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苯二氮䓬受体结合的调节:对药理疗效的深入了解。

Modulation of benzodiazepine receptor binding: insight into pharmacological efficacy.

作者信息

Ehlert F J, Ragan P, Chen A, Roeske W R, Yamamura H I

出版信息

Eur J Pharmacol. 1982 Feb 26;78(2):249-53. doi: 10.1016/0014-2999(82)90246-1.

Abstract

The effects of GABA on the binding of analogues of benzodiazepines, triazolopyridazines, beta-carbolines and imidazodiazepines were examined in ligand/[3H] flunitrazepam competition experiments. GABA increased the potency of anxiolytics, like flunitrazepam, whereas the potency of benzodiazepine antagonists, like Ro15-1788, was largely insensitive to the influence of GABA. Several other agents including pyrazolopyridines, barbiturates and etomidate caused a chloride dependent enhancement of [3H] flunitrazepam binding but not an enhancement of [3H] propyl-beta-carboline-3-carboxylate binding.

摘要

在配体/[³H]氟硝西泮竞争实验中,研究了γ-氨基丁酸(GABA)对苯二氮䓬类、三唑并哒嗪类、β-咔啉类和咪唑并二氮䓬类类似物结合的影响。GABA增强了如氟硝西泮等抗焦虑药的效力,而像Ro15 - 1788这类苯二氮䓬拮抗剂的效力在很大程度上不受GABA影响。包括吡唑并吡啶类、巴比妥类和依托咪酯在内的其他几种药物可引起[³H]氟硝西泮结合的氯离子依赖性增强,但不会增强[³H]丙基-β-咔啉-3-羧酸盐的结合。

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