Brain Glucose Metabolism: Integration of Energetics with Function

Fluctuations in Cytosolic Calcium Regulate the Neuronal Malate–Aspartate NADH Shuttle: Implications for Neuronal Energy Metabolism

Satrústegui, J., & Bak, L. K. (2015) · Neurochemical Research · doi:10.1007/s11064-015-1652-8 · Cited by 33

Involvement of cellular metabolism in age-related LTP modifications in rat hippocampal slices

Drulis‐Fajdasz, D., Wójtowicz, T., Wawrzyniak, M., Włodarczyk, J., Mozrzymas, J. W., & Rakus, D. (2015) · Oncotarget · doi:10.18632/oncotarget.4188 · Cited by 32

Metabolites of 2-Deoxy-[ 14 C]Glucose in Plasma and Brain: Influence on Rate of Glucose Utilization Determined with Deoxyglucose Method in Rat Brain

Dienel, G. A., Cruz, N. F., & Sokoloff, L. (1993) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.1993.40 · Cited by 32

Interaction between mammalian glyceraldehyde‐3‐phosphate dehydrogenase and L ‐lactate dehydrogenase from heart and muscle

Svedružić, Ž. M., & Spivey, H. O. (2006) · Proteins Structure Function and Bioinformatics · doi:10.1002/prot.20862 · Cited by 32

Acid Lability of Metabolites of 2‐Deoxyglucose in Rat Brain: Implications for Estimates of Kinetic Parameters of Deoxyglucose Phosphorylation and Transport Between Blood and Brain

Dienel, G. A., Cruz, N. F., Mori, K., & Sokoloff, L. (1990) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.1990.tb01981.x · Cited by 32

Longitudinal changes of cerebral glutathione (GSH) levels associated with the clinical course of disease progression in patients with secondary progressive multiple sclerosis

Choi, I., Lee, P., Hughes, A. J., Denney, D. R., & LYNCH, S. G. (2016) · Multiple Sclerosis Journal · doi:10.1177/1352458516669441 · Cited by 32

The Kety–Schmidt technique for repeated measurements of global cerebral blood flow and metabolism in the conscious rat

Linde, Schmalbruch, Paulson, O. B., & Madsen (1999) · Acta Physiologica Scandinavica · doi:10.1046/j.1365-201x.1999.00522.x · Cited by 31

Glycolytic and oxidative metabolic contributions to potassium ion transport in rat cerebral cortex

Rosenthal, M., & Sick, T. J. (1992) · Canadian Journal of Physiology and Pharmacology · doi:10.1139/y92-258 · Cited by 31

Astrocyte-Neuron Interactions during Learning May Occur by Lactate Signaling Rather than Metabolism

DiNuzzo, M. (2016) · Frontiers in Integrative Neuroscience · doi:10.3389/fnint.2016.00002 · Cited by 31

Negligible Glucose‐6‐Phosphatase Activity in Cultured Astroglia

Gotoh, J., Itoh, Y., Kuang, T., Cook, M., Law, M. J., & Sokoloff, L. (2000) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.2000.0741400.x · Cited by 30

Decreased levels of free d-aspartic acid in the forebrain of serine racemase (Srr) knock-out mice

Horio, M., Ishima, T., Fujita, Y., Inoue, R., Mori, H., & Hashimoto, K. (2013) · Neurochemistry International · doi:10.1016/j.neuint.2013.02.015 · Cited by 30

Characterization of the Enzymatic and Structural Properties of Human D-Aspartate Oxidase and Comparison with Those of the Rat and Mouse Enzymes

Katane, M., Kawata, T., Nakayama, K., Saitoh, Y., Kaneko, Y., Matsuda, S., Saitoh, Y., Miyamoto, T., Sekine, M., & Homma, H. (2015) · Biological and Pharmaceutical Bulletin · doi:10.1248/bpb.b14-00690 · Cited by 30

Comparison of glucose and lactate as substrates during NMDA-induced activation of hippocampal slices

Chih, C.-P., He, J., Sly, T. S., & Roberts, E. L. (2001) · Brain Research · doi:10.1016/s0006-8993(00)03306-0 · Cited by 30

Evidence for a Lactate Pool in the Rat Brain That is Not Used as an Energy Supply under Normoglycemic Conditions

Leegsma‐Vogt, G., Venema, K., & Korf, J. (2003) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1097/01.wcb.0000080650.64357.8f · Cited by 30

