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RHC 3659:一种在正常志愿者中具有口服活性的新型血管紧张素转换酶抑制剂。

RHC 3659: a new orally active angiotensin converting enzyme inhibitor in normal volunteers.

作者信息

Burnier M, Turini G A, Brunner H R, Porchet M, Kruithof D, Vukovich R A, Gavras H

出版信息

Br J Clin Pharmacol. 1981 Dec;12(6):893-9. doi: 10.1111/j.1365-2125.1981.tb01327.x.

Abstract

1 The new converting enzyme inhibitor RHC 3659 was tested in 15 male volunteers. The study consisted of two parts: first, the ability of a single oral dose (5, 10, 20, 40 or 80 mg) to inhibit the pressor response to exogenous angiotensin I was tested with blood pressure and heart rate monitored continuously through an intraarterial catheter. A dose-related shift to the right of the pressor response curve to angiotensin I was observed with a peak occurring within 0.5 to 1 h. The pressor response to angiotensin II was unaffected. 2 In the second part, plasma renin and converting enzyme activity, angiotensin II and aldosterone were measured serially before and up to 8 h after administration of a single oral dose of RHC 3659. As expected. plasma angiotensin II and aldosterone fell within 30 min while plasma renin activity increased. Plasma converting enzyme activity was suppressed at 0.5 h in a dose-related manner with levels still below 30% of control 4 h following 80 mg of the inhibitor. 3 However, in vitro the enzyme-inhibitor complex seemed quited fragile since during storage of the plasma samples at -20 degrees C, converting enzyme activity increased significantly already within days (P less than 0.001, n = 28) and continued to rise for more than 2 months. This fragility may explain the seemingly lower potency of RHC 3659 when compared to captopril. No side effects were observed.

摘要
  1. 新型转化酶抑制剂RHC 3659在15名男性志愿者身上进行了测试。该研究包括两个部分:首先,通过动脉内导管连续监测血压和心率,测试单次口服剂量(5、10、20、40或80毫克)抑制对外源性血管紧张素I的升压反应的能力。观察到血管紧张素I升压反应曲线向右的剂量相关偏移,峰值出现在0.5至1小时内。对血管紧张素II的升压反应未受影响。2. 在第二部分中,在单次口服RHC 3659之前及给药后长达8小时连续测量血浆肾素和转化酶活性、血管紧张素II和醛固酮。正如预期的那样,血浆血管紧张素II和醛固酮在30分钟内下降,而血浆肾素活性增加。血浆转化酶活性在0.5小时时以剂量相关方式受到抑制,在服用80毫克抑制剂后4小时,其水平仍低于对照的30%。3. 然而,在体外,酶 - 抑制剂复合物似乎相当脆弱,因为在血浆样本于 -20℃储存期间,转化酶活性在数天内就已显著增加(P < 0.001,n = 28),并持续上升超过2个月。这种脆弱性可能解释了与卡托普利相比,RHC 3659看似较低的效力。未观察到副作用。

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