生理和病理条件下内源性大麻素水平的调节。一个迷你回顾

V. Marzo
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引用次数: 3

摘要

在内源性大麻素受体配体“内源性大麻素”anandamide (n -花生四烯醇乙醇胺)和2-花生四烯醇甘油)被发现后,一些研究已经开展,以阐明这些化合物在动物组织中水平调节的分子机制。已经提出了一种以上的苯胺和2-花生四烯醇甘油的生物合成途径,并确定了几种使这些物质失活的途径。已经设计了特异性的阿南胺失活抑制剂。最近,这些化合物的水平与一些生理和病理情况的发生有关,如细胞损伤、休克、神经系统疾病、疼痛和炎症、大脑发育和药物耐受性。本文简要回顾了其中的一些研究,并提出了使用内源性大麻素衍生物质作为镇痛和神经保护药物的建议,并提出了anandamide和2-花生四烯醇甘油在运动障碍中的作用。
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Regulation of Endocannabinoid Levels under Physiological and Pathological Conditions. A Mini‐review
After the discovery of the endogenous ligands of cannabinoid receptors, the “endocannabinoids” anandamide (N-arachidonoyl-ethanolamine) and 2-arachidonoylglycerol, several studies have been carried out to clarify the molecular mechanisms underlying the regulation of the levels of these compounds in animal tissues. More than one biosynthetic pathway has been proposed for anandamide and 2-arachidonoylglycerol, and several routes for the inactivation of these substances have been identified also. Specific inhibitors of anandamide inactivation have been designed. More recently, the levels of these compounds have been correlated to the occurrence of some physiological and pathological situations, such as cell damage, shock, neurological disorders, pain and inflammation, brain development, and drug tolerance. Some of these studies are reviewed briefly here and have led to the proposal of the use of endocannabinoid-derived substances as analgesic and neuroprotective drugs, and to suggest a role for anandamide and 2-arachidonoylglycerol in motor disorders.
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