Brain Slice Glucose Utilization

Newman, G. C., Hospod, F. E., & Patlak, C. S. (1988) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.1988.tb01160.x · Cited by 30

Glyceraldehyde-3-Phosphate Dehydrogenase Activity and F-Actin Associations in Synaptosomes and Postsynaptic Densities of Porcine Cerebral Cortex

Rogalski, A. A., & Cohen, R. S. (1997) · Cellular and Molecular Neurobiology · doi:10.1023/a:1026377004261 · Cited by 30

Cerebral glycogen in humans following acute and recurrent hypoglycemia: Implications on a role in hypoglycemia unawareness

Öz, G., DiNuzzo, M., Kumar, A. F., Moheet, A. A., Khowaja, A. A., Kubisiak, K. M., Eberly, L. E., & Seaquist, E. R. (2016) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1177/0271678x16678240 · Cited by 30

Brain Nonoxidative Carbohydrate Consumption is Not Explained by Export of an Unknown Carbon Source: Evaluation of the Arterial and Jugular Venous Metabolome

Rasmussen, P., Nyberg, N. T., Jaroszewski, J. W., Krogh‐Madsen, R., Secher, N. H., & Quistorff, B. (2010) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.2010.25 · Cited by 29

Global Cerebral Blood Flow and Metabolism during Acute Hyperketonemia in the Awake and Anesthetized Rat

Linde, R., Hasselbalch, S. G., Topp, S., Paulson, O. B., & Madsen, P. L. (2005) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/sj.jcbfm.9600177 · Cited by 29

Synthesis of Deoxyglucose‐1‐Phosphate, Deoxyglucose‐1,6‐Bisphosphate, and Other Metabolites of 2‐Deoxy‐D‐[14C]Glucose in Rat Brain In Vivo: Influence of Time and Tissue Glucose Level

Dienel, G. A., & Cruz, N. F. (1993) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.1993.tb03508.x · Cited by 29

Cotransport of Glyceraldehyde-3-Phosphate Dehydrogenase and Actin in Axons of Chicken Motoneurons

Yuan, A., Mills, R. G., Bamburg, J. R., & Bray, J. J. (1999) · Cellular and Molecular Neurobiology · doi:10.1023/a:1006953022763 · Cited by 28

Cerebral Metabolism and Visualization of Cerebral Activity

Sokoloff, L. (1996) · Springer eBooks · doi:10.1007/978-3-642-60946-6_30 · Cited by 28

Activation of mammalian phosphofructokinases by ribose 1,5-bisphosphate.

Ishikawa, E., Ogushi, S., Ishikawa, T., & Uyeda, K. (1990) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(17)30596-3 · Cited by 28

Astrocyte activation in vivo during graded photic stimulation

Dienel, G. A., Schmidt, K., & Cruz, N. F. (2007) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2007.04859.x · Cited by 28

Pyruvate incubation enhances glycogen stores and sustains neuronal function during subsequent glucose deprivation

Shetty, P. K., Sadgrove, M. P., Galeffi, F., & Turner, D. A. (2011) · Neurobiology of Disease · doi:10.1016/j.nbd.2011.08.002 · Cited by 27

The effect of glycogen phosphorolysis on basal glutaminergic transmission

Mozrzymas, J. W., Szczęsny, T. J., & Rakus, D. (2010) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2010.12.033 · Cited by 27

Noninvasive assessment of the relative roles of cerebral antioxidant enzymes by quantitation of pentose phosphate pathway activity

Ben‐Yoseph, O., Boxer, P. A., & Ross, B. D. (1996) · Neurochemical Research · doi:10.1007/bf02532410 · Cited by 27

Analysis of Glutamine Accumulation in Rat Brain Mitochondria in the Presence of a Glutamine Uptake Inhibitor, Histidine, Reveals Glutamine Pools With a Distinct Access to Deamidation

Ziemińska, E., Hilgier, W., Waagepetersen, H. S., Hertz, L., Sonnewald, U., Schousboe, A., & Albrecht, J. (2004) · Neurochemical Research · doi:10.1007/s11064-004-6885-x · Cited by 27

Determination of local brain glucose level with [14C]methylglucose: effects of glucose supply and demand

Dienel, G. A., Cruz, N. F., Adachi, K., Sokoloff, L., & Holden, J. E. (1997) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.1997.273.5.e839 · Cited by 27

