We studied brain redox capacity using ascorbate-derived hyperpolarized (HP) 13C MR and 11C PET probes. We first demonstrated the molecular transport and biodistribution features of the ascorbic acid (VitC)-dehydroascorbate (DHA) pair by leveraging both HP MR and PET modalities. We then showed that HP 13C DHA could detect redox modulation of the brain in a pharmacologic glutathione-depletion rat model. In conclusion, HP 13C DHA MR has the potential for non-invasive evaluation of brain redox capacity.
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