首页> 美国卫生研究院文献>American Journal of Physiology - Heart and Circulatory Physiology >Localization of the novel angiotensin peptide angiotensin-(1-12) in heart and kidney of hypertensive and normotensive rats
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Localization of the novel angiotensin peptide angiotensin-(1-12) in heart and kidney of hypertensive and normotensive rats

机译:新型血管紧张素肽血管紧张素-(1-12)在高血压和正常血压大鼠的心脏和肾脏中的定位

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摘要

A low expression of angiotensinogen in the heart has been construed as indicating a circulating uptake mechanism to explain the local effects of angiotensin II on tissues. The recent identification of angiotensin-(1–12) in an array of rat organs suggests this propeptide may be an alternate substrate for local angiotensin production. To test this hypothesis, tissues from 11-wk-old spontaneously hypertensive rats (SHR) and Wistar-Kyoto (WKY) rats (n = 14) were stained with purified antibodies directed to the COOH terminus of angiotensin-(1–12). Robust angiotensin-(1–12) staining was predominantly found in ventricular myocytes with less staining found in the medial layer of intracoronary arteries and vascular endothelium. In addition, angiotensin-(1–12) immunoreactivity was present in the proximal, distal, and collecting renal tubules within the deep cortical and outer medullary zones in both strains. Preadsorption of the antibody with angiotensin-(1–12) abolished staining in both tissues. Corresponding tissue measurements by radioimmunoassay showed 47% higher levels of angiotensin-(1–12) in the heart of SHR compared with WKY rats (P < 0.05). In contrast, renal angiotensin-(1–12) levels were 16.5% lower in SHR compared with the WKY rats (P < 0.05). This study shows for first time the localization of angiotensin-(1–12) in both cardiac myocytes and renal tubular components of WKY and SHR. In addition, we show that increased cardiac angiotensin-(1–12) concentrations in SHR is associated with a small, but statistically significant, reduction in renal angiotensin-(1–12) levels.
机译:心脏中血管紧张素原的低表达被认为指示了循环摄取机制,以解释血管紧张素II对组织的局部作用。最近在一系列大鼠器官中鉴定出血管紧张素-(1-12),表明该前肽可能是局部血管紧张素生成的另一种底物。为了验证这一假设,对11周大的自发性高血压大鼠(SHR)和Wistar-Kyoto(WKY)大鼠(n = 14)的组织进行了染色,这些纯化的抗体直接针对血管紧张素-(1-12)的COOH末端。健壮的血管紧张素-(1-12)染色主要在心室肌细胞中发现,而在冠状动脉内层和血管内皮的中间层中发现较少。此外,两种菌株的近端,远端和深部皮质和髓外区域的肾小管中都存在血管紧张素-(1-12)免疫反应。血管紧张素(1–12)对抗体的前吸附消除了两个组织的染色。通过放射免疫分析法进行的相应组织测量显示,与WKY大鼠相比,SHR心脏的血管紧张素-(1–12)水平高47%(P <0.05)。相比之下,与WKY大鼠相比,SHR的肾血管紧张素-(1-12)水平降低了16.5%(P <0.05)。这项研究首次显示了血管紧张素-(1-12)在WKY和SHR的心肌细胞和肾小管成分中的定位。此外,我们显示SHR中心脏血管紧张素(1–12)浓度升高与肾脏血管紧张素(1–12)水平的降低(但有统计学意义)相关。

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