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Determination of the rate of the glutamate/glutamine cycle in the human brain by in vivo 13 C NMR
Author(s) -
Jun Shen,
Kitt Falk Petersen,
Kevin L. Behar,
Peter B. Brown,
Terrence W. Nixon,
Graeme F. Mason,
Ognen A. C. Petroff,
Gerald I. Shulman,
Robert G. Shulman,
Douglas L. Rothman
Publication year - 1999
Publication title -
proceedings of the national academy of sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.96.14.8235
Subject(s) - glutamine , citric acid cycle , glutamate receptor , tricarboxylic acid , glutamatergic , glutamic acid , biochemistry , metabolism , biology , in vivo , chemistry , amino acid , receptor , microbiology and biotechnology
Recent 13C NMR studies in rat models have shown that the glutamate/glutamine cycle is highly active in the cerebral cortex and is coupled to incremental glucose oxidation in an approximately 1:1 stoichiometry. To determine whether a high level of glutamatergic activity is present in human cortex, the rates of the tricarboxylic acid cycle, glutamine synthesis, and the glutamate/glutamine cycle were determined in the human occipital/parietal lobe at rest. During an infusion of [1-13C]-glucose, in vivo 13C NMR spectra were obtained of the time courses of label incorporation into [4-13C]-glutamate and [4-13C]-glutamine. Using a metabolic model we have validated in the rat, we calculated a total tricarboxylic acid cycle rate of 0.77 +/- 0.07 micromol/min/g (mean +/- SD, n = 6), a glucose oxidation rate of 0.39 +/- 0.04 micromol/min/g, and a glutamate/glutamine cycle rate of 0.32 +/- 0.05 micromol/min/g (mean +/- SD, n = 6). In agreement with studies in rat cerebral cortex, the glutamate/glutamine cycle is a major metabolic flux in the resting human brain with a rate approximately 80% of glucose oxidation.

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