Effects of Perfluorooctanoic Acid on Metabolic Profiles in Brain and Liver of Mouse Revealed by a High-throughput Targeted Metabolomics Approach

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作者
Nanyang Yu
Si Wei
Meiying Li
Jingping Yang
Kan Li
Ling Jin
Yuwei Xie
John P. Giesy
Xiaowei Zhang
Hongxia Yu
机构
[1] State Key Laboratory of Pollution Control and Resource Reuse,Department of Civil and Environmental Engineering
[2] School of the Environment,Department of Biomedical Veterinary Sciences and Toxicology Centre
[3] Nanjing University,undefined
[4] Laboratory of Immunology and Reproductive Biology,undefined
[5] School of Medicine,undefined
[6] Nanjing University,undefined
[7] The Hong Kong Polytechnic University,undefined
[8] University of Saskatchewan,undefined
[9] School of Biology Sciences,undefined
[10] University of Hong Kong,undefined
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Perfluorooctanoic acid (PFOA), a perfluoroalkyl acid, can result in hepatotoxicity and neurobehavioral effects in animals. The metabolome, which serves as a connection among transcriptome, proteome and toxic effects, provides pathway-based insights into effects of PFOA. Since understanding of changes in the metabolic profile during hepatotoxicity and neurotoxicity were still incomplete, a high-throughput targeted metabolomics approach (278 metabolites) was used to investigate effects of exposure to PFOA for 28 d on brain and liver of male Balb/c mice. Results of multivariate statistical analysis indicated that PFOA caused alterations in metabolic pathways in exposed individuals. Pathway analysis suggested that PFOA affected metabolism of amino acids, lipids, carbohydrates and energetics. Ten and 18 metabolites were identified as potential unique biomarkers of exposure to PFOA in brain and liver, respectively. In brain, PFOA affected concentrations of neurotransmitters, including serotonin, dopamine, norepinephrine and glutamate in brain, which provides novel insights into mechanisms of PFOA-induced neurobehavioral effects. In liver, profiles of lipids revealed involvement of β-oxidation and biosynthesis of saturated and unsaturated fatty acids in PFOA-induced hepatotoxicity, while alterations in metabolism of arachidonic acid suggesting potential of PFOA to cause inflammation response in liver. These results provide insight into the mechanism and biomarkers for PFOA-induced effects.
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