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三种不同强效肾素抑制剂在灵长类动物中的比较效果。

Comparative effects of three different potent renin inhibitors in primates.

作者信息

Clozel J P, Fischli W

机构信息

Pharma Division, Preclinical Research, F. Hoffmann-La Roche Ltd, Basel, Switzerland.

出版信息

Hypertension. 1993 Jul;22(1):9-17. doi: 10.1161/01.hyp.22.1.9.

Abstract

The goal of the present study was to compare the effects of three potent reference renin inhibitors (remikiren, CGP 38560A, and enalkiren) in sodium-depleted normotensive squirrel monkeys. In these monkeys, arterial pressure was measured in the conscious state with a telemetry system. Oral and intravenous maximal effective doses of the three renin inhibitors were compared in parallel groups of monkeys. In additional experiments, remikiren was given on top of either CGP 38560A or enalkiren in the same animals. Finally, the three drugs were compared with the angiotensin converting enzyme inhibitor cilazapril. The effects of the three drugs on the plasma components of the renin-angiotensin system (plasma renin activity, immunoreactive renin, and immunoreactive angiotensin II concentrations) were also measured. Our results show that remikiren was as effective as cilazapril and markedly more effective than CGP 38560A or enalkiren in reducing arterial pressure in our monkey model. Interestingly, these differences in arterial pressure could not be explained by differences of in vitro potency or different biochemical changes of the plasma components of the renin-angiotensin system, because the inhibitors all reduced immunoreactive angiotensin II to similarly low levels. One possible explanation is that, in our model, remikiren in contrast to CGP 38560A and enalkiren is able to inhibit renin in a functionally important extraplasmatic compartment.

摘要

本研究的目的是比较三种强效参考肾素抑制剂(瑞米吉仑、CGP 38560A和依那吉仑)对钠缺乏的正常血压松鼠猴的影响。在这些猴子中,使用遥测系统在清醒状态下测量动脉血压。在平行分组的猴子中比较了三种肾素抑制剂的口服和静脉注射最大有效剂量。在额外的实验中,在同一动物中,在CGP 38560A或依那吉仑之上给予瑞米吉仑。最后,将这三种药物与血管紧张素转换酶抑制剂西拉普利进行比较。还测量了这三种药物对肾素-血管紧张素系统血浆成分(血浆肾素活性、免疫反应性肾素和免疫反应性血管紧张素II浓度)的影响。我们的结果表明,在我们的猴子模型中,瑞米吉仑在降低动脉血压方面与西拉普利一样有效,且明显比CGP 38560A或依那吉仑更有效。有趣的是,动脉血压的这些差异无法用体外效力的差异或肾素-血管紧张素系统血浆成分的不同生化变化来解释,因为这些抑制剂都将免疫反应性血管紧张素II降低到了相似的低水平。一种可能的解释是,在我们的模型中,与CGP 38560A和依那吉仑相比,瑞米吉仑能够在功能重要的细胞外间隙抑制肾素。

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