Department of Physiology, Medical College of Wisconsin, Milwaukee, Wisconsin.
Department of Integrative Biology and Pharmacology, University of Texas Health Science Center, Houston, Texas, USA.
Curr Opin Nephrol Hypertens. 2018 Sep;27(5):373-378. doi: 10.1097/MNH.0000000000000437.
Multiple clinical and translational evidence support benefits of high potassium diet; however, there many uncertainties underlying the molecular and cellular mechanisms determining effects of dietary potassium. Kir4.1 and Kir5.1 proteins form a functional heteromer (Kir4.1/Kir5.1), which is the primary inwardly rectifying potassium channel on the basolateral membrane of both distal convoluted tubule (DCT) and the collecting duct principal cells. The purpose of this mini-review is to summarize latest advances in our understanding of the evolution, physiological relevance and mechanisms controlling these channels.
Kir4.1 and Kir5.1 channels play a critical role in determining electrolyte homeostasis in the kidney and blood pressure, respectively. It was reported that Kir4.1/Kir5.1 serves as potassium sensors in the distal nephron responding to variations in dietary intake and hormonal stimuli. Global and kidney specific knockouts of either channel resulted in hypokalemia and severe cardiorenal phenotypes. Furthermore, knock out of Kir5.1 in Dahl salt-sensitive rat background revealed the crucial role of the Kir4.1/Kir5.1 channel in salt-induced hypertension.
Here, we focus on reviewing novel experimental evidence of the physiological function, expression and hormonal regulation of renal basolateral inwardly rectifying potassium channels. Further investigation of molecular and cellular mechanisms controlling Kir4.1 and Kir4.1/Kir5.1-mediating pathways and development of specific compounds targeting these channels function is essential for proper control of electrolyte homeostasis and blood pressure.
多项临床和转化证据支持高钾饮食的益处,但饮食钾确定作用的分子和细胞机制背后存在许多不确定性。Kir4.1 和 Kir5.1 蛋白形成功能性异聚体(Kir4.1/Kir5.1),这是远曲小管(DCT)和集合管主细胞基底外侧膜上的主要内向整流钾通道。本综述的目的是总结我们对这些通道的进化、生理相关性和调控机制的最新认识。
Kir4.1 和 Kir5.1 通道分别在确定肾脏电解质稳态和血压方面起着关键作用。据报道,Kir4.1/Kir5.1 作为远曲小管中的钾传感器,对饮食摄入和激素刺激的变化作出反应。通道的全局和肾脏特异性敲除导致低钾血症和严重的心肾表型。此外,Dahl 盐敏感大鼠背景下的 Kir5.1 敲除揭示了 Kir4.1/Kir5.1 通道在盐诱导高血压中的关键作用。
本文重点综述了肾脏基底外侧内向整流钾通道的生理功能、表达和激素调节的新实验证据。进一步研究调控 Kir4.1 和 Kir4.1/Kir5.1 介导途径的分子和细胞机制以及开发针对这些通道功能的特异性化合物对于电解质稳态和血压的适当控制至关重要。