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通过驾驶模拟器表现测量氯美扎酮、硫酸美哌隆和地西泮的酒精相互作用。

Alcohol interaction of lormetazepam, mepindolol sulphate and diazepam measured by performance on the driving simulator.

作者信息

Willumeit H P, Ott H, Neubert W, Hemmerling K G, Schratzer M, Fichte K

出版信息

Pharmacopsychiatry. 1984 Mar;17(2):36-43. doi: 10.1055/s-2007-1017405.

Abstract

Sixteen healthy volunteers of a mean age of means = 26.4 years took part in a driving simulator test in an eightfold crossover study under double-blind conditions. The additional influence of alcohol was tested acutely after a single administration of 2 mg lormetazepam, a new, highly effective derivative from the benzodiazepine class, 10 mg mepindolol sulphate, a new betablocker without sedating properties, and 10 mg diazepam. All drugs were compared with placebo and the test was performed 1, 2 and 3 hours after oral intake. The aim was to investigate particularly the risks relevant in road traffic caused by simultaneous intake of these substances with alcohol. For this purpose, besides the driving simulator, an accurate reaction test ( WDG ) and self-rating scales were used, the latter in order to assess subjective stress and anxiety levels. Lormetazepam, due to its strong sedating property, showed a reduction in driving performance and an increase in reaction time and pulse rate as compared with placebo, and these effects were highly potentiated by alcohol. Mepindolol sulphate expectedly reduced pulse rate when compared with placebo, otherwise there were no significant differences. Diazepam, when compared with placebo, like lormetazepam caused a reduction in driving performance and reaction capacity and an increase in pulse rate, but intensity and duration of this effect were less than with lormetazepam and did not reach statistical significance. No significant potentiating effects were observed after the additional application of alcohol.

摘要

16名平均年龄为26.4岁的健康志愿者参与了一项在双盲条件下进行的八交叉研究中的驾驶模拟器测试。在单次服用2毫克氯美扎酮(一种新型高效苯二氮䓬类衍生物)、10毫克甲吲哚心安硫酸盐(一种无镇静作用的新型β受体阻滞剂)和10毫克地西泮后,急性测试了酒精的额外影响。所有药物均与安慰剂进行比较,并在口服后1、2和3小时进行测试。目的是特别调查同时摄入这些物质与酒精所导致的道路交通相关风险。为此,除了驾驶模拟器外,还使用了精确反应测试(WDG)和自评量表,后者用于评估主观压力和焦虑水平。氯美扎酮由于其强大的镇静特性,与安慰剂相比,驾驶性能下降,反应时间和脉搏率增加,并且这些影响因酒精而显著增强。与安慰剂相比,甲吲哚心安硫酸盐预期会降低脉搏率,除此之外没有显著差异。与安慰剂相比,地西泮与氯美扎酮一样,会导致驾驶性能和反应能力下降以及脉搏率增加,但这种影响的强度和持续时间小于氯美扎酮,且未达到统计学显著性。额外应用酒精后未观察到显著的增强作用。

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