• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

相似文献

1
Perfluorooctanesulfonic Acid and Perfluorohexanesulfonic Acid Alter the Blood Lipidome and the Hepatic Proteome in a Murine Model of Diet-Induced Obesity.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。
Toxicol Sci. 2020 Dec 1;178(2):311-324. doi: 10.1093/toxsci/kfaa148.
2
The role of maternal high fat diet on mouse pup metabolic endpoints following perinatal PFAS and PFAS mixture exposure.母体高脂肪饮食对围产期全氟烷基物质和全氟烷基物质混合物暴露后小鼠幼仔代谢终点的影响。
Toxicology. 2021 Oct;462:152921. doi: 10.1016/j.tox.2021.152921. Epub 2021 Aug 28.
3
Perfluorooctanesulfonic acid (PFOS) administration shifts the hepatic proteome and augments dietary outcomes related to hepatic steatosis in mice.全氟辛烷磺酸(PFOS)给药会改变肝脏蛋白质组,并增强与小鼠肝脂肪变性相关的饮食结果。
Toxicol Appl Pharmacol. 2020 Dec 1;408:115250. doi: 10.1016/j.taap.2020.115250. Epub 2020 Sep 23.
4
An 'Omics Approach to Unraveling the Paradoxical Effect of Diet on Perfluorooctanesulfonic Acid (PFOS) and Perfluorononanoic Acid (PFNA)-Induced Hepatic Steatosis.一种“组学”方法揭示饮食对全氟辛烷磺酸(PFOS)和全氟壬酸(PFNA)诱导肝脂肪变性的矛盾作用。
Toxicol Sci. 2021 Apr 12;180(2):277-294. doi: 10.1093/toxsci/kfaa172.
5
Perfluoroalkyl sulfonates cause alkyl chain length-dependent hepatic steatosis and hypolipidemia mainly by impairing lipoprotein production in APOE*3-Leiden CETP mice.全氟磺酸化合物通过损害 APOE*3-Leiden CETP 小鼠的脂蛋白生成,导致肝脂肪变性和血脂降低,主要与烷基链长度有关。
Toxicol Sci. 2011 Sep;123(1):290-303. doi: 10.1093/toxsci/kfr142. Epub 2011 Jun 24.
6
An Environmentally Relevant Mixture of Perfluorooctanesulfonic Acid and Perfluorohexanesulfonic Acid Does Not Conform to Additivity in Northern Leopard Frogs Exposed Through Metamorphosis.全氟辛烷磺酸和全氟己烷磺酸的环境相关混合物在通过变态暴露于北豹蛙时不符合加和性。
Environ Toxicol Chem. 2022 Dec;41(12):3007-3016. doi: 10.1002/etc.5486. Epub 2022 Nov 2.
7
Investigation of Peroxisome Proliferator-Activated Receptor Genes as Requirements for Visual Startle Response Hyperactivity in Larval Zebrafish Exposed to Structurally Similar Per- and Polyfluoroalkyl Substances (PFAS).研究过氧化物酶体增殖物激活受体基因作为结构相似的全氟和多氟烷基物质 (PFAS) 暴露的幼期斑马鱼视觉惊跳反应过度的需求。
Environ Health Perspect. 2024 Jul;132(7):77007. doi: 10.1289/EHP13667. Epub 2024 Jul 24.
8
Association of Perfluoroalkyl and Polyfluoroalkyl Substances With Premature Ovarian Insufficiency in Chinese Women.中文妇女中全氟和多氟烷基物质与卵巢早衰的关联。
J Clin Endocrinol Metab. 2018 Jul 1;103(7):2543-2551. doi: 10.1210/jc.2017-02783.
9
Exposure to a PFOA, PFOS and PFHxS Mixture during Gestation and Lactation Alters the Liver Proteome in Offspring of CD-1 Mice.孕期和哺乳期暴露于全氟辛酸、全氟辛烷磺酸和全氟己烷磺酸混合物会改变CD-1小鼠后代的肝脏蛋白质组。
Toxics. 2024 May 9;12(5):348. doi: 10.3390/toxics12050348.
10
Sensitivity and Accumulation of Perfluorooctanesulfonate and Perfluorohexanesulfonic Acid in Fathead Minnows (Pimephales promelas) Exposed over Critical Life Stages of Reproduction and Development.在繁殖和发育的关键生命阶段暴露的黑头呆鱼(Pimephales promelas)中全氟辛烷磺酸和全氟己烷磺酸的敏感性与蓄积情况。
Environ Toxicol Chem. 2021 Mar;40(3):811-819. doi: 10.1002/etc.4936. Epub 2021 Jan 29.

