Lee Dongoh, Ahn Changhwan, Hong Eui-Ju, An Beum-Soo, Hyun Sang-Hwan, Choi Kyung-Chul, Jeung Eui-Bae
Laboratory of Veterinary Biochemistry and Molecular Biology, College of Veterinary Medicine, Chungbuk National University, Cheongju, Chungbuk 362-763, Korea.
Laboratory of Veterinary Biochemistry, College of Veterinary Medicine, Chungnam National University, Daejeon 305-764, Korea.
Int J Environ Res Public Health. 2016 Jul 12;13(7):697. doi: 10.3390/ijerph13070697.
2,4,6-Tribromophenol (TBP) is a brominated flame retardant (BFR). Based on its affinity for transthyretin, TBP could compete with endogenous thyroid hormone. In this study, the effects of TBP on the thyroid hormone system were assessed in mice. Briefly, animals were exposed to 40 and 250 mg/kg TBP. Thyroid hormones were also administered with or without TBP. When mice were treated with TBP, deiodinase 1 (Dio1) and thyroid hormone receptor β isoform 2 (Thrβ2) decreased in the pituitary gland. The levels of deiodinase 2 (Dio2) and growth hormone (Gh) mRNA increased in response to 250 mg/kg of TBP, and the relative mRNA level of thyroid stimulating hormone β (Tshβ) increased in the pituitary gland. Dio1 and Thrβ1 expression in the liver were not altered, while Dio1 decreased in response to co-treatment with thyroid hormones. The thyroid gland activity decreased in response to TBP, as did the levels of free triiodothyronine and free thyroxine in serum. Taken together, these findings indicate that TBP can disrupt thyroid hormone homeostasis and the presence of TBP influenced thyroid actions as regulators of gene expression. These data suggest that TBP interferes with thyroid hormone systems.
2,4,6-三溴苯酚(TBP)是一种溴化阻燃剂(BFR)。基于其对转甲状腺素蛋白的亲和力,TBP可能会与内源性甲状腺激素竞争。在本研究中,评估了TBP对小鼠甲状腺激素系统的影响。简而言之,将动物暴露于40和250mg/kg的TBP中。同时也在给予或不给予TBP的情况下给予甲状腺激素。当用TBP处理小鼠时,垂体中的脱碘酶1(Dio1)和甲状腺激素受体β亚型2(Thrβ2)减少。脱碘酶2(Dio2)和生长激素(Gh)mRNA的水平在给予250mg/kg TBP后升高,垂体中促甲状腺激素β(Tshβ)的相对mRNA水平升高。肝脏中Dio1和Thrβ1的表达未改变,而在与甲状腺激素联合处理时Dio1减少。甲状腺活性因TBP而降低,血清中游离三碘甲状腺原氨酸和游离甲状腺素的水平也降低。综上所述,这些发现表明TBP可破坏甲状腺激素稳态,并且TBP的存在会影响甲状腺作为基因表达调节因子的作用。这些数据表明TBP会干扰甲状腺激素系统。