Böhm R O, van Baak M A, Rahn K H
Eur J Clin Pharmacol. 1986;30(5):541-7. doi: 10.1007/BF00542412.
The time course of the blood pressure lowering effect and the dose-response relationship of the new angiotensin converting enzyme inhibitor ramipril (HOE 498) were studied in 8 patients, with essential hypertension. As compared with placebo, a single oral dose of 2.5 mg ramipril lowered systolic and diastolic blood pressure. The antihypertensive action of single oral doses of 5, 7.5 and 10 mg ramipril was more pronounced. No change in heart rate occurred. Angiotensin converting enzyme activity was suppressed after all doses of ramipril studied. Plasma renin activity increased after 2.5 mg and 5 mg ramipril. Plasma aldosterone was not affected by 2.5 mg, but it fell after 5 mg ramipril. Thus, ramipril produced prolonged inhibition (more than 12 hours) of angiotensin converting enzyme activity and lowered blood pressure in patients with essential hypertension.
在8例原发性高血压患者中研究了新型血管紧张素转换酶抑制剂雷米普利(HOE 498)的降压作用时程和剂量反应关系。与安慰剂相比,单次口服2.5mg雷米普利可降低收缩压和舒张压。单次口服5mg、7.5mg和10mg雷米普利的降压作用更显著。心率无变化。在所研究的所有雷米普利剂量后,血管紧张素转换酶活性均受到抑制。口服2.5mg和5mg雷米普利后血浆肾素活性升高。2.5mg雷米普利对血浆醛固酮无影响,但5mg雷米普利后血浆醛固酮下降。因此,雷米普利可对血管紧张素转换酶活性产生长期抑制作用(超过12小时),并降低原发性高血压患者的血压。