Roelandt L, Todaro A, Thomé J P, Kremers P
Université de Liege, Laboratoire de Chimie Médicale, Sart Tilman, Belgium.
Toxicology. 1995 Apr 12;98(1-3):95-103. doi: 10.1016/0300-483x(94)02972-w.
Polychlorinated biphenyls (PCBs) are widespread residual micropollutants which accumulate in living organisms, probably as a consequence of their high lipophilicity. Cultured foetal rat hepatocytes used as target cells constitute an interesting in vitro model for studying the mechanisms of action of PCBs. In this paper, and the accompanying one (Toxicology 98 (1995) 83-94), we have used this model to investigate the effects of PCBs on several cellular parameters. The inducibility of CYPIA1 is the most sensitive parameter studied, as shown by the induction of ethoxycoumarin-O-deethylase and ethoxyresorufin-O-deethylase activities at PCB concentrations as low as 1 microM. Dexamethasone treatment of the cells potentiates this induction. PCB induction is reversible and occurs even in cells cultured for several days. CYP2B and CYP3A seem unaffected by PCBs in this experimental system. By inducing CYP1A1, PCBs can trigger the 'activation' of xenobiotics, such as polycyclic hydrocarbons, into mutagenic compounds.
多氯联苯(PCBs)是广泛存在的残留微污染物,可能由于其高亲脂性而在生物体内蓄积。用作靶细胞的培养胎鼠肝细胞构成了一个研究多氯联苯作用机制的有趣体外模型。在本文以及随附的论文(《毒理学》98(1995)83 - 94)中,我们使用该模型研究了多氯联苯对几个细胞参数的影响。CYPIA1的诱导性是所研究的最敏感参数,在低至1 microM的多氯联苯浓度下,乙氧基香豆素 - O - 脱乙基酶和乙氧基试卤灵 - O - 脱乙基酶活性的诱导就表明了这一点。用 dexamethasone 处理细胞可增强这种诱导作用。多氯联苯诱导是可逆的,甚至在培养数天的细胞中也会发生。在该实验系统中,CYP2B 和 CYP3A 似乎不受多氯联苯影响。通过诱导 CYP1A1,多氯联苯可引发多环芳烃等外源性物质“激活”为致突变化合物。