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DA-9601 decreases immediate-type allergic reaction and tumor necrosis factor-α production

  • Hyo Hyun Park
  • , Sug Hyun Kim
  • , Soyoung Lee
  • , Jin Young Moon
  • , Won Hwan Park
  • , Cheorl Ho Kim
  • , Myung Chung Jae
  • , Tae Young Oh
  • , Chang Duk Jun
  • , Sang Hyun Kim
  • Kyungpook National University
  • Dongguk University
  • Dong-A Pharmaceutical Company
  • Gwangju Institute of Science and Technology

Research output: Contribution to journalArticlepeer-review

Abstract

The immediate-type allergic reaction is involved in many allergic diseases such as asthma, allergic rhinitis, and sinusitis. The discovery of drugs for the treatment of immediate-type allergic disease is a very important subject in human health. The formulated ethanol extract of Artemisia asiatica Nakai (DA-9601) has been reported to have antioxidative and anti-inflammatory activities. In this report, we investigated the effect of DA-9601 on the immediate-type allergic reaction and studied its possible mechanisms of action, focusing on the mast cell-mediated allergic reaction. DA-9601 inhibited compound 48/80-induced systemic anaphylactic reactions and serum histamine release in mice. DA-9601 decreased the IgE-mediated passive cutaneous anaphylaxis, the model of local allergic reaction in vivo. DA-9601 dose-dependently reduced histamine release from mast cells activated by compound 48/80 or IgE. Furthermore, DA-9601 decreased the gene expression and production of tumor necrosis factor (TNF)-α in phorbol 12-myristate 13-acetate plus A23187-stimulated mast cells. These findings provide evidence that DA-9601 could be a candidate as an anti-allergic agent.

Original languageEnglish
Pages (from-to)383-389
Number of pages7
JournalJournal of Health Science
Volume52
Issue number4
DOIs
StatePublished - 2006

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • DA-9601
  • Immediate-type allergic reaction
  • Mast cells
  • Tumor necrosis factor-α

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