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酒精对N-甲基-D-天冬氨酸受体通道功能的抑制作用。

Alcohol inhibition of NMDA channel function.

作者信息

Weight F F, Lovinger D M, White G

机构信息

Section of Electrophysiology, National Institute on Alcohol Abuse and Alcoholism, Rockville, MD 20852.

出版信息

Alcohol Alcohol Suppl. 1991;1:163-9.

PMID:1726982
Abstract

In mammalian central neurons, intoxicating concentrations of ethanol inhibit the ion current activated by the glutamate agonist N-methyl-D-aspartate (NMDA). Electrophysiologic analysis of the molecular mechanism involved in this inhibition indicates that ethanol does not inhibit NMDA-activated ion current by voltage-dependent block of the channel, altering the ion selectivity of the channel, or altering the affinity of binding sites for NMDA, glycine or substances known to regulate the function of this channel (Mg2+, Zn2+ and ketamine). The potency for inhibiting the NMDA-activated current by different alcohols is linearly related to their hydrophobicity, suggesting that alcohols may inhibit the NMDA-activated current by a novel type of interaction with a hydrophobic region of the channel.

摘要

在哺乳动物中枢神经元中,达到中毒浓度的乙醇会抑制由谷氨酸激动剂N-甲基-D-天冬氨酸(NMDA)激活的离子电流。对这种抑制作用所涉及分子机制的电生理分析表明,乙醇并非通过电压依赖性阻断通道、改变通道的离子选择性或改变NMDA、甘氨酸或已知调节该通道功能的物质(Mg2+、Zn2+和氯胺酮)结合位点的亲和力来抑制NMDA激活的离子电流。不同醇类抑制NMDA激活电流的效力与其疏水性呈线性相关,这表明醇类可能通过与通道疏水区域的一种新型相互作用来抑制NMDA激活的电流。

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