Dickstein K, Aarsland T, Woie L, Kremer D, Abrahamsen A M
Scand J Urol Nephrol Suppl. 1984;79:125-7.
The acute hemodynamic and hormonal effects of the oral angiotensin converting enzyme (ACE) inhibitor MK-521 were assessed over a period of 96 hours in 6 patients with heart failure. This compound is the lysine analogue of enalapril diacid (MK-422) and is biologically active following absorption. Dosages ranging from 1.25 mg to 5.0 mg were administered on days 1 and 3, followed by 48 hours intensive hemodynamic observation. Marked reduction in mean arterial pressure (25.2%), pulmonary capillary wedge pressure (47.3%), and systemic vascular resistance (34.5%) was observed. Arterial blood was sampled at frequent intervals for angiotensin I (AI), angiotensin II (AII), plasma renin activity, renin substrate, plasma aldosterone, urinary aldosterone, ACE activity, and serum drug levels. Right atrial blood was sampled simultaneously for AI and AII thus permitting reliable assessment of the degree of pulmonary conversion to angiotensin II. Prolonged inhibition of the renin-angiotensin-aldosterone system was confirmed and corresponded to drug concentration. The results indicate hemodynamic efficacy and potent ACE inhibition over a period exceeding 24 hours.
在6例心力衰竭患者中,对口服血管紧张素转换酶(ACE)抑制剂MK - 521的急性血流动力学和激素效应进行了为期96小时的评估。该化合物是依那普利二酸(MK - 422)的赖氨酸类似物,吸收后具有生物活性。在第1天和第3天给予1.25毫克至5.0毫克的剂量,随后进行48小时的强化血流动力学观察。观察到平均动脉压(降低25.2%)、肺毛细血管楔压(降低47.3%)和全身血管阻力(降低34.5%)显著下降。每隔一段时间采集动脉血样,检测血管紧张素I(AI)、血管紧张素II(AII)、血浆肾素活性、肾素底物、血浆醛固酮、尿醛固酮、ACE活性和血清药物水平。同时采集右心房血样检测AI和AII,从而能够可靠地评估肺脏转化为血管紧张素II的程度。证实了肾素 - 血管紧张素 - 醛固酮系统受到长期抑制,且与药物浓度相关。结果表明,在超过24小时的时间段内,该药物具有血流动力学疗效并能有效抑制ACE。