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Perinatal exposure to perfluorooctane sulfonate and the risk of hepatic inflammation in rat offspring: Perturbation of gut-liver crosstalk.

Publication ,  Journal Article
Liu, Y; Yu, G; Medsker, H; Luo, T; Meng, X; Wang, C; Feng, L; Zhang, J
Published in: Environ Res
October 15, 2024

Perfluorooctane sulfonate (PFOS) exposure is associated with harmful hepatic outcomes. Growing evidence indicates that crosstalk between the gut microbiome, immune system, and liver plays a vital role in the pathogenesis of liver diseases. However, the underlying mechanism is not fully understood. In the present study, we aimed to investigate the effects of PFOS exposure during pregnancy and lactation on hepatic inflammation in rat offspring. Features of hepatic inflammation and increased levels of aspartate-amino transferase (AST) were found in pups on postnatal day 28 (PND28) in PFOS-exposed groups. Gut microbiota analysis identified Chitinophaga, Ralstonia, and Alloprevotella as the key genera in distinguishing the PFOS-exposed group from the control group. Metabolic and transcriptomic analyses found that PFOS exposure resulted in 48 differentially expressed metabolites (DEMs) in the serum, 62 DEMs in the liver, and 289 differentially expressed genes (DEGs) in the liver of PND28 pups. The immune response is significantly enriched in PFOS-exposed liver on PND28; multi-omics analysis indicated that PFOS might lead to immune response perturbation by disturbing the metabolic profiling in the liver. The changed gut microbiota was significantly related to the serum level of the liver function index. Specifically, Alloprevotella, Chitinophage, Ruminococcus, and Allobaculum were significantly associated with the metabolic abundance changes of 4-Hydroxydebrisoquine, L-Norvaline, and Eremopetasinorol, and the gene expression changes of Acat211, Msmol, Idi1, Sqle, and Gadd45b in the liver. These findings suggest that early-life PFOS exposure may be associated with adverse hepatic inflammation in young offspring via disruption of the gut-liver crosstalk, which may provide mechanistic clues for clarifying the hepatotoxicity in offspring associated with perinatal PFOS exposure.

Duke Scholars

Published In

Environ Res

DOI

EISSN

1096-0953

Publication Date

October 15, 2024

Volume

259

Start / End Page

119442

Location

Netherlands

Related Subject Headings

  • Toxicology
  • Rats, Sprague-Dawley
  • Rats
  • Prenatal Exposure Delayed Effects
  • Pregnancy
  • Maternal Exposure
  • Male
  • Liver
  • Inflammation
  • Gastrointestinal Microbiome
 

Citation

APA
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ICMJE
MLA
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Liu, Y., Yu, G., Medsker, H., Luo, T., Meng, X., Wang, C., … Zhang, J. (2024). Perinatal exposure to perfluorooctane sulfonate and the risk of hepatic inflammation in rat offspring: Perturbation of gut-liver crosstalk. Environ Res, 259, 119442. https://doi.org/10.1016/j.envres.2024.119442
Liu, Yongjie, Guoqi Yu, Hannah Medsker, Tingyu Luo, Xi Meng, Cuiping Wang, Liping Feng, and Jun Zhang. “Perinatal exposure to perfluorooctane sulfonate and the risk of hepatic inflammation in rat offspring: Perturbation of gut-liver crosstalk.Environ Res 259 (October 15, 2024): 119442. https://doi.org/10.1016/j.envres.2024.119442.
Liu, Yongjie, et al. “Perinatal exposure to perfluorooctane sulfonate and the risk of hepatic inflammation in rat offspring: Perturbation of gut-liver crosstalk.Environ Res, vol. 259, Oct. 2024, p. 119442. Pubmed, doi:10.1016/j.envres.2024.119442.
Liu Y, Yu G, Medsker H, Luo T, Meng X, Wang C, Feng L, Zhang J. Perinatal exposure to perfluorooctane sulfonate and the risk of hepatic inflammation in rat offspring: Perturbation of gut-liver crosstalk. Environ Res. 2024 Oct 15;259:119442.
Journal cover image

Published In

Environ Res

DOI

EISSN

1096-0953

Publication Date

October 15, 2024

Volume

259

Start / End Page

119442

Location

Netherlands

Related Subject Headings

  • Toxicology
  • Rats, Sprague-Dawley
  • Rats
  • Prenatal Exposure Delayed Effects
  • Pregnancy
  • Maternal Exposure
  • Male
  • Liver
  • Inflammation
  • Gastrointestinal Microbiome