Suppr超能文献

乙醇与γ-氨基丁酸-苯二氮䓬受体复合物

Ethanol and the gamma-aminobutyric acid-benzodiazepine receptor complex.

作者信息

Greenberg D A, Cooper E C, Gordon A, Diamond I

出版信息

J Neurochem. 1984 Apr;42(4):1062-8. doi: 10.1111/j.1471-4159.1984.tb12711.x.

Abstract

Ethanol appears to enhance gamma-aminobutyric acid (GABA)-mediated synaptic transmission. Using radioligand binding techniques, we investigated the possibility that the GABA-benzodiazepine receptor complex is the site responsible for this effect. Ethanol at concentrations up to 100 mM failed to alter binding of [3H]flunitrazepam (FNZ), [3H]Ro 15-1788, or [3H]methyl-beta-carboline-3-carboxylate (MBCC) to benzodiazepine receptors, or of [3H]muscimol to GABA receptors in rat brain membranes. Scatchard analyses of the binding of these radioligands at 4 degrees C and 37 degrees C revealed no significant effects of 100 mM ethanol on receptor affinity or number. A variety of drugs as well as chloride ion increased binding of [3H]FNZ and/or [3H]muscimol, but these influences were not modified by ethanol. These findings indicate that ethanol probably potentiates GABAergic neurotransmission at a signal transduction site beyond the GABA-benzodiazepine receptor complex.

摘要

乙醇似乎能增强γ-氨基丁酸(GABA)介导的突触传递。我们运用放射性配体结合技术,研究了GABA-苯二氮䓬受体复合物是否是产生这一效应的位点。浓度高达100 mM的乙醇未能改变[³H]氟硝西泮(FNZ)、[³H]Ro 15-1788或[³H]甲基-β-咔啉-3-羧酸(MBCC)与大鼠脑膜中苯二氮䓬受体的结合,也未改变[³H]蝇蕈醇与GABA受体的结合。在4℃和37℃下对这些放射性配体结合进行的Scatchard分析表明,100 mM乙醇对受体亲和力或数量无显著影响。多种药物以及氯离子可增加[³H]FNZ和/或[³H]蝇蕈醇的结合,但这些影响不受乙醇的改变。这些发现表明,乙醇可能在GABA-苯二氮䓬受体复合物之外的信号转导位点增强GABA能神经传递。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验