["The Journal of Physiology, Volume 604, Issue 10, Page 3934-3963, 15 May 2026. ", "\nAbstract figure legend Astrocyte‐derived lactate enhances neuronal NMDA receptor (NMDAR) function and synaptic plasticity through a redox‐ and CaMKII‐dependent mechanism. Lactate enters neurons via monocarboxylate transporters (MCTs) and is oxidized by lactate dehydrogenase (LDH) to pyruvate, generating NADH and increasing the intracellular NADH/NAD+ ratio. This redox shift promotes Ca2+ release from ryanodine‐sensitive stores (RyR) and the recruitment of Ca2+/calmodulin‐dependent protein kinase II (CaMKII) to GluN2B‐containing NMDARs. The interaction occurs at intracellular redox‐sensitive cysteine residues of GluN2B, leading to enhanced NMDAR currents and prolonged decay kinetics. Consequently the strengthened NMDAR–CaMKII signalling is associated with increased NMDAR presence at postsynaptic sites, thereby facilitating the molecular processes underlying long‐term synaptic plasticity and memory formation.\n\n\n\n\n\n\n\n\n\nAbstract\nAstrocyte‐derived lactate, through the astrocyte–neuron lactate shuttle, fuels neuronal energy demands and acts as a signalling molecule promoting synaptic plasticity and memory consolidation. Lactate regulates neuronal excitability and expression of genes related to synaptic plasticity and neuroprotection, but the molecular mechanisms remain unclear. Using patch‐clamp recordings in cultured cortical neurons we found that lactate enhances NMDA receptor currents (INMDAR), increasing their amplitude and decay time constant. Not reproduced by HCAR1 agonists, this modulation depends on monocarboxylate transporters and lactate dehydrogenase, requiring lactate entry, metabolic conversion to pyruvate and NADH formation within neurons. Disruption of intracellular calcium dynamics or inhibition of Ca2+/calmodulin‐dependent protein kinase II (CaMKII) diminishes lactate's effects on INMDAR. Two redox‐sensitive cysteine‐containing sequences in the intracellular C‐terminal domain of GluN2B subunit play a crucial role in the potentiation of NMDAR by lactate. Experiments in HEK cells demonstrate that functional CaMKII and GluN2B‐containing NMDARs are necessary for lactate's effects. Mutations in GluN2B, that disrupt either CaMKII binding or cysteine‐mediated redox regulation, abolish lactate's modulatory action. Immunoprecipitation experiments in neurons show that lactate promotes CaMKII‐GluN2B association, which is critical for increasing INMDAR amplitude. Proximity ligation assays between GluN2B and PSD‐95 reveal that lactate induces GluN2B accumulation in dendritic spines, an effect a CaMKII inhibitor prevents. These findings elucidate a pathway whereby lactate enhances NMDAR function through metabolic conversion and redox‐sensitive interactions requiring CaMKII, linking astrocyte energy metabolism to synaptic modulation.\n\n\n\n\n\n\n\n\n\nKey points\n\nAstrocytes produce lactate, traditionally seen as an energy source, which also acts as a signalling molecule in the brain, influencing memory and synaptic plasticity by modulating NMDA receptor (NMDAR) function.\nLactate enhances NMDAR responses specifically by increasing current amplitude through changes in cellular redox balance, which requires the entry of lactate into neurons and its conversion to pyruvate, producing NADH.\nLactate‐induced potentiation of NMDARs depends on calcium signalling involving Ca2+/calmodulin‐dependent protein kinase II (CaMKII), which interacts directly with the GluN2B subunit of the receptor.\nLactate strengthens the interaction between CaMKII and GluN2B through redox‐sensitive cysteine residues in GluN2B, facilitating synaptic localization of this complex and enhancing synaptic responses.\nThese findings reveal a molecular pathway by which lactate, produced by astrocytes, can significantly influence neuronal activity and synaptic function, linking brain metabolism with learning and memory processes.\n\n\n"]