Ligresti Alessia, Cascio Maria Grazia, Di Marzo Vincenzo
Endocannabinoid Research Group, Institute of Biomolecular Chemistry, Consiglio Nazionale delle Ricerche, Via Campi Flegrei 34, Comprensorio Olivetti, Fabbr. 70, 80078 Pozzuoli (NA), Italy.
Curr Drug Targets CNS Neurol Disord. 2005 Dec;4(6):615-23. doi: 10.2174/156800705774933104.
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.
内源性大麻素于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参与这些途径的酶(“内源性大麻素酶”)是本综述的主题。一种通用策略似乎适用于调节两种主要内源性大麻素——花生四烯乙醇胺和2-花生四烯酸甘油酯(2-AG)的水平。迄今为止,已克隆出五种内源性大麻素酶:两种分别负责花生四烯乙醇胺的生物合成和降解,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的生物合成和降解,即sn-1选择性二酰基甘油脂肪酶α和β以及单酰基甘油脂肪酶。本文讨论了这五种蛋白质的主要特征、它们在决定内源性大麻素水平方面的相对权重、其中一些用于治疗目的的可能靶向性,以及是否存在替代合成代谢和分解代谢途径的可能性。