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dc.contributor.authorLam, Virginie
dc.contributor.authorPhillips, Juliette
dc.contributor.authorHarrild, Elizabeth
dc.contributor.authorTidy, Rebecca J.
dc.contributor.authorHollings, Ashley
dc.contributor.authorCodd, L.
dc.contributor.authorRichardson, K.
dc.contributor.authorCelliers, L.
dc.contributor.authorTakechi, Ryu
dc.contributor.authorMamo, John
dc.contributor.authorHackett, Mark
dc.date.accessioned2023-01-24T04:40:54Z
dc.date.available2023-01-24T04:40:54Z
dc.date.issued2022
dc.identifier.citationLam, V. and Phillips, J. and Harrild, E. and Tidy, R.J. and Hollings, A.L. and Codd, L. and Richardson, K. et al. 2022. Association between ageing, brain chemistry and white matter volume revealed with complementary MRI and FTIR brain imaging. Analyst. 147 (23): pp. 5274-5282.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/90107
dc.identifier.doi10.1039/d2an01271e
dc.description.abstract

Magnetic resonance imaging (MRI) is the gold standard method to study brain anatomy in vivo. Using MRI, subtle alterations to white matter structures in the brain are observed prior to cognitive decline associated with the ageing process, and neurodegenerative diseases such as Alzheimer's disease. Detection of such alterations provides hope for early clinical diagnosis. While MRI is essential to detect subtle alterations to brain structure in vivo, the technique is less suited to study and image the distribution of biochemical markers within specific brain structures. Consequently, the chemical changes that drive, or are associated with MRI-detectable alterations to white matter are not well understood. Herein, we describe (to the best of our knowledge) the first application of a complementary imaging approach that incorporates in vivo MRI with ex vivo Fourier transform infrared (FTIR) spectroscopic imaging on the same brain tissue. The combined workflow is used to detect and associate markers of altered biochemistry (FTIR) with anatomical changes to brain white matter (MRI). We have applied this combination of techniques to the senescence accelerated murine prone strain 8 (SAMP8) mouse model (n = 6 animals in each group, analysed across two ageing time points, 6 and 12 months). The results have demonstrated alterations to lipid composition and markers of disturbed metabolism during ageing are associated with loss of white matter volume.

dc.languageEnglish
dc.publisherROYAL SOC CHEMISTRY
dc.subjectScience & Technology
dc.subjectPhysical Sciences
dc.subjectChemistry, Analytical
dc.subjectChemistry
dc.subjectAGE-RELATED-CHANGES
dc.subjectALZHEIMERS-DISEASE
dc.subjectMURINE MODEL
dc.subjectMOUSE
dc.subjectDAMAGE
dc.subjectSAMP8
dc.subjectMICROSPECTROSCOPY
dc.subjectRESOLUTION
dc.subjectMEMORY
dc.subjectMICE
dc.titleAssociation between ageing, brain chemistry and white matter volume revealed with complementary MRI and FTIR brain imaging
dc.typeJournal Article
dcterms.source.volume147
dcterms.source.number23
dcterms.source.startPage5274
dcterms.source.endPage5282
dcterms.source.issn0003-2654
dcterms.source.titleAnalyst
dc.date.updated2023-01-24T04:40:54Z
curtin.departmentCurtin School of Population Health
curtin.departmentSchool of Molecular and Life Sciences (MLS)
curtin.departmentCurtin Health Innovation Research Institute(CHIRI)
curtin.accessStatusFulltext not available
curtin.facultyFaculty of Health Sciences
curtin.facultyFaculty of Science and Engineering
curtin.contributor.orcidTakechi, Ryu [0000-0001-6359-3382]
curtin.contributor.orcidLam, Virginie [0000-0001-8463-645X]
curtin.contributor.orcidHollings, Ashley [0000-0001-7829-4932]
curtin.contributor.orcidHackett, Mark [0000-0002-3296-7270]
curtin.contributor.orcidMamo, John [0000-0002-5741-7849]
curtin.contributor.researcheridTakechi, Ryu [D-3692-2012] [T-9970-2019]
dcterms.source.eissn1364-5528
curtin.contributor.scopusauthoridTakechi, Ryu [24173759200]
curtin.contributor.scopusauthoridLam, Virginie [36096751600]
curtin.contributor.scopusauthoridHackett, Mark [35240056500] [57999521300]
curtin.contributor.scopusauthoridMamo, John [7006456735]


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