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营养保健品水飞蓟宾可对抗非酒精性脂肪性肝病进展模型中的脂质过度积累和持续氧化应激。

The Nutraceutic Silybin Counteracts Excess Lipid Accumulation and Ongoing Oxidative Stress in an Model of Non-Alcoholic Fatty Liver Disease Progression.

作者信息

Vecchione Giulia, Grasselli Elena, Cioffi Federica, Baldini Francesca, Oliveira Paulo J, Sardão Vilma A, Cortese Katia, Lanni Antonia, Voci Adriana, Portincasa Piero, Vergani Laura

机构信息

DISTAV, Department of Earth, Environment and Life Sciences, University of Genova, Genoa, Italy.

Department of Science and Technology, University of Sannio, Benevento, Italy.

出版信息

Front Nutr. 2017 Sep 19;4:42. doi: 10.3389/fnut.2017.00042. eCollection 2017.

Abstract

Non-alcoholic fatty liver disease (NAFLD) is a major cause of liver-related morbidity and mortality. Oxidative stress and release of pro-inflammatory cytokines, such as tumor necrosis factor α (TNFα), are major consequences of hepatic lipid overload, which can contribute to progression of NAFLD to non-alcoholic steatohepatitis (NASH). Also, mitochondria are involved in the NAFLD pathogenesis for their role in hepatic lipid metabolism. Definitive treatments for NAFLD/NASH are lacking so far. Silybin, the extract of the milk thistle seeds, has previously shown beneficial effects in NAFLD. Sequential exposure of hepatocytes to high concentrations of fatty acids (FAs) and TNFα resulted in fat overload and oxidative stress, which mimic the progression of NAFLD from simple steatosis (SS) to steatohepatitis (SH). The exposure to 50 µM silybin for 24 h reduced fat accumulation in the model of NAFLD progression. The progression of NAFLD from SS to SH resulted in reduced hepatocyte viability, increased apoptosis and oxidative stress, reduction in lipid droplet size, and up-regulation of IκB kinase β-interacting protein and adipose triglyceride lipase expressions. The direct action of silybin on SS or SH cells and the underlying mechanisms were assessed. Beneficial action of silybin was sustained by changes in expression/activity of peroxisome proliferator-activated receptors and enzymes for FA oxidation. Moreover, silybin counteracted the FA-induced mitochondrial damage by acting on complementary pathways: (i) increased the mitochondrial size and improved the mitochondrial cristae organization; (ii) stimulated mitochondrial FA oxidation; (iii) reduced basal and maximal respiration and ATP production in SH cells; (iv) stimulated ATP production in SS cells; and (v) rescued the FA-induced apoptotic signals and oxidative stress in SH cells. We provide new insights about the direct protective effects of the nutraceutic silybin on hepatocytes mimicking NAFLD progression.

摘要

非酒精性脂肪性肝病(NAFLD)是肝脏相关发病和死亡的主要原因。氧化应激和促炎细胞因子如肿瘤坏死因子α(TNFα)的释放是肝脏脂质过载的主要后果,这可能导致NAFLD进展为非酒精性脂肪性肝炎(NASH)。此外,线粒体因其在肝脏脂质代谢中的作用而参与NAFLD发病机制。迄今为止,尚无针对NAFLD/NASH的确定性治疗方法。水飞蓟宾是水飞蓟种子的提取物,此前已显示对NAFLD有有益作用。肝细胞先后暴露于高浓度脂肪酸(FAs)和TNFα会导致脂肪过载和氧化应激,这模拟了NAFLD从单纯性脂肪变性(SS)进展为脂肪性肝炎(SH)的过程。在NAFLD进展模型中,暴露于50μM水飞蓟宾24小时可减少脂肪积累。NAFLD从SS进展为SH导致肝细胞活力降低、凋亡增加和氧化应激,脂滴大小减小,以及IκB激酶β相互作用蛋白和脂肪甘油三酯脂肪酶表达上调。评估了水飞蓟宾对SS或SH细胞的直接作用及其潜在机制。水飞蓟宾的有益作用通过过氧化物酶体增殖物激活受体和FA氧化酶的表达/活性变化得以维持。此外,水飞蓟宾通过作用于互补途径抵消了FA诱导的线粒体损伤:(i)增加线粒体大小并改善线粒体嵴的组织;(ii)刺激线粒体FA氧化;(iii)降低SH细胞的基础呼吸和最大呼吸以及ATP产生;(iv)刺激SS细胞中的ATP产生;(v)挽救SH细胞中FA诱导的凋亡信号和氧化应激。我们提供了关于营养保健品水飞蓟宾对模拟NAFLD进展的肝细胞的直接保护作用的新见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ae0/5609553/d2386d97b695/fnut-04-00042-g001.jpg

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