Department of Psychology, University of Connecticut, Storrs, CT 06269-1020, USA.
Pharmacol Biochem Behav. 2010 Nov;97(1):179-84. doi: 10.1016/j.pbb.2010.07.021. Epub 2010 Aug 14.
Drugs that interfere with cannabinoid CB1 transmission suppress food-motivated behaviors, and may be useful clinically as appetite suppressants. However, there may also be undesirable side effects (e.g., nausea, malaise, anxiety, and depression) that are produced by the current generation of CB1 inverse agonists such as rimonabant and taranabant. For that reason, it is important to continue research on novel cannabinoid antagonists. The present studies examined the effects of the novel compound AM6545, which is a neutral antagonist of CB1 receptors that is thought to have relatively poor penetrability into the central nervous system. Intraperitoneal administration of AM6545 significantly reduced food-reinforced operant responding at doses of 4.0, 8.0 and 16.0 mg/kg. AM6545 also produced a strong suppression of the intake of high-carbohydrate and high-fat diets in the same dose range, but only produced a mild suppression of lab chow intake at the highest dose (16.0 mg/kg). Although AM6545 did not affect food handling, it did reduce time spent feeding and feeding rate. Taken together, these results suggest that AM6545 is a compound that warrants further study as a potential appetite suppressant drug.
干扰大麻素 CB1 传递的药物会抑制与食物相关的行为,并且可能作为食欲抑制剂在临床上有用。然而,当前一代的 CB1 反向激动剂(例如利莫那班和塔兰班坦)可能会产生不良的副作用(例如恶心、不适、焦虑和抑郁)。因此,继续研究新型大麻素拮抗剂非常重要。本研究检查了新型化合物 AM6545 的作用,该化合物是 CB1 受体的中性拮抗剂,据认为其对中枢神经系统的穿透力相对较差。腹腔内给予 AM6545 可显著减少 4.0、8.0 和 16.0 mg/kg 剂量的食物强化操作性反应。AM6545 还在相同剂量范围内强烈抑制高碳水化合物和高脂肪饮食的摄入,但在最高剂量(16.0 mg/kg)时仅轻度抑制实验室饲料的摄入。尽管 AM6545不影响食物处理,但它确实减少了进食时间和进食速度。总的来说,这些结果表明 AM6545 是一种值得进一步研究作为潜在食欲抑制剂药物的化合物。