Goparaju S K, Ueda N, Yamaguchi H, Yamamoto S
Department of Biochemistry, Tokushima University, School of Medicine, Japan.
FEBS Lett. 1998 Jan 23;422(1):69-73. doi: 10.1016/s0014-5793(97)01603-7.
Two endogenous ligands for cannabinoid receptors, anandamide (arachidonylethanolamide) and 2-arachidonoylglycerol, lose their biological activities by enzymatic hydrolysis. A cDNA for a rat liver enzyme hydrolyzing anandamide as well as oleamide was overexpressed in COS-7 cells. When the particulate fraction was allowed to react with 2-arachidonoylglycerol, arachidonic acid was produced. In contrast, this hydrolytic reaction did not occur with the control cells. The hydrolysis of 2-arachidonoylglycerol proceeded about 4-fold faster than the anandamide hydrolysis with a Km value as low as 6 microM and an optimal pH of 10. Phenylmethylsulfonyl fluoride and methyl arachidonyl fluorophosphonate inhibited the hydrolysis of both anandamide and 2-arachidonoylglycerol in parallel. Furthermore, the hydrolysis of [14C]2-arachidonoylglycerol was inhibited by anandamide dose-dependently. These results suggest that anandamide and 2-arachidonoylglycerol can be inactivated by the same enzyme.
大麻素受体的两种内源性配体,花生四烯酸乙醇胺(N-花生四烯酸乙醇胺)和2-花生四烯酸甘油酯,通过酶促水解失去其生物活性。一种水解花生四烯酸乙醇胺以及油酰胺的大鼠肝脏酶的cDNA在COS-7细胞中过表达。当微粒体部分与2-花生四烯酸甘油酯反应时,会产生花生四烯酸。相比之下,对照细胞未发生这种水解反应。2-花生四烯酸甘油酯的水解速度比花生四烯酸乙醇胺的水解速度快约4倍,Km值低至6微摩尔,最适pH为10。苯甲基磺酰氟和甲基花生四烯酰基氟磷酸酯同时抑制花生四烯酸乙醇胺和2-花生四烯酸甘油酯的水解。此外,[14C]2-花生四烯酸甘油酯的水解受到花生四烯酸乙醇胺的剂量依赖性抑制。这些结果表明,花生四烯酸乙醇胺和2-花生四烯酸甘油酯可被同一种酶灭活。