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Diet induced obesity in rats reduces NHE 3 and Na + /K + ‐ ATP ase expression in the kidney
Author(s) -
Briffa JF,
Grinfeld E,
Jenkin KA,
Mathai ML,
Poronnik P,
McAinch AJ,
Hryciw DH
Publication year - 2015
Publication title -
clinical and experimental pharmacology and physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.752
H-Index - 103
eISSN - 1440-1681
pISSN - 0305-1870
DOI - 10.1111/1440-1681.12452
Subject(s) - reabsorption , medicine , endocrinology , renal sodium reabsorption , chemistry , sodium , sodium–hydrogen antiporter , kidney , western blot , albuminuria , renal physiology , biology , biochemistry , organic chemistry , gene
Summary The consumption of a high fat diet ( HFD ) is associated with proteinuria and altered sodium handling and excretion, which can lead to kidney disease. In the proximal tubule, the Na + /H + Exchanger 3 ( NHE 3) is responsible for normal protein reabsorption and the reabsorption of approximately 70% of the renal sodium load. It is the Na + /K + ‐ ATP ase that provides the driving force for the reabsorption of sodium and its exit across the basolateral membrane. This study investigates the effects that consumption of a HFD for 12 weeks has on NHE 3 and Na + /K + ‐ ATP ase expression in the kidney. Western blot analysis identified a significant reduction in NHE 3 and its modulator, phosphorylated protein kinase B, in renal lysate from obese rats. In the obese rats, a reduction in NHE 3 expression in the proximal tubule may impact on the acidification of endosomes which are responsible for albumin uptake, suggesting a key role for the exchanger in protein endocytosis in obesity. Western blot analysis identified a reduction in Na + /K + ‐ ATP ase which could also potentially impact on albumin uptake and sodium reabsorption. This study demonstrates that consumption of a HFD for 12 weeks reduces renal NHE 3 and Na + /K + ‐ ATP ase expression, an effect that may contribute to the albuminuria associated with obesity. Furthermore the reduction in these transporters is not likely to contribute to the reduced sodium excretion in obesity. These data highlight a potential link between NHE 3 and Na + /K + ‐ ATP ase in the pathophysiological changes in renal protein handling observed in obesity.