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双硫死亡在非酒精性脂肪性肝病中的作用机制

严丽沙 陈煜 王学士 冯宪敏 孙洁

引用本文:
Citation:

双硫死亡在非酒精性脂肪性肝病中的作用机制

DOI: 10.12449/JCH241223
基金项目: 

吉林省自然科学基金 (YDZJ202201ZYTS145);

吉林省教育厅科学技术研究项目 (JJKH20210488KJ);

吉林医药学院国家级大学生创新创业训练计划项目 (202313706002)

利益冲突声明:本文不存在任何利益冲突。
作者贡献声明:严丽沙、陈煜负责查阅文献,撰写论文;严丽沙、孙洁、冯宪敏负责资料分析,设计课题;陈煜、王学士参与论文撰写及修改;孙洁和冯宪敏指导论文撰写、修改及校阅。
详细信息
    通信作者:

    冯宪敏, fengxianmin28@163.com (ORCID: 0000-0002-5079-350X)

    孙洁, sunjie1014@163.com (ORCID: 0009-0008-5226-9366)

Mechanism of action of disulfidptosis in nonalcoholic fatty liver disease

Research funding: 

Jilin Natural Science Foundation Project (YDZJ202201ZYTS145);

Jilin Provincial Education Department Project (JJKH20210488KJ);

Program for College Students’ Innovation and Entrepreneurship Training of Jilin Medical University (202313706002)

More Information
    Corresponding author: FENG Xianmin, fengxianmin28 @163.com (ORCID: 0000-0002-5079-350X); SUN Jie, sunjie1014@163.com (ORCID: 0009-0008-5226-9366)
  • 摘要: 双硫死亡是近年来提出的一种新型细胞死亡方式,其本质为烟酰胺腺嘌呤二核苷酸磷酸不足而导致的二硫化物应激性死亡。非酒精性脂肪性肝病(NAFLD)是一类以脂肪浸润为主要病理特征,与胰岛素抵抗和遗传易感性密切相关的代谢性疾病。最新研究显示,双硫死亡产生的二硫化物应激可导致肝细胞死亡,从而加快NAFLD的进展。本文就双硫死亡在NAFLD中的最新研究予以总结和分析,以期探讨双硫死亡在NAFLD中的应用潜力,为NAFLD的防治提供新思路。

     

  • 图  1  双硫死亡的作用机制(本图由Figdraw绘制)

    注: GLUT,葡萄糖转运体;SLC3A2,溶质载体家族3成员2;NADP+,烟酰胺腺嘌呤二核苷磷酸;G6P,葡萄糖-6-磷酸;G6PD,葡萄糖-6-磷酸酶;6PG,6-磷酸葡萄糖酸;PGD,磷酸葡萄糖酸脱氢酶;R5P,核糖-5-磷酸;F-actin,丝状肌动蛋白。

    Figure  1.  Biological mechanisms of disulfidptosis (By Figdraw)

    图  2  NADPH在正常肝脏和NAFLD肝脏中的作用机制(本图由Figdraw绘制)

    注: a,NADPH在正常肝脏中的作用;b,NADPH在NAFLD肝脏中的作用。GLU,葡萄糖;PPP,磷酸戊糖途径;IRS-PI3K-AKT,胰岛素受体底物-磷脂酰肌醇3-激酶-蛋白激酶B通路;InsR,胰岛素受体;TG,甘油三酯;FFA,游离脂肪酸;Acyl-CoA,脂酰辅酶A;FATP-1,脂肪酸转运蛋白1。

    Figure  2.  NADPH’s mechanism in the liver and the NAFLD liver (By Figdraw)

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  • 收稿日期:  2024-08-21
  • 录用日期:  2024-09-10
  • 出版日期:  2024-12-25
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