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衰老过程中的内源性大麻素系统:药物研发的新靶点。

The endocannabinoid system in ageing: a new target for drug development.

作者信息

Paradisi A, Oddi S, Maccarrone M

机构信息

Department of Biomedical Sciences, University of Teramo, Piazza A. Moro 45, 64100 Teramo, Italy.

出版信息

Curr Drug Targets. 2006 Nov;7(11):1539-52. doi: 10.2174/1389450110607011539.

Abstract

Endocannabinoids are a new class of lipids, which include amides, esters and ethers of long chain polyunsaturated fatty acids. Anandamide (N-arachidonoylethanolamine; AEA) and 2-arachidonoylglycerol are the main endogenous agonists of cannabinoid receptors able to mimic several pharmacological effects of Delta(9)-tetrahydrocannabinol, the active principle of Cannabis sativa preparations like hashish and marijuana. AEA is released "on demand" from membrane lipids, and its activity at the receptors is limited by cellular uptake followed by intracellular hydrolysis. Together with AEA and congeners, the proteins which bind, synthesize, transport and hydrolyze AEA form the "endocannabinoid system". Endogenous cannabinoids are present in the central nervous system and in peripheral tissues, suggesting a physiological role as broad spectrum modulators. This review summarizes the main features of the endocannabinoid system, and the latest advances on its involvement in ageing of central and peripheral cells. In addition, the therapeutic potential of recently developed drugs able to modulate the endocannabinoid tone for the treatment of ageing and age-related human pathologies will be reviewed.

摘要

内源性大麻素是一类新型脂质,包括长链多不饱和脂肪酸的酰胺、酯和醚。花生四烯酸乙醇胺(N-花生四烯酰乙醇胺;AEA)和2-花生四烯酸甘油酯是大麻素受体的主要内源性激动剂,能够模拟大麻(如哈希什和大麻)制剂中的活性成分Δ⁹-四氢大麻酚的多种药理作用。AEA从膜脂中“按需”释放,其在受体上的活性受细胞摄取及随后的细胞内水解限制。与AEA及其同系物一起,结合、合成、转运和水解AEA的蛋白质构成了“内源性大麻素系统”。内源性大麻素存在于中枢神经系统和外周组织中,提示其作为广谱调节剂的生理作用。本文综述了内源性大麻素系统的主要特征,以及其在中枢和外周细胞衰老过程中的最新研究进展。此外,还将综述近期开发的能够调节内源性大麻素水平的药物在治疗衰老及与年龄相关的人类疾病方面的治疗潜力。

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