Callicarpa japonica Thunb. ameliorates allergic airway inflammation by suppressing NF-κB activation and upregulating HO-1 expression

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dc.contributor.authorSung-Man Kim-
dc.contributor.authorHyung Won Ryu-
dc.contributor.authorOk-Kyoung Kwon-
dc.contributor.authorDaseul Hwang-
dc.contributor.authorMin Gu Kim-
dc.contributor.authorJae-Hong Min-
dc.contributor.authorZ Zhang-
dc.contributor.authorSoo Yong Kim-
dc.contributor.authorJin Hyub Paik-
dc.contributor.authorSei-Ryang Oh-
dc.contributor.authorKyung Seop Ahn-
dc.contributor.authorJae-Won Lee-
dc.date.accessioned2021-01-01T03:30:42Z-
dc.date.available2021-01-01T03:30:42Z-
dc.date.issued2021-
dc.identifier.issn0378-8741-
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/23965-
dc.description.abstractEthnopharmacological relevance: Callicarpa japonica Thunb., as an herbal medicine has been used for the treatment of inflammatory diseases in China and Korea. Materials and methods: Ultra performance liquid chromatography-photodiode array-quadrupole time-of-flight mass spectrometer (UPLC-PDA-QTof MS) was used to detect the major phenylethanoid glycosides in the C. japonica extract. BALB/c mice were intraperitoneally sensitized by ovalbumin (OVA) (on days 0 and 7) and challenged by OVA aerosol (on days 11-13) to induce airway inflammatory response. The mice were also administered with C. japonica Thunb. (CJT) (20 and 40 mg/kg Per oral) on days 9-13. CJT pretreatment was conducted in lipopolysaccharide (LPS)-stimulated RAW264.7 or phorbol 12-myristate 13-acetate (PMA)-stimulated A549 cells. Results: CJT administration significantly reduced the secretion of Th2 cytokines, TNF-α, IL-6, immunoglobulin E (IgE) and histamine, and the recruitment of eosinophils in an OVA-exposed mice. In histological analyses, the amelioration of inflammatory cell influx and mucus secretion were observed with CJT. The OVA-induced airway hyperresponsiveness (AHR), iNOS expression and NF-κB activation were effectively suppressed by CJT administration. In addition, CJT led to the upregulation of HO-1 expression. In an in vitro study, CJT pretreatment suppressed the LPS-induced TNF-α secretion in RAW264.7 cells and attenuated the PMA-induced IL-6, IL-8 and MCP-1 secretion in A549 cells. These effects were accompanied by downregulated NF-κB phosphorylation and by upregulated HO-1 expression. Conclusion: These results suggested that CJT has protective activity against OVA-induced airway inflammation via downregulation of NF-κB activation and upregulation of HO-1, suggesting that CJT has preventive potential for the development of allergic asthma.-
dc.publisherElsevier-
dc.titleCallicarpa japonica Thunb. ameliorates allergic airway inflammation by suppressing NF-κB activation and upregulating HO-1 expression-
dc.title.alternativeCallicarpa japonica Thunb. ameliorates allergic airway inflammation by suppressing NF-κB activation and upregulating HO-1 expression-
dc.typeArticle-
dc.citation.titleJournal of Ethnopharmacology-
dc.citation.number0-
dc.citation.endPage113523-
dc.citation.startPage113523-
dc.citation.volume267-
dc.contributor.affiliatedAuthorSung-Man Kim-
dc.contributor.affiliatedAuthorHyung Won Ryu-
dc.contributor.affiliatedAuthorOk-Kyoung Kwon-
dc.contributor.affiliatedAuthorDaseul Hwang-
dc.contributor.affiliatedAuthorMin Gu Kim-
dc.contributor.affiliatedAuthorJae-Hong Min-
dc.contributor.affiliatedAuthorSoo Yong Kim-
dc.contributor.affiliatedAuthorJin Hyub Paik-
dc.contributor.affiliatedAuthorSei-Ryang Oh-
dc.contributor.affiliatedAuthorKyung Seop Ahn-
dc.contributor.affiliatedAuthorJae-Won Lee-
dc.contributor.alternativeName김성만-
dc.contributor.alternativeName류형원-
dc.contributor.alternativeName권옥경-
dc.contributor.alternativeName황다슬-
dc.contributor.alternativeName김민구-
dc.contributor.alternativeName민재홍-
dc.contributor.alternativeNameZhang-
dc.contributor.alternativeName김수용-
dc.contributor.alternativeName백진협-
dc.contributor.alternativeName오세량-
dc.contributor.alternativeName안경섭-
dc.contributor.alternativeName이재원-
dc.identifier.bibliographicCitationJournal of Ethnopharmacology, vol. 267, pp. 113523-113523-
dc.identifier.doi10.1016/j.jep.2020.113523-
dc.subject.keywordAllergic asthma-
dc.subject.keywordCallicarpa japonica Thunb.-
dc.subject.keywordTh2 cytokines-
dc.subject.keywordEosinophil-
dc.subject.keywordNF-κB-
dc.subject.keywordHO-1-
dc.subject.localAllergic asthma-
dc.subject.localallergic asthma-
dc.subject.localCallicarpa japonica Thunb.-
dc.subject.localTh2 cytokines-
dc.subject.localeosinophil-
dc.subject.localEosinophil-
dc.subject.localEosinophils-
dc.subject.localNuclear factor-kappa B-
dc.subject.localnuclear factor κB-
dc.subject.localNf-κb-
dc.subject.localNF-kB-
dc.subject.localnuclear factor kappa B-
dc.subject.localNF-κB (nuclear factor kappa-B)-
dc.subject.localNF-kappaB-
dc.subject.localNuclear factor-κb-
dc.subject.localNF-κ B-
dc.subject.localNF-κB-
dc.subject.localNF-kappa B-
dc.subject.localNuclear factor κB (NF-κB)-
dc.subject.localNuclear factor κB-
dc.subject.localNFκB-
dc.subject.localNf-κB-
dc.subject.localNuclear factor-κB-
dc.subject.localnuclear factorκB-
dc.subject.localNuclear factor (NF)-κB-
dc.subject.localNuclear factor kappa B-
dc.subject.localnuclear factor-κB-
dc.subject.localNF-ΚB-
dc.subject.localNuclear factor-kappa B (NF-κB)-
dc.subject.localNuclear factor-kappaB-
dc.subject.localnuclear factor-kappaB-
dc.subject.localnuclear factor-kappaB (NF-κB)-
dc.subject.localNFkappaB-
dc.subject.localNuclear factor kappaB-
dc.subject.localHO-1-
dc.description.journalClassY-
Appears in Collections:
Ochang Branch Institute > Natural Product Research Center > 1. Journal Articles
Ochang Branch Institute > Division of National Bio-Infrastructure > Bio-Resource Central Bank > 1. Journal Articles
Ochang Branch Institute > Division of National Bio-Infrastructure > International Biological Material Research Center > 1. Journal Articles
Ochang Branch Institute > 1. Journal Articles
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