Igarashi A, Iijima H, Tamura G, Shirato K
First Department of Internal Medicine, Tohoku University School of Medicine, Sendai, Japan.
Am J Respir Crit Care Med. 1998 May;157(5 Pt 1):1531-5. doi: 10.1164/ajrccm.157.5.9707049.
We studied the inhibitory effect of tazanolast, a selective mast-cell-stabilizing drug, on ozone-induced airway hyperresponsiveness in guinea pigs. Airway responsiveness to methacholine peaked at 2 h after ozone exposure (2.0 ppm for 2 h) and the number of neutrophils in bronchoalveolar lavage (BAL) fluid continued to increase until 6 h. Tazanolast administered before ozone exposure at doses of 30, 100, or 300 mg/kg inhibited ozone-induced airway hyperresponsiveness in a dose-dependent manner. However, tazanolast administered after ozone exposure did not inhibit the airway hyperresponsiveness. Tazanolast did not significantly change the cell distribution of BAL cells at 2 h after the exposure. We conclude that tazanolast significantly inhibits ozone-induced airway hyperresponsiveness in guinea pigs. This result suggests that mast cells may play an important role in its development.
我们研究了选择性肥大细胞稳定剂他扎司特对豚鼠臭氧诱导的气道高反应性的抑制作用。气道对乙酰甲胆碱的反应性在臭氧暴露(2.0 ppm,持续2小时)后2小时达到峰值,支气管肺泡灌洗(BAL)液中的中性粒细胞数量持续增加直至6小时。在臭氧暴露前以30、100或300 mg/kg的剂量给予他扎司特,以剂量依赖的方式抑制臭氧诱导的气道高反应性。然而,在臭氧暴露后给予他扎司特并不能抑制气道高反应性。他扎司特在暴露后2小时并未显著改变BAL细胞的细胞分布。我们得出结论,他扎司特可显著抑制豚鼠臭氧诱导的气道高反应性。该结果表明肥大细胞可能在其发展中起重要作用。