Xenobiotic-Induced Aggravation of Metabolic-Associated Fatty Liver Disease

被引:29
作者
Massart, Julie [1 ]
Begriche, Karima [1 ]
Corlu, Anne [1 ]
Fromenty, Bernard [1 ]
机构
[1] Univ Rennes, Inst NUMECAN Nutr Metabolisms & Canc, INRAE, INSERM,UMR A 1341,UMR S 1241, F-35000 Rennes, France
基金
欧盟地平线“2020”;
关键词
obesity; fatty liver; NASH; drugs; environmental contaminants; endocrine disruptors; ethanol; PERFLUOROOCTANOIC ACID EXPOSURE; ENDOPLASMIC-RETICULUM STRESS; HEPATIC GENE-EXPRESSION; DIET-INDUCED OBESITY; BISPHENOL-A; NONALCOHOLIC STEATOHEPATITIS; LIPID-ACCUMULATION; ALCOHOL-CONSUMPTION; BINGE ETHANOL; IN-VITRO;
D O I
10.3390/ijms23031062
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
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页数:23
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