Effect of triclosan, triclocarban, 2,2′,4′,-tetrabromodiphenyl ether, and bisphenol A on the iodide uptake, thyroid peroxidase activity, and expression of genes involved in thyroid hormone synthesis

被引:97
作者
Wu, Yuanfeng [1 ]
Beland, Frederick A. [1 ]
Fang, Jia-Long [1 ]
机构
[1] US FDA, Div Biochem Toxicol, Natl Ctr Toxicol Res, Jefferson, AR 72079 USA
关键词
Thyroid disruptors; Iodide uptake; Thyroid hormone synthesis; Thyroid peroxidase; POLYBROMINATED DIPHENYL ETHERS; IN-VIVO EXPOSURE; SODIUM/IODIDE SYMPORTER; FLAME RETARDANTS; VITAMIN-A; RAT; DISRUPTION; THYROXINE; INHIBITION; VITRO;
D O I
10.1016/j.tiv.2016.01.014
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Triclosan, triclocarban, 2,2',4,4'-tetrabromodiphenyl ether (BDE-47), and bisphenol A (BPA) have been reported to disturb thyroid hormone (TH) homeostasis. We have examined the effects of these chemicals on sodium/iodide symporter (NIS)-mediated iodide uptake and the expression of genes involved in TH synthesis in rat thyroid follicular FRTL-5 cells, and on the activity of thyroid peroxidase (TPO) using rat thyroid microsomes. All four chemicals inhibited NIS-mediated iodide uptake in a concentration-dependent manner. A decrease in the iodide uptake was also observed in the absence of sodium iodide. Kinetic studies showed that all four chemicals were non-competitive inhibitors of NIS, with the order of K-i values being triclosan < triclocarban < BDE-47 < BPA. The transcriptional expression of three genes involved in TH synthesis, Slc5a5, Tpo, and Tgo, and three thyroid transcription factor genes, Pax8, Foxe1, and Nkx2-1, was examined using quantitative real-time PCR. No significant changes in the expression of any genes were observed with triclosan or triclocarban. BDE-47 decreased the level of Tpo, while BPA altered the expression of all six genes. Triclosan and triclocarban inhibited the activity of TPO at 166 and >300 mu M, respectively. Neither BDE-47 nor BPA affected TPO activity. In conclusion, triclosan, triclocarban, BDE-47, and BPA inhibited iodide uptake, but had differential effects on the expression of TH synthesis-related genes and the activity of TPO. Published by Elsevier Ltd.
引用
收藏
页码:310 / 319
页数:10
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