Yoshiyama Y, Grenier L, Gourde P, Simard M, Lin L, Morin N J, Bergeron M G, Labrecque G, Beauchamp D
Department of Clinical Pharmacy, Kyoritsu College of Pharmacy, Tokyo, Japan.
Antimicrob Agents Chemother. 1996 Mar;40(3):802-6. doi: 10.1128/AAC.40.3.802.
The temporal variation in the nephrotoxicity of low doses of isepamicin was studied in male Sprague-Dawley rats treated with a single daily intraperitoneal injection of saline (NaCl, 0.9%) or isepamicin (80 mg/kg of body weight) at either 0800, 1400, 2000, or 0200 h for 4 and 10 days. On day 10, the cellular regeneration (incorporation of [3H] thymidine into DNA of renal cortex) and cortical accumulation of isepamicin were significantly higher in animals treated at 1400 h than at 0200 h (P < 0.01). Immunogold labeling studies showed that isepamicin was essentially localized in the lysosomes of proximal tubular cells in all treated groups, but the density of the gold particles over the lysosomes was higher in animals treated at 1400 than at 0200 h. The results of the present study show that the renal toxicity of isepamicin was maximal at 1400 h (midlight period) and minimal at 0200 h (middark period).
在雄性斯普拉格 - 道利大鼠中研究了低剂量异帕米星肾毒性的时间变化。大鼠每天于08:00、14:00、20:00或02:00进行一次腹腔注射生理盐水(0.9% NaCl)或异帕米星(80 mg/kg体重),持续4天和10天。在第10天,14:00接受治疗的动物的细胞再生([3H]胸腺嘧啶掺入肾皮质DNA)和异帕米星在皮质中的蓄积显著高于02:00接受治疗的动物(P < 0.01)。免疫金标记研究表明,在所有治疗组中,异帕米星主要定位于近端肾小管细胞的溶酶体中,但14:00接受治疗的动物溶酶体上的金颗粒密度高于02:00接受治疗的动物。本研究结果表明,异帕米星的肾毒性在14:00(光照中期)最大,在02:00(黑暗中期)最小。