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全氟辛烷磺酸和全氟己烷磺酸改变饮食诱导肥胖小鼠的血液脂质组和肝蛋白质组。

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

机构信息

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

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

出版信息

Toxicol Sci. 2020 Dec 1;178(2):311-324. doi: 10.1093/toxsci/kfaa148.

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.

摘要

全氟烷基物质(PFAS)是一类环境毒物,已渗透到生物界中。本研究探讨了饮食与 PFAS 的相互作用,以及全氟辛烷磺酸(PFOS)和全氟己烷磺酸(PFHxS)对肝脏蛋白质组和血液脂质组谱的影响。雄性 C57BL/6J 小鼠喂食低脂肪(10.5%的热量来自脂肪)或高脂肪(58%的热量来自脂肪)高碳水化合物(42g/l)饮食,或在饲料中添加(0.0003%wt/wt)PFOS 或 PFHxS,持续 29 周。通过测定脂质组学、蛋白质组学和基因表达谱,探索脂质代谢和肝脏的机制途径。用高脂肪高碳水化合物饮食处理后,PFOS 和 PFHxS 增加了与脂质代谢和氧化应激相关的肝脏靶基因的表达。在血液中,PFOS 和 PFHxS 改变了血清磷脂酰胆碱、磷脂酰乙醇胺、血浆蛋白、神经鞘磷脂和甘油三酯。此外,在 PFOS 和 PFHxS 处理的小鼠的血液脂质组中,氧化脂质种类丰富。这些数据支持了这样一种假说,即 PFOS 和 PFHxS 通过诱导失调的脂质代谢和氧化应激,增加了饮食引起的代谢和炎症性疾病的风险。

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