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Diabetes, Vol 43, Issue 5 629-633, Copyright © 1994 by American Diabetes Association
Increased renal metabolism in diabetes. Mechanism and functional implications
A Korner, AC Eklof, G Celsi and A Aperia
Department of Pediatrics, Karolinska Institute, St. Goran's Children's Hospital, Stockholm, Sweden.
The coupling between the Na+/glucose cotransporter and Na(+)-K(+)-ATPase
(NKA) described for epithelial cells (1) prompted us to study in rats with
streptozocin-induced diabetes the effect of increased tubular glucose load
on tubular Na+ reabsorption, NKA-dependent O2 consumption (QO2), and NKA
activity. Filtered glucose is mainly reabsorbed in the proximal tubuli via
the phlorizin-sensitive Na+/glucose cotransporter. In this study, the
diabetic rats had a significantly higher renal blood flow (RBF), glomerular
filtration rate (GFR), and Na+ reabsorption than the control rats. Total
renal QO2 as well as QO2 in cortical tissue, which consists mainly of
proximal tubular cells, was significantly higher in diabetic than in
control rats. The increase in tissue QO2 was entirely caused by increased
NKA-dependent QO2. NKA activity, measured as rate of ATP hydrolysis, was
increased in cortical tubular but not glomerular tissue from diabetic rats.
Phlorizin treatment abolished the increase in NKA activity, Na+
reabsorption, and QO2, as well as the increase in RBF and GFR in diabetic
rats. We conclude that diabetes is associated with increased renal O2
metabolism secondary to the increase in coupled Na+ reabsorption via the
Na+/glucose cotransporter and NKA. The increased oxygen consumption might
contribute to the hyperperfusion and hyperfiltration in the diabetic
kidney.

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Copyright © 1994 by the American Diabetes Association.
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