Smolarek T A, Moynihan C G, Salmon C P, Baird W M
Cancer Lett. 1986 Mar;30(3):243-9. doi: 10.1016/0304-3835(86)90048-0.
Co-administration of benz[a]anthracene (BA) with benzo[a]pyrene (B[a]P) to hamster embryo cell cultures for 24 h resulted in a decrease in the metabolism of benzo[a]pyrene by 40%, a decrease in the level of binding of B[a]P to DNA by 70% and a 10-fold reduction in mutation induction in a hamster embryo cell-mediated V79 cell mutation assay. This data indicates that the biological effects of co-administration of BA with B[a]P result from inhibition of the metabolic activation of B[a]P rather than induction of enzymes that detoxify the B[a]P.
将苯并[a]蒽(BA)与苯并[a]芘(B[a]P)共同作用于仓鼠胚胎细胞培养物24小时,结果显示苯并[a]芘的代谢减少了40%,B[a]P与DNA的结合水平降低了70%,并且在仓鼠胚胎细胞介导的V79细胞突变试验中,突变诱导减少了10倍。该数据表明,BA与B[a]P共同给药的生物学效应是由于抑制了B[a]P的代谢活化,而非诱导了使B[a]P解毒的酶。