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首页> 外文期刊>American Journal of Physiology >Metabolic acidosis regulates rat renal Na-Si cotransport activity.
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Metabolic acidosis regulates rat renal Na-Si cotransport activity.

机译:代谢性酸中毒调节大鼠肾脏Na-Si共转运活性。

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Recently, we cloned a cDNA (NaSi-1) localized to rat renal proximal tubules and encoding the brush-border membrane (BBM) Na gradient-dependent inorganic sulfate (Si) transport protein (Na-Si cotransporter). The purpose of the present study was to determine the effect of metabolic acidosis (MA) on Na-Si cotransport activity and NaSi-1 protein and mRNA expression. In rats with MA for 24 h (but not 6 or 12 h), there was a significant increase in the fractional excretion of Si, which was associated with a 2.4-fold decrease in BBM Na-Si cotransport activity. The decrease in Na-Si cotransport correlated with a 2.8-fold decrease in BBM NaSi-1 protein abundance and a 2.2-fold decrease in cortical NaSi-1 mRNA abundance. The inhibitory effect of MA on BBM Na-Si cotransport was also sustained in rats with chronic (10 days) MA. In addition, in Xenopus laevis oocytes injected with mRNA from kidney cortex, there was a significant reduction in the induced Na-Si cotransport in rats with MA compared with control rats, suggesting that MA causes a decrease in the abundance of functional mRNA encoding the NaSi-1 cotransporter. These findings indicate that MA reduces Si reabsorption by causing decreases in BBM Na-Si cotransport activity and that decreases in the expression of NaSi-1 protein and mRNA abundance, at least in part, play an important role in the inhibition of Na-Si cotransport activity during MA.
机译:最近,我们克隆了定位于大鼠肾近端小管的cDNA(NaSi-1),并编码刷边界膜(BBM)Na梯度依赖性无机硫酸盐(Si)转运蛋白(Na-Si cotransporter)。本研究的目的是确定代谢性酸中毒(MA)对Na-Si共转运活性以及NaSi-1蛋白和mRNA表达的影响。在MA持续24小时(而不是6或12小时)的大鼠中,Si的分数排泄显着增加,这与BBM Na-Si共转运活性降低了2.4倍有关。 Na-Si共转运的减少与BBM NaSi-1蛋白丰度下降2.8倍和皮质NaSi-1 mRNA丰度下降2.2倍相关。在患有慢性(10天)MA的大鼠中,MA对BBM Na-Si共转运的抑制作用也得以维持。此外,在注射了来自肾皮质的mRNA的非洲爪蟾卵母细胞中,与对照组相比,MA的大鼠中诱导的Na-Si共转运显着减少,这表明MA导致编码NaSi的功能性mRNA丰度下降。 -1共转运体。这些发现表明,MA通过引起BBM Na-Si共转运活性降低而减少了Si重吸收,并且NaSi-1蛋白和mRNA丰度的降低至少部分在抑制Na-Si共转运中起重要作用。 MA期间的活动。

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