Ridout F, Meadows R, Johnsen S, Hindmarch I
HPRU Medical Research Centre, University of Surrey, Egerton Road, Guildford GU2 7XP, UK.
Hum Psychopharmacol. 2003 Jun;18(4):261-9. doi: 10.1002/hup.494.
To assess the effects of paroxetine and mirtazapine on psychometric performance related to car driving, including an on-the-road test of BRT.
In a 4-way, double blind randomised crossover study, 12 healthy volunteers received paroxetine 20mg mane, mirtazapine 15mg/30mg nocte (comparator), mirtazapine 15mg mane/15 mg b.i.d.(verum) and placebo over a 5 day period with a washout period of 7 days between treatments. Psychometric assessments included 'on-the-road' BRT (BRT), CFF (CFF), CRT (CRT) and subjective measures of sedation and sleep parameters.
Paroxetine had no significant effect on BRT compared with placebo. Although subjective ratings of sleep quality and sedation were impaired, there were significant improvements in both CFF and the recognition reaction component of CRT with paroxetine. Mirtazapine 15mg/30mg nocte impaired laboratory performance and some subjective tests. Mirtazapine 15mg mane/15mg b.i.d. improved sleep, but significantly impaired all other measures.
Paroxetine 20 mg/day has no psychomotor or behavioural toxicity and has no negative impact on BRT. Further research into the chronic and sub-chronic effects of mirtazapine is needed to establish the clinical significance of these results.
评估帕罗西汀和米氮平对与汽车驾驶相关的心理测量表现的影响,包括BRT的道路测试。
在一项4组双盲随机交叉研究中,12名健康志愿者在5天内接受20mg晨服的帕罗西汀、15mg/30mg睡前服用的米氮平(对照)、15mg晨服/15mg每日两次的米氮平(试验组)和安慰剂,治疗之间有7天的洗脱期。心理测量评估包括“道路上”的BRT(BRT)、临界闪光融合频率(CFF)、选择反应时(CRT)以及镇静和睡眠参数的主观测量。
与安慰剂相比,帕罗西汀对BRT没有显著影响。虽然睡眠质量和镇静的主观评分受损,但帕罗西汀使CFF和CRT的识别反应成分均有显著改善。15mg/30mg睡前服用的米氮平损害了实验室表现和一些主观测试。15mg晨服/15mg每日两次的米氮平改善了睡眠,但显著损害了所有其他测量指标。
每日20mg的帕罗西汀没有精神运动或行为毒性,对BRT没有负面影响。需要对米氮平的慢性和亚慢性影响进行进一步研究,以确定这些结果的临床意义。