Magnussen H, Reuss G, Jörres R, Aurich R
Grosshansdorf Hospital, Center for Pneumology and Thoracic Surgery, Frankfurt, West Germany.
J Allergy Clin Immunol. 1989 Feb;83(2 Pt 1):467-71. doi: 10.1016/0091-6749(89)90135-8.
We studied the duration of the protective effect of azelastine against histamine-induced bronchoconstriction in six subjects with asymptomatic asthma. The study was performed in two periods of five consecutive days each. After a histamine inhalation test, we randomly administered either placebo or a single oral dose of 8.8 mg azelastine in a double-blind crossover fashion. Histamine challenges were repeated 5 hours after ingestion and at 1 PM on the following four days. The geometric means of the dose of histamine (in cumulative breath units [cbu]) necessary to increase specific airway resistance by 100% as compared with baseline (PD100SRaw) were 8.7 and 8.5 cbu before placebo and azelastine, respectively. Placebo did not significantly influence PD100SRaw within 99 hours after treatment. Five and 27 hours after azelastine, PD100SRaw increased to 178.2 and 46.7 cbu, respectively (p less than 0.05). Two patients showed a highly significant protection against the airway effect of histamine even 99 hours after ingestion (p less than 0.01). These data demonstrate a variable duration of the antihistaminic property of azelastine. The prolonged therapeutic effect in some patients may be beneficial in the timing of medication intervals.
我们研究了氮卓斯汀对6名无症状哮喘患者组胺诱导的支气管收缩的保护作用持续时间。该研究分两个阶段进行,每个阶段连续5天。在进行组胺吸入试验后,我们以双盲交叉方式随机给予安慰剂或单次口服8.8毫克氮卓斯汀。在服药后5小时以及接下来4天的下午1点重复进行组胺激发试验。与基线相比,使特定气道阻力增加100%所需的组胺剂量(以累积呼吸单位[cbu]计)的几何平均值,在服用安慰剂和氮卓斯汀之前分别为8.7和8.5 cbu。安慰剂在治疗后99小时内对PD100SRaw没有显著影响。在服用氮卓斯汀后5小时和27小时,PD100SRaw分别增至178.2和46.7 cbu(p<0.05)。两名患者甚至在服药99小时后对组胺的气道效应仍表现出高度显著的保护作用(p<0.01)。这些数据表明氮卓斯汀抗组胺特性的持续时间存在差异。在某些患者中延长的治疗效果可能对确定给药间隔时间有益。