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Perfluorooctane sulfonate (PFOS) and benzo[a]pyrene (BaP) synergistically induce neurotoxicity in C6 rat glioma cells via the activation of neurotransmitter and Cyp1a1-mediated steroid hormone synthesis pathways

文献类型：外文期刊

第一作者： Lu, Yu-Shun

作者： Lu, Yu-Shun;Chen, Ju;He, Xiao-Rong;Yang, Shang-Lin;Ma, Bing-Jie;Qiu, Jing;Qian, Yong-Zhong;Xu, Yan-Yang;Lu, Yu-Shun;Yu, Jiang

作者机构：

关键词： Perfluorooctane sulfonates; Benzo[a]pyrene; C6 cell; Combined toxicity; Molecular mechanism

期刊名称：FOOD AND CHEMICAL TOXICOLOGY （影响因子：3.5；五年影响因子：4.1 ）

ISSN： 0278-6915

年卷期： 2024 年 193 卷

页码：

收录情况： SCI

摘要： Humans are often exposed to complex mixtures of multiple pollutants rather than a single pollutant. However, the combined toxic effects and the molecular mechanism of PFOS and BaP remain poorly understood. In this study, two typical environmental pollutants, perfluorooctane sulfonate acid (PFOS) and benzo [a]pyrene (BaP), were selected to investigate their combined neurotoxic effects on rat C6 glioma cells at environmentally relevant concentrations. The results showed that coexposure to low-dose PFOS and BaP induced greater toxicity (synergistic effect) than did single exposure. PFOS-BaP coexposure had stronger toxic effects on inducing oxidative stress and promoting early apoptosis. Targeted metabolomics confirmed that increased levels of the neurotransmitters 5-hydroxytryptophan, dopamine, tryptophan and serotonin disturb the phenylalanine, tyrosine and tryptophan biosynthesis pathways. Mechanistically, exposure to a low-dose PFOS-BaP binary mixture induces steroid hormone synthesis disorder through the activation of Cyp1a1 and Hsd17b8 (steroid hormone synthesis genes) and Dhcr24 and Dhcr7 (cholesterol synthesis genes). These findings are useful for comprehensively and systematically elucidating the biological safety of PFOS-BaP and its potential threats to human health.

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