Upregulation of Fatty Acid Synthesis Genes in the Livers of Adolescent Female Rats Caused by Inhalation Exposure to PCB52 (2,2',5,5'-Tetrachlorobiphenyl).

Fatty acid synthesis Inhalation exposure PCB52 Persistent organic pollutant Polychlorinated biphenyl Steatosis

Journal

Environmental toxicology and pharmacology
ISSN: 1872-7077
Titre abrégé: Environ Toxicol Pharmacol
Pays: Netherlands
ID NLM: 9612020

Informations de publication

Date de publication:
25 Jul 2024
Historique:
received: 10 06 2024
revised: 23 07 2024
accepted: 24 07 2024
medline: 28 7 2024
pubmed: 28 7 2024
entrez: 27 7 2024
Statut: aheadofprint

Résumé

Elevated airborne PCB levels in older schools are concerning due to their health impacts, including cancer, metabolic dysfunction-associated steatotic liver disease (MASLD), cardiovascular issues, neurodevelopmental diseases, and diabetes. During a four-week inhalation exposure to PCB52, an air pollutant commonly found in school environments, adolescent rats exhibited notable presence of PCB52 and its hydroxylated forms in their livers, alongside changes in gene expression. Female rats exhibited more pronounced changes in gene expression compared to males, particularly in fatty acid synthesis genes regulated by the transcription factor SREBP1. In vitro studies with human liver cells showed that the hydroxylated metabolite of PCB52, 4-OH-PCB52, but not the parent compound, upregulated genes involved in fatty acid biosynthesis similar to in vivo exposure. These findings highlight the sex-specific effects of PCB52 exposure on livers, particularly in females, suggesting a potential pathway for increased MASLD susceptibility.

Identifiants

pubmed: 39067718
pii: S1382-6689(24)00160-1
doi: 10.1016/j.etap.2024.104520
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

104520

Informations de copyright

Copyright © 2024 Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper CONFLICTS OF INTEREST The authors declare no conflict of interest.

Auteurs

Brynn Kyleakin Helm-Kwasny (BK)

Molecular Medicine Graduate Program, The University of Iowa, Iowa City, Iowa, USA.

Amanda Bullert (A)

Interdisciplinary Graduate Program in Neuroscience, The University of Iowa, Iowa City, Iowa, USA; Department of Occupational and Environmental Health, The University of Iowa, Iowa City, Iowa, USA.

Hui Wang (H)

Department of Occupational and Environmental Health, The University of Iowa, Iowa City, Iowa, USA.

Michael S Chimenti (MS)

Iowa Institute of Human Genetics, Bioinformatics Division, The University of Iowa, Iowa City, Iowa, USA.

Andrea Adamcakova-Dodd (A)

Department of Occupational and Environmental Health, The University of Iowa, Iowa City, Iowa, USA.

Xuefang Jing (X)

Department of Occupational and Environmental Health, The University of Iowa, Iowa City, Iowa, USA.

Xueshu Li (X)

Department of Occupational and Environmental Health, The University of Iowa, Iowa City, Iowa, USA.

David K Meyerholz (DK)

Department of Pathology, Carver College of Medicine, The University of Iowa, Iowa City, Iowa, USA.

Peter S Thorne (PS)

Department of Occupational and Environmental Health, The University of Iowa, Iowa City, Iowa, USA.

Hans-Joachim Lehmler (HJ)

Department of Occupational and Environmental Health, The University of Iowa, Iowa City, Iowa, USA.

James A Ankrum (JA)

Roy J. Carver Department of Biomedical Engineering, The University of Iowa, Iowa City, Iowa, USA; Fraternal Order of Eagles Diabetes Research Center, The University of Iowa, Iowa City, Iowa, USA.

Aloysius J Klingelhutz (AJ)

Department of Microbiology and Immunology, Carver College of Medicine, The University of Iowa, Iowa City, Iowa, USA; Fraternal Order of Eagles Diabetes Research Center, The University of Iowa, Iowa City, Iowa, USA.

Classifications MeSH