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More Rapid Sleep Onset with Lingual-Spray vs Oral-Tablet Delivery Zolpidem

机译:舌喷雾比口服片剂递送唑吡坦更能迅速入睡

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Insomnia and related sleep disorders (somnipathies) affect a large segment of the population, and result in a significant negative impact on quality of life and reduced or lost productivity. The speed of sleep onset is a critical characteristic of successful pharmacotherapeutic intervention for insomnia. Zolpidem, a non-benzodiazepine benzodiazepine receptor agonist (nBzRA) is widely used to treat insomnia. Although not itself a benzodiazepine (BZD), zolpidem has high binding affinity for the benzodiazepine receptor, which acts as a positive allosteric modulator of the GABAA receptor complex. It therefore increases the neuronal transmembrane influx of Cl~(-) ions, thereby decreasing neuronal excitability and promoting sleep. In this four-way crossover, dose-ranging, multiple-treatment study, a lingual spray formulation of zolpidem was safe and well - tolerated and yielded more rapid pharmacokinetics (mean plasma concentration) and efficacy (visual analog scale and digit symbol substitution test) compared to oral tablets.
机译:失眠症和相关的睡眠障碍(神志不清)会影响大部分人口,并对生活质量产生重大负面影响,并降低或丧失生产力。睡眠开始的速度是成功的失眠药物治疗干预的关键特征。非苯二氮卓类苯并二氮杂receptor受体激动剂(nBzRA)唑吡坦被广泛用于治疗失眠症。唑吡坦虽然本身不​​是苯二氮卓类药物(BZD),但对苯二氮卓类受体具有高结合亲和力,该受体充当GABAA受体复合物的正变构调节剂。因此,它增加了Cl〜(-)离子的神经元跨膜流入,从而降低了神经元兴奋性并促进了睡眠。在这项四次交叉,剂量范围,多次治疗研究中,唑吡坦的舌喷剂安全,耐受性良好,并能产生更快的药代动力学(平均血浆浓度)和功效(视觉模拟量表和数字符号替代测试)相比口服片剂。

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