Journal
NEUROSCIENCE LETTERS
Volume 421, Issue 1, Pages 37-41Publisher
ELSEVIER IRELAND LTD
DOI: 10.1016/j.neulet.2007.05.017
Keywords
glia; inflammation; ginsenosides; NF-kappa B; JNK; tumor necrosis factor
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Ginsenosides, the main component of Panax ginseng, have been known for the anti-inflammatory and anti-proliferative activities. In this study, we investigated the molecular mechanisms responsible for the anti-inflammatory effects of ginsenosides on activated astroglial cells. Among 13 different ginsenosides. intestinal bacterial metabolites Rh and compound K (C-K) showed a significant inhibitory effect on tumor necrosis factor-alpha (TNF-alpha)-induced expression of intercellular adhesion molecule-1 in human astroglial cells. Pretreatment with C-K or Rh-2 suppressed TNF-alpha-induced phosphorylation Of I kappa B alpha. kinase and the subsequent phosphorylation and degradation Of I kappa B alpha. Additionally, the same treatment inhibited TNF-alpha-induced phosphorylation of MKK4 and the subsequent activation of the JNK-AP-1 pathway. The inhibitory effect of ginsenosides on TNF-alpha-induced activation of the NF-kappa B and JNK pathways was not observed in human monocytic U937 cells. These results collectively indicate that ginsenoside metabolites C-K and Rh-2 exert anti-inflammatory effects by the inhibition of both NF-kappa B and JNK pathways in a cell-specific manner. (c) 2007 Elsevier Ireland Ltd. All rights reserved.
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