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

Author:

Pfohl Marisa1,Ingram Lishann23,Marques Emily1,Auclair Adam1ORCID,Barlock Benjamin1,Jamwal Rohitash1ORCID,Anderson Dwight1,Cummings Brian S24,Slitt Angela L1ORCID

Affiliation:

1. Department of Biomedical and Pharmaceutical Sciences, College of Pharmacy, University of Rhode Island, Kingston, Rhode Island 02881

2. Department of Pharmaceutical and Biomedical Sciences, College of Pharmacy, University of Georgia, Athens, Georgia 30602

3. Department of Embryology, Carnegie Institution for Science, Baltimore, Maryland 21218

4. Interdisciplinary Toxicology Program, College of Pharmacy, University of Georgia, Athens, Georgia 30602

Abstract

Abstract 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.

Funder

National Institutes of Health

NIH

University of Rhode Island

Rhode Island National Science Foundation

NSF

Established Program to Stimulate Competitive Research

Molecular Characterization Facility

National Science Foundation EPSCoR Cooperative

Publisher

Oxford University Press (OUP)

Subject

Toxicology

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