Show simple item record

dc.contributor.authorRivera Tapia, ED
dc.contributor.authorMeakin, JR
dc.contributor.authorHolsgrove, TP
dc.date.accessioned2022-08-31T14:23:37Z
dc.date.issued2022-08-17
dc.date.updated2022-08-31T13:36:40Z
dc.description.abstractThe intervertebral disc (IVD) provides flexibility, acts as a shock absorber, and transmits load. Degeneration of the IVD includes alterations in the biomechanics, extracellular matrix (ECM), and cellular activity. These changes are not always perceived, however, IVD degeneration can lead to severe health problems including long-term disability. To understand the pathogenesis of IVD degeneration and suitable testing methods for emerging treatments and therapies, this review documents in-vitro models of IVD degeneration including physical disruption, hyperphysiological loading, ECM degradation by enzyme digestion, or a combination of these methods. This paper reviews and critically analyses the models of degeneration published since the year 2000 in either in human or animal specimens. The results are categorised in terms of the IVD biomechanics, physical attributes, ECM composition, tissue damage and cellularity to evaluate the models with respect to natural human degeneration, and to provide recommendations for clinically relevant models for the various stages of degeneration. There is no one model that replicates the wide range of degenerative changes that occur as part of normal degeneration. However, cyclic overloading replicates many aspects of degeneration, with the advantage of a dose-response allowing the tuning of damage initiated. Models of severe degeneration are currently lacking, but there is potential that combining cyclic overloading and enzymatic digestion will provide model that closely resembles human IVD degeneration. This will provide an effective way to investigate the effects of severe degeneration, and the evaluation of treatments for the IVD, which would generally be indicated at this advanced stage of degeneration.en_GB
dc.format.extent111260-
dc.format.mediumPrint-Electronic
dc.identifier.citationVol. 142, article 111260en_GB
dc.identifier.doihttps://doi.org/10.1016/j.jbiomech.2022.111260
dc.identifier.urihttp://hdl.handle.net/10871/130625
dc.identifierORCID: 0000-0003-2832-4958 (Holsgrove, TP)
dc.identifierScopusID: 22634311700 (Holsgrove, TP)
dc.language.isoenen_GB
dc.publisherElsevieren_GB
dc.relation.urlhttps://www.ncbi.nlm.nih.gov/pubmed/36027637en_GB
dc.rights.embargoreasonUnder embargo until 17 August 2023 in compliance with publisher policyen_GB
dc.rights© 2022. This version is made available under the CC-BY-NC-ND 4.0 license:https://creativecommons.org/licenses/by-nc-nd/4.0/en_GB
dc.subjectDegenerationen_GB
dc.subjectIn-vitro testingen_GB
dc.subjectIntervertebral discen_GB
dc.subjectResearch methodsen_GB
dc.subjectSpineen_GB
dc.titleIn-vitro models of disc degeneration - A review of methods and clinical relevance.en_GB
dc.typeArticleen_GB
dc.date.available2022-08-31T14:23:37Z
dc.identifier.issn0021-9290
exeter.article-number111260
exeter.place-of-publicationUnited States
dc.descriptionThis is the author accepted manuscript. The final version is available from Elsevier via the DOI in this recorden_GB
dc.identifier.eissn1873-2380
dc.identifier.journalJournal of Biomechanicsen_GB
dc.relation.ispartofJ Biomech, 142
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/en_GB
dcterms.dateAccepted2022-08-11
rioxxterms.versionAMen_GB
rioxxterms.licenseref.startdate2022-08-17
rioxxterms.typeJournal Article/Reviewen_GB
refterms.dateFCD2022-08-31T14:15:35Z
refterms.versionFCDAM
refterms.dateFOA2023-08-16T23:00:00Z
refterms.panelBen_GB
refterms.dateFirstOnline2022-08-17


Files in this item

This item appears in the following Collection(s)

Show simple item record

© 2022. This version is made available under the CC-BY-NC-ND 4.0 license:https://creativecommons.org/licenses/by-nc-nd/4.0/
Except where otherwise noted, this item's licence is described as © 2022. This version is made available under the CC-BY-NC-ND 4.0 license:https://creativecommons.org/licenses/by-nc-nd/4.0/