Black Shawn C
Cardiovascular and Metabolic Diseases, MS 8220-3119, Pfizer Global Research and Development, Eastern Point Road, Groton, CT 06340, USA.
Curr Opin Investig Drugs. 2004 Apr;5(4):389-94.
The cannabinoid-1 (CB1) receptor plays a role in the regulation of appetitive behavior. Exogenously administered cannabinoid receptor agonists stimulate food consumption in animals and humans. Endogenous cannabinoid receptor agonists are present in the brain, and the brain level of these agonists increases with greater demand of food by rodents. Specific CB1 receptor antagonist compounds have been discovered that display high affinity and selectivity for the CB1 receptor. CB1 receptor antagonists inhibit both acute and long-term food intake in rodents. Chronic treatment with CB1 antagonists results in a sustained reduction in body weight in rodents (5 weeks), and weight loss in humans (16 weeks). Patent literature indicates CB1 receptor antagonist discovery efforts at a number of pharmaceutical companies. The CB1 receptor antagonist, rimonabant (SR-141716), discovered by Sanofi-Synthélabo, is in phase III clinical trials for the treatment of obesity and has been found to decrease appetite and body weight in humans.
大麻素-1(CB1)受体在调节食欲行为中发挥作用。外源性给予的大麻素受体激动剂会刺激动物和人类的食物消耗。内源性大麻素受体激动剂存在于大脑中,并且这些激动剂在啮齿动物对食物需求增加时大脑中的水平会升高。已发现对CB1受体具有高亲和力和选择性的特定CB1受体拮抗剂化合物。CB1受体拮抗剂可抑制啮齿动物的急性和长期食物摄入。用CB1拮抗剂进行慢性治疗会导致啮齿动物体重持续下降(5周)以及人类体重减轻(16周)。专利文献表明多家制药公司都在进行CB1受体拮抗剂的研发工作。赛诺菲-圣德拉堡公司发现的CB1受体拮抗剂利莫那班(SR-141716)正处于治疗肥胖症的III期临床试验阶段,并且已发现它能降低人类的食欲和体重。