4.3 Article

Changes in Key Mitochondrial Lipids Accompany Mitochondrial Dysfunction and Oxidative Stress in NAFLD

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HINDAWI LTD
DOI: 10.1155/2021/9986299

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  1. INSERM
  2. French Regional Council of Pays de la Loire [2017-08542, 2017-02946/02947]
  3. scholarship Allocation de Recherche SFD jeune chercheur Francophone 2018 from the Societe Francophone du Diabete
  4. INSERM ATIP-Avenir [R16067NS-RSE17002NSA]
  5. Fondation Genavie

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NAFLD is a dysmetabolic hepatic damage that progresses through stages of increasing severity, with oxidative stress and specific hepatic lipid species playing potential roles in disease progression. A study on mouse livers with NAFLD induced by a western diet revealed time-dependent changes in mitochondrial lipid composition, suggesting mitochondrial lipid modifications may act as an early event in mitochondrial dysfunction and disease progression.
Nonalcoholic fatty liver disease (NAFLD) is a dysmetabolic hepatic damage of increasing severity: simple fat accumulation (steatosis), nonalcoholic steatohepatitis (NASH), and hepatic fibrosis. Oxidative stress is considered an important factor in producing hepatocyte injury associated with NAFLD progression. Studies also suggest a link between the accumulation of specific hepatic lipid species, mitochondrial dysfunction, and the progression of NAFLD. However, it is unclear whether mitochondrial lipid modifications are involved in NAFLD progression. To gain insight into the relationship between mitochondrial lipids and disease progression through different stages of NAFLD, we performed lipidomic analyses on mouse livers at different stages of western diet-induced NAFLD, with or without hepatic fibrosis. After organelle separation, we studied separately the mitochondrial and the nonmitochondrial hepatic lipidomes. We identified 719 lipid species from 16 lipid families. Remarkably, the western diet triggered time-dependent changes in the mitochondrial lipidome, whereas the nonmitochondrial lipidome showed little difference with levels of hepatic steatosis or the presence of fibrosis. In mitochondria, the changes in the lipidome preceded hepatic fibrosis. In particular, two critical phospholipids, phosphatidic acid (PA) and cardiolipin (CL), displayed opposite responses in mitochondria. Decrease in CL and increase in PA were concurrent with an increase of coenzyme Q. Electron paramagnetic resonance spectroscopy superoxide spin trapping and Cu2+ measurement showed the progressive increase in oxidative stress in the liver. Overall, these results suggest mitochondrial lipid modifications could act as an early event in mitochondrial dysfunction and NAFLD progression.

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