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顶端H-K交换和基底外侧K通道在大鼠远端结肠隐窝细胞内pH调节中的作用

Role of apical H-K exchange and basolateral K channel in the regulation of intracellular pH in rat distal colon crypt cells.

作者信息

Ikuma M, Binder H J, Geibel J

机构信息

Department of Internal Medicine, Yale University School of Medicine, New Haven, CT 06520, USA.

出版信息

J Membr Biol. 1998 Dec 1;166(3):205-12. doi: 10.1007/s002329900462.

Abstract

An apical membrane ouabain-sensitive H-K exchange and a barium-sensitive basolateral membrane potassium channel are present in colonic crypt cells and may play a role in both K absorption and intracellular pH (pHi) regulation. To examine the possible interrelationship between apical membrane H-K exchange and basolateral membrane K movement in rat distal colon in the regulation of pHi, experiments were designed to assess whether changes in extracellular potassium can alter pHi. pHi in isolated rat crypts was determined using microspectrofluorimetric measurements of the pH-sensitive dye BCECF-AM (2', 7'-bis(carboxyethyl-5(6)-carboxy-fluorescein acetoxy methylester). After loading with the dye, crypts were superfused with a Na-free solution which resulted in a rapid and reversible fall in pHi (7.36 +/- 0.02 to 6.98 +/- 0.03). Following an increase in extracellular [K] to 20 mm, in the continued absence of Na, there was a further decrease in pHi (0.20 +/- 0.02, P < 0.01). K-induced acidification was blocked both by 2 mm bath barium, a K channel blocker, and by 0. 5 mm lumen ouabain. K-induced acidification was also observed when intracellular acidification was induced by a NH4Cl prepulse. These observations suggest that increased basolateral K movement increases intracellular [K] resulting in a decrease in pHi that is mediated by a ouabain-sensitive apical membrane H,K-ATPase. Our results demonstrate an interrelationship between basolateral K movement and apical H-K exchange in the regulation of pHi and apical K entry in rat distal colon.

摘要

结肠隐窝细胞存在顶端膜哇巴因敏感的H-K交换和钡敏感的基底外侧膜钾通道,它们可能在钾吸收和细胞内pH(pHi)调节中发挥作用。为了研究大鼠远端结肠顶端膜H-K交换与基底外侧膜钾转运在pHi调节中的可能相互关系,设计实验评估细胞外钾变化是否能改变pHi。使用对pH敏感的染料BCECF-AM(2',7'-双(羧乙基-5(6)-羧基-荧光素乙酰氧基甲酯)的显微分光荧光测定法测定分离的大鼠隐窝中的pHi。用该染料加载后,用无钠溶液对隐窝进行灌流,导致pHi迅速且可逆地下降(从7.36±0.02降至6.98±0.03)。在细胞外[K]增加到20 mM且持续无钠的情况下,pHi进一步下降(0.20±0.02,P<0.01)。钾诱导的酸化被2 mM浴液钡(一种钾通道阻滞剂)和0.5 mM管腔哇巴因阻断。当通过NH4Cl预脉冲诱导细胞内酸化时,也观察到钾诱导的酸化。这些观察结果表明,基底外侧钾转运增加会增加细胞内[K],导致pHi下降,这是由哇巴因敏感的顶端膜H,K-ATP酶介导的。我们的结果证明了大鼠远端结肠在pHi调节和顶端钾进入中基底外侧钾转运与顶端H-K交换之间的相互关系。

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