Skip to main content

Research Repository

Advanced Search

Glycogen synthase kinase-3 is increased in white cells early in Alzheimer's disease

Hye, Abdul; Kerr, Fiona; Archer, Nicola; Foy, Catherine; Poppe, Michaela; Brown, Richard; Hamilton, Gillian; Powell, John; Anderton, Brian; Lovestone, Simon

Authors

Abdul Hye

Nicola Archer

Catherine Foy

Michaela Poppe

Richard Brown

Gillian Hamilton

John Powell

Brian Anderton

Simon Lovestone



Abstract

Alzheimer's disease (AD) is a disorder without a molecular marker in peripheral tissues or a disease modifying treatment. As increasing evidence has suggested a role for glycogen synthase kinase-3 (GSK-3) in the pathogenesis of the condition we measured total GSK-3 protein (alpha and beta isoforms) and GSK-3 activity (serine 9 phosphorylation) in a group of healthy elderly people, in AD and in mild cognitive impairment (MCI). Total GSK-3 protein was increased in both AD and in MCI without a compensatory decrease in activity. These data suggest that GSK-3 assays might be a useful diagnostic marker in a readily available tissue and moreover that GSK-3 activity is increased in the prodromal phase of the disorder suggesting that inhibition of GSK-3 might be a useful therapeutic strategy.

Citation

Hye, A., Kerr, F., Archer, N., Foy, C., Poppe, M., Brown, R., Hamilton, G., Powell, J., Anderton, B., & Lovestone, S. (2004). Glycogen synthase kinase-3 is increased in white cells early in Alzheimer's disease. Neuroscience Letters, 373(1), 1-4. https://doi.org/10.1016/j.neulet.2004.10.031

Journal Article Type Article
Acceptance Date Oct 13, 2004
Online Publication Date Nov 11, 2004
Publication Date Dec 13, 2004
Deposit Date Oct 27, 2016
Journal Neuroscience Letters
Print ISSN 0304-3940
Publisher Elsevier
Peer Reviewed Peer Reviewed
Volume 373
Issue 1
Pages 1-4
DOI https://doi.org/10.1016/j.neulet.2004.10.031
Keywords Alzheimer's disease; Glycogen synthase kinase-3 (GSK-3); Biomarker; Lymphocytes; White cells; Mild cognitive impairment (MCI)
Public URL http://researchrepository.napier.ac.uk/Output/409203