A comparison of the thyroid disruption induced by decabrominated diphenyl ethers (BDE-209) and decabromodiphenyl ethane (DBDPE) in rats

• Published in: Ecotoxicology and environmental safety Vol. 174; pp. 224 - 235
• Main Authors: Wang, Yuwei, Chen, Tian, Sun, Yanmin, Zhao, Xuezhen, Zheng, Dan, Jing, Li, Zhou, Xianqing, Sun, Zhiwei, Shi, Zhixiong
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier Inc 15.06.2019
• Subjects: Brominated flame retardants; Decabrominated diphenyl ether; Decabromodiphenyl ethane; Hypothalamic-pituitary-thyroid axis; Rat; Thyroid function; Decabrominated diphenyl ether; Decabromodiphenyl ethane; Rat; Thyroid function; Hypothalamic-pituitary-thyroid axis; Brominated flame retardants
• ISSN: 0147-6513; 1090-2414; 1090-2414
• DOI: 10.1016/j.ecoenv.2019.02.080

In recent years, decabromodiphenyl ethane (DBDPE), a new alternative flame retardant to the decabrominated diphenyl ethers (BDE-209), is widely used in a variety of products. Previous studies have indicated that DBDPE, like BDE-209, could disrupt thyroid function. However, compared with BDE-209, the degrees of thyrotoxicosis induced by DBDPE were not clear. In addition, the mechanism of thyrotoxicosis induced by DBDPE or BDE-209 was still under further investigation. In this study, male rats as a model were orally exposed to DBDPE or BDE-209 by 5, 50, 500 mg/kg bw/day for 28 days. Then, we assessed the thyrotoxicosis of DBDPE versus BDE-209 and explored the mechanisms of DBDPE and BDE-209-induced thyrotoxicosis. Results showed that decreased free triiodothyronine (FT3) and increased thyroid-stimulating hormone (TSH) and thyrotropin-releasing hormone (TRH) in serum were observed in both 500 mg/kg bw/day BDE-209 and DBDPE group. Decreased total thyroxine (TT4), total T3 (TT3), and free T4 (FT4) were only observed in BDE-209 group but not in DBDPE group. Histological examination and transmission electron microscope examination showed that high level exposure to BDE-209 and DBDPE both caused significant changes in histological structure and ultrastructure of the thyroid gland. Additionally, oxidative damages of thyroid gland (decreased SOD and GSH activities, and increased MDA content) were also observed in both BDE-209 and DBDPE groups. TG contents in the thyroid gland was reduced in BDE-209 group but not in DBDPE group. Both BDE-209 and DBDPE affected the expression of hypothalamic-pituitary-thyroid (HPT) axis related genes. These findings suggested that both BDE-209 and DBDPE exposure could disrupt thyroid function in the direction of hypothyroidism and the underlying mechanism was likely to be oxidative stress and perturbations of HPT axis. However, DBDPE was found to be less toxic than BDE-209. •Thyroid disruption induced by BDE-209 and DBDPE in rats was studied and compared.•Both BDE-209 and DBDPE can disrupt thyroid function in the direction of hypothyroidism.•Both BDE-209 and DBDPE induced oxidative stress but DBDPE is less toxic than BDE-209.