Sphingolipid metabolism in non-alcoholic fatty liver diseases

Non-alcoholic fatty liver disease (NAFLD) involves a panel of pathologies starting with hepatic steatosis and continuing to irreversible and serious conditions like steatohepatitis (NASH) and hepatocarcinoma. NAFLD is multifactorial in origin and corresponds to abnormal fat deposition in liver. Even...

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Veröffentlicht in:Biochimie 2019-04, Vol.159 (159), p.9-22
Hauptverfasser: Régnier, Marion, Polizzi, Arnaud, Guillou, Hervé, Loiseau, Nicolas
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Sprache:eng
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Zusammenfassung:Non-alcoholic fatty liver disease (NAFLD) involves a panel of pathologies starting with hepatic steatosis and continuing to irreversible and serious conditions like steatohepatitis (NASH) and hepatocarcinoma. NAFLD is multifactorial in origin and corresponds to abnormal fat deposition in liver. Even if triglycerides are mostly associated with these pathologies, other lipid moieties seem to be involved in the development and severity of NAFLD. That is the case with sphingolipids and more particularly ceramides. In this review, we explore the relationship between NAFLD and sphingolipid metabolism. After providing an analysis of complex sphingolipid metabolism, we focus on the potential involvement of sphingolipids in the different pathologies associated with NAFLD. An unbalanced ratio between ceramides and terminal metabolic products in the liver and plasma promotes weight gain, inflammation, and insulin resistance. In the etiology of NAFLD, some sphingolipid species such as ceramides may be potential biomarkers for NAFLD. We review the clinical relevance of sphingolipids in liver diseases. •This review covers a hot topic in the development of NAFLD in humans.•Overview of sphingolipid metabolism in mammals and their role in the development of non-alcoholic fatty liver diseases.•The levels of some sphingolipid metabolites are key players in the development of NAFLD.•Sphingolipid metabolites play key role in weight-gain, inflammation and insulin-resistance.•Sphingolipid metabolites could also play as mediators in organ cross-talk which seemed to play a role in NAFLD.
ISSN:0300-9084
1638-6183
DOI:10.1016/j.biochi.2018.07.021