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大鼠近端小管中钠钾泵的分化受钠氢交换体调节。

Differentiation of Na+-K+ pump in rat proximal tubule is modulated by Na+-H+ exchanger.

作者信息

Fukuda Y, Aperia A

机构信息

Department of Pediatrics, St. Göran's Children's Hospital, Karolinska Institute, Stockholm, Sweden.

出版信息

Am J Physiol. 1988 Sep;255(3 Pt 2):F552-7. doi: 10.1152/ajprenal.1988.255.3.F552.

Abstract

This study examines the effect of in vivo modulation of Na+-H+ exchange activity on the development of Na+-K+-ATPase in rat kidney proximal convoluted tubule (PCT) segments. To stimulate Na+-H+ exchanger (major entry pathway for Na in PCT), weanling rats were fed NH4Cl for 4 days to induce metabolic acidosis (MA). In vehicle (Vh)-fed rats PCT Na+-K+-ATPase activity (pmol Pi.mm tubule-1.h-1 +/- SE) increased from 481 +/- 78 at 16 days to 1,122 +/- 119 at 20 days. In 20-day-old chronic MA rats, PCT Na+-K+-ATPase activity was 1,717 +/- 109, i.e., significantly higher (P less than 0.01) relative to controls. Chronic MA had no effect on PCT Mg ATPase activity and on Na+-K+-ATPase in the medullary thick ascending limb (MTAL). To inhibit the Na+-H+ exchanger, weanling rats received amiloride (30 micrograms.100 g body wt-1.day-1) via osmotic minipump for 4 days. In Vh-treated rats PCT Na+-K+-ATPase increased from 481 +/- 78 at 16 days to 1,428 +/- 81 at 20 days. In rats given chronic amiloride, PCT Na+-K+-ATPase was significantly lower (858 +/- 75) at 20 days relative to controls but PCT Mg ATPase and MTAL Na+-K+-ATPase activity was the same as in controls. Chronic MA and amiloride had no significant effect on PCT Na+-K+-ATPase activity in adult rats. Acute MA and acute amiloride injection had no significant effect on PCT Na+-K+-ATPase in weanling rats.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

本研究检测了体内调节钠氢交换活性对大鼠肾近端曲管(PCT)节段钠钾ATP酶发育的影响。为刺激钠氢交换体(PCT中钠的主要进入途径),给断奶大鼠喂食氯化铵4天以诱导代谢性酸中毒(MA)。在喂食赋形剂(Vh)的大鼠中,PCT钠钾ATP酶活性(pmol Pi·mm小管⁻¹·h⁻¹±标准误)从16天时的481±78增加到20天时的1122±119。在20日龄的慢性MA大鼠中,PCT钠钾ATP酶活性为1717±109,即相对于对照组显著更高(P<0.01)。慢性MA对PCT镁ATP酶活性以及髓质厚升支(MTAL)中的钠钾ATP酶无影响。为抑制钠氢交换体,给断奶大鼠通过渗透微型泵给予氨氯吡脒(30μg·100g体重⁻¹·天⁻¹),持续4天。在Vh处理的大鼠中,PCT钠钾ATP酶从16天时的481±78增加到20天时的1428±81。在给予慢性氨氯吡脒的大鼠中,20天时PCT钠钾ATP酶相对于对照组显著更低(858±75),但PCT镁ATP酶和MTAL钠钾ATP酶活性与对照组相同。慢性MA和氨氯吡脒对成年大鼠PCT钠钾ATP酶活性无显著影响。急性MA和急性注射氨氯吡脒对断奶大鼠PCT钠钾ATP酶无显著影响。(摘要截短于第250词)

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