F1F0-ATPase, early target of the radical initiator 2,2'-azobis-(2-amidinopropane) dihydrochloride in rat liver mitochondria in vitro

Biochem J. 1996 Dec 1;320 ( Pt 2)(Pt 2):571-6. doi: 10.1042/bj3200571.

Abstract

This study was designed to determine which enzyme activities were first impaired in mitochondria exposed to 2,2'-azobis-(2-amidinopropane) dihydrochloride (AAPH), a known radical initiator. EPR spin-trapping revealed generation of reactive oxygen species although malondialdehyde formation remained very low. With increasing AAPH concentrations, State-3 respiration was progressively depressed with unaltered ADP/O ratios. A top-down approach demonstrated that alterations were located at the phosphorylation level. As shown by inhibitor titrations, ATP/ADP translocase activity was unaffected in the range of AAPH concentrations used. In contrast, AAPH appeared to exert a deleterious effect at the level of F1F0-ATPase, comparable with dicyclohexylcarbodi-imide, which alters Fo proton channel. A comparison of ATP hydrolase activity in uncoupled and broken mitochondria reinforced this finding. In spite of its pro-oxidant properties, AAPH was shown to act as a dose-dependent inhibitor of cyclosporin-sensitive permeability transition initiated by Ca2+, probably as a consequence of its effect on F1F0-ATPase. Resveratrol, a potent antiperoxidant, completely failed to prevent the decrease in State-3 respiration caused by AAPH. The data suggest that AAPH, when used under mild conditions, acted as a radical initiator and was capable of damaging F1F0-ATPase, thereby slowing respiratory chain activity and reducing mitochondrial antioxidant defences.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amidines / pharmacology*
  • Animals
  • Atractyloside / analogs & derivatives
  • Atractyloside / pharmacology
  • Carbonyl Cyanide m-Chlorophenyl Hydrazone / pharmacology
  • Cyclic N-Oxides
  • Dicyclohexylcarbodiimide / pharmacology
  • Electron Spin Resonance Spectroscopy
  • Female
  • Free Radicals / metabolism
  • Intracellular Membranes / drug effects
  • Intracellular Membranes / physiology*
  • Kinetics
  • Lipid Peroxidation / drug effects
  • Malondialdehyde / analysis
  • Membrane Potentials / physiology
  • Mitochondria, Liver / drug effects
  • Mitochondria, Liver / metabolism*
  • Oxidative Phosphorylation / drug effects*
  • Oxygen Consumption / drug effects
  • Proton-Translocating ATPases / drug effects
  • Proton-Translocating ATPases / metabolism*
  • Rats
  • Rats, Wistar
  • Spin Labels
  • Succinates / metabolism

Substances

  • Amidines
  • Cyclic N-Oxides
  • Free Radicals
  • Spin Labels
  • Succinates
  • Atractyloside
  • Malondialdehyde
  • Dicyclohexylcarbodiimide
  • Carbonyl Cyanide m-Chlorophenyl Hydrazone
  • 5,5-dimethyl-1-pyrroline-1-oxide
  • 2,2'-azobis(2-amidinopropane)
  • Proton-Translocating ATPases
  • carboxyatractyloside