血管紧张素的产生和调控。

Blood vessels Pub Date : 1991-01-01 DOI:10.1159/000158863
K F Hilgers, J F Mann, U Hilgenfeldt, D Ganten
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引用次数: 10

摘要

为了验证血管紧张素(Ang) I和Ang II是由血管产生的假设,我们在离体灌注大鼠后腿中研究了Ang I和Ang II的形成。为了进一步表征这种产生的性质,我们通过全肾或次全肾切除术来调节血浆肾素,并测试了外源性肾素和肾素底物对血管Ang形成的影响。用高效液相色谱法和放射免疫法对灌注液进行分析,证实了Ang I和Ang II从后肢血管中自发释放。后节血管中Ang I向Ang II的转化约为75%,卡托普利完全抑制了这种转化。双侧肾切除术可消除Ang肽的自发形成,但5/6次全肾切除术不影响Ang肽的自发形成。在制剂中加入纯化的大鼠血管紧张素原可提高Ang II水平。肾素输注后肢血管后,局部Ang形成显著增加,灌注压力升高。这两种效应均对卡托普利和肾素抑制剂H-142敏感。数据表明Ang I和Ang II在血管内局部产生。然而,血管肾素的来源仍有争议。我们的结果表明,部分酶是从血浆中吸收的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Vascular production and regulation of angiotensin.

To test the hypothesis that angiotensin (Ang) I and II are produced by blood vessels, we investigated the formation of both Ang I and Ang II in isolated, perfused rat hindquarters. To characterize the nature of this production further, we modulated plasma renin by total or subtotal nephrectomy and tested the effects of exogenous renin and renin substrate on vascular Ang formation. Assays of the perfusate by high-performance liquid chromatography and radioimmunoassay demonstrated the spontaneous release of Ang I and Ang II from the hindlimb vasculature. Conversion of Ang I to Ang II in hindquarter vasculature was approximately 75% and was totally suppressed by captopril. The spontaneous formation of Ang peptides was abolished by bilateral nephrectomy but was not affected by subtotal 5/6 nephrectomy. The addition of purified rat angiotensinogen to the preparation increased Ang II levels. The infusion of renin into the hindlimb vasculature led to substantial increases in local Ang formation and also raised the perfusion pressure. Both effects were sensitive to captopril and to the renin inhibitor H-142. The data indicate that Ang I and Ang II are produced locally within blood vessels. However, the origin of vascular renin remains controversial. Our results suggest that part of the enzyme is taken up from plasma.

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