Additive combination studies of captopril and ditekiren, a renin inhibitor, in nonhuman primates.

D T Pals, G L DeGraaf, S J Couch, M N Brunden
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引用次数: 6

Abstract

Additive combination studies of an angiotensin converting enzyme (ACE) inhibitor, captopril, and a renin inhibitor, ditekiren (U-71038), were carried out in conscious sodium-depleted and sodium replete cynomolgus monkeys. The agents elicited dose-additive hypotensive responses regardless of the order of drug administration in sodium-depleted monkeys. A dose-additive blood pressure response was also observed when the administration of captopril was preceded by ditekiren in conscious sodium replete monkeys. None of the animals in these groups exhibited significant alterations of heart rate. An apparent over-additive hypotensive response, accompanied by tachycardia, occurred in sodium replete monkeys when ditekiren was administered after captopril. It was proposed that the captopril-induced hyperreninemia may have allowed the blood pressure to become partially renin-dependent and therefore susceptible to the inhibitory action of ditekiren. The results of these studies suggested that both ditekiren and captopril elicited cardiovascular effects in conscious cynomolgus monkeys via a decreased formation of angiotensin II.

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卡托普利和肾素抑制剂迪特克伦在非人灵长类动物中的加性联合研究。
血管紧张素转换酶(ACE)抑制剂卡托普利(captopril)和肾素抑制剂迪特克伦(ditekiren, U-71038)的添加剂组合研究在有意识的缺钠和补钠食猴中进行。在钠耗尽的猴子中,无论药物给药顺序如何,这些药物都能引起剂量加性降压反应。在清醒的充满钠的猴子中,在给予卡托普利之前使用迪特克伦也观察到剂量加性血压反应。这些组中没有一只动物表现出明显的心率变化。在卡托普利给药后,钠充足的猴子出现明显的过度添加性降压反应,并伴有心动过速。有人提出,卡托普利引起的高肾素血症可能使血压变得部分依赖肾素,因此对迪特克伦的抑制作用敏感。这些研究结果表明,迪特克伦和卡托普利通过减少血管紧张素II的形成,在有意识的食蟹猴中引起心血管效应。
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