Trafficking of amino acids between neurons and glia in vivo. Effects of inhibition of glial metabolism by fluoroacetate

Glial-neuronal interchange of amino acids was studied by C-13 nuclear magnetic resonance spectroscopy of brain extracts from fluoroacetate-treated mice that received [1,2-C-13]acetate and [1-C-13]glucose simultaneously. [C-13]Acetate was found to be a specific marker for glial metabolism even with thr large doses necessary for nuclear magnetic resonance spectroscopy. Fluoroacetate, 100 mg/kg, blocked the glial, but not the neuronal tricarboxylic acid cycles as seen from the C-13 labeling of glutamine, glutamate, and gamma-aminobutyric acid. Glutamine, but not citrate, was the only glial metabolite that could account for the transfer of C-13 from glia to neurons. Massive glial uptake of transmitter glutamate was indicated by the labeling of glutamine from [1-C-13]glucose in fluoroacetate-treated mice. The C-3/C-4 enrichment ratio, which indicates the degree of cycling of label, was higher in glutamine than in glutamate in the presence of fluoroacetate, suggesting that transmitter glutamate (which was converted to glutamine after release) is associated with a tricarboxylic acid cycle that turns more rapidly than the overall cerebral tricarboxylic acid cycle.