Tsubosaki M, Irie Y, Ito K, Handa J, Ezura H, Kumagai M, Irie Y, Suzuki A, Yamashita T, Miyamoto K, Matsuda A, Konoha N
Jpn J Antibiot. 1978 Dec;31(12):738-65.
Studies on subactute toxicity and its recovery of pepleomycin sulfate (NK631) were carried out in both sexes of rats. NK 631 was administered intraperitoneally in dose levels of 0.3, 0.9, 2.7. 8.1 and 24.3 mg/kg/day for 30 days. After finishing administration of NK 631 for 30 days, 5 animals of each group were proceeded to recovery test for 35 days. During the course of the experiment, the body weight gains were suppressed in all dose levels except in 0.3 mg/kg group of male rats. The deaths were found in the animals treated with doses over 24.3 mg/kg during treatment period and in those over 2.7 mg/kg during recovery period. In biochemical and urinary analysis, the increases of serum GPT, BUN, Mg, Ca and urine glucose were moderately recognized in 8.1 mg/kg group. Additionally, in macroscopical and histopathological findings, bone damage was found in the animals treated with doses over 2.7 mg/kg during treatment and recovery periods. From these results, the maximum safety dose of NK 631 in subacute toxicity using rats were estimated to be about 0.3 mg/kg.
对硫酸培普利欧霉素(NK631)进行了大鼠亚急性毒性及其恢复情况的研究,实验对象为雌雄大鼠。NK631按0.3、0.9、2.7、8.1和24.3毫克/千克/天的剂量水平腹腔注射给药,持续30天。在NK631给药30天后,每组选取5只动物进行为期35天的恢复试验。在实验过程中,除0.3毫克/千克组的雄性大鼠外,所有剂量水平的动物体重增加均受到抑制。在治疗期间,剂量超过24.3毫克/千克的动物出现死亡,在恢复期间,剂量超过2.7毫克/千克的动物出现死亡。在生化和尿液分析中,8.1毫克/千克组血清谷丙转氨酶、尿素氮、镁、钙以及尿糖均有适度升高。此外,在大体和组织病理学检查中,治疗期和恢复期剂量超过2.7毫克/千克的动物出现骨损伤。根据这些结果,估计NK631在大鼠亚急性毒性实验中的最大安全剂量约为0.3毫克/千克。