Proton Fall or Bicarbonate Rise

Theparambil, S. M., Weber, T., Schmälzle, J., Ruminot, I., & Deitmer, J. W. (2016) · Journal of Biological Chemistry · doi:10.1074/jbc.m116.730143 · Cited by 27

Futile cycling of lactate through the plasma membrane of C6 glioma cells as detected by (13C, 2H) NMR

Rodrigues, T. B., Gray, H. L., Benito, M., Garrido, S., Sierra, A., Geraldes, C. F. G. C., Ballesteros, P., & Cerdán, S. (2004) · Journal of Neuroscience Research · doi:10.1002/jnr.20308 · Cited by 26

Non‐invasive quantification of brain glycogen absolute concentration

Morgenthaler, F. D., van Heeswijk, R. B., Xin, L., Laus, S., Frenkel, H., Lei, H., & Rolf Gruetter, A. (2008) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2008.05717.x · Cited by 26

Glycogen Supercompensation in the Rat Brain After Acute Hypoglycemia is Independent of Glucose Levels During Recovery

Duarte, J. M. N., Morgenthaler, F. D., & Rolf Gruetter, A. (2017) · Neurochemical Research · doi:10.1007/s11064-017-2178-z · Cited by 26

Functional impact of glycogen degradation on astrocytic signalling

Müller, M. S. (2014) · Biochemical Society Transactions · doi:10.1042/bst20140157 · Cited by 25

β-Hydroxybutyrate is the preferred substrate for GABA and glutamate synthesis while glucose is indispensable during depolarization in cultured GABAergic neurons

Lund, T. M., Obel, L. F., Risa, Ø., & Sonnewald, U. (2011) · Neurochemistry International · doi:10.1016/j.neuint.2011.06.002 · Cited by 25

Effects of metabolic inhibitors on evoked activity and the energy state of hippocampal slices superfused in vitro

COX, D. W. G., Drower, J., & Bachelard, H. S. (1985) · Experimental Brain Research · doi:10.1007/bf00237833 · Cited by 25

[3H]glycogenolysis in brain slices mediated by β-adrenoceptors: Comparison of physiological response and [3H]dihydroalprenolol binding parameters

Quach, T. (1988) · Neuropharmacology · doi:10.1016/0028-3908(88)90185-2 · Cited by 25

13C metabolic flux analysis in neurons utilizing a model that accounts for hexose phosphate recycling within the pentose phosphate pathway

Gebril, H. M., Avula, B., Wang, Y., Khan, I. A., & Jekabsons, M. B. (2015) · Neurochemistry International · doi:10.1016/j.neuint.2015.12.008 · Cited by 25

Astrocyte Cultures Mimicking Brain Astrocytes in Gene Expression, Signaling, Metabolism and K+ Uptake and Showing Astrocytic Gene Expression Overlooked by Immunohistochemistry and In Situ Hybridization

Hertz, L., Chen, Y., & Song, D. (2016) · Neurochemical Research · doi:10.1007/s11064-016-1828-x · Cited by 25

An Isozyme-specific Redox Switch in Human Brain Glycogen Phosphorylase Modulates Its Allosteric Activation by AMP

Mathieu, C., Duval, R., Cocaign, A., Petit, E., Bui, L. C., Haddad, I., Vinh, J., Etchebest, C., Dupret, J., & Rodrigues‐Lima, F. (2016) · Journal of Biological Chemistry · doi:10.1074/jbc.m116.757062 · Cited by 25

Alternative Fuels in Epilepsy and Amyotrophic Lateral Sclerosis

Tefera, T. W., Tan, K. N., McDonald, T. S., & Borges, K. (2016) · Neurochemical Research · doi:10.1007/s11064-016-2106-7 · Cited by 25

Silent information regulator 1 modulator resveratrol increases brain lactate production and inhibits mitochondrial metabolism, whereas SRT1720 increases oxidative metabolism

Rowlands, B. D., Lau, C. L., Ryall, J. G., Thomas, D. S., Klugmann, M., Beart, P. M., & Rae, C. D. (2015) · Journal of Neuroscience Research · doi:10.1002/jnr.23570 · Cited by 24

Glutamate stimulates 2-deoxyglucose uptake in rat cerebellar granule cells

Minervini, M., Atlante, A., Gagliardi, S., Ciotti, M. T., Marra, E., & Calissano, P. (1997) · Brain Research · doi:10.1016/s0006-8993(97)00547-7 · Cited by 23

