Hokkaido Institute of Public Health, Kita-19, Nishi-12, Kita-ku, Sapporo 060-0819, Japan.
Toxicology. 2011 Nov 18;289(2-3):112-21. doi: 10.1016/j.tox.2011.08.001. Epub 2011 Aug 6.
Hydroxylated polychlorinated biphenyls (OH-PCBs), major metabolites of PCBs, have been reported to act as estrogen receptor α (ERα) agonists or antagonists. However, little concern has been paid to the ability of OH-PCBs to interfere with other steroid hormone receptors such as ERβ, androgen receptor (AR) or glucocorticoid receptor (GR). In this study, we characterized the agonistic and antagonistic activities of available 100 OH-PCBs (39 ortho-, 24 meta-, and 37 para-OH compounds), including some congeners identified in humans, against human ERα/β, AR, and GR using in vitro reporter gene assays. In the ERα assay, 45 and 9 of the 100 OH-PCBs tested showed agonistic and antagonistic activities, respectively. In the ERβ assay, 45 and 6 compounds showed agonistic and antagonistic activities, respectively. In the AR and GR assays, although none of the compounds tested showed agonistic activity, 83 and 30 of the 100 OH-PCBs showed antagonistic activity, respectively. These AR and/or GR antagonistic compounds had various patterns of substituent in the structure, while relatively potent ERα/β agonistic and antagonistic compounds possessed para- and ortho-OH structures, respectively. Three OH-PCBs, predominantly identified in human tissues, showed little ERα/β or AR activities, apart from the weak ERα and/or GR antagonistic activity observed in 4-OH-CB107 and 4-OH-CB187. Taken together, these results suggest that a large number of OH-PCBs might act as agonists and/or antagonists against ERα/β, AR and GR.
羟基多氯联苯(OH-PCBs)是多氯联苯的主要代谢物,据报道其具有雌激素受体α(ERα)激动剂或拮抗剂的作用。然而,人们对 OH-PCBs 干扰其他甾体激素受体(如 ERβ、雄激素受体(AR)或糖皮质激素受体(GR))的能力关注甚少。在本研究中,我们使用体外报告基因检测法,对现有的 100 种 OH-PCBs(39 种邻位、24 种间位和 37 种对位 OH 化合物),包括一些在人体内鉴定出的同系物,对人 ERα/β、AR 和 GR 的激动和拮抗活性进行了特征描述。在 ERα 检测中,100 种 OH-PCBs 中有 45 种表现出激动活性,9 种表现出拮抗活性。在 ERβ 检测中,45 种和 6 种化合物分别表现出激动和拮抗活性。在 AR 和 GR 检测中,虽然没有一种测试化合物表现出激动活性,但 100 种 OH-PCBs 中有 83 种和 30 种化合物分别表现出拮抗活性。这些 AR 和/或 GR 拮抗化合物在结构上具有不同的取代模式,而相对有效的 ERα/β 激动和拮抗化合物分别具有对位和邻位 OH 结构。三种 OH-PCBs 主要在人体组织中被鉴定出,除了在 4-OH-CB107 和 4-OH-CB187 中观察到的微弱 ERα 和/或 GR 拮抗活性外,对 ERα/β 或 AR 活性几乎没有作用。综上所述,这些结果表明,大量的 OH-PCBs 可能对 ERα/β、AR 和 GR 表现出激动剂和/或拮抗剂作用。