MacGregor G A, Markandu N D, Bayliss J, Roulston J E, Squires M, Morton J J
Br Med J (Clin Res Ed). 1981 Aug 8;283(6288):401-3. doi: 10.1136/bmj.283.6288.401.
A non-sulfhydryl-containing inhibitor of angiotensin-converting enzyme (MK421) was given as a single dose in a randomised double-blind cross-over trial using 20 mg and 5 mg of MK-421 or matched placebo to nine normotensive volunteers receiving a sodium intake of 150 mmol (mEq) daily. The two dosages of MK-421 caused similar, significant falls in supine and standing blood pressure, which were maximum four to six hours after dosing (9.5-11.0% fall). With this fall in blood pressure there was a significant fall in activity of angiotensin-converting enzyme and in concentrations of plasma angiotensin II and aldosterone and a rise in plasma renin activity. Placebo caused no significant change in blood pressure or blood measurements. The study showed that MK-421 inhibits angiotensin-converting enzyme activity and lowers blood pressure in normotensive subjects. It strongly suggested that the renin system plays an important part in maintaining blood pressure in normotensive subjects receiving normal sodium intake. The results also suggest that this non-sulfhydryl-containing converting-enzyme inhibitor will be an effective blood-pressure-lowering drug in patients with blood pressure. A single dose of 5 mg was as effective at lowering blood pressure as a single dose of 20 mg.
在一项随机双盲交叉试验中,给9名每日钠摄入量为150毫摩尔(毫当量)的血压正常志愿者单次服用一种不含巯基的血管紧张素转换酶抑制剂(MK421),分别给予20毫克和5毫克的MK - 421或匹配的安慰剂。两种剂量的MK - 421均导致仰卧位和站立位血压出现相似的显著下降,给药后4至6小时降幅最大(下降9.5 - 11.0%)。随着血压下降,血管紧张素转换酶活性、血浆血管紧张素II和醛固酮浓度显著降低,血浆肾素活性升高。安慰剂对血压或血液检测指标无显著影响。该研究表明,MK - 421可抑制血压正常受试者的血管紧张素转换酶活性并降低血压。这有力地表明,肾素系统在每日钠摄入量正常的血压正常受试者维持血压方面起着重要作用。结果还表明,这种不含巯基的转换酶抑制剂对高血压患者将是一种有效的降压药物。5毫克单次剂量降压效果与20毫克单次剂量相同。