Oxidative stress induces vascular heme oxygenase-1 expression in ovariectomized rats

Free Radic Biol Med. 2005 Jul 1;39(1):108-17. doi: 10.1016/j.freeradbiomed.2005.02.033. Epub 2005 Mar 24.

Abstract

Heme oxygenase-1 (HO-1), an inducible stress protein, has been implicated in cytoprotection against oxidative stress in vitro and in vivo. Estrogens also have antioxidant effects. This study investigated the time course of HO-1 and inducible nitric oxide synthase (iNOS) expression in the aortas of ovariectomized rats, and the regulatory relationship between the NO/NOS and the carbon monoxide/HO systems. HO-1 and iNOS protein expression was induced by ovariectomy (Ovx) and was extremely high 2-6 weeks after Ovx compared with the sham-operated group. Expression of the constitutive enzymes HO-2 and endothelial NOS did not differ significantly between sham-operated and Ovx rats. 17beta-Estradiol (E(2)) replacement reversed these changes in rats after Ovx. Long-term treatment with the antioxidant tempol significantly inhibited HO-1 and iNOS expression. The iNOS inhibitor aminoguanidine significantly suppressed the induction of HO-1. Oxidized glutathione in the hearts of Ovx rats increased gradually, with significant elevation at 3-6 weeks after Ovx compared with the sham-operated group, whereas plasma levels of NO metabolites were significantly reduced 4-6 weeks after Ovx. Treatment with the HO inhibitor zinc protoporphyrin IX blocked HO-1 induction, but significantly increased the plasma levels of NO metabolites. In conclusion, HO-1 is induced by oxidative stress resulting from E(2) depletion. The NO/iNOS system contributes to the induction of HO-1, which may subsequently suppress iNOS activity to modulate vasculoprotective effects after menopause.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Aorta, Thoracic / enzymology*
  • Body Weight
  • Cyclic N-Oxides / pharmacology
  • Enzyme Induction
  • Estradiol / blood
  • Estradiol / pharmacology
  • Female
  • Glutathione Disulfide / metabolism
  • Guanidines / pharmacology
  • Heat-Shock Proteins / antagonists & inhibitors
  • Heat-Shock Proteins / biosynthesis*
  • Heme Oxygenase (Decyclizing)
  • Nitrates / blood
  • Nitric Oxide Synthase / antagonists & inhibitors
  • Nitric Oxide Synthase / biosynthesis
  • Nitric Oxide Synthase Type II
  • Nitric Oxide Synthase Type III
  • Nitrites / blood
  • Organ Size
  • Ovariectomy
  • Ovary / physiology*
  • Oxidative Stress / physiology*
  • Oxygenases / antagonists & inhibitors
  • Oxygenases / biosynthesis*
  • Protoporphyrins / pharmacology
  • Rats
  • Spin Labels
  • Time Factors
  • Uterus / anatomy & histology

Substances

  • Cyclic N-Oxides
  • Guanidines
  • Heat-Shock Proteins
  • Nitrates
  • Nitrites
  • Protoporphyrins
  • Spin Labels
  • zinc protoporphyrin
  • Estradiol
  • Oxygenases
  • Nitric Oxide Synthase
  • Nitric Oxide Synthase Type II
  • Nitric Oxide Synthase Type III
  • Nos2 protein, rat
  • Nos3 protein, rat
  • Heme Oxygenase (Decyclizing)
  • Hmox1 protein, rat
  • pimagedine
  • tempol
  • Glutathione Disulfide