评价人肾素抑制剂的大鼠模型

Donald T. Pals, Judy A. Lawson, Sally J. Couch
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引用次数: 11

摘要

一个大鼠模型提供了一个快速的方法来体内评估潜在的人肾素抑制剂已经开发和验证。将重组人肾素静脉注射到麻醉、肾切除、神经节阻滞的大鼠体内。结果血压有大约60毫米汞柱人肾素依赖成分。血管紧张素I到血管紧张素II转换酶抑制剂卡托普利和肾素抑制剂迪特克仑(U-71038)在口服后能够消除该成分。与猪肾素输注大鼠相比,人肾素输注大鼠口服didekiren引起了剂量依赖性的降压反应,其强度更大,持续时间更长。在输注肾素的大鼠中进行的观察反映了体外动力学研究的结果,该研究表明,迪特克伦对人肾素的结合亲和力高于对猪肾素的结合亲和力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Rat model for evaluating inhibitors of human renin

A rat model that provides a rapid method for the in vivo evaluation of potential inhibitors of human renin has been developed and validated. Recombinant human renin was infused intravenously into anesthetized, nephrectomized, ganglion-blocked rats. The resulting blood pressure had an approximate 60 mm Hg human renin-dependent component. The angiotensin I to angiotensin II converting enzyme inhibitor, captopril, and the renin inhibitor, ditekiren (U-71038), were capable of abolishing this component after oral administration. Oral administration of ditekiren to rats receiving human renin infusions evoked dose-dependent hypotensive responses that were greater in magnitude and longer in duration than those elicited in rats receiving hog renin infusions. Observations made in the renin-infused rats reflected the results of in vitro kinetic studies that had indicated a greater binding affinity of ditekiren for human renin than for hog renin.

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