TY - JOUR
T1 - Quantitative proton spectroscopy of canine brain
T2 - in Vivo and in Vitro correlations
AU - Barker, Peter B.
AU - Breiter, Steven N.
AU - Soher, Brian J.
AU - Chatham, John C.
AU - Forder, John R.
AU - Samphilipo, Michael A.
AU - Magee, Carolyn A.
AU - Anderson, James H.
PY - 1994/8
Y1 - 1994/8
N2 - Quantitative, single‐voxel proton NMR spectroscopy of normal brain was performed in five adult beagle dogs using the cerebral water signal as an internal intensity reference. The same brain regions were then rapidly isolated and frozen using a pneumatic biopsy drill, perchloric acid extracted, and analyzed by biochemical assay and high‐resolution NMR spectroscopy. The concentrations of the major resonances in the in vivo and in vitro spectra were compared, and good agreement was found between the different measurements. The in vivo spectra contained three peaks at 3.21, 3.04, and 2.02 ppm, which are usually assigned to trimethylamines (TMA), creatines, and N‐acetyl derivatives (NAc), which corresponded to be the following metabolite concentration values: 1.7 ± 0.6, 7.7 ± 2.1, and 10.9 ± 2.7 μmol/g wet weight respectively. In vitro, the following metabolite concentrations were measured: glycerophosphocholine (GPC) 1.3 ± 0.2, phosphocholine (PC) 0.5 ± 0.1, phosphocreatine (PCr) 2.6 ± 0.4, creatine (Cr) 5.9 ± 1.4, and N‐Acetyl aspartate (NAA) 8.9 ± 1.8 μmol/g wet weight. Therefore, the 3.21 ppm resonance observed in the in vivo spectrum is predominantly GPC and PC in a ratio of 2.6:1, the 3.04 ppm resonance is Cr and PCr in a ratio of 2.3:1, and the 2.02 ppm resonance is predominantly (≈80%) NAA with small contributions from N‐acetylaspartyl‐glutamate (NAAG) and glutamate. The data presented here validate the technique of water referencing as a simple and convenient means of quantitating single‐voxel in vivo proton NMR spectra of the brain.
AB - Quantitative, single‐voxel proton NMR spectroscopy of normal brain was performed in five adult beagle dogs using the cerebral water signal as an internal intensity reference. The same brain regions were then rapidly isolated and frozen using a pneumatic biopsy drill, perchloric acid extracted, and analyzed by biochemical assay and high‐resolution NMR spectroscopy. The concentrations of the major resonances in the in vivo and in vitro spectra were compared, and good agreement was found between the different measurements. The in vivo spectra contained three peaks at 3.21, 3.04, and 2.02 ppm, which are usually assigned to trimethylamines (TMA), creatines, and N‐acetyl derivatives (NAc), which corresponded to be the following metabolite concentration values: 1.7 ± 0.6, 7.7 ± 2.1, and 10.9 ± 2.7 μmol/g wet weight respectively. In vitro, the following metabolite concentrations were measured: glycerophosphocholine (GPC) 1.3 ± 0.2, phosphocholine (PC) 0.5 ± 0.1, phosphocreatine (PCr) 2.6 ± 0.4, creatine (Cr) 5.9 ± 1.4, and N‐Acetyl aspartate (NAA) 8.9 ± 1.8 μmol/g wet weight. Therefore, the 3.21 ppm resonance observed in the in vivo spectrum is predominantly GPC and PC in a ratio of 2.6:1, the 3.04 ppm resonance is Cr and PCr in a ratio of 2.3:1, and the 2.02 ppm resonance is predominantly (≈80%) NAA with small contributions from N‐acetylaspartyl‐glutamate (NAAG) and glutamate. The data presented here validate the technique of water referencing as a simple and convenient means of quantitating single‐voxel in vivo proton NMR spectra of the brain.
KW - canine brain
KW - proton NMR spectroscopy
KW - quantitation
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U2 - 10.1002/mrm.1910320202
DO - 10.1002/mrm.1910320202
M3 - Article
C2 - 7968436
AN - SCOPUS:0028122325
SN - 0740-3194
VL - 32
SP - 157
EP - 163
JO - Magnetic resonance in medicine
JF - Magnetic resonance in medicine
IS - 2
ER -