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The Journal of Neuroscience, August 13, 2003, 23(19):7337-7342
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BRIEF COMMUNICATION
Glutamate Triggers Rapid Glucose Transport Stimulation in Astrocytes as Evidenced by Real-Time Confocal Microscopy
Anitsi Loaiza,
Omar H. Porras, and
Luis Felipe Barros
Centro de Estudios Científicos, Casilla 1469, Valdivia,
Chile
Glutamate stimulates glycolysis in astrocytes, a phenomenon that couples
astrocytic metabolism with neuronal activity. However, it is not known whether
glutamate also affects glucose transporter-1 (GLUT1), the transporter
responsible for glucose entry into astrocytes. To address this question, two
different real-time single-cell hexose uptake assays were applied to cultured
hippocampal astrocytes using confocal epifluorescence microscopy. Glutamate
caused a twofold to threefold increase in the zero-trans uptake rates of the
fluorescent hexoses
2-[N-(7-nitrobenz-2-oxa-1,3-diazol-4-yl)amino]-2-deoxyglucose
(2-NBDG) and
6-[N-(7-nitrobenz-2-oxa-1,3-diazol-4-yl)amino]-6-deoxyglucose
(6-NBDG). Galactose uptake, determined by the calcein volumetric assay, was
stimulated to a similar extent, confirming the fluorescent hexose data, and
also demonstrating that glutamate stimulation is a Vmax
effect. Remarkably, glucose transport stimulation developed fully inside 10
sec, which is 100 times faster than acute stimulations of glucose transport in
other cell types. Glutamate did not significantly affect the rate of 6-NBDG
uptake by GLUT1-expressing epithelial Clone 9 cells, suggesting that an
astrocyte-specific factor is required for transport stimulation. We conclude
that glucose transport stimulation occurs early during astrocytic activation
by glutamate, which provides a novel regulatory node to current models of
brain energy metabolism. This mechanism should also be considered for the
interpretation of functional imaging data based on hexoses.
Key words: glucose; galactose; membrane transport; 2-NBDG; 6-NBDG; calcein
Received Apr. 16, 2003;
revised May. 30, 2003;
accepted Jun. 3, 2003.
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