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

被引:111
作者
Gureviciene, I
Ikonen, S
Gurevicius, K
Sarkaki, A
van Groen, T
Pussinen, R
Ylinen, A
Tanila, H
机构
[1] Univ Kuopio, Dept Neurol & Neurosci, FIN-70211 Kuopio, Finland
[2] Med Sch Basic Sci, Dept Physiol, Ahvaz 61355189, Iran
[3] Kuopio Univ Hosp, Dept Neurol, Kuopio 70211, Finland
基金
芬兰科学院;
关键词
long-term potentiation; synaptic plasticity; Alzheimer's disease; hippocampus; spatial memory;
D O I
10.1016/j.nbd.2003.11.011
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
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.
引用
收藏
页码:188 / 195
页数:8
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