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10.1152/ajprenal.00615.2013

http://scihub22266oqcxt.onion/10.1152/ajprenal.00615.2013
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C4080160!4080160!24785188
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suck abstract from ncbi


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pmid24785188      Am+J+Physiol+Renal+Physiol 2014 ; 307 (1): F58-63
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  • Sodium and potassium regulate endothelial phospholipase C-? and Bmx #MMPMID24785188
  • Ying WZ; Aaron KJ; Sanders PW
  • Am J Physiol Renal Physiol 2014[Jul]; 307 (1): F58-63 PMID24785188show ga
  • The amount of Na+ and K+ in the diet promotes significant changes in endothelial cell function. In the present study, a series of in vitro and in vivo experiments determined the role of Na+ and K+ in the regulation of two pleckstrin homology domain-containing intracellular signaling molecules, phospholipase C (PLC)-?1 and epithelial and endothelial tyrosine kinase/bone marrow tyrosine kinase on chromosome X (Bmx), and agonist-generated Ca2+ signaling in the endothelium. Extracellular K+ concentration regulated the levels of activated PLC-?1, Bmx, and carbachol-stimulated intracellular Ca2+ mobilization in human endothelial cells. Additional experiments confirmed that high-conductance Ca2+-activated K+ channels and phosphatidylinositol 3-kinase mediated these effects. The content of Na+ and K+ in the diet also regulated Bmx levels in endothelial cells and activated PLC-?1 levels in rats in vivo. The effects of dietary K+ on Bmx were more pronounced in rats fed a high-salt diet compared with rats fed a low-salt diet. These experiments elucidated an endothelial cell signaling mechanism regulated by electrolytes, further demonstrating an integral relationship between endothelial cell function and dietary Na+ and K+ content.
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