High‐resolution one‐and two‐dimensional 1 H MRS of human brain tumor and normal glial cells

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‐correl...

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Veröffentlicht in:NMR in biomedicine 1994-05, Vol.7 (3), p.111-120
Hauptverfasser: Kotitschke, Klaus, Jung, Hans, Nekolla, Stephan, Haase, Axel, Bauer, Albrech, Bogdahn, Ulrich
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Sprache:eng
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Zusammenfassung: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.
ISSN:0952-3480
1099-1492
DOI:10.1002/nbm.1940070303