Betuletol, a Propolis Component, Suppresses IL-33 Gene Expression and Effective against Eosinophilia.


Journal

Molecules (Basel, Switzerland)
ISSN: 1420-3049
Titre abrégé: Molecules
Pays: Switzerland
ID NLM: 100964009

Informations de publication

Date de publication:
25 Aug 2022
Historique:
received: 29 07 2022
revised: 19 08 2022
accepted: 23 08 2022
entrez: 9 9 2022
pubmed: 10 9 2022
medline: 14 9 2022
Statut: epublish

Résumé

Propolis, a resinous substance produced by honeybees, has been used in folk medicine since ancient times due to its many biological benefits such as antitumor, antioxidant, antimicrobial, anti-inflammatory, and immunomodulatory effects. Propolis contains flavonoids, terpenoids, aromatic aldehydes, and alcohols, which vary with different climate and environmental conditions. In our study, we examined the antiallergic activity of Brazilian green propolis (BGP) and isolated the active compound that can suppress an allergy-sensitive gene, IL-33, expression and eosinophilia. Ethanolic extract of BGP freeze-dried powder was fractionated with several solvent systems, and the active fractions were collected based on activity measurement. The single active compound was found by thin-layer chromatography. Using column chromatography and NMR, the active compound was isolated and identified as 3,5,7-trihydroxy-6,4'-dimethoxyflavone, also known as betuletol. Further, the antiallergic activity of that has been examined in PMA-induced up-regulation of IL-33 gene expression in Swiss 3T3 cells. Our data showed the IL-33 gene suppression both by BGP and the isolated active compound, betuletol. We also found that betuletol suppressed ERK phosphorylation, suggesting it could be effective in suppressing IL-33 mediated eosinophilic chronic inflammation and will provide new insights to develop potent therapeutics against allergic inflammations.

Identifiants

pubmed: 36080225
pii: molecules27175459
doi: 10.3390/molecules27175459
pmc: PMC9457836
pii:
doi:

Substances chimiques

Anti-Allergic Agents 0
Interleukin-33 0
Propolis 9009-62-5

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Japan Society for the Promotion of Science
ID : 24659474, 22580132
Organisme : Osaka Medical Research Foundation for Intractable Diseases
ID : 26-22, 21-2-24
Organisme : Yamada Research Grant
ID : 0188

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Auteurs

Aurpita Shaha (A)

Department of Molecular Pharmacology, Institute of Biomedical Sciences, Tokushima University Graduate School, Tokushima 770-8503, Japan.
Laboratory of Tumor Microenvironment and Metastasis, The Hormel Institute, University of Minnesota, Austin, MN 55912, USA.

Rezwanul Islam (R)

Department of Molecular Pharmacology, Institute of Biomedical Sciences, Tokushima University Graduate School, Tokushima 770-8503, Japan.
Department of Biomedical Sciences, Charles E. Schmidt College of Medicine, Florida Atlantic University, Boca Raton, FL 33431, USA.

Naonobu Tanaka (N)

Department of Parmacognosy, Institute of Biomedical Sciences, Tokushima University Graduate School, Tokushima 770-8503, Japan.

Yoshiki Kashiwada (Y)

Department of Parmacognosy, Institute of Biomedical Sciences, Tokushima University Graduate School, Tokushima 770-8503, Japan.

Hiroyuki Fukui (H)

Laboratory of Pharmacology, Faculty of Pharmacy, Osaka Ohtani University, Osaka 584-8540, Japan.
Medical Corporation Kinshukai, Osaka 558-0011, Japan.

Noriaki Takeda (N)

Department of Otolaryngology, Institute of Biomedical Sciences, Tokushima University Graduate School, Tokushima 770-8503, Japan.

Yoshiaki Kitamura (Y)

Department of Otolaryngology, Institute of Biomedical Sciences, Tokushima University Graduate School, Tokushima 770-8503, Japan.

Hiroyuki Mizuguchi (H)

Laboratory of Pharmacology, Faculty of Pharmacy, Osaka Ohtani University, Osaka 584-8540, Japan.

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Classifications MeSH