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Polyozellin blocks tumor necrosis factor α-induced interleukin 8 and matrix metalloproteinase 7 production in the human intestinal epithelial cell line HT-29.

Abstract
Polyozellin isolated from Polyozellus multiplex (Thelephoraceae) displays potent anti-inflammatory effects in murine macrophages. Here we evaluated whether polyozellin has the potential to ameliorate diseases characterized by mucosal inflammation in intestinal epithelial HT-29 cells. Polyozellin significantly inhibited tumor necrosis factor (TNF)-α-induced interleukin-8 secretion and mRNA expression. Moreover, polyozellin suppressed the expression of matrix metalloproteinase-7 mRNA and extracellular pro-matrix metalloproteinase-7 secretion. A signal transduction study revealed that polyozellin significantly attenuates TNF-α-mediated p38 phosphorylation, inhibitory factor κBα degradation, and nuclear factor-κB-mediated transcriptional activation. Collectively, these results suggest that polyozellin has the potential to attenuate intestinal inflammation and shed light on the novel signal pathway evoked by TNF-α during intestinal inflammation.
AuthorsSung Hee Lee, Kyung-Sik Song, Dong Hwan Sohn, Geom Seog Seo
JournalArchives of pharmacal research (Arch Pharm Res) Vol. 34 Issue 1 Pg. 91-7 (Jan 2011) ISSN: 1976-3786 [Electronic] Korea (South)
PMID21468920 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Furans
  • I-kappa B Proteins
  • Interleukin-8
  • NF-kappa B
  • NFKBIA protein, human
  • RNA, Messenger
  • Tumor Necrosis Factor-alpha
  • polyozellin
  • NF-KappaB Inhibitor alpha
  • p38 Mitogen-Activated Protein Kinases
  • Matrix Metalloproteinase 7
Topics
  • Basidiomycota (chemistry)
  • Furans (isolation & purification, pharmacology)
  • HT29 Cells
  • Humans
  • I-kappa B Proteins (drug effects, metabolism)
  • Inflammation (drug therapy, physiopathology)
  • Interleukin-8 (drug effects, metabolism)
  • Intestinal Mucosa (drug effects, pathology)
  • Matrix Metalloproteinase 7 (drug effects, metabolism)
  • NF-KappaB Inhibitor alpha
  • NF-kappa B (drug effects, metabolism)
  • Phosphorylation (drug effects)
  • RNA, Messenger (metabolism)
  • Signal Transduction (drug effects)
  • Tumor Necrosis Factor-alpha (antagonists & inhibitors)
  • p38 Mitogen-Activated Protein Kinases (drug effects, metabolism)

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