Literature DB >> 8851591

Effects of fasting on temporal variations in nephrotoxicity of gentamicin in rats.

D Beauchamp1, P Collin, L Grenier, M LeBrun, M Couture, L Thibault, G Labrecque, M G Bergeron.   

Abstract

Evidence for temporal variations in the nephrotoxicity of low doses of aminoglycosides were recently shown by using specific and sensitive parameters of renal toxicity. The aim of the present study was to evaluate the effect of a short period of fasting on the temporal variations in the renal toxicity of gentamicin. Twenty-eight normally fed (i.e., food and water were available ad libitum throughout the experiment) female Sprague-Dawley rats (weight, 175 to 220 g) and 28 fasted rats (i.e., only water was available during a 12-h fast before and a 24-h fast after gentamicin injection) were used. The animals were synchronized on a 14-h light, 10-h dark cycle (lights on at 0600 h) for 1 week before gentamicin administration. In July 1993, each group of animals was treated with a single intraperitoneal injection of saline (NaCl, 0.9%) or gentamicin (150 mg/kg of body weight) at either the peak (1400 h) or the trough (0200 h) of the previously determined toxicity. On day 1, the 24-h urinary excretion of beta-galactosidase, N-acetyl-beta-D-glucosaminidase, and gamma-glutamyltransferase was significantly higher in normally fed animals treated with gentamicin at 1400 h than in their time-matched controls and in normally fed animals treated at 0200 h (P < 0.01), which had normal levels of these enzymes. By contrast, the urinary excretion of these enzymes was significantly higher in both groups of gentamicin-treated, fasted rats than in their time-matched control groups (P < 0.01), reaching levels similar to those measured in normally fed rats treated at 1400 h. The accumulation of gentamicin was significantly lower in the renal cortex of normally fed rats treated at 0200 h than in rats treated at 1400 h (P < 0.05), but this time-dependent difference was not found in fasted rats treated at 0200 and 1400 h. Immunogold labeling done on ultrathin sections and observed by electron microscopy showed a similar subcellular localization of gentamicin in normally fed and fasted rats treated at either 1400 or 0200 h. These results suggest that the feeding period is of crucial importance in the temporal variations of the nephrotoxicity of gentamicin in rats.

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Year:  1996        PMID: 8851591      PMCID: PMC163178     

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


  30 in total

Review 1.  Once-daily aminoglycoside therapy.

Authors:  D N Gilbert
Journal:  Antimicrob Agents Chemother       Date:  1991-03       Impact factor: 5.191

2.  Chronotoxical study of gentamicin induced nephrotoxicity in rats.

Authors:  Y Yoshiyama; T Kobayashi; F Tomonaga; S Nakano
Journal:  J Antibiot (Tokyo)       Date:  1992-05       Impact factor: 2.649

3.  Incidence of and significant risk factors for aminoglycoside-associated nephrotoxicity in patients dosed by using individualized pharmacokinetic monitoring.

Authors:  J S Bertino; L A Booker; P A Franck; P L Jenkins; K R Franck; A N Nafziger
Journal:  J Infect Dis       Date:  1993-01       Impact factor: 5.226

4.  Effects of dietary protein conditioning on gentamicin-induced nephrotoxicosis in healthy male dogs.

Authors:  G F Grauer; D S Greco; E N Behrend; M J Fettman; R S Jaenke; T A Allen
Journal:  Am J Vet Res       Date:  1994-01       Impact factor: 1.156

5.  Circadian variation in amikacin clearance and its effects on efficacy and toxicity in mice with and without immunosuppression.

Authors:  H Hosokawa; S Nyu; K Nakamura; K Mifune; S Nakano
Journal:  Chronobiol Int       Date:  1993-08       Impact factor: 2.877

6.  Chrononephrotoxicity in rat of a vancomycin and gentamicin combination.

Authors:  B Fauconneau; E De Lemos; C Pariat; S Bouquet; P Courtois; A Piriou
Journal:  Pharmacol Toxicol       Date:  1992-07

7.  Influence of circadian-stage-dependent dosing schedule on nephrotoxicity and pharmacokinetics of isepamicin in rats.

Authors:  Y Yoshiyama; S Nishikawa; T Sugiyama; T Kobayashi; H Shimada; F Tomonaga; S Ohdo; N Ogawa; S Nakano
Journal:  Antimicrob Agents Chemother       Date:  1993-09       Impact factor: 5.191

8.  Subcellular distribution of gentamicin in proximal tubular cells, determined by immunogold labeling.

Authors:  D Beauchamp; P Gourde; M G Bergeron
Journal:  Antimicrob Agents Chemother       Date:  1991-11       Impact factor: 5.191

9.  Influence of feeding schedule on chronopharmacological aspects of gentamicin in mice.

Authors:  J Song; S Ohdo; N Ogawa; S Nakano
Journal:  Chronobiol Int       Date:  1993-10       Impact factor: 2.877

10.  Subcellular localization of tobramycin and vancomycin given alone and in combination in proximal tubular cells, determined by immunogold labeling.

Authors:  D Beauchamp; P Gourde; M Simard; M G Bergeron
Journal:  Antimicrob Agents Chemother       Date:  1992-10       Impact factor: 5.191

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  3 in total

1.  Effectiveness and toxicity of gentamicin in an experimental model of pyelonephritis: effect of the time of administration.

Authors:  M LeBrun; L Grenier; P Gourde; M G Bergeron; G Labrecque; D Beauchamp
Journal:  Antimicrob Agents Chemother       Date:  1999-05       Impact factor: 5.191

2.  Pharmacologic Basis for the Treatment of Pyelonephritis.

Authors: 
Journal:  Curr Infect Dis Rep       Date:  1999-10       Impact factor: 3.725

3.  Time-restricted feeding schedules modify temporal variation of gentamicin experimental nephrotoxicity.

Authors:  D Beauchamp; C Guimont; L Grenier; M LeBrun; D Tardif; P Gourde; M G Bergeron; L Thibault; G Labrecque
Journal:  Antimicrob Agents Chemother       Date:  1997-07       Impact factor: 5.191

  3 in total

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