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Article type: Short Communication
Authors: Saab, Bechara J.a; b; * | Luca, Ruxandra M.b; 1 | Yuen, Wing B.b; 1 | Saab, Adam M.P.b; c | Roder, John C.a; b
Affiliations: [a] Department of Molecular and Medical Genetics, Program in Neuroscience, University of Toronto, Toronto, Canada | [b] Samuel Lunenfeld Research Institute, Mount Sinai Hospital, Toronto, Canada | [c] University of British Columbia, Okanagan Campus, Kelowna, Canada
Correspondence: [*] Correspondence to: Bechara J. Saab, Brain Research Institute, Swiss Federal Institute of Technology, University of Zurich, Winterthurerstrasse 190, CH-8057 Zurich, Switzerland. Tel.: +41 44 635 3309; Fax: +41 44 635 3303; E-mail: saab@hifo.uzh.ch.
Note: [1] These authors contributed equally to the manuscript.
Abstract: Alzheimer's disease (AD) is multi-factorial mental disorder characterized by a copious array of congruent features cumulating in disrupted memory and dysthymia. Though the mechanism remains elusive, the highly unspecific pharmaceutical, memantine, provides modest benefits for patients with moderate-to-severe AD. A greater understanding of how memantine affects cognitive function promises to facilitate the search for better therapeutics. We therefore examined cognitive flexibility of mice following 5 and 10 mg/kg memantine administration using a platform re-location water maze. Strikingly, subjects receiving memantine demonstrated memory impairment relative to controls when re-trained off drug, revealing a novel and unusual disruption of cognitive flexibility.
Keywords: Alzheimer's disease, cognitive disorder, cognitive flexibility, dopamine, excitotoxicity, GABA(A), hippocampus, learning and memory, memantine, mental flexibility, mice, mouse, muscarinic cholinergic system, neurotoxicity, NMDAR, platform re-location water maze, prefrontal cortex
DOI: 10.3233/JAD-2011-110650
Journal: Journal of Alzheimer's Disease, vol. 27, no. 3, pp. 477-482, 2011
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