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首页> 外文期刊>Biochimica et biophysica acta. Biomembranes >Effects of angiotensin II on NaPi-IIa co-transporter expression and activity in rat renal cortex
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Effects of angiotensin II on NaPi-IIa co-transporter expression and activity in rat renal cortex

机译:血管紧张素II对大鼠肾皮质NaPi-IIa共转运蛋白表达和活性的影响

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摘要

The kidney plays a major role in reabsorption of phosphate with the majority occurring in the proximal tubule (PT). The type IIa sodium-phosphate co-transporter (NaPi-IIa) is the main player in PT. The purpose of current study was to determine the effect of angiotensin II (A-II) on membrane expression of NaPi-IIa in the rat renal cortex. A-II (500 ng/kg/min) was chronically infused into the Sprague-Dawley rats by miniosmotic pump for 7 days. The arterial pressure and circulating plasma A-II level along with urine output were markedly increased in A-II rats. There was diuresis but no natriuresis. The phosphate excretion increased sevenfold on day 4 and 5.7-fold on day 7. There was no change in Na-dependent Pi uptake in brush-border membrane (BBM) vesicles between A-II-treated group and control on day 4, however, there was a 43% increase on day 7. Western blot analysis of NaPi-IIa protein abundance showed a parallel pattern: no change after 4 days of treatment and a 48% increase after 7 days of treatment. However, Northern blot analysis of cortical RNA showed no change in NaPi-IIa mRNA abundance on day 7. A-II stimulation of Na/Pi co-transport activity is a result of increases in the expression of BBM NaPi-IIa protein level and that stimulation is most likely mediated by posttranscriptional mechanisms. (C) 2004 Elsevier B.V. All rights reserved.
机译:肾脏在磷酸盐的重吸收中起主要作用,大部分发生在近端小管(PT)中。 IIa型磷酸钠共转运蛋白(NaPi-IIa)是PT的主要参与者。本研究的目的是确定血管紧张素II(A-II)对大鼠肾皮质中NaPi-IIa膜表达的影响。通过微型渗透泵将A-II(500 ng / kg / min)长期注入Sprague-Dawley大鼠中,持续7天。在A-II大鼠中,动脉压和循环血浆A-II水平以及尿量显着增加。有利尿但无利尿。磷酸盐排泄在第4天增加了7倍,在第7天增加了5.7倍。在A-II处理组和对照组之间,刷状边界膜(BBM)囊泡中Na依赖的Pi吸收没有变化,但是在第4天,第7天增加了43%。NaPi-IIa蛋白丰度的蛋白质印迹分析显示出一种平行的模式:治疗4天后无变化,治疗7天后增加48%。然而,皮质RNA的Northern印迹分析显示,第7天NaPi-IIa mRNA的丰度没有变化。A-II刺激Na / Pi共转运活性是BBM NaPi-IIa蛋白水平表达增加的结果,并且刺激很可能是由转录后机制介导的。 (C)2004 Elsevier B.V.保留所有权利。

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