EFFECTS OF A THROMBOXANE-RECEPTOR ANTAGONIST, BAY U 3405, ON PROSTAGLANDIN-D2-INDUCED AND EXERCISE-INDUCED BRONCHOCONSTRICTION

JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY

卷:89

Article

MAGNUSSEN, H ; BOERGER, S ; TEMPLIN, K ; BAUNACK, AR

关键词: BAY U 3405;    THROMBOXANE-RECEPTOR ANTAGONIST;    PGD2 CHALLENGE;    EXERCISE CHALLENGE;    PATIENTS WITH ASTHMA;   

DOI  :  10.1016/0091-6749(92)90295-D

来源: Elsevier

【 摘 要 】

In the pathogenesis of exercise-induced bronchoconstriction (EIB), prostaglandin D2 (PGD2) may play a role as a newly generated, mast cell-derived mediator. As the bronchoconstrictor effects of PGD2 are predominantly mediated via stimulation of thromboxane receptors in the lung, we studied a novel, orally effective, thromboxane-receptor antagonist, BAY u 3405, on EIB in 12 male subjects with mild asthma. On 4 study days, we determined, in a randomized, double-blind, placebo-controlled, crossover fashion, the effects of 20 mg of BAY u 3405 administered orally 1 hour before PGD, and exercise challenges, respectively. Increasing dosages of PGD2 were inhaled to establish dose-response curves that allowed determination of the provocative concentration necessary to decrease FEV1 by at least 20% (PC20) and to increase specific airway resistance (SR(aw)) by 100% (PC100). EIB was measured as a maximal fall/increase in postexertional FEV1/SR(aw) after bicycle exercise and cold-air breathing. Prechallenge lung-function values were similar on all four occasions. BAY u 3405 did not elicit any effect on resting bronchial tone. After placebo, the geometric means (SD) of PC20 and PC100 were 0.0380 (2.6) and 0.0266 (2.4) mg/ml, increasing to 0.554 (5.9) and 0.143 (8.1) mg/ml after BAY u 3405 (p = 0.0002). Mean (SD) maximal postexertional decrease in FEV1 and increase in SR(aw) after placebo was 29.4% (16.4%) and 280% (135%), and after BAY u 3405, 31.4% (18.1%) and 379% (281%) (not significant). No clinically relevant BAY u 3405-related side effects were observed. From these results we conclude that RAY u 3405 is highly effective in attenuating PGD2-induced bronchoconstriction. However, BAY u 3405 does not modulate EIB, suggesting that the mast cell-derived mediator, PGD2, does not play an important role in the pathogenesis of exercise-induced asthma.

【 授权许可】

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