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褪黑素激动剂与失眠。

Melatonin agonists and insomnia.

机构信息

Centre for Sleep Research, University of South Australia, GPO Box 2471, Adelaide, SA 5001, Australia.

出版信息

Expert Rev Neurother. 2010 Feb;10(2):305-18. doi: 10.1586/ern.10.1.

Abstract

The ability of melatonin to shift biological rhythms is well known. As a result, melatonin has been used in the treatment of various circadian rhythm sleep disorders, such as advanced and delayed sleep phase disorders, jet lag and shiftwork disorder. The current evidence for melatonin being efficacious in the treatment of primary insomnia is less compelling. The development of agents that are selective for melatonin receptors provides opportunity to further elucidate the actions of melatonin and its receptors and to develop novel treatments for specific types of sleep disorders. The agonists reviewed here - ramelteon, tasimelteon and agomelatine - all appear to be efficacious in the treatment of circadian rhythm sleep disorders and some types of insomnia. However, further studies are required to understand the mechanisms of action, particularly for insomnia. Clinical application of the agonists requires a good understanding of their phase-dependent properties. Long-term effects of melatonin should be evaluated in large-scale, independent randomized controlled trials.

摘要

褪黑素转移生物节律的能力是众所周知的。因此,褪黑素已被用于治疗各种昼夜节律睡眠障碍,如提前和延迟睡眠阶段障碍、时差和轮班工作障碍。目前,褪黑素在治疗原发性失眠方面的疗效证据并不那么有说服力。选择性褪黑素受体药物的开发为进一步阐明褪黑素及其受体的作用以及开发特定类型睡眠障碍的新疗法提供了机会。这里回顾的激动剂 - ramelteon、tasimelteon 和 agomelatine - 似乎都能有效治疗昼夜节律睡眠障碍和某些类型的失眠。然而,需要进一步的研究来了解它们的作用机制,特别是对失眠症的作用机制。激动剂的临床应用需要很好地了解它们的时相依赖性特性。褪黑素的长期作用应在大规模、独立的随机对照试验中进行评估。

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