LeBrun M, Grenier L, Bergeron M G, Thibault L, Labrecque G, Beauchamp D
Centre de Recherche en Infectiologie, Faculté de Médecine, Université Laval, Sainte-Foy, Québec, Canada.
Antimicrob Agents Chemother. 1999 Mar;43(3):520-4. doi: 10.1128/AAC.43.3.520.
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-beta-D-glucosaminidase and beta-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.
最近在实验动物中报道了两性霉素B肾毒性存在时间变化的证据。通过研究短期禁食对两性霉素B肾毒性时间变化的影响,确定了食物在这些变化中的作用。使用了28只正常喂食和28只禁食的雌性Sprague-Dawley大鼠。喂食的大鼠可随意获取食物,而禁食的动物在两性霉素B注射前12小时和注射后24小时禁食,以尽量减少动物的应激。两组大鼠均可随意获取水,它们维持在14小时光照、10小时黑暗的饲养方案(0600时开灯)。通过比较腹腔注射单剂量葡萄糖(5%;对照组)或两性霉素B(50mg/kg体重;治疗组)后大鼠在最大肾毒性(0700时)或最小肾毒性(1900时)时肾酶排泄水平、血清肌酐和血尿素氮(BUN)水平来确定肾毒性。将一天中两个时间点给予两性霉素B后获得的肾毒性与时间匹配对照组观察到的肾毒性进行比较。在喂食的动物中,当在0700时和1900时注射两性霉素B时,N-乙酰-β-D-氨基葡萄糖苷酶和β-半乳糖苷酶的24小时尿排泄量显著更高。在禁食大鼠中,这两种酶的排泄量显著降低(P<0.05),且这种作用在0700时(P<0.05)比在1900时更大。在0700时治疗的喂食动物中,血清肌酐水平也显著高于在1900时治疗的喂食动物(P<0.05)。禁食显著降低(P<0.05)了血清肌酐水平的升高,且这种作用在0700时治疗的动物中更大。BUN水平也获得了类似的数据。喂食大鼠肾皮质中两性霉素B的蓄积显著高于禁食动物(P<0.05),但根据注射时间没有差异。这些结果表明,禁食可降低两性霉素B的肾毒性,并且食物供应在大鼠两性霉素B肾毒性的时间变化中至关重要。