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食欲素受体拮抗剂:治疗失眠的新型治疗药物。

Orexin Receptor Antagonists: New Therapeutic Agents for the Treatment of Insomnia.

作者信息

Roecker Anthony J, Cox Christopher D, Coleman Paul J

机构信息

Department of Medicinal Chemistry, Merck Research Laboratories , P.O. Box 4, 770 Sumneytown Pike, WP14-2, West Point, Pennsylvania 19486, United States.

出版信息

J Med Chem. 2016 Jan 28;59(2):504-30. doi: 10.1021/acs.jmedchem.5b00832. Epub 2015 Sep 15.

Abstract

Since its discovery in 1998, the orexin system, composed of two G-protein coupled receptors, orexins 1 and 2, and two neuropeptide agonists, orexins A and B, has captured the attention of the scientific community as a potential therapeutic target for the treatment of obesity, anxiety, and sleep/wake disorders. Genetic evidence in rodents, dogs, and humans was revealed between 1999 and 2000, demonstrating a causal link between dysfunction or deletion of the orexin system and narcolepsy, a disorder characterized by hypersomnolence during normal wakefulness. These findings encouraged efforts to discover agonists to treat narcolepsy and, alternatively, antagonists to treat insomnia. This perspective will focus on the discovery and development of structurally diverse orexin antagonists suitable for preclinical pharmacology studies and human clinical trials. The work described herein culminated in the 2014 FDA approval of suvorexant as a first-in-class dual orexin receptor antagonist for the treatment of insomnia.

摘要

自1998年被发现以来,由两种G蛋白偶联受体(食欲素1和2)以及两种神经肽激动剂(食欲素A和B)组成的食欲素系统,作为治疗肥胖症、焦虑症和睡眠/觉醒障碍的潜在治疗靶点,引起了科学界的关注。1999年至2000年间,在啮齿动物、狗和人类中发现了基因证据,证明食欲素系统功能障碍或缺失与发作性睡病之间存在因果关系,发作性睡病是一种在正常清醒状态下表现为过度嗜睡的疾病。这些发现促使人们努力寻找治疗发作性睡病的激动剂,以及治疗失眠的拮抗剂。本文将重点关注结构多样的食欲素拮抗剂的发现和开发,这些拮抗剂适用于临床前药理学研究和人体临床试验。本文所述的工作最终促成了2014年美国食品药品监督管理局(FDA)批准苏沃雷生作为首个用于治疗失眠的双食欲素受体拮抗剂。

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