Mattila M J, Mattila M, Konno K
Eur J Clin Pharmacol. 1986;31(3):291-8. doi: 10.1007/BF00981126.
Thirteen healthy subjects participated in a combined acute and subacute double-blind, cross-over trial of two H1-antihistamines diphenhydramine (DPH) and temelastine (SKF) against placebo. The doses were DPH 50 mg b.d. and SKF 100 mg b.d. Objective (digit symbol substitution, flicker fusion, Maddox wing, attention, tracking, choice reaction) and subjective (visual analogue scales, side-effects on questionnaire) tests were done on Days 1, 4 and 5, on each occasion before drug intake and after 90 min and 3 h. On Day 1 DPH caused clear sedation of unpleasant character and impaired flicker fusion, attention and digit symbol substitution. SKF shifted the VAS assessment "drowsy/alert" towards drowsiness at 90 min, without objective impairment. On Day 4 DPH reduced exophoria and impaired flicker fusion without subjective sedation. On Day 5, diazepam 0.3 mg/kg (DZ) given with the other drugs caused subjective sedation of pleasant character and impaired various functions in the objective tests. Neither SKF nor DPH increased the effects of DZ; DPH slightly counteracted the effect of DZ on exophoria. At home, SKF did not differ from placebo while DPH proved sedative. DPH did not improve sleep but caused dry mouth and blurred vision. Measurement of plasma levels of antihistamines on each test day revealed the development of tolerance to antihistamine-induced sedation. The concentration of DZ measured by bioassay was somewhat elevated in the presence of DPH. Since the majority of the performance tests were not influenced by temelastine, it appears to be an acceptable, novel H1-antihistamine for the treatment of allergic disorders.
13名健康受试者参与了一项联合急性和亚急性双盲、交叉试验,比较两种H1抗组胺药苯海拉明(DPH)和替美斯汀(SKF)与安慰剂的效果。剂量分别为DPH每日两次,每次50毫克,SKF每日两次,每次100毫克。在第1、4和5天,在每次服药前、服药后90分钟和3小时进行客观测试(数字符号替换、闪烁融合、马多克斯翼试验、注意力、跟踪、选择反应)和主观测试(视觉模拟量表、问卷中的副作用)。第1天,DPH引起明显的令人不适的镇静作用,并损害闪烁融合、注意力和数字符号替换能力。SKF在90分钟时使视觉模拟量表评估的“困倦/警觉”向困倦方向转变,但无客观功能损害。第4天,DPH减少了外隐斜并损害了闪烁融合能力,但无主观镇静作用。第5天,与其他药物一起给予0.3毫克/千克的地西泮(DZ)引起了令人愉悦的主观镇静作用,并在客观测试中损害了各种功能。SKF和DPH均未增强DZ的作用;DPH略微抵消了DZ对外隐斜的作用。在家中,SKF与安慰剂无差异,而DPH具有镇静作用。DPH没有改善睡眠,但导致口干和视力模糊。在每个测试日测量抗组胺药的血浆水平,发现对抗组胺药引起的镇静作用产生了耐受性。在存在DPH的情况下,通过生物测定法测得的DZ浓度有所升高。由于大多数性能测试不受替美斯汀的影响,因此它似乎是一种可接受的新型H1抗组胺药,可用于治疗过敏性疾病。