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本文引用的文献

1
Differential effects of a dual orexin receptor antagonist (SB-649868) and zolpidem on sleep initiation and consolidation, SWS, REM sleep, and EEG power spectra in a model of situational insomnia.在情境性失眠模型中,双重食欲素受体拮抗剂(SB-649868)和唑吡坦对睡眠起始和巩固、慢波睡眠、快速眼动睡眠和 EEG 功率谱的差异影响。
Neuropsychopharmacology. 2012 Apr;37(5):1224-33. doi: 10.1038/npp.2011.310. Epub 2012 Jan 11.
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Phase I studies on the safety, tolerability, pharmacokinetics and pharmacodynamics of SB-649868, a novel dual orexin receptor antagonist.SB-649868,一种新型双重食欲素受体拮抗剂的安全性、耐受性、药代动力学和药效学的 I 期研究。
J Psychopharmacol. 2012 Aug;26(8):1058-70. doi: 10.1177/0269881111408954. Epub 2011 Jul 5.
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Prevalence and perceived health associated with insomnia based on DSM-IV-TR; International Statistical Classification of Diseases and Related Health Problems, Tenth Revision; and Research Diagnostic Criteria/International Classification of Sleep Disorders, Second Edition criteria: results from the America Insomnia Survey.基于 DSM-IV-TR;国际疾病分类与相关健康问题第十版;以及研究诊断标准/睡眠障碍国际分类第二版标准的失眠症患病率和与健康相关的感知:来自美国失眠调查的结果。
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Disposition and metabolism of [14C]SB-649868, an orexin 1 and 2 receptor antagonist, in humans.食欲素1和2受体拮抗剂[14C]SB-649868在人体内的处置与代谢
Drug Metab Dispos. 2011 Feb;39(2):215-27. doi: 10.1124/dmd.110.035386. Epub 2010 Nov 2.
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Neurobehavioral dynamics following chronic sleep restriction: dose-response effects of one night for recovery.慢性睡眠限制后的神经行为动力学:恢复一夜的剂量反应效应。
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Slow-wave sleep deficiency and enhancement: implications for insomnia and its management.慢波睡眠不足与增强:对失眠及其治疗的影响。
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Effect of gaboxadol on patient-reported measures of sleep and waking function in patients with Primary Insomnia: results from two randomized, controlled, 3-month studies.加巴喷丁在原发性失眠患者中对患者报告的睡眠和觉醒功能测量指标的影响:两项随机、对照、为期 3 个月的研究结果。
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Melatonin agonists and insomnia.褪黑素激动剂与失眠。
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The memory function of sleep.睡眠的记忆功能。
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食欲素拮抗剂 SB-649868 可促进和维持原发性失眠男性的睡眠。

The orexin antagonist SB-649868 promotes and maintains sleep in men with primary insomnia.

机构信息

Neuroscience CEDD Discovery Medicine, GlaxoSmithKline, Verona, Italy.

出版信息

Sleep. 2012 Aug 1;35(8):1097-104. doi: 10.5665/sleep.1996.

DOI:10.5665/sleep.1996
PMID:22851805
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3397789/
Abstract

STUDY OBJECTIVES

To assess the acute effects of SB-649868 in male subjects with Primary Insomnia with regard to (1) objective and subjective sleep parameters, (2) safety and tolerability, (3) next-day residual effects.

DESIGN

Multicenter, randomized, double-blind, placebo-controlled crossover study using a complete set of Williams orthogonal Latin Squares

SETTING

9 sleep centers in Germany

PATIENTS

52 male subjects with a diagnosis of primary insomnia (difficulty in sleep initiation and maintenance) confirmed by polysomnography

INTERVENTIONS

SB-649868 (10, 30, 60 mg) and placebo administered after dinner 90 minutes before bedtime

MEASUREMENTS AND RESULTS

Sleep effects assessed by polysomnography during 2 consecutive nights and by sleep questionnaires completed by subjects after each night at the sleep laboratory. Safety and tolerability were assessed by adverse events collection, electrocardiogram (ECG), vital signs, laboratory tests. Next-day residual effects were assessed by Digit Symbol Substitution Test, and modified Verbal Learning Memory Test administered at "lights on" after night 2. SB-649868 significantly reduced latency to persistent sleep, wake after sleep onset (WASO), and increased total sleep time (TST) compared to placebo. A dose-dependent effect was observed. A dose-dependent increase in absolute and percent REM sleep and reduction in REM sleep latency was observed mainly at the 60-mg dose. SB-649868 was well tolerated with inconsistent next day residual effects. SB-649868 sleep effects were correlated with SB-649868 circulating levels.

CONCLUSION

The data demonstrate the sleep-promoting properties of the orexin antagonist SB-649868 in male patients with insomnia.

摘要

研究目的

评估 SB-649868 在原发性失眠男性患者中的急性影响,具体涉及(1)客观和主观睡眠参数、(2)安全性和耐受性、(3)次日残留效应。

设计

采用完整的威廉姆斯正交拉丁方,进行多中心、随机、双盲、安慰剂对照交叉研究。

设置

德国 9 个睡眠中心

患者

52 名男性原发性失眠患者(入睡和维持睡眠困难),经多导睡眠图(PSG)确诊

干预措施

SB-649868(10、30、60mg)和安慰剂,于睡前 90 分钟晚餐后给药

测量和结果

通过连续 2 晚的多导睡眠图评估睡眠效果,并通过每位受试者在睡眠实验室后每夜填写的睡眠问卷进行评估。通过不良事件收集、心电图(ECG)、生命体征、实验室检查评估安全性和耐受性。次日残留效应通过数字符号替换测试和改良词语学习记忆测试进行评估,在第 2 夜“开灯”后进行。与安慰剂相比,SB-649868 显著缩短了入睡潜伏期、睡眠起始后觉醒(WASO)时间,并增加了总睡眠时间(TST)。观察到剂量依赖性效应。主要在 60mg 剂量下观察到 REM 睡眠时间的绝对和百分比增加以及 REM 睡眠潜伏期缩短。SB-649868 耐受性良好,次日残留效应不一致。SB-649868 的睡眠效应与 SB-649868 的循环水平相关。

结论

数据表明,食欲素拮抗剂 SB-649868 具有促进睡眠的特性,可改善男性失眠患者的睡眠。