Oxidative Phosphorylation, Not Glycolysis, Powers Presynaptic and Postsynaptic Mechanisms Underlying Brain Information Processing

Neural activity has been suggested to initially trigger ATP production by glycolysis, rather than oxidative phosphorylation, for three reasons: glycolytic enzymes are associated with ion pumps; neurons may increase their energy supply by activating glycolysis in astrocytes to generate lactate; and activity increases glucose uptake more than O2 uptake. In rat hippocampal slices, neuronal activity rapidly decreased the levels of extracellular O2 and intracellular NADH (reduced nicotinamide adenine dinucleotide), even with lactate dehydrogenase blocked to prevent lactate generation, or with only 20% superfused O2 to mimic physiological O2 levels. Pharmacological analysis revealed an energy budget in which 11% of O2 use was on presynaptic action potentials, 17% was on presynaptic Ca2+ entry and transmitter release, 46% was on postsynaptic glutamate receptors, and 26% was on postsynaptic action potentials, in approximate accord with theoretical brain energy budgets. Thus, the major mechanisms mediating brain information processing are all initially powered by oxidative phosphorylation, and an astrocyte–neuron lactate shuttle is not needed for this to occur.

[1]  M. Prins,et al.  Cerebral Metabolic Adaptation and Ketone Metabolism after Brain Injury , 2008, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[2]  P. Nair,et al.  Mass transfer, storage, and utilization of O2 in cat cerebral cortex. , 1970, The American journal of physiology.

[3]  P. Magistretti,et al.  Glutamate uptake into astrocytes stimulates aerobic glycolysis: a mechanism coupling neuronal activity to glucose utilization. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[4]  E. Gozal,et al.  Aerobic Production and Utilization of Lactate Satisfy Increased Energy Demands Upon Neuronal Activation in Hippocampal Slices and Provide Neuroprotection Against Oxidative Stress , 2012, Front. Pharmacol..

[5]  R G Shulman,et al.  Energy on Demand , 1999, Science.

[6]  G. Dahlquist,et al.  The Rate of Cerebral Utilization of Glucose, Ketone Bodies, and Oxygen: A Comparative in Vivo Study of Infant and Adult Rats , 1976, Pediatric Research.

[7]  J. Deitmer,et al.  Glucose and lactate supply to the synapse , 2010, Brain Research Reviews.

[8]  P. Hare Advance Online Publication , 2002, Nature Medicine.

[9]  B CHANCE,et al.  Respiratory enzymes in oxidative phosphorylation. III. The steady state. , 1955, The Journal of biological chemistry.

[10]  B. Chance ENZYMES IN OXIDATIVE PHOSPHORYLATION , 2003 .

[11]  S. Matsugo,et al.  The lactate-dependent enhancement of hydroxyl radical generation by the Fenton reaction , 2000, Free radical research.

[12]  M. Duchen,et al.  Ca(2+)-dependent changes in the mitochondrial energetics in single dissociated mouse sensory neurons. , 1992, The Biochemical journal.

[13]  G. Dienel,et al.  Imaging Brain Activation , 2008, Annals of the New York Academy of Sciences.

[14]  L. Sokoloff,et al.  Cerebral Oxygen/Glucose Ratio is Low during Sensory Stimulation and Rises above Normal during Recovery: Excess Glucose Consumption during Stimulation is Not Accounted for by Lactate Efflux from or Accumulation in Brain Tissue , 1999, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[15]  C. Iadecola,et al.  Nitric oxide and adenosine mediate vasodilation during functional activation in cerebellar cortex , 1994, Neuropharmacology.

[16]  Yuchio Yanagawa,et al.  Glial Nax Channels Control Lactate Signaling to Neurons for Brain [Na+] Sensing , 2007, Neuron.

[17]  M. Jüptner,et al.  Review: Does Measurement of Regional Cerebral Blood Flow Reflect Synaptic Activity?—Implications for PET and fMRI , 1995, NeuroImage.

[18]  Mauro DiNuzzo,et al.  Response to ‘Comment on Recent Modeling Studies of Astrocyte—Neuron Metabolic Interactions’: Much ado about Nothing , 2011, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[19]  B CHANCE,et al.  Respiratory enzymes in oxidative phosphorylation. II. Difference spectra. , 1955, The Journal of biological chemistry.

[20]  S. Laughlin,et al.  An Energy Budget for Signaling in the Grey Matter of the Brain , 2001, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[21]  W. Webb,et al.  Neural Activity Triggers Neuronal Oxidative Metabolism Followed by Astrocytic Glycolysis , 2004, Science.

