Acetaminophen-Induced Hepatotoxicity in Obesity and Nonalcoholic Fatty Liver Disease: A Critical Review.

acetaminophen cytochrome P450 2E1 diabetes drug-induced liver injury fatty acids mitochondria nonalcoholic fatty liver disease nonalcoholic steatohepatitis obesity steatosis

Journal

Livers
ISSN: 2673-4389
Titre abrégé: Livers
Pays: Switzerland
ID NLM: 9918230902806676

Informations de publication

Date de publication:
Mar 2023
Historique:
entrez: 30 1 2023
pubmed: 31 1 2023
medline: 31 1 2023
Statut: ppublish

Résumé

The epidemic of obesity, type 2 diabetes and nonalcoholic liver disease (NAFLD) favors drug consumption, which augments the risk of adverse events including liver injury. For more than 30 years, a series of experimental and clinical investigations reported or suggested that the common pain reliever acetaminophen (APAP) could be more hepatotoxic in obesity and related metabolic diseases, at least after an overdose. Nonetheless, several investigations did not reproduce these data. This discrepancy might come from the extent of obesity and steatosis, accumulation of specific lipid species, mitochondrial dysfunction and diabetes-related parameters such as ketonemia and hyperglycemia. Among these factors, some of them seem pivotal for the induction of cytochrome P450 2E1 (CYP2E1), which favors the conversion of APAP to the toxic metabolite N-acetyl-

Identifiants

pubmed: 36713231
doi: 10.3390/livers3010003
pmc: PMC9879315
mid: NIHMS1866665
doi:

Types de publication

Journal Article

Langues

eng

Pagination

33-53

Subventions

Organisme : NIGMS NIH HHS
ID : P20 GM103549
Pays : United States

Déclaration de conflit d'intérêts

Conflicts of Interest: The authors declare no conflict of interest.

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Auteurs

Karima Begriche (K)

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

Clémence Penhoat (C)

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

Pénélope Bernabeu-Gentey (P)

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

Julie Massart (J)

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

Bernard Fromenty (B)

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

Classifications MeSH