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双酚A作为一种拮抗剂会干扰甲状腺激素的作用。

Thyroid hormone action is disrupted by bisphenol A as an antagonist.

作者信息

Moriyama Kenji, Tagami Tetsuya, Akamizu Takashi, Usui Takeshi, Saijo Misa, Kanamoto Naotetsu, Hataya Yuji, Shimatsu Akira, Kuzuya Hideshi, Nakao Kazuwa

机构信息

Department of Medicine and Clinical Science, Graduate School of Medicine, Kyoto University, Kyoto 606-8507, Japan.

出版信息

J Clin Endocrinol Metab. 2002 Nov;87(11):5185-90. doi: 10.1210/jc.2002-020209.

Abstract

Bisphenol A (BPA), a monomer of polycarbonate plastics, has been shown to possess estrogenic properties and act as an agonist for the estrogen receptors. Although an epidemiologically based investigation has suggested that some chemicals could disrupt thyroid function in animals, the effects on thyroid hormone receptors (TRs) are unknown. We show here that BPA inhibits TR-mediated transcription by acting as an antagonist. In the transient gene expression experiments, BPA suppressed transcriptional activity that is stimulated by thyroid hormone (T(3)) in a dose-dependent manner. The inhibitory effects were observed in the presence of physiological concentrations of T(3). In contrast, in the case of negatively regulated TSHalpha promoter, BPA activated the gene transcription that is suppressed by T(3). To elucidate possible mechanisms of the antagonistic action of BPA, the effects on T(3) binding and cofactor interaction with TR were examined. The K(i) value for BPA was 200 micro M when assessed by inhibition of [(125)I]T(3) binding to rat hepatic nuclear TRs. In a mammalian two-hybrid assay, BPA recruited the nuclear corepressor to the TR. These results suggest that BPA could displace T(3) from the TR and recruit a transcriptional repressor, resulting in gene suppression. This is the first report that BPA can antagonize T(3) action at the transcriptional level. BPA may disrupt the function of various types of nuclear hormone receptors and their cofactors to disturb our internal hormonal environment.

摘要

双酚A(BPA)是聚碳酸酯塑料的单体,已被证明具有雌激素特性,并可作为雌激素受体的激动剂。尽管一项基于流行病学的调查表明某些化学物质可能会干扰动物的甲状腺功能,但对甲状腺激素受体(TRs)的影响尚不清楚。我们在此表明,BPA通过作为拮抗剂来抑制TR介导的转录。在瞬时基因表达实验中,BPA以剂量依赖性方式抑制甲状腺激素(T3)刺激的转录活性。在生理浓度的T3存在下观察到了这种抑制作用。相反,在负调控的促甲状腺激素α(TSHα)启动子的情况下,BPA激活了被T3抑制的基因转录。为了阐明BPA拮抗作用的可能机制,研究了其对T3与TR结合以及辅助因子相互作用的影响。通过抑制[125I]T3与大鼠肝细胞核TRs的结合来评估时,BPA的抑制常数(Ki)值为200μM。在哺乳动物双杂交试验中,BPA将核共抑制因子募集到TR上。这些结果表明,BPA可以从TR上取代T3并募集转录抑制因子,从而导致基因抑制。这是关于BPA可在转录水平拮抗T3作用的首次报道。BPA可能会破坏各种类型的核激素受体及其辅助因子的功能,从而扰乱我们体内的激素环境。

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