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Anti-Atopic Effect of Isatidis Folium Water Extract in TNF-α/IFN-γ-Induced HaCaT Cells and DNCB-Induced Atopic Dermatitis Mouse Model

Molecules, ISSN: 1420-3049, Vol: 28, Issue: 9
2023
  • 5
    Citations
  • 0
    Usage
  • 3
    Captures
  • 2
    Mentions
  • 48
    Social Media
Metric Options:   Counts1 Year3 Year

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  • Citations
    5
  • Captures
    3
  • Mentions
    2
    • Blog Mentions
      1
      • Blog
        1
    • News Mentions
      1
      • News
        1
  • Social Media
    48
    • Shares, Likes & Comments
      48
      • Facebook
        48

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Molecules, Vol. 28, Pages 3960: Anti-Atopic Effect of Isatidis Folium Water Extract in TNF-α/IFN-γ-Induced HaCaT Cells and DNCB-Induced Atopic Dermatitis Mouse Model

Molecules, Vol. 28, Pages 3960: Anti-Atopic Effect of Isatidis Folium Water Extract in TNF-α/IFN-γ-Induced HaCaT Cells and DNCB-Induced Atopic Dermatitis Mouse Model Molecules doi: 10.3390/molecules28093960

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Research on Tumor Necrosis Factors Detailed by Researchers at Korea Institute of Oriental Medicine (Anti-Atopic Effect of Isatidis Folium Water Extract in TNF-a/IFN-g-Induced HaCaT Cells and DNCB-Induced Atopic Dermatitis Mouse Model)

2023 MAY 29 (NewsRx) -- By a News Reporter-Staff News Editor at NewsRx Life Science Daily -- New research on tumor necrosis factors is the

Article Description

Isatidis folium or Isatis tinctoria L. is a flowering plant of the Brassicaceae family, commonly known as woad, with an ancient and well-documented history as an indigo dye and medicinal plant. This study aimed to evaluate the anti-atopic dermatitis (AD) effects of Isatidis folium water extract (WIF) using a 2,4-dinitrochlorobenzene (DNCB)-induced AD-like mouse model and to investigate the underlying mechanism using tumor necrosis factor-α (TNF-α) and interferon-γ (IFN-γ)-activated HaCaT cells. Oral administration of WIF reduced spleen weight, decreased serum IgE and TNF-α levels, reduced epidermal and dermal thickness, and inhibited eosinophil and mast cell recruitment to the dermis compared to DNCB-induced control groups. Furthermore, oral WIF administration suppressed extracellular signal-regulated kinase and p38 mitogen-activated protein kinase protein expression levels, p65 translocation from the cytoplasm to the nucleus, and mRNA expression of TNF-α, IFN-γ, interleukin (IL)-6, and IL-13 in skin lesion tissues. In HaCaT cells, WIF suppressed the production of regulated upon activation, normal T cell expressed and secreted (RANTES), thymus and activation-regulated chemokine (TARC), macrophage-derived chemokine (MDC), MCP-1, and MIP-3a, which are inflammatory cytokines and chemokines related to AD, and inhibited the mRNA expression of RANTES, TARC, and MDC in TNF-α/IFN-γ-stimulated HaCaT cells. Overall, the results revealed that WIF ameliorated AD-like skin inflammation by suppressing proinflammatory cytokine and chemokine production via nuclear factor-κB pathway inhibition, suggesting WIF as a potential candidate for AD treatment.

Bibliographic Details

Min, Ga-Yul; Kim, Tae In; Kim, Ji-Hye; Cho, Won-Kyung; Yang, Ju-Hye; Ma, Jin Yeul

MDPI AG

Chemistry; Biochemistry, Genetics and Molecular Biology; Pharmacology, Toxicology and Pharmaceutics

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