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Seomae mugwort and jaceosidin attenuate osteoarthritic cartilage damage by blocking IkappaB degradation in mice
DC Field | Value | Language |
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dc.contributor.author | Lee, H | - |
dc.contributor.author | Jang, D | - |
dc.contributor.author | Jeon, J | - |
dc.contributor.author | Cho, C | - |
dc.contributor.author | Choi, S | - |
dc.contributor.author | Han, SJ | - |
dc.contributor.author | Oh, E | - |
dc.contributor.author | Nam, J | - |
dc.contributor.author | Park, CH | - |
dc.contributor.author | Shin, YS | - |
dc.contributor.author | Yun, SP | - |
dc.contributor.author | Yang, S | - |
dc.contributor.author | Kang, LJ | - |
dc.date.accessioned | 2022-11-29T01:43:24Z | - |
dc.date.available | 2022-11-29T01:43:24Z | - |
dc.date.issued | 2020 | - |
dc.identifier.issn | 1582-1838 | - |
dc.identifier.uri | http://repository.ajou.ac.kr/handle/201003/22982 | - |
dc.description.abstract | Seomae mugwort, a Korean native variety of Artemisia argyi, exhibits physiological effects against various diseases. However, its effects on osteoarthritis (OA) are unclear. In this study, a Seomae mugwort extract prevented cartilage destruction in an OA mouse model. In vitro and ex vivo analyses revealed that the extract suppressed MMP3, MMP13, ADAMTS4 and ADAMTS5 expression induced by IL-1beta, IL-6 and TNF-alpha and inhibited the loss of extracellular sulphated proteoglycans. In vivo analysis revealed that oral administration of the extract suppressed DMM-induced cartilage destruction. We identified jaceosidin in Seomae mugwort and showed that this compound decreased MMP3, MMP13, ADAMTS4 and ADAMTS5 expression levels, similar to the action of the Seomae mugwort extract in cultured chondrocytes. Interestingly, jaceosidin and eupatilin combined had similar effects to Seomae mugwort in the DMM-induced OA model. Induction of IkappaB degradation by IL-1beta was blocked by the extract and jaceosidin, whereas JNK phosphorylation was only suppressed by the extract. These results suggest that the Seomae mugwort extract and jaceosidin can attenuate cartilage destruction by suppressing MMPs, ADAMTS4/5 and the nuclear factor-kappaB signalling pathway by blocking IkappaB degradation. Thus, the findings support the potential application of Seomae mugwort, and particularly jaceosidin, as natural therapeutics for OA. | - |
dc.language.iso | en | - |
dc.subject.MESH | Animals | - |
dc.subject.MESH | Artemisia | - |
dc.subject.MESH | Arthritis, Experimental | - |
dc.subject.MESH | Biomarkers | - |
dc.subject.MESH | Cartilage, Articular | - |
dc.subject.MESH | Cell Survival | - |
dc.subject.MESH | Cells, Cultured | - |
dc.subject.MESH | Chondrocytes | - |
dc.subject.MESH | Disease Models, Animal | - |
dc.subject.MESH | Flavonoids | - |
dc.subject.MESH | Gene Expression | - |
dc.subject.MESH | I-kappa B Proteins | - |
dc.subject.MESH | Immunohistochemistry | - |
dc.subject.MESH | Interleukin-1beta | - |
dc.subject.MESH | Matrix Metalloproteinases | - |
dc.subject.MESH | Mice | - |
dc.subject.MESH | Models, Biological | - |
dc.subject.MESH | NF-kappa B | - |
dc.subject.MESH | Osteoarthritis | - |
dc.subject.MESH | Plant Extracts | - |
dc.subject.MESH | Proteoglycans | - |
dc.subject.MESH | Proteolysis | - |
dc.subject.MESH | Signal Transduction | - |
dc.title | Seomae mugwort and jaceosidin attenuate osteoarthritic cartilage damage by blocking IkappaB degradation in mice | - |
dc.type | Article | - |
dc.identifier.pmid | 32529755 | - |
dc.identifier.url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7348148 | - |
dc.subject.keyword | cartilage destruction | - |
dc.subject.keyword | IκB | - |
dc.subject.keyword | jaceosidin | - |
dc.subject.keyword | matrix metalloproteinase | - |
dc.subject.keyword | nuclear factor‐kappa B | - |
dc.subject.keyword | osteoarthritis | - |
dc.subject.keyword | Seomae mugwort | - |
dc.contributor.affiliatedAuthor | Yang, S | - |
dc.contributor.affiliatedAuthor | Kang, LJ | - |
dc.type.local | Journal Papers | - |
dc.identifier.doi | 10.1111/jcmm.15471 | - |
dc.citation.title | Journal of cellular and molecular medicine | - |
dc.citation.volume | 24 | - |
dc.citation.number | 14 | - |
dc.citation.date | 2020 | - |
dc.citation.startPage | 8126 | - |
dc.citation.endPage | 8137 | - |
dc.identifier.bibliographicCitation | Journal of cellular and molecular medicine, 24(14). : 8126-8137, 2020 | - |
dc.identifier.eissn | 1582-4934 | - |
dc.relation.journalid | J015821838 | - |
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