Effect of dehydroepiandrosterone (DHEA) treatment on oxidative energy metabolism in rat liver and brain mitochondria. A dose-response study

Clin Biochem. 2007 Jan;40(1-2):57-65. doi: 10.1016/j.clinbiochem.2006.08.014. Epub 2006 Sep 14.

Abstract

Objectives: Effects of treatment with dehydroepiandrosterone (DHEA) on oxidative energy metabolism in rat liver and brain mitochondria were examined.

Design and methods: Young adult rats were administered DHEA (0.1, 0.2, 1.0 or 2.0 mg/kg body weight) by subcutaneous route for 7 consecutive days.

Results: DHEA treatment resulted in general, in stimulation of state 3 respiration rates without having any uncoupling effect on ADP/O ratios. The stimulation of state 3 respiration rate for a given substrate was dose dependent in a tissue-specific manner. Parallel increases in the contents of cytochromes aa(3) and b were also noted. DHEA treatment stimulated the glutamate dehydrogenase (GDH) and succinate DCIP reductase (SDR) activities. Under the treatment conditions, mitochondrial ATPase activity was also stimulated.

Conclusions: Treatment with DHEA significantly stimulated oxidative energy metabolism in liver and brain mitochondria.

MeSH terms

  • Adenosine Triphosphatases / metabolism
  • Animals
  • Ascorbic Acid / metabolism
  • Brain / drug effects*
  • Brain / enzymology
  • Cytochromes / metabolism
  • Cytosol / drug effects
  • Cytosol / enzymology
  • Dehydroepiandrosterone / administration & dosage
  • Dehydroepiandrosterone / pharmacology*
  • Glutamic Acid / metabolism
  • Malates / metabolism
  • Male
  • Mitochondria / drug effects*
  • Mitochondria / enzymology
  • Mitochondria, Liver / drug effects*
  • Mitochondria, Liver / enzymology
  • Oxidative Phosphorylation / drug effects*
  • Oxidoreductases / metabolism
  • Pyruvic Acid / metabolism
  • Rats
  • Substrate Specificity / drug effects
  • Succinic Acid / metabolism
  • Tetramethylphenylenediamine / metabolism

Substances

  • Cytochromes
  • Malates
  • Glutamic Acid
  • Dehydroepiandrosterone
  • malic acid
  • Pyruvic Acid
  • Succinic Acid
  • Oxidoreductases
  • Adenosine Triphosphatases
  • Tetramethylphenylenediamine
  • Ascorbic Acid