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In Vitro and In Vivo Anti-Allergic and Anti-Inflammatory Effects of eBV, a Newly Developed Derivative of Bee Venom, through Modulation of IRF3 Signaling Pathway in a Carrageenan-Induced Edema Model
- Source :
- PLoS ONE, PLoS ONE, Vol 11, Iss 12, p e0168120 (2016), PLOS ONE(11): 12
- Publication Year :
- 2016
- Publisher :
- Public Library of Science, 2016.
-
Abstract
- Background Bee venom (BV), a type of toxin extracted from honeybees (Apis mellifera), has been empirically and widely used to treat inflammatory diseases throughout Asia. Essential BV (eBV) was developed by removing phospholipase A2 (PLA2) and histamine to lower occurrence of allergic reaction. This study investigated the anti-allergic and anti-inflammatory activities of eBV in vitro and in vivo and its underlying mechanism of action. Methods The anti-inflammatory potential of eBV was assessed in vivo using a carrageenan-induced paw edema model. To further investigate the mechanism by which eBV exerts anti-allergic and anti-inflammatory effects, compound 48/80-stimulated RBL-2H3 cells and lipopolysaccharide (LPS)-stimulated RAW 264.7 murine macrophage cells were studied in vitro. Results Release of beta-hexosaminidase and histamine was increased by eBV in a dose-dependent manner, but these levels were lower in eBV compared to original BV at the same concentration. In addition, eBV suppressed compound 48/80-induced expression of tumor necrosis factor-alpha (TNF-alpha) and interleukin-1 beta (IL-1 beta) in RBL-2H3 cells. eBV was also shown to suppress nitric oxide (NO) production by down-regulating mRNA expression and subsequent protein expression of inflammatory mediators in LPS-induced RAW 264.7 cells. Phosphorylation of activators and signal transducers of transcription 1/interferon regulatory factor 3 (STAT1/IRF3) was attenuated by eBV treatment. eBV significantly inhibited carrageenan-induced acute edema in vivo. Serum levels of prostaglandin E2 (PGE2), TNF-alpha, and IL-1 beta were also down-regulated by eBV. Conclusions These results demonstrate that eBV inhibits allergic and inflammatory response by reducing inflammatory mediator production via regulation of the STAT1/IRF3 signaling pathway, suggesting that eBV is a feasible candidate for regulation of allergic-inflammatory response in complementary and alternative medicine.
- Subjects :
- 0301 basic medicine
Male
Lipopolysaccharide
Physiology
Protein Expression
lcsh:Medicine
Pathology and Laboratory Medicine
Carrageenan
Biochemistry
Cell Degranulation
Rats, Sprague-Dawley
chemistry.chemical_compound
White Blood Cells
Mice
0302 clinical medicine
Animal Cells
Immune Physiology
Medicine and Health Sciences
Edema
STAT1
Post-Translational Modification
Phosphorylation
lcsh:Science
Immune Response
Chromatography, High Pressure Liquid
Innate Immune System
Multidisciplinary
Organic Compounds
Neurochemistry
Neurotransmitters
Chemistry
Bee Venoms
STAT1 Transcription Factor
Physical Sciences
Cytokines
Tumor necrosis factor alpha
medicine.symptom
Cellular Types
Histamine
Research Article
Signal Transduction
Biogenic Amines
Cell Physiology
Immune Cells
Immunology
Blotting, Western
Inflammation
Biology
Research and Analysis Methods
Real-Time Polymerase Chain Reaction
Dinoprostone
03 medical and health sciences
Signs and Symptoms
In vivo
Diagnostic Medicine
medicine
Gene Expression and Vector Techniques
Hypersensitivity
Animals
Molecular Biology Techniques
Molecular Biology
Molecular Biology Assays and Analysis Techniques
Blood Cells
Tumor Necrosis Factor-alpha
Macrophages
lcsh:R
Organic Chemistry
Chemical Compounds
Biology and Life Sciences
Proteins
Cell Biology
Molecular Development
Rats
Disease Models, Animal
030104 developmental biology
RAW 264.7 Cells
chemistry
Immune System
Cancer research
biology.protein
lcsh:Q
Interferon Regulatory Factor-3
Interleukin-4
IRF3
030217 neurology & neurosurgery
Interferon regulatory factors
Neuroscience
Developmental Biology
Subjects
Details
- Language :
- English
- ISSN :
- 19326203
- Volume :
- 11
- Issue :
- 12
- Database :
- OpenAIRE
- Journal :
- PLoS ONE
- Accession number :
- edsair.doi.dedup.....abf6fe3a574418b8076e8cc8806e3060