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1 Department of Biochemistry
and Molecular Biology,
The anomalous increase in charge selectivity as previously
observed with reduced dextran sulfate clearances in diabetic rats (L. D. Michels, M. Davidman, and W. F. Keane. Kidney
Int. 21: 699-705, 1982) was confirmed in 4-wk
streptozotocin (STZ) diabetic Sprague-Dawley rats using the isolated
perfused kidney technique. The apparent charge selectivity in both
control and diabetic rats could be abolished by increasing the dextran
sulfate concentration to 200 µg/ml in the perfusate. This was
demonstrated by a high rate of processing of dextran sulfate (~1,700
ng · min
1 · kidney
1)
by glomeruli in both control and diabetic kidneys and by the fact that
charge interaction could not explain the concentration dependence. The amount of urinary desulfation of dextran sulfate was
also found to be significantly less in the diabetic kidney as was
glomerular sulfatase activity compared with controls. Dextran sulfate
glomerular processing is therefore altered in the STZ diabetic rat
kidney but could be rationalized in terms of previous models of
endothelial cell receptor-mediated uptake of dextran sulfate. The
results are consistent with recent work demonstrating that there is
little or no electrostatic charge interaction operating on dextran
sulfate or other negatively charged molecules at the glomerular
capillary wall.
dextran sulfate; isolated perfused kidney; glomerular cell uptake; fractional clearance; sulfatase; streptozotocin diabetes; charge selectivity
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