PUBLICATION

Dimethyl fumarate reduces hepatocyte senescence following paracetamol exposure

Authors
Meseguer-Ripolles, J., Lucendo-Villarin, B., Tucker, C., Ferreira-Gonzalez, S., Homer, N., Wang, Y., Starkey Lewis, P.J., M Toledo, E., Mellado-Gomez, E., Simpson, J., Flint, O., Jaiswal, H., Beer, N.L., Karlsen, A.E., Forbes, S.J., Dear, J.W., Hughes, J., Hay, D.C.
ID
ZDB-PUB-210622-47
Date
2021
Source
iScience   24: 102552 (Journal)
Registered Authors
Keywords
Cell biology, Molecular biology, Toxicology, Transcriptomics
MeSH Terms
none
PubMed
34151225 Full text @ iScience
Abstract
Liver disease is a major cause of premature death. Oxidative stress in the liver represents a key disease driver. Compounds, such as dimethyl fumarate (DMF), can activate the antioxidant response and are used clinically to treat disease. In this study, we tested the protective properties of DMF before or after paracetamol exposure. Following DMF administration, Nrf2 nuclear translocation was tracked at the single-cell level and target gene transactivation confirmed. Next, the protective properties of DMF were examined following paracetamol exposure. Transcriptomic and biochemical analysis revealed that DMF rescue was underpinned by reduced Nf-kB and TGF-β signaling and cell senescence. Following on from these studies, we employed a Zebrafish model to study paracetamol exposure in vivo. We combined a genetically modified Zebrafish model, expressing green fluorescent protein exclusively in the liver, with automated microscopy. Pre-treatment with DMF, prior to paracetamol exposure, led to reduced liver damage in Zebrafish demonstrating protective properties.
Genes / Markers
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Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping