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首页> 外文期刊>International immunopharmacology >Combined ischemic and rapamycin preconditioning alleviated liver ischemia and reperfusion injury by restoring autophagy in aged mice
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Combined ischemic and rapamycin preconditioning alleviated liver ischemia and reperfusion injury by restoring autophagy in aged mice

机译:结合缺血性和雷帕霉素预处理缓解肝脏缺血和再灌注损伤通过恢复老年小鼠的自噬

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摘要

Old livers are more damaged by hepatic ischemia and reperfusion (IR) injury than young livers. The aim of this study was to investigate the effects of ischemic and rapamycin preconditioning on IR injury in old livers. Young (8-week-old) and aged (60-week-old) mice were subjected to IR or a sham control procedure. The aged mice were randomly divided into six groups: IR (CON), IR with ischemic preconditioning (IPC), IR with rapamycin preconditioning (RAPA), IR with combined ischemic and rapamycin preconditioning (IPC + RAPA), IR with 3-methyladenine (3-MA), IR with combined ischemic and rapamycin preconditioning with 3-MA pretreatment (IPC + RAPA +3-MA). Liver injury was evaluated 6 h after reperfusion. Hepatocellular autophagy induction was also analyzed by western blotting. The results revealed that aged mice had aggravated liver IR injury as compared to young mice. In aged mice following IR, IPC + RAPA but not IPC or RAPA alleviated liver injury, as evidenced by lower levels of serum ALT, improved preservation of liver architecture with lower Suzuki scores, and decreased caspase-3 activity compared with CON. In addition, western blot analysis revealed increased LC3B II but decreased p62 protein expression levels in the IPC + RAPA group, indicating that autophagic flux was restored by combined ischemic and rapamycin preconditioning. Furthermore, autophagy inhibition by the inhibitor 3-MA abrogated the protective role in the IPC + RAPA group, while no significant effects were observed in the CON group. In conclusions, our results demonstrated that combined ischemic and rapamycin preconditioning protected old livers against IR injury, which was likely attributed to restored autophagy activation.
机译:肝脏缺血和再灌注(IR)伤害而不是年轻肝脏的旧肝脏更受损。本研究的目的是探讨缺血性和雷帕霉素预处理对旧肝脏IR损伤的影响。杨(8周龄)和年龄(60周龄)小鼠进行IR或假控制程序。将老年的小鼠随机分为六组:IR(CON),IR,缺血预处理(IPC),IR与雷帕霉素预处理(RAPA),IR组合缺血性和雷帕霉素预处理(IPC + RAPA),IR与3-甲基腺嘌呤( 3- mA),IR具有组合缺血性和雷帕霉素预处理,具有3 mA预处理(IPC + Rapa + 3-mA)。再灌注后6小时评估肝损伤。蛋白质印迹还分析了肝细胞癌诱导。结果表明,与幼小小鼠相比,老年小鼠肝脏红外损伤加剧。在IR,IPC + Rapa之后的老年小鼠,而不是IPC或Rapa缓解肝损伤,如血清ALT水平的较低,改善了肝脏结构的保护,与孔相比降低了Caspase-3活性。此外,Western印迹分析显示IPC + RAPA组的LC3B II增加,但降低了P62蛋白表达水平,表明通过组合缺血和雷帕霉素预处理恢复自噬助焊剂。此外,抑制剂3-mA的自噬抑制废除了IPC + RAPA组中的保护作用,而在CON组中没有观察到显着影响。在结论中,我们的结果表明,组合缺血和雷帕霉素预处理保护的旧肝脏免受IR伤害,这可能归因于恢复的自噬激活。

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  • 来源
    《International immunopharmacology》 |2019年第2019期|共6页
  • 作者单位

    Nanjing Med Univ Affiliated Hosp 1 Hepatobiliary Liver Transplantat Ctr Nanjing 210029 Jiangsu;

    Nanjing Med Univ Affiliated Hosp 1 Hepatobiliary Liver Transplantat Ctr Nanjing 210029 Jiangsu;

    Nanjing Med Univ Affiliated Hosp 1 Dept Anesthesiol Nanjing Jiangsu Peoples R China;

    Nanjing Med Univ Affiliated Hosp 1 Dept Anesthesiol Nanjing Jiangsu Peoples R China;

    Nanjing Med Univ Affiliated Hosp 1 Hepatobiliary Liver Transplantat Ctr Nanjing 210029 Jiangsu;

    Nanjing Med Univ Affiliated Hosp 1 Hepatobiliary Liver Transplantat Ctr Nanjing 210029 Jiangsu;

    Nanjing Med Univ Affiliated Hosp 1 Hepatobiliary Liver Transplantat Ctr Nanjing 210029 Jiangsu;

    Nanjing Med Univ Affiliated Hosp 1 Hepatobiliary Liver Transplantat Ctr Nanjing 210029 Jiangsu;

    Nanjing Med Univ Affiliated Hosp 1 Hepatobiliary Liver Transplantat Ctr Nanjing 210029 Jiangsu;

    Nanjing Med Univ Affiliated Hosp 1 Hepatobiliary Liver Transplantat Ctr Nanjing 210029 Jiangsu;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 药理学;
  • 关键词

    Liver ischemia and reperfusion injury; Ischemic preconditioning; Rapamycin preconditioning; Autophagy; Aging;

    机译:肝脏缺血和再灌注损伤;缺血预处理;雷帕霉素预处理;自噬;老龄化;

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