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苯二氮䓬类药物的中枢作用:概述

Central actions of benzodiazepines: general introduction.

作者信息

Haefely W E

出版信息

Br J Psychiatry. 1978 Sep;133:231-8. doi: 10.1192/bjp.133.3.231.

Abstract

After a brief review of the characteristic somatic and psychotropic effects of benzodiazepines evidence is presented which supports a specific facilitatory action of these drugs on GABA ergic synapses within the mammalian central nervous system. Benzodiazepines enhance presynaptic inhibition in the spinal cord and dorsal column nuclei as well as postsynaptic inhibition in dorsal column nuclei, hippocampus, hypothalamus, cerebral cortex, cerebellar cortex, which are all examples of recurrent and collateral inhibition mediated by GABA ergic intrinsic neurones. In addition, the compounds also enhance the inhibitory effect of GABA ergic long projection neurones in the substantia nigra and the lateral vestibular nucleus of Deiters. Several problems remain to be solved, such as the exact site at which benzodiazepines initiate their action (pre-synaptically at GABA ergic nerve endings or postsynaptically at the target cells) and the possible existence of endogenous ligands for the benzodiazepine receptor. Some suspected implications which studies on benzodiazepine binding sites could have for a deeper understanding of the mode of action of these drugs are discussed.

摘要

在简要回顾了苯二氮䓬类药物的典型躯体和精神作用后,本文提供了证据,支持这些药物对哺乳动物中枢神经系统内γ-氨基丁酸(GABA)能突触具有特定的促进作用。苯二氮䓬类药物增强脊髓和薄束核的突触前抑制以及薄束核、海马体、下丘脑、大脑皮层、小脑皮层的突触后抑制,这些都是由GABA能内在神经元介导的返回性抑制和侧支抑制的例子。此外,这些化合物还增强了黑质和Deiters外侧前庭核中GABA能长投射神经元的抑制作用。仍有几个问题有待解决,例如苯二氮䓬类药物开始发挥作用的确切部位(在GABA能神经末梢的突触前还是在靶细胞的突触后)以及苯二氮䓬受体可能存在的内源性配体。本文讨论了关于苯二氮䓬类结合位点的研究对更深入理解这些药物作用方式可能产生的一些潜在影响。

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