Lai C, Alberti D, Onnis E, Orani E, Soro A, Pirisi R, Cadeddu M, Lai G, Cherchi A
Istituto di Cardiologia, Università degli Studi, Cagliari.
Cardiologia. 1991 Oct;36(10):785-92.
The aim of this study was to evaluate the anti-ischemic efficacy of 2 different doses of benazepril (B), a new ACE-inhibitor, 10 and 20 mg, given per os. Fifteen male patients gave informed, written consent; they were aged 40-67 years, with stable effort angina pectoris and were randomly given, in double-blind condition, a tablet containing B 10 mg, B 20 mg or placebo (PL), once a day, according to a 3 x 3 latin square design. Bicycle exercise tests were performed on the same day, 2 and 10 hours after the last drug intake. B 10 mg and B 20 mg, in patients with stable effort angina, compared to placebo, increased ischemic threshold and decreased ischemic ST depression at maximal work, after 2 hours but not after 10 hours. In conclusion B 10 mg and B 20 mg showed anti-ischemic activity 2 hours after drug intake.
本研究旨在评估两种不同剂量(10毫克和20毫克)的新型血管紧张素转换酶抑制剂贝那普利经口服给药后的抗缺血疗效。15名男性患者签署了知情书面同意书;他们年龄在40至67岁之间,患有稳定型劳力性心绞痛,并根据3×3拉丁方设计,在双盲条件下随机每天服用一次含有10毫克贝那普利、20毫克贝那普利或安慰剂的片剂。在最后一次服药后当天、2小时和10小时进行自行车运动试验。与安慰剂相比,10毫克和20毫克贝那普利在患有稳定型劳力性心绞痛的患者中,服药2小时后而非10小时后,增加了缺血阈值并降低了最大运动量时的缺血性ST段压低。总之,10毫克和20毫克贝那普利在服药2小时后显示出抗缺血活性。