Spatial learning in transgenic mice expressing human presenilin 1 (PS1) transgenes

被引:72
作者
Janus, C
D'Amelio, S
Amitay, O
Chishti, MA
Strome, R
Fraser, P
Carlson, GA
Roder, JC
St George-Hyslop, P
Westaway, D
机构
[1] Univ Toronto, Ctr Res Neurodegenerat Dis, Toronto, ON M5S 3H2, Canada
[2] Mt Sinai Hosp, Samuel Lunenfeld Res Inst, Toronto, ON M5G 1X5, Canada
[3] McLaughlin Res Inst, Great Falls, MT USA
[4] York Univ, Dept Psychol, Toronto, ON M3J 2R7, Canada
基金
英国医学研究理事会;
关键词
presenilin; 1; transgenic mouse; Alzheimer's disease; behavior; spatial learning;
D O I
10.1016/S0197-4580(00)00107-X
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
Dominant mutations in the Presenilin 1 gene are linked to an aggressive, early-onset form of familial Alzheimer's Disease (FAD). Spatial memory of transgenic (Tg) mice expressing either mutant (lines Tg(M146L)1, Tg(M146L)76, Tg(L286V)198) or wild type (line Tg(PS1wt)195) human PS1 transgenes was investigated in the Morris water maze (WM) test at 6 and 9 months of age. The results showed that the mutated Tg mice had increased swim speed when compared to non-Tg littermates or Tg PSI wild type mice. The swim speed difference did not, however, significantly affect the spatial learning in the WM test and all groups showed comparable search paths during training and similar spatial bias during probe trials. When re-tested at 9 months, all mice showed significantly improved learning acquisition of spatial information. The lack of progressive spatial learning impairment in mice expressing the mutated human PSI transgene in the WM does not preclude impairments in other cognitive tasks but suggests that full phenotypic expression of mutant PS1 alleles may require co-expression of human versions of other AD-associated genes. (C) 2000 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:541 / 549
页数:9
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