Ioli F, Donner C F, Fracchia C, Patessio A, Aprile C
Respiration. 1984;46(1):105-13. doi: 10.1159/000194677.
A number of drugs have been taken into consideration as to their efficacy in preventing exercise-induced asthma (EIA), which may be a reliable model for the investigation of bronchodilating agents. 15 asthmatic patients (mean age 21.1 +/- 10.7), EIA positive (free running test), were selected for a double-blind cross-over study of a sustained-release theophylline preparation against placebo. Patients underwent four subsequent bronchoprovocation tests by means of free running, at a 3-hours' interval, with a prior administration (3 h before the first test) of the drug at the dose of 7-8 mg/kg or the placebo. Lung function was tested (FEV1.0, FEF50, FEF25, sGaw) after the four induction tests as regards to the plasma concentrations of theophylline. After 6, 9 and 12 h, respectively, from administration of the drug, theophylline plasma levels between 7 and 9 micrograms/ml were found, which are to be considered more than satisfactory after an acute administration. A continuous protective activity has been noted against the exercise stress, with a significant difference between drug and placebo, for all lung function parameters with the obvious exception of the first one in which a satisfactory level of theophylline absorption was not reached. The finding of this new positive aspect of the drug investigated appears to be extremely interesting, particularly if added to the already well-known therapeutic activity, and to the fact that often other classes of drugs do not show a good correlation of protective action against EIA and prevention of spontaneous asthmatic attacks.
关于多种药物预防运动诱发哮喘(EIA)的疗效已被纳入考量,EIA可能是研究支气管扩张剂的可靠模型。选取15名哮喘患者(平均年龄21.1±10.7岁),EIA阳性(自由跑步试验),进行一项关于缓释茶碱制剂与安慰剂的双盲交叉研究。患者以3小时的间隔进行四次连续的自由跑步支气管激发试验,在第一次试验前3小时给予7 - 8mg/kg剂量的药物或安慰剂。在四次激发试验后,根据茶碱的血浆浓度测试肺功能(FEV1.0、FEF50、FEF25、sGaw)。分别在给药后6、9和12小时,发现茶碱血浆水平在7至9微克/毫升之间,急性给药后该水平被认为是相当令人满意的。对于所有肺功能参数,除第一个参数因未达到令人满意的茶碱吸收水平外,均观察到对运动应激的持续保护作用,药物与安慰剂之间存在显著差异。所研究药物这一新的积极方面的发现似乎极其有趣,特别是如果将其与已为人熟知的治疗活性相加,以及考虑到其他类药物通常在预防EIA和自发性哮喘发作的保护作用方面没有良好的相关性这一事实。