内源性大麻素代谢途径和酶。

Alessia Ligresti, Maria Grazia Cascio, Vincenzo Di Marzo
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引用次数: 78

摘要

内源性大麻素在1995年被定义为大麻素受体的内源性激动剂,其合成代谢和分解代谢途径以及这些途径中涉及的酶(“内源性大麻素酶”)是本综述的主题。一般策略似乎适用于调节两种主要内源性大麻素,anandamide和2-花生四烯醇甘油(2-AG)的水平。迄今为止,已经克隆了5种内源性大麻素酶:2种分别负责anandamide的生物合成和降解,即nape选择性磷脂酶D和脂肪酸酰胺水解酶;另外三种分别催化2-AG、sn-1选择性二酰基甘油脂肪酶α和β和单酰基甘油脂肪酶的生物合成和降解。本文讨论了这五种蛋白的主要特征,它们在决定内源性大麻素水平中的相对权重,以及其中一些蛋白的可能靶向治疗目的,以及存在替代合成代谢和分解代谢途径的可能性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Endocannabinoid metabolic pathways and enzymes.
Endocannabinoids, defined in 1995 as endogenous agonists of cannabinoid receptors, their anabolic and catabolic pathways, and the enzymes involved in these pathways (the "endocannabinoid enzymes"), are the subject of this review. A general strategy seems to apply to the regulation of the levels of the two major endocannabinoids, anandamide and 2-arachidonoylglycerol (2-AG). Five endocannabinoid enzymes have been cloned to date: two are responsible for the biosynthesis and degradation of anandamide, the NAPE-selective phospholipase D and the fatty acid amide hydrolase, respectively; the other three catalyse the biosynthesis and degradation of 2-AG, the sn-1-selective diacylglycerol lipases alpha and beta and the monoacylglycerol lipase, respectively. The major features of these five proteins, their relative weight in determining endocannabinoid levels, and the possible targeting of some of them for therapeutic purpose, as well as the possibility of the existence of alternative anabolic and catabolic pathways are discussed.
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