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用烷基化苯二氮卓类药物肯那西平证明中枢神经系统中苯二氮卓受体的异质性。

Heterogeneity of benzodiazepine receptors in the central nervous system demonstrated with kenazepine, an alkylating benzodiazepine.

作者信息

Williams E F, Rice K C, Paul S M, Skolnick P

出版信息

J Neurochem. 1980 Sep;35(3):591-7. doi: 10.1111/j.1471-4159.1980.tb03695.x.

Abstract

Binding studies using the alkylating benzodiazepine kenazepine strongly suggest the existence of several populations of benzodiazepine receptors in the CNS. Kenazepine reacts noncompetitively and irreversibly with some receptors and competitively (reversibly) with others. Cerebellum contains the largest proportion (approx. 80%) of the noncompetitive type, while hippocampus and cortex contain a preponderance of competitive-type receptors (approx. 80 and 50%, respectively). The Hill coefficients for kenazepine are approx. 0.7 in cortex and cerebellum, and near unity in dorsal hippocampus. Different populations of benzodiazepine receptors may mediate different physiologic and pharmacologic effects in vivo.

摘要

使用烷基化苯二氮䓬类药物凯那西平进行的结合研究有力地表明,中枢神经系统中存在几种不同类型的苯二氮䓬受体。凯那西平与某些受体发生非竞争性和不可逆反应,与其他受体发生竞争性(可逆性)反应。小脑含有最大比例(约80%)的非竞争性类型受体,而海马体和皮质则主要是竞争性类型受体(分别约为80%和50%)。凯那西平在皮质和小脑中的希尔系数约为0.7,在背侧海马体中接近1。不同类型的苯二氮䓬受体可能在体内介导不同的生理和药理作用。

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