关键词: Human Hypocretin Insomnia NREM sleep Non-rapid eye movement sleep Orexin Orexin receptor antagonists REM sleep Rapid eye movement sleep Sleep architecture

Mesh : Azepines / pharmacology therapeutic use Healthy Volunteers Humans Orexin Receptor Antagonists / pharmacology therapeutic use Polysomnography Sleep / drug effects Sleep Initiation and Maintenance Disorders / drug therapy Sleep Stages Sleep, REM / drug effects Triazoles / pharmacology therapeutic use

来  源:   DOI:10.1016/j.smrv.2020.101332   PDF(Sci-hub)

Abstract:
Orexin receptor antagonists are a relatively new hypnotic principle. Their influence on human sleep architecture is a point of debate that has not been systematically evaluated. Thus, we performed a systematic review to assess how these compounds effect sleep architecture in healthy and clinical human samples. Relevant articles were identified via searches of PubMed, Embase, the Cochrane central register of controlled trials, and clinicaltrials. gov. From 1147 retrieved records, 18 satisfied inclusion criteria and formed the basis of this review. Of these, fifteen studies administered dual orexin receptor antagonists (DORA) in a healthy control (five studies) or clinical sample (ten studies). By contrast, three studies administered selective orexin receptor-2 antagonists (2-SORA) in either a healthy control (one study) or clinical sample (two studies). Results reveal DORAs increase total sleep time primarily by promoting REM sleep, without affecting, or even decreasing, non-REM sleep, especially in clinical samples. Therefore, the clinical utility of DORAs may depend on the specific sample being treated. For 2-SORAs, limited evidence available precludes firm conclusions about their influence on human sleep architecture and, thus, further investigation of 2-SORAs is required to define their effects and make comparisons on this basis with DORAs.
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