Peroxidative damage of mitochondrial respiration is substrate-dependent

Physiol Res. 2009;58(5):685-692. doi: 10.33549/physiolres.931635. Epub 2008 Nov 4.

Abstract

The concentration-dependence of tert-butyl hydroperoxide (BHP) inhibitory effect on oxygen consumption in isolated rat liver mitochondria was measured in the presence of various respiratory substrates. Strong inhibitory effect at low concentrations of BHP (15-30 microM) was found for oxoglutarate and palmitoyl carnitine oxidation. Pyruvate and glutamate oxidation was inhibited at higher concentrations of BHP (100-200 microM). Succinate oxidation was not affected even at 3.3 mM BHP. Determination of mitochondrial membrane potential has shown that in the presence of NADH-dependent substrates the membrane potential was dissipated by BHP but was completely restored after addition of succinate. Our data thus indicate that beside peroxidative damage of complex I also various mitochondrial NADH-dependent dehydrogenases are inhibited, but to a different extent and with different kinetics. Our data also show that succinate could be an important nutritional substrate protecting hepatocytes during peroxidative damage.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Respiration
  • Glutamic Acid / metabolism
  • Ketoglutaric Acids / metabolism
  • Male
  • Membrane Potential, Mitochondrial
  • Mitochondria, Liver / metabolism*
  • Oxidative Stress*
  • Oxygen Consumption
  • Palmitoylcarnitine / metabolism
  • Pyruvic Acid / metabolism
  • Rats
  • Rats, Wistar
  • Succinic Acid / metabolism
  • tert-Butylhydroperoxide / pharmacology

Substances

  • Ketoglutaric Acids
  • Palmitoylcarnitine
  • Glutamic Acid
  • Pyruvic Acid
  • tert-Butylhydroperoxide
  • Succinic Acid