首页> 外文期刊>International journal of clinical pharmacology and therapeutics >Influence of an antivertiginous combination preparation of cinnarizine and dimenhydrinate on event-related potentials, reaction time and psychomotor performance--a randomized, double-blind, 3-way crossover study in healthy volunteers.
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Influence of an antivertiginous combination preparation of cinnarizine and dimenhydrinate on event-related potentials, reaction time and psychomotor performance--a randomized, double-blind, 3-way crossover study in healthy volunteers.

机译:抗眩晕的肉桂那嗪和苯海拉明联合制剂对事件相关电位,反应时间和心理运动能力的影响-健康志愿者的一项随机,双盲,三向交叉研究。

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摘要

In the present comparative, double-blind, 3-way crossover study, possible effects of an antivertiginous combination preparation on event-related potentials (ERPs) and performance were investigated. Twenty-one healthy volunteers received 4 doses (within 24 h) of a fixed combination of cinnarizine 20 mg and dimenhydrinate 40 mg (Arlevert, ARL), dimenhydrinate 50 mg, or a placebo, in randomized order at 1-week intervals. Auditory event-related potentials (ERPs), reaction time (RT) and psychometric tests were assessed before as well as 60 and 150 minutes after the intake of the 1st (Day 1) and the 4th (Day 2) dose of study medication. The evaluation was primarily based on the difference in the outcomes measured 150 min after the 4th dose (t5) and those before the start of medication intake (t0). None of the medications affected the latency and amplitude of the sensory ERP component N100, neither under passive listening nor under discrimination task conditions. The latency of P300 in response to the rare target tones (oddball paradigm and binary series), showed significant (p < 0.05) delays after 4 doses of dimenhydrinate (18-24 ms), and no significant differences between ARL (3-17 ms) and either dimenhydrinate or placebo (4-13 ms). Responses to nontarget tones remained almost unaffected after medication intake. The secondary analysis of the P300 amplitude showed the greatest decreases under DH in both active series, with no significant differences between ARL and either DH or placebo. The 3 medications did not significantly prolong RT nor did they impair the performance of psychometric tests, or cause significant shifts of current mood. The combination preparation ARL showed the lowest rate of adverse events (n = 1), followed by dimenhydrinate (n = 3) and placebo (n = 6). Two subjects withdrew because of adverse events, both after the intake of placebo. In conclusion, the results gave no evidence for an impairment of central information processing and psychomotor performance after multiple dosing with the fixed combination ARL in healthy volunteers, which might, when present, represent an adverse reaction limiting its use in antivertiginous therapy. No significant differences were found between ARL and placebo.
机译:在目前的比较,双盲,三向交叉研究中,研究了抗蛇纹复合制剂对事件相关电位(ERP)和性能的可能影响。 21名健康志愿者在1周间隔内随机接受4剂量的肉桂酸20 mg和苯海拉明40 mg(Arlevert,ARL),苯海拉明50 mg或安慰剂的固定组合(24小时内)。在服用第一剂(第一天)和第四剂(第二天)之前以及之后60分钟和150分钟,评估听觉事件相关电位(ERP),反应时间(RT)和心理测试。评估主要基于第四次给药后150分钟(t5)和开始服用药物之前(t0)测得的结果的差异。在被动聆听和辨别任务条件下,没有任何一种药物会影响感觉性ERP组件N100的潜伏时间和幅度。 P300对稀有靶标音(oddball范式和二元数列)的响应潜伏期显示,在4次苯海马因剂量(18-24 ms)后,显着(p <0.05)延迟,而ARL之间(3-17 ms)无显着差异)和去甲海因或安慰剂(4-13毫秒)。服用药物后,对非目标音调的反应几乎不受影响。对P300幅度的二次分析显示,在两个活动系列中,DH下的下降幅度最大,ARL与DH或安慰剂之间无明显差异。这三种药物均不能显着延长放疗时间,也不会损害心理测验的性能,也不会引起当前情绪的明显变化。组合制剂ARL的不良事件发生率最低(n = 1),其次是苯海二海因(n = 3)和安慰剂(n = 6)。服用安慰剂后,两名受试者均因不良事件而退出。总之,在健康志愿者中,使用固定组合ARL多次给药后,结果没有证据表明中枢信息处理和精神运动能力受到损害,这可能表示不良反应,限制了其在抗眩晕治疗中的使用。在ARL和安慰剂之间未发现明显差异。

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