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High‐resolution one‐and two‐dimensional 1 H MRS of human brain tumor and normal glial cells
Author(s) -
Kotitschke Klaus,
Jung Hans,
Nekolla Stephan,
Haase Axel,
Bauer Albrech,
Bogdahn Ulrich
Publication year - 1994
Publication title -
nmr in biomedicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.278
H-Index - 114
eISSN - 1099-1492
pISSN - 0952-3480
DOI - 10.1002/nbm.1940070303
Subject(s) - phosphocreatine , glutamine , choline , in vivo , creatine , taurine , phosphocholine , chemistry , nuclear magnetic resonance , glutamate receptor , inositol , biology , biochemistry , amino acid , endocrinology , phospholipid , phosphatidylcholine , physics , receptor , microbiology and biotechnology , membrane , energy metabolism
Astrocytoma (WHO grade II, III), glioblastoma, malignant melanoma, and normal glial cell cultures, established from biopsies, were investigated by 1 H MRS. At a 1 H resonance frequency of 500 MHz (11.75 T) a high spectral resolution was achieved in 1D 1 H spectra; in conjunction with 2D shift‐correlated (COSY) MRS, resonances of alanine, aspartate, choline, creatine, glutamate, glutamine, hypotaurine, myo ‐inositol, phosphocreatine, phosphoryl‐ethanolamine, phosphoryl‐choline, lactate, lysine, N ‐acetylaspartate, taurine, threonine and valine could be identified. T 1 relaxation times for the most prominent compounds are presented. T 1 values of lactate ranged between 450 ms and 850 ms. The intensity of the lactate signal revealed differences between individual spectra, but exhibited no correlation between different tumor specimens or degree of malignancy. It was shown that the lactate signal at 1.3 ppm is covered by peaks arising from threonine and fatty acids. The choline signal level varied among spectra of different tumors, among tumors with similar degree of malignancy, and within the same tumor. Further preliminary differences due to aspartate, inositol and glutamine/glutamate were found in 1D and 2D COSY spectra between normal glial cells as well as different tumors. These results indicate that some differences observed in in vivo spectra may be attributable to secondary macroscopic structural changes (hypoxia, necrosis) and not to tumor inherent characteristics. Further correlation between in vivo and in vitro spectroscopy is therefore required.