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Antimicrobial Agents and Chemotherapy, March 1999, p. 520-524, Vol. 43, No. 3
Centre de Recherche en Infectiologie,
Received 11 June 1998/Returned for modification 12 September
1998/Accepted 20 December 1998
Evidence for temporal variation in the nephrotoxicity of
amphotericin B was recently reported in experimental animals. The role
of food in these variations was determined by studying the effect of a
short fasting period on the temporal variation in the renal toxicity of
amphotericin B. Twenty-eight normally fed and 28 fasted female
Sprague-Dawley rats were used. Food was available ad libitum to the fed
rats, while the fasted animals were fasted 12 h before and 24 h after amphotericin B injection to minimize stress for the animals.
Water was available ad libitum to both groups of rats, which were
maintained on a 14-h light, 10-h dark regimen (light on at 0600 h). Renal toxicity was determined by comparing the levels of excretion
of renal enzyme and the serum creatinine and blood urea nitrogen (BUN)
levels at the time of the maximal (0700 h) or the minimal (1900 h)
nephrotoxicity after the intraperitoneal administration of a single
dose of dextrose (5%; control group) or amphotericin B (50 mg/kg of
body weight; treated group) to the rats. The nephrotoxicities obtained
after amphotericin B administration at both times of day were compared to the nephrotoxicities observed for time-matched controls. In fed
animals, the 24-h urinary excretion of
N-acetyl-
0066-4804/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Effect of Fasting on Temporal Variation in the
Nephrotoxicity of Amphotericin B in Rats
-D-glucosaminidase and
-galactosidase was significantly higher when amphotericin B was
injected at 0700 and 1900 h. The excretion of these two enzymes
was reduced significantly (P < 0.05) in fasting
rats, and this effect was larger at 0700 h (P < 0.05) than at 1900 h. The serum creatinine level was also
significantly higher (P < 0.05) in fed animals
treated at 0700 h than in fed animals treated at 1900 h.
Fasting reduced significantly (P < 0.05) the
increase in the serum creatinine level, and this effect was larger in
the animals treated at 0700 h. Similar data were obtained for BUN levels. Amphotericin B accumulation was significantly higher
(P < 0.05) in the renal cortexes of fed rats
than in those of fasted animals, but there was no difference according
to the time of injection. These results demonstrated that fasting
reduces the nephrotoxicity of amphotericin B and that food availability
is of crucial importance in the temporal variation in the renal
toxicity of amphotericin B in rats.
*
Corresponding author. Mailing address: Centre de
Recherche en Infectiologie, Centre de Recherche du CHUL, 2705 Boul.
Laurier, Ste-Foy, Québec, Canada G1V 4G2. Phone: (418) 654-2705. Fax: (418) 654-2715. E-mail:
denis.beauchamp{at}crchul.ulaval.ca.
Antimicrobial Agents and Chemotherapy, March 1999, p. 520-524, Vol. 43, No. 3
0066-4804/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
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