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Ethanol inhibits glutamate-induced currents in heteromeric NMDA receptor subtypes.

作者信息

Kuner T, Schoepfer R, Korpi E R

机构信息

Laboratory of Molecular Neuroendocrinology, University of Heidelberg, Germany.

出版信息

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.

摘要

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