## 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 com
Developmental and regional changes in the neurochemical profile of the rat brain determined by in vivo 1H NMR spectroscopy
✍ Scribed by Ivan Tkáč; Raghavendra Rao; Michael K. Georgieff; Rolf Gruetter
- Publisher
- John Wiley and Sons
- Year
- 2003
- Tongue
- English
- Weight
- 896 KB
- Volume
- 50
- Category
- Article
- ISSN
- 0740-3194
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Sixteen metabolites were quantified from 11–24 μl volumes in three different brain regions (hippocampus, striatum, and cerebral cortex) during postnatal development. Rat pups from the same litter were repeatedly measured on postnatal days 7, 10, 14, 21, and 28 using a completely noninvasive and longitudinal study design. Metabolite quantification was based on ultra‐short echo‐time ^1^H NMR spectroscopy at 9.4 T and LCModel processing. Most of the brain metabolites were quantified with Cramer‐Rao lower bounds (CRLB) less than 20%, which corresponded to an estimated concentration error <0.2 μmol/g. Taurine and total creatine were quantified with CRLB ≤ 5% from all 114 processed spectra. The resulting high reliability and reproducibility revealed significant regional and age‐related changes in metabolite concentrations. The most sensitive markers for developmental and regional variations between hippocampus, striatum, and cerebral cortex were N‐acetylaspartate, myo‐inositol, taurine, glutamate, and choline compounds. Absolute values of metabolite concentrations were in very good agreement with previously published in vitro results based on chromatographic measurements of brain extracts. The current data may serve as a reference for studies focused on developmental defects and pathologies using neonatal rat models. Magn Reson Med 50:24–32, 2003. © 2003 Wiley‐Liss, Inc.
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