Dent J G, Netter K J, Gibson J E
Res Commun Chem Pathol Pharmacol. 1976 Jan;13(1):75-82.
Parameters relating to hepatic microsomal drug metabolism were measured in vitro following 2 weeks exposure of rats to polybrominated biphenyls (PBB) as a dietary supplement at 4.69, 18.75, 75 and 300 ppm. The mixture of PBB was a potent inducer of hepatic microsomal drug metabolism. The pattern of induction seen after PBB exposure was compared with that produced by phenobarbital and 3-methyl-cholanthrene and the pattern of induction observed shared similarities with both of these agents.
将大鼠作为饮食补充剂暴露于4.69、18.75、75和300 ppm的多溴联苯(PBB)两周后,在体外测量了与肝脏微粒体药物代谢相关的参数。PBB混合物是肝脏微粒体药物代谢的强效诱导剂。将PBB暴露后观察到的诱导模式与苯巴比妥和3-甲基胆蒽产生的诱导模式进行了比较,观察到的诱导模式与这两种药物都有相似之处。