Differential activation of the mTOR/autophagy pathway predicts cognitive performance in APP/PS1 mice

被引:21
|
作者
Vartak, Rasika S. [1 ]
Rodin, Alexis [1 ]
Oddo, Salvatore [1 ,2 ]
机构
[1] Arizona State Univ, Biodesign Inst, Banner Neurodegenerat Dis Res Ctr, Tempe, AZ USA
[2] Arizona State Univ, Sch Life Sci, Tempe, AZ USA
基金
美国国家卫生研究院;
关键词
Alzheimer's disease; AD; Plaques; Tangles; tau; A beta; CENTRAL INSULIN DYSREGULATION; ALZHEIMERS-DISEASE; MAMMALIAN TARGET; AMYLOID-BETA; MOUSE MODEL; LIFE-SPAN; SYNAPTIC PLASTICITY; S6; KINASE; RAPAMYCIN; MTOR;
D O I
10.1016/j.neurobiolaging.2019.08.018
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
The molecular bases underlying cognitive impairments in Alzheimer's disease remain elusive. In this study, we sought to determine the molecular correlates of memory deficits in APP/PS1 mice, a widely used animal model of Alzheimer's disease. To this end, we tested 18-month-old APP/PS1 mice in the Morris water maze and ranked them by their spatial memory performance. We found that some APP/PS1 mice performed poorly, whereas others performed as well as nontransgenic mice. We took advantage of this intragroup variability to identify the best predictor of cognitive deficits. In this APP/PS1 cohort, soluble and insoluble amyloid-beta levels did not correlate significantly with cognitive performance. However, we found that cognitive performance within the APP/PS1 group had a strong inverse correlation with A beta plaque load and mammalian target of rapamycin activation and positively correlated with autophagy activation. Our data suggest that mammalian target of rapamycin signaling may account cognitive performance in APP/PS1 mice. (C) 2019 Elsevier Inc. All rights reserved.
引用
收藏
页码:105 / 113
页数:9
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