4.7 Article

Normal induction but accelerated decay of LTP in APP+PS1 transgenic mice

Journal

NEUROBIOLOGY OF DISEASE
Volume 15, Issue 2, Pages 188-195

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.nbd.2003.11.011

Keywords

long-term potentiation; synaptic plasticity; Alzheimer's disease; hippocampus; spatial memory

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Mice carrying mutated human APPswe and PSI (A246E) transgenes (A/P mice) show age-dependent memory impairment in hippocampus-dependent tasks. Moreover, the mice show normal learning in the water maze within a day but impairment across days. We recorded LTP in a slice preparation (CA1) and in chronically implanted animals (dentate gyrus, or DG) at 17-18 months of age. The genotypes did not differ in the basal synaptic transmission. Also, LTP induction and its maintenance over 60 min did not differ between A/P and control mice. However, the fEPSP enhancement in vivo decayed to 77% of its maximum in 24 h in A/P mice while remaining at 96% in control mice. The time course of the LTP decay in the A/P mice corresponds to their behavioral impairment and indicates that Abeta accumulation in the dentate gyrus may interfere with the signal transduction pathways responsible for memory consolidation. (C) 2004 Elsevier Inc. All rights reserved.

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