Antiasthmic effect of fermented Artemisia princeps in asthmic mice induced by ovalbumin
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Updated: Jul 9, 2026

Murine Model of Allergen Induced Asthma
Published on: May 14, 2012
Eun-Ah Bae1, Sung-Won Min, Bomi Lee
1Department of Life and Nanopharmaceutical Sciences, Kyung Hee University, Seoul 130-701, Korea.
Abstract:
Artemisia princeps Pampanini (AP) was fermented with Bifidobacterium infantis K-525 and its antiasthmic effect investigated. AP and fermented AP (FAP) reduced the IgE level in the blood of ovalbumin-induced asthmic mice. Moreover, FAP reduced the IgE, proinflammatory cytokine IL-6, and IL-4 levels in the trachea, as well as in the lung of the experimental asthmic mice, whereas AP only reduced the IgE and IL-6 levels in the lungs. Nonetheless, AP and FAP both inhibited the mRNA expression of IL-6 and TNF-alpha in IgE-induced RBL-2H3 cells. The in vivo antiasthmic effect of FAP was more potent than that of AP. Therefore, these findings suggest that the enhanced antiasthmic effect of AP after bifidus fermentation was possibly due to the regulation of the proinflammatory cytokine biosynthesis of IL-6 and TNF-alpha.
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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