In vivo metabolite differences between the basal ganglia and cerebellum of the rat brain detected with proton MRS at 3T

被引:16
作者
Mayer, Dirk
Zahr, Natalie M.
Sullivan, Edith V.
Pfefferbaum, Adolf
机构
[1] Stanford Univ, Radiol Dept Lucas MRS I Ctr, Stanford, CA 94305 USA
[2] SRI Int, Neurosci Program, Menlo Pk, CA 94025 USA
关键词
MRS; glutamate; single-voxel; in vivo; rat; CT-PRESS;
D O I
10.1016/j.pscychresns.2006.11.005
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
In vivo magnetic resonance spectroscopy (MRS) enables non-invasive longitudinal tracking of brain chemistry changes that can accompany aging, neurodegenerative disease, drug addiction and experimental manipulations in animals modeling such conditions. J-coupled resonances, such as glutamate, which are highly relevant to neuropsychiatric conditions are difficult to resolve on a clinical 3T MR scanner using conventional one-dimensional MRS sequences. We, therefore, implemented Constant Time PRESS (CT-PRESS) to quantify major metabolite and neurotransmitter biochemical signals, including glutamate, in two brain regions of the rat, basal ganglia and cerebellum. We acquired spectra at two distinct time points in two independent groups of six rats and analyzed metabolite levels using either creatine or water as a reference. Our results provide evidence that CT-PRESS at 3T is adequate and reliable for in vivo detection and quantification of glutamate in the rat brain and that regional differences occur in the signal intensities of the major metabolites. That the directionality of the differences depends on whether creatine or water is used as a reference for metabolite levels emphasizes the benefit to in vivo MRS of incorporating methods to establish absolute baseline metabolite concentrations. (C) 2006 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:267 / 273
页数:7
相关论文
共 44 条
[1]   In vivo 2D J-resolved magnetic resonance spectroscopy of rat brain with a 3-T clinical human scanner [J].
Adalsteinsson, E ;
Hurd, RE ;
Mayer, D ;
Sailasuta, N ;
Sullivan, EV ;
Pfefferbaum, A .
NEUROIMAGE, 2004, 22 (01) :381-386
[2]  
ADALSTEINSSON E, 2006, IN PRESS NEUROP 0111
[3]  
ADALSTEINSSON E, 2002, METH NE FRO NEUROSCI, P345
[4]  
Bendszus M, 2001, AM J NEURORADIOL, V22, P1926
[5]  
BOTTOMLEY PA, 1989, CLIN CHEM, V35, P392
[6]   Axonal damage correlates with disability in patients with relapsing-remitting multiple sclerosis - Results of a longitudinal magnetic resonance spectroscopy study [J].
De Stefano, N ;
Matthews, PM ;
Fu, LQ ;
Narayanan, S ;
Stanley, J ;
Francis, GS ;
Antel, JP ;
Arnold, DL .
BRAIN, 1998, 121 :1469-1477
[7]   Detection of homonuclear decoupled in vivo proton NMR spectra using constant time chemical shift encoding: CT-PRESS [J].
Dreher, W ;
Leibfritz, D .
MAGNETIC RESONANCE IMAGING, 1999, 17 (01) :141-150
[8]  
Fein G., 1994, NIAAA RES MONOGRAPH, V27, P227
[9]   A longitudinal study comparing the sensitivity of CSE and rare sequences in detecting new multiple sclerosis lesions [J].
Filippi, M ;
Rovaris, M ;
Pereira, C ;
Comi, G .
MAGNETIC RESONANCE IMAGING, 1999, 17 (03) :457-458
[10]   Chemical heterogeneity of the living human brain: A proton MR spectroscopy study on the effects of sex, age, and brain region [J].
Grachev, ID ;
Apkarian, AV .
NEUROIMAGE, 2000, 11 (05) :554-563