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首页> 外文期刊>The Journal of Clinical Pharmacology: Official Journal of the American College of Clinical Pharmacology >Opioid receptor modulation of hedonic taste preference and food intake: A single-dose safety, pharmacokinetic, and pharmacodynamic investigation with GSK1521498, a novel μ-opioid receptor inverse agonist
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Opioid receptor modulation of hedonic taste preference and food intake: A single-dose safety, pharmacokinetic, and pharmacodynamic investigation with GSK1521498, a novel μ-opioid receptor inverse agonist

机译:阿片受体对享乐主义口味和食物摄取的调节:使用新型μ阿片受体反向激动剂GSK1521498进行单剂量安全性,药代动力学和药效学研究

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摘要

Endogenous opioids and μ-opioid receptors have been linked to hedonic and rewarding aspects of palatable food intake. The authors examined the safety, pharmacokinetic, and pharmacodynamic profile of GSK1521498, a μ-opioid receptor inverse agonist that is being investigated primarily for the treatment of overeating behavior in obesity. In healthy participants, GSK1521498 oral solution and capsule formulations were well tolerated up to a dose of 100 mg. After single doses (10-150 mg), the maximum concentration (Cmax) and area under the curve (AUC) in plasma increased in a dose-proportional manner. GSK1521498 selectively reduced sensory hedonic ratings of high-sugar and high-fat dairy products and caloric intake of high-fat/high-sucrose snack foods. These findings provide encouraging data in support of the development of GSK1521498 for the treatment of disorders of maladaptive ingestive behavior or compulsive consumption.
机译:内源性阿片和阿片受体与可口食物摄入的享乐和有益方面有关。作者研究了GSK1521498(一种μ阿片类受体反向激动剂)的安全性,药代动力学和药效学特征,目前正在研究其主要用于治疗肥胖症中的暴饮暴食行为。在健康参与者中,GSK1521498口服溶液和胶囊制剂的耐受性高达100 mg。单剂量(10-150 mg)后,血浆中的最大浓度(Cmax)和曲线下面积(AUC)以剂量比例方式增加。 GSK1521498有选择地降低了高糖和高脂乳制品的享乐享乐率,以及高脂/高蔗糖休闲食品的热量摄入。这些发现提供了令人鼓舞的数据,以支持GSK1521498的开发,用于治疗适应不良的吞咽行为或强迫性进食障碍。

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