Correlation of behavior changes and BOLD signal in Alzheimer-like rat model

被引:17
作者
Hu, ZH
Wang, XC
Li, LY
Liu, ML
Liu, R
Ling, ZQ
Tian, Q
Tang, XW
Wu, YG
Wang, JZ [1 ]
机构
[1] Huazhong Univ Sci & Technol, Tongji Med Coll, Dept Pathophysiol, Wuhan 430030, Peoples R China
[2] Zhejiang Univ, Dept Phys, Hangzhou 310027, Peoples R China
[3] Zhejiang Univ, BioX Disciplinary Lab, Hangzhou 310027, Peoples R China
[4] Chinese Acad Sci, Inst High Energy Phys, Beijing 100039, Peoples R China
[5] Chinese Acad Sci, Key Lab Nucl Anal Tech, Beijing 100039, Peoples R China
[6] Chinese Acad Sci, Wuhan Inst Phys & Math, State Key Lab Magnet Resonance & Atom & Mol Phys, Wuhan 430071, Peoples R China
关键词
Alzheimer disease (AD); functional magnetic resonance imaging (fMRI); isoproterenol (IP); Morris Water Maze; diagnosis;
D O I
10.1093/abbs/36.12.803
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
To explore a potential means for the early diagnosis of Alzheimer disease, we studied the relationship of resting T2* signal and tau hyperphosphorylation/spatial memory deficit. The rat model with tau hyperphosphorylation and spatial memory deficit was established by bilateral hippocampi injection of isoproterenol (IP). Then, the correlative alteration between resting T2* signal and spatial memory retention was assessed with blood oxygenation level dependent (BOLD) functional magnetic resonance imaging (fMRI) study and Morris Water Maze test, and Western blot was employed to confirm tau hyperphosphorylation. The analysis showed following results. (1) Tau phosphorylation at Ser(396)/Ser(404) and Ser(199)/Ser(202) was significantly increased in IP-injected rats as detected by PHF-1 and tau-1, respectively. (2) An AD-like spatial memory retention disturbance was induced at 24 h after isoproterenol injection. (3) A sensitivity threshold of resting T2* signal intensity, which separated the IP-treated rats from vehicle control, was obtained by applying linear regression analysis, and an estimated sensitivity statistical threshold was at 32.62. These results suggest that resting T2* signal may serve as a noninvasive quantitative marker in predicting AD-like spatial memory deficits and tau hyperphosphorylation.
引用
收藏
页码:803 / 810
页数:8
相关论文
共 24 条
[1]   Tau aggregation in the hippocampal formation: an ageing or a pathological process? [J].
Delacourte, A ;
Sergeant, N ;
Wattez, A ;
Maurage, CA ;
Lebert, F ;
Pasquier, F ;
David, JP .
EXPERIMENTAL GERONTOLOGY, 2002, 37 (10-11) :1291-1296
[2]   Neurodegenerative disorders with extensive tau pathology: A comparative study and review [J].
Feany, MB ;
Dickson, DW .
ANNALS OF NEUROLOGY, 1996, 40 (02) :139-148
[3]   Differential diagnosis and clinical assessment of patients with severe Alzheimer disease [J].
Ferris, SH ;
Yan, B .
ALZHEIMER DISEASE & ASSOCIATED DISORDERS, 2003, 17 :S92-S95
[4]  
Friston K.J., 1994, Human Brain Mapping, V2, P189, DOI DOI 10.1002/HBM.460020402
[5]   THE RELATIONSHIP BETWEEN GLOBAL AND LOCAL CHANGES IN PET SCANS [J].
FRISTON, KJ ;
FRITH, CD ;
LIDDLE, PF ;
DOLAN, RJ ;
LAMMERTSMA, AA ;
FRACKOWIAK, RSJ .
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 1990, 10 (04) :458-466
[6]   Formation of neurofibrillary tangles in P301L tau transgenic mice induced by Aβ42 fibrils [J].
Götz, J ;
Chen, F ;
van Dorpe, J ;
Nitsch, RM .
SCIENCE, 2001, 293 (5534) :1491-1495
[7]   Default-mode network activity distinguishes Alzheimer's disease from healthy aging: Evidence from functional MRI [J].
Greicius, MD ;
Srivastava, G ;
Reiss, AL ;
Menon, V .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (13) :4637-4642
[8]  
GRUNDKEIQBAL I, 1986, J BIOL CHEM, V261, P6084
[9]   Advances in the development of biomarkers for Alzheimer's disease:: from CSF total tau and Aβ1-42 proteins to phosphorylated tau protein [J].
Hampel, H ;
Goernitz, A ;
Buerger, K .
BRAIN RESEARCH BULLETIN, 2003, 61 (03) :243-253
[10]   Levels of nonphosphorylated and phosphorylated tau in cerebrospinal fluid of Alzheimer's disease patients - An ultrasensitive bienzyme-substrate-recycle enzyme-linked Immunosorbent assay [J].
Hu, YY ;
He, SS ;
Wang, XC ;
Duan, QH ;
Grundke-Iqbal, I ;
Iqbal, K ;
Wang, JZ .
AMERICAN JOURNAL OF PATHOLOGY, 2002, 160 (04) :1269-1278