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Role of Mesencephalic Astrocyte-Derived Neurotrophic Factor in Alcohol-Induced Liver Injury

机译:中脑星形胶质细胞衍生神经营养因子在醇诱导的肝损伤中的作用

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Consumption of alcohol in immoderate quantity induces endoplasmic reticulum (ER) stress response (alcohol-induced ER stress). Mesencephalic astrocyte-derived neurotrophic factor (MANF), an ER stress-inducible protein, works as an evolutionarily conserved regulator of systemic and liver metabolic homeostasis. In this study, the effects of MANF on alcohol-induced liver injury were explored by using hepatocyte-specific MANF-knockout mice (MANFΔHep) in a chronic-plus-binge alcohol feeding model. We found that alcohol feeding upregulated MANF expression and MANFΔHep mice exhibited more severe liver injury with extra activated ER stress after alcohol feeding. In addition, we found that MANF deficiency activated iNOS and p65 and increased the production of NO and anti-inflammatory cytokines, which was further enhanced after alcohol treatment. Meanwhile, MANF deletion upregulated the levels of CYP2E1, 4-HNE, and MDA and downregulated the levels of GSH and SOD. These results indicate that MANF has potential protection on alcohol-induced liver injury, and the underlying mechanisms may be associated with meliorating the overactivated ER stress triggered by inflammation and oxidative stress via inhibiting and reducing NO/NF-κB and CYP2E1/ROS, respectively. Therefore, MANF might be a negative regulator in alcohol-induced ER stress and participate in the crosstalk between the NF-κB pathway and oxidative stress in the liver. Conclusions. This study identifies a specific role of MANF in alcohol-induced liver injury, which may provide a new approach for the treatment of ALI.
机译:在不加工量中消耗醇诱导内质网(ER)应激反应(醇诱导的ER应力)。成分术星形胶质细胞衍生的神经营养因子(MANF),ER应激诱导蛋白,作为全身和肝脏代谢稳态的进化保护稳压因子。在这项研究中,通过使用慢性加液饮料喂养模型中的肝细胞特异性曼夫敲除小鼠(MANFΔHEP)探讨了MANF对酒精诱导的肝损伤的影响。我们发现酒精喂养上调的MANF表达和ManfδHep小鼠表现出更严重的肝损伤,并在饮食后额外的活化ER应激。此外,我们发现曼菲缺乏激活INOS和P65并增加了NO和抗炎细胞因子的产生,在醇处理后进一步提高。同时,曼夫缺失上调CYP2E1,4-HNE和MDA的水平,并下调了GSH和SOD的水平。这些结果表明,MANF对醇诱导的肝损伤具有潜在的保护,并且潜在的机制可以分别通过抑制和减少NO / NF-κB和CYP2E1 / RO来改变通过炎症和氧化应激引发的过度活化的ER应力。因此,MANF可能是醇诱导的ER应激中的负调节剂,并参与肝脏中NF-κB途径和氧化应激之间的串扰。结论。该研究识别人类在醇诱导的肝损伤中的特定作用,这可以为治疗ALI提供一种新方法。

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