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Triptolide inhibits TNF-α, IL-Iβ and NO production in primary microglial cultures

  • Hui Fang Zhou
  • , Dong Bin Niu
  • , Bing Xue
  • , Feng Qiao Li
  • , Xian Yu Liu
  • , Qi Hua He
  • , Xin Hong Wang
  • , Xiao Min Wang

Research output: Contribution to journalArticlepeer-review

Abstract

Microglia are believed to participate in the mediation of neuro-degeneration through producing a variety of cytotoxic factors upon activation. Pharmacological intervention in microglial activation may therefore exert a neuroprotective effect. In exploring pharmacological agents that can affect microglial activation, we found in this study that triptolide possesses a powerful inhibitory influence over microglia. Pretreatment with triptolide was able to dose-dependently reduce the lipopolysaccharide (LPS)-induced nitrite accumulation and tumor necrosis factor-α and interleukin-Iβ release from LPS-activated microglia as revealed by Griess reaction and ELISA, respectively. Triptolide reduced LPS-stimulated mRNA expression of all three inflammatory factors. The results obtained from this study demonstrate that triptolide can inhibit inflammatory responses of microglia to inflammatory stimulation via a mechanism involving the inhibition of the synthesis and release of inflammatory factors.

Original languageEnglish
Pages (from-to)1091-1095
Number of pages5
JournalNeuroReport
Volume14
Issue number7
DOIs
StatePublished - May 2003

Keywords

  • Inflammation
  • Microglia
  • Neuroprotection
  • Nitric oxide
  • Proinflammatory cytokines
  • Tripterygium wilfordii Hook F.
  • Triptolide

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