Metabolism of glucose into glutamate via the hexose monophosphate shunt and its inhibition by 6-aminonicotinamide in rat brain in vivo

Gaitonde, M. K., Jones, J. M., & Evans, G. (1987) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.1987.0036 · Cited by 23

Vesicular Glutamate Uptake

Ueda, T. (2016) · Advances in neurobiology · doi:10.1007/978-3-319-45096-4_7 · Cited by 23

Metabolic Effects of Blocking Lactate Transport in Brain Cortical Tissue Slices Using an Inhibitor Specific to MCT1 and MCT2

Rae, C. D., Nasrallah, F. A., & Bröer, S. (2009) · Neurochemical Research · doi:10.1007/s11064-009-9973-0 · Cited by 22

Measurement of 10−7 to 10−12 mol of potassium by stimulation of pyruvate kinase

Outlaw, W. H., & Lowry, O. H. (1979) · Analytical Biochemistry · doi:10.1016/0003-2697(79)90673-0 · Cited by 22

Microdialysate concentration changes do not provide sufficient information to evaluate metabolic effects of lactate supplementation in brain-injured patients

Dienel, G. A., Rothman, D. L., & Nordström, C. (2016) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1177/0271678x16666552 · Cited by 22

Axon‐glia interactions in the crayfish: Glial cell oxygen consumption is tightly coupled to axon metabolism

Hargittai, P. T., & Lieberman, E. M. (1991) · Glia · doi:10.1002/glia.440040410 · Cited by 21

Interrelationships (Between Glucose Metabolism, Energy State, and the Cytosolic Free Calcium Concentration in Cortical Synjaptosomes from the Guinea Pig

Kauppinen, R. A., Taipale, H., & Komulainen, H. (1989) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.1989.tb11771.x · Cited by 21

Behavioral characterization of a mutant mouse strain lacking d-amino acid oxidase activity

Zhang, M., Ballard, M. E., Basso, A. M., Bratcher, N. A., Browman, K. E., Curzon, P., Konno, R., Meyer, A. H., & Rueter, L. E. (2010) · Behavioural Brain Research · doi:10.1016/j.bbr.2010.09.030 · Cited by 21

2.1 The Support of Energy Metabolism in the Central Nervous System with Substrates Other than Glucose

Roberts, E. L. (2007) · Springer eBooks · doi:10.1007/978-0-387-30411-3_7 · Cited by 21

Monoaminergic Control of Cellular Glucose Utilization by Glycogenolysis in Neocortex and Hippocampus

DiNuzzo, M., Giove, F., Maraviglia, B., & Mangia, S. (2015) · Neurochemical Research · doi:10.1007/s11064-015-1656-4 · Cited by 20

Characterization of neurochemically specific projections from the locus coeruleus with respect to somatosensory‐related barrels

Simpson, K. L., Waterhouse, B. D., & Lin, R. C. S. (2006) · The Anatomical Record Part A Discoveries in Molecular Cellular and Evolutionary Biology · doi:10.1002/ar.a.20287 · Cited by 20

1.2 Glucose, Oxidative Energy Metabolism, and Neural Function in Brain Slices—Glycolysis Plays a Key Role in Neural Activity

Okada, Y., & Lipton, P. (2007) · Springer eBooks · doi:10.1007/978-0-387-30411-3_2 · Cited by 20

Effective Mechanism for Synthesis of Neurotransmitter Glutamate and its Loading into Synaptic Vesicles

Takeda, K., & Ueda, T. (2016) · Neurochemical Research · doi:10.1007/s11064-016-2037-3 · Cited by 19

Energy Metabolism in the Brain

Dienel, G. A. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-397179-1.00003-8 · Cited by 18

Activity-related increases of glucose utilization associated with reduced incorporation of glucose into its derivatives

Sharp, F. R. (1976) · Brain Research · doi:10.1016/0006-8993(76)90157-8 · Cited by 18

Enzyme complexity in intermediary metabolism

SCHAFTINGEN, E. V., Veiga‐da‐Cunha, M., & Linster, C. L. (2015) · Journal of Inherited Metabolic Disease · doi:10.1007/s10545-015-9821-0 · Cited by 18

Glucose, Lactate and Glutamine but not Glutamate Support Depolarization-Induced Increased Respiration in Isolated Nerve Terminals

