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核因子E2相关因子2/血红素加氧酶-1(Nrf2/HO-1)信号通路在酒精性肝病中的作用

马成 杨慧

引用本文:
Citation:

核因子E2相关因子2/血红素加氧酶-1(Nrf2/HO-1)信号通路在酒精性肝病中的作用

DOI: 10.3969/j.issn.1001-5256.2023.07.028
基金项目: 

山西省省筹资金资助留学人员科研项目 (2020-168)

利益冲突声明:本文不存在任何利益冲突。
作者贡献声明:马成负责收集文献,撰写论文;杨慧负责拟定写作思路,指导撰写文章,最后定稿及经费支持。
详细信息
    通信作者:

    杨慧,576371816@qq.com (ORCID:0000-0002-9162-6951)

Role of the nuclear factor erythroid 2-related factor 2/heme oxygenase-1 signaling pathway in alcoholic liver disease

Research funding: 

Scientific Research Project of Shanxi Province Raises Funds to Support Overseas Students (2020-168)

More Information
  • 摘要: 酒精性肝病(ALD)在我国的发病率逐年上升,国民的疾病负担日益增加。肝细胞的氧化应激反应是ALD的重要致病机制。核因子E2相关因子2/血红素加氧酶-1(Nrf2/HO-1)信号通路是人体重要的内源性抗氧化应激通路,在氧化应激作用下,Nrf2被激活并发挥其转录活性诱导HO-1高表达。HO-1是体内重要的氧化应激反应蛋白,与其血红素酶解产物(胆红素、CO、铁)共同发挥着抗炎、抗氧化及调控细胞凋亡的作用。本文将对近年来Nrf2/HO-1信号通路在ALD中的研究进展进行综述,力求为ALD的发生发展寻找理论依据及治疗切入点。

     

  • 图  1  Nrf2和Keap1分子的结构域

    注:a,Nrf2;b,Keap1。

    Figure  1.  The schematic diagram of Nrf2 and Keap1 domain structure

    图  2  Nrf2/HO-1信号通路的调控机制

    Figure  2.  The illustration of regulatory mechanisms for Nrf2/HO-1 signaling pathway

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  • 收稿日期:  2022-09-20
  • 录用日期:  2022-11-21
  • 出版日期:  2023-07-20
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