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

Toxicol In Vitro. 2016 Apr:32:310-9. doi: 10.1016/j.tiv.2016.01.014. Epub 2016 Jan 29.

Abstract

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 Ki 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 μM, 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.

Keywords: Iodide uptake; Thyroid disruptors; Thyroid hormone synthesis; Thyroid peroxidase.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Benzhydryl Compounds / toxicity*
  • Carbanilides / toxicity*
  • Cell Line
  • Cell Survival / drug effects
  • Endocrine Disruptors / toxicity*
  • Forkhead Transcription Factors / genetics
  • Gene Expression Regulation / drug effects
  • Halogenated Diphenyl Ethers / toxicity*
  • Iodide Peroxidase / genetics
  • Iodide Peroxidase / metabolism
  • Iodides / metabolism
  • Male
  • Microsomes / drug effects
  • Microsomes / metabolism
  • Nuclear Proteins / genetics
  • PAX8 Transcription Factor / genetics
  • Phenols / toxicity*
  • Rats, Wistar
  • Symporters / genetics
  • Thyroglobulin / genetics
  • Thyroid Epithelial Cells / drug effects*
  • Thyroid Epithelial Cells / metabolism
  • Thyroid Hormones / metabolism
  • Thyroid Nuclear Factor 1
  • Transcription Factors / genetics
  • Triclosan / toxicity*

Substances

  • Benzhydryl Compounds
  • Carbanilides
  • Endocrine Disruptors
  • Forkhead Transcription Factors
  • FoxE1 protein, rat
  • Halogenated Diphenyl Ethers
  • Iodides
  • Nkx2-1 protein, rat
  • Nuclear Proteins
  • PAX8 Transcription Factor
  • Pax8 protein, rat
  • Phenols
  • Symporters
  • Thyroid Hormones
  • Thyroid Nuclear Factor 1
  • Transcription Factors
  • 2,2',4,4'-tetrabromodiphenyl ether
  • Triclosan
  • sodium-iodide symporter
  • Thyroglobulin
  • triclocarban
  • Iodide Peroxidase
  • bisphenol A