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吸入性钙通道阻滞剂加洛帕米(D600)在减轻气道对乙酰甲胆碱和运动的反应性方面的剂量反应。

Dose response of inhaled gallopamil (D600), a calcium channel blocker, in attenuating airway reactivity to methacholine and exercise.

作者信息

Massey K L, Hill M, Harman E, Rutledge D R, Ahrens R, Hendeles L

机构信息

Department of Pharmacy Practice, College of Pharmacy, University of Florida, Gainesville 32610.

出版信息

J Allergy Clin Immunol. 1988 May;81(5 Pt 1):912-8. doi: 10.1016/0091-6749(88)90950-5.

Abstract

To determine if there is a dose-response relationship for calcium channel blockers in preventing experimentally induced bronchoconstriction, we evaluated the effects of inhaled gallopamil (D600), a potent methoxy derivative of verapamil, on airway reactivity to methacholine and exercise in volunteers with mild asthma. Methacholine challenges were completed by 11 subjects 2 hours before and 20 minutes after placebo, and 1, 2, 5, 10, and 20 mg of inhaled gallopamil administered in a single-blind, randomized manner on different days. Gallopamil did not significantly alter FVC, FEV1, or forced expiratory flow rate between 25% and 75% of FVC, but increased the dose of methacholine required to produce a 20% decrease in FEV1 from baseline (p less than 0.0001). The mean +/- SEM fold increase in the dose of methacholine required to produce a 20% decrease in FEV1 from baseline was 1.0 +/- 0.1 after placebo, 2.4 +/- 0.2 after 1 mg, 2.2 +/- 0.2 after 2 mg, 2.5 +/- 0.2 after 5 mg, 2.5 +/- 0.3 after 10 mg, and 2.3 +/- 0.2 after 20 mg. Thirty minutes before a standardized exercise challenge, 10 subjects inhaled 1 and 10 mg of gallopamil or placebo in a randomized, double-blind, crossover manner. The mean +/- SEM maximum decrease in FEV1 after exercise was 25.1 +/- 5% after 10 mg of gallopamil (p less than 0.01), 34.4 +/- 5% after 1 mg (p greater than 0.05), and 39.0 +/- 6% after placebo. We conclude that inhaled gallopamil only modestly alters airway reactivity to methacholine; increasing the dose greater than 1 mg did not provide greater benefit.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

为确定钙通道阻滞剂在预防实验性诱导的支气管收缩中是否存在剂量反应关系,我们评估了吸入维拉帕米的强效甲氧基衍生物加洛帕米(D600)对轻度哮喘志愿者气道对乙酰甲胆碱和运动的反应性的影响。11名受试者在安慰剂给药前2小时和给药后20分钟,以及在不同日期以单盲、随机方式吸入1、2、5、10和20毫克加洛帕米后完成乙酰甲胆碱激发试验。加洛帕米未显著改变用力肺活量(FVC)、第1秒用力呼气容积(FEV1)或FVC的25%至75%之间的用力呼气流量,但增加了使FEV1从基线下降20%所需的乙酰甲胆碱剂量(p小于0.0001)。与基线相比,使FEV1下降20%所需的乙酰甲胆碱剂量的平均±标准误增加倍数在安慰剂后为1.0±0.1,1毫克后为2.4±0.2,2毫克后为2.2±0.2,5毫克后为2.5±0.2,10毫克后为2.5±0.3,20毫克后为2.3±0.2。在标准化运动激发试验前30分钟,10名受试者以随机、双盲、交叉方式吸入1毫克和10毫克加洛帕米或安慰剂。吸入10毫克加洛帕米后运动后FEV1的平均±标准误最大下降为25.1±5%(p小于0.01),1毫克后为34.4±5%(p大于0.05),安慰剂后为39.0±6%。我们得出结论,吸入加洛帕米仅适度改变气道对乙酰甲胆碱的反应性;剂量增加超过1毫克并未带来更大益处。(摘要截短于250字)

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