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双酚A及其结构类似物对雌激素受体转录激活的混合效应

Mixture Effects of Bisphenol A and Its Structural Analogs on Estrogen Receptor Transcriptional Activation.

作者信息

Lee Handule, Park Juyoung, Park Kwangsik

机构信息

College of Pharmacy, Dongduk Women's University, Seoul 02748, Republic of Korea.

出版信息

Toxics. 2023 Dec 4;11(12):986. doi: 10.3390/toxics11120986.

DOI:10.3390/toxics11120986
PMID:38133387
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10747781/
Abstract

Bisphenol A (BPA) exposure has been widely linked to endocrine-disrupting effects. Recently, many substitutes for BPA have been developed as safe structural analogs. However, they have still been reported to have similar adverse effects. The current study evaluated the effects of bisphenol A and eight structural analogs on the transcription of estrogen receptor alpha (ERα). The effects of binary and ternary mixtures prepared from different combinations of BPA analogs were also evaluated for transcription activity. The measured data of the mixtures were compared to the predicted data obtained by the full logistic model, and the model deviation ratio (MDR) was calculated to determine whether the effects were synergistic, antagonistic, or additive. Overall, the results suggest that the effect of bisphenol compound are additive in binary and ternary mixtures.

摘要

双酚A(BPA)暴露已被广泛认为与内分泌干扰效应有关。最近,许多双酚A的替代品已被开发为安全的结构类似物。然而,仍有报道称它们具有类似的不良影响。本研究评估了双酚A及其八种结构类似物对雌激素受体α(ERα)转录的影响。还评估了由双酚A类似物的不同组合制备的二元和三元混合物对转录活性的影响。将混合物的实测数据与通过完全逻辑模型获得的预测数据进行比较,并计算模型偏差率(MDR)以确定这些效应是协同的、拮抗的还是相加的。总体而言,结果表明双酚化合物在二元和三元混合物中的效应是相加的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c36/10747781/7e4faebdf83d/toxics-11-00986-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c36/10747781/f7c9262185f0/toxics-11-00986-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c36/10747781/31be1cb00237/toxics-11-00986-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c36/10747781/520b985bdcdb/toxics-11-00986-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c36/10747781/dc6119169422/toxics-11-00986-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c36/10747781/e0d30703f84f/toxics-11-00986-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c36/10747781/7e4faebdf83d/toxics-11-00986-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c36/10747781/f7c9262185f0/toxics-11-00986-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c36/10747781/31be1cb00237/toxics-11-00986-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c36/10747781/520b985bdcdb/toxics-11-00986-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c36/10747781/dc6119169422/toxics-11-00986-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c36/10747781/e0d30703f84f/toxics-11-00986-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c36/10747781/7e4faebdf83d/toxics-11-00986-g006.jpg

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Prenatal exposure to bisphenol A and neonatal health outcomes: A systematic review.产前暴露于双酚 A 与新生儿健康结局:系统评价。
Environ Pollut. 2023 Oct 15;335:122295. doi: 10.1016/j.envpol.2023.122295. Epub 2023 Jul 31.
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Current Evidence on Bisphenol A Exposure and the Molecular Mechanism Involved in Related Pathological Conditions.
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双酚A暴露的当前证据及相关病理状况涉及的分子机制
Pharmaceutics. 2023 Mar 10;15(3):908. doi: 10.3390/pharmaceutics15030908.
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Bisphenol A and bisphenol S both disrupt ovine granulosa cell steroidogenesis but through different molecular pathways.双酚 A 和双酚 S 均可干扰绵羊颗粒细胞的类固醇生成,但作用的分子途径不同。
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Comparison of toxicokinetic properties of eleven analogues of Bisphenol A in pig after intravenous and oral administrations.双酚A的十一种类似物在猪体内静脉注射和口服给药后的毒代动力学特性比较。
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