Karlberg Bengt E, Fyhrquist Frej, Grönhagen-Riska Carola, Tikkanen Ilkka, Öhman K Peter
a Hypertension-Endocrine Unit , University Hospital , Helsinki , Finland.
b University Hospital, Linköping , Sweden and IV Medical Clinic , Helsinki , Finland.
Scand J Urol Nephrol. 1984 Jul;18(sup79):103-106. doi: 10.1080/00365599.1984.11783725.
We assessed the antihypertensive and hormonal effects of two new angiotensin converting enzyme (ACE) inhibitors. enalapril (MK-421) and lisinopril (MK-521) in 22 patients with renovascular hypertension. All patients had angiographically verified renal artery lesions, 3 had bilateral renal artery stenosis and one a stenosis in a single kidney, and the rest had unilateral renal artery stenosis. After placebo treatment for 3 days in hospital, increasing doses from 5 to 40 mg daily, of both ACE-inhibitors were given. Both drugs induced a significant fall in blood pressure (BP). Significant BP reductions were seen after 2 h with a maximum fall for the enalapril group at a dose of 40 mg 4 h after drug intake (mean supine BP decrease-31/24 mm Hg, standing-29/16 mmHg). The corresponding maximal BP reductions were for the lisinopril group at a dose of 40 mg o.d. at 6 h: mean supine BP fall-25/28 mmHg and standing-33/31 mm Hg. Both drugs significantly inhibited serum ACE to about 5 to 10% of initial values and with a duration for more than 24 h. Both drugs also caused a decrease in plasma All levels and also in plasma aldosterone concentrations. There were no toxic effects and no serious side effects. Careful monitoring of biochemical variables showed no significant changes. We conclude that both enalapril and lisinopril are effective and very Safe agents for the treatment of renovascular hypertension and with a long duration of action and with very good tolerance.
我们评估了两种新型血管紧张素转换酶(ACE)抑制剂依那普利(MK - 421)和赖诺普利(MK - 521)对22例肾血管性高血压患者的降压及激素效应。所有患者均经血管造影证实存在肾动脉病变,3例为双侧肾动脉狭窄,1例为单肾狭窄,其余为单侧肾动脉狭窄。患者在医院接受3天安慰剂治疗后,给予两种ACE抑制剂,剂量从每日5毫克增至40毫克。两种药物均使血压显著下降。用药2小时后血压明显降低,依那普利组在服药后4小时剂量为40毫克时血压下降最大(平均仰卧位血压下降31/24毫米汞柱,站立位29/16毫米汞柱)。赖诺普利组在每日一次剂量为40毫克时,6小时出现相应最大血压下降:平均仰卧位血压下降25/28毫米汞柱,站立位33/31毫米汞柱。两种药物均显著抑制血清ACE至初始值的约5%至10%,且作用持续时间超过24小时。两种药物还导致血浆血管紧张素I水平及血浆醛固酮浓度降低。未出现毒性作用及严重副作用。对生化指标的仔细监测未显示明显变化。我们得出结论,依那普利和赖诺普利都是治疗肾血管性高血压的有效且非常安全的药物,作用持续时间长,耐受性良好。