YC-1 reduces inflammatory responses by inhibiting nuclear factor-?B translocation in mice subjected to transient focal cerebral ischemia

Wei Ting Lee, Shih Huang Tai, Yu Wen Lin, Tian Shung Wu, E. Jian Lee

研究成果: Article同行評審

4 引文 斯高帕斯(Scopus)

摘要

3-(5-hydroxymethyl-2-furyl)-1-benzyl-indazole (YC-1) is understood to protect against ischemic stroke, but the molecular basis for its neuroprotection remains to be fully characterized. The present study investigated the influence of YC-1 on inflammatory responses following experimental stroke. Previous studies indicated that nuclear factor (NF)-?B-driven signals serve a pivotal role in mediating inflammatory responses following stroke. Ischemic stroke results in activation of NF-?B to induce gene expression of factors including inducible nitric oxide synthase, interleukin (IL)-1ß, IL-6 and matrix metalloproteinases (MMPs). The results of the present study demonstrated that YC-1 effectively reduced brain infarction and brain edema, and improved blood-brain barrier leakage. Additionally, animals treated with YC-1 exhibited significant reductions in neutrophil and macrophage infiltration into the ischemic brain. Furthermore, YC-1 effectively inhibited NF-?B translocation and binding activity, and the activity and expression of MMP-9 following ischemic stroke. In conclusion, YC-1 may effectively attenuate NF-?B-induced inflammatory damage following cerebral ischemia-reperfusion.

原文English
頁(從 - 到)2043-2051
頁數9
期刊Molecular Medicine Reports
18
發行號2
DOIs
出版狀態Published - 2018 八月

All Science Journal Classification (ASJC) codes

  • 生物化學
  • 分子醫學
  • 分子生物學
  • 遺傳學
  • 腫瘤科
  • 癌症研究

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