Callicarpa japonica Thunb. reduces inflammatory responses: A mouse model of lipopolysaccharide-induced acute lung injury = 캘리카파의 항염증 효과

Cited 24 time in scopus
Metadata Downloads

Full metadata record

DC FieldValueLanguage
dc.contributor.authorNa Rae Shin-
dc.contributor.authorIn Sik Shin-
dc.contributor.authorHyuk-Hwan Song-
dc.contributor.authorJu Mi Hong-
dc.contributor.authorOk-Kyoung Kwon-
dc.contributor.authorChan Mi Jeon-
dc.contributor.authorJung Hee Kim-
dc.contributor.authorSang Woo Lee-
dc.contributor.authorJoongku Lee-
dc.contributor.authorH Jin-
dc.contributor.authorW Y Li-
dc.contributor.authorSei-Ryang Oh-
dc.contributor.authorK W Hahn-
dc.contributor.authorKyung Seop Ahn-
dc.date.accessioned2017-04-19T10:03:03Z-
dc.date.available2017-04-19T10:03:03Z-
dc.date.issued2015-
dc.identifier.issn1567-5769-
dc.identifier.uri10.1016/j.intimp.2015.01.025ko
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/12565-
dc.description.abstractCallicarpa japonica Thunb. (CJT) is traditionally used as an herbal remedy for the treatment of inflammatory diseases. This study aimed to investigate the anti-inflammatory response of CJT in lipopolysaccharide (LPS)-stimulated RAW264.7 cells and LPS-induced acute lung injury (ALI) in mice. The C57BL/6 mice were administered 30 mg/kg of CJT by oral gavage for 3 days. LPS is applied to animals by intranasal administration 1 h after final CJT treatment. LPS is applied to animals by intranasal administration 1 h after final CJT treatment. LPS was delivered intranasally 1 h after the final CJT treatment. In the LPS-stimulated RAW264.7 cells, CJT significantly decreased nitric oxide (NO) and interleukin (IL)-6 in a concentration-dependent manner by reducing inducible NO synthase (iNOS) and IL-6 mRNA levels. In the ALI model, CJT decreased the inflammatory cell count in the bronchoalveolar lavage fluid (BALF) while IL-6 levels were reduced in CJT-treated mice compared with the ALI control mice. CJT also inhibited airway inflammation by reducing iNOS expression in lung tissue. In conclusion, our results indicate that CJT inhibits inflammatory responses in LPS-stimulated RAW264.7 cells and in the LPS-induced ALI model. Therefore, we suggest that CJT has the potential to treat inflammatory diseases such as pneumonia.-
dc.publisherElsevier-
dc.titleCallicarpa japonica Thunb. reduces inflammatory responses: A mouse model of lipopolysaccharide-induced acute lung injury = 캘리카파의 항염증 효과-
dc.title.alternativeCallicarpa japonica Thunb. reduces inflammatory responses: A mouse model of lipopolysaccharide-induced acute lung injury-
dc.typeArticle-
dc.citation.titleInternational Immunopharmacology-
dc.citation.number1-
dc.citation.endPage180-
dc.citation.startPage174-
dc.citation.volume26-
dc.contributor.affiliatedAuthorNa Rae Shin-
dc.contributor.affiliatedAuthorIn Sik Shin-
dc.contributor.affiliatedAuthorHyuk-Hwan Song-
dc.contributor.affiliatedAuthorJu Mi Hong-
dc.contributor.affiliatedAuthorOk-Kyoung Kwon-
dc.contributor.affiliatedAuthorChan Mi Jeon-
dc.contributor.affiliatedAuthorJung Hee Kim-
dc.contributor.affiliatedAuthorSang Woo Lee-
dc.contributor.affiliatedAuthorJoongku Lee-
dc.contributor.affiliatedAuthorSei-Ryang Oh-
dc.contributor.affiliatedAuthorKyung Seop Ahn-
dc.contributor.alternativeName신나래-
dc.contributor.alternativeName신인식-
dc.contributor.alternativeName송혁환-
dc.contributor.alternativeName홍주미-
dc.contributor.alternativeName권옥경-
dc.contributor.alternativeName전찬미-
dc.contributor.alternativeName김정희-
dc.contributor.alternativeName이상우-
dc.contributor.alternativeName이중구-
dc.contributor.alternativeNameJin-
dc.contributor.alternativeNameLi-
dc.contributor.alternativeName오세량-
dc.contributor.alternativeName한규웅-
dc.contributor.alternativeName안경섭-
dc.identifier.bibliographicCitationInternational Immunopharmacology, vol. 26, no. 1, pp. 174-180-
dc.identifier.doi10.1016/j.intimp.2015.01.025-
dc.subject.keywordAcute lung injury-
dc.subject.keywordCallicarpa japonica-
dc.subject.keywordInducible nitric oxide synthase-
dc.subject.keywordInterleukin-6-
dc.subject.keywordThunb.-
dc.subject.localAcute lung injury-
dc.subject.localacute lung injury-
dc.subject.localAcute Lung Injury-
dc.subject.localacute lung injury (ALI)-
dc.subject.localCallicarpa japonica-
dc.subject.localInducible nitric oxide synthase (iNOS)-
dc.subject.localInducible nitric oxide synthase-
dc.subject.localinducible nnitric oxide synthase-
dc.subject.localiNOS-
dc.subject.localInducible nitric oxide synthease (iNOS)-
dc.subject.localINOS-
dc.subject.localinducible nitric oxide synthase-
dc.subject.localIL6-
dc.subject.localinterukin -6-
dc.subject.localInterleukin-6 (IL-6)-
dc.subject.localIL-6-
dc.subject.localIl-6-
dc.subject.localinterleukin-6-
dc.subject.localinterleukin-6 (IL-6)-
dc.subject.localInterleukin-6-
dc.subject.localThunb.-
dc.description.journalClassY-
Appears in Collections:
Ochang Branch Institute > Natural Product Research Center > 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
Files in This Item:
  • There are no files associated with this item.


Items in OpenAccess@KRIBB are protected by copyright, with all rights reserved, unless otherwise indicated.