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Endocannabinoids: synthesis and degradation

机译:内源性大麻素:合成和降解

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Endocannabinoids were defined in 1995 as endogenous agonists of cannabi-noid receptors, i.e. of the G protein-coupled receptors for cannabis's psychoactive principle, A9-tetrahydrocannabinol Although there appear to be several endocannabinoids, only two of such endogenous mediators have been thoroughly studied so far: anandamide and 2-arachidonoylglycerol (2-AG). A general strategy seems to apply to the biosynthesis and degradation of anandamide and 2-AG, although the levels of these two compounds appear to be regulated in different, and sometimes even opposing, ways "Endocannabinoid enzymes", that is to say enzymes that catalyse endocannabinoid biosynthesis or degradation, have been identified and in some cases cloned, and will be described in this review together with their possible pharmacological targeting for therapeutic purposes. The cellular and subcellular localization and the modes for the regulation of the expression and activity of these enzymes play an important role in the functions played by the endocannabinoids under physiological and pathological conditions.
机译: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,即大麻精神活性成分A9-四氢大麻酚的G蛋白偶联受体。 :anandamide和2-花生四烯酰基甘油(2-AG)。尽管这两种化合物的水平似乎以不同的,有时甚至是相反的方式“内源性大麻素酶”来调节,这似乎是一种通用策略似乎适用于阿南酰胺和2-AG的生物合成和降解。内源性大麻素的生物合成或降解已被鉴定,在某些情况下已被克隆,并将在本综述中进行描述,并结合其可能的药理作用进行治疗。这些酶在细胞和亚细胞中的定位以及表达方式和活性的调控方式在生理和病理条件下对内源性大麻素发挥的功能起着重要作用。

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