Enrichment improves cognition in AD mice by amyloid-related and unrelated mechanisms

被引:176
作者
Costa, David A.
Craechiolo, Jennifer R.
Bachstetter, Adam D.
Hughes, Tiffany F.
Bales, Kelly R.
Paul, Steven M.
Mervis, Ronald F.
Arendash, Gary W.
Potter, Huntington
机构
[1] Johnnie B Byrd Sr Alzheimers Ctr & Res Inst, Tampa, FL 33647 USA
[2] Univ S Florida, Dept Mol Med, Tampa, FL 33612 USA
[3] Univ S Florida, Suncoast Gerontol Ctr, Tampa, FL 33612 USA
[4] Univ S Florida, Florida Alzheimers Dis Res Ctr, Tampa, FL 33612 USA
[5] Univ S Florida, Memory & Aging Res Lab, Tampa, FL 33620 USA
[6] Neurostruct Res Labs, Tampa, FL 33612 USA
[7] Univ S Florida, Ctr Aging & Brain Repair, Tampa, FL 33612 USA
[8] Lilly Res Labs, Neurosci Discovery Res, Indianapolis, IN 46285 USA
关键词
Alzheimer's disease; environmental enrichment; amyloid; microarray;
D O I
10.1016/j.neurobiolaging.2006.04.009
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
Lifelong cognitive stimulation is associated with a lower risk of Alzheimer's disease (AD), but causality is difficult to prove. We therefore sought to investigate the preventative potential of environmental enrichment (EE) using mice expressing both human mutant presenilin-1 and the amyloid precursor protein (PS1/PDAPP). At weaning, mice were placed into either an enriched or standard housing environment. Behavioral testing at 4.5-6 months showed that environmentally enriched PS1/PDAPP mice outperformed mice in standard housing, and were behaviorally indistinguishable from non-transgenic mice across multiple cognitive domains. PS1/PDAPP mice exposed to both environmental enrichment and behavioral testing, but not to EE alone, showed 50% less brain beta-amyloid without improved dendritic morphology. Microarray analysis revealed large enrichment-induced changes in hippocampal expression of genes/proteins related to A beta sequestration and synaptic plasticity. These results indicate that EE protects against cognitive impairment in AD transgenic mice through a dual mechanism, including both amyloid dependent and independent mechanisms. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:831 / 844
页数:14
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