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Enhancement of cutaneous immune response to bacterial infection after low-level light therapy with 1072 nm infrared light: A preliminary study

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dc.contributor.authorLee, Seung Yoon Celine-
dc.contributor.authorSeong, In-Wha-
dc.contributor.authorKim, Ji-Seon-
dc.contributor.authorCheon, Kyeong-A-
dc.contributor.authorGu, Se Hun-
dc.contributor.authorKim, Hee Hwan-
dc.contributor.authorPark, Ki Ho-
dc.date.accessioned2021-09-07T05:17:42Z-
dc.date.available2021-09-07T05:17:42Z-
dc.date.created2021-06-19-
dc.date.issued2011-12-02-
dc.identifier.issn1011-1344-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/110925-
dc.description.abstractWe investigated the photobiomodulation effects of 1072 nm infrared light on the natural immune response involved in anti-bacterial and wound healing processes. Thirty mice infected with MRSA on the skin were divided into two groups. The experimental group was treated with 1072 nm infrared light (irradiance: 20 mW/cm(2), fluence: 12 J/cm(2) for 10 min) at 2, 4, 8, 12, 24 h, 3 and 5 days after inoculation and the control group with sham light. Serial changes of the mRNA levels of TLR2, IL-1 beta, INF-alpha. IL-6, iNOS, MCP-1. TGF-beta, bFGF and VEGF were studied by real time RT-PCR and those of the expression level of VEGF, bFGF, TGF-beta and NF-kappa B by immunohistochemistry. The mRNA levels of the cytokines involved in the early phase of anti-bacterial immune response (IL-1 beta, TNF-alpha, IL-6, MCP-1) increased significantly in the 1072 nm group, peaking between 12 and 24 h post-inoculation. These levels normalized after 3-5 days. Immunohistochemistry revealed a notably stronger expression of VEGF in the 1072 nm group from 8-h post-inoculation to 5-day post-inoculation. We concluded that 1072 nm infrared light had a photobiomodulation effect which resulted in an enhanced biological immune response to the bacterial infection by MRSA and also increased the expression of VEGF to a significant level. (C) 2011 Elsevier B.V. All rights reserved.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherELSEVIER SCIENCE SA-
dc.subjectENDOTHELIAL GROWTH-FACTOR-
dc.subjectNITRIC-OXIDE SYNTHASE-
dc.subjectEMITTING DIODE IRRADIATION-
dc.subjectPHOTODYNAMIC THERAPY-
dc.subjectACNE-VULGARIS-
dc.subjectPROPIONIBACTERIUM-ACNES-
dc.subjectSTAPHYLOCOCCUS-AUREUS-
dc.subjectHERPES LABIALIS-
dc.subjectANGIOGENESIS-
dc.subjectMECHANISMS-
dc.titleEnhancement of cutaneous immune response to bacterial infection after low-level light therapy with 1072 nm infrared light: A preliminary study-
dc.typeArticle-
dc.contributor.affiliatedAuthorSeong, In-Wha-
dc.identifier.doi10.1016/j.jphotobiol.2011.08.009-
dc.identifier.scopusid2-s2.0-80855132682-
dc.identifier.wosid000297891800002-
dc.identifier.bibliographicCitationJOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY B-BIOLOGY, v.105, no.3, pp.175 - 182-
dc.relation.isPartOfJOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY B-BIOLOGY-
dc.citation.titleJOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY B-BIOLOGY-
dc.citation.volume105-
dc.citation.number3-
dc.citation.startPage175-
dc.citation.endPage182-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaBiophysics-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryBiophysics-
dc.subject.keywordPlusENDOTHELIAL GROWTH-FACTOR-
dc.subject.keywordPlusNITRIC-OXIDE SYNTHASE-
dc.subject.keywordPlusEMITTING DIODE IRRADIATION-
dc.subject.keywordPlusPHOTODYNAMIC THERAPY-
dc.subject.keywordPlusACNE-VULGARIS-
dc.subject.keywordPlusPROPIONIBACTERIUM-ACNES-
dc.subject.keywordPlusSTAPHYLOCOCCUS-AUREUS-
dc.subject.keywordPlusHERPES LABIALIS-
dc.subject.keywordPlusANGIOGENESIS-
dc.subject.keywordPlusMECHANISMS-
dc.subject.keywordAuthorPhotobiomodulation-
dc.subject.keywordAuthor1072 nm-
dc.subject.keywordAuthorLow level light therapy-
dc.subject.keywordAuthorLED-
dc.subject.keywordAuthorAntibacterial-
dc.subject.keywordAuthorVEGF-
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