Revisiting voltage-coupled H+ secretion in the collecting duct.

Niklas Ayasse, Peder Berg, Mads V Sørensen, Samuel L Svendsen, Alan M Weinstein, Jens Leipziger
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Abstract

Experimental studies have shown that V-type ATPase-driven H+ secretion is dependent on transepithelial voltage. On this basis, the "voltage hypothesis" of urinary acidification by the collecting duct was derived. Accordingly, it has been supposed that the lumen-negative potential created by the reabsorption of Na+ via the epithelial Na+ channel (ENaC) enhances electrogenic H+ secretion via V-type H+-ATPase. This concept continues to be widely used to explain acid/base disorders. Importantly, however, a solid proof of principle for the voltage hypothesis in physiologically relevant situations has not been reached. Rather, it has been challenged by recent in vivo functional studies. In this review, we outline the arguments and experimental observations explaining why voltage-coupled H+ secretion in the collecting duct often appears poorly applicable for rationalizing changes in H+ secretion as a function of more or less ENaC function in the collecting duct.

重新审视集合管中的电压耦合 H+ 分泌。
实验研究表明,V 型 ATP 酶驱动的 H+ 分泌取决于跨上皮细胞电压。在此基础上,产生了集尿管尿液酸化的 "电压假说"。因此,人们认为通过上皮钠通道(ENaC)重吸收 Na+ 所产生的管腔负电位会增强通过 V 型 H+-ATP 酶的电原 H+ 分泌。这一概念仍被广泛用于解释酸碱紊乱。但重要的是,在生理相关的情况下,电压假说尚未得到可靠的原理证明。相反,最近的体内功能研究对其提出了挑战。在这篇综述中,我们概述了一些论点和实验观察结果,这些论点和观察结果解释了为什么集合管中的电压耦合 H+ 分泌往往不能很好地解释 H+ 分泌的变化与集合管中 ENaC 功能的多寡有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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