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| Q30429932 | Astrocytic energetics during excitatory neurotransmission: What are contributions of glutamate oxidation and glycolysis? |
| Q35846489 | Astroglial pentose phosphate pathway rates in response to high-glucose environments. |
| Q38770428 | Bioenergetics and redox adaptations of astrocytes to neuronal activity. |
| Q21129443 | Brain glycogen-new perspectives on its metabolic function and regulation at the subcellular level |
| Q30452931 | Brain lactate metabolism: the discoveries and the controversies |
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| Q47813249 | Comparative Examination of Temporal Glyoxalase 1 Variations Following Perforant Pathway Transection, Excitotoxicity, and Controlled Cortical Impact Injury. |
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| Q47887507 | CrossTalk opposing view: lack of evidence supporting an astrocyte-to-neuron lactate shuttle coupling neuronal activity to glucose utilisation in the brain |
| Q35858095 | Demonstrated brain insulin resistance in Alzheimer's disease patients is associated with IGF-1 resistance, IRS-1 dysregulation, and cognitive decline |
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| Q58759828 | Dual action of L-Lactate on the activity of NR2B-containing NMDA receptors: from potentiation to neuroprotection |
| Q52151944 | Dynamic Changes in Cytosolic ATP Levels in Cultured Glutamatergic Neurons During NMDA-Induced Synaptic Activity Supported by Glucose or Lactate. |
| Q59136352 | Dysregulated Glucose Metabolism as a Therapeutic Target to Reduce Post-traumatic Epilepsy |
| Q35013625 | Energy metabolism and glutamate-glutamine cycle in the brain: a stoichiometric modeling perspective |
| Q58753940 | Estimation of intracellular fluxes in cerebellar neurons after hypoglycemia: Importance of the pyruvate recycling pathway and glutamine oxidation |
| Q38542199 | Fluctuations in Cytosolic Calcium Regulate the Neuronal Malate-Aspartate NADH Shuttle: Implications for Neuronal Energy Metabolism. |
| Q30465578 | Fueling and imaging brain activation |
| Q88645870 | Fueling thought: Management of glycolysis and oxidative phosphorylation in neuronal metabolism |
| Q34278619 | Gabapentin reverses central hypersensitivity and suppresses medial prefrontal cortical glucose metabolism in rats with neuropathic pain |
| Q34033057 | Glutamate reduces glucose utilization while concomitantly enhancing AQP9 and MCT2 expression in cultured rat hippocampal neurons |
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| Q30938714 | Glycolysis and the significance of lactate in traumatic brain injury |
| Q42498674 | Glycolysis selectively shapes the presynaptic action potential waveform |
| Q39114928 | Misconceptions regarding basic thermodynamics and enzyme kinetics have led to erroneous conclusions regarding the metabolic importance of lactate dehydrogenase isoenzyme expression |
| Q90690062 | Neurons rely on glucose rather than astrocytic lactate during stimulation |
| Q42556097 | Novel model of neuronal bioenergetics: postsynaptic utilization of glucose but not lactate correlates positively with Ca2+ signalling in cultured mouse glutamatergic neurons. |
| Q48325187 | Rebuttal from L. F. Barros and B. Weber. |
| Q33852904 | Response to 'comment on recent modeling studies of astrocyte-neuron metabolic interactions': much ado about nothing. |
| Q37382205 | Synaptic activity and bioenergy homeostasis: implications in brain trauma and neurodegenerative diseases. |
| Q90259961 | The Response to Stimulation in Neurons and Astrocytes |
| Q26766023 | The Role of Lactate-Mediated Metabolic Coupling between Astrocytes and Neurons in Long-Term Memory Formation |
| Q38254907 | The metabolic response to excitotoxicity - lessons from single-cell imaging. |
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| Q48511211 | Valine but not leucine or isoleucine supports neurotransmitter glutamate synthesis during synaptic activity in cultured cerebellar neurons. |