Alcohol inhibits the depolarization-induced stimulation of oxidative phosphorylation in synaptosomes

J Neurochem. 1996 Apr;66(4):1691-7. doi: 10.1046/j.1471-4159.1996.66041691.x.

Abstract

The effects of alcohol and Ca2+ transport inhibitors on depolarization-induced stimulation of oxidative phosphorylation and free-Ca2+ concentrations in rat synaptosomes were investigated. Glucose oxidation was stimulated by depolarization with K+ or veratridine and by the Ca2+ ionophore ionomycin. The stimulation by K+, veratridine, and ionomycin was correlated with elevation of synaptosomal free Ca2+. Depolarization-stimulated respiration was inhibited by verapamil, Cd2+, and ruthenium red but not by diltiazem. Synaptosomal Ca2+ elevation was inhibited by verapamil but not by ruthenium red. These results indicate that the stimulation depends on elevation of mitochondrial free Ca2+. Ethanol, at pharmacological concentrations (50-200 mM), inhibited the Ca2+-dependent stimulation of oxidative phosphorylation. This inhibition resulted, in part, from the inhibition of voltage-gated Ca2+ channels, which inhibited the elevation of synaptosomal free Ca2+, and, in part, from the stimulation of the mitochondrial Ca2+/Na+ antiporter, which inhibited the elevation of the mitochondrial matrix free Ca2+. The inhibition by ethanol of the excitation-induced stimulation of oxidative phosphorylation in the synapse may contribute to the depressant and narcotic effects of alcohol and enhance excitotoxicity.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adenosine Triphosphate / biosynthesis
  • Animals
  • Cadmium / pharmacology
  • Calcium / metabolism
  • Calcium Channel Blockers / pharmacology
  • Cell Respiration / drug effects
  • Coloring Agents
  • Diltiazem / pharmacology
  • Ethanol / pharmacology*
  • Glucose / metabolism
  • Ionomycin / pharmacology
  • Ionophores / pharmacology
  • Male
  • Membrane Potentials / drug effects
  • Mitochondria / enzymology
  • Oxidative Phosphorylation / drug effects*
  • Oxygen Consumption / physiology
  • Potassium Chloride / pharmacology
  • Rats
  • Rats, Sprague-Dawley
  • Ruthenium Red / pharmacology
  • Signal Transduction / physiology
  • Synaptosomes / drug effects*
  • Synaptosomes / metabolism
  • Verapamil / pharmacology
  • Veratridine / pharmacology

Substances

  • Calcium Channel Blockers
  • Coloring Agents
  • Ionophores
  • Cadmium
  • Ruthenium Red
  • Ethanol
  • Ionomycin
  • Potassium Chloride
  • Veratridine
  • Adenosine Triphosphate
  • Verapamil
  • Diltiazem
  • Glucose
  • Calcium