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首页> 外文期刊>Food & Function >Protection of hepatocyte mitochondrial function by blueberry juice and probiotics via SIRT1 regulation in non-alcoholic fatty liver disease
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Protection of hepatocyte mitochondrial function by blueberry juice and probiotics via SIRT1 regulation in non-alcoholic fatty liver disease

机译:非酒精脂肪肝病中的蓝莓汁和益生菌对肝细胞线粒体功能的保护

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摘要

Mitochondrial dysfunction has been implicated in the pathogenesis of nonalcoholic fatty liver disease (NAFLD). Our previous study has firstly reported that blueberry juice and probiotics (BP) effectively protect liver function in NAFLD. However, the role of BP in hepatic mitochondria is unknown. Here, we aimed to investigate the effects and mechanisms of BP on the mitochondrial function and oxidative stress of rats with NAFLD. The NAFLD rat models were established and treated with BP and SIRT1 siRNA. The mitochondrial ultrastructure was analyzed by electron microscopy, reactive oxygen species (ROS) was detected by immunofluorescence, and biomarkers of mitochondrial function and oxidative stress were examined via quantitative reverse transcription-PCR, western blot, and immunohistochemistry. Results revealed that BP significantly reversed the NAFLD-induced hepatic mitochondrial damage, mitochondrial swelling, and hepatic necrosis. In particular, BP significantly restored the mitochondrial respiratory function of NAFLD rats by decreasing state 4 and 3 respiration rates, by increasing the respiration control ratio (RCR) and the ADP/O ratio, and by enhancing ATP, ADP, AMP, and EC syntheses. Moreover, BP reduced mitochondrial oxidative stress in NAFLD by decreasing the MDA level, elevating the GSH and SOD levels, and suppressing the ROS activity. Importantly, SIRT1 deficiency significantly abolished the effects of BP on the mitochondria and oxidative stress. Furthermore, BP reversed the decline of PGC-1 expression induced by NAFLD, while SIRT1 silencing significantly suppressed the effects of BP on PGC-1. In conclusion, BP might effectively protect rats against mitochondrial dysfunction during NAFLD as potential ingredients of functional food, by modulating the SIRT1 expression. Potential endogenous modulators of NAFLD pathogenesis may ultimately provide novel tools for therapeutic intervention.
机译:线粒体功能障碍涉及非酒精性脂肪肝疾病(NAFLD)的发病机制。我们以前的研究首先报道,蓝莓汁和益生菌(BP)有效保护NAFLD肝功能。然而,BP在肝线粒体中的作用是未知的。在这里,我们旨在探讨BP对NAFLD大鼠线粒体功能和氧化应激的影响和机制。建立并用BP和SIRT1 siRNA建立并治疗NAFLD大鼠模型。通过电子显微镜分析线粒体超微结构,通过免疫荧光检测反应性氧物质(ROS),通过定量逆转录-PCR,Western印迹和免疫组化检查线粒体功能和氧化胁迫的生物标志物。结果表明,BP显着逆转了NAFLD诱导的肝线粒体损伤,线粒体肿胀和肝脏坏死。特别地,通过增加呼吸控制比(RCR)和ADP / O比率,通过增加呼吸控制比率(RCR)和增强ATP,ADP,AMP和EC合成,BP通过降低状态4和3呼吸速率显着恢复NAFLD大鼠的线粒体呼吸功能。 。此外,BP通过降低MDA水平,升高GSH和SOD水平,抑制ROS活性,BP降低了NAFLD中的线粒体氧化应激。重要的是,SIRT1缺陷显着消除了BP对线粒体和氧化应激的影响。此外,BP逆转NAFLD诱导的PGC-1表达的下降,而SIRT1沉默显着抑制了BP对PGC-1的影响。总之,通过调节SIRT1表达,BP可以有效地保护大鼠NAFLD作为功能性食物的潜在成分。 NAFLD发病机制的潜在内源性调节剂最终可能是用于治疗干预的新型工具。

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  • 来源
    《Food & Function》 |2019年第3期|共12页
  • 作者单位

    Guizhou Med Univ Affiliated Hosp Dept Physiol &

    Chem Guiyang 550004 Guizhou Peoples R China;

    Guizhou Med Univ Affiliated Hosp Dept Blood Transfus Guiyang 550004 Guizhou Peoples R China;

    Guizhou Med Univ Grad Sch Guiyang 550004 Guizhou Peoples R China;

    Guizhou Med Univ Baiyun Hosp Dept Blood Transfus Guiyang 550004 Guizhou Peoples R China;

    Guizhou Med Univ Affiliated Hosp Dept Clin Examinat Guiyang 550004 Guizhou Peoples R China;

    Guiyang Dent Hosp Guiyang 550003 Guizhou Peoples R China;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 食品工业;
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