Enhanced neurochemical profile of the rat brain using in vivo 1H NMR spectroscopy at 16.4 T |
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Authors: | Sung‐Tak Hong Dávid Zsolt Balla G. Shajan Changho Choi Kâmil Uğurbil Rolf Pohmann |
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Affiliation: | 1. High‐Field Magnetic Resonance Center, Max‐Planck Institute for Biological Cybernetics, 72076 Tübingen, Germany;2. Advanced Imaging Research Center, University of Texas Southwestern Medical Center, Dallas, Texas, USA;3. Center for Magnetic Resonance Research, University of Minnesota, Minneapolis, Minnesota, USA |
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Abstract: | Single voxel magnetic resonance spectroscopy with ultrashort echo time was implemented at 16.4 T to enhance the neurochemical profile of the rat brain in vivo. A TE of 1.7 msec was achieved by sequence optimization and by using short‐duration asymmetric pulses. Macromolecular signal components were parameterized individually and included in the quantitative analysis, replacing the use of a metabolite‐nulled spectrum. Because of the high spectral dispersion, several signals close to the water line could be detected, and adjacent peaks could be resolved. All 20 metabolites detected in this study were quantified with Cramér‐Rao lower bounds below 20%, implying reliable quantification accuracy. The signal of acetate was detected for the first time in rat brain in vivo with Cramér‐Rao lower bounds of 16% and a concentration of 0.52 μmol/g. The absolute concentrations of most metabolites showed close agreement with values previously measured using in vivo 1H NMR spectroscopy and in vitro biochemical assay. Magn Reson Med, 2010. © 2010 Wiley‐Liss, Inc. |
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Keywords: | 1H magnetic resonance spectroscopy (MRS) STEAM ultrashort TE LCModel parameterization macromolecular ultrahigh‐field |
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