In vivo 2D J-resolved magnetic resonance spectroscopy of rat brain with a 3-T clinical human scanner

被引:33
作者
Adalsteinsson, E
Hurd, RE
Mayer, D
Sailasuta, N
Sullivan, EV
Pfefferbaum, A
机构
[1] SRI Int, Program Neurosci, Menlo Pk, CA 94025 USA
[2] Stanford Univ, Sch Med, Dept Psychiat & Behav Sci, Stanford, CA 94305 USA
[3] GE Co, Med Syst, Menlo Pk, CA USA
[4] Stanford Univ, Sch Med, Dept Radiol, Stanford, CA 94305 USA
关键词
animal model; rat; brain; magnetic resonance; 2D J-resolved; spectroscopy;
D O I
10.1016/j.neuroimage.2003.12.046
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
A clinical 3-T scanner equipped with a custom-made transmit/receive birdcage coil was used to collect 2D J-resolved single-voxel spectroscopy in vivo of rat brain. Four adult Wistar rats were scanned twice each, with a 2-week interval. Voxel size was approximately 5 x 10 x 5 mm(3). Total spectroscopic acquisition time was 14 min for collection of two 4:20 min water-suppressed acquisitions and one 4:20 min acquisition acquired in the absence of water suppression. The unsuppressed water data were used in post-processing to reduce residual water side bands, as well as for metabolite signal normalization to account for variations in coil loading and voxel size. Peak areas were estimated for resonances from N-acetyl aspartate (NAA), creatine, choline, taurine, glutamate, and combined glutamate and glutamine. T-2-relaxation times were estimated for NAA and creatine. The average deviation from the mean of repeated measures for glutamate, combined glutamate and glutamine, and taurine ranged from 7.6% to 18.3%, while for NAA, creatine, and choline, the deviation was less than 3%. The estimated T-2 values for NAA (mean +/- SD = 330 +/- 57 ms) and creatine (174 +/- 27 ms) were similar to those reported previously for rat brain and for human gray and white matter. These results indicate that reliable, small animal brain MR spectroscopy can be performed on a human clinical 3-T scanner. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:381 / 386
页数:6
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