Cognitive impairment in the Tg6590 transgenic rat model of Alzheimer's disease

被引:18
|
作者
Kloskowska, Ewa
Pham, Therese M.
Nilsson, Tatjana
Zhu, Shunwei
Oberg, Johanna [2 ]
Codita, Alina
Pedersen, Lars O. [3 ]
Pedersen, Jan T. [3 ]
Malkiewicz, Katarzyna
Winblad, Bengt
Folkesson, Ronnie
Benedikz, Eirikur [1 ]
机构
[1] Karolinska Inst, Novum, Dept Neurobiol Care Sci & Soc, Div Neurodegenerat, S-14186 Stockholm, Sweden
[2] Karolinska Inst, Dept Clin Neurosci, MR Ctr, S-14186 Stockholm, Sweden
[3] H Lundbeck & Co AS, Copenhagen, Denmark
基金
瑞典研究理事会;
关键词
Alzheimer's disease; transgenic; animal model; rat; behaviour; AMYLOID PRECURSOR PROTEIN; HIPPOCAMPAL-NEURONS; A-BETA; MUTATION; DYSFUNCTION; MEMORY; APP; PATHOLOGY; DECLINE;
D O I
10.1111/j.1582-4934.2009.00809.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Recently, interest in the rat as an animal model of Alzheimer's disease (AD) has been growing. We have previously described the Tg6590 transgenic rat line expressing the amyloid precursor protein containing the Swedish AD mutation (K670M/N671L) that shows early stages of A beta deposition, predominantly in cerebrovascular blood vessels, after 15 months of age. Here we show that by the age of 9 months, that is long before the appearance of A beta deposits, the Tg6590 rats exhibit deficits in the Morris water maze spatial navigation task and altered spontaneous behaviour in the open-field test. The levels of soluble A beta were elevated both in the hippocampus and cortex of transgenic animals. Magnetic resonance imaging showed no major changes in the brains of transgenic animals, although they tended to have enlarged lateral ventricles when compared to control animals. The Tg6590 transgenic rat line should prove a suitable model of early AD for advanced studies including serial cerebrospinal fluid sampling, electrophysiology, neuroimaging or complex behavioural testing.
引用
收藏
页码:1816 / 1823
页数:8
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