引用本文的文献

1
Importance of post-translational protein modifications in PFAS toxicity.翻译后蛋白质修饰在全氟和多氟烷基物质毒性中的重要性。
Toxicology. 2025 Aug 8;518:154260. doi: 10.1016/j.tox.2025.154260.
2
An oat fiber intervention for reducing PFAS body burden: A pilot study in male C57Bl/6 J mice.一项关于降低全氟烷基和多氟烷基物质(PFAS)体内负荷的燕麦纤维干预研究:对雄性C57Bl/6 J小鼠的初步研究。
Toxicol Appl Pharmacol. 2025 Feb;495:117188. doi: 10.1016/j.taap.2024.117188. Epub 2024 Dec 6.
3
Mid-Childhood Plasma Concentrations of Per- and Polyfluoroalkyl Substances, Modifiable Lifestyle Factors, and Bone Mineral Density Through Late Adolescence.青少年中期全氟和多氟烷基物质的血浆浓度、可改变的生活方式因素与青少年后期的骨矿物质密度。
Environ Sci Technol. 2024 Nov 12;58(45):19970-19980. doi: 10.1021/acs.est.4c08480. Epub 2024 Nov 1.
4
Sex and obesity influence the relationship between perfluoroalkyl substances and lean body mass: NHANES 2011-2018.性别和肥胖影响全氟烷基物质与去脂体重之间的关系:2011 - 2018年美国国家健康与营养检查调查(NHANES)
Heliyon. 2024 Aug 8;10(17):e35888. doi: 10.1016/j.heliyon.2024.e35888. eCollection 2024 Sep 15.
5
Exposure to a PFOA, PFOS and PFHxS Mixture during Gestation and Lactation Alters the Liver Proteome in Offspring of CD-1 Mice.孕期和哺乳期暴露于全氟辛酸、全氟辛烷磺酸和全氟己烷磺酸混合物会改变CD-1小鼠后代的肝脏蛋白质组。
Toxics. 2024 May 9;12(5):348. doi: 10.3390/toxics12050348.
6
Associations of perfluoroalkyl substances with metabolic-associated fatty liver disease and non-alcoholic fatty liver disease: NHANES 2017-2018.全氟烷基物质与代谢相关脂肪性肝病和非酒精性脂肪性肝病的关联:NHANES 2017-2018。
Cancer Causes Control. 2024 Sep;35(9):1271-1282. doi: 10.1007/s10552-024-01865-5. Epub 2024 May 19.
7
Hepatic Transcriptome Comparative In Silico Analysis Reveals Similar Pathways and Targets Altered by Legacy and Alternative Per- and Polyfluoroalkyl Substances in Mice.肝脏转录组的计算机模拟比较分析揭示了传统和替代全氟及多氟烷基物质在小鼠体内改变的相似途径和靶点。
Toxics. 2023 Nov 28;11(12):963. doi: 10.3390/toxics11120963.
8
A review of cardiovascular effects and underlying mechanisms of legacy and emerging per- and polyfluoroalkyl substances (PFAS).对传统和新兴的全氟和多氟烷基物质(PFAS)的心血管效应及其潜在机制的综述。
Arch Toxicol. 2023 May;97(5):1195-1245. doi: 10.1007/s00204-023-03477-5. Epub 2023 Mar 22.
9
Plasma concentrations of per- and polyfluoroalkyl substances are associated with perturbations in lipid and amino acid metabolism.全氟和多氟烷基物质的血浆浓度与脂质和氨基酸代谢的紊乱有关。
Chemosphere. 2023 May;324:138228. doi: 10.1016/j.chemosphere.2023.138228. Epub 2023 Mar 4.
10
Isomer-Specific Serum Concentrations of Perfluorooctane Sulfonic Acid among U.S. Adults: Results from the National Health and Nutrition Examination Survey (NHANES) and the Study of Women's Health Across the Nation Multi-Pollutant Study (SWAN-MPS).美国成年人中全氟辛烷磺酸的立体异构体特异性血清浓度:来自国家健康和营养检查调查(NHANES)和全国妇女健康多污染物研究(SWAN-MPS)的结果。
Environ Sci Technol. 2023 Jan 10;57(1):385-394. doi: 10.1021/acs.est.2c04501. Epub 2022 Dec 19.

