Glutamatergic and GABAergic TCA cycle and neurotransmitter cycling fluxes in different regions of mouse brain

The C-13 nuclear magnetic resonance (NMR) studies together with the infusion of C-13-labeled substrates in rats and humans have provided important insight into brain energy metabolism. In the present study, we have extended a three-compartment metabolic model in mouse to investigate glutamatergic and GABAergic tricarboxylic acid (TCA) cycle and neurotransmitter cycle fluxes across different regions of the brain. The C-13 turnover of amino acids from [1,6-C-13(2)]glucose was monitored ex vivo using H-1-[C-13]-NMR spectroscopy. The astroglial glutamate pool size, one of the important parameters of the model, was estimated by a short infusion of [2-C-13]acetate. The ratio V-cyc/V-TCA was calculated from the steady-state acetate experiment. The C-13 turnover curves of [4-C-13]/[3-C-13]glutamate, [4-C-13]glutamine, [2-C-13]/[3-C-13]GABA, and [3-C-13]aspartate from [1,6-C-13(2)]glucose were analyzed using a three-compartment metabolic model to estimate the rates of the TCA cycle and neurotransmitter cycle associated with glutamatergic and GABAergic neurons. The glutamatergic TCA cycle rate was found to be highest in the cerebral cortex (0.91 +/- 0.05 mu mol/g per minute) and least in the hippocampal region (0.64 +/- 0.07 mu mol/g per minute) of the mouse brain. In contrast, the GABAergic TCA cycle flux was found to be highest in the thalamus-hypothalamus (0.28 +/- 0.01 mu mol/g per minute) and least in the cerebral cortex (0.24 +/- 0.02 mmol/g per minute). These findings indicate that the energetics of excitatory and inhibitory function is distinct across the mouse brain.