Chick T W, Jenne J W
Chest. 1977 Dec;72(6):719-23. doi: 10.1378/chest.72.6.719.
We have compared bronchodilator responses to atropine and terbutaline in 39 chronic bronchitics and 16 stable asthmatics. Fasting subjects were given either 1.05 mg atropine of 5.0 mg terbutaline orally. Pulmonary function was assessed using the peak responses, namely: three 60-minute intervals for terbutaline and three 30-minute intervals for atropine. A subgroup of five reactive bronchitis patients was given a placebo with no response. Areas under the percent response-time interval curve were compared. Both patient groups responded to the same degree to atropine and terbutaline with respect to reduction of airway resistance. However, the FEV1 and V50 responses to terbutaline were markedly enhanced compared to atropine in the asthmatics while equal to the atropine response in the bronchitis patients. Thus, atropine appears to exert its effect upon both large and small airways in bronchitis, but predominantly on large airways in asthma. The results are consistent with a state of enhanced vagal tone in small airways in bronchitis compared to asthma, but other explanations are conceivable.
我们比较了39名慢性支气管炎患者和16名稳定期哮喘患者对阿托品和特布他林的支气管扩张反应。空腹受试者口服1.05毫克阿托品或5.0毫克特布他林。使用峰值反应评估肺功能,即:特布他林为三个60分钟时间段,阿托品为三个30分钟时间段。五名反应性支气管炎患者的一个亚组服用安慰剂后无反应。比较了反应百分比-时间间隔曲线下的面积。两组患者在降低气道阻力方面对阿托品和特布他林的反应程度相同。然而,与阿托品相比,哮喘患者对特布他林的FEV1和V50反应明显增强,而在支气管炎患者中与阿托品反应相当。因此,阿托品似乎对支气管炎的大、小气道均有作用,但在哮喘中主要作用于大气道。结果与支气管炎患者小气道迷走神经张力增强的状态一致,但也可以设想其他解释。