California Environmental Protection Agency (CalEPA) Office of Environmental Health Hazard Assessment (OEHHA), Sacramento, California 95814, United States.
CalEPA OEHHA, Oakland, California 94612, United States.
Chem Res Toxicol. 2021 Nov 15;34(11):2319-2330. doi: 10.1021/acs.chemrestox.1c00205. Epub 2021 Oct 27.
There is growing evidence from human and animal studies indicating an association between exposure to synthetic food dyes and adverse neurobehavioral outcomes in children. However, data gaps persist for potential mechanisms by which the synthetic food dyes could elicit neurobehavioral impacts. We developed an approach to evaluate seven US FDA-batch-certified food dyes using publicly available high-throughput screening (HTS) data from the US EPA's Toxicity Forecaster to assess potential underlying molecular mechanisms that may be linked to neurological pathway perturbations. The dyes were screened through 270 assays identified based on whether they had a neurological-related gene target and/or were mapped to neurodevelopmental processes or neurobehavioral outcomes, and were conducted in brain tissue, targeted specific hormone receptors, or targeted oxidative stress and inflammation. Some results provided support for neurological impacts found in human and animal studies, while other results showed a lack of correlation with findings. The azo dyes had a range of activity in assays mapped to G-protein-coupled receptors and were active in assays targeting dopaminergic, serotonergic, and opioid receptors. Assays mapped to nuclear receptors (androgen, estrogen, and thyroid hormone) also exhibited activity with the food dyes. Other molecular targets included the aryl hydrocarbon receptor, acetylcholinesterase, and monoamine oxidase. The Toxicological Prioritization Index tool was used to visualize the results of the Novascreen assays. Our results highlight certain limitations of HTS assays but provide insight into potential underlying mechanisms of neurobehavioral effects observed in animal toxicology studies and human clinical studies.
越来越多的人类和动物研究证据表明,儿童接触合成食用色素与不良神经行为结果之间存在关联。然而,对于合成食用色素如何引发神经行为影响的潜在机制,仍存在数据空白。我们开发了一种方法,使用美国环保署毒性预测器提供的公开高通量筛选 (HTS) 数据,评估美国食品药品监督管理局批次认证的七种食用色素,以评估可能与神经通路扰动相关的潜在分子机制。这些染料通过 270 种基于是否具有神经相关基因靶标和/或是否映射到神经发育过程或神经行为结果的检测进行筛选,并且在脑组织中进行,针对特定激素受体,或针对氧化应激和炎症。一些结果为人类和动物研究中发现的神经影响提供了支持,而其他结果则显示与发现缺乏相关性。偶氮染料在映射到 G 蛋白偶联受体的检测中具有一系列活性,并且在针对多巴胺能、血清素能和阿片受体的检测中具有活性。映射到核受体(雄激素、雌激素和甲状腺激素)的检测也表现出与食用染料的活性。其他分子靶标包括芳香烃受体、乙酰胆碱酯酶和单胺氧化酶。使用毒性优先指数工具可视化 Novascreen 检测的结果。我们的结果突出了 HTS 检测的某些局限性,但为动物毒理学研究和人类临床研究中观察到的神经行为效应的潜在机制提供了一些见解。