Nakamura M, Fort F L, Kikuchi Y
Drug Safety Research Laboratory, Takeda Chemical Industries Ltd., Osaka, Japan.
Mutat Res. 1993 Feb;291(1):29-34.
The cytogenetic effects of 5-fluorouracil (5-FU), 1-hexyl-carbamoyl-5- fluorouracil (HCFU) and 1-(2-tetrahydrofuryl)-5-fluorouracil (TF) were examined with the fetal liver micronucleus assay in mice. The frequencies of micronucleated polychromatic erythrocytes (MNPCEs) in fetal liver peaked at 27, 24 and 27 h, respectively, after single intraperitoneal injections into pregnant mice on day 13 of gestation. The highest frequency of MNPCEs by 5-FU treatment in fetal liver was 13.6%, whereas the frequency in maternal bone marrow was only 0.4%. The micronucleus frequency and the number of micronuclei per individual polychromatic erythrocyte were clearly dose-dependent. These results suggest that the micronucleus test in fetal liver has particular advantages compared to maternal bone marrow for evaluating the cytogenetic effects of 5-FU and related compounds after a single treatment. The cytogenetic effect was ranked 5-FU = HCFU > TF, in both a time-course study and a dose-response study of micronucleus distribution.
采用小鼠胎肝微核试验检测了5-氟尿嘧啶(5-FU)、1-己基-氨基甲酰基-5-氟尿嘧啶(HCFU)和1-(2-四氢呋喃基)-5-氟尿嘧啶(TF)的细胞遗传学效应。在妊娠第13天对怀孕小鼠进行单次腹腔注射后,胎肝中微核多染红细胞(MNPCEs)的频率分别在27、24和27小时达到峰值。5-FU处理组胎肝中MNPCEs的最高频率为13.6%,而母体骨髓中的频率仅为0.4%。微核频率和单个多染红细胞中的微核数量明显呈剂量依赖性。这些结果表明,与母体骨髓相比,胎肝微核试验在单次处理后评估5-FU及相关化合物的细胞遗传学效应方面具有特殊优势。在微核分布的时间进程研究和剂量反应研究中,细胞遗传学效应的排序均为5-FU = HCFU > TF。