Hohnholt, M. C., Andersen, V. H., Bak, L. K., & Waagepetersen, H. S. (2016) · Neurochemical Research · doi:10.1007/s11064-016-2036-4 · Cited by 18

Trajectories of Brain Lactate and Re-visited Oxygen-Glucose Index Calculations Do Not Support Elevated Non-oxidative Metabolism of Glucose Across Childhood

Benveniste, H., Dienel, G. A., Jacob, Z., Lee, H., Makaryus, R., GJEDDE, A. H., Hyder, F., & Rothman, D. L. (2018) · Frontiers in Neuroscience · doi:10.3389/fnins.2018.00631 · Cited by 18

Metabolic studies on perinatal human brain

Himwich, W. A., Benaron, H. B. W., Tucker, B. E., et al. (1959) · Journal of Applied Physiology · doi:10.1152/jappl.1959.14.6.873 · Cited by 17

Modification of Astrocyte Metabolism as an Approach to the Treatment of Epilepsy: Triheptanoin and Acetyl-l-Carnitine

Hadera, M. G., McDonald, T. S., Smeland, O. B., Meisingset, T. W., Eloqayli, H., Jaradat, S. A., Borges, K., & Sonnewald, U. (2015) · Neurochemical Research · doi:10.1007/s11064-015-1728-5 · Cited by 16

Role of fructose 2,6-bisphosphate in the regulation of glycolysis in various types of cultivated brain cell

Pauwels, P. J., & Trouet, A. (1984) · Neuroscience Letters · doi:10.1016/0304-3940(84)90437-3 · Cited by 16

Updates to a 13 C metabolic flux analysis model for evaluating energy metabolism in cultured cerebellar granule neurons from neonatal rats

Jekabsons, M. B., Gebril, H. M., Wang, Y., Avula, B., & Khan, I. A. (2017) · Neurochemistry International · doi:10.1016/j.neuint.2017.03.020 · Cited by 16

Maintained cerebral metabolic ratio during exercise in patients with β‐adrenergic blockade

Gam, C. M. B. F., Rasmussen, P. V., Secher, N. H., Seifert, T., Larsen, F. S., & Nielsen, H. B. (2009) · Clinical Physiology and Functional Imaging · doi:10.1111/j.1475-097x.2009.00889.x · Cited by 15

Cellular Origin of [ 18 F]FDG-PET Imaging Signals During Ceftriaxone-Stimulated Glutamate Uptake: Astrocytes and Neurons

Dienel, G. A., Behar, K. L., & Rothman, D. L. (2017) · The Neuroscientist · doi:10.1177/1073858417749375 · Cited by 15

Determination of Glucose Utilization Rates in Cultured Astrocytes and Neurons with [14C]deoxyglucose: Progress, Pitfalls, and Discovery of Intracellular Glucose Compartmentation

Dienel, G. A., Cruz, N. F., Sokoloff, L., & Driscoll, B. F. (2015) · Neurochemical Research · doi:10.1007/s11064-015-1650-x · Cited by 12

Nitrous oxide and xenon increase noradrenaline release in the cerebral cortex in vivo and in vitro

Yoshida, H., Kushikata, T., Tose, R., Kudo, M., Kudo, T., & Hirota, K. (2009) · Neuroscience Letters · doi:10.1016/j.neulet.2009.11.074 · Cited by 12

4.1 Cytoplasmic Glycolytic Enzymes. Synaptic Vesicle-Associated Glycolytic ATP-Generating Enzymes: Coupling to Neurotransmitter Accumulation

Ueda, T., & Ikemoto, A. (2007) · Springer eBooks · doi:10.1007/978-0-387-30411-3_10 · Cited by 11

Activation of muscle phosphofructokinase by α-glucose 1,6-bisphosphate and fructose 2,6-bisphosphate is differently affected by other allosteric effectors and by pH

Andrés, V., Carreras, J., & Cussó, R. (1988) · Biochemical and Biophysical Research Communications · doi:10.1016/s0006-291x(88)80301-2 · Cited by 11

K+ Homeostasis in the Brain: A New Role for Glycogenolysis

Mangia, S., Giove, F., & DiNuzzo, M. (2013) · Neurochemical Research · doi:10.1007/s11064-012-0962-3 · Cited by 11

Techniques and strategies in neurocritical care originating from Southern Scandinavia

Nordström, C., Nielsen, T. H., & Jacobsen, A. (2013) · Journal of Rehabilitation Medicine · doi:10.2340/16501977-1157 · Cited by 11

