Laboratory of Biology and Physiology of Organisms/Molecular Modelling Endothlial Dysfunction and Diabetes, Faculty of Biological Sciences, University of Science and Technology Houari Boumediene (USTHB), P.O. Box 32, El Alia, Dar El Beida, 16111 Alger, Algeria.
Laboratory of Biology and Physiology of Organisms/Molecular Modelling Endothlial Dysfunction and Diabetes, Faculty of Biological Sciences, University of Science and Technology Houari Boumediene (USTHB), P.O. Box 32, El Alia, Dar El Beida, 16111 Alger, Algeria.
C R Biol. 2019 Jun-Aug;342(5-6):209-219. doi: 10.1016/j.crvi.2019.04.003.
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.
本研究旨在首次展示高热量饮食对沙鼠肝细胞中线粒体重排的影响,沙鼠是代谢综合征的典型动物模型。通过标准实验室饮食(SD)喂养动物 9 个月来诱导代谢和氧化应激。评估了代谢参数、肝丙二醛(MDA)和谷胱甘肽(GSH)。通过使用 CD3 和 CD20 抗体进行组织病理学和免疫组织化学检查,研究了病理演变。通过透射电子显微镜观察线粒体结构的动态。SD 导致了这种动物的脂肪变性,在氧化和代谢应激的影响下,适应性炎症和纤维化的出现导致动物发展到肝硬化阶段,严重的肝细胞损伤引发了最初的线粒体融合-分裂循环,试图保持线粒体完整和功能,但肝细胞的氧化损伤增加,导致线粒体改变和功能障碍的恶性循环,并通过线粒体自噬消除它们。P. obesus 是治疗研究的优秀动物模型,针对的是脂肪变性进展中线粒体功能障碍。