Rodríguez de Fonseca F, Navarro M, Gómez R, Escuredo L, Nava F, Fu J, Murillo-Rodríguez E, Giuffrida A, LoVerme J, Gaetani S, Kathuria S, Gall C, Piomelli D
Department of Psychobiology, Complutense University, 28233 Madrid, Spain.
Nature. 2001 Nov 8;414(6860):209-12. doi: 10.1038/35102582.
Oleylethanolamide (OEA) is a natural analogue of the endogenous cannabinoid anandamide. Like anandamide, OEA is produced in cells in a stimulus-dependent manner and is rapidly eliminated by enzymatic hydrolysis, suggesting a function in cellular signalling. However, OEA does not activate cannabinoid receptors and its biological functions are still unknown. Here we show that, in rats, food deprivation markedly reduces OEA biosynthesis in the small intestine. Administration of OEA causes a potent and persistent decrease in food intake and gain in body mass. This anorexic effect is behaviourally selective and is associated with the discrete activation of brain regions (the paraventricular hypothalamic nucleus and the nucleus of the solitary tract) involved in the control of satiety. OEA does not affect food intake when injected into the brain ventricles, and its anorexic actions are prevented when peripheral sensory fibres are removed by treatment with capsaicin. These results indicate that OEA is a lipid mediator involved in the peripheral regulation of feeding.
油酰乙醇胺(OEA)是内源性大麻素花生四烯酸乙醇胺的天然类似物。与花生四烯酸乙醇胺一样,OEA在细胞中以刺激依赖的方式产生,并通过酶促水解迅速消除,这表明其在细胞信号传导中发挥作用。然而,OEA并不激活大麻素受体,其生物学功能仍然未知。在此我们表明,在大鼠中,食物剥夺显著降低小肠中OEA的生物合成。给予OEA会导致食物摄入量和体重显著且持续下降。这种厌食作用具有行为选择性,并且与参与饱腹感控制的脑区(室旁下丘脑核和孤束核)的离散激活有关。将OEA注入脑室时不影响食物摄入量,并且当用辣椒素处理去除外周感觉纤维时,其厌食作用会被阻止。这些结果表明,OEA是一种参与进食外周调节的脂质介质。