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dc.contributor.authorRa, Ho Jong-
dc.contributor.authorOh, Mi Young-
dc.contributor.authorKim, Hee Ju-
dc.contributor.authorLee, Seung Yong-
dc.contributor.authorEom, Dae Woon-
dc.contributor.authorLee, Suk Kyu-
dc.contributor.authorKim, Su-Nam-
dc.contributor.authorChung, Kyu Sung-
dc.contributor.authorJang, Hyuk Jai-
dc.date.accessioned2024-01-19T23:04:59Z-
dc.date.available2024-01-19T23:04:59Z-
dc.date.created2021-09-03-
dc.date.issued2018-03-
dc.identifier.issn1226-4512-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/121651-
dc.description.abstractPRF001 is a fragmented DNA polymer extracted from the testes of salmon. The purpose of this study was to assess the anti-inflammatory effect of PRF001 in vitro as well as the protective effect of PRF001 intake against arthritis in a rat model. In vitro, cell survival and inflammatory markers after H2O2 treatment to induce cell damage were investigated in CHON-001 cells treated with different concentrations of PRF001. In vivo, osteoarthritis was induced by intra-articular injection of monosodium iodoacetate (MIA) into the knee joints of rats. After consumption of PRF001 (10, 50, or 100 mg/kg) for 4 weeks, inflammatory mediators and cytokines in articular cartilage were investigated. In vitro, the levels of inflammatory markers, IL-1 beta, TNF-alpha, COX-2, iNOS, and PGE2, were significantly suppressed by PRF001 treatment. In vivo, the inflammatory mediators and cytokines, IL-1 beta, p-Erk1/2, NF-kappa B, TNF-alpha, COX-2, and PGE2, as well as MMP3 and MMP7, which have catabolic activity in chondrocytes, were decreased in the MIA-induced osteoarthritic rats following intake of PRF001. Histological analysis revealed that PRF001 had a protective effect on the articular cartilage. Altogether, these results demonstrated that the anti-inflammatory property of PRF001 contributes to its protective effects in osteoarthritis through deregulating IL1 beta, TNF-alpha, and subsequent signals, such as p-Erk1/2, NF-kappa B, COX-2, PGE2, and MMPs.-
dc.languageEnglish-
dc.publisherKOREAN JOURNAL OF PHYSIOLOGY & PHARMACOLOGY-
dc.subjectARTERY OCCLUSIVE DISEASE-
dc.subjectNECROSIS-FACTOR-ALPHA-
dc.subjectDIABETIC FOOT ULCERS-
dc.subjectPOLYDEOXYRIBONUCLEOTIDE PDRN-
dc.subjectARTICULAR-CARTILAGE-
dc.subjectHUMAN CHONDROCYTES-
dc.subjectPROSTAGLANDIN E-2-
dc.subjectAPOPTOSIS-
dc.subjectCYTOKINES-
dc.subjectINFLAMMATION-
dc.titleEffects of salmon DNA fraction in vitro and in a monosodium iodoacetate-induced osteoarthritis rat model-
dc.typeArticle-
dc.identifier.doi10.4196/kjpp.2018.22.2.163-
dc.description.journalClass1-
dc.identifier.bibliographicCitationKOREAN JOURNAL OF PHYSIOLOGY & PHARMACOLOGY, v.22, no.2, pp.163 - 172-
dc.citation.titleKOREAN JOURNAL OF PHYSIOLOGY & PHARMACOLOGY-
dc.citation.volume22-
dc.citation.number2-
dc.citation.startPage163-
dc.citation.endPage172-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
dc.identifier.kciidART002323920-
dc.identifier.wosid000426608800006-
dc.identifier.scopusid2-s2.0-85043363759-
dc.relation.journalWebOfScienceCategoryPharmacology & Pharmacy-
dc.relation.journalWebOfScienceCategoryPhysiology-
dc.relation.journalResearchAreaPharmacology & Pharmacy-
dc.relation.journalResearchAreaPhysiology-
dc.type.docTypeArticle-
dc.subject.keywordPlusARTERY OCCLUSIVE DISEASE-
dc.subject.keywordPlusNECROSIS-FACTOR-ALPHA-
dc.subject.keywordPlusDIABETIC FOOT ULCERS-
dc.subject.keywordPlusPOLYDEOXYRIBONUCLEOTIDE PDRN-
dc.subject.keywordPlusARTICULAR-CARTILAGE-
dc.subject.keywordPlusHUMAN CHONDROCYTES-
dc.subject.keywordPlusPROSTAGLANDIN E-2-
dc.subject.keywordPlusAPOPTOSIS-
dc.subject.keywordPlusCYTOKINES-
dc.subject.keywordPlusINFLAMMATION-
dc.subject.keywordAuthorChondrocyte-
dc.subject.keywordAuthorCytokine-
dc.subject.keywordAuthorInflammation-
dc.subject.keywordAuthorOsteoarthritis-
dc.subject.keywordAuthorPolydeoxyribonucleotide-
dc.subject.keywordAuthorPRF001-
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