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Division of Nephrology, Medical and Research Services, Sepulveda Veterans Affairs Medical Center, University of California at Los Angeles School of Medicine, Los Angeles, California 91343
In our present
study, we examined the effect of
Cl
on rabbit renal
brush-border membrane (BBM) phosphate
(Pi) uptake. It was found that
the Na+-dependent BBM
32P uptake was significantly
inhibited by Cl
replacement
in the uptake solution with other anions, or by
Cl
transport inhibitors,
including DIDS, SITS, diphenylamine-2-carboxylate (DPC), niflumic acid
(NF), and 5-nitro-2-(3-phenylpropylamino)benzoate (NPPB).
Intravesicular formate or
Cl
increased BBM
36Cl
uptake but did not affect BBM 32P
uptake. BBM
22Na+
uptake was lowered by Cl
replacement in the uptake solution but not by
Cl
transport inhibitors.
Changes in transmembrane electrical potential altered BBM
36Cl
and 32P uptake in directions
consistent with a net inward movement of negative and positive charges,
respectively. However, the
Cl
-dependent BBM
Pi uptake was not affected by
changes in transmembrane electrical potential. Finally, a similar
Cl
dependency of
Pi uptake was also found with BBM
derived from rat and mouse kidneys. In summary, our study showed that a
component of Na+-dependent
Pi uptake was also
Cl
dependent in rabbit,
rat, and mouse renal BBM. The mechanism underlying this
Cl
dependency remains to be identified.
proximal tubule; chloride channel; chloride channel inhibitor; sodium cotransport; hereditary nephrolithiasis
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