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dc.contributor.authorBeattie, James Renwick
dc.contributor.authorSophocleous, Antonia
dc.contributor.authorCaraher, M. Clare
dc.contributor.authorO’Driscoll, Olive M.
dc.contributor.authorCummins, Niamh Maria
dc.contributor.authorBell, Steven E.J.
dc.contributor.authorTowler, Mark R.
dc.contributor.authorRahimnejad Yazdi, Alireza
dc.contributor.authorRalston, Stuart H.
dc.contributor.authorIdris, Aymen I.
dc.creatorBeattie, James Renwick
dc.date.accessioned2019-02-23T08:10:08Z
dc.date.available2019-02-23T08:10:08Z
dc.date.issued2019-02-01
dc.identifierSCOPUS_ID:85061366083
dc.identifier.issn09574530
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85061366083&origin=inward
dc.identifier.urihttps://repo.euc.ac.cy/handle/123456789/1868
dc.description.abstractPharmacological therapy of osteoporosis reduces bone loss and risk of fracture in patients. Modulation of bone mineral density cannot explain all effects. Other aspects of bone quality affecting fragility and ways to monitor them need to be better understood. Keratinous tissue acts as surrogate marker for bone protein deterioration caused by oestrogen deficiency in rats. Ovariectomised rats were treated with alendronate (ALN), parathyroid hormone (PTH) or estrogen (E2). MicroCT assessed macro structural changes. Raman spectroscopy assessed biochemical changes. Micro CT confirmed that all treatments prevented ovariectomy-induced macro structural bone loss in rats. PTH induced macro structural changes unrelated to ovariectomy. Raman analysis revealed ALN and PTH partially protect against molecular level changes to bone collagen (80% protection) and mineral (50% protection) phases. E2 failed to prevent biochemical change. The treatments induced alterations unassociated with the ovariectomy; increased beta sheet with E2, globular alpha helices with PTH and fibrous alpha helices with both ALN and PTH. ALN is closest to maintaining physiological status of the animals, while PTH (comparable protective effect) induces side effects. E2 is unable to prevent molecular level changes associated with ovariectomy. Raman spectroscopy can act as predictive tool for monitoring pharmacological therapy of osteoporosis in rodents. Keratinous tissue is a useful surrogate marker for the protein related impact of these therapies.The results demonstrate utility of surrogates where a clear systemic causation connects the surrogate to the target tissue. It demonstrates the need to assess broader biomolecular impact of interventions to examine side effects. [Figure not available: see fulltext.].
dc.relation.ispartofJournal of Materials Science: Materials in Medicine
dc.titleRaman spectroscopy as a predictive tool for monitoring osteoporosis therapy in a rat model of postmenopausal osteoporosis
elsevier.identifier.doi10.1007/s10856-019-6226-x
elsevier.identifier.eid2-s2.0-85061366083
elsevier.identifier.scopusidSCOPUS_ID:85061366083
elsevier.volume30
elsevier.issue.identifier2
elsevier.coverdate2019-02-01
elsevier.coverdisplaydate1 February 2019
elsevier.openaccess0
elsevier.openaccessflagfalse
elsevier.aggregationtypeJournal


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