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   <subfield code="a">Invivo &lt;sup&gt;13&lt;/sup&gt;C MRS in the mouse brain at 14.1 Tesla and metabolic flux quantification under infusion of</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[M. Lai, B. Lanz, C. Poitry-Yamate, J.F. Romero, C.M. Berset, C. Cudalbu, R. Gruetter]</subfield>
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   <subfield code="a">1,6-&lt;sup&gt;13&lt;/sup&gt;C&lt;sub&gt;2&lt;/sub&gt;</subfield>
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   <subfield code="a">Invivo &amp;lt;sup&amp;gt;13&amp;lt;/sup&amp;gt; C magnetic resonance spectroscopy (MRS) enables the investigation of cerebral metabolic compartmentation while, e.g. infusing &amp;lt;sup&amp;gt;13&amp;lt;/sup&amp;gt; C-labeled glucose. Metabolic flux analysis of &amp;lt;sup&amp;gt;13&amp;lt;/sup&amp;gt; C turnover previously yielded quantitative information of glutamate and glutamine metabolism in humans and rats, while the application to invivo mouse brain remains exceedingly challenging. In the present study, &amp;lt;sup&amp;gt;13&amp;lt;/sup&amp;gt; C direct detection at 14.1 T provided highly resolved invivo spectra of the mouse brain while infusing [1,6- &amp;lt;sup&amp;gt;13&amp;lt;/sup&amp;gt; C &amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt; ]glucose for up to 5 h. &amp;lt;sup&amp;gt;13&amp;lt;/sup&amp;gt; C incorporation to glutamate and glutamine C4, C3, and C2 and aspartate C3 were detected dynamically and fitted to a two-compartment model: flux estimation of neuron-glial metabolism included tricarboxylic acid cycle (TCA) flux in astrocytes (V &amp;lt;sub&amp;gt;g&amp;lt;/sub&amp;gt;  = 0.16 ± 0.03 µmol/g/min) and neurons (V &amp;lt;sub&amp;gt;TCA&amp;lt;/sub&amp;gt; &amp;lt;sup&amp;gt;n &amp;lt;/sup&amp;gt; = 0.56 ± 0.03 µmol/g/min), pyruvate carboxylase activity (V &amp;lt;sub&amp;gt;PC&amp;lt;/sub&amp;gt;  = 0.041 ± 0.003 µmol/g/min) and neurotransmission rate (V &amp;lt;sub&amp;gt;NT&amp;lt;/sub&amp;gt;  = 0.084 ± 0.008 µmol/g/min), resulting in a cerebral metabolic rate of glucose (CMR &amp;lt;sub&amp;gt;glc&amp;lt;/sub&amp;gt; ) of 0.38 ± 0.02 µmol/g/min, in excellent agreement with that determined with concomitant &amp;lt;sup&amp;gt;18&amp;lt;/sup&amp;gt; F-fluorodeoxyglucose positron emission tomography ( &amp;lt;sup&amp;gt;18&amp;lt;/sup&amp;gt; FDG PET).We conclude that modeling of neuron-glial metabolism invivo is accessible in the mouse brain from &amp;lt;sup&amp;gt;13&amp;lt;/sup&amp;gt; C direct detection with an unprecedented spatial resolution under [1,6- &amp;lt;sup&amp;gt;13&amp;lt;/sup&amp;gt; C &amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt; ]glucose infusion.</subfield>
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   <subfield code="t">Journal of cerebral blood flow and metabolism</subfield>
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