Literature DB >> 7305324

Gentamicin pharmacokinetic changes in induced acute canine nephrotoxic glomerulonephritis.

J E Riviere, G L Coppoc, E J Hinsman, W W Carlton.   

Abstract

Most clinical schemes used to adjust gentamicin dosage regimens in renal insufficiency assume that the volume of distribution remains constant. The purpose of this investigation was to determine the pharmacokinetic parameters of gentamicin (two-compartment open model) before and at two points during the acute phase of experimentally induced nephrotoxic (injection of anti-glomerular basement membrane antibody) glomerulonephritis in beagle dogs. Disease was verified by decreased 24-h creatinine clearance, increased 24-h urinary protein excretion, and characteristic immunofluorescent, light- and electron-microscopic lesions. After disease induction, the concentration of drug in serum at time zero (Cp0) was significantly decreased and the volume of the central compartment (Vc) and the volume of distribution (Vd(area)) were increased in all treated dogs. These findings suggest that the assumption of unchanged volume of distribution in acute glomerulonephritis could lead to a serious overestimation of serum drug concentration.

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Year:  1981        PMID: 7305324      PMCID: PMC181706          DOI: 10.1128/AAC.20.3.387

Source DB:  PubMed          Journal:  Antimicrob Agents Chemother        ISSN: 0066-4804            Impact factor:   5.191


  27 in total

1.  Studies of nephrotoxic nephritis. II. The fine structure of the glomerulus in acute nephrotoxic nephritis of dogs.

Authors:  H Z MOVAT; D D McGREGOR; J W STEINER
Journal:  Am J Clin Pathol       Date:  1961-10       Impact factor: 2.493

2.  Canine nephrotoxic glomerulonephritis. A combined light, immunofluorescent, and ultrastructural study.

Authors:  N G Wright; H Thompson; H J Cornwell
Journal:  Vet Pathol       Date:  1973       Impact factor: 2.221

Review 3.  Glomerulonephritis (third of three parts).

Authors:  J P Merrill
Journal:  N Engl J Med       Date:  1974-02-14       Impact factor: 91.245

4.  Binding of antibiotics to tissue homogenates.

Authors:  C M Kunin
Journal:  J Infect Dis       Date:  1970-01       Impact factor: 5.226

5.  Renal parenchymal accumulation of aminoglycoside antibiotics in rats.

Authors:  F C Luft; S A Kleit
Journal:  J Infect Dis       Date:  1974-12       Impact factor: 5.226

6.  Serum protein binding of the aminoglycoside antibiotics.

Authors:  R C Gordon; C Regamey; W M Kirby
Journal:  Antimicrob Agents Chemother       Date:  1972-09       Impact factor: 5.191

7.  Drug dosage in patients with renal disease.

Authors:  L C Dettli
Journal:  Clin Pharmacol Ther       Date:  1974-07       Impact factor: 6.875

8.  The unpredictability of serum concentrations of gentamicin: pharmacokinetics of gentamicin in patients with normal and abnormal renal function.

Authors:  D Kaye; M E Levison; E D Labovitz
Journal:  J Infect Dis       Date:  1974-08       Impact factor: 5.226

9.  Effects of change in elimination on varous parameters of the two-compartment open model.

Authors:  W J Jusko; M Gibaldi
Journal:  J Pharm Sci       Date:  1972-08       Impact factor: 3.534

10.  Drug elimination and apparent volume of distribution in multicompartment systems.

Authors:  M Gibaldi; D Perrier
Journal:  J Pharm Sci       Date:  1972-06       Impact factor: 3.534

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  2 in total

1.  Effect of Enterococcus faecalis pyelonephritis on the intracortical accumulation kinetics of gentamicin in rats.

Authors:  M Jullien; G Thériault; M G Bergeron; D Beauchamp
Journal:  Can J Infect Dis       Date:  1990

2.  An experimental model for pharmacokinetic analysis in renal failure.

Authors:  N E Duffee; R F Bevill; G D Koritz; D J Schaeffer
Journal:  J Pharmacokinet Biopharm       Date:  1990-02
  2 in total

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