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首页> 外文期刊>The Tohoku Journal of Experimental Medicine >Water Deprivation Increases (Pro)renin Receptor Levels in the Kidney and Decreases Plasma Concentrations of Soluble (Pro)renin Receptor
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Water Deprivation Increases (Pro)renin Receptor Levels in the Kidney and Decreases Plasma Concentrations of Soluble (Pro)renin Receptor

机译:缺水会增加肾脏中肾素原受体的水平,降低血浆可溶性肾素原受体的浓度

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摘要

Water deprivation activates the renin-angiotensin system. We have hypothesized that the renal expression of (pro)renin receptor ((P)RR), a specific receptor for renin and prorenin, could be changed under dehydration. Moreover, plasma levels of soluble (P)RR (s(P)RR) comprising of the extracellular domain of (P)RR may reflect the renal (P)RR expression. In the present study, we therefore aimed to clarify changes of plasma s(P)RR concentrations and kidney tissue (P)RR levels using rats with dehydration. Male Wister-Kyoto rats were divided into two groups; dehydrated (DH) rats deprived of water for 72 hours with free access to food, and control rats. Plasma s(P)RR concentrations measured by enzyme-linked immunosorbent assay were significantly lower in DH rats (6.94 +/- 2.08 ng/mL, mean +/- SD, n = 5) than in control (12.54 +/- 2.00 ng/mL, n = 5) (p < 0.05). Western blot analysis confirmed lower expression levels of s(P)RR in plasma in DH rats than in control. By contrast, western blot analysis showed higher levels of full-length (P)RR and lower levels of furin (an enzyme responsible for generation of s(P)RR from full-length (P)RR) in the kidney tissues obtained from DH rats compared to control. There was no significant difference in the renal (P)RR mRNA levels between DH rats and control. These findings suggest that water deprivation may elevate the renal full-length (P)RR levels via reducing the expression of furin. Increased full-length (P)RR may contribute to the up-regulation of the renal renin-angiotensin system and the production of concentrated urine under dehydration.
机译:缺水激活肾素-血管紧张素系统。我们假设,脱水状态下肾素和肾素原的特异性受体肾上腺素原受体(PRR)的肾脏表达可能会改变。而且,由(P)RR的胞外域组成的可溶性(P)RR(s(P)RR)的血浆水平可以反映肾脏(P)RR的表达。因此,在本研究中,我们旨在阐明使用脱水大鼠的血浆s(P)RR浓度和肾脏组织(P)RR水平的变化。将雄性Wister-Kyoto大鼠分为两组;每组1只。脱水(DH)的大鼠缺水72小时,可自由进食,而对照组则为对照组。通过酶联免疫吸附法测定的血浆s(P)RR浓度在DH大鼠(6.94 +/- 2.08 ng / mL,平均值+/- SD,n = 5)中明显低于对照组(12.54 +/- 2.00 ng) / mL,n = 5)(p <0.05)。 Western印迹分析证实DH大鼠血浆中s(P)RR的表达水平低于对照组。相比之下,蛋白质印迹分析显示,从DH获得的肾脏组织中全长(P)RR较高,而弗林蛋白酶(负责从全长(P)RR产生s(P)RR的酶)含量较低。大鼠与对照组相比。 DH大鼠与对照组之间的肾脏(P)RR mRNA水平没有显着差异。这些发现表明,缺水可能通过减少弗林蛋白酶的表达来提高肾脏的全长(P)RR水平。全长(P)RR的增加可能有助于肾脏肾素-血管紧张素系统的上调和脱水时浓缩尿液的产生。

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