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Metabolomic, Lipidomic, Transcriptomic, and Metagenomic Analyses in Mice Exposed to PFOS and Fed Soluble and Insoluble Dietary Fibers

  • Pan Deng
  • , Jerika Durham
  • , Jinpeng Liu
  • , Xiaofei Zhang
  • , Chi Wang
  • , Dong Li
  • , Taesik Gwag
  • , Murong Ma
  • , Bernhard Hennig

Producción científica: Articlerevisión exhaustiva

41 Citas (Scopus)

Resumen

BACKGROUND: Perfluorooctane sulfonate (PFOS) is a persistent environmental pollutant that has become a significant concern around the world. Exposure to PFOS may alter gut microbiota and liver metabolic homeostasis in mammals, thereby increasing the risk of cardiometabolic diseases. Diets high in soluble fibers can ameliorate metabolic disease risks. OBJECTIVES: We aimed to test the hypothesis that soluble fibers (inulin or pectin) could modulate the adverse metabolic effects of PFOS by affecting microbe-liver metabolism and interactions. METHODS: Male C57BL/6J mice were fed an isocaloric diet containing different fibers: a) inulin (soluble), b) pectin (soluble), or c) cellulose (control, insoluble). The mice were exposed to PFOS in drinking water (3 lg=g per day) for 7 wk. Multi-omics was used to analyze mouse liver and cecum contents. RESULTS: In PFOS-exposed mice, the number of differentially expressed genes associated with atherogenesis and hepatic hyperlipidemia were lower in those that were fed soluble fiber than those fed insoluble fiber. Shotgun metagenomics showed that inulin and pectin protected against differences in microbiome community in PFOS-exposed vs. control mice. It was found that the plasma PFOS levels were lower in inulin-fed mice, and there was a trend of lower liver accumulation of PFOS in soluble fiber-fed mice compared with the control group. Soluble fiber intake ameliorated the effects of PFOS on host hepatic metabolism gene expression and cecal content microbiome structure. DISCUSSIONS: Results from metabolomic, lipidomic, and transcriptomic studies suggest that inulin-and pectin-fed mice were less susceptible to PFOS-induced liver metabolic disturbance, hepatic lipid accumulation, and transcriptional changes compared with control diet-fed mice. Our study advances the understanding of interaction between microbes and host under the influences of environmental pollutants and nutrients. The results provide new insights into the microbe-liver metabolic network and the protection against environmental pollutant-induced metabolic diseases by high-fiber diets. https://doi.org/10.1289/EHP11360.

Idioma originalEnglish
Número de artículo117003
PublicaciónEnvironmental Health Perspectives
Volumen130
N.º11
DOI
EstadoPublished - nov 2022

Nota bibliográfica

Publisher Copyright:
© 2022, Public Health Services, US Dept of Health and Human Services. All rights reserved.

Financiación

This work was supported by the National Institute of Environmental Health Sciences, National Institutes of Health (NIH; P42 ES007380, to B.H.), the Markey Cancer Center Biostatistics and Bioinformatics Core Facility (P30 CA177558, to C.W.), the Emory University Human Exposome Research Center (HERCULES; P30 ES019776), the University of Kentucky Agricultural Experiment Station, and the Priority Academic Program Development of Jiangsu Higher Education Institutes (PAPD). The content is solely the responsibility of the authors and does not necessarily represent the official views of the NIH.

FinanciadoresNúmero del financiador
Emory University Human Exposome Research Center
National Institutes of Health/National Institute of Environmental Health Sciences
Priority Academic Program Development of Jiangsu Higher Education Institutions
University of Kentucky Agricultural Experiment Station
Markey Cancer Center Biostatistics and Bioinformatics Core FacilityP30 CA177558
HERCULESP30 ES019776
National Institutes of Health (NIH)P42 ES007380
National Institutes of Health (NIH)

    ODS de las Naciones Unidas

    Este resultado contribuye a los siguientes Objetivos de Desarrollo Sostenible

    1. Good health and well being
      Good health and well being

    ASJC Scopus subject areas

    • Public Health, Environmental and Occupational Health
    • Health, Toxicology and Mutagenesis

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