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Anti-inflammatory activity of 3,5,6,7,3 ',4 '-hexamethoxyflavone via repression of the NF-kappa B and MAPK signaling pathways in LPS-stimulated RAW264.7 cells

Authors
Son, E.S.Park, J.-W.Kim, S.-H.Park, H.R.Han, W.Kwon, O.C.Nam, J.Y.Jeong, S.H.Lee, C.S.
Issue Date
Sep-2020
Publisher
SPANDIDOS PUBL LTD
Citation
Molecular medicine reports, v.22, no.3, pp.1985 - 1993
Journal Title
Molecular medicine reports
Volume
22
Number
3
Start Page
1985
End Page
1993
URI
https://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/78177
DOI
10.3892/mmr.2020.11252
ISSN
1791-2997
Abstract
Citrus peel has been used as a Traditional medicine in Asia to treat coughs, asthma and bronchial disorders. Therefore, the anti‑inflammatory effects of 3,5,6,7,3',4'‑hexamethoxyflavone (quercetogetin, QUE) isolated from Citrus unshiu peel were investigated in lipopolysaccharide (LPS)‑induced RAW 264.7 macrophage cells. The results showed that QUE repressed the production of prostaglandin E2 and nitric oxide by suppressing LPS‑induced expression of cyclooxygenase‑2 and inducible nitric oxide synthase. It also suppressed the production of interleukin (IL)‑6, IL‑1β, and tumor necrosis factor‑α cytokines, and decreased the nuclear translocation of NF‑κB by interrupting the phosphorylation of NF‑κB inhibitor α in macrophage cells. Based on the finding that QUE inhibited the phosphorylation of ERK protein expression in LPS‑induced RAW264.7 cells, it was confirmed that inhibition of inflammatory responses by QUE was mediated via the ERK pathway. Therefore, this study suggests that QUE has strong anti‑inflammatory effects, making it a promising compound for use as a therapeutic agent in treating inflammatory lung diseases, such as emphysema.
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