首页> 美国卫生研究院文献>American Journal of Physiology - Renal Physiology >Renal Acid-Base Physiology: Proximal tubule Na+/H+ exchanger activity in adult NHE8−/− NHE3−/− and NHE3−/−/NHE8−/− mice
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Renal Acid-Base Physiology: Proximal tubule Na+/H+ exchanger activity in adult NHE8−/− NHE3−/− and NHE3−/−/NHE8−/− mice

机译:肾酸碱生理:成年NHE8-/-NHE3-/-和NHE3-/-/ NHE8-/-小鼠的近端小管Na + / H +交换子活性

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摘要

NHE3 is the predominant Na+/H+ exchanger on the brush-border membrane (BBM) of the proximal tubule in adults. However, NHE3 null mice still have significant renal BBM Na+/H+ activity. NHE8 has been localized to the BBM of proximal tubules and is more highly expressed in neonates than adult animals. The relative role of NHE8 in adult renal H+ transport is unclear. This study examined whether there was compensation by NHE8 in NHE3−/− mice and by NHE3 in NHE8−/− mice. NHE3−/− mice had significant metabolic acidosis, and renal BBM NHE8 protein abundance was greater in NHE3−/− mice than control mice, indicating that there may be compensation by NHE8 in NHE3−/− mice. NHE8−/− mice had serum bicarbonate levels and pH that were not different from controls. NHE3 protein expression on the BBM was greater in NHE8−/− mice than in wild-type mice, indicating that there may be compensation by NHE3 in NHE8−/− mice. Both BBM NHE3 and NHE8 protein abundance increased in response to acidosis. Blood pressure and Na+/H+ exchanger activity were comparable in NHE8−/− mice to that of controls, but both were significantly lower in NHE3−/− mice compared with control mice. Compared with NHE3−/− mice, NHE3−/−/NHE8−/− mice had lower blood pressures. While serum bicarbonate was comparable in NHE3−/− mice and NHE3−/−/NHE8−/− mice, proximal tubule Na+/H+ exchange activity was less in NHE3−/−/NHE8−/− mice compared with NHE3−/− mice. In conclusion, NHE3 is the predominant Na+/H+ exchanger in adult mice. NHE8 may play a compensatory role in renal acidification and blood pressure regulation in NHE3−/− mice.
机译:NHE3是成人近端肾小管刷状膜(BBM)上主要的Na + / H + 交换子。但是,NHE3缺失的小鼠仍然具有明显的肾BBM Na + / H + 活性。 NHE8已定位于近端肾小管的BBM,并且在新生婴儿中比成年动物更高度表达。 NHE8在成人肾脏H + 转运中的相对作用尚不清楚。这项研究检查了NHE3 -/-小鼠中是否存在NHE8的补偿以及NHE8 -/-小鼠中是否存在NHE3的补偿。 NHE3 -/-小鼠具有明显的代谢性酸中毒,并且NHE3 -/-小鼠的肾BBM NHE8蛋白丰度高于对照组,表明NHE8可能有补偿在NHE3 -/-小鼠中。 NHE8 -/-小鼠的血清碳酸氢盐水平和pH与对照组无差异。在NHE8 -/-小鼠中,BBM上的NHE3蛋白表达高于野生型小鼠,这表明NHE8 -/-小鼠中可能存在NHE3的补偿。 BBM NHE3和NHE8蛋白质丰度均随着酸中毒而增加。在NHE8 -/-小鼠中,血压和Na + / H + 交换子活性与对照组相当,但在对照组中,两者均显着降低NHE3 -/-小鼠与对照小鼠相比。与NHE3 -/-小鼠相比,NHE3 -/- / NHE8 -/-小鼠的血压更低。尽管NHE3 -/-小鼠和NHE3 -/- / NHE8 -/-小鼠的血清碳酸氢盐具有可比性,但近端小管Na 与NHE3 相比,NHE3 -/- / NHE8 -// 小鼠的+ / H + 交换活性较小-/-小鼠。总之,NHE3是成年小鼠中主要的Na + / H + 交换子。 NHE8可能在NHE3 -/-小鼠的肾脏酸化和血压调节中起补偿作用。

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