首页> 外文期刊>Biochemistry and Cell Biology >Formononetin protects against concanavalin-A-induced autoimmune hepatitis in mice through its anti-apoptotic and anti-inflammatory properties
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Formononetin protects against concanavalin-A-induced autoimmune hepatitis in mice through its anti-apoptotic and anti-inflammatory properties

机译:通过其抗凋亡和抗炎特性,Formononetin通过抗凋亡和抗炎性质来保护针对小鼠的自身免疫性肝炎

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摘要

Autoimmune hepatitis (AIH) is a chronic inflammatory liver disease that seriously threatens the health of humans globally. Formononetin (FMN) is a natural herb extract with multiple biological functions. In this study, an experimental model of AIH was established in mice through the use of concanavalin A (ConA). To investigate the effects of FMN on ConA-induced hepatitis, the mice were pretreated with 50 or 100 mg/kg body mass of FMN. The results show that FMN alleviated ConA-induced liver injury of mice in a dose-dependent manner. Moreover, pretreatment with FMN inhibited the apoptosis of hepatocytes in the ConA-treated mice through downregulating the expression of pro-apoptotic proteins (Bax, cleaved caspase 9, and cleaved caspase 3) and upregulating the expression of anti-apoptotic protein (Bcl-2). It was also found that the levels of proinflammatory cytokines were greatly reduced in the serum and liver tissues of mice pretreated with FMN. Further studies showed that FMN reduced the level of phosphorylated nuclear factor kappa B (p-NF-kappa B) p65 and enhanced the level of I kappa B alpha (inhibitor of NF-kappa B), suggesting that FMN inhibits the activation of the NF-kappa B signaling pathway. In addition, FMN inhibited activation of the NOD-like receptor protein 3 (NLRP3) inflammasome. Therefore, FMN could be a promising agent for the treatment of AIH.
机译:自身免疫性肝炎(AIH)是一种严重威胁全球人类健康的慢性炎症性肝病。 Formononetin(FMN)是一种具有多种生物学功能的天然草药提取物。在这项研究中,通过使用Concanavalin A(Cona)在小鼠中建立了AIH的实验模型。为了探讨FMN对Cona诱导的肝炎的影响,用50或100mg / kg体重的FMN预处理小鼠。结果表明,FMN以剂量依赖性方式缓解了Cona诱导的小鼠肝损伤。此外,通过下调促凋亡蛋白(Bax,Cleave Caspase 9和Cleaved Caspase 3)的表达,对FMN的预处理抑制了Cona处理的小鼠中肝细胞的凋亡并上调了抗凋亡蛋白的表达(Bcl-2 )。还发现,在用FMN预处理的小鼠的血清和肝组织中大大降低了促炎细胞因子的水平。进一步的研究表明,FMN降低了磷酸化核因子κB(P-NF-Kappa B)P65的水平,并增强了IκBα的水平(NF-Kappa B的抑制剂),表明FMN抑制了NF的激活-Kappa B信号通路。此外,FMN抑制了NOD样受体蛋白3(NLRP3)炎症的活化。因此,FMN可能是治疗AIH的有希望的剂。

著录项

  • 来源
    《Biochemistry and Cell Biology》 |2021年第2期|共10页
  • 作者单位

    Henan Univ Chinese Med Affiliated Hosp 1 Spleen Stomach &

    Hepatobiliary Dept Zhengzhou 450004;

    Henan Univ Chinese Med Affiliated Hosp 1 Spleen Stomach &

    Hepatobiliary Dept Zhengzhou 450004;

    Henan Univ Chinese Med Spleen Stomach &

    Hepatobiliary Dept Zhengzhou 450046 Peoples R China;

    Henan Univ Chinese Med Affiliated Hosp 1 Spleen Stomach &

    Hepatobiliary Dept Zhengzhou 450004;

    Henan Univ Chinese Med Affiliated Hosp 1 Spleen Stomach &

    Hepatobiliary Dept Zhengzhou 450004;

    Henan Univ Chinese Med Sch Basic Med Sci Zhengzhou 450046 Peoples R China;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 生物化学;
  • 关键词

    autoimmune hepatitis; formononetin; anti-apoptosis; anti-inflammation;

    机译:自身免疫性肝炎;蛋白质蛋白;抗细胞凋亡;抗炎;

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