[22]  L. Raeymaekers,et al.  Preferential support of Ca2+ uptake in smooth muscle plasma membrane vesicles by an endogenous glycolytic cascade , 1989, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

[23]  S. Ogawa,et al.  The sensitivity of magnetic resonance image signals of a rat brain to changes in the cerebral venous blood oxygenation , 1993, Magnetic resonance in medicine.

[24]  D. Beard,et al.  Faculty Opinions recommendation of Calcium signaling in brain mitochondria: interplay of malate aspartate NADH shuttle and calcium uniporter/mitochondrial dehydrogenase pathways. , 2010 .

[25]  J. Tepper,et al.  Endogenous Hydrogen Peroxide Regulates the Excitability of Midbrain Dopamine Neurons via ATP-Sensitive Potassium Channels , 2005, The Journal of Neuroscience.

[26]  R. Rej Measurement of aspartate aminotransferase activity: effects of oxamate. , 1979, Clinical chemistry.

[27]  Á. Martín-Requero,et al.  Interaction of oxamate with the gluconeogenic pathway in rat liver. , 1986, Archives of biochemistry and biophysics.

[28]  J. Aubin Autofluorescence of viable cultured mammalian cells. , 1979, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

[29]  R. Ichord,et al.  MK801 decreases glutamate release and oxidative metabolism during hypoglycemic coma in piglets. , 2001, Brain research. Developmental brain research.

[30]  S. Kety,et al.  THE GENERAL METABOLISM OF THE BRAIN IN VIVO , 1957 .

[31]  R. S. Payne,et al.  Lactate, not pyruvate, is neuronal aerobic glycolysis end product: An in vitro electrophysiological study , 2007, Neuroscience.

[32]  N. Akgören,et al.  Importance of nitric oxide for local increases of blood flow in rat cerebellar cortex during electrical stimulation. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[33]  J. Connor,et al.  NAD(P)H Fluorescence Transients after Synaptic Activity in Brain Slices: Predominant Role of Mitochondrial Function , 2006, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[34]  A. Grinvald,et al.  Interactions Between Electrical Activity and Cortical Microcirculation Revealed by Imaging Spectroscopy: Implications for Functional Brain Mapping , 1996, Science.

[35]  R. Freeman,et al.  Single-Neuron Activity and Tissue Oxygenation in the Cerebral Cortex , 2003, Science.

[36]  Gordon M Shepherd,et al.  Odor-Evoked Oxygen Consumption by Action Potential and Synaptic Transmission in the Olfactory Bulb , 2009, The Journal of Neuroscience.

[37]  K. Gunter,et al.  Calcium and mitochondria , 2004, FEBS letters.

[38]  Pierre J Magistretti,et al.  Sweet Sixteen for ANLS , 2012, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[39]  C. Cooper Competitive, Reversible, Physiological? Inhibition of Mitochondrial Cytochrome Oxidase by Nitric Oxide , 2003, IUBMB life.

[40]  P. Magistretti,et al.  Activity‐dependent regulation of energy metabolism by astrocytes: An update , 2007, Glia.

[41]  S. Schultz,et al.  Colocalization of glycolytic enzyme activity and KATP channels in basolateral membrane of Necturusenterocytes. , 1998, American journal of physiology. Cell physiology.

[42]  H. Koch,et al.  Prostaglandin E2-Induced Synaptic Plasticity in Neocortical Networks of Organotypic Slice Cultures , 2010, The Journal of Neuroscience.

[43]  M. Mintun,et al.  Nonoxidative glucose consumption during focal physiologic neural activity. , 1988, Science.

[44]  J Meixensberger,et al.  Clinical experience with 118 brain tissue oxygen partial pressure catheter probes. , 1998, Neurosurgery.

[45]  Yi Zhang,et al.  Noninvasive and Three-Dimensional Imaging of CMRO2 in Rats at 9.4 T: Reproducibility Test and Normothermia/Hypothermia Comparison Study , 2007, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[46]  Sarah A. Stern,et al.  Astrocyte-Neuron Lactate Transport Is Required for Long-Term Memory Formation , 2011, Cell.

[47]  Martin Lauritzen,et al.  Dissociation of spikes, synaptic activity, and activity-dependent increments in rat cerebellar blood flow by tonic synaptic inhibition , 2003, Proceedings of the National Academy of Sciences of the United States of America.

[48]  S. Schultz,et al.  Colocalization of glycolytic enzyme activity and KATP channels in basolateral membrane of Necturus enterocytes. , 1998, The American journal of physiology.

[49]  P. Dunham,et al.  Membrane-bound ATP fuels the Na/K pump. Studies on membrane-bound glycolytic enzymes on inside-out vesicles from human red cell membranes , 1981, The Journal of general physiology.

[50]  H. Knull Association of glycolytic enzymes with particulate fractions from nerve endings. , 1978, Biochimica et biophysica acta.

