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肝脂肪变性小鼠的线粒体适应。

Mitochondrial adaptation in steatotic mice.

机构信息

Institute of Molecular Toxicology and Pharmacology, Helmholtz Center Munich, German Research Center for Environmental Health, 85764 Neuherberg, Germany.

Department of Medicine II, Liver Center Munich, University Hospital LMU Munich, 81377 Munich, Germany.

出版信息

Mitochondrion. 2018 May;40:1-12. doi: 10.1016/j.mito.2017.08.015. Epub 2017 Sep 19.

Abstract

Western lifestyle-associated malnutrition causes steatosis that may progress to liver inflammation and mitochondrial dysfunction has been suggested as a key factor in promoting this disease. Here we have molecularly, biochemically and biophysically analyzed mitochondria from steatotic wild type and immune-compromised mice fed a Western diet (WD) - enriched in saturated fatty acids (SFAs). WD-mitochondria demonstrated lipidomic changes, a decreased mitochondrial ATP production capacity and a significant sensitivity to calcium. These changes preceded hepatocyte damage and were not associated with enhanced ROS production. Thus, WD-mitochondria do not promote steatohepatitis per se, but demonstrate bioenergetic deficits and increased sensitivity to stress signals.

摘要

西方生活方式相关的营养不良导致脂肪变性,可能进展为肝炎症和线粒体功能障碍,被认为是促进这种疾病的关键因素。在这里,我们从喂食富含饱和脂肪酸(SFAs)的西式饮食(WD)的肥胖野生型和免疫功能低下的小鼠中进行了线粒体的分子、生化和生物物理分析。WD-线粒体表现出脂质组学变化、线粒体 ATP 产生能力降低以及对钙的显著敏感性。这些变化先于肝细胞损伤,与增强的 ROS 产生无关。因此,WD-线粒体本身并不促进脂肪性肝炎,但表现出生物能量缺陷和对应激信号的敏感性增加。

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