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血管紧张素的血管生成与调节

Vascular production and regulation of angiotensin.

作者信息

Hilgers K F, Mann J F, Hilgenfeldt U, Ganten D

机构信息

Department of Medicine-Nephrology, University of Erlangen-Nürnberg, FRG.

出版信息

Blood Vessels. 1991;28(1-3):201-9. doi: 10.1159/000158863.

Abstract

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.

摘要

为了验证血管能产生血管紧张素(Ang)I和II这一假说,我们研究了分离的灌注大鼠后肢中Ang I和Ang II的形成。为了进一步明确这种产生的性质,我们通过全肾切除或次全肾切除来调节血浆肾素,并测试外源性肾素和肾素底物对血管Ang形成的影响。通过高效液相色谱法和放射免疫分析法对灌注液进行检测,结果表明后肢血管系统能自发释放Ang I和Ang II。后肢血管系统中Ang I向Ang II的转化率约为75%,并被卡托普利完全抑制。双侧肾切除可消除Ang肽的自发形成,但5/6次全肾切除对此无影响。向制剂中添加纯化的大鼠血管紧张素原可提高Ang II水平。向后肢血管系统中输注肾素可导致局部Ang形成显著增加,同时也会升高灌注压力。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是在血管内局部产生的。然而,血管肾素的来源仍存在争议。我们的结果提示部分酶是从血浆中摄取的。

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