Given the issues of chemical shift displacement error, B1 inhomogeneity and short T2 at high field, a semi-adiabatic SPECIAL-based MRSI sequence was implemented at 9.4T, which is equipped with a pair of broad-band hyperbolic secant adiabatic full passage pulses for refocusing, and yet, allows a minimum TE of as short as 4.98 ms. In phantom, the effect of the prolonged minimum TE on the J-evolution of coupled spins is negligible. In a rat brain, preliminary quantitative results are in close agreement with the previous results obtained by using single-voxel MRS.
The animal study was approved by IACUC. All data were acquired on a 9.4T scanner with a 1H Tx/Rx surface coil (Agilent). A PRESS sequence (a MAO refocusing pulse; duration=1 ms, bandwidth=8 kHz) was modified to a PRESS-MRSI sequence. A SPECIAL sequence (a SLR refocusing pulse; duration=0.82 ms, bandwidth=7.8 kHz) was modified to a SPECIAL-MRSI and a semi-SPECIAL-MRSI sequences. For the semi-SPECIAL-MRSI sequence, a pair of broad-band hyperbolic secant adiabatic full passage (HS-AFP) pulses (duration=1 ms, bandwidth=16 kHz) were used for refocusing. The minimum TEs were 12.41, 3.30, and 4.98 ms for PRESS-, SPECIAL-, and semi-SPECIAL-MRSI sequences.
To investigate the impact of the different minimum TEs of the sequences on the J-evolution of coupled spins, spectra were collected from a phantom (an aqueous solution of Cr, GABA, Gln, Glu, mI, NAA, PCho and Tau) using all MRSI sequences in single-voxel MRS mode (i.e., without phase encoding). After acquisition of T2-weighted scout images, in vivo MRSI data were collected from a rat brain using semi-SPECIAL-MRSI (TR/TE=2000/4.98 ms, VOI size=10x10x2.5mm3, FOV=16x16 mm2, matrix size=16x16 (nominal voxel size=2.5mm3), and 16 signal averages). Two voxels in the imaging plane were selected, one from the striatum (STR) and the other from the hippocampus (Hip) for metabolite quantification. For these two voxels, water-unsuppressed spectra (2 signal averages) and metabolite-nulled spectra as a surrogate of spectral baseline (double inversion; TI1/TI2/TR=2830/680/4650ms, 160 signal averages) 4 were also acquired in single-voxel MRS mode for metabolite quantification.
Using the acquired MRSI data, individual metabolite maps were generated by peak integration (VNMRJ, Agilent). Those spectra from the STR and Hip were quantitatively analyzed using QUEST 5 with 19 simulated metabolite bases and the metabolite-nulled spectra.4
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