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Daytime wakefulness following a bedtime oral dose of zolpidem 20 mg flunitrazepam 2 mg and placebo.

机译:睡前口服唑吡坦20 mg氟尼西epa 2 mg和安慰剂就寝后的白天清醒。

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摘要

1. The effects of zolpidem 20 mg, flunitrazepam 2 mg and placebo, administered at bed time, were studied in 12 healthy young male volunteers. 2. The assessments included, at awakening, subjective ratings of overnight sleep, cognitive function, psychomotor performance (digit symbol substitution, choice reaction time, flicker fusion threshold), subjective ratings of alertness, and plasma assay of residual drug concentration. Daytime sleep propensity during the day after dosing was evaluated with the multiple sleep latency test. 3. Compared with placebo, both active drugs improved subjective assessment of the ease of getting to sleep. At awakening, under flunitrazepam treatment, the reduction of performance, on memory and psychomotor tests, paralleled an increased subjective rating of sleepiness, but zolpidem treatment left subjects unimpaired compared with placebo. Similarly, daytime sleep propensity was enhanced throughout the following day under flunitrazepam treatment, but not under zolpidem treatment. Plasma assay for residual drug concentration at awakening found significant amounts of flunitrazepam and marginal amounts of zolpidem. 4. Results indicate that zolpidem 20 mg is devoid of residual effects in a range of tasks that were sensitive enough to demonstrate a prolonged wakefulness impairment following flunitrzepam 2 mg in healthy volunteers.
机译:1.在睡前服用唑吡坦20 mg,氟硝西epa 2 mg和安慰剂,在12位健康的年轻男性志愿者中进行了研究。 2.评估包括在醒来时的过夜睡眠,认知功能,精神运动表现(数字符号替代,选择反应时间,闪烁融合阈值)的主观评分,警觉性的主观评分以及残留药物浓度的血浆分析。用多次睡眠潜伏期试验评估服药后一天中白天的睡眠倾向。 3.与安慰剂相比,两种活性药物均改善了对入睡难易度的主观评估。醒来时,在氟硝西epa治疗下,记忆力和精神运动测试的表现降低,与主观嗜睡程度的提高平行,但唑吡坦治疗与安慰剂相比无损。同样,氟尼西epa治疗后第二天的白天睡眠倾向增强,但唑吡坦治疗则没有。觉醒时残留药物浓度的血浆分析发现大量的氟尼西epa和少量的唑吡坦。 4.结果表明,在健康志愿者中,20 mg唑吡坦在一系列敏感度足以证明长期服用氟硝西p后的觉醒受损的任务中,没有残留作用。

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