Citrus hallabong [(Citrus unshiu × C. sinensis) × C. reticulata)] exerts potent anti-inflammatory properties in murine splenocytes and TPA-induced murine ear oedema model

Publication Overview
TitleCitrus hallabong [(Citrus unshiu × C. sinensis) × C. reticulata)] exerts potent anti-inflammatory properties in murine splenocytes and TPA-induced murine ear oedema model
AuthorsHerath KH, Bing SJ, Cho J, Kim A, Kim GO, Lee JC, Jee Y
TypeJournal Article
Journal NamePharmaceutical biology
Year2016
Page(s)1-12
CitationHerath KH, Bing SJ, Cho J, Kim A, Kim GO, Lee JC, Jee Y. Citrus hallabong [(Citrus unshiu × C. sinensis) × C. reticulata)] exerts potent anti-inflammatory properties in murine splenocytes and TPA-induced murine ear oedema model. Pharmaceutical biology. 2016 Jun 22; 1-12.

Abstract

CONTEXT
Hallabong [(Citrus unshiu × C. sinensis) X C. reticulata)] (Rutaceae) is a hybrid citrus cultivated in temperate regions of South Korea. Its fruit is well-known for pharmacological properties.

OBJECTIVE
This study examined the anti-inflammatory effect of 80% ethanol extract of Hallabong (HE) on concanavalin A (Con A)-stimulated splenocytes and mouse oedema model induced by 12-O-tetradecanoylphorbal acetate (TPA).

MATERIALS AND METHODS
Murine splenocytes treated with HE were stimulated with Con A (10 μg/mL, for 24 h) were evaluated for T-cell population and production of inflammatory cytokines IL-2, IL-4 and IFN-γ. Anti-inflammatory effect of topically applied HE (100 μg/20 μL) on TPA (4 μg/20 μL/ear)-induced ear oedema was investigated in mouse model.

RESULTS
HE-treated Con A-stimulated murine splenocytes showed a marked decrease in CD44/CD62L(+) memory T-cell population, an important marker for anti-inflammatory activity, and a significant inhibition in the production of IL-2 and IFN-γ. HE treatment had reduced the mouse skin oedema (47%) and myeloperoxidase (MPO) activity significantly (40%) in TPA-challenged tissues. More importantly, immunohistochemical localization revealed the suppressed (p < 0.05) expression of inducible nitric oxide (iNOS), cyclooxygenase-2 (COX2). HE decreased the infiltration of CD3(+) T cells and F4/80(+) macrophages to the site of inflammation and a topical application of HE significantly suppressed the expression of TNF-α (20.2%).

DISCUSSION AND CONCLUSION
A topical application of HE can exert a potential anti-inflammatory effect and HE can be explored further as a putative alternative therapeutic agent for inflammatory oedema.

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Properties
Additional details for this publication include:
Property NameValue
LanguageEnglish
Language AbbrENG
Publication TypeJournal Article
Publication ModelPrint-Electronic
ISSN1744-5116
eISSN1744-5116
Publication Date2016 Jun 22
Journal AbbreviationPharm Biol