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健康受试者中两种抗组胺药(咪唑斯汀和西替利嗪)与乙醇在精神运动和驾驶性能方面缺乏相互作用。

Lack of interaction between two antihistamines, mizolastine and cetirizine, and ethanol in psychomotor and driving performance in healthy subjects.

作者信息

Patat A, Stubbs D, Dunmore C, Ulliac N, Sexton B, Zieleniuk I, Irving A, Jones W

机构信息

Synthélabo Recherche, Clinical Research Department, Bagneux, France.

出版信息

Eur J Clin Pharmacol. 1995;48(2):143-50. doi: 10.1007/BF00192740.

Abstract

The pharmacodynamic interaction between mizolastine, a new H1 antihistamine, and ethanol was assessed in a randomized, double-blind, three-way crossover, placebo-controlled study. Eighteen healthy young male volunteers received mizolastine 10 mg, or cetirizine 10 mg or placebo once daily for 7 days with a 1-week wash-out interval. An oral dose of ethanol or ethanol placebo, given 2 h after dosing on days 5 or 7 of each treatment period, was administered to achieve a peak blood alcohol concentration (BAC) of 0.7 g/l then maintained for 1 h by two further doses of ethanol. Driving ability and psychomotor performance were evaluated using actual and simulated driving tests, critical flicker fusion threshold (CFF), adaptive tracking and divided attention (DAT) tasks. Ethanol produced a significant decrement in all tasks up to 5.5 h after administration: an increase in steering movements of 4.6, in lateral deviation of 0.45 m, in braking reaction time of 80 ms, in driving test and DAT performance of + 3.2; and a decrease in CFF and in tracking speed of 2.6 m.s-1. Neither mizolastine nor cetirizine significantly impaired driving ability or arousal (CFF) compared with the placebo. However, both drugs significantly impaired DAT performance 6:00 h post-dose (increase of + 2.1 for mizolastine and + 2.4 for cetirizine). The tracking speed was significantly decreased 7:50 h after mizolastine administration (-1.3 m.s-1) and more consistently from 1:30 to 7:50 h after cetirizine administration (-1.4 m.s-1). No significant adverse interaction, i.e. potentiation, occurred between ethanol and either antihistamine.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在一项随机、双盲、三交叉、安慰剂对照研究中,评估了新型H1抗组胺药咪唑斯汀与乙醇之间的药效学相互作用。18名健康年轻男性志愿者每天服用10毫克咪唑斯汀、或10毫克西替利嗪或安慰剂,共7天,中间有1周的洗脱期。在每个治疗期的第5天或第7天给药后2小时,口服一定剂量的乙醇或乙醇安慰剂,使血酒精浓度(BAC)峰值达到0.7克/升,然后通过再服用两剂乙醇维持1小时。使用实际驾驶和模拟驾驶测试、临界闪烁融合阈值(CFF)、自适应跟踪和注意力分散(DAT)任务来评估驾驶能力和精神运动表现。乙醇在给药后长达5.5小时内使所有任务出现显著下降:转向运动增加4.6次,横向偏差增加0.45米,制动反应时间增加80毫秒,驾驶测试和DAT表现增加3.2;CFF和跟踪速度降低2.6米/秒。与安慰剂相比,咪唑斯汀和西替利嗪均未显著损害驾驶能力或觉醒(CFF)。然而,两种药物在给药后6小时均显著损害DAT表现(咪唑斯汀增加2.1,西替利嗪增加2.4)。咪唑斯汀给药后7小时50分跟踪速度显著降低(-1.3米/秒),西替利嗪给药后1小时30分至7小时50分更持续降低(-1.4米/秒)。乙醇与任何一种抗组胺药之间均未发生显著的不良相互作用,即增强作用。(摘要截选至250字)

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