Effect of nitric oxide on hydrogen peroxide-induced damage in isolated rabbit gastric glands

Pharmacology. 1998 Dec;57(6):323-30. doi: 10.1159/000028258.

Abstract

The present study aims at investigating the effects of nitric oxide (NO) on hydrogen peroxide (H2O2)-induced damage in isolated rabbit gastric glands. NO synthesis modulators such as L-arginine and NG-nitro-L-arginine methyl ester (L-NAME) and an NO donor, sodium nitroprusside, were added to isolated rabbit gastric glands exposed to H2O2, generated by glucose oxidase acting on beta-D-glucose. As a result, glucose/glucose oxidase caused an increase in lipid peroxide production and decreases in reduced glutathione (GSH) content, GSH peroxidase activity, nitrite release, and mucus secretion in gastric glands. The alterations in lipid peroxide production, GSH content, and mucus secretion were prevented by pretreatment with L-arginine, a substrate for NO synthase and sodium nitroprusside, but not by L-NAME. In conclusion, NO protects gastric glands from H2O2 by inhibiting lipid peroxidation and maintaining cellular GSH content and mucus secretion.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Drug Interactions
  • Enzyme Inhibitors / pharmacology
  • Gastric Mucosa / drug effects*
  • Gastric Mucosa / enzymology
  • Gastric Mucosa / metabolism
  • Glutathione Peroxidase / metabolism
  • Hydrogen Peroxide / toxicity*
  • Lipid Peroxides / biosynthesis*
  • NG-Nitroarginine Methyl Ester / pharmacology
  • Nitric Oxide / pharmacology*
  • Nitroprusside / pharmacology
  • Peroxidases / pharmacology
  • Rabbits

Substances

  • Enzyme Inhibitors
  • Lipid Peroxides
  • Nitroprusside
  • Nitric Oxide
  • Hydrogen Peroxide
  • Peroxidases
  • glucose peroxidase
  • Glutathione Peroxidase
  • NG-Nitroarginine Methyl Ester