Suppression of Th2-driven, allergen-induced airway inflammation by sauchinone

  • Hyun Jung Min
  • , Hee Yeon Won
  • , Young Choong Kim
  • , Sang Hyun Sung
  • , Mi Ran Byun
  • , Jun Ha Hwang
  • , Jeong Ho Hong
  • , Eun Sook Hwang

Research output: Contribution to journalArticlepeer-review

24 Scopus citations

Abstract

Sauchinone, a lignan compound isolated from the root of Saururus chinensis, has been recently demonstrated to exhibit anti-inflammatory activity via the suppression of NF-kB p65 activity in vitro. In an effort to evaluate the in vivo anti-inflammatory function of sauchinone, we have evaluated the effects of sauchinone on allergen-induced airway inflammation using a murine model of allergic asthma. We observed that marked eosinophilic and lymphocyte infiltration in the BAL fluid were suppressed to a significant degree by sauchinone, and that mucus-secreting goblet cell hyperplasia and collagen deposition in the airways were also ameliorated by administration of sauchinone treatment. Moreover, gene expression of the inflammatory cytokines, IL-13, and IL-5 and eotaxin in the lung, and IL-5 in the draining lymph node were significantly decreased in sauchinone-treated mice. We demonstrated that sauchinone repressed Th2 cell development in vitro and IL-4 production by Th2 cells, and also inhibited GATA-3-mediated IL-5 promoter activity in a dose-dependent manner. Collectively, sauchinone ameliorated allergen-induced airway inflammation, in part, by repressing GATA-3 activity for Th2 cell development, indicating the possible therapeutic potential of sauchinone in airway inflammatory diseases including allergic asthma and rhinitis.

Original languageEnglish
Pages (from-to)204-209
Number of pages6
JournalBiochemical and Biophysical Research Communications
Volume385
Issue number2
DOIs
StatePublished - 24 Jul 2009

Bibliographical note

Funding Information:
This work was supported by NCRC Program of MEST and KOSEF (R15-2006-020, E.S.H.) and also by a Korea Research Foundation Grant funded by MOEHRD (KRF-2007-314-C00239, J.H.H), and the Research Program for New Drug Target Discovery of MEST (M10748000286-07N4800-28610, J.H.H.).

Keywords

  • Airway inflammatory diseases
  • Allergen-induced airway inflammation
  • GATA-3
  • Sauchinone
  • Th2 cell development

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