脂肪变性
氧化应激
脂肪性肝炎
内科学
生物
内分泌学
胰岛素抵抗
肝硬化
线粒体
脂肪肝
线粒体分裂
粒体自噬
肝细胞
胰岛素
医学
细胞生物学
生物化学
自噬
细胞凋亡
体外
疾病
作者
Ouahiba Sihali-Beloui,Djamila Aroune,Fella Benazouz,Adile Hadji,Salima El-Aoufi,Sergio Marco
标识
DOI:10.1016/j.crvi.2019.04.003
摘要
The aim of this study was to show, for the first time, the effect of a hypercaloric diet on the mitochondrial reshuffle of hepatocytes during the progression from steatosis to steatohepatitis to cirrhosis in Psammomys obesus, a typical animal model of the metabolic syndrome. Metabolic and oxidative stresses were induced by feeding the animal through a standard laboratory diet (SD) for nine months. Metabolic parameters, liver malondialdehyde (MDA) and glutathione (GSH), were evaluated. The pathological evolution was examined by histopathology and immunohistochemistry, using CD3 and CD20 antibodies. The dynamics of the mitochondrial structure was followed by transmission electron microscopy. SD induced a steatosis in this animal that evolved under the effect of oxidative and metabolic stress by the appearance of adaptive inflammation and fibrosis leading the animal to the cirrhosis stage with serious hepatocyte damage by the triggering, at first the mitochondrial fusion-fission cycles, which attempted to maintain the mitochondria intact and functional, but the hepatocellular oxidative damage was increased inducing a vicious circle of mitochondrial alteration and dysfunction and their elimination by mitophagy. P. obesus is an excellent animal model of therapeutic research that targets mitochondrial dysfunction in the progression of steatosis.
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