Kleberg Karen, Hassing Helle A, Hansen Harald S
Department of Drug Design and Pharmacology, Faculty of Health and Medical Sciences, University of Copenhagen, Denmark.
Biofactors. 2014 Jul-Aug;40(4):363-72. doi: 10.1002/biof.1158. Epub 2014 Feb 14.
Endocannabinoid-like compounds are structurally related to the true endocannabinoids but do not contain highly unsaturated fatty acids, and they do not bind the cannabinoid receptors. The classical endocannabinoid-like compounds include N-acylethanolamines and 2-monoacylglycerols, and their structural resemblance to the endocannabinoids makes them players in the endocannabinoid system, where they can interfere with the actions of the true endocannabinoids, because they in several cases engage the same synthesizing and degrading enzymes. In addition they have pharmacological actions of their own, which are particularly interesting in a nutritional and metabolic context. Exogenously supplied oleoylethanolamide, palmitoylethanolamide, and linoleoylethanolamide have anorexic effects, and the endogenous formation of these N-acylethanolamines in the small intestine may serve an important role in regulating food intake, through signaling via PPARα and the vagus nerve to the brain appetite center. A chronic high-fat diet will decrease intestinal levels of these anorectic N-acylethanolamines and this may contribute to the hyperphagic effect of high-fat diet; 2-monoacylglycerols mediate endocrine responses in the small intestine; probably trough activation of GPR119 on enteroendocrine cells, and diet-derived 2-monoacylglycerols, for example, 2-oleoylglycerol and 2-palmitoylglycerol might be important for intestinal fat sensing. Whether these 2-monoacylglycerols have signaling functions in other tissues is unclear at present.
内源性大麻素样化合物在结构上与真正的内源性大麻素相关,但不含高度不饱和脂肪酸,且它们不与大麻素受体结合。经典的内源性大麻素样化合物包括N-酰基乙醇胺和2-单酰甘油,它们与内源性大麻素的结构相似性使其成为内源性大麻素系统中的参与者,在该系统中它们可以干扰真正内源性大麻素的作用,因为在某些情况下它们使用相同的合成和降解酶。此外,它们自身具有药理作用,在营养和代谢方面尤其引人关注。外源性提供的油酰乙醇胺、棕榈酰乙醇胺和亚油酰乙醇胺具有厌食作用,这些N-酰基乙醇胺在小肠中的内源性形成可能通过过氧化物酶体增殖物激活受体α(PPARα)和迷走神经向大脑食欲中枢发出信号,从而在调节食物摄入中发挥重要作用。长期高脂饮食会降低这些厌食性N-酰基乙醇胺的肠道水平,这可能导致高脂饮食的贪食效应;2-单酰甘油介导小肠中的内分泌反应;可能是通过激活肠内分泌细胞上的G蛋白偶联受体119(GPR119),饮食来源的2-单酰甘油,例如2-油酰甘油和2-棕榈酰甘油,可能对肠道脂肪感知很重要。目前尚不清楚这些2-单酰甘油在其他组织中是否具有信号传导功能。