Shionoiri H, Takasaki I, Minamisawa K, Ueda S, Kihara M, Shindo K, Hiroto S, Sugimoto K, Himeno H, Naruse M, Nagamochi I, Yasuda G
Second Department of Internal Medicine, Yokohama City University School of Medicine, Japan.
J Clin Pharmacol. 1998 May;38(5):442-6. doi: 10.1002/j.1552-4604.1998.tb04451.x.
This study was conducted to examine whether imidaprilat, an active diacid of the angiotensin-converting enzyme (ACE) inhibitor imidapril, preferentially inhibits angiotensin I degradation rather than bradykinin degradation, and whether imidapril is less active than other ACE inhibitors in inducing cough in patients with hypertension. The effect of imidaprilat on the inhibition of pressor response to angiotensin I and augmentation of depressor response to bradykinin was compared with that of enalaprilat and captopril in anesthetized rats. To determine the incidence of cough associated with imidapril, patients with a history of ACE inhibitor-induced dry cough were enrolled in a randomized, open-labeled, crossover trial with two 6-week periods to be treated with imidapril or amlodipine, a calcium-channel blocker. The recurrence of cough was assessed during both treatments. In the animal study, there were no significant differences in the ratio of inhibition of pressor response to angiotensin I and the augmentation of depressor response to bradykinin among the ACE inhibitors. In the cough-challenge trial, a total of 60 patients with hypertension were enrolled in the study. Cough and cough related symptoms recurred in 98.3% of the patients (59/ 60) during imidapril therapy. In contrast, only two patients reported cough during treatment with amlodipine. These results indicate that imidapril has no selectivity in inhibiting angiotensin I- and bradykinin-degradation in rats, and that clinically it is not different from other ACE inhibitors in inducing cough in patients with hypertension.
本研究旨在探讨血管紧张素转换酶(ACE)抑制剂咪达普利的活性二酸代谢产物咪达普利拉是否优先抑制血管紧张素I降解而非缓激肽降解,以及咪达普利在高血压患者中诱发咳嗽的活性是否低于其他ACE抑制剂。在麻醉大鼠中,比较了咪达普利拉与依那普利拉和卡托普利对血管紧张素I升压反应的抑制作用以及对缓激肽降压反应的增强作用。为了确定与咪达普利相关的咳嗽发生率,将有ACE抑制剂诱发干咳病史的患者纳入一项随机、开放标签、交叉试验,试验为期两个6周,分别接受咪达普利或钙通道阻滞剂氨氯地平治疗。在两种治疗期间均评估咳嗽的复发情况。在动物研究中,ACE抑制剂之间对血管紧张素I升压反应的抑制率和对缓激肽降压反应的增强率无显著差异。在咳嗽激发试验中,共有60例高血压患者纳入研究。在咪达普利治疗期间,98.3%的患者(59/60)出现咳嗽及与咳嗽相关的症状。相比之下,氨氯地平治疗期间只有2例患者报告咳嗽。这些结果表明,咪达普利在大鼠中对血管紧张素I和缓激肽降解的抑制无选择性,且在临床上,其在高血压患者中诱发咳嗽的情况与其他ACE抑制剂无异。