DC Field | Value | Language |
---|---|---|
dc.contributor.author | Yu-Bin Kim | - |
dc.contributor.author | Eun-Jung Kang | - |
dc.contributor.author | Jung Ran Noh | - |
dc.contributor.author | J P An | - |
dc.contributor.author | J T Park | - |
dc.contributor.author | W K Oh | - |
dc.contributor.author | Yong-Hoon Kim | - |
dc.contributor.author | Chul-Ho Lee | - |
dc.date.accessioned | 2023-08-25T16:32:32Z | - |
dc.date.available | 2023-08-25T16:32:32Z | - |
dc.date.issued | 2023 | - |
dc.identifier.issn | 1792-0981 | - |
dc.identifier.uri | https://oak.kribb.re.kr/handle/201005/32530 | - |
dc.description.abstract | As 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.publisher | Spandidos Publ Ltd | - |
dc.title | Humulus japonicus ameliorates irritant contact dermatitis by suppressing NF-κB p65-dependent inflammatory responses in mice | - |
dc.title.alternative | Humulus japonicus ameliorates irritant contact dermatitis by suppressing NF-κB p65-dependent inflammatory responses in mice | - |
dc.type | Article | - |
dc.citation.title | Experimental and Therapeutic Medicine | - |
dc.citation.number | 3 | - |
dc.citation.endPage | 446 | - |
dc.citation.startPage | 446 | - |
dc.citation.volume | 26 | - |
dc.contributor.affiliatedAuthor | Yu-Bin Kim | - |
dc.contributor.affiliatedAuthor | Eun-Jung Kang | - |
dc.contributor.affiliatedAuthor | Jung Ran Noh | - |
dc.contributor.affiliatedAuthor | Yong-Hoon Kim | - |
dc.contributor.affiliatedAuthor | Chul-Ho Lee | - |
dc.contributor.alternativeName | 김유빈 | - |
dc.contributor.alternativeName | 강은정 | - |
dc.contributor.alternativeName | 노정란 | - |
dc.contributor.alternativeName | 안진표 | - |
dc.contributor.alternativeName | 박종태 | - |
dc.contributor.alternativeName | 오원근 | - |
dc.contributor.alternativeName | 김용훈 | - |
dc.contributor.alternativeName | 이철호 | - |
dc.identifier.bibliographicCitation | Experimental and Therapeutic Medicine, vol. 26, no. 3, pp. 446-446 | - |
dc.identifier.doi | 10.3892/etm.2023.12145 | - |
dc.subject.keyword | Humulus japonicus | - |
dc.subject.keyword | Irritant contact dermatitis | - |
dc.subject.keyword | Luteolin | - |
dc.subject.keyword | 12-O-tetradecanoylphorbol-13-acetate | - |
dc.subject.keyword | NF-κB | - |
dc.subject.keyword | p65 | - |
dc.subject.local | Humulus japonicas | - |
dc.subject.local | Humulus japonicus | - |
dc.subject.local | humulus japonicus | - |
dc.subject.local | irritant contact dermatitis | - |
dc.subject.local | Irritant contact dermatitis | - |
dc.subject.local | luteolin | - |
dc.subject.local | Luteolin | - |
dc.subject.local | 12-O-tetradecanoylphorbol-13-acetate | - |
dc.subject.local | NFkappaB | - |
dc.subject.local | NFκB | - |
dc.subject.local | Nf-κB | - |
dc.subject.local | Nf-κb | - |
dc.subject.local | Nuclear factor (NF)-κB | - |
dc.subject.local | Nuclear factor kappa B | - |
dc.subject.local | Nuclear factor kappaB | - |
dc.subject.local | Nuclear factor κB | - |
dc.subject.local | Nuclear factor κB (NF-κB) | - |
dc.subject.local | Nuclear factor-kappa B | - |
dc.subject.local | Nuclear factor-kappa B (NF-κB) | - |
dc.subject.local | Nuclear factor-kappaB | - |
dc.subject.local | Nuclear factor-κB | - |
dc.subject.local | Nuclear factor-κb | - |
dc.subject.local | NF-kB | - |
dc.subject.local | NF-kappa B | - |
dc.subject.local | NF-kappaB | - |
dc.subject.local | NF-ΚB | - |
dc.subject.local | NF-κ B | - |
dc.subject.local | NF-κB | - |
dc.subject.local | NF-κB (nuclear factor kappa-B) | - |
dc.subject.local | nuclear factor kappa B | - |
dc.subject.local | nuclear factor κB | - |
dc.subject.local | nuclear factor-kappaB | - |
dc.subject.local | nuclear factor-kappaB (NF-κB) | - |
dc.subject.local | nuclear factor-κB | - |
dc.subject.local | nuclear factorκB | - |
dc.subject.local | P65 | - |
dc.subject.local | p65 | - |
dc.description.journalClass | Y | - |
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