Chongqing Key Laboratory of Animal Biology, School of Life Sciences, Chongqing Normal University, Chongqing 401331, China.
CAS Key Laboratory of Separation Sciences for Analytical Chemistry, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian 116023, Liaoning, China.
Environ Sci Technol. 2021 Oct 5;55(19):13122-13131. doi: 10.1021/acs.est.1c03948. Epub 2021 Sep 15.
Due to commercial uses and environmental degradation of aryl phosphate esters, diphenyl phosphate (DPhP) is frequently detected in environmental matrices and is thus of growing concern worldwide. However, information on potential adverse effects of chronic exposure to DPhP at environmentally realistic concentrations was lacking. Here, we investigated the effects of life cycle exposure to DPhP on zebrafish at environmentally relevant concentrations of 0.8, 3.9, or 35.6 μg/L and employed a dual-omics approach (metabolomics and transcriptomics) to characterize potential modes of action. Exposure to DPhP at 35.6 μg/L for 120 days resulted in significant reductions in body mass and length of male zebrafish, but did not cause those same effects to females. Predominant toxicological mechanisms, including inhibition of oxidative phosphorylation, down-regulation of fatty acid oxidation, and up-regulation of phosphatidylcholine degradation, were revealed by integrated dual-omics analysis and successfully linked to adverse outcomes. Activity of succinate dehydrogenase and protein content of carnitine -palmitoyltransferase 1 were significantly decreased in livers of male fish exposed to DPhP, which further confirmed the proposed toxicological mechanisms. This study is the first to demonstrate that chronic, low-level exposure to DPhP can retard growth via inhibiting energy output in male zebrafish.
由于芳基磷酸酯的商业用途和环境降解,磷酸二苯酯(DPhP)经常在环境基质中被检测到,因此在全球范围内受到越来越多的关注。然而,关于在环境现实浓度下慢性暴露于 DPhP 可能产生的不利影响的信息还很缺乏。在这里,我们研究了在环境相关浓度 0.8、3.9 或 35.6 μg/L 下,全生命周期暴露于 DPhP 对斑马鱼的影响,并采用双组学方法(代谢组学和转录组学)来描述潜在的作用模式。暴露于 35.6 μg/L DPhP 120 天导致雄性斑马鱼的体重和体长显著减少,但对雌性没有同样的影响。通过整合的双组学分析揭示了主要的毒理学机制,包括氧化磷酸化抑制、脂肪酸氧化下调和磷脂酰胆碱降解上调,并成功将其与不良结果联系起来。暴露于 DPhP 的雄性鱼肝脏中的琥珀酸脱氢酶活性和肉碱棕榈酰转移酶 1 的蛋白质含量显著降低,进一步证实了所提出的毒理学机制。这项研究首次表明,慢性低水平暴露于 DPhP 可以通过抑制雄性斑马鱼的能量输出来减缓生长。