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We generated mice with deletion of the glucose transporter 3 (GLUT3cKO) or pyruvate kinase 1 (PKM1cKO) in CA1 hippocampal neurons. GLUT3cKO and PKM1cKO mice showed memory impairment. Hyperpolarized (HP) 13C magnetic resonance spectroscopic imaging showed that female, but not male, PKM1cKO mice had increased HP 1-13Cpyruvate-to-lactate conversion, while female GLUT3cKO mice had decreased conversion and brain volume, evaluated by T2-MRI. Fluorine-18-fluorodeoxyglucose (18F-FDG) positron emission tomography imaging did not detect changes, highlighting HP 1-13Cpyruvate’s potential to detect downstream alterations in brain glucose metabolism. Altogether, our findings demonstrated that neurons metabolize glucose through glycolysis in vivo, and require glycolysis for normal function.
Guglielmetti et al. (Wed,) studied this question.