Anti-inflammatory mechanism of ginseng saponins in activated microglia

J Neuroimmunol. 2009 Apr 30;209(1-2):40-9. doi: 10.1016/j.jneuroim.2009.01.020. Epub 2009 Feb 15.

Abstract

In the present study, we investigated the effect of ginseng extract (KRG) and total saponins (GTS) on microglial activation. KRG and GTS inhibited LPS-induced expression of iNOS, MMP-9 and proinflammatory cytokines in microglial cells. Suppression of microglial activation by ginseng was also observed in the mouse brain inflamed by LPS. Furthermore, KRG and GTS significantly suppressed NF-kappaB and MAP kinase activities, which are upstream signaling molecules in inflammation. Among the individual ginsenosides tested, Rh2, Rh3 and compound K significantly inhibited LPS-induced iNOS and cytokine expressions. Therefore, the inhibition of microglial activation by ginseng saponins may a good potential therapeutic modality for neurodegenerative diseases.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Anti-Inflammatory Agents / pharmacology*
  • Anti-Inflammatory Agents / therapeutic use
  • Cell Line, Transformed
  • Cell Line, Tumor
  • Cell Proliferation / drug effects
  • Cytokines / antagonists & inhibitors
  • Cytokines / metabolism
  • Drugs, Chinese Herbal / pharmacology
  • Drugs, Chinese Herbal / therapeutic use
  • Encephalitis / drug therapy*
  • Encephalitis / immunology
  • Encephalitis / physiopathology
  • Ginsenosides / pharmacology*
  • Ginsenosides / therapeutic use
  • Gliosis / drug therapy*
  • Gliosis / immunology
  • Gliosis / physiopathology
  • Lipopolysaccharides / antagonists & inhibitors
  • Male
  • Matrix Metalloproteinase 9 / metabolism
  • Matrix Metalloproteinase Inhibitors
  • Mice
  • Mice, Inbred C57BL
  • Microglia / drug effects*
  • Microglia / immunology
  • Neurodegenerative Diseases / drug therapy
  • Neurodegenerative Diseases / immunology
  • Neurodegenerative Diseases / physiopathology
  • Nitric Oxide Synthase Type II / antagonists & inhibitors
  • Nitric Oxide Synthase Type II / metabolism
  • Rats
  • Saponins / pharmacology*
  • Saponins / therapeutic use
  • Signal Transduction / drug effects
  • Signal Transduction / physiology

Substances

  • Anti-Inflammatory Agents
  • Cytokines
  • Drugs, Chinese Herbal
  • Ginsenosides
  • Lipopolysaccharides
  • Matrix Metalloproteinase Inhibitors
  • Saponins
  • Nitric Oxide Synthase Type II
  • Matrix Metalloproteinase 9