Baughman R P, Loudon R G
Department of Medicine, University of Cincinnati.
Chest. 1988 Feb;93(2):285-8. doi: 10.1378/chest.93.2.285.
Patients with nocturnal asthma have their lowest pulmonary function and lowest serum epinephrine level at 4 to 6 AM. We studied a new long-acting beta-adrenergic agonist, procaterol, in ten patients with nocturnal asthma. The patients received 0.1 mg of procaterol one night and a placebo the other night in random order. Pulmonary function tests were performed every two hours from 10 PM to 8 AM. Pulmonary sounds were recorded using a modified stethoscope and were subsequently analyzed to estimate the proportion of time occupied by wheezing (est Tw/Ttot). The forced expiratory volume in one second (FEV1) while receiving the placebo and procaterol were similar at 10 PM (placebo, 1.35 +/- 0.18 L [mean +/- SE]; procaterol, 1.48 +/- 0.20 L); however, by 4 AM, the FEV1 had dropped significantly lower on the night with the placebo (1.01 +/- 0.14 L) than the night with procaterol (1.30 +/- 0.19 L; p less than 0.05). The est Tw/Ttot was similar at 12 AM for both nights, but at 4 AM, there was a significant increase in the est Tw/Ttot for the group with placebo but not the group with procaterol. The use of a long-acting beta-adrenergic sympathomimetic agent reversed the obstruction of the airways seen with nocturnal asthma.
夜间哮喘患者在凌晨4点至6点时肺功能最低,血清肾上腺素水平也最低。我们对10名夜间哮喘患者研究了一种新型长效β-肾上腺素能激动剂丙卡特罗。患者随机在某一晚服用0.1毫克丙卡特罗,另一晚服用安慰剂。从晚上10点到早上8点,每两小时进行一次肺功能测试。使用改良听诊器记录肺部声音,随后进行分析以估计哮鸣音所占时间比例(估计Tw/Ttot)。晚上10点时,服用安慰剂和丙卡特罗时的一秒用力呼气量(FEV1)相似(安慰剂组,1.35±0.18升[平均值±标准误];丙卡特罗组,1.48±0.20升);然而,到凌晨4点时,服用安慰剂的那一晚FEV1显著低于服用丙卡特罗的那一晚(1.01±0.14升对1.30±0.19升;p<0.05)。两晚凌晨12点时的估计Tw/Ttot相似,但凌晨4点时,安慰剂组的估计Tw/Ttot显著增加,而丙卡特罗组则没有。使用长效β-肾上腺素能拟交感神经药可逆转夜间哮喘所见的气道阻塞。