MTM Research Center, University of Örebro, Örebro, Sweden.
Department of Environmental Toxicology, University of California, Davis, California, USA.
Environ Toxicol Chem. 2018 Feb;37(2):385-397. doi: 10.1002/etc.3958. Epub 2017 Nov 6.
In the present study 42 polycyclic aromatic compounds (PACs) were investigated for their estrogenic potential using the VM7Luc4E2 transactivation assay. Relative potencies were determined for mass-balance analysis. In addition, compounds were tested in combination with the estrogen receptor (ER) antagonist ICI182,780 (ICI) and the aryl hydrocarbon receptor antagonist/CYP1A1 inhibitor α-naphthoflavone. Luciferase induction and CYP1A1-dependent ethoxyresorufin-O-deethylase (EROD) activity were measured to assess whether the estrogenic activity was elicited by the compound itself and/or by its metabolites. Relative potencies ranged between 10 and 10 . The ability of ICI to decrease luciferase activity stimulated by all compounds indicated that the induction responses were ER-dependent. The aryl hydrocarbon receptor antagonist/CYP1A1 inhibitor α-naphthoflavone decreased luciferase induction and EROD activity by several compounds, including the methylated chrysenes, suggesting that metabolites of these chemicals contributed to ER activation. Several PACs, such as acridine and its derivatives, appear to directly activate the ER. Furthermore, extracts of soils from industrial areas were examined using this bioassay, and estrogenic activity was detected in all soil samples. Mass-balance analysis using a combination of relative potencies and chemical analysis of the samples suggested that polycyclic aromatic hydrocarbons (PAHs) and alkylated PAHs, such as 1- and 3-methylchrysene, are important contributors to the overall estrogenic activity. However, these results revealed that a considerable proportion of the estrogenic activity in the soil remained unexplained, indicating the presence of other significant estrogenic compounds. Environ Toxicol Chem 2018;37:385-397. © 2017 SETAC.
在本研究中,使用 VM7Luc4E2 转录激活测定法研究了 42 种多环芳烃(PACs)的雌激素潜力。为了进行质量平衡分析,确定了相对效力。此外,还测试了化合物与雌激素受体(ER)拮抗剂 ICI182,780(ICI)和芳烃受体拮抗剂/CYP1A1 抑制剂α-萘黄酮的组合。测量荧光素酶诱导和 CYP1A1 依赖性乙氧基荧光素-O-去乙基酶(EROD)活性,以评估雌激素活性是由化合物本身及其代谢物引起的。相对效力范围在 10 和 10 之间。ICI 降低所有化合物刺激的荧光素酶活性的能力表明诱导反应依赖于 ER。芳烃受体拮抗剂/CYP1A1 抑制剂α-萘黄酮降低了几种化合物的荧光素酶诱导和 EROD 活性,包括甲基化的 chrysenes,表明这些化学物质的代谢物有助于 ER 激活。几种多环芳烃,如吖啶及其衍生物,似乎可以直接激活 ER。此外,还使用这种生物测定法检查了来自工业区的土壤提取物,并在所有土壤样本中检测到雌激素活性。使用相对效力的组合和对样品的化学分析进行的质量平衡分析表明,多环芳烃(PAHs)和烷基化 PAHs,如 1-和 3-甲基 chrysene,是总雌激素活性的重要贡献者。然而,这些结果表明,土壤中相当一部分雌激素活性仍未得到解释,表明存在其他重要的雌激素化合物。环境毒理化学 2018;37:385-397。©2017 SETAC。