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Pflugers Arch. 2009 May;458(1):157-68. doi: 10.1007/s00424-008-0593-3. Epub 2008 Oct 7.

Regulation of potassium (K) handling in the renal collecting duct.

Author information

1
Department of Pharmacology, New York Medical College, Valhalla, 10595, USA. wenhui_wang@nymc.edu

Abstract

This review provides an overview of the molecular mechanisms of K transport in the mammalian connecting tubule (CNT) and cortical collecting duct (CCD), both nephron segments responsible for the regulation of renal K secretion. Aldosterone and dietary K intake are two of the most important factors regulating K secretion in the CNT and CCD. Recently, angiotensin II (AngII) has also been shown to play a role in the regulation of K secretion. In addition, genetic and molecular biological approaches have further identified new mechanisms by which aldosterone and dietary K intake regulate K transport. Thus, the interaction between serum-glucocorticoid-induced kinase 1 (SGK1) and with-no-lysine kinase 4 (WNK4) plays a significant role in mediating the effect of aldosterone on ROMK (Kir1.1), an important apical K channel modulating K secretion. Recent evidence suggests that WNK1, mitogen-activated protein kinases such as P38, ERK, and Src family protein tyrosine kinase are involved in mediating the effect of low K intake on apical K secretory channels.

PMID:
18839206
PMCID:
PMC2730119
DOI:
10.1007/s00424-008-0593-3
[Indexed for MEDLINE]
Free PMC Article

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