阿那达胺
大麻素受体
大麻素
内大麻素系统
化学
花生四烯酸
去极化抑制抑制
大麻素受体2型
受体
生物化学
药理学
生物
酶
敌手
作者
William A. Devane,Lumir Hanuš,Aviva Breuer,Roger G. Pertwee,Lesley Stevenson,Graeme Griffin,Dan Gibson,Asher Mandelbaum,Alexander Etinger,Raphael Mechoulam
出处
期刊:Science
[American Association for the Advancement of Science]
日期:1992-12-18
卷期号:258 (5090): 1946-1949
被引量:5614
标识
DOI:10.1126/science.1470919
摘要
Arachidonylethanolamide, an arachidonic acid derivative in porcine brain, was identified in a screen for endogenous ligands for the cannabinoid receptor. The structure of this compound, which has been named "anandamide," was determined by mass spectrometry and nuclear magnetic resonance spectroscopy and was confirmed by synthesis. Anandamide inhibited the specific binding of a radiolabeled cannabinoid probe to synaptosomal membranes in a manner typical of competitive ligands and produced a concentration-dependent inhibition of the electrically evoked twitch response to the mouse vas deferens, a characteristic effect of psychotropic cannabinoids. These properties suggest that anandamide may function as a natural ligand for the cannabinoid receptor.
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