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[VP 16-213的生殖研究(三)——在胎儿器官形成期对家兔进行口服给药]

[Reproduction studies of VP 16-213 (III)--Oral administration to rabbits during the period of fetal organogenesis].

作者信息

Takahashi N, Kai S, Kohmura H, Ishikawa K, Kuroyanagi K, Hamajima Y, Ohta S, Kadota T, Kawano S, Ohta K

出版信息

J Toxicol Sci. 1986 Apr;11 Suppl 1:227-39. doi: 10.2131/jts.11.supplementi_227.

Abstract

VP 16-213 (etoposide, abbr. to VP), an oncostatic drug, was administered orally to pregnant JW-NIBS rabbits from day 6 through 18 of gestation at dose levels of 0.3, 1, 3 and 10 mg/kg/day. The summarized results obtained are as follows: VP 3 and 10 mg/kg elevated the maternal mortality dose-responsively. VP 3 mg/kg and lower doses failed to affect the fetal growth and ossification processes, and did not induce drug-dependent external and visceral anomalies as well as skeletal variations and anomalies. Based on these results, the no-effect dose levels of VP under the present experimental condition were estimated to be 1 mg/kg/day against dams and 3 mg/kg/day against fetuses.

摘要

依托泊苷(VP 16 - 213,简称VP)是一种抗癌药物,在妊娠第6天至18天期间,以0.3、1、3和10毫克/千克/天的剂量水平口服给予怀孕的JW - NIBS兔。获得的总结结果如下:3毫克/千克和10毫克/千克的VP剂量依赖性地提高了母体死亡率。3毫克/千克及更低剂量的VP未能影响胎儿生长和骨化过程,也未诱发药物依赖性的外部和内脏异常以及骨骼变异和异常。基于这些结果,在当前实验条件下,VP对母兔的无作用剂量水平估计为1毫克/千克/天,对胎儿为3毫克/千克/天。

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