本文引用的文献

1
Phospholipid Levels Predict the Tissue Distribution of Poly- and Perfluoroalkyl Substances in a Marine Mammal.磷脂水平可预测海洋哺乳动物体内多氟和全氟烷基物质的组织分布。
Environ Sci Technol Lett. 2019 Mar 12;6(3):119-125. doi: 10.1021/acs.estlett.9b00031. Epub 2019 Feb 20.
2
Perfluorooctanoic acid activates multiple nuclear receptor pathways and skews expression of genes regulating cholesterol homeostasis in liver of humanized PPARα mice fed an American diet.全氟辛酸激活多种核受体通路,并改变了喂食美式饮食的人源化 PPARα 小鼠肝脏中胆固醇稳态调节基因的表达。
Toxicol Appl Pharmacol. 2020 Oct 15;405:115204. doi: 10.1016/j.taap.2020.115204. Epub 2020 Aug 19.
3
Temporal trends of suspect- and target-per/polyfluoroalkyl substances (PFAS), extractable organic fluorine (EOF) and total fluorine (TF) in pooled serum from first-time mothers in Uppsala, Sweden, 1996-2017.1996-2017 年瑞典乌普萨拉首次生育母亲血清中可疑和目标多氟/全氟烷基物质(PFAS)、可提取有机氟(EOF)和总氟(TF)的时间趋势。
Environ Sci Process Impacts. 2020 Apr 29;22(4):1071-1083. doi: 10.1039/c9em00502a.
4
Assessing the human health risks of perfluorooctane sulfonate by in vivo and in vitro studies.通过体内和体外研究评估全氟辛烷磺酸对人类健康的风险。
Environ Int. 2019 May;126:598-610. doi: 10.1016/j.envint.2019.03.002. Epub 2019 Mar 8.
5
Nrf2 Signaling Elicits a Neuroprotective Role Against PFOS-mediated Oxidative Damage and Apoptosis.Nrf2 信号对全氟辛烷磺酸介导的氧化损伤和细胞凋亡发挥神经保护作用。
Neurochem Res. 2018 Dec;43(12):2446-2459. doi: 10.1007/s11064-018-2672-y. Epub 2018 Oct 31.
6
Identification of metabolic profiles associated with human exposure to perfluoroalkyl substances.鉴定与人类接触全氟烷基物质相关的代谢特征。
J Expo Sci Environ Epidemiol. 2019 Mar;29(2):196-205. doi: 10.1038/s41370-018-0060-y. Epub 2018 Sep 5.
7
Large-scale plasma lipidomic profiling identifies lipids that predict cardiovascular events in secondary prevention.大规模血浆脂质组学分析鉴定出可预测二级预防中心血管事件的脂质。
JCI Insight. 2018 Sep 6;3(17). doi: 10.1172/jci.insight.121326.
8
Partitioning and Accumulation of Perfluoroalkyl Substances in Model Lipid Bilayers and Bacteria.全氟烷基物质在模型脂质双层和细菌中的分配与积累
Environ Sci Technol. 2018 Sep 18;52(18):10433-10440. doi: 10.1021/acs.est.8b02912. Epub 2018 Sep 10.
9
Paradoxical Protective Effect of Perfluorooctanesulfonic Acid Against High-Fat Diet-Induced Hepatic Steatosis in Mice.全氟辛烷磺酸对高脂饮食诱导的小鼠肝脂肪变性的矛盾保护作用。
Int J Toxicol. 2018 Sep/Oct;37(5):383-392. doi: 10.1177/1091581818790934. Epub 2018 Aug 22.
10
Molecular mechanisms of hepatic lipid accumulation in non-alcoholic fatty liver disease.非酒精性脂肪性肝病中肝脏脂质积累的分子机制。
Cell Mol Life Sci. 2018 Sep;75(18):3313-3327. doi: 10.1007/s00018-018-2860-6. Epub 2018 Jun 23.

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.

DOI:10.1093/toxsci/kfaa148
PMID:32991729
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7751193/
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。