T2 measurement and quantification of glutamate in human brain in vivo
Changho Choia b✉, Nicholas J. Couplandc d, Paramjit P. Bhardwajc d, Sanjay Kalrad e, Colin A. Casaultc d, Kim Reidd e, Peter S. Allenb d
- aDepartment of Biomedical Engineering, University of Alberta, Edmonton, Alberta, Canada. changho.choi@ualberta.ca
- bDepartment of Biomedical Engineering, University of Alberta, Edmonton, Alberta, Canada
- cDepartment of Psychiatry, University of Alberta, Edmonton, Alberta, Canada
- dUniversity of Alberta
- eDepartment of Medicine (Neurology), University of Alberta, Edmonton, Alberta, Canada
- ✉Corresponding author
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Abstract
The proton NMR transverse relaxation time T(2) of glutamate (Glu) in human brain was measured by means of spectrally selective refocusing at 3.0 T in vivo. An 81.4-ms-long dual-band Gaussian 180 degrees RF pulse, designed for refocusing at 2.35 and 3.03 ppm, was employed within point-resolved spectroscopy (PRESS) to generate the Glu C4-proton target multiplet and the total creatine (tCr) singlet. Six optimal echo times (TEs) between 128 and 380 ms were selected from numerical analysis of the filtering performance for effective detection of the Glu signal with minimal contamination from glutamine (Gln), N-acetylaspartate (NAA), and glutathione (GSH). The magnetization of Glu and tCr was extracted from spectral fitting of experimental and calculated spectra. Apparent T(2) values of Glu and tCr were estimated as 201 +/- 18 and 164 +/- 12 ms for the medial prefrontal (PF) cortex, and 198 +/- 22 and 169 +/- 15 ms (mean +/- SD, N = 5) for the left frontal (LF) cortex, respectively. With water segmentation data, the magnetization values of Glu and tCr of the two adjacent voxels, calculated from the T(2) values and spectra following the thermal equilibrium magnetization, were combined to give the Glu and tCr concentrations as 10.37 +/- 1.06 and 8.87 +/- 0.56 mM for gray matter (GM), and 5.06 +/- 0.57 and 5.16 +/- 0.45 mM (mean +/- SD, N = 5) for white matter (WM), respectively.