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PMID: 8755523 Published · ppublish English Comparative Study Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Increased tricarboxylic acid cycle flux in rat brain during forepaw stimulation detected with 1H[13C]NMR.

Hyder F, Chase JR, Behar KL, Mason GF, Siddeek M, Rothman DL, Shulman RG

Abstract

NMR spectroscopy was used to test recent proposals that the additional energy required for brain activation is provided through nonoxidative glycolysis. Using localized NMR spectroscopic methods, the rate of C4-glutamate isotopic turnover from infused [1-(13)C]glucose was measured in the somatosensory cortex of rat brain both at rest and during forepaw stimulation. Analysis of the glutamate turnover data using a mathematical model of cerebral glucose metabolism showed that the tricarboxylic acid cycle flux [(V(TCA)] increased from 0.49 +/- 0.03 at rest to 1.48 +/- 0.82 micromol/g/min during stimulation (P < 0.01). The minimum fraction of C4-glutamate derived from C1-glucose was approximately 75%, and this fraction was found in both the resting and stimulated rats. Hence, the percentage increase in oxidative cerebral metabolic rate of glucose use (CMRglc) equals the percentage increases in V(TCA) and cerebral metabolic rate of oxygen consumption (CMRO2). Comparison with previous work for the same rat model, which measured total CMRglc [Ueki, M., Linn, F. & Hossman, K. A. (1988) J. Cereb. Blood Flow Metab. 8, 486-4941, indicates that oxidative CMRglc supplies the majority of energy during sustained brain activation.

MeSH Terms
Animals Brain/metabolism,physiology Carbon Isotopes Citric Acid Cycle Electric Stimulation Forelimb Glucose/metabolism Glutamic Acid/metabolism Hydrogen Kinetics Magnetic Resonance Spectroscopy/methods Male Models, Theoretical Motor Cortex/metabolism Occipital Lobe/metabolism Rats Rats, Sprague-Dawley Skin/innervation Somatosensory Cortex/metabolism
Chemicals
Carbon Isotopes Glutamic Acid Hydrogen Glucose
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Hyder F
Department of Molecular Biophysics and Biochemistry, Yale University, New Haven, CT 06520-8043, USA.
Chase J R
Behar K L
Mason G F
Siddeek M
Rothman D L
Shulman R G
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Article Info
Journal
Proceedings of the National Academy of Sciences of the United States of America
Abbr.
Proc Natl Acad Sci U S A
ISSN
0027-8424
Published
1996-07-23
Pages
7612-7
Language
English
Region
United States
NLM ID
7505876
PMCID
PMC38794
Subset
IM
Grants
NIDDK NIH HHS · DK27121 · United States
NICHD NIH HHS · HD-32573 · United States
NCRR NIH HHS · RR-07723 · United States
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