Manhem P J, Ball S G, Morton J J, Murray G D, Leckie B J, Fraser R, Robertson J I
Br J Clin Pharmacol. 1985 Jul;20(1):27-35. doi: 10.1111/j.1365-2125.1985.tb02794.x.
The effect of different oral doses of HOE 498, a new non-sulphydryl containing converting enzyme inhibitor, was investigated in a double-blind, placebo-controlled study in normotensive volunteers. Dose-related reductions in serum converting enzyme activity, plasma angiotensin II and aldosterone were seen, greater at 4 h than at 12 h after drug ingestion. Converse dose-related increases in blood angiotensin I and plasma active renin concentration occurred. Falls of angiotensin II were as great with 20 mg as with 50 mg of HOE 498, although the effect was more prolonged with 50 mg. The reductions in concentrations of plasma angiotensin II and serum converting enzyme activity and the increases in plasma renin concentration were correlated with the concentration of HOE 498 - diacid in plasma. Dose-related falls in both supine and erect blood pressure were maximal 2-3.5 h after dosing. Pulse rate increased marginally but insignificantly in the supine; slightly and significantly in the upright position, concomitantly with the blood pressure reduction at all doses of active drug. We conclude that effects of single doses of HOE 498 on the renin-angiotensin system are maximal within 4 h, but are still apparent after 24 h. Thus it is likely that once daily administration will be adequate for treatment of high blood pressure in patients.
在一项针对血压正常志愿者的双盲、安慰剂对照研究中,研究了新型不含巯基的转换酶抑制剂HOE 498不同口服剂量的效果。观察到血清转换酶活性、血浆血管紧张素II和醛固酮呈剂量相关降低,服药后4小时比12小时降低更明显。相反,出现了血中血管紧张素I和血浆活性肾素浓度的剂量相关升高。20毫克HOE 498与50毫克HOE 498使血管紧张素II下降的幅度相同,尽管50毫克的作用持续时间更长。血浆血管紧张素II浓度和血清转换酶活性的降低以及血浆肾素浓度的升高与血浆中HOE 498 -二酸的浓度相关。给药后2 - 3.5小时,仰卧位和直立位血压的剂量相关下降最大。仰卧位时脉搏率略有增加但无统计学意义;直立位时略有增加且有统计学意义,与所有活性药物剂量下的血压降低同时出现。我们得出结论,单剂量HOE 498对肾素 - 血管紧张素系统的作用在4小时内最大,但24小时后仍很明显。因此,每日给药一次可能足以治疗高血压患者。