U. Sonnewald et al., NUCLEAR-MAGNETIC-RESONANCE SPECTROSCOPY - BIOCHEMICAL EVALUATION OF BRAIN-FUNCTION IN-VIVO AND IN-VITRO, Neurotoxicology, 15(3), 1994, pp. 579-590
Nuclear magnetic resonance spectroscopy (MRS) offers a unique opportun
ity to monitor mmolar concentrations of high energy phosphates, glucos
e, lactate and amino acids. The possibility oi obtaining information a
bout chemical constituents noninvasively is of great importance. MRS a
nd chemical shift imaging (CSI) are emerging as tools for tumor gradin
g, monitoring of treatment, ischemia research, in pediatric research f
or follow-up of children with borderline mental retardation, for defin
ing brain death and to define epileptic foci. It is important to know
which cell type (neuronal or glial) shows changes as a result of exter
nal manipulations (e.g. excitotoxins) or intern al changes (brain path
ology). Metabolic studies have been carried out on brain cell cultures
. By using C-13 labeled glucose and acetate in combination with C-13 M
RS it Was shown that astrocytes release lactate, glutamine, citrate an
d alanine and that cerebral cortical neurons use glutamine released fr
om astrocytes as a precursor for GABA synthesis. An important feature
in MRS is the localization of N-acetyl aspartate in neurons, since thi
s enables monitoring of neuronal reactions, such as survival after neu
rotoxic insults. Recent advances have yielded high speed functional ec
ho planar imaging (EPI) techniques that are sensitive to changes in ce
rebral blood volume, blood flow and blood oxygenation (Functional MRI)
. During cognitive cask performance, local alterations in neuronal act
ivity induce local changes in cerebral metabolism and cerebral perfusi
on, which can now be detected with MRI. (C) 1994 Intox Press, Inc.