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大鼠严重乙醇中毒及戒断过程中的苯二氮䓬/GABA受体复合物

The benzodiazepine/GABA receptor complex during severe ethanol intoxication and withdrawal in the rat.

作者信息

Hemmingsen R, Braestrup C, Nielsen M, Barry D I

出版信息

Acta Psychiatr Scand. 1982 Feb;65(2):120-6. doi: 10.1111/j.1600-0447.1982.tb00830.x.

Abstract

The benzodiazepine/GABA (gammaaminobutyric acid) receptor complex was investigated during severe ethanol intoxication and withdrawal in the rat. The intragastric intubation technique was used to establish physical ethanol dependence in the animals. Cerebral cortex from male Wistar rats was studied 1) after 3 1/2 days of severe ethanol intoxication, 2) during the ethanol withdrawal reaction and 3) in a control group. The effect of GABA-ergic activation by muscimol and THIP (4,5,6,7-tetrahydroisoxazole(5,4-c)pyridin-3-01) on 3H-diazepam binding was unchanged during ethanol intoxication and withdrawal, as was the affinity constant (KD) and the maximal number of binding sites (Bmax) for 3H-flunitrazepam. In conclusion, the benzodiazepine/GABA receptor complex is unlikely to play any causal part in physical ethanol dependence.

摘要

在大鼠严重乙醇中毒及戒断过程中,对苯二氮卓/γ-氨基丁酸(GABA)受体复合物进行了研究。采用胃内插管技术使动物产生身体对乙醇的依赖性。对雄性Wistar大鼠的大脑皮层进行了研究:1)在严重乙醇中毒3.5天后;2)在乙醇戒断反应期间;3)设立对照组。在乙醇中毒和戒断期间,蝇蕈醇和THIP(4,5,6,7-四氢异恶唑并[5,4-c]吡啶-3-醇)对GABA能的激活作用对3H-地西泮结合的影响未变,3H-氟硝西泮的亲和常数(KD)和最大结合位点数(Bmax)也是如此。总之,苯二氮卓/GABA受体复合物不太可能在身体对乙醇的依赖性中起任何因果作用。

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