Finnerty J P, Holgate S T
Immunopharmacology Group, Southampton General Hospital, UK.
Eur Respir J. 1990 May;3(5):540-7.
We investigated the effects of terfenadine, a histamine H1-receptor antagonist, and flurbiprofen, a cyclooxygenase inhibitor, on exercise-induced bronchoconstriction to assess the contribution of the mast cell products histamine and prostaglandins. Eight asthmatics were studied on 4 occasions with treadmill exercise tests. Terfenadine or placebo was administered 3 h prior to exercise, and flurbiprofen or placebo was administered 2 h prior to exercise, in a double-blind randomized trial. Airway calibre was determined by measurement of the forced expiratory volume in one second (FEV1) immediately prior to exercise challenge, and over 30 min post-exercise. Following placebo, the mean maximum percentage fall in FEV1 was 39%. This fell to 25% after terfenadine (p less than 0.05), 27% after flurbiprofen (p less than 0.05), and 30% after the active combination (NS). Analysis of the areas under curves of percentage falls in FEV1 over 30 min showed significant inhibition on all 3 active drug days (p less than 0.05). We conclude that histamine release and prostaglandin generation contribute to exercise-induced bronchoconstriction, although the interaction between these mediators appears complex.
我们研究了组胺H1受体拮抗剂特非那定和环氧化酶抑制剂氟比洛芬对运动诱发性支气管收缩的影响,以评估肥大细胞产物组胺和前列腺素的作用。对8名哮喘患者进行了4次跑步机运动试验研究。在一项双盲随机试验中,运动前3小时给予特非那定或安慰剂,运动前2小时给予氟比洛芬或安慰剂。通过在运动激发前及运动后30分钟测量一秒用力呼气量(FEV1)来确定气道口径。服用安慰剂后,FEV1的平均最大下降百分比为39%。服用特非那定后降至25%(p<0.05),服用氟比洛芬后为27%(p<0.05),服用活性组合药物后为30%(无统计学意义)。对运动后30分钟内FEV1下降百分比的曲线下面积分析显示,在所有3个使用活性药物的日子里均有显著抑制作用(p<0.05)。我们得出结论,组胺释放和前列腺素生成均参与运动诱发性支气管收缩,尽管这些介质之间的相互作用似乎很复杂。