Quantitative in vivo measurement of early axonal transport deficits in a triple transgenic mouse model of Alzheimer's disease using manganese-enhanced MRI

被引:50
作者
Kim, Jieun [1 ]
Choi, In-Young [1 ,2 ,3 ]
Michaelis, Mary L. [4 ]
Lee, Phil [1 ,3 ]
机构
[1] Univ Kansas, Med Ctr, Hoglund Brain Imaging Ctr, Kansas City, KS 66160 USA
[2] Univ Kansas, Med Ctr, Dept Neurol, Kansas City, KS 66160 USA
[3] Univ Kansas, Med Ctr, Dept Mol & Integrat Physiol, Kansas City, KS 66160 USA
[4] Univ Kansas, Dept Pharmacol & Toxicol, Lawrence, KS 66045 USA
基金
美国国家卫生研究院;
关键词
Axonal transport; Alzheimer's disease; MEMRI; Triple transgenic mouse model; T-1; mapping; NEURODEGENERATIVE DISEASES; A-BETA; DEMENTIA; TAU; DYSFUNCTION; AXONOPATHY; DECREASE; DEFECTS; BRAIN; MEMRI;
D O I
10.1016/j.neuroimage.2011.02.039
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Impaired axonal transport has been linked to the pathogenic processes of Alzheimer's disease (AD) in which axonal swelling and degeneration are prevalent. The development of non-invasive neuroimaging methods to quantitatively assess in vivo axonal transport deficits would be enormously valuable to visualize early, yet subtle, changes in the AD brain, to monitor the disease progression and to quantify the effect of drug intervention. A triple transgenic mouse model of AD closely resembles human AD neuropathology. In this study, we investigated age-dependent alterations of the axonal transport rate in the triple transgenic mouse olfactory system, using fast multi-sliced T-1 mapping with manganese-enhanced MRI. The data show that impairment in axonal transport is a very early event in AD pathology in these mice, preceding both deposition of A beta, plaques and formation of Tau fibrils. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:1286 / 1292
页数:7
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