[51]  F. Striggow,et al.  Extramitochondrial Ca2+ in the Nanomolar Range Regulates Glutamate-Dependent Oxidative Phosphorylation on Demand , 2009, PloS one.

[52]  R. Gerard Handbook of physiology, section I: Neurophysiology , 1960 .

[53]  Peter T Fox,et al.  Nonlinear coupling between cerebral blood flow, oxygen consumption, and ATP production in human visual cortex , 2010, Proceedings of the National Academy of Sciences.

[54]  Albert Gjedde,et al.  Neuronal–Glial Glucose Oxidation and Glutamatergic–GABAergic Function , 2006, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[55]  M. Reivich,et al.  THE [14C]DEOXYGLUCOSE METHOD FOR THE MEASUREMENT OF LOCAL CEREBRAL GLUCOSE UTILIZATION: THEORY, PROCEDURE, AND NORMAL VALUES IN THE CONSCIOUS AND ANESTHETIZED ALBINO RAT 1 , 1977, Journal of neurochemistry.

[56]  V. Schuster,et al.  Identification of lactate as a driving force for prostanoid transport by prostaglandin transporter PGT. , 2002, American journal of physiology. Renal physiology.

[57]  D. Attwell,et al.  Assessing the physiological concentration and targets of nitric oxide in brain tissue , 2008, The Journal of physiology.

[58]  Grant R. Gordon,et al.  Brain metabolism dictates the polarity of astrocyte control over arterioles , 2008, Nature.

[59]  Jörg R. P. Geiger,et al.  Energy-Efficient Action Potentials in Hippocampal Mossy Fibers , 2009, Science.

[60]  F. Striggow,et al.  The regulation of OXPHOS by extramitochondrial calcium. , 2010, Biochimica et biophysica acta.

[61]  A. Volterra,et al.  Astrocytes: Powering Memory , 2011, Cell.

[62]  P. Lipton,et al.  Glycolysis and brain function: [K+]o stimulation of protein synthesis and K+ uptake require glycolysis. , 1983, Federation proceedings.

[63]  Nikolas Offenhauser,et al.  Activity‐induced tissue oxygenation changes in rat cerebellar cortex: interplay of postsynaptic activation and blood flow , 2005, The Journal of physiology.

[64]  Min Wu,et al.  Multiparameter metabolic analysis reveals a close link between attenuated mitochondrial bioenergetic function and enhanced glycolysis dependency in human tumor cells. , 2007, American journal of physiology. Cell physiology.

[65]  L. Janssen,et al.  Determination of the diffusion coefficient of oxygen in sodium chloride solutions with a transient pulse technique , 1993 .

[66]  V. Routh,et al.  Differential effects of glucose and lactate on glucosensing neurons in the ventromedial hypothalamic nucleus. , 2005, Diabetes.

[67]  M. Lu,et al.  Interaction between Aldolase and Vacuolar H+-ATPase , 2001, The Journal of Biological Chemistry.

[68]  C. Pournaras,et al.  Microinjection of L-lactate in the preretinal vitreous induces segmental vasodilation in the inner retina of miniature pigs. , 1993, Investigative ophthalmology & visual science.

[69]  R. Paul,et al.  Vascular smooth muscle: aerobic glycolysis linked to sodium and potassium transport processes. , 1979, Science.

[70]  M. Moser,et al.  Pattern Separation in the Dentate Gyrus and CA3 of the Hippocampus , 2007, Science.

[71]  I. Jang,et al.  Feed-forward facilitation of glutamate release by presynaptic GABAA receptors , 2005, Neuroscience.

[72]  C. Mathiesen,et al.  Activity-dependent Increases in Local Oxygen Consumption Correlate with Postsynaptic Currents in the Mouse Cerebellum In Vivo , 2011, The Journal of Neuroscience.

[73]  D. Attwell,et al.  Intracellular pH changes produced by glutamate uptake in rat hippocampal slices. , 1994, Journal of neurophysiology.

[74]  V. Mootha,et al.  Ca2+ activation of heart mitochondrial oxidative phosphorylation: role of the F0/F1-ATPase , 2000 .

[75]  J. Adams,et al.  High-performance liquid chromatography analysis of oxidized and reduced pyridine dinucleotides in specific brain regions. , 1995, Analytical biochemistry.

[76]  V. Mootha,et al.  Ca(2+) activation of heart mitochondrial oxidative phosphorylation: role of the F(0)/F(1)-ATPase. , 2000, American journal of physiology. Cell physiology.

[77]  Zhen-Dan Shi,et al.  Mitochondrial NADH fluorescence is enhanced by complex I binding. , 2008, Biochemistry.

[78]  Albert Gjedde,et al.  The pathways of oxygen in brain. I. Delivery and metabolism of oxygen. , 2005, Advances in experimental medicine and biology.