Xenobiotic-Induced Aggravation of Metabolic-Associated Fatty Liver Disease.


Journal

International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791

Informations de publication

Date de publication:
19 Jan 2022
Historique:
received: 14 12 2021
revised: 11 01 2022
accepted: 15 01 2022
entrez: 15 2 2022
pubmed: 16 2 2022
medline: 9 4 2022
Statut: epublish

Résumé

Metabolic-associated fatty liver disease (MAFLD), which is often linked to obesity, encompasses a large spectrum of hepatic lesions, including simple fatty liver, steatohepatitis, cirrhosis and hepatocellular carcinoma. Besides nutritional and genetic factors, different xenobiotics such as pharmaceuticals and environmental toxicants are suspected to aggravate MAFLD in obese individuals. More specifically, pre-existing fatty liver or steatohepatitis may worsen, or fatty liver may progress faster to steatohepatitis in treated patients, or exposed individuals. The mechanisms whereby xenobiotics can aggravate MAFLD are still poorly understood and are currently under deep investigations. Nevertheless, previous studies pointed to the role of different metabolic pathways and cellular events such as activation of de novo lipogenesis and mitochondrial dysfunction, mostly associated with reactive oxygen species overproduction. This review presents the available data gathered with some prototypic compounds with a focus on corticosteroids and rosiglitazone for pharmaceuticals as well as bisphenol A and perfluorooctanoic acid for endocrine disruptors. Although not typically considered as a xenobiotic, ethanol is also discussed because its abuse has dire consequences on obese liver.

Identifiants

pubmed: 35162986
pii: ijms23031062
doi: 10.3390/ijms23031062
pmc: PMC8834714
pii:
doi:

Substances chimiques

Xenobiotics 0

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : European Union
ID : 825489

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Auteurs

Julie Massart (J)

Institut NUMECAN (Nutrition Metabolisms and Cancer), UMR_A 1341, UMR_S 1241, INSERM, University Rennes, INRAE, F-35000 Rennes, France.

Karima Begriche (K)

Institut NUMECAN (Nutrition Metabolisms and Cancer), UMR_A 1341, UMR_S 1241, INSERM, University Rennes, INRAE, F-35000 Rennes, France.

Anne Corlu (A)

Institut NUMECAN (Nutrition Metabolisms and Cancer), UMR_A 1341, UMR_S 1241, INSERM, University Rennes, INRAE, F-35000 Rennes, France.

Bernard Fromenty (B)

Institut NUMECAN (Nutrition Metabolisms and Cancer), UMR_A 1341, UMR_S 1241, INSERM, University Rennes, INRAE, F-35000 Rennes, France.

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