Literature DB >> 2052528

Sulfate homeostasis. IV. Probenecid-induced alterations of inorganic sulfate in rats.

I M Darling1, M E Morris.   

Abstract

Homeostasis of inorganic sulfate is maintained by the capacity-limited renal reabsorption of sulfate in the proximal tubule. The purpose of the present investigation was to determine if probenecid, the classical inhibitor of renal organic anion secretion, may affect sulfate renal clearance. Two groups of rats were administered in a randomized crossover design, an i.v. bolus dose (20.6 or 92.4 mg/kg) and 4-hr infusion (0.28 or 0.59 mg/min/kg) of probenecid or vehicle, and blood and urine samples were collected. At a steady-state serum concentration of 0.45 mM, probenecid had no significant effect on the serum concentrations or renal clearance of inorganic sulfate, whereas at a serum concentration of 1.4 mM, probenecid treatment caused a significant decrease in serum sulfate concentrations (0.57 +/- 0.11 vs 0.96 +/- 0.19 mM in controls, mean +/- SD, n = 6, P less than 0.001) due to an increase in the renal clearance of sulfate (3.88 +/- 1.18 vs 2.13 +/- 0.84 ml/min/kg in controls, P less than 0.01). The fraction of the filtered sulfate that was reabsorbed was significantly decreased (0.38 +/- 0.23, vs 0.74 +/- 0.09 in controls, P less than 0.01). Therefore, probenecid treatment results in the inhibition of the renal reabsorption of inorganic sulfate in rats in vivo.

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Year:  1991        PMID: 2052528     DOI: 10.1023/a:1015805918168

Source DB:  PubMed          Journal:  Pharm Res        ISSN: 0724-8741            Impact factor:   4.200


  25 in total

1.  Mean residence time concepts for pharmacokinetic systems with nonlinear drug elimination described by the Michaelis-Menten equation.

Authors:  H Y Cheng; W J Jusko
Journal:  Pharm Res       Date:  1988-03       Impact factor: 4.200

2.  Dose-dependent pharmacokinetics of probenecid in the rat.

Authors:  B M Emanuelsson; L K Paalzow
Journal:  Biopharm Drug Dispos       Date:  1988 Jan-Feb       Impact factor: 1.627

Review 3.  Renal organic anion transport system: pharmacological, physiological, and biochemical aspects.

Authors:  J V Møller; M I Sheikh
Journal:  Pharmacol Rev       Date:  1982-12       Impact factor: 25.468

4.  Dose- and time-dependent elimination of acetaminophen in rats: pharmacokinetic implications of cosubstrate depletion.

Authors:  R E Galinsky; G Levy
Journal:  J Pharmacol Exp Ther       Date:  1981-10       Impact factor: 4.030

5.  Determination of probenecid in serum by high-performance liquid chromatography.

Authors:  R K Harle; T Cowen
Journal:  Analyst       Date:  1978-05       Impact factor: 4.616

6.  Sulphate-ion/sodium-ion co-transport by brush-border membrane vesicles isolated from rat kidney cortex.

Authors:  H Lücke; G Stange; H Murer
Journal:  Biochem J       Date:  1979-07-15       Impact factor: 3.857

7.  Contraluminal sulfate transport in the proximal tubule of the rat kidney. IV. Specificity: salicylate analogs.

Authors:  K J Ullrich; G Rumrich; S Klöss
Journal:  Pflugers Arch       Date:  1985-08       Impact factor: 3.657

8.  Renal sulfate transport at the basolateral membrane is mediated by anion exchange.

Authors:  J B Pritchard; J L Renfro
Journal:  Proc Natl Acad Sci U S A       Date:  1983-05       Impact factor: 11.205

9.  Renal clearance of inorganic sulfate in rats: effect of acetaminophen-induced depletion of endogenous sulfate.

Authors:  J H Lin; G Levy
Journal:  J Pharm Sci       Date:  1983-03       Impact factor: 3.534

10.  EFFECT ON KIDNEY S35O4 UPTAKE OF COMPOUNDS RELATED TO SO4 TRANSPORT AND METABOLISM.

Authors:  I J DEYRUP
Journal:  Am J Physiol       Date:  1964-07
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