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1 Department of Pharmaceutics, State University of New York at Buffalo, Amherst, New York 14260; and 2 Institute of Physiology, University of Zurich, CH-8057 Zurich, Switzerland
Decreased serum
sulfate concentrations are observed in hypothyroid patients. However,
the mechanism involved in thyroid hormone-induced alterations of renal
sulfate homeostasis is unknown. The objectives of this investigation
were to determine the effect of 6-propyl-2-thiouracil (PTU)-induced
hypothyroidism in rats on 1) the in
vivo serum concentrations, renal clearance, and renal reabsorption of
sulfate, 2) the in vitro renal
transport in brush-border membrane (BBM) and basolateral membrane (BLM)
vesicles, and 3) the cellular
mechanism of the hypothyroid-induced alteration in sulfate renal
transport. Serum sulfate concentrations, renal fractional reabsorption
of sulfate, and creatinine clearance were decreased significantly in
the hypothyroid group. The
Vmax values for
sodium-sulfate cotransport in BBM were significantly decreased in the
kidney cortex from the hypothyroid animals (0.90 ± 0.31 vs. 0.49 ± 0.08 nmol · mg
1 · 10 s
1,
n = 5-6,
P < 0.05) without
changes in Km.
There were no significant differences in
Vmax and
Km for
sulfate/anion exchange transport in BLM. Sodium-dependent sulfate
transporter (NaSi-1) mRNA and protein levels were
significantly lower in the kidney cortex from hypothyroid rats.
Hypothyroidism did not alter the membrane motional order (fluidity) in
BBM and BLM, which indicates that the changes in the membrane fluidity
do not represent the mechanism for the altered renal transport. These
results demonstrate that PTU-induced hypothyroidism decreases
sodium-sulfate cotransport by downregulation of the NaSi-1 gene.
inorganic sulfate; sodium sulfate cotransport; NaSi-1; kidney
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