Perfluorooctanesulfonic Acid and Perfluorohexanesulfonic Acid Alter the Blood Lipidome and the Hepatic Proteome in a Murine Model of Diet-Induced Obesity

被引:45
作者
Pfohl, Marisa [1 ]
Ingram, Lishann [2 ,3 ]
Marques, Emily [1 ]
Auclair, Adam [1 ]
Barlock, Benjamin [1 ]
Jamwal, Rohitash [1 ]
Anderson, Dwight [1 ]
Cummings, Brian S. [2 ,4 ]
Slitt, Angela L. [1 ]
机构
[1] Univ Rhode Isl, Dept Biomed & Pharmaceut Sci, Coll Pharm, Kingston, RI 02881 USA
[2] Univ Georgia, Dept Pharmaceut & Biomed Sci, Coll Pharm, Athens, GA 30602 USA
[3] Carnegie Inst Sci, Dept Embryol, Baltimore, MD 21218 USA
[4] Univ Georgia, Interdisciplinary Toxicol Program, Coll Pharm, Athens, GA 30602 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
proteomics; lipidomics; PFHxS; PFOS; PFAS; high-fat diet; OXIDIZED PHOSPHOLIPIDS; COMPARATIVE PHARMACOKINETICS; POLYFLUOROALKYL SUBSTANCES; OXIDATIVE STRESS; BETA-OXIDATION; HIGH-FAT; IN-VIVO; LIVER; MICE; PFOS;
D O I
10.1093/toxsci/kfaa148
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Perfluoroalkyl substances (PFAS) represent a family of environmental toxicants that have infiltrated the living world. This study explores diet-PFAS interactions and the impact of perfluorooctanesulfonic acid (PFOS) and perfluorohexanesulfonic (PFHxS) on the hepatic proteome and blood lipidomic profiles. Male C57BL/6J mice were fed with either a low-fat diet (10.5% kcal from fat) or a high fat (58% kcal from fat) high carbohydrate (42 g/l) diet with or without PFOS or PFHxS in feed (0.0003% wt/wt) for 29 weeks. Lipidomic, proteomic, and gene expression profiles were determined to explore lipid outcomes and hepatic mechanistic pathways. With administration of a high-fat high-carbohydrate diet, PFOS and PFHxS increased hepatic expression of targets involved in lipid metabolism and oxidative stress. In the blood, PFOS and PFHxS altered serum phosphatidylcholines, phosphatidylethanolamines, plasmogens, sphingomyelins, and triglycerides. Furthermore, oxidized lipid species were enriched in the blood lipidome of PFOS and PFHxS treated mice. These data support the hypothesis that PFOS and PFHxS increase the risk of metabolic and inflammatory disease induced by diet, possibly by inducing dysregulated lipid metabolism and oxidative stress.
引用
收藏
页码:311 / 324
页数:14
相关论文
共 65 条
  • [1] [Anonymous], 2015, AM CHILDR ENV
  • [2] [Anonymous], 2019, PER POL SUBST PFAS F
  • [3] Perfluorooctane Sulfonate-Induced Hepatic Steatosis in Male Sprague Dawley Rats Is Not Attenuated by Dietary Choline Supplementation
    Bagley, Bradford D.
    Chang, Shu-Ching
    Ehresman, David J.
    Eveland, Alan
    Zitzow, Jeremiah D.
    Parker, George A.
    Peters, Jeffrey M.
    Wallace, Kendall B.
    Butenhoff, John L.
    [J]. TOXICOLOGICAL SCIENCES, 2017, 160 (02) : 284 - 298
  • [4] BARTLETT GR, 1959, J BIOL CHEM, V234, P466
  • [5] Multiplicity of nuclear receptor activation by PFOA and PFOS in primary human and rodent hepatocytes
    Bjork, J. A.
    Butenhoff, J. L.
    Wallace, K. B.
    [J]. TOXICOLOGY, 2011, 288 (1-3) : 8 - 17
  • [6] BLIGH EG, 1959, CAN J BIOCHEM PHYS, V37, P911
  • [7] Phosphatidylethanolamine Metabolism in Health and Disease
    Calzada, Elizabeth
    Onguka, Ouma
    Claypool, Steven M.
    [J]. INTERNATIONAL REVIEW OF CELL AND MOLECULAR BIOLOGY, VOL 321, 2016, 321 : 29 - 88
  • [8] CDC-Centers of Disease Control ans Prevention, 2019, 4 CDC NAT CTR ENV HL, P866
  • [9] Comparative pharmacokinetics of perfluorooctanesulfonate (PFOS) in rats, mice, and monkeys
    Chang, Shu-Ching
    Noker, Patricia E.
    Gorman, Gregory S.
    Gibson, Sheila J.
    Hart, Jill A.
    Ehresman, David J.
    Butenhoff, John L.
    [J]. REPRODUCTIVE TOXICOLOGY, 2012, 33 (04) : 428 - 440
  • [10] Evaluation of Serum Lipid, Thyroid, and Hepatic Clinical Chemistries in Association With Serum Perfluorooctanesulfonate (PFOS) in Cynomolgus Monkeys After Oral Dosing With Potassium PFOS
    Chang, Sue
    Allen, Bruce C.
    Andres, Kara L.
    Ehresman, David J.
    Falvo, Ria
    Provencher, Anne
    Olsen, Geary W.
    Butenhoff, John L.
    [J]. TOXICOLOGICAL SCIENCES, 2017, 156 (02) : 387 - 401