Naya M, Noguchi M, Mataki Y, Deguchi T, Yasuda M
Kyowa Toxicological Research Laboratories, Yamaguchi, Japan.
Hiroshima J Med Sci. 1990 Sep;39(3):79-82.
Embryotoxicity and teratogenicity of 5-fluorouracil (5-FU) and modulation of its effect by L-2-oxothiazolidine-4-carboxylate (OTC), a cysteine pro-drug, were evaluated in mice. Pregnant ICR mice were intraperitoneally (i.p.) injected with 25 mg/kg of 5-FU on day 11 of gestation (vaginal plug = day 0). Mice were pretreated i.p. with 950 mg/kg of OTC 4 hours before dosing with 5-FU. Dams were killed on day 17 of gestation. Fetuses were examined for external malformations, especially limb malformations. Pretreatment with OTC decreased the frequency and severity of oligodactyly induced by 5-FU, although the differences were not significant statistically. There was little difference in either liver glutathione levels, or body weight gain during gestation of dams between the 5-FU group and the 5-FU plus OTC group. Fetal mortality and fetal weight of the group treated with 5-FU alone were comparable with those of the group pretreated with OTC. In the present study, teratogenicity of 5-FU seemed to be slightly mitigated with OTC pretreatment.
在小鼠中评估了5-氟尿嘧啶(5-FU)的胚胎毒性和致畸性,以及半胱氨酸前药L-2-氧代噻唑烷-4-羧酸(OTC)对其作用的调节。妊娠第11天(阴道栓出现日=第0天),对怀孕的ICR小鼠腹腔注射25mg/kg的5-FU。在给予5-FU前4小时,对小鼠进行腹腔注射950mg/kg的OTC预处理。在妊娠第17天处死母鼠。检查胎儿的外部畸形,尤其是肢体畸形。OTC预处理降低了5-FU诱导的少指畸形的频率和严重程度,尽管差异无统计学意义。5-FU组和5-FU加OTC组母鼠在妊娠期间的肝脏谷胱甘肽水平或体重增加几乎没有差异。单独使用5-FU治疗组的胎儿死亡率和胎儿体重与OTC预处理组相当。在本研究中,5-FU的致畸性似乎因OTC预处理而略有减轻。