Thust R, Kneist S
Mutat Res. 1979 Aug;67(4):321-30. doi: 10.1016/0165-1218(79)90028-4.
The mycotoxin citrinin is a potent inducer of chromosomal aberrations in the clastogenicity assay on V79-E cells when metabolized by rat and human liver microsomes. Rat and human liver microsomes, standardized on protein content, activate citrinin at equal levels. 5 X 10(-4) M citrinin induces complex translocations in a high frequency as well as defects of chromosomal coiling. Higher concentrations are cytotoxic, lower ones are almost inactive. After metabolization of mycotoxin by rat-kidney microsomes or an S9 mix fraction containing rat liver and kidney microsomes, toxic effects predominate and chromosomal aberrations are diminished. Clastogenic citrinin concentrations do not induce an increase of SCE frequency. Although the mode of action of this mycotoxin on chromosomal structure remains obscure, possible explanations are discussed.
在对V79-E细胞进行的致突变性试验中,当被大鼠和人肝微粒体代谢时,霉菌毒素桔霉素是染色体畸变的强效诱导剂。以蛋白质含量标准化的大鼠和人肝微粒体以相同水平激活桔霉素。5×10(-4)M的桔霉素可高频诱导复杂易位以及染色体螺旋缺陷。较高浓度具有细胞毒性,较低浓度几乎无活性。在大鼠肾脏微粒体或含有大鼠肝脏和肾脏微粒体的S9混合组分代谢霉菌毒素后,毒性作用占主导,染色体畸变减少。具有致突变性的桔霉素浓度不会诱导姐妹染色单体交换频率增加。尽管这种霉菌毒素对染色体结构的作用方式仍不清楚,但讨论了可能的解释。