Blumeatin inhibits LPS-induced inflammation of TLR4/NF-κB signaling pathway via targeting TLR4/MD-2

被引:0
|
作者
Peng, Jun-Chao [1 ]
Qi, Wei-Jin [1 ]
Wang, Hong-Ying [1 ,2 ]
Zhou, Wei [3 ]
Yu, Xing-Jian [4 ]
Wang, Lu [1 ]
机构
[1] Minist Educ Dev & Utilizat Southwest Characterist, Engn Res Ctr, Guiyang 550025, Peoples R China
[2] Guizhou Univ, Coll Pharm, Guiyang 550025, Peoples R China
[3] Guizhou Med Univ, Guiyang 550025, Peoples R China
[4] Univ Calif Davis, Sch Med, Dept Biochem & Mol Med, Davis, CA 95817 USA
基金
中国国家自然科学基金;
关键词
Blumeatin; anti-inflammatory; target; TLR4/MD-2; signaling pathway; LPS; SMALL-MOLECULE; TLR4; MD-2; ENDOTOXIN; TAK-242;
D O I
10.1080/10286020.2025.2469690
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
TLR4/MD-2, a protein complex to recognize LPS, has become an ideal target for the treatment of inflammation-related diseases. Blumeatin (BL), which is isolated from Blumea balsamifera (L.) DC has rarely been reported in the inflammation field. In this article, we targeted the TLR4/MD-2 complex to explore how BL regulates the TLR4/NF-kappa B inflammatory signaling pathway and inhibits LPS-induced inflammation. BL can target the hydrophobic pocket of TLR4/MD-2, inhibit the binding of LPS to TLR4/MD-2, the dimerization of TLR4 and MD-2, and the TLR4/NF-kappa B signaling pathway activation and the secretion of downstream inflammatory factors. BL may be used as a molecular target of TLR4/MD-2 for the treatment of inflammation-related diseases.
引用
收藏
页数:14
相关论文
共 50 条
  • [31] Aloperine suppresses LPS-induced macrophage activation through inhibiting the TLR4/NF-κB pathway
    Yinyin Ye
    Yuwei Wang
    Yanlang Yang
    Liangfei Tao
    Inflammation Research, 2020, 69 : 375 - 383
  • [32] Aloperine suppresses LPS-induced macrophage activation through inhibiting the TLR4/NF-κB pathway
    Ye, Yinyin
    Wang, Yuwei
    Yang, Yanlang
    Tao, Liangfei
    INFLAMMATION RESEARCH, 2020, 69 (04) : 375 - 383
  • [33] Safinamide prevents lipopolysaccharide (LPS)-induced inflammation in macrophages by suppressing TLR4/NF-κB signaling
    Qian, LuLu
    Li, Jun-Zhao
    Sun, XueMei
    Chen, Jie-Bin
    Dai, Ying
    Huang, Qiu-Xiang
    Jin, Ying-Ji
    Duan, Qing-Ning
    INTERNATIONAL IMMUNOPHARMACOLOGY, 2021, 96
  • [34] Fosinoprilat alleviates lipopolysaccharide (LPS)-induced inflammation by inhibiting TLR4/NF-κB signaling in monocytes
    Yang, Shuansuo
    Li, Ruogu
    Qu, Xinkai
    Tang, Lei
    Ge, Guanghao
    Fang, Weiyi
    Qiao, Zengyong
    Ma, Jiangwei
    Hou, Yuemei
    Liu, Huajin
    CELLULAR IMMUNOLOGY, 2013, 284 (1-2) : 182 - 186
  • [35] NF-κB inhibition attenuates LPS-induced TLR4 activation in monocyte cells
    Wan, Jian
    Shan, Yi
    Fan, Yibo
    Fan, Conghui
    Chen, Song
    Sun, Jie
    Zhu, Lili
    Qin, Long
    Yu, Mengjin
    Lin, Zhaofen
    MOLECULAR MEDICINE REPORTS, 2016, 14 (05) : 4505 - 4510
  • [36] Nerolidol Protects Against LPS-induced Acute Kidney Injury via Inhibiting TLR4/NF-κB Signaling
    Zhang, Lu
    Sun, Dandan
    Bao, Yan
    Shi, Yan
    Cui, Yan
    Guo, Minghao
    PHYTOTHERAPY RESEARCH, 2017, 31 (03) : 459 - 465
  • [37] Plasminogen Activator Inhibitor-1 Regulates LPS-Induced TLR4/MD-2 Pathway Activation and Inflammation in Alveolar Macrophages
    Ren, Weiying
    Wang, Zhonghui
    Hua, Feng
    Zhu, Lei
    INFLAMMATION, 2015, 38 (01) : 384 - 393
  • [38] Plasminogen Activator Inhibitor-1 Regulates LPS-Induced TLR4/MD-2 Pathway Activation and Inflammation in Alveolar Macrophages
    Weiying Ren
    Zhonghui Wang
    Feng Hua
    Lei Zhu
    Inflammation, 2015, 38 : 384 - 393
  • [39] Electroacupuncture Inhibits TLR4/NF-κB Signaling Pathway and Alleviates Trauma in Frostbite
    Kong, Xiang-yi
    Yang, Xue-song
    Luo, Guangyun
    Wang, Zhimin
    Xia, Shuangli
    Mu, Jing
    Wang, Fang
    Ye, Jian-zhou
    JOURNAL OF BIOLOGICAL REGULATORS AND HOMEOSTATIC AGENTS, 2023, 37 (02): : 917 - 925
  • [40] Cryptotanshinone inhibits LPS-induced proinflammatory mediators via TLR4 and TAK1 signaling pathway
    Li, Xin
    Lian, Li-Hua
    Bai, Ting
    Wu, Yan-Ling
    Wan, Ying
    Xie, Wen-Xue
    Jin, Xuejun
    Nan, Ji-Xing
    INTERNATIONAL IMMUNOPHARMACOLOGY, 2011, 11 (11) : 1871 - 1876