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Evaluation of tetrabromobisphenol A effects on human glucocorticoid and androgen receptors: a comparison of results from human- with yeast-based in vitro assays

机译:评价四溴双酚A对人糖皮质激素和雄激素受体的作用:基于人和酵母的体外测定结果的比较

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摘要

The incidence of immune-related diseases increased over the last years in industrialized countries, suggesting a contribution of environmental factors. Impaired glucocorticoid action has been associated with immune disorders. Thus, there is an increasing interest to identify chemicals disrupting glucocorticoid action. The widely used flame retardant tetrabromobisphenol A (TBBPA) was reported earlier to potently inhibit glucocorticoid receptor (GR) and moderately androgen receptor (AR) activity in yeast-based reporter gene assays. To further characterize possible GR disrupting effects of TBBPA, transactivation experiments using a human HEK-293 cell-based reporter gene assay and cell-free receptor binding experiments were performed in the present study. Both, transactivation and GR binding experiments failed to detect any activity of TBBPA on GR function. Molecular docking calculations supported this observation. Additionally, the current study could confirm the antiandrogenic activity of TBBPA seen in the yeast assay, although the effect was an order of magnitude less pronounced in the HEK-293 cell-based system. In conclusion, TBBPA does not directly affect GR function and, considering its rapid metabolism and low concentrations found in humans, it is unlikely to cause adverse effects by acting through AR. This study emphasizes the use of cell-free assays in combination with cell-based assays for the in vitro evaluation of endocrine disrupting chemicals.
机译:在工业化国家中,免疫相关疾病的发病率在过去几年中有所增加,这表明环境因素的影响。糖皮质激素作用受损与免疫疾病有关。因此,越来越需要鉴定破坏糖皮质激素作用的化学物质。据报道,在基于酵母的报告基因检测中,广泛使用的阻燃剂四溴双酚A(TBBPA)能有效抑制糖皮质激素受体(GR)和中度雄激素受体(AR)活性。为了进一步表征TBBPA的可能的GR破坏作用,在本研究中进行了使用基于人类HEK-293细胞的报告基因基因测定的反式激活实验和无细胞受体结合实验。反式激活和GR结合实验均未能检测到TBBPA对GR功能的任何活性。分子对接计算支持该观察。另外,尽管在基于HEK-293细胞的系统中该作用不明显,但目前的研究可以证实在酵母分析中发现的TBBPA具有抗雄激素活性。总之,TBBPA不会直接影响GR功能,并且考虑到其在人体中的快速代谢和低浓度,不太可能通过AR作用而引起不良反应。这项研究强调将无细胞测定法与基于细胞的测定法结合用于体外评估内分泌干扰物。

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