食欲素受体
增食欲素
失眠症
睡眠(系统调用)
睡眠诱导
非快速眼动睡眠
化学
敌手
药理学
原发性失眠
对抗
心理学
神经科学
睡眠障碍
受体
医学
催眠药
神经肽
眼球运动
生物化学
计算机科学
操作系统
作者
Claudia Betschart,Samuel Hintermann,Dirk Behnke,Simona Cotesta,Markus Fendt,Christine E. Gee,Laura H. Jacobson,Grit Laue,Silvio Ofner,Vinod D. Chaudhari,Sangamesh Badiger,Chetan Pandit,Juergen Wagner,Daniël Hoyer
摘要
Dual orexin receptor (OXR) antagonists (DORAs) such as almorexant, 1 (SB-649868), or suvorexant have shown promise for the treatment of insomnias and sleep disorders in several recent clinical trials in volunteers and primary insomnia patients. The relative contribution of antagonism of OX1R and OX2R for sleep induction is still a matter of debate. We therefore initiated a drug discovery project with the aim of creating both OX2R selective antagonists and DORAs. Here we report that the OX2R selective antagonist 26 induced sleep in mice primarily by increasing NREM sleep, whereas the DORA suvorexant induced sleep largely by increasing REM sleep. Thus, OX2R selective antagonists may also be beneficial for the treatment of insomnia.
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