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内源性大麻素的生物合成与失活:与其作为神经调质的假定作用的相关性。

Biosynthesis and inactivation of endocannabinoids: relevance to their proposed role as neuromodulators.

作者信息

Di Marzo V

机构信息

Istituto per la Chimica di Molecole di Interesse Biologico, C.N.R., Napoli, Italy.

出版信息

Life Sci. 1999;65(6-7):645-55. doi: 10.1016/s0024-3205(99)00287-8.

Abstract

The two putative endogenous ligands of cannabinoid receptors, anandamide and 2-arachidonoylglycerol, are synthesized by and released from neurons in a Ca2+-dependent fashion, and re-uptaken and catabolized by both neurons and astrocytes. These biochemical features of the endocannabinoids, as well as some of their pharmacological effects in both central and peripheral nervous systems, suggest a role as neuromodulators for these metabolites. This neuromodulatory role is supported by the brain regional distribution of anandamide, its biosynthetic precursor and its major inactivating enzyme, and by the existence of possible regulatory mechanisms for the biosynthesis and inactivation of endocannabinoids, which are reviewed in this article.

摘要

大麻素受体的两种假定内源性配体,花生四烯乙醇胺和2-花生四烯酸甘油酯,以钙离子依赖的方式由神经元合成并释放,然后被神经元和星形胶质细胞重新摄取并分解代谢。内源性大麻素的这些生化特性,以及它们在中枢和外周神经系统中的一些药理作用,表明这些代谢产物具有神经调质的作用。花生四烯乙醇胺、其生物合成前体及其主要失活酶在脑区的分布,以及内源性大麻素生物合成和失活可能存在的调节机制,都支持了这种神经调节作用,本文将对此进行综述。

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