F. Hyder et al., INCREASED TRICARBOXYLIC-ACID CYCLE FLUX IN RAT-BRAIN DURING FOREPAW STIMULATION DETECTED WITH H-1 [C-13] NMR, Proceedings of the National Academy of Sciences of the United Statesof America, 93(15), 1996, pp. 7612-7617
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-C-13]glucose was measured
in the somatosensory cortex of rat brain both at rest and during fore
paw stimulation, Analysis of the glutamate turnover data using a mathe
matical model of cerebral glucose metabolism showed that the tricarbox
ylic acid cycle flux (V-TCA) increased from 0.49 +/- 0.03 at rest to 1
.48 +/- 0.82 mu mol/g/min during stimulation (P < 0.01), The minimum f
raction of C4-glutamate derived from C1-glucose was approximate to 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 (CMR(gIc)) equals the percentage increases in V-TCA and c
erebral metabolic rate of oxygen consumption (CMR(o2)). Comparison wit
h previous work for the same rat model, which measured total CMR(gIc)
[Ueki, M., Linn, F. & Hossman, K. A. (1988) J. Cereb. Blood Flow Metab
. 8, 486-494], indicates that oxidative CMR(gIc) supplies the majority
of energy during sustained brain activation.