Hotchkiss Brain Institute and Snyder Institute of Infection, Immunity and Inflammation, Department of Physiology and Pharmacology, University of Calgary, Calgary, Alberta, Canada.
Pharmacol Biochem Behav. 2011 Jan;97(3):537-43. doi: 10.1016/j.pbb.2010.10.013. Epub 2010 Nov 4.
The aim of this study was to determine if the neutral cannabinoid CB₁ receptor antagonist, AM4113, regulates body weight in the rat via changes in food intake. We confirmed that the AM4113-induced reduction in food intake is mediated by CB₁ receptors using CB₁ receptor knockout mice. In rats, intraperitoneally administered AM4113 (2, 10 mg kg⁻¹) had a transient inhibitory effect on food intake, while body weight gain was suppressed for the duration of the study. AM4113-induced hypophagia was no longer observed once the inhibitory effect of AM4113 on body weight stabilized, at which time rats gained weight at a similar rate to vehicle-treated animals, yet at a lower magnitude. Pair-feeding produced similar effects to treatment with AM4113. Food intake and body weight gain were also inhibited in rats by oral administration of AM4113 (50 mg kg⁻¹). Dual energy x-ray absorptiometry (DEXA) was used to measure lean and fat mass. The AM4113 treated group had 29.3±11.4% lower fat mass than vehicle-treated rats; this trend did not reach statistical significance. There were no differences in circulating levels of the endogenous cannabinoid 2-arachidonoyl glycerol (2-AG), glucose, triglycerides, or cholesterol observed between treatment groups. Similarly, 2-AG hypothalamic levels were not modified by AM4113 treatment. These data suggest that blockade of an endocannabinoid tone acting at CB₁ receptors induces an initial, transient reduction in food intake which results in long-term reduction of body weight gain.
本研究旨在确定中性大麻素 CB₁ 受体拮抗剂 AM4113 是否通过改变食物摄入量来调节大鼠体重。我们通过 CB₁ 受体基因敲除小鼠证实,AM4113 诱导的食物摄入量减少是由 CB₁ 受体介导的。在大鼠中,腹腔内给予 AM4113(2、10mg/kg)对食物摄入量有短暂的抑制作用,而在研究期间体重增加受到抑制。一旦 AM4113 对体重的抑制作用稳定,即当大鼠不再出现 AM4113 诱导的食欲减退时,它们的体重增加速度与对照组相似,但幅度较低。与 AM4113 治疗一样,限食也产生了类似的效果。口服 AM4113(50mg/kg)也抑制了大鼠的食物摄入量和体重增加。双能 X 射线吸收法(DEXA)用于测量瘦体重和脂肪量。与对照组相比,AM4113 治疗组的脂肪量减少了 29.3±11.4%;这一趋势没有达到统计学意义。在治疗组之间,没有观察到循环中内源性大麻素 2-花生四烯酸甘油(2-AG)、葡萄糖、甘油三酯或胆固醇水平的差异。同样,AM4113 治疗也没有改变下丘脑的 2-AG 水平。这些数据表明,阻断作用于 CB₁ 受体的内源性大麻素张力会引起初始的、短暂的食物摄入量减少,从而导致长期体重增加减少。