摘要
用妊娠第14天大鼠胚胎中脑神经细胞作微团培养,培养物接触维生素A(VitA)和3-甲基胆蒽(3-MCA)后,微团中的集落形成率明显降低,半数分化抑制浓度分别为10ng/ml和1.0ng/ml,有明显的致畸性。在培养12小时内,还原型谷胱甘肽(GSH)和谷胱甘肽S-转移酶(GST)水平明显降低,24小时后逐步快复正常,而GST活性继续升高,于48小时达最大值。这两种化学物的体外致畸作用可能与GSH耗竭有一定关系。
The teratogenicity of vit A and 3-MCA was studied in a micromass culture system in vitro. The teratogenicity was expressed as decrement of counts of differentiated foci. The differentiating rat embryo midbrain cells exposing to nontoxic doses of vit A or 3-MCA showed inhibition on subsequent differentiation. It was observed that glutathione was depleted and glutathione S-transferase was inhibited by vit A or 3-MCA in the cultures at 12h, and then both were reversed and increased after 24h. The concentration-response relationship of the varieties was apparent. The results in present study indicated the possibility that the varieties of glutathione system would affect the subsequent differentiation of midbrain cells.
出处
《卫生毒理学杂志》
CSCD
1991年第3期164-166,共3页
Journal of Health Toxicology
基金
国家自然科学基金
关键词
维生素A
甲基胆蒽
致畸性
Teratogenicity in vitro
Micromass Culture, GSH
GST