臭氧对毒蕈碱支气管反应性的影响。

J H Roum, C Murlas
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引用次数: 40

摘要

我们研究了臭氧(O3)对豚鼠毒蕈碱支气管反应性的影响,并比较了两种不同的激动剂递送途径所确定的反应性。通过测量34只未麻醉、自主呼吸的动物静脉注射乙酰胆碱和/或雾化吸入甲胆碱时的气道阻力,测定O3暴露(3.0 ppm, 2 h)前和暴露后4 h至2天的反应性。在暴露前,我们观察到静脉注射激动剂的结果更加渐进和可重复。暴露后,对肠外激动剂的高反应性持续发生,但对吸入激动剂无高反应性。两种途径的高反应性在暴露14h内的程度和时间过程相似。2天后,吸入激动剂的高反应性缓解;静脉注射药物持续存在。我们的结果表明,臭氧诱导的吸入激动剂高反应性的发生和时间过程的变化可能是所采用技术的结果。注射肠外激动剂后O3持续出现高反应性,表明这种高反应性不是由气道粘膜高渗透性引起的。
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Ozone-induced changes in muscarinic bronchial reactivity by different testing methods.

We examined the effect of ozone (O3) on muscarinic bronchial reactivity in the guinea pig and compared reactivity determined by two different routes of agonist delivery. Reactivity before and from 4 h to 2 days after O3 exposure (3.0 ppm, 2 h) was determined by measuring specific airway resistance upon administration of intravenous acetylcholine and/or aerosolized methacholine challenge in 34 unanesthetized, spontaneously breathing animals. Before exposure, we observed more gradual and reproducible results to intravenous agonist. After exposure, hyperreactivity to parenteral agonist occurred consistently, but not to inhaled agonist. Hyperreactivity demonstrable by either route was similar in magnitude and time course within 14 h of exposure. Two days later, hyperreactivity to inhaled agonist had remitted; that to intravenous drug persisted. Our results indicate that variability in the occurrence and time course of O3-induced hyperreactivity to inhaled agonist may be a consequence of the technique employed. The consistent occurrence of hyperreactivity after O3 to parenteral agonist suggests mechanisms other than airway mucosal hyperpermeability are responsible for this hyperreactivity.

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