Ghosh S K, Rafferty P, De Vos C, Patel K R
Department of Respiratory Medicine, Western Infirmary, Glasgow, U.K.
Clin Exp Allergy. 1993 Jun;23(6):524-7. doi: 10.1111/j.1365-2222.1993.tb03241.x.
Effect of cetirizine, a potent and specific H1 receptor antagonist, was examined on platelet activating factor-induced bronchoconstriction in 10 patients (5 male, mean [s.e.m.] aged 37.4 [3.6] years) with mild asthma in a placebo controlled, double-blind cross-over study. Airway responses were assessed by measuring specific airway conductance (SGaw). Patients were challenged with a single dose (12-96 micrograms) of PAF that had previously produced a 35% fall in SGaw. PAF challenges were performed after single dose (15 mg) and 1 week's treatment (15 mg twice daily) of cetirizine. There was no significant difference in pre- and post-treatment baseline values of SGaw on different study days and the percentage changes after cetirizine were 38.7 (7.01) and 45.6 (5.52) compared to 50.2 (2.89) and 43.9 (7.26) with placebo respectively. Similarly mean (s.e.m.) area under curve (AUC-SGaw/time course response) was 391 (143) and 514 (85) with cetirizine compared to 565 (37) and 461 (94) with placebo respectively. The difference was not statistically significant. There was no difference in facial flushing and feeling of warmth between cetirizine and placebo. We conclude that PAF induced bronchoconstriction in humans is not mediated by histamine release and that H1 receptor antagonists do not modify PAF induced bronchoconstriction.
在一项安慰剂对照、双盲交叉研究中,对10例(5例男性,平均年龄[标准误]为37.4[3.6]岁)轻度哮喘患者,研究了强效特异性H1受体拮抗剂西替利嗪对血小板活化因子诱导的支气管收缩的影响。通过测量特异性气道传导率(SGaw)评估气道反应。患者接受单剂量(12 - 96微克)的血小板活化因子(PAF)激发,该剂量此前会使SGaw下降35%。在单剂量(15毫克)及1周治疗(每日2次,每次15毫克)西替利嗪后进行PAF激发试验。不同研究日中西替利嗪治疗前后SGaw的基线值无显著差异,西替利嗪治疗后的百分比变化分别为38.7(7.01)和45.6(5.52),而安慰剂组分别为50.2(2.89)和43.9(7.26)。同样,西替利嗪组曲线下平均(标准误)面积(AUC - SGaw/时间过程反应)分别为391(143)和514(85),安慰剂组分别为565(37)和461(94)。差异无统计学意义。西替利嗪组与安慰剂组在面部潮红和温热感方面无差异。我们得出结论,人类中PAF诱导的支气管收缩不是由组胺释放介导的,且H1受体拮抗剂不会改变PAF诱导的支气管收缩。