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Determination of in vitro relative potency (REP) values for mono-ortho polychlorinated biphenyls after purification with active charcoal

机译:活性炭纯化后测定单邻多氯联苯的体外相对效能(REP)值

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摘要

The TEF system for dioxin-like compounds has included assignment of TEF values for mono-ortho polychlorinated biphenyls (MO-PCBs). Small traces of aryl hydrocarbon receptor (AhR)-active impurities could result in artifactually higher relative potency (REP) values. MO-PCBs -105, -118, -156, and -167 were purified on an active charcoal column to remove AhR agonists that could be present as impurities. Activation or inhibition of AhR-dependent gene expression by purified MO-PCBs was studied in stably transfected cell lines (H1G1.1c3 mouse, H4G1.1c2 rat hepatoma), containing an AhR-responsive (AhR-EGFP) reporter gene. In addition, EROD activity was used as marker for CYP1A1 activity in these cell lines. MO-PCBs -105, -118, -156 induced AhR-EGFP expression in both rodent cell lines, with PCB-156 (10 μM) being most effectively; inducing gene expression to ~27% of TCDD (mouse cells) and 62.5 ± 3.4% (rat cells) of TCDD. This concurred with increased EROD activity in both cell lines to maxima of 20.5 ± 1.5% and 68 ± 3.2% of TCDD, respectively. No induction was observed for PCB-167. In the H1G1.1c3 mouse cells, PCB-105, -118 and -156 (10 μM) significantly reduced TCDD-induced AhR-EGFP expression to 50.9 ± 2.9%, 58.3 ± 2.2% and 70.8 ± 1.3% of TCDD. Reduced EROD activity was also observed, of 39.3 ± 2.8%, 67 ± 5% and 48.3 ± 4% compared to TCDD. PCB-167 did not result in significant reduction. In rat cells, only PCB-156 resulted in significant decrease in TCDD-induced AhR-EGFP expression of 35%, suggesting species differences play a role. Our results suggest that purification of MO-PCBs is an essential step in determining accurate REP values, and could very likely lead to lower TEF values than those presently assigned by the WHO.
机译:二恶英样化合物的TEF系统已包括单邻多氯联苯(MO-PCB)的TEF值分配。微量的芳烃受体(AhR)活性杂质可能会导致人为地提高相对效能(REP)值。 MO-PCBs -105,-118,-156和-167在活性炭柱上进行纯化,以去除可能作为杂质存在的AhR激动剂。在含有AhR反应性(AhR-EGFP)报告基因的稳定转染的细胞系(H1G1.1c3小鼠,H4G1.1c2大鼠肝癌)中研究了纯化MO-PCB对AhR依赖性基因表达的激活或抑制。另外,EROD活性被用作这些细胞系中CYP1A1活性的标记。 MO-PCBs -105,-118,-156诱导了两种啮齿动物细胞系中的AhR-EGFP表达,其中PCB-156(10μM)最有效;诱导基因表达达到TCDD的〜27%(小鼠细胞)和62.5±3.4%(大鼠细胞)。这与两种细胞系中的EROD活性增加分别达到TCDD的最大值分别为20.5±1.5%和68±3.2%有关。对于PCB-167,未观察到感应。在H1G1.1c3小鼠细胞中,PCB-105,-118和-156(10μM)将TCDD诱导的AhR-EGFP表达显着降低至TCDD的50.9±2.9%,58.3±2.2%和70.8±1.3%。与TCDD相比,还发现EROD活性降低,分别为39.3±2.8%,67±5%和48.3±4%。 PCB-167并未显着减少。在大鼠细胞中,只有PCB-156导致TCDD诱导的AhR-EGFP表达显着下降35%,这表明物种差异发挥了作用。我们的结果表明,MO-PCBs的纯化是确定准确REP值的重要步骤,并且很可能导致TEF值低于WHO目前指定的值。

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