Devane W A, Hanus L, Breuer A, Pertwee R G, Stevenson L A, Griffin G, Gibson D, Mandelbaum A, Etinger A, Mechoulam R
Department of Natural Products, Medical Faculty, Hebrew University, Jerusalem, Israel.
Science. 1992 Dec 18;258(5090):1946-9. doi: 10.1126/science.1470919.
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.
花生四烯酸乙醇酰胺是猪脑中的一种花生四烯酸衍生物,在对大麻素受体的内源性配体进行的筛选中被鉴定出来。这种已被命名为“阿南德酰胺”的化合物的结构通过质谱和核磁共振光谱确定,并经合成得到证实。阿南德酰胺以竞争性配体的典型方式抑制放射性标记的大麻素探针与突触体膜的特异性结合,并对小鼠输精管的电诱发抽搐反应产生浓度依赖性抑制,这是精神活性大麻素的典型效应。这些特性表明阿南德酰胺可能作为大麻素受体的天然配体发挥作用。