Billings P C, Heidelberger C, Landolph J R
Toxicol Appl Pharmacol. 1985 Jan;77(1):58-65. doi: 10.1016/0041-008x(85)90267-4.
The use of a rat liver S-9 metabolic activation system to enhance aflatoxin B1-mediated transformation of C3H/10T1/2 cells was studied. Under conditions of metabolic activation, the cytotoxicity of Aflatoxin B1 (AFB) was increased approximately 10-fold over that observed in the absence of activation. Similarly, activation increased the transformation of these cells treated with 1 microgram/ml AFB1 greater than 10-fold when cells were treated in the absence of activation with 1 microgram/ml AFB1 for 3 hr, and four-to-fivefold over the transformation observed when cells were treated for 48 hr with 1 microgram/ml AFB1. This same activation procedure also induced the transformation of these cells treated with 10 and 20 micrograms/ml cyclophosphamide in the absence of activation. The use of S-9 metabolic activation greatly increased the sensitivity of AFB1-mediated transformation of C3H/10T1/2 cells, and should expand the range of chemical carcinogens, requiring metabolic activation, in particular mycotoxins related to AFB1, that can be effectively detected and studied in the C3H/10T1/2 cell transformation assay.
研究了使用大鼠肝脏S-9代谢活化系统来增强黄曲霉毒素B1介导的C3H/10T1/2细胞转化。在代谢活化条件下,黄曲霉毒素B1(AFB)的细胞毒性比未活化时观察到的增加了约10倍。同样,当细胞在无活化条件下用1微克/毫升AFB1处理3小时时,活化使这些用1微克/毫升AFB1处理的细胞的转化率提高了10倍以上,而在用1微克/毫升AFB1处理48小时时,转化率比观察到的提高了四到五倍。相同的活化程序也诱导了这些在无活化条件下用10和20微克/毫升环磷酰胺处理的细胞的转化。S-9代谢活化的使用大大提高了C3H/10T1/2细胞对AFB1介导转化的敏感性,并且应该扩大需要代谢活化的化学致癌物的范围,特别是与AFB1相关的霉菌毒素,这些物质可以在C3H/10T1/2细胞转化试验中得到有效检测和研究。