Humulus japonicus ameliorates irritant contact dermatitis by suppressing NF-κB p65-dependent inflammatory responses in mice

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dc.contributor.authorYu-Bin Kim-
dc.contributor.authorEun-Jung Kang-
dc.contributor.authorJung Ran Noh-
dc.contributor.authorJ P An-
dc.contributor.authorJ T Park-
dc.contributor.authorW K Oh-
dc.contributor.authorYong-Hoon Kim-
dc.contributor.authorChul-Ho Lee-
dc.date.accessioned2023-08-25T16:32:32Z-
dc.date.available2023-08-25T16:32:32Z-
dc.date.issued2023-
dc.identifier.issn1792-0981-
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/32530-
dc.description.abstractAs a type of contact dermatitis (CD), irritant CD (ICD) is an acute skin inflammation caused by external irritants, such as soap, water and chemicals. Humulus japonicus (HJ) is a herbal medicine widely distributed in Asian countries and has anti-inflammatory, antimicrobial and antioxidant effects. The current study aimed to investigate the anti-dermatitis effect of HJ on ICD and determine the molecular basis of this effect using 12-O-tetradecanoylphorbol-13-acetate (TPA)-induced dermatitis mice models and lipopolysaccharide (LPS)-stimulated RAW264.7 cells. Mice were orally administered HJ and luteolin, the major compound in HJ, and topically administered TPA on the right ear to induce dermatitis. Topical application of TPA induced ear redness, oedema and increased infiltration of neutrophils and macrophages, which ameliorated following HJ and luteolin administration. The gene expression levels of inflammatory cell migrating chemokines, chemokine ligand 3 (CCL3) and chemokine (C-X-C motif) ligand 2 (CXCL2), and pro-inflammatory cytokine, IL-1β, were reduced in the ears of HJ- and luteolin-treated mice. HJ and luteolin also inhibited the gene expression of chemokines, CCL3 and CXCL2, and pro-inflammatory cytokines, IL-1β, IL-6 and TNF-α, in LPS-stimulated RAW264.7 cells. Moreover, HJ and luteolin decreased the expression levels of two key inflammatory enzymes, cyclooxygenase-2 (COX2) and inducible nitric oxide synthase (iNOS), and total and active phosphorylation of NF-κB p65. These results suggest that HJ could have a protective effect against ICD by suppressing inflammatory responses; therefore, HJ is a promising therapeutic strategy for ICD treatment.-
dc.publisherSpandidos Publ Ltd-
dc.titleHumulus japonicus ameliorates irritant contact dermatitis by suppressing NF-κB p65-dependent inflammatory responses in mice-
dc.title.alternativeHumulus japonicus ameliorates irritant contact dermatitis by suppressing NF-κB p65-dependent inflammatory responses in mice-
dc.typeArticle-
dc.citation.titleExperimental and Therapeutic Medicine-
dc.citation.number3-
dc.citation.endPage446-
dc.citation.startPage446-
dc.citation.volume26-
dc.contributor.affiliatedAuthorYu-Bin Kim-
dc.contributor.affiliatedAuthorEun-Jung Kang-
dc.contributor.affiliatedAuthorJung Ran Noh-
dc.contributor.affiliatedAuthorYong-Hoon Kim-
dc.contributor.affiliatedAuthorChul-Ho Lee-
dc.contributor.alternativeName김유빈-
dc.contributor.alternativeName강은정-
dc.contributor.alternativeName노정란-
dc.contributor.alternativeName안진표-
dc.contributor.alternativeName박종태-
dc.contributor.alternativeName오원근-
dc.contributor.alternativeName김용훈-
dc.contributor.alternativeName이철호-
dc.identifier.bibliographicCitationExperimental and Therapeutic Medicine, vol. 26, no. 3, pp. 446-446-
dc.identifier.doi10.3892/etm.2023.12145-
dc.subject.keywordHumulus japonicus-
dc.subject.keywordIrritant contact dermatitis-
dc.subject.keywordLuteolin-
dc.subject.keyword12-O-tetradecanoylphorbol-13-acetate-
dc.subject.keywordNF-κB-
dc.subject.keywordp65-
dc.subject.localHumulus japonicas-
dc.subject.localHumulus japonicus-
dc.subject.localhumulus japonicus-
dc.subject.localirritant contact dermatitis-
dc.subject.localIrritant contact dermatitis-
dc.subject.localluteolin-
dc.subject.localLuteolin-
dc.subject.local12-O-tetradecanoylphorbol-13-acetate-
dc.subject.localNFkappaB-
dc.subject.localNFκB-
dc.subject.localNf-κB-
dc.subject.localNf-κb-
dc.subject.localNuclear factor (NF)-κB-
dc.subject.localNuclear factor kappa B-
dc.subject.localNuclear factor kappaB-
dc.subject.localNuclear factor κB-
dc.subject.localNuclear factor κB (NF-κB)-
dc.subject.localNuclear factor-kappa B-
dc.subject.localNuclear factor-kappa B (NF-κB)-
dc.subject.localNuclear factor-kappaB-
dc.subject.localNuclear factor-κB-
dc.subject.localNuclear factor-κb-
dc.subject.localNF-kB-
dc.subject.localNF-kappa B-
dc.subject.localNF-kappaB-
dc.subject.localNF-ΚB-
dc.subject.localNF-κ B-
dc.subject.localNF-κB-
dc.subject.localNF-κB (nuclear factor kappa-B)-
dc.subject.localnuclear factor kappa B-
dc.subject.localnuclear factor κB-
dc.subject.localnuclear factor-kappaB-
dc.subject.localnuclear factor-kappaB (NF-κB)-
dc.subject.localnuclear factor-κB-
dc.subject.localnuclear factorκB-
dc.subject.localP65-
dc.subject.localp65-
dc.description.journalClassY-
Appears in Collections:
Ochang Branch Institute > Division of National Bio-Infrastructure > Laboratory Animal Resource & Research Center > 1. Journal Articles
Ochang Branch Institute > Division of National Bio-Infrastructure > 1. Journal Articles
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