ausblenden:
Schlagwörter:
LONG-TERM POTENTIATION; SYNAPTIC-TRANSMISSION; MITOCHONDRIAL TRANSPORT;
PROTEOMIC ANALYSIS; ENERGY-METABOLISM; MEMORY FORMATION;
GENE-EXPRESSION; MOUSE-BRAIN; PROTEIN; AGENeurosciences & Neurology; aging; energy metabolism; hippocampal proteome;
Zusammenfassung:
Lactate derived from astrocytic glycogen has been shown to support memory formation in hippocampi of young animals, inhibiting it in old animals. Here we show, using quantitative mass spectrometry-based proteomics, immunofluorescence, and qPCR that aging is associated with an increase of glycogen metabolism enzymes concentration and shift in their localization from astrocytes to neurons. These changes are accompanied with reorganization of hippocampal energy metabolism which is manifested by elevated capacity of aging neurons to oxidize glucose in glycolysis and mitochondria, and decreased ability for fatty acids utilization. Our observations suggest that astrocyte-to-neuron lactate shuttle may operate in young hippocampi, however, during aging neurons become independent on astrocytic lactate and the metabolic crosstalk between the brain's cells is disrupted.
