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Vol. 290, Issue 2, 496-504, August 1999
Departments of Pharmacology and Therapeutics (K.B.G., D.D.S.,
D.S.S.), Internal Medicine (D.D.S., D.S.S.), and Pediatrics and Child
Health (D.S.S.), and Centre on Aging (D.S.S.), University of Manitoba,
Winnipeg, Manitoba, Canada
Amantadine transport into renal proximal and distal tubules is
bicarbonate dependent. In the present study, we addressed the effects
of bicarbonate on renal clearance and urinary excretion of amantadine.
Renal clearance of kynurenic acid was also studied to determine whether
bicarbonate effects are specific for organic base transport by the
kidney. After a moderate diuresis was established, animals received
i.v. [3H]amantadine or [3H]kynurenic acid
followed by an acute dose of sodium bicarbonate or physiological
saline. Urine and blood samples were analyzed for
[3H]amantadine or [3H]kynurenic acid, blood
gases, and pH. Amantadine and kynurenic acid were excreted by the
kidneys, and both compounds underwent renal tubular secretion.
Amantadine metabolism occurred, and one metabolite was detected in the
urine. In the bicarbonate-treated rats, the total amount of amantadine
excreted in the urine was decreased, whereas the amount of metabolite
recovered was similar in both groups. Bicarbonate treatment caused a
sustained increase in blood bicarbonate levels, a mild increase in
blood pH, and a decrease in amantadine renal clearance and in the
amantadine/creatinine clearance ratio. Only a transient decrease in the
renal clearance of kynurenic acid and the kynurenic acid/creatinine
clearance ratio was observed. This study demonstrates that short-term
changes in bicarbonate concentration may have significant effects on
renal organic cation elimination. Coupled with our previous in vitro demonstration of bicarbonate-dependent organic cation transport, the
present study suggests that bicarbonate inhibition of renal tubule
organic cation secretion may explain the previous observation that
bicarbonate dosing decreases amantadine excretion by the kidney.
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