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中性大麻素 CB₁ 受体拮抗剂 AM4113 通过改变大鼠的能量摄入来调节体重。

The neutral cannabinoid CB₁ receptor antagonist AM4113 regulates body weight through changes in energy intake in the rat.

机构信息

Hotchkiss Brain Institute and Snyder Institute of Infection, Immunity and Inflammation, Department of Physiology and Pharmacology, University of Calgary, Calgary, Alberta, Canada.

出版信息

Pharmacol Biochem Behav. 2011 Jan;97(3):537-43. doi: 10.1016/j.pbb.2010.10.013. Epub 2010 Nov 4.

Abstract

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.

摘要

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。

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6
The endocannabinoid system: role in glucose and energy metabolism.
Pharmacol Res. 2009 Aug;60(2):93-8. doi: 10.1016/j.phrs.2009.04.004. Epub 2009 Apr 14.
7
Food intake-independent effects of CB1 antagonism on glucose and lipid metabolism.
Obesity (Silver Spring). 2009 Aug;17(8):1641-5. doi: 10.1038/oby.2009.84. Epub 2009 Mar 26.
8
Endogenous cannabinoids and appetite.
Nutr Res Rev. 2001 Jun;14(1):65-86. doi: 10.1079/NRR200118.

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