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Inhibition of interleukin-8 production in the human colonic epithelial cell line HT-29 by 18 beta-glycyrrhetinic acid.

  • Ok Hwa Kang*
  • , Jin A. Kim
  • , Yeon A. Choi
  • , Hye Jung Park
  • , Dae Ki Kim
  • , Yong Hwan An
  • , Suck Chei Choi
  • , Ki Jung Yun
  • , Yong Ho Nah
  • , Xing Fu Cai
  • , Young Ho Kim
  • , Ki Hwan Bae
  • , Young Mi Lee
  • *Corresponding author for this work
  • Wonkwang University

Research output: Contribution to journalJournal articlepeer-review

Abstract

Interleukin (IL)-8 plays a central role in the initiation and maintenance of inflammatory responses in the inflammatory bowel disease. The proinflammatory cytokine-mediated production of IL-8 requires activation of various kinases, which leads to the I kappa B degradation and NF-kappa B activation. We investigated the role of 18 beta-glycyrrhetinic acid (GA), a saponin isolated from licorice roots, on TNF-alpha-induced IL-8 production in human colonic epithelial cells. HT29 cells were stimulated with TNF-alpha in the presence or absence of GA (1, 5 or 10 microM). IL-8 production was measured by enzyme-linked immunosorbent assay (ELISA) and reverse transcriptase-polymerase chain reaction analysis, and the mitogen-activated protein kinases (MAPKs) activation and I kappa B alpha degradation were determined by Western blot analysis. GA suppressed TNF-alpha-induced IL-8 production in a concentration-dependent manner. In addition, GA inhibited TNF-alpha-induced phosphorylation of p38 MAPK and extracellular-regulated kinases (ERK), I kappa B alpha degradation, and NF-kappa B activation. These results suggest that GA has the inhibitory effects on TNF-alpha-induced IL-8 production in the intestinal epithelial cells through blockade in the phosphorylation of MAPKs, following I kappa B alpha degradation and NF-kappa B activation.

Original languageEnglish
Pages (from-to)981-985
Number of pages5
JournalInternational Journal of Molecular Medicine
Volume15
Issue number6
StatePublished - 2005.06

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