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Oral Administration of beta-Glucan and Lactobacillus plantarum Alleviates Atopic Dermatitis-Like Symptoms

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dc.contributor.authorKim, In Sung-
dc.contributor.authorLee, Seung Ho-
dc.contributor.authorKwon, Young Min-
dc.contributor.authorAdhikari, Bishnu-
dc.contributor.authorKim, Jeong A.-
dc.contributor.authorYu, Da Yoon-
dc.contributor.authorKim, Gwang Il-
dc.contributor.authorLim, Jong Min-
dc.contributor.authorKim, Sung Hak-
dc.contributor.authorLee, Sang Suk-
dc.contributor.authorMoon, Yang Soo-
dc.contributor.authorChoi, In Soon-
dc.contributor.authorCho, Kwang Keun-
dc.date.accessioned2022-12-26T14:18:19Z-
dc.date.available2022-12-26T14:18:19Z-
dc.date.issued2019-11-
dc.identifier.issn1017-7825-
dc.identifier.issn1738-8872-
dc.identifier.urihttps://scholarworks.gnu.ac.kr/handle/sw.gnu/8530-
dc.description.abstractAtopic dermatitis ( AD) is a chronic inflammatory skin disease of mainly infants and children. Currently, the development of safe and effective treatments for AD is urgently required. The present study was conducted to investigate the immunomodulatory effects of yeast-extracted beta-1,3/1,6-glucan and/or Lactobacillus plantarum (L. plantarum) LM1004 against AD-like symptoms. To purpose, beta-1,3/1,6-glucan and/or L. plantarum LM1004 were orally administered to AD-induced animal models of rat (histamine-induced vasodilation) and mouse (pruritus and contact dermatitis) exhibiting different symptoms of AD. We then investigated the treatment effects on AD-like symptoms, gene expression of immune-related factors, and gut microbiomes. Oral administration of beta-1,3/1,6-glucan (0.01 g/kg initial body weight) and/or 2 x 10(12) cells/g L. plantarum LM1004 (0.01 g/kg initial body weight) to AD-induced animal models showed significantly reduced vasodilation in the rat model, and pruritus, edema, and serum histamine in the mouse models (p < 0.05). Interestingly, beta-1,3/1,6-glucan and/or L. plantarum LM1004 significantly decreased the mRNA levels of Th2 and Th17 cell transcription factors, while the transcription factors of Th1 and Treg cells, galactin-9, filaggrin increased, which are indicative of enhanced immunomodulation (p < 0.05). Moreover, in rats with no AD induction, the same treatments significantly increased the relative abundance of phylum Bacteroidetes and the genus Bacteroides. Furthermore, bacterial taxa associated with butyrate production such as, Lachnospiraceae and Ruminococcaceae at family, and Roseburia at genus level were increased in the treated groups. These findings suggest that the dietary supplementation of beta-1,3/1,6-glucan and/or L. plantarum LM1004 has a great potential for treatment of AD as well as obesity in humans through mechanisms that might involve modulation of host immune systems and gut microbiota.-
dc.format.extent14-
dc.language영어-
dc.language.isoENG-
dc.publisher한국미생물·생명공학회-
dc.titleOral Administration of beta-Glucan and Lactobacillus plantarum Alleviates Atopic Dermatitis-Like Symptoms-
dc.typeArticle-
dc.publisher.location대한민국-
dc.identifier.doi10.4014/jmb.1907.07011-
dc.identifier.scopusid2-s2.0-85075962899-
dc.identifier.wosid000499146400002-
dc.identifier.bibliographicCitationJournal of Microbiology and Biotechnology, v.29, no.11, pp 1693 - 1706-
dc.citation.titleJournal of Microbiology and Biotechnology-
dc.citation.volume29-
dc.citation.number11-
dc.citation.startPage1693-
dc.citation.endPage1706-
dc.type.docTypeArticle-
dc.identifier.kciidART002529163-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
dc.relation.journalResearchAreaBiotechnology & Applied Microbiology-
dc.relation.journalResearchAreaMicrobiology-
dc.relation.journalWebOfScienceCategoryBiotechnology & Applied Microbiology-
dc.relation.journalWebOfScienceCategoryMicrobiology-
dc.subject.keywordPlusGUT MICROBIOTA-
dc.subject.keywordPlusT-CELLS-
dc.subject.keywordPlusSCRATCHING BEHAVIOR-
dc.subject.keywordPlusBINDING LECTIN-
dc.subject.keywordPlusANIMAL-MODELS-
dc.subject.keywordPlusMAST-CELLS-
dc.subject.keywordPlusSKIN-
dc.subject.keywordPlusRESPONSES-
dc.subject.keywordPlusGALECTIN-9-
dc.subject.keywordPlusIGE-
dc.subject.keywordAuthorGut microbiota-
dc.subject.keywordAuthorimmunomodulation-
dc.subject.keywordAuthorTh1 cells-
dc.subject.keywordAuthorTh2 cells-
dc.subject.keywordAuthortreg cells-
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