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Clinical evaluation of zaleplon in the treatment of insomnia

机译:扎来普隆治疗失眠的临床评价

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摘要

Zaleplon is a pyrazolopyrimidine hypnotic used for the treatment of insomnia. Zaleplon binds preferentially at the α1β2γ2 subunit of gamma aminobutyric acid type A (GABAA) receptors in the central nervous system, and has a half-life of about one hour. Efficacy studies show that zaleplon is a suitable hypnotic for sleep initiation purposes. However, because of its short half-life, zaleplon is less effective in sleep maintenance when compared with other hypnotics. Nevertheless, zaleplon does increase total sleep time. No rebound effects are observed after treatment discontinuation. The use of zaleplon is relatively safe. Adverse effects are mild and of short duration. No important interactions have been reported, and there is no evidence of abuse potential. Relative to benzodiazepine hypnotics, the biggest advantage of zaleplon is that current evidence suggests it does not produce residual next-day effects. As early as four hours after intake of zaleplon, no effects on cognitive, memory, psychomotor performance, and the ability to drive a car have been reported. Future studies should confirm these findings, and comparisons with new nonbenzodiazepine hypnotics should determine the importance of zaleplon in the future treatment of insomnia.
机译:Zaleplon是吡唑并嘧啶的催眠药,用于治疗失眠症。 Zaleplon优先结合中枢神经系统中A型γ氨基丁酸(GABAA)受体的α1β2γ2亚基,并具有约一小时的半衰期。功效研究表明,扎来普隆是适合入睡目的的催眠药。但是,由于扎来普隆的半衰期短,与其他催眠药相比,在维持睡眠方面效果较差。然而,扎来普隆确实会增加总睡眠时间。停药后未观察到反弹作用。使用扎来普隆相对安全。不良反应轻微,持续时间短。没有重要相互作用的报道,也没有滥用潜力的证据。相对于苯二氮卓类催眠药,扎来普隆的最大优势在于当前证据表明它不会产生残留的次日效应。早在服用扎来普仑后四个小时,就没有对认知,记忆,精神运动表现和驾驶汽车的能力产生影响。未来的研究应证实这些发现,与新型非苯二氮卓类催眠药的比较应确定扎来普隆在未来失眠治疗中的重要性。

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