Dose-related protection of exercise bronchoconstriction by montelukast, a cysteinyl leukotriene-receptor antagonist, at the end of a once-daily dosing interval

被引:66
作者
Bronsky, EA
Kemp, JP
Zhang, J
Guerreiro, D
Reiss, TF
机构
[1] MERCK & CO INC, MERCK SHARP & DOHME RES LABS, RAHWAY, NJ 07065 USA
[2] CALIF RES GRP, SAN DIEGO, CA USA
[3] AAAA MED RES GRP, SALT LAKE CITY, UT USA
关键词
D O I
10.1016/S0009-9236(97)90051-5
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The dose-related protective effects of montelukast, a potent and selective cysteinyl leukotriene-receptor antagonist, against exercise-induced bronchoconstriction were investigated in a five-period, randomized, incomplete-block, crossover study with montelukast (0.4, 2, 10, 50 mg) and placebo. The study subjects were 27 nonsmoking, healthy stable patients with asthma (mean forced expiratory volume in 1 second [FEV1], 82.0% predicted) who demonstrated a a greater than or equal to 20% decrease in FEV1 while beta-agonist was withheld for 6 hours before treadmill exercise. The standard exercise challenge was performed 20 to 24 hours, and again 32 to 36 hours, after the second of two once-daily doses. The effect of oral montelukast on exercise was measured by the area above the postexercise percentage decrease in FEV1 versus time curve from 0 to 60 minutes [AUC(0-60)], the maximal percentage decrease in FEV1 after exercise, and time after maximal decrease to recovery of FEV1, to within 5% of the preexercise baseline. Twenty to 24 hours after administration, montelukast caused dose-related protection, while providing similar protection against exercise-induced bronchoconstriction at the two highest doses. The AUC(0-60) values (mean +/-SD) were 637 +/- 898, 715 +/- 870, 988 +/- 1147, and 927 +/- 968 min % for 50, 10, 2, and 0.4 mg montelukast, respectively, and 1193 +/- 1097 min % for placebo (p = 0.003). No important clinical effect was present 36 hours after dosing. Montelukast was generally well tolerated at all dose levels. In conclusion, montelukast caused dose-related protection against exercise-induced bronchoconstriction at the end of a once-daily dosing interval. Protection against exercise-induced bronchoconstriction can be used to determine appropriate dose selection.
引用
收藏
页码:556 / 561
页数:6
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