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首页> 外文期刊>Psychopharmacology >Residual effect of zolpidem 10 mg and zopiclone 7.5 mg versus flunitrazepam 1 mg and placebo on driving performance and ocular saccades.
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Residual effect of zolpidem 10 mg and zopiclone 7.5 mg versus flunitrazepam 1 mg and placebo on driving performance and ocular saccades.

机译:唑吡坦10毫克和佐匹克隆7.5毫克相对于氟尼西epa 1毫克和安慰剂对驾驶性能和眼球扫视的残留作用。

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RATIONALE: Studies report contradictory results concerning the residual effects of zolpidem and zopiclone. Moreover, residual effects of these compounds on healthy subjects have not yet been simultaneously assessed. OBJECTIVE: The present study with healthy subjects investigated the residual effects of zolpidem 10 mg and zopiclone 7.5 mg on driving performance and on ocular saccade and compared them to those under flunitrazepam 1 mg and placebo. METHODS: The study involved 16 subjects divided into two groups, a 9:00 a.m. group and a 11:00 a.m. group, in a balanced, double-blind, cross-over design. RESULTS: In the 9:00 a.m. group, zolpidem had no residual effects while zopiclone and flunitrazepam both impaired driving performance (P < 0.001 for both) and increased saccadic latency (P < 0.005; P = 0.052, respectively). Zopiclone impaired driving performance 5 times less than did flunitrazepam. In the 11:00 a.m. group, zolpidem and zopiclone had no residual effects, while flunitrazepam increased saccadic latency (P = 0.065) but did not impair driving performance. CONCLUSIONS: Zopiclone and flunitrazepam had residual effects in the first part of the morning, whereas zolpidem had no residual effects. The hierarchical character of the effects of the molecules differed according to the test administered. This is probably linked more to drug-induced specific alterations than to different sensitivities of the tests.
机译:理由:研究报告了关于唑吡坦和佐匹克隆的残留影响的矛盾结果。此外,尚未同时评估这些化合物对健康受试者的残留作用。目的:本研究针对健康受试者,研究了唑吡坦10 mg和佐匹克隆7.5 mg对驾驶性能和眼球扫视的残留作用,并将其与氟硝西epa 1 mg和安慰剂的残留作用进行了比较。方法:研究采用平衡,双盲,交叉设计,将16名受试者分为两组,上午9:00组和上午11:00组。结果:在上午9:00的组中,唑吡坦没有残留作用,而佐匹克隆和氟硝西epa既损害了驾驶性能(两者均P <0.001)又增加了后排潜伏期(P <0.005; P = 0.052)。佐匹克隆的驾驶性能比氟硝西epa低5倍。在上午11:00组,唑吡坦和佐匹克隆没有残留作用,而氟尼西epa增加了排球潜伏期(P = 0.065),但没有损害驾驶性能。结论:佐匹克隆和氟尼西epa在早晨的第一部分具有残留作用,而唑吡坦没有残留作用。分子作用的等级特征根据所进行的测试而不同。这可能与药物诱导的特异性改变有关,而不是与测试的不同敏感性有关。

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