Ethanol inhibits glutamate-induced currents in heteromeric NMDA receptor subtypes

Neuroreport. 1993 Dec 13;5(3):297-300. doi: 10.1097/00001756-199312000-00029.

Abstract

Maximal L-glutamate/glycine-evoked currents were inhibited by ethanol in Xenopus laevis oocytes expressing recombinant heteromeric NMDA receptors consisting of NR1-NR2A, NR1-NR2B, and NR1-NR2C subunit combinations. Concentration-dependent inhibition was observed at ethanol concentrations of > or = 50 mM both in Ca(2+)-containing and Ca(2+)-deficient, Ba(2+)-containing Mg(2+)-free media. The NR1-NR2C channels were slightly less sensitive to ethanol inhibition than the other heteromeric channels in Ca(2+)-deficient, Ba(2+)-containing medium. The inhibition was unaffected by the clamping-voltage and by a mutation [NR1-NR2A(N595Q)] that prevents the Mg(2+)-blockade of the channels, indicating that the mechanism of action of ethanol differs from that of Mg2+. The results are consistent with the hypothesis that the NMDA receptor subtypes can mediate many behavioural actions of ethanol.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cloning, Molecular
  • Ethanol / pharmacology*
  • Excitatory Amino Acid Antagonists*
  • Glutamates / pharmacology
  • Glutamic Acid
  • Glycine / pharmacology
  • Oocytes / drug effects
  • Oocytes / metabolism
  • Receptors, N-Methyl-D-Aspartate / antagonists & inhibitors*
  • Xenopus

Substances

  • Excitatory Amino Acid Antagonists
  • Glutamates
  • Receptors, N-Methyl-D-Aspartate
  • Ethanol
  • Glutamic Acid
  • Glycine