Department of Environmental Health Sciences, Arnold School of Public Health, University of South Carolina, Columbia, South Carolina, USA.
Toxicol Sci. 2013 May;133(1):144-56. doi: 10.1093/toxsci/kft020. Epub 2013 Feb 1.
Firemaster 550 (FM550) is an additive flame retardant formulation of brominated and aryl phosphate ester (APE) components introduced as a major replacement product for the commercial polybrominated diphenyl ether mixture (known as PentaBDE) used primarily in polyurethane foam. However, little is known about the potential effects of FM550-based ingredients during early vertebrate development. Therefore, we first screened the developmental toxicity of each FM550 component using zebrafish as an animal model. Based on these initial screening assays, we found that exposure to the brominated components as high as 10µM resulted in no significant effects on embryonic survival or development, whereas exposure to triphenyl phosphate (TPP) or mono-substituted isopropylated triaryl phosphate (mono-ITP)-two APEs comprising almost 50% of FM550-resulted in targeted effects on cardiac looping and function during embryogenesis. As these cardiac abnormalities resembled aryl hydrocarbon receptor (AHR) agonist-induced phenotypes, we then exposed developing embryos to TPP or mono-ITP in the presence or absence of an AHR antagonist (CH223191) or AHR2-specific morpholino. Based on these studies, we found that CH223191 blocked heart malformations following exposure to mono-ITP but not TPP, whereas AHR2 knockdown failed to block the cardiotoxic effects of both components. Finally, using a cell-based human AHR reporter assay, we found that mono-ITP (but not TPP) exposure resulted in a significant increase in human AHR-driven luciferase activity at similar nominal concentrations as a potent reference AHR agonist (β-naphthoflavone). Overall, our findings suggest that two major APE components of FM550 induce severe cardiac abnormalities during early vertebrate development.
Firemaster 550 (FM550) 是一种含溴和芳基磷酸酯 (APE) 成分的阻燃剂配方,作为商业多溴二苯醚混合物 (俗称五溴二苯醚) 的主要替代品推出,主要用于聚氨酯泡沫。然而,对于 FM550 基成分在早期脊椎动物发育过程中的潜在影响知之甚少。因此,我们首先使用斑马鱼作为动物模型筛选每个 FM550 成分的发育毒性。基于这些初步筛选试验,我们发现,暴露于高达 10µM 的溴化成分对胚胎存活率或发育没有显著影响,而暴露于三苯基磷酸酯 (TPP) 或单取代异丙基三芳基磷酸酯 (单 ITP) - FM550 中几乎 50%的两种 APE-导致胚胎发生期间心脏环化和功能的靶向效应。由于这些心脏异常类似于芳基烃受体 (AHR) 激动剂诱导的表型,我们随后在存在或不存在 AHR 拮抗剂 (CH223191) 或 AHR2 特异性 morpholino 的情况下,将发育中的胚胎暴露于 TPP 或单 ITP。基于这些研究,我们发现 CH223191 阻断了暴露于单 ITP 后的心脏畸形,但不能阻断 TPP 的心脏畸形,而 AHR2 敲低未能阻断两种成分的心脏毒性作用。最后,使用基于细胞的人 AHR 报告基因测定,我们发现单 ITP(而不是 TPP)暴露在与强效参考 AHR 激动剂 (β-萘黄酮) 相似的名义浓度下导致人 AHR 驱动的荧光素酶活性显著增加。总的来说,我们的研究结果表明,FM550 的两个主要 APE 成分在早期脊椎动物发育过程中诱导严重的心脏异常。