Antiasthmic effect of fermented Artemisia princeps in asthmic mice induced by ovalbumin

Eun-Ah Bae1, Sung-Won Min, Bomi Lee

  • 1Department of Life and Nanopharmaceutical Sciences, Kyung Hee University, Seoul 130-701, Korea.

Insights

Fermented Artemisia princeps Pampanini (FAP) shows a stronger antiasthmic effect than unfermented AP. FAP effectively reduced allergic inflammation markers in asthma models, suggesting improved therapeutic potential.

Area of Science:

  • Immunology
  • Microbiology
  • Pharmacology

Background:

  • Asthma is a chronic respiratory disease characterized by airway inflammation and elevated immunoglobulin E (IgE) levels.
  • Artemisia princeps Pampanini (AP) has demonstrated potential anti-inflammatory properties.
  • Probiotics, such as Bifidobacterium infantis K-525, are known to modulate immune responses.

Purpose of the Study:

  • To investigate the antiasthmic effects of Artemisia princeps Pampanini (AP) fermented with Bifidobacterium infantis K-525 (FAP).
  • To compare the efficacy of FAP with unfermented AP in an ovalbumin-induced asthma mouse model.
  • To explore the underlying mechanisms of FAP's antiasthmic activity, focusing on cytokine regulation.

Main Methods:

  • Ovalbumin-induced asthma model in mice.
  • Administration of AP and FAP.
  • Measurement of IgE levels in blood.
  • Analysis of inflammatory cytokine levels (IL-6, IL-4) in trachea and lungs.
  • Assessment of mRNA expression of IL-6 and TNF-alpha in RBL-2H3 cells.

Main Results:

  • Both AP and FAP reduced IgE levels in asthmatic mice.
  • FAP demonstrated a more potent reduction in IgE, IL-6, and IL-4 in the trachea and lungs compared to AP.
  • AP and FAP inhibited the mRNA expression of IL-6 and TNF-alpha in IgE-induced RBL-2H3 cells.
  • The in vivo antiasthmic effect of FAP was superior to that of AP.

Conclusions:

  • Fermentation of AP with Bifidobacterium infantis K-525 enhances its antiasthmic properties.
  • FAP effectively regulates key inflammatory mediators involved in asthma pathogenesis.
  • The enhanced efficacy of FAP is likely attributed to its ability to modulate the biosynthesis of proinflammatory cytokines IL-6 and TNF-alpha.

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