Omagari Ryo, Yagishita Mayuko, Shiraishi Fujio, Kamata Ryo, Terasaki Masanori, Kubo Takuya, Nakajima Daisuke
Health and Environmental Risk Division, National Institute for Environmental Studies, Japan.
Department of Life and Environmental Science, Prefectural University of Hiroshima, Japan.
Data Brief. 2022 May 21;42:108303. doi: 10.1016/j.dib.2022.108303. eCollection 2022 Jun.
The human thyroid receptor (hTR)-antagonist activities of 691 compounds were evaluated using a yeast two-hybrid assay with Y190 introduced hTRα and coactivator. In parallel, those YTOX tests were conducted to evaluate whether those compounds affected either antagonism or toxicity. This is the first report that focuses on the hTR-antagonist activity of many chemical compounds suspected to be endocrine disruptor. In this study, 46 compounds exhibited antagonist activity at 50% of the maximum activity (IC × 50) within 11-9940 nM. In particular, 10,10-Oxybisphenoxarsine, triphenyltin fluoride, triphenyltin hydroxide, and chlorothalonil had strong hTR-antagonist activities. This knowledge gained from the present study will boost chemical regulation strategies for human and wildlife health.
使用导入hTRα和共激活因子的Y190酵母双杂交试验评估了691种化合物的人甲状腺受体(hTR)拮抗活性。同时,进行了那些YTOX测试以评估这些化合物是否影响拮抗作用或毒性。这是第一份关注许多疑似内分泌干扰物的化合物的hTR拮抗活性的报告。在本研究中,46种化合物在11 - 9940 nM范围内表现出50%最大活性(IC₅₀)的拮抗活性。特别是,双(对氯苯基)氧胂、三苯基氟化锡、三苯基氢氧化锡和百菌清具有很强的hTR拮抗活性。从本研究中获得的这些知识将推动针对人类和野生动物健康的化学监管策略。