PFOA and PFOS promote diabetic renal injury in vitro by impairing the metabolisms of amino acids and purines

被引:63
作者
Gong, Xun [1 ,2 ]
Yang, Chunxue [1 ]
Hong, Yanjun [1 ,2 ]
Chung, Arthur C. K. [1 ,2 ]
Cai, Zongwei [1 ,2 ]
机构
[1] Hong Kong Baptist Univ, Dept Chem, State Key Lab Environm & Biol Anal, Hong Kong, Peoples R China
[2] HKBU Inst Res & Continuing Educ, Shenzhen, Peoples R China
基金
中国国家自然科学基金;
关键词
PFOA; PFOS; Fibrosis; diabetic kidney disease; Purine metabolism; Amino acid metabolism; PERFLUOROOCTANE SULFONATE; NUCLEOSIDE PHOSPHORYLASE; REDUCTASE INHIBITORS; PERFLUOROALKYL ACIDS; ARGININE METABOLISM; PROTEOMIC ANALYSIS; OXIDATIVE STRESS; DNA-DAMAGE; KIDNEY; DYSFUNCTION;
D O I
10.1016/j.scitotenv.2019.04.208
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Background: Environmental pollutants, perfluotooctanoic acid (PFOA) and perfluorooctane sulfonate (PFOS), are common surfactants in various consumer products. Epidemiological studies have demonstrated the association of diabetic kidney diseases with PFOA and PFOS. However, mechanisms of metabolic alterations involved are still unclear. Methods: Considering their involvement of glomerular hemodynamics, rat mesangial cells (MCs) are used as an in vitro model of diabetic kidney diseases for exposure to PFOS/PFOA under diabetic condition. Non-targeted meta-bolomics studies based on liquid chromatography-high resolution mass spectrometry were conducted to determine how PFOA/PFOS promoted fibrotic and proinflammatory responses in the MCs under diabetic condition. Results: Exposure of PFOA/PFOS (10 mu M) increased oxidative stress and the levels of fibrotic and proinflammatory markers in MCs under diabetic condition. We demonstrated for the first time that PFOA and PFOS altered amino acid biosynthesis, citrate cycle ; and purine metabolism in MCs under diabetic condition. Compared with diabetic condition, the exposure of PFOA and PFOS under diabetic condition more significantly altered the levels of 13 intracellular metabolites, including L-tyrosine, L-phenylalanine, L-arginine, L-tryptophan, AMP, ADP, UMP, inosine, and hypoxanthine, which have been reported to be related to kidney injury. In addition, PFOA/PFOS treatment significantly altered the expression levels of key enzymes involved in these metabolisms. Treatment with L-tyrosine, L-phenylalanine, L-arginine, and L-tryptophan reduced the levels of fibrotic and inflammatory markers induced by PFOA/PFOS. Conclusion: Our results suggest that under diabetic condition, exposure of PFOA or PFOS aggravated diabetic kidney injury in vitro by impairing metabolisms of amino acids and purines to induce more fibrosis and inflammation in MCs. (C) 2019 Elsevier B.V. All rights reserved.
引用
收藏
页码:72 / 86
页数:15
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