Dehydroepiandrosterone and alpha-estradiol limit the functional alterations of rat brain mitochondria submitted to different experimental stresses

Neuroscience. 2002;115(2):415-24. doi: 10.1016/s0306-4522(02)00416-5.

Abstract

The effects of dehydroepiandrosterone (DHEA), dehydroepiandrosterone-sulfate (DHEA-S), alpha-estradiol and beta-estradiol on the main functions of purified rat brain mitochondria were investigated in basal conditions and after being submitted to various stresses including anoxia-reoxygenation, uncoupling and apoptosis. In basal conditions, DHEA (1 microM) and alpha-estradiol (1 microM) inhibited the respiratory control ratio (RCR) from 3.1 to 2.3 (25%). After anoxia-reoxygenation, DHEA (1 microM) and alpha-estradiol (1 microM) reversed significantly (P<0.01) the RCR decrease from 1.4 to 2.0 (21.5%) by restoring the state 4. This effect was observed when DHEA was added either before anoxia or before reoxygenation and when alpha-estradiol was added before anoxia. The mitochondrial membranes damaged after the anoxia-reoxygenation were 70 and 50%, respectively, protected by DHEA and alpha-estradiol at 1 microM. They also limited by about 50%, the cytochrome c release induced by the anoxia-reoxygenation. The oxygen consumption of mitochondria in presence of NADH (130 microM) and cytochrome c (5 microM) was significantly inhibited by DHEA and alpha-estradiol with high EC(50) of 30 and 22 pM, respectively. At 1 microM, they also inhibited the 10 microM carbonyl cyanide m-chlorophenylhydrazone-induced uncoupling to about 35% whereas beta-estradiol only decreased it to 9%. Our results indicated that DHEA and alpha-estradiol partly preserved the mitochondrial functions altered by an anoxia-reoxygenation with a concentration-dependent effect. The mechanism involved was independent of the classical genomic effect of steroids, the antioxidant properties but implicated a direct action on the mitochondrial membranes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine Triphosphatases / metabolism
  • Adjuvants, Immunologic / pharmacology*
  • Animals
  • Apoptosis / drug effects
  • Brain / metabolism*
  • Carbonyl Cyanide m-Chlorophenyl Hydrazone / pharmacology
  • Carrier Proteins*
  • Cell Hypoxia / drug effects
  • Cytochrome c Group / metabolism
  • Dehydroepiandrosterone / pharmacology*
  • Electron Transport / drug effects
  • Electron Transport / physiology
  • Electron Transport Complex I
  • Electron Transport Complex II
  • Electron Transport Complex III / metabolism
  • Electron Transport Complex IV / metabolism
  • Estradiol / pharmacology*
  • Free Radicals / metabolism
  • Lipid Peroxidation / drug effects
  • Membrane Fluidity / drug effects
  • Membrane Proteins / metabolism
  • Mitochondria / drug effects
  • Mitochondria / metabolism*
  • Mitochondrial Proton-Translocating ATPases
  • Multienzyme Complexes / metabolism
  • NADH, NADPH Oxidoreductases / metabolism
  • Oxidative Stress / drug effects
  • Oxidoreductases / metabolism
  • Oxygen / pharmacology
  • Oxygen Consumption / drug effects
  • Rats
  • Reactive Oxygen Species / metabolism
  • Succinate Dehydrogenase / metabolism
  • Uncoupling Agents / pharmacology

Substances

  • Adjuvants, Immunologic
  • Carrier Proteins
  • Cytochrome c Group
  • Free Radicals
  • Membrane Proteins
  • Multienzyme Complexes
  • Reactive Oxygen Species
  • Uncoupling Agents
  • Dehydroepiandrosterone
  • Estradiol
  • Carbonyl Cyanide m-Chlorophenyl Hydrazone
  • Oxidoreductases
  • Electron Transport Complex II
  • Succinate Dehydrogenase
  • NADH, NADPH Oxidoreductases
  • Electron Transport Complex IV
  • Adenosine Triphosphatases
  • Mitochondrial Proton-Translocating ATPases
  • Electron Transport Complex I
  • Electron Transport Complex III
  • oligomycin sensitivity-conferring protein
  • Oxygen