1H MRS detection of glycine residue of reduced glutathione in vivo

被引:41
作者
Kaiser, Lana G. [1 ]
Marjanska, Malgorzata [2 ,3 ]
Matson, Gerald B. [4 ,5 ]
Iltis, Isabelle [2 ,3 ]
Bush, Seth D. [6 ]
Soher, Brian J. [7 ]
Mueller, Susanne [4 ,8 ]
Young, Karl [4 ,8 ]
机构
[1] Varian Inc, Palo Alto, CA USA
[2] Univ Minnesota, Ctr Magnet Resonance Res, Minneapolis, MN 55455 USA
[3] Univ Minnesota, Dept Radiol, Minneapolis, MN 55455 USA
[4] VA Med Ctr 114M, Dept Vet Affairs Med Ctr, Ctr Imaging Neurodegenerat Dis, San Francisco, CA 94121 USA
[5] Univ Calif San Francisco, Dept Pharmaceut Chem, San Francisco, CA 94143 USA
[6] Calif Polytech State Univ San Luis Obispo, San Luis Obispo, CA 93407 USA
[7] Duke Univ, Dept Radiol, Durham, NC 27710 USA
[8] Univ Calif San Francisco, Dept Radiol, San Francisco, CA 94143 USA
关键词
Brain; Spectral editing; MEGA-PRESS; PRESS+4; H-1-NMR SPECTROSCOPY; BRAIN; NMR; PRESS; NEURODEGENERATION; SCHIZOPHRENIA; ERYTHROCYTES; SPECTRA; 4T;
D O I
10.1016/j.jmr.2009.11.013
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Glutathione (GSH) is a powerful antioxidant found inside different kinds of cells, including those of the central nervous system. Detection of GSH in the human brain using H-1 MR spectroscopy is hindered by low concentration and spectral overlap with other metabolites. Previous MRS methods focused mainly on the detection of the cysteine residue (GSH-Cys) via editing schemes. This Study focuses on the detection of the glycine residue (GSH-Gly), which is overlapped by glutamate and glutamine (Glx) under physiological pH and temperature. The first goal of the study was to obtain the spectral parameters for characterization of the GSH-Gly signal under physiological conditions. The second goal was to investigate a new method of separating GSH-Gly from Glx in vivo. The characterization of the signal was carried out by utilization of numerical simulations as well as experiments over a wide range of magnetic fields (4.0-14 T). The proposed separation scheme utilizes J-difference editing to quantify the Glx contribution to separate it from the GSH-Gly signal. The presented method retains 100% of the GSH-Gly signal. The overall increase in signal to noise ratio of the targeted resonance is calculated to yield a significant SNR improvement compared to previously used methods that target GSH-Cys residue. This allows shorter acquisition times for in vivo human clinical studies. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:259 / 266
页数:8
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