Taytard A, Vergeret J, Guenard H, Vaida P, Bellvert P, Freour P
Clinique de Pneumologie, Centre Hospitalo-Universitaire de Bordeaux, Hopital X. Arnozan, Pessac, France.
Eur J Clin Pharmacol. 1987;33(5):455-8. doi: 10.1007/BF00544234.
A vagal mechanism appears to be involved in the development of exercise-induced asthma (EIA), although previous studies have failed to demonstrate a protective effect of anticholinergic drugs against post-exercise bronchoconstriction. To reassess this hypothesis the effect of a new anticholinergic drug, Oxitropium Bromide (OTB) has been studied in ten subjects with documented EIA. There was no change after inhalation of a placebo. Administration of OTB led to bronchodilatation and totally blocked post-exercise bronchoconstriction in 7 patients, and it did so partly in 2. The response to the drug appeared to depend on pretest respiratory function. Thus, the anticholinergic drug OTB may protect against EIA in most patients, confirming the role of a vagal cholinergic mechanism in EIA.
尽管先前的研究未能证明抗胆碱能药物对运动后支气管收缩有保护作用,但迷走神经机制似乎参与了运动诱发哮喘(EIA)的发病过程。为了重新评估这一假设,我们对10名有EIA记录的受试者研究了一种新型抗胆碱能药物氧托溴铵(OTB)的效果。吸入安慰剂后无变化。给予OTB导致7例患者支气管扩张并完全阻断运动后支气管收缩,2例患者部分阻断。对药物的反应似乎取决于测试前的呼吸功能。因此,抗胆碱能药物OTB可能对大多数患者预防EIA有保护作用,证实了迷走胆碱能机制在EIA中的作用。