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dc.contributor.authorKocinaj, Altinpt_BR
dc.contributor.authorChaudhury, Tabassumpt_BR
dc.contributor.authorUddin, Mohammed S.pt_BR
dc.contributor.authorJunaid, Rashad R.pt_BR
dc.contributor.authorRamsden, David B.pt_BR
dc.contributor.authorHondhamuni, Geshanthipt_BR
dc.contributor.authorKlamt, Fabiopt_BR
dc.contributor.authorParsons, Lindapt_BR
dc.contributor.authorParsons, Richard B.pt_BR
dc.date.accessioned2021-05-04T04:27:53Zpt_BR
dc.date.issued2021pt_BR
dc.identifier.issn0893-7648pt_BR
dc.identifier.urihttp://hdl.handle.net/10183/220502pt_BR
dc.description.abstractWe have previously shown that the expression of nicotinamide N-methyltransferase (NNMT) is significantly increased in the brains of patients who have died of Parkinson’s disease (PD). In this study, we have compared the expression of NNMT in post-mortem medial temporal lobe, hippocampus and cerebellum of 10 Alzheimer’s disease (AD) and 9 non-disease control subjects using a combination of quantitative Western blotting, immunohistochemistry and dual-label confocal microscopy coupled with quantitative analysis of colocalisation. NNMT was detected as a single protein of 29 kDa in both AD and non-disease control brains, which was significantly increased in AD medial temporal lobe compared to non-disease controls (7.5-fold, P < 0.026). There was no significant difference in expression in the cerebellum (P = 0.91). NNMT expression in AD medial temporal lobe and hippocampus was present in cholinergic neurones with no glial localisation. Cell-type expression was identical in both non-disease control and AD tissues. These results are the first to show, in a proof-of-concept study using a small patient cohort, that NNMT protein expression is increased in the AD brain and is present in neurones which degenerate in AD. These results suggest that the elevation of NNMT may be a common feature of many neurodegenerative diseases. Confirmation of this overexpression using a larger AD patient cohort will drive the future development of NNMT-targetting therapeutics which may slow or stop the disease pathogenesis, in contrast to current therapies which solely address AD symptoms.en
dc.format.mimetypeapplication/pdfpt_BR
dc.language.isoengpt_BR
dc.relation.ispartofMolecular neurobiology. Clifton. Vol. 58, no. 4 (Apr. 2021), p. 1769-1781pt_BR
dc.rightsOpen Accessen
dc.subjectDoença de Alzheimerpt_BR
dc.subjectAlzheimer’s diseaseen
dc.subjectNicotinamida N-metiltransferasept_BR
dc.subjectNicotinamide N-methyltransferaseen
dc.subjectPathogenic processen
dc.subjectLobo temporalpt_BR
dc.subjectOverexpressionen
dc.subjectHipocampopt_BR
dc.subjectTherapiesen
dc.subjectHomocysteineen
dc.subjectStress responseen
dc.titleHigh expression of nicotinamide N-methyltransferase in patients with sporadic Alzheimer’s diseasept_BR
dc.typeArtigo de periódicopt_BR
dc.identifier.nrb001124672pt_BR
dc.type.originEstrangeiropt_BR


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