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Anti-inflammatory effect of Ishige okamurae ethanolic extract via inhibition of NF-kappaB transcription factor in RAW 264.7 cells.

Abstract
Nowadays, much attention has been paid to the development of anti-inflammatory agents from marine natural resources. As a result of screening anti-inflammatory agents from marine algae using immunoassay, we found for the first time that ethanolic extract of Ishige okamurae (IO) classified into brown algae was effective in inhibiting the production of inflammatory mediators, such as tumor necrosis factor-alpha, interleukin-1beta, interleukin-6 and prostaglandin E(2), in RAW264.7 cells stimulated by lipopolysaccharide, compared with dexamethasone and aspirin used as positive control in this study. Moreover, transcriptional activation of NF-kappaB transcription factor that regulates the expression of these inflammatory mediators was also examined using reporter gene assay and western blot analysis. It was observed that IO extract exerted anti-inflammatory effect via inactivation of NF-kappaB transcription factor in macrophages. In addition, the expression and activity of matrix metalloproteinase-2 and 9 that play an important role in chronic inflammation were decreased in dose-dependent manner in the presence of IO extract in HT1080 cells. The above results suggest that IO extract can inhibit inflammation through inactivation of NF-kappaB transcription factor in macrophage.
AuthorsMoon-Moo Kim, Niranjan Rajapakse, Se-Kwon Kim
JournalPhytotherapy research : PTR (Phytother Res) Vol. 23 Issue 5 Pg. 628-34 (May 2009) ISSN: 1099-1573 [Electronic] England
PMID19117331 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Anti-Inflammatory Agents
  • Interleukin-1beta
  • Interleukin-6
  • NF-kappa B
  • Plant Extracts
  • Tumor Necrosis Factor-alpha
  • Matrix Metalloproteinase 2
  • Matrix Metalloproteinase 9
  • Dinoprostone
Topics
  • Animals
  • Anti-Inflammatory Agents (pharmacology)
  • Cell Line
  • Dinoprostone (metabolism)
  • Humans
  • Interleukin-1beta (metabolism)
  • Interleukin-6 (metabolism)
  • Matrix Metalloproteinase 2 (metabolism)
  • Matrix Metalloproteinase 9 (metabolism)
  • Mice
  • NF-kappa B (antagonists & inhibitors)
  • Phaeophyta (chemistry)
  • Plant Extracts (pharmacology)
  • Tumor Necrosis Factor-alpha (metabolism)

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