Myou S, Fujimura M, Nishi K, Ohka T, Matsuda T
Division of Respiratory Medicine, Ishikawa Prefectural Central Hospital, Kanazawa, Japan.
Eur Respir J. 1995 Apr;8(4):619-23.
We wanted to evaluate the effect of terfenadine, a selective H1-receptor antagonist, on alcoholic beverage-induced bronchoconstriction. Eight patients with alcohol-induced asthma received terfenadine (60 mg, twice on the test day) or placebo, with the last dosing 2 h before the test in a double-blind, randomized, cross-over manner. On two separate study days, each subject drank the same brand and volume of alcoholic beverage (beer or Japanese saké), and bronchoconstriction was assessed as change in peak expiratory flow (PEF) over 120 min postchallenge. Inhalation challenges were performed with the same alcoholic beverage with which they had been orally challenged. The mean (SEM) percentage fall in PEF 15, 30, 45, 60, 90 and 120 min after the oral alcohol challenge was significantly reduced from 12.0 (3.1), 17.0 (1.7), 15.8 (2.3), 15.2 (3.4), 16.6 (4.8) and 14.7 (5.2)%, to 2.6 (1.8), 2.1 (1.6), 3.9 (1.2), 5.7 (2.2), 6.5 (2.6), 5.1 (1.6)%, respectively, by terfenadine. No significant bronchoconstriction was observed after the inhalation challenge. We conclude that the release of histamine makes a major contribution to alcoholic beverage-induced bronchoconstriction in Japanese asthmatic patients, and that histamine H1 antagonists may be effective in preventing alcoholic beverage-induced bronchoconstriction.
我们想要评估特非那定(一种选择性H1受体拮抗剂)对酒精饮料诱发的支气管收缩的影响。八名酒精诱发哮喘患者以双盲、随机、交叉方式接受特非那定(60毫克,测试日服用两次)或安慰剂,最后一次给药在测试前2小时。在两个不同的研究日,每位受试者饮用相同品牌和体积的酒精饮料(啤酒或日本清酒),并将支气管收缩评估为激发后120分钟内呼气峰值流速(PEF)的变化。吸入激发使用与口服激发相同的酒精饮料进行。口服酒精激发后15、30、45、60、90和120分钟时,PEF平均(SEM)下降百分比从12.0(3.1)、17.0(1.7)、15.8(2.3)、15.2(3.4)、16.6(4.8)和14.7(5.2)%显著降低至2.6(1.8)、2.1(1.6)、3.9(1.2)、5.7(2.2)、6.5(2.6)和5.1(1.6)%。吸入激发后未观察到明显的支气管收缩。我们得出结论,组胺的释放对日本哮喘患者酒精饮料诱发的支气管收缩起主要作用,并且组胺H1拮抗剂可能有效预防酒精饮料诱发的支气管收缩。