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中枢神经系统苯二氮䓬受体:生理学研究与假定的内源性配体

CNS benzodiazepine receptors: physiological studies and putative endogenous ligands.

作者信息

Skolnick P, Marangos P J, Syapin P, Goodwin F K, Paul S M

出版信息

Pharmacol Biochem Behav. 1979 May;10(5):815-23. doi: 10.1016/0091-3057(79)90340-x.

Abstract

The recent demonstration of benzodiazepine receptors in the mammalian CNS has provided new information on the mechanism of action of this important class of drugs. In addition, the presence of these receptors has prompted studies on their physiological significance, including attempts at isolating an endogenous ligand. The isolation of a number of substances from bovine brain that competitively inhibit (3H)-diazepam binding to synaptosomal membrane suggests the presence of an endogenous ligand. Two of these substances have been identified as the purines inosine and hypoxanthine. Pharmacological studies of these purines suggest that they may have diazepam-like effect in vivo. The possibility that the brain may contain its own benzodiazepine-like compound is currently being studied.

摘要

最近在哺乳动物中枢神经系统中苯二氮䓬受体的发现,为这一重要类别的药物作用机制提供了新信息。此外,这些受体的存在促使人们对其生理意义进行研究,包括尝试分离内源性配体。从牛脑中分离出多种竞争性抑制(3H)-地西泮与突触体膜结合的物质,提示存在内源性配体。其中两种物质已被鉴定为嘌呤肌苷和次黄嘌呤。对这些嘌呤的药理学研究表明,它们在体内可能具有地西泮样作用。目前正在研究大脑中可能含有自身苯二氮䓬样化合物的可能性。

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