[Inhibitory effects of acteoside on LPS-induced inflammatory response on BV-2 microglial cells]

Zhongguo Zhong Yao Za Zhi. 2016 Jul;41(13):2506-2510. doi: 10.4268/cjcmm20161322.
[Article in Chinese]

Abstract

To investigate the inhibitory effects of acteoside (ACT) on BV-2 microglial cells and the potential mechanism,LPS was used to treat BV-2 cells with or without ACT (12.5,25,50 μmol•L ⁻¹). Then, the expressions of inflammatory factors (NO,TNF-α,IL-6) and inflammation related proteins (iNOS,COX-2,p-IKKβ,IKKβ,p-ⅠκB,ⅠκB) were detected. In addition,the nuclear translocation of NF-κB was explored. The results showed that ACT could significantly suppress the inflammatory response against LPS stimulation by decreasing the expressions of NO,IL-6,TNF-α,iNOS,COX-2 and the phosphorylations of IKKβ and IκB. Moreover,the nuclear translocation of NF-κB p65 was inhibited by ACT. Taken together, ACT could significantly inhibit the inflammatory response of BV-2 microglial cells which were induced by LPS via inhibition of NF-κB signaling pathway.

Keywords: NF-κB signal pathway; acteoside; lipopolysaccharide; microglial cells; neuroinflammation.

MeSH terms

  • Animals
  • Anti-Inflammatory Agents / pharmacology*
  • Cell Line
  • Cyclooxygenase 2 / metabolism
  • Glucosides
  • Inflammation / chemically induced
  • Lipopolysaccharides
  • Mice
  • Microglia / drug effects*
  • Nitric Oxide
  • Nitric Oxide Synthase Type II / metabolism
  • Phenols
  • Transcription Factor RelA / metabolism

Substances

  • Anti-Inflammatory Agents
  • Glucosides
  • Lipopolysaccharides
  • Phenols
  • Rela protein, mouse
  • Transcription Factor RelA
  • Nitric Oxide
  • acteoside
  • Nitric Oxide Synthase Type II
  • Nos2 protein, mouse
  • Ptgs2 protein, mouse
  • Cyclooxygenase 2