人参
TLR4型
化学
信号转导
三七
炎症
磷酸化
药理学
受体
人参皂甙
细胞生物学
对接(动物)
Toll样受体
激酶
脂多糖
生物化学
生物
免疫学
医学
先天免疫系统
替代医学
病理
护理部
作者
Honglin Xu,Guang‐Hong Chen,Yuting Wu,Lingpeng Xie,Zhang‐Bin Tan,Bin Liu,Huijie Fan,Hongmei Chen,Guiqiong Huang,Min Liu,Yingchun Zhou
标识
DOI:10.1016/j.jgr.2021.05.011
摘要
BACKGROUND: against inflammation and elucidate underlying mechanisms. METHODS: Inflammation model was constructed by lipopolysaccharide (LPS) in C57BL/6 mice and RAW264.7 macrophages. Molecular docking, molecular dynamics, surface plasmon resonance imaging (SPRi) and immunofluorescence were utilized to predict active component. RESULTS: M). GRo significantly inhibited LPS488 binding to cell membranes. Further studies showed that GRo markedly suppressed LPS-triggered lung injury, the transcription and secretion levels of TNF-α, IL-6 and IL-1β. Moreover, the phosphorylation of NF-κB and MAPKs as well as the p65 subunit nuclear translocation were inhibited by GRo dose-dependently. CONCLUSION: Our results suggest that GRo exerts anti-inflammation actions by direct inhibition of TLR4 signaling pathway.
科研通智能强力驱动
Strongly Powered by AbleSci AI