Stellera chamaejasme and its main compound luteolin 7-O-glucoside alleviates skin lesions in oxazolone- and 2,4-dinitrochlorobenzene-stimulated murine models of atopic dermatitis

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dc.contributor.authorB G Jo-
dc.contributor.authorN J Park-
dc.contributor.authorJ Jegal-
dc.contributor.authorSangho Choi-
dc.contributor.authorSang Woo Lee-
dc.contributor.authorL W Yi-
dc.contributor.authorS N Kim-
dc.contributor.authorM H Yang-
dc.date.accessioned2019-07-10T01:23:21Z-
dc.date.available2019-07-10T01:23:21Z-
dc.date.issued2019-
dc.identifier.issn0032-0943-
dc.identifier.uri10.1055/a-0746-8698ko
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/18757-
dc.description.abstractStellera chamaejasme, also known as Langdu , has been traditionally used for the management of skin-related diseases such as psoriasis and skin ulcers. The aim of this study was to determine whether S. chamaejasme and its major component, luteolin 7- O -glucoside, have a preventive effect on the development of atopic dermatitis in oxazolone-treated BALB/c mice and 2,4-dinitrochlorobenzene-treated hairless mice. The epicutaneous applications of oxazolone and 2,4-dinitrochlorobenzene evoke an experimental murine atopic dermatitis-like reaction in BALB/c mouse ears and SKH-1 hairless mice. Atopic skin symptoms, including erythema (redness), pruritus (itching), exudation (weeping), excoriation (peeling), and lichenification (skin thickening), responded to treatment with S. chamaejasme aerial parts EtOH extract for 2 or 3 weeks. Histopathological examination revealed S. chamaejasme aerial parts EtOH extract significantly reduced inflammatory cell infiltration when applied to atopic dermatitis mice. In addition, luteolin 7- O -glucoside, the major active compound of the S. chamaejasme aerial parts EtOH extract, decreased serum IgE and IL-4 levels and transepidermal water loss and increased skin hydration, therefore exhibiting strong anti-atopic dermatitis activity in 2,4-dinitrochlorobenzene-induced atopic dermatitis mice. In this study, we confirmed antipruritic and antidermatitic effects of S. chamaejasme extract and its main component luteolin 7- O -glucoside in atopic dermatitis murine models. The study shows S. chamaejasme aerial parts EtOH extract and luteolin 7- O -glucoside are most likely to be potential drug candidates for atopic dermatitis treatment.-
dc.publisherGeorg Thieme Verlag Kg-
dc.titleStellera chamaejasme and its main compound luteolin 7-O-glucoside alleviates skin lesions in oxazolone- and 2,4-dinitrochlorobenzene-stimulated murine models of atopic dermatitis-
dc.title.alternativeStellera chamaejasme and its main compound luteolin 7-O-glucoside alleviates skin lesions in oxazolone- and 2,4-dinitrochlorobenzene-stimulated murine models of atopic dermatitis-
dc.typeArticle-
dc.citation.titlePlanta Medica-
dc.citation.number7-
dc.citation.endPage590-
dc.citation.startPage583-
dc.citation.volume85-
dc.contributor.affiliatedAuthorSangho Choi-
dc.contributor.affiliatedAuthorSang Woo Lee-
dc.contributor.alternativeName조범근-
dc.contributor.alternativeName박노준-
dc.contributor.alternativeName제갈종환-
dc.contributor.alternativeName최상호-
dc.contributor.alternativeName이상우-
dc.contributor.alternativeNameYi-
dc.contributor.alternativeName김수남-
dc.contributor.alternativeName양민혜-
dc.identifier.bibliographicCitationPlanta Medica, vol. 85, no. 7, pp. 583-590-
dc.identifier.doi10.1055/a-0746-8698-
dc.subject.keywordStellera chamaejasme-
dc.subject.keywordThymelaeaceae-
dc.subject.keywordluteolin 7Oglucoside-
dc.subject.keywordatopic dermatitis-
dc.subject.keywordskin barrier function-
dc.subject.keywordinterleukin 4-
dc.subject.keywordimmunoglobulin E-
dc.subject.localStellera chamaejasme-
dc.subject.localStellera chamaejasme L.-
dc.subject.localThymelaeaceae-
dc.subject.localluteolin 7Oglucoside-
dc.subject.localAtopic Dermatitis-
dc.subject.localAtopic dermatitis-
dc.subject.localatopic dermatitis-
dc.subject.localatopic dermatitis (AD)-
dc.subject.localAtopic dermatitis (AD)-
dc.subject.localSkin barrier function-
dc.subject.localskin barrier function-
dc.subject.localInterleukin 4-
dc.subject.localInterleukin-4-
dc.subject.localinterleukin 4-
dc.subject.localInterleukin 4 (IL-4)-
dc.subject.localImmunoglobulin E-
dc.subject.localimmunoglobulin E-
dc.subject.localImmunoglobulin E (IgE)-
dc.description.journalClassY-
Appears in Collections:
Ochang Branch Institute > Division of National Bio-Infrastructure > International Biological Material Research Center > 1. Journal Articles
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