奥卡西泮
安定
氯二氮杂环氧化物
化学
药理学
γ-氨基丁酸受体
佐匹克隆
苯二氮卓
硝西泮
氟马西尼
结合位点
氯硝西泮
敌手
GABA受体拮抗剂
受体
生物化学
催眠药
荷包牡丹碱
医学
作者
John H. Skerritt,Graham A.R. Johnston
标识
DOI:10.1016/0014-2999(83)90494-6
摘要
Several benzodiazepines (chlordiazepoxide, clonazepam, diazepam, midazolam, nitrazepam and oxazepam) produced a concentration-dependent enhancement of low affinity GABA binding to fresh, washed brain membranes in 50 mM Tris-citrate buffer at concentrations comparable to those displacing [3H]diazepam binding in vitro. The nonbenzodiazepine anxiolytics CL218872 and zopiclone also enhanced GABA binding, while the centrally inactive benzodiazepine Ro5-4864 failed to alter GABA binding. The benzodiazepine antagonist, Ro15-1788 did not alter GABA binding but potently antagonised stimulation of GABA binding by 100 nM diazepam. These pharmacological characteristics suggest than an enhancement of the binding of GABA to low affinity receptor sites may give rise to many of the in vivo actions of the benzodiazepines.
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