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Published on: May 27, 2015
Vigna angularis inhibits mast cell-mediated allergic inflammation
Hui-Hun Kim1, Sung-Wan Kim, Duk-Sil Kim
1Korean Traditional Medicine Agency, Korea Promotion Institute for Traditional Medicine Industry, Gyeongsan 712‑210, Republic of Korea.
Vigna angularis extracts (EVA) effectively inhibit allergic inflammation by reducing histamine release and pro-inflammatory cytokine production from mast cells. These findings suggest EVA
Area of Science:
- Immunology
- Pharmacology
- Natural Product Research
Background:
- Allergic inflammatory reactions involve mast cell activation and the release of mediators like histamine and cytokines.
- Understanding the mechanisms underlying mast cell degranulation is crucial for developing anti-allergic therapies.
Purpose of the Study:
- To investigate the inhibitory effects of Vigna angularis extracts (EVA) on allergic inflammatory responses.
- To elucidate the molecular mechanisms by which EVA modulates mast cell activity.
Main Methods:
- Assessed histamine release and pro-inflammatory cytokine (TNF-α, IL-6) expression in human mast cells (HMC-1).
- Investigated intracellular calcium levels, nuclear factor (NF)-κB, and mitogen-activated protein kinases (MAPKs) activation.
- Utilized in vivo mouse models for systemic and local allergic reactions.
Main Results:
- EVA dose-dependently inhibited histamine release induced by PMACI.
- EVA's histamine inhibition was linked to reduced intracellular calcium levels.
- EVA suppressed PMACI-stimulated pro-inflammatory cytokine gene expression and secretion.
- Inhibition of cytokines was dependent on NF-κB and MAPK pathways.
- EVA attenuated compound 48/80-induced systemic anaphylaxis and IgE-mediated cutaneous anaphylaxis in mice.
Conclusions:
- Vigna angularis extracts demonstrate potent anti-allergic properties by inhibiting mast cell degranulation and mediator release.
- EVA exerts its effects through modulation of intracellular calcium, NF-κB, and MAPK signaling pathways.
- EVA holds potential as a therapeutic agent for managing allergic inflammatory disorders.
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Allergic Reactions
Inflammation
