Gene expression and DNA methylation as mechanisms of disturbed metabolism in offspring after exposure to a prenatal HF diet.


Journal

Journal of lipid research
ISSN: 1539-7262
Titre abrégé: J Lipid Res
Pays: United States
ID NLM: 0376606

Informations de publication

Date de publication:
07 2019
Historique:
received: 21 01 2019
revised: 03 05 2019
pubmed: 9 5 2019
medline: 14 7 2020
entrez: 9 5 2019
Statut: ppublish

Résumé

Exposure to a prenatal high-fat (HF) diet leads to an impaired metabolic phenotype in mouse offspring. The underlying mechanisms, however, are not yet fully understood. Therefore, this study investigated whether the impaired metabolic phenotype may be mediated through altered hepatic DNA methylation and gene expression. We showed that exposure to a prenatal HF diet altered the offspring's hepatic gene expression of pathways involved in lipid synthesis and uptake (SREBP), oxidative stress response [nuclear factor (erythroid-derived 2)-like 2 (Nrf2)], and cell proliferation. The downregulation of the SREBP pathway related to previously reported decreased hepatic lipid uptake and postprandial hypertriglyceridemia in the offspring exposed to the prenatal HF diet. The upregulation of the Nrf2 pathway was associated with increased oxidative stress levels in offspring livers. The prenatal HF diet also induced hypermethylation of transcription factor (TF) binding sites upstream of lipin 1 (

Identifiants

pubmed: 31064776
pii: S0022-2275(20)31057-9
doi: 10.1194/jlr.M092593
pmc: PMC6602131
doi:

Substances chimiques

DNA 9007-49-2
Lpin1 protein, mouse EC 3.1.3.4
Phosphatidate Phosphatase EC 3.1.3.4

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1250-1259

Informations de copyright

Copyright © 2019 Rouschop et al. Published by The American Society for Biochemistry and Molecular Biology, Inc.

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Auteurs

Sven H Rouschop (SH)

Department of Pharmacology and Toxicology, NUTRIM School of Nutrition and Translational Research in Metabolism, Maastricht University, Maastricht, The Netherlands.

Tanja Karl (T)

Department of Biosciences University of Salzburg, Salzburg, Austria.

Angela Risch (A)

Department of Biosciences University of Salzburg, Salzburg, Austria.

Petronella A van Ewijk (PA)

Department of Radiology and Nuclear Medicine Maastricht University Medical Center, Maastricht, The Netherlands.

Vera B Schrauwen-Hinderling (VB)

Department of Radiology and Nuclear Medicine Maastricht University Medical Center, Maastricht, The Netherlands.

Antoon Opperhuizen (A)

Department of Pharmacology and Toxicology, NUTRIM School of Nutrition and Translational Research in Metabolism, Maastricht University, Maastricht, The Netherlands.
Netherlands Food and Consumer Product Safety Authority (NVWA), Utrecht, The Netherlands.

Frederik J van Schooten (FJ)

Department of Pharmacology and Toxicology, NUTRIM School of Nutrition and Translational Research in Metabolism, Maastricht University, Maastricht, The Netherlands.

Roger W Godschalk (RW)

Department of Pharmacology and Toxicology, NUTRIM School of Nutrition and Translational Research in Metabolism, Maastricht University, Maastricht, The Netherlands r.godschalk@maastrichuniversity.nl.

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