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Biol Psychiatry 85(9):769781

Mitochondria enriched in cardiomyocytes are essential for processing these metabolites into a steady-state ATP pool through catabolic pathways, oxidation, glycolysis, ketosis, and ultimately, the TCA cycle and oxidative phosphorylation (OXPHOS)

In Huntingtons disease, an inherited neurodegenerative disorder, reduced expression of EAAT2 was observed in postmortem brain samples (Faideau et al., To date, exploration of how gliotransmission contributes to neural information processing and behavior focused mostly on physiological conditions

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