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氯卡色林用于治疗肥胖症。

Lorcaserin for the treatment of obesity.

作者信息

Redman L M, Ravussin E

机构信息

Pennington Biomedical Research Center, Baton Rouge, Louisiana 70808, USA.

出版信息

Drugs Today (Barc). 2010 Dec;46(12):901-10. doi: 10.1358/dot.2010.46.12.1556433.

Abstract

Obesity is a worldwide epidemic and there is an urgent need for the development of effective pharmacological therapies that target the metabolic and behavioral factors of body weight regulation. Serotonin (5-HT) has been implicated as a critical factor in the short-term (meal-by-meal) regulation of food intake and pharmaceutical companies have invested millions of dollars to discover and develop drug targets for the serotonergic pathway. Lorcaserin is a novel selective agonist of the 5-HT(2C) receptor for weight loss therapy. Preclinical and clinical studies indicate lorcaserin is well tolerated and not associated with cardiac valvulopathy or pulmonary hypertension suggesting that lorcaserin is a selective 5-HT(2C) receptor agonist and has little or no activation of the 5-HT(2B) and 5-HT(2A) receptors, respectively. Lorcaserin acts to alter energy balance through a reduction in energy intake and without an increase in energy expenditure and achieved the U.S. Food and Drug Administration guidelines for weight loss efficacy. It remains to be determined whether or not lorcaserin will be approved for the long-term management of obesity.

摘要

肥胖是一种全球性的流行病,迫切需要开发针对体重调节的代谢和行为因素的有效药物疗法。血清素(5-羟色胺,5-HT)被认为是食物摄入短期(逐餐)调节中的关键因素,制药公司已投入数百万美元来发现和开发血清素能途径的药物靶点。氯卡色林是一种用于减肥治疗的新型5-HT(2C)受体选择性激动剂。临床前和临床研究表明,氯卡色林耐受性良好,与心脏瓣膜病或肺动脉高压无关,这表明氯卡色林是一种选择性5-HT(2C)受体激动剂,分别对5-HT(2B)和5-HT(2A)受体几乎没有或没有激活作用。氯卡色林通过减少能量摄入来改变能量平衡,而不会增加能量消耗,并达到了美国食品药品监督管理局的减肥疗效指南。氯卡色林是否会被批准用于肥胖的长期管理还有待确定。

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