Cushley M J, Tattersfield A E, Holgate S T
Am Rev Respir Dis. 1984 Mar;129(3):380-4. doi: 10.1164/arrd.1984.129.3.380.
Inhaled adenosine causes bronchoconstriction in asthmatic patients. Antagonism of the bronchoconstrictor effect of endogenous adenosine has been proposed as a possible mechanism of action of theophylline in asthma. To directly investigate this, we have compared the airway responses to inhaled adenosine and histamine, with and without the prior administration of inhaled theophylline in 8 allergic asthmatic subjects. Airway response was measured both as forced expiratory volume in one second (FEV1) and as specific airway conductance (SGaw). Inhaled adenosine was less potent than histamine in producing bronchoconstriction, with geometric mean concentrations required to produce a 20% fall of FEV1 (PCf20) and a 40% fall of SGaw (PCs40) being 0.27 and 0.25 mg/ml for adenosine and 0.10 and 0.09 mg/ml for histamine. In a total nebulized dose of 37.5 mg, inhaled theophylline was a weak bronchodilator that caused maximal increases in FEV1 of 2 +/- 2% (mean +/- SE, p less than 0.05) and in SGaw of 8 +/- 4% (p greater than 0.05). However, theophylline significantly inhibited adenosine-induced bronchoconstriction, increasing the PCf20 and PCs40 values for adenosine to 1.66 (p less than 0.001) and 2.34 (p less than 0.005) mg/ml, respectively. Inhibition of histamine-induced bronchoconstriction was less marked, with PCf20 and PCs40 values of 0.19 (p greater than 0.05) and 0.21 (p less than 0.05) mg/ml. Thus, adenosine is a bronchoconstrictor in asthma whose effects are preferentially antagonized by concentrations of theophylline that cause little change in baseline airway caliber.(ABSTRACT TRUNCATED AT 250 WORDS)
吸入腺苷可使哮喘患者发生支气管收缩。内源性腺苷支气管收缩作用的拮抗被认为是茶碱治疗哮喘可能的作用机制。为直接研究这一机制,我们比较了8名过敏性哮喘患者在吸入茶碱前后对吸入腺苷和组胺的气道反应。气道反应通过一秒用力呼气量(FEV1)和比气道传导率(SGaw)来测量。吸入腺苷诱发支气管收缩的作用比组胺弱,使FEV1下降20%(PCf20)和使SGaw下降40%(PCs40)的几何平均浓度,腺苷分别为0.27和0.25mg/ml,组胺分别为0.10和0.09mg/ml。吸入37.5mg茶碱时,其为弱支气管扩张剂,使FEV1最大增加2±2%(均值±标准误,p<0.05),使SGaw最大增加8±4%(p>0.05)。然而,茶碱显著抑制腺苷诱发的支气管收缩,使腺苷的PCf20和PCs40值分别增至1.66(p<0.001)和2.34(p<0.005)mg/ml。对组胺诱发支气管收缩的抑制作用较弱,PCf20和PCs40值分别为0.19(p>0.05)和0.21(p<0.05)mg/ml。因此,腺苷是哮喘中的支气管收缩剂,其作用优先被对基线气道管径影响较小的茶碱浓度所拮抗。(摘要截短于250词)