Paul Michel A, MacLellan Mike, Gray Gary
Defence Research and Development Canada, Toronto, North York, Ontario, Canada.
Aviat Space Environ Med. 2005 Jun;76(6):560-5.
Motion sickness remains a significant problem for aircrew both in the flying environment (airsickness) and for aircrew deployed at sea (seasickness). While some anti-motion-sickness medications provide reasonable efficacy, adverse neurocognitive effects limit their use in military personnel engaged in safety-sensitive operational roles such as flying. The purpose of this study was to assess the impact on psychomotor performance of promethazine, meclizine, and dimenhydrinate and to determine if the addition of pseudoephedrine or damphetamine to promethazine would ameliorate its adverse effects.
There were 21 subjects (11 men, 10 women), aged 22-59, who were assessed for psychomotor performance on 4 tasks as well as with sleepiness and drug side-effects questionnaires. Psychomotor testing was conducted prior to, and for 7 h after, ingestion of a single dose of each of placebo, promethazine 25 mg, meclizine 50 mg, dimenhydrinate 50 mg, promethazine 25 mg plus pseudoephedrine 60 mg, and promethazine 25 mg plus d-amphetamine 10 mg.
Relative to placebo, promethazine, meclizine, and promethazine plus pseudoephedrine impaired performance on all four tasks [serial reaction time (SRT), logical reasoning (LRT), serial subraction (SST), and multitask (MT)]. Dimenhydrinate impaired performance on the SRT only. Promethazine plus d-amphetamine did not impair performance on any task nor did it result in increased sleepiness. The times to recovery of normal performance for SRT with promethazine, meclizine, dimenhydrinate, and promethazine plus pseudoephedrine were > 7.25, 7.25, 4.25, and 7.25 h, respectively; for LRT were > 7.25, > 7.25, ns, and 7.25 h; for SST were > 7.25, > 7.25, ns, and 7.25 h; for MT were 7.25, 7.25, ns, and 7.25 h. Recovery times to baseline sleepiness levels for promethazine, meclizine, dimenhydrinate, and promethazine plus pseudoephedrine were 7.25, > 7.25, 6.25, and > 7.25 h.
Only promethazine plus d-amphetamine was free from impact on psychomotor performance and did not increase sleepiness.
晕动病对于飞行环境中的空勤人员(晕机)以及部署在海上的空勤人员(晕船)而言,仍然是一个重大问题。虽然一些抗晕动病药物具有一定疗效,但不良的神经认知效应限制了它们在从事飞行等安全敏感作战任务的军事人员中的使用。本研究的目的是评估异丙嗪、茶苯海明和乘晕宁对精神运动表现的影响,并确定在异丙嗪中添加伪麻黄碱或右苯丙胺是否会改善其不良反应。
共有21名受试者(11名男性,10名女性),年龄在22 - 59岁之间,通过4项任务评估其精神运动表现,并使用嗜睡和药物副作用问卷进行调查。在服用安慰剂、25毫克异丙嗪、50毫克茶苯海明、50毫克乘晕宁、25毫克异丙嗪加60毫克伪麻黄碱以及25毫克异丙嗪加10毫克右苯丙胺的单剂量之前及之后7小时进行精神运动测试。
相对于安慰剂,异丙嗪、茶苯海明以及异丙嗪加伪麻黄碱在所有四项任务[序列反应时间(SRT)、逻辑推理(LRT)、连续减法(SST)和多任务(MT)]上均损害了表现。乘晕宁仅在SRT任务上损害了表现。异丙嗪加右苯丙胺在任何任务上均未损害表现,也未导致嗜睡增加。异丙嗪、茶苯海明、乘晕宁以及异丙嗪加伪麻黄碱恢复正常SRT表现的时间分别>7.25、7.25、4.25和7.25小时;LRT任务分别为>7.25、>7.25、无显著差异(ns)和7.25小时;SST任务分别为>7.25、>7.25、无显著差异和7.25小时;MT任务分别为7.25、7.25、无显著差异和7.25小时。异丙嗪、茶苯海明、乘晕宁以及异丙嗪加伪麻黄碱恢复至基线嗜睡水平的时间分别为7.25、>7.25、6.25和>7.25小时。
只有异丙嗪加右苯丙胺对精神运动表现无影响且不会增加嗜睡。