Age-related changes in brain metabolites and cognitive function in APP/PS1 transgenic mice

被引:54
作者
Chen, Shuang-qing [1 ]
Cai, Qing [1 ]
Shen, Yu-ying [1 ]
Wang, Pei-jun [2 ]
Teng, Gao-jun [3 ,4 ]
Zhang, Wei [2 ]
Zang, Feng-chao [4 ]
机构
[1] Nanjing Med Univ, Suzhou Hosp, Dept Radiol, Suzhou 215001, Jiangsu, Peoples R China
[2] Tongji Univ, Tongji Hosp, Dept Radiol, Shanghai 200065, Peoples R China
[3] Southeast Univ, Zhongda Hosp, Dept Radiol, Nanjing 210009, Jiangsu, Peoples R China
[4] Southeast Univ, Mol Imaging Laboratoryl, Nanjing 210009, Jiangsu, Peoples R China
关键词
Alzheimer's disease (AD); Magnetic resonance spectroscopy (MRS); Morris water maze (MWM); Metabolite; MAGNETIC-RESONANCE-SPECTROSCOPY; ALZHEIMERS-DISEASE; MOUSE-BRAIN; MR SPECTROSCOPY; AMYLOID-BETA; WATER MAZE; IN-VIVO; H-1; MRS; MODEL; DEFICITS;
D O I
10.1016/j.bbr.2012.07.016
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
Proton magnetic resonance spectroscopy (H-1-MRS) and the Morris water maze (MWM) have played an important role in Alzheimer's disease (AD) research. The aim of this study was to determine whether H-1-MRS and the MWM can detect for early AD in APP/PS1 transgenic (tg) mice. H-1-MRS was performed in 20 tg mice and 15 wild-type mice at 3,5 and 8 months of age. The concentration of N-acetylaspartate (NAA), glutamate (Glu), myo-inositol (ml), choline (Cho) and creatine (Cr) in the hippocampus were measured, and the NAA/Cr. Glu/Cr, ml/Cr and Cho/Cr ratios were quantified. Additionally, the spatial learning and memory of the mice were evaluated by MWM. The H-1-MRS revealed that ml levels in tg mice were significantly higher at 3 months of age compared to wt mice, while the NAA and Glu levels in 5- and 8-month-old tg mice were significantly decreased (p < 0.05). Additionally, significant cognitive changes only occurred at 8 months of age in APP/PS1 tg mice. These results indicated that metabolic changes preceded overt cognitive dysfunctions in early-stage AD, suggesting that H-1-MRS is a more sensitive biomarker for assessing early AD. (c) 2012 Elsevier B.V. All rights reserved.
引用
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页码:1 / 6
页数:6
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