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NH4+/NH3对来自髓袢升支粗段新鲜分离细胞的胞质pH及钾通道的影响。

Effect of NH4+/NH3 on cytosolic pH and the K+ channels of freshly isolated cells from the thick ascending limb of Henle's loop.

作者信息

Bleich M, Köttgen M, Schlatter E, Greger R

机构信息

Physiologisches Institut Albert-Ludwigs-Universität, Freiburg, Germany.

出版信息

Pflugers Arch. 1995 Jan;429(3):345-54. doi: 10.1007/BF00374149.

Abstract

The conductance properties of the luminal membrane of cells from the thick ascending limb of Henle's loop of rat kidney (TAL) are dominated by K+. In excised membrane patches the luminal K+ channel is regulated by pH changes on the cytosolic side. To examine this pH regulation in intact cells of freshly isolated TAL segments we measured the membrane voltage (Vm) in slow-whole-cell (SWC) recordings and the open probability (Po) of K+ channels in the cell-attached nystatin (CAN) configuration, where channel activity and part of Vm can be recorded. The pipette solution contained K+ 125 mmol/l and Cl- 32 mmol/l. Intracellular pH was determined by 2',7'bis(2-carboxyethyl)-5,(6)-carboxyfluorescein (BCECF) fluorescence. pH changes were induced by the addition of 10 mmol/l NH4+/NH3 to the bath. In the presence of NH4+/NH3 intracellular pH acidified by 0.53 +/- 0.11 units (n = 7). Inhibition of the Na+2Cl-K+ cotransporter by furosemide (0.1 mmol/l) reversed this effect and led to a transient alkalinisation by 0.62 +/- 0.14 units (n = 7). In SWC experiments Vm of TAL cells was -72 +/- 1 mV (n = 70). NH4+/NH3 depolarised Vm by 22 +/- 2 mV (n = 25). In 11 SWC experiments furosemide (0.1 mmol/l) attenuated the depolarising effect of NH4+ from 24 +/- 3 mV to 7 +/- 3 mV. Under control conditions the single-channel conductance of TAL K+ channels in CAN experiments was 66 +/- 5 pS and the reversal voltage for K+ currents was 70 +/- 2 mV (n = 35). The Po of K+ channels in CAN patches was reduced by NH4+/NH3 from 0.45 +/- 0.15 to 0.09 +/- 0.07 (n = 7). NH4+/NH3 exposure depolarised the zero current voltage of the permeabilised patches by -9.7 +/- 3.6 mV (n = 5). The results show that TAL K+ channels are regulated by cytosolic pH in the intact cell. The cytosolic pH is acidified by NH4+/NH3 exposure at concentrations which are physiologically relevant because Na+2Cl-K+(NH4+) cotransporter-mediated import of NH4+ exceeds the rate of NH3 diffusion into the TAL. K+ channels are inhibited by this acidification and the cells depolarise. In the presence of furosemide TAL cells alkalinise proving that NH4+ uptake occurs by the Na+2Cl-K+ cotransporter. The findings that, in the presence of NH4+/NH3 and furosemide, Vm is not completely repolarised and that K+ channels are not activated suggest that the respective K+ channels may in addition to their pH regulation be inhibited directly by NH4+/NH3.

摘要

大鼠肾髓袢升支粗段(TAL)细胞管腔膜的电导特性主要由K⁺决定。在切除的膜片上,管腔K⁺通道受胞质侧pH变化的调节。为了在新鲜分离的TAL节段的完整细胞中研究这种pH调节,我们在慢全细胞(SWC)记录中测量膜电压(Vm),并在细胞贴附制霉菌素(CAN)模式下测量K⁺通道的开放概率(Po),在该模式下可以记录通道活性和部分Vm。移液管溶液含有125 mmol/L的K⁺和32 mmol/L的Cl⁻。通过2',7'-双(2-羧乙基)-5,(6)-羧基荧光素(BCECF)荧光测定细胞内pH。通过向浴中添加10 mmol/L的NH₄⁺/NH₃诱导pH变化。在存在NH₄⁺/NH₃的情况下,细胞内pH酸化0.53±0.11个单位(n = 7)。呋塞米(0.1 mmol/L)抑制Na⁺2Cl-K⁺协同转运体可逆转这种效应,并导致短暂碱化0.62±0.14个单位(n = 7)。在SWC实验中,TAL细胞的Vm为-72±1 mV(n = 70)。NH₄⁺/NH₃使Vm去极化22±2 mV(n = 25)。在11次SWC实验中,呋塞米(0.1 mmol/L)将NH₄⁺的去极化作用从24±3 mV减弱至7±3 mV。在对照条件下,CAN实验中TAL K⁺通道的单通道电导为66±5 pS,K⁺电流的反转电压为70±2 mV(n = 35)。CAN膜片中K⁺通道的Po被NH₄⁺/NH₃从0.45±0.15降低至0.09±0.07(n = 7)。暴露于NH₄⁺/NH₃使通透膜片的零电流电压去极化-9.7±3.6 mV(n = 5)。结果表明,TAL K⁺通道在完整细胞中受胞质pH的调节。在生理相关浓度下,暴露于NH₄⁺/NH₃会使胞质pH酸化,因为Na⁺2Cl-K⁺(NH₄⁺)协同转运体介导的NH₄⁺导入超过了NH₃扩散到TAL中的速率。K⁺通道被这种酸化抑制,细胞去极化。在存在呋塞米的情况下,TAL细胞碱化,证明NH₄⁺通过Na⁺2Cl-K⁺协同转运体摄取。在存在NH₄⁺/NH₃和呋塞米的情况下,Vm没有完全复极化且K⁺通道没有被激活,这一发现表明,各自的K⁺通道除了其pH调节外,可能还被NH₄⁺/NH₃直接抑制。

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