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In Vivo, Ex Vivo, and In Vitro One‐ and Two‐Dimensional Nuclear Magnetic Resonance Spectroscopy of an Intracerebral Glioma in Rat Brain: Assignment of Resonances
Author(s) -
Rémy C.,
Arús C.,
Ziegler A.,
Lai E. Sam,
Moreno A.,
Fur Y. Le,
Décorps M.
Publication year - 1994
Publication title -
journal of neurochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.75
H-Index - 229
eISSN - 1471-4159
pISSN - 0022-3042
DOI - 10.1046/j.1471-4159.1994.62010166.x
Subject(s) - ex vivo , in vivo , glioma , nuclear magnetic resonance , nuclear magnetic resonance spectroscopy , magnetic resonance imaging , in vitro , spectroscopy , resonance (particle physics) , chemistry , biology , cancer research , physics , medicine , biochemistry , atomic physics , genetics , radiology , quantum mechanics
An in vivo study of intracerebral rat glioma using proton‐localized NMR spectroscopy showed important modifications of the spectra in the tumor as compared with the contralateral brain. To carry out the assignment of the resonances of the glioma spectra, tumoral and normal rat brain tissues were studied in vivo, ex vivo, and in vitro by one‐dimensional and two‐dimensional proton spectroscopy. N ‐Acetylaspartate was found at an extremely low level in the glioma. The change of peak ratio total creatine/3.2 ppm peak was found to be due to a simultaneous decrease of the total creatine content and an increase of the 3.2 ppm peak. The 3.2 ppm resonance in the glioma spectra has been shown to originate from choline, phosphocholine, glycerophosphocholine, taurine, inositol, and phosphoethanolamine. The increase of the 3.2 ppm peak in the glioma was found to result from the increase of taurine and phosphoethanolamine contents. The peak in the 1.3 ppm region of the glioma spectra was due to both lactate and mobile fatty acids. Moreover, two‐dimensional spectroscopy of excised tissues and extracts showed the presence of hypotaurine only in the tumor.