well as tissue injury. In this review, we examine the protective role of HO-1 and its downstream effectors in modulating inflammatory diseases of the upper (esophagus and stomach) and lower (small and large intestine) gastrointestinal tract, the liver, and the pancreas. Cytoprotective, anti-inflammatory, anti-proliferative, antioxidant, and anti-apoptotic activities of HO-1 make it a promising if not ideal therapeutic target for inflammatory diseases of the gastrointestinal system.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Biliverdine / immunology
  • Carbon Monoxide / immunology
  • Gastrointestinal Diseases / drug therapy
  • Gastrointestinal Diseases / genetics
  • Gastrointestinal Diseases / immunology*
  • Gastrointestinal Diseases / pathology
  • Gastrointestinal Tract / drug effects
  • Gastrointestinal Tract / immunology*
  • Gastrointestinal Tract / metabolism
  • Gastrointestinal Tract / pathology
  • Gene Expression Regulation
  • Heme Oxygenase-1 / analysis
  • Heme Oxygenase-1 / genetics
  • Heme Oxygenase-1 / immunology*
  • Humans
  • Inflammation / drug therapy
  • Inflammation / genetics
  • Inflammation / immunology*
  • Inflammation / pathology
  • Molecular Targeted Therapy

Substances

  • Carbon Monoxide
  • Heme Oxygenase-1
  • Biliverdine