Detailed Information

Cited 28 time in webofscience Cited 27 time in scopus
Metadata Downloads

Knee osteoarthritis accelerates amyloid beta deposition and neurodegeneration in a mouse model of Alzheimer’s disease

Full metadata record
DC Field Value Language
dc.contributor.authorGupta, D.P.-
dc.contributor.authorLee, Y.-S.-
dc.contributor.authorChoe, Y.-
dc.contributor.authorKim, K.-T.-
dc.contributor.authorSong, G.J.-
dc.contributor.authorHwang, S.-C.-
dc.date.accessioned2023-01-13T01:21:01Z-
dc.date.available2023-01-13T01:21:01Z-
dc.date.issued2023-01-
dc.identifier.issn1756-6606-
dc.identifier.issn1756-6606-
dc.identifier.urihttps://scholarworks.gnu.ac.kr/handle/sw.gnu/30093-
dc.description.abstractKnee osteoarthritis (OA) is characterized by knee cartilage degeneration and secondary bone hyperplasia, resulting in pain, stiffness, and gait disturbance. The relationship between knee OA and neurodegenerative diseases is still unclear. This study used an Alzheimer’s disease (AD) mouse model to observe whether osteoarthritis accelerates dementia progression by analyzing brain histology and neuroinflammation. Knee OA was induced by destabilizing the medial meniscus (DMM) in control (WT) and AD (5xFAD) mice before pathological symptoms. Mouse knee joints were scanned with a micro-CT scanner. A sham operation was used as control. Motor and cognitive abilities were tested after OA induction. Neurodegeneration, β-amyloid plaque formation, and neuroinflammation were analyzed by immunostaining, Western blotting, and RT-PCR in brain tissues. Compared with sham controls, OA in AD mice increased inflammatory cytokine levels in brain tissues. Furthermore, OA significantly increased β-amyloid deposition and neuronal loss in AD mice compared to sham controls. In conclusion, knee OA accelerated amyloid plaque deposition and neurodegeneration in AD-OA mice, suggesting that OA is a risk factor for AD. © 2023, The Author(s).-
dc.language영어-
dc.language.isoENG-
dc.publisherBioMed Central Ltd-
dc.titleKnee osteoarthritis accelerates amyloid beta deposition and neurodegeneration in a mouse model of Alzheimer’s disease-
dc.typeArticle-
dc.publisher.location영국-
dc.identifier.doi10.1186/s13041-022-00986-9-
dc.identifier.scopusid2-s2.0-85145492545-
dc.identifier.wosid000906722800001-
dc.identifier.bibliographicCitationMolecular Brain, v.16, no.1-
dc.citation.titleMolecular Brain-
dc.citation.volume16-
dc.citation.number1-
dc.type.docTypeArticle-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaNeurosciences & Neurology-
dc.relation.journalWebOfScienceCategoryNeurosciences-
dc.subject.keywordPlusINFLAMMATION-
dc.subject.keywordPlusNEUROINFLAMMATION-
dc.subject.keywordPlusPATHOGENESIS-
dc.subject.keywordPlusPROGRESSION-
dc.subject.keywordAuthorAlzheimer’s disease-
dc.subject.keywordAuthorAmyloid deposition-
dc.subject.keywordAuthorKnee osteoarthritis-
dc.subject.keywordAuthorNeurodegeneration-
dc.subject.keywordAuthorNeuroinflammation-
Files in This Item
There are no files associated with this item.
Appears in
Collections
College of Medicine > Department of Medicine > Journal Articles

qrcode

Items in ScholarWorks are protected by copyright, with all rights reserved, unless otherwise indicated.

Related Researcher

Altmetrics

Total Views & Downloads

BROWSE