血管紧张素转换酶抑制剂对肾素-血管紧张素系统动态平衡的影响。

Journal of applied biochemistry Pub Date : 1985-12-01
T Aoyagi, T Wada, H Iinuma, K Ogawa, F Kojima, M Nagai, H Kuroda, A Obayashi, H Umezawa
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引用次数: 0

摘要

为了了解血管紧张素转换酶(ACE)抑制剂的体内作用,在兔子身上进行了一项为期半年的长期研究,使用其中一种抑制剂,氧甲氧嘧啶。在使用抑制剂的最初2个月,血清ACE水平被抑制。此后,可能是由此引起的血浆肾素活性(PRA)水平的急剧升高引起的,ACE水平恢复其初始值。因此,这种抑制剂完全打破了对照动物中PRA和ACE水平之间的密切相关性。一项多变量研究表明,该抑制剂显著改变了体内正常的肽代谢网络。这些结果与ACE抑制剂在体内阻断肾素-血管紧张素系统调节机制的观点是一致的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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Influence of angiotensin-converting enzyme inhibitor, foroxymithine, on dynamic equilibrium around the renin-angiotensin system in vivo.

To understand the in vivo actions of angiotensin-converting enzyme (ACE) inhibitors, a prolonged study was performed in rabbits over a half year, using one of such inhibitors, foroxymithine. During the initial 2 months of the inhibitor administration, the serum level of ACE was suppressed. Thereafter, probably triggered by the consequent sharp rise in the plasma renin activity (PRA) level, the ACE level regained its initial value. Thus the close correlation between the levels of PRA and ACE seen in the control animal was entirely broken by this inhibitor. A multivariate study indicated that the inhibitor drastically changed the normal networks of peptide metabolism in vivo. These results are compatible with the notion that the ACE inhibitor blocks the regulatory mechanisms of the renin-angiotensin system in vivo.

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Influence of angiotensin-converting enzyme inhibitor, foroxymithine, on dynamic equilibrium around the renin-angiotensin system in vivo. Assessment of internal primary structure of polypeptides newly translated in vitro by reticulocyte lysate: a study with cytochrome b5. Immunosorbent consisting of DNA immobilized on oxirane-activated sepharose. Syntheses and effects of a thymopoietin II fragment and its analogs on the impaired T-cell transformation in a patient with common variable immunodeficiency. Simplified separation of myosin from rabbit liver.
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