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内源性大麻素的生物合成和失活,从简单到复杂。

Endocannabinoid biosynthesis and inactivation, from simple to complex.

机构信息

Bioanalysis and Pharmacology of Bioactive Lipids Laboratory, CHAM7230, Louvain Drug Research Institute, Université catholique de Louvain, Av. E. Mounier 72, B-1200 Bruxelles, Belgium.

出版信息

Drug Discov Today. 2010 Jun;15(11-12):474-83. doi: 10.1016/j.drudis.2010.03.007. Epub 2010 Mar 19.

Abstract

Cannabinoid receptors, the primary molecular targets of the endocannabinoid system, are activated by specific bioactive lipids termed 'endocannabinoids'. These lipid transmitters are synthesized from cell membrane phospholipids through multiple pathways and are inactivated by enzymatic hydrolysis, and their levels are the major parameter driving the endocannabinoid system activity. An in-depth understanding of their metabolic pathways is essential to unravel the endocannabinoid system's role in physiological and pathological situations and to devise new therapeutic strategies based on the endocannabinoid system. Major advances both in the characterization of anandamide's and 2-arachidonoylglycerol's biosynthesis and inactivation pathways and in the discovery of pharmacological tools used to interfere with their metabolism have been made and are discussed in this review.

摘要

大麻素受体是内源性大麻素系统的主要分子靶标,它们被特定的生物活性脂质激活,这些脂质递质是通过多种途径从细胞膜磷脂合成的,并通过酶水解失活,它们的水平是驱动内源性大麻素系统活性的主要参数。深入了解它们的代谢途径对于揭示内源性大麻素系统在生理和病理情况下的作用以及基于内源性大麻素系统设计新的治疗策略至关重要。本文综述了在鉴定花生四烯酸乙醇胺和 2-花生四烯酰甘油生物合成和失活途径以及发现用于干扰其代谢的药理学工具方面取得的重大进展,并对这些进展进行了讨论。

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