On the relationship between the excitability of dentate granule cell field potentials and their sensitivity to low glucose

COX, D. W. G., & Bachelard, H. S. (1988) · Brain Research · doi:10.1016/0006-8993(88)91177-8 · Cited by 10

Amobarbital inhibits K+-stimulated glucose oxidation in cerebellar granule neurons by two mechanisms

Peng, L., & Hertz, L. (2002) · European Journal of Pharmacology · doi:10.1016/s0014-2999(02)01794-6 · Cited by 9

Membrane Transport

Albers, R. W., Siegel, G. J., & Xie, Z. (2012) · Elsevier eBooks · doi:10.1016/b978-0-12-374947-5.00003-1 · Cited by 9

Synaptic Plasticity

Heidelberger, R., Shouval, H. Z., Zucker, R. S., & Byrne, J. H. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-397179-1.00018-x · Cited by 8

4.3 Coupling of Neuronal Function to Oxygen and Glucose Metabolism Through Changes in Neurotransmitter Dynamics as Revealed with Aging, Hypoglycemia, and Hypoxia

Joseph, J. A., & Gibson, G. E. (2007) · Springer eBooks · doi:10.1007/978-0-387-30411-3_12 · Cited by 8

7.2 Genetics and Gene Expression of Glycolysis

LaManna, J. C., Pichiule, P., & Chavez, J. C. (2007) · Springer eBooks · doi:10.1007/978-0-387-30411-3_28 · Cited by 8

Astrocytic Vesicle‐based Exocytosis in Cultures and Acutely Isolated Hippocampal Rodent Slices

Jorgačevski, J., Potokar, M., Kreft, M., Guček, A., Mothet, J., & Zorec, R. (2017) · Journal of Neuroscience Research · doi:10.1002/jnr.24051 · Cited by 8

Fructose 2,6-bisphosphate in developing rat brain

Ambrosio, S., Ventura, F., & Bartrons, R. (1992) · Developmental Brain Research · doi:10.1016/0165-3806(92)90092-b · Cited by 5

Hexose diphosphates and phosphofructokinase in rat brain during development

Dombrowski, G. J., Swiatek, K. R., & Chao, K. (1994) · Neurochemical Research · doi:10.1007/bf01006822 · Cited by 4

Assessment of Mitochondrial Protein Glutathionylation as Signaling for CO Pathway

Almeida, A. S., Figueiredo-Pereira, C., & Vieira, H. L. A. (2021) · Methods in molecular biology · doi:10.1007/978-1-0716-1266-8_19 · Cited by 2

Assessment of Mitochondrial Protein Glutathionylation as Signaling for CO Pathway

Almeida, A. S., & Vieira, H. L. A. (2015) · Methods in molecular biology · doi:10.1007/978-1-4939-2257-4_30 · Cited by 1

Lactate metabolism in human health and disease

Li, X., Yang, Y., Zhang, B., Lin, X., Fu, X., An, Y., Zou, Y., Wang, J.-X., Wang, Z., & Yu, T. (2022) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-022-01151-3 · Cited by 1,454

Brain energy rescue: an emerging therapeutic concept for neurodegenerative disorders of ageing

Cunnane, S. C., Trushina, E., Morland, C., Prigione, A., Casadesus, G., Andrews, Z. B., Beal, M. F., Bergersen, L. H., Brinton, R. D., de la Monte, S., et al. (2020) · Nature Reviews Drug Discovery · doi:10.1038/s41573-020-0072-x · Cited by 1,003

Astrocyte-neuron metabolic cooperation shapes brain activity

Bonvento, G., & Bolaños, J. P. (2021) · Cell Metabolism · doi:10.1016/j.cmet.2021.07.006 · Cited by 580

Lactate and lactylation in cancer

Chen, J., Huang, Z., Chen, Y., Tian, H., Chai, P., Shen, Y., Yao, Y., Xu, S., Ge, S., & Jia, R. (2025) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-024-02082-x · Cited by 477

Glutamate metabolism and recycling at the excitatory synapse in health and neurodegeneration

Andersen, J. V., Markussen, K. H., Jakobsen, E., Schousboe, A., Waagepetersen, H. S., Rosenberg, P. A., & Aldana, B. I. (2021) · Neuropharmacology · doi:10.1016/j.neuropharm.2021.108719 · Cited by 371