NYMC Faculty Publications

Inwardly Rectifying K Channels 4.1 and 5.1 (Kir4.1/Kir5.1) in the Renal Distal Nephron

Author Type(s)

Faculty

DOI

10.1152/ajpcell.00096.2022

Journal Title

American Journal of Physiology. Cell Physiology

First Page

C277

Last Page

C288

Document Type

Article

Publication Date

8-1-2022

Department

Pharmacology

Abstract

The inwardly rectifying potassium channel (Kir) 4.1 (encoded by ) interacts with Kir5.1 (encoded by ) to form a major basolateral K channel in the renal distal convoluted tubule (DCT), connecting tubule (CNT), and the cortical collecting duct (CCD). Kir4.1/Kir5.1 heterotetramer plays an important role in regulating Na and K transport in the DCT, CNT, and CCD. A recent development in the field has firmly established the role of Kir4.1/Kir5.1 heterotetramer of the DCT in the regulation of thiazide-sensitive Na-Cl cotransporter (NCC). Changes in Kir4.1/Kir5.1 activity of the DCT are an essential step for the regulation of NCC expression/activity induced by dietary K and Na intakes and play a role in modulating NCC by type 2 angiotensin II receptor (AT2R), bradykinin type II receptor (BK2R), and β-adrenergic receptor. Since NCC activity determines the Na delivery rate to the aldosterone-sensitive distal nephron (ASDN), a distal nephron segment from late DCT to CCD, Kir4.1/Kir5.1 activity plays a critical role not only in the regulation of renal Na absorption but also in modulating renal K excretion and maintaining K homeostasis. Thus, Kir4.1/Kir5.1 activity serves as an important component of renal K sensing mechanism. The main focus of this review is to provide an overview regarding the role of Kir4.1 and Kir5.1 of the DCT and CCD in the regulation of renal K excretion and Na absorption.

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