In vivo H-1 NMR measurement of glycine in rat brain at 9.4 T at short echo time
Glycine is an amino acid present in mammalian brain, where it acts as an inhibitory and excitatory neurotransmitter. The two detectable protons of glycine give rise to a singlet at 3.55 ppm that overlaps with the more intense myo-inositol resonances, and its measurement has traditionally required specific editing efforts. The aim of the current study was to reduce the signal intensity of myo-inositol relative to that of glycine by exploiting the fast signal J-evolution of the myo-inositol spin system when using a single spin-echo localization method we recently introduced. Glycine was detected at TE = 20 ms with an average Cramer-Rao lower bound (CRLB) of 8.6% +/- 1.5% in rat brain (N = 5), at 9.4 T. The concentration of glycine was determined using LCModel analysis at 1.1 +/- 0.1 mM, in good agreement with biochemical measurements previously reported. We conclude that at high magnetic fields, glycine can be measured at a relatively short echo time (TE) without additional editing efforts.
Keywords: glycine ; strongly coupled spin system ; NMR spectroscopy ; density matrix simulations ; rat brain ; Magnetic-Resonance-Spectroscopy ; Free Amino Acids ; Spin Systems ; Spectra ; Schizophrenia ; Metabolites ; Sequences ; Vitro ; CIBM-AIT
Record created on 2010-11-30, modified on 2016-08-09