The DOI matches its Crossref record; 134 of the 135 references it cites were found in a registry or an index.
Brain Energy Metabolism: Focus on Astrocyte-Neuron Metabolic Cooperation
Open accessAbstract
The energy requirements of the brain are very high, and tight regulatory mechanisms operate to ensure adequate spatial and temporal delivery of energy substrates in register with neuronal activity. Astrocytes-a type of glial cell-have emerged as active players in brain energy delivery, production, utilization, and storage. Our understanding of neuroenergetics is rapidly evolving from a "neurocentric" view to a more integrated picture involving an intense cooperativity between astrocytes and neurons. This review focuses on the cellular aspects of brain energy metabolism, with a particular emphasis on the metabolic interactions between neurons and astrocytes.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“As the major lipid carrier in the brain, secreted ApoE is generally presumed to be converted into HDL-like LNPs by astrocytes.”
From ApoE is Secreted as a Lipid Nanoparticle by Mammalian Cells: Implications for Alzheimer’s Disease Pathogenesis (2025) · cites this paper as [47]
In the citing paper
“In turn, these LNPs undergo receptor-mediated endocytosis in neurons and glia cells where their lipid constituents are disassembled in lysosomes to supply these constituents to the recipient cells.22, 44–47”
From ApoE is Secreted as a Lipid Nanoparticle by Mammalian Cells: Implications for Alzheimer’s Disease Pathogenesis (2025) · cites this paper as [47]
In the citing paper
“Astrocytes provide critical support to neurons for synapse formation/pruning, neurotransmitter modulation, and metabolic homeostasis (Bélanger et al., 2011; Jha and Morrison, 2018).”
From ApoE4 Impairs Neuron-Astrocyte Coupling of Fatty Acid Metabolism (2021) · cites this paper as Bélanger et al., 2011
In the citing paper
“Compared with neurons, astrocytes are relatively resistant to oxidative stress (Bélanger et al. 2011; Wilson 1997).”
From LDL Cholesterol Modulates Astrocyte Metabolism, Lipid Handling, and Morphology: Evidence From In Vitro and In Vivo Models (2026) · cites this paper as Bélanger et al. 2011
In the citing paper
“Neuronal cells in the brain have a particularly high metabolism, using 20% and 25% of the total consumed oxygen and glucose,34 this makes neurons and their mitochondria particularly susceptible to ROS damage.”
From Bacopa monnieri (L.) wettst. Extract protects against glutamate toxicity and increases the longevity of Caenorhabditis elegans (2020) · cites this paper as [34]
Citations
Cites
Sokoloff, L., Reivich, M., Kennedy, C., Rosiers, M. H. D., Patlak, C. S., Pettigrew, K. D., Sakurada, O., & Shinohara, M. (1977) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.1977.tb10649.x · Cited by 6,000
Ogawa, S., Tank, D. W., Menon, R., Ellermann, J. M., Kim, S. G., Merkle, H., & Ugurbil, K. (1992) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.89.13.5951 · Cited by 3,681
An Energy Budget for Signaling in the Grey Matter of the Brain
Attwell, D., & Laughlin, S. B. (2001) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1097/00004647-200110000-00001 · Cited by 3,543
Searching for a baseline: Functional imaging and the resting human brain
Gusnard, D. A., & Raichle, M. E. (2001) · Nature Reviews Neuroscience · doi:10.1038/35094500 · Cited by 3,371
Cahoy, J. D., Emery, B., Kaushal, A., Foo, L. C., Zamanian, J. L., Christopherson, K. S., Xing, Y., Lubischer, J. L., Krieg, P. A., Krupenko, S. A., et al. (2008) · The Journal of Neuroscience · doi:10.1523/jneurosci.4178-07.2008 · Cited by 3,129
Pellerin, L., & Magistretti, P. J. (1994) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.91.22.10625 · Cited by 2,927 · cited 2×
“The stimulation of astrocytic glucose utilization by glutamate was subsequently confirmed by several independent groups (reviewed in Pellerin et al., 2007; Barros and Deitmer, 2010).”
BackgroundSelf-citationGlial and neuronal control of brain blood flow
Attwell, D., Buchan, A. M., Charpak, S., Lauritzen, M., MacVicar, B. A., & Newman, E. A. (2010) · Nature · doi:10.1038/nature09613 · Cited by 2,511
Fox, P. T., & Raichle, M. E. (1986) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.83.4.1140 · Cited by 2,056
Astrocytes, from brain glue to communication elements: the revolution continues
Volterra, A., & Meldolesi, J. (2005) · Nature reviews. Neuroscience · doi:10.1038/nrn1722 · Cited by 1,837
Nonoxidative Glucose Consumption During Focal Physiologic Neural Activity
Fox, P. T., Raichle, M. E., Mintun, M. A., & Dence, C. (1988) · Science · doi:10.1126/science.3260686 · Cited by 1,796
Flagged first, then by citations
1 of the 135 references couldn’t be matched to a known paper.
Cited by
Sorted by citations
Items 601–700 of 1,008
Ludikhuize, M. C., & Colman, M. J. R. (2020) · Antioxidants and Redox Signaling · doi:10.1089/ars.2020.8126 · Cited by 45
Yang, W., Pang, D., Chen, M., Du, C., Jia, L., Wang, L., He, Y., Jiang, W., Luo, L., Yu, Z., et al. (2021) · Developmental Cell · doi:10.1016/j.devcel.2021.02.022 · Cited by 47
Tseng, Y., Liu, S., Hu, M. Y., Chen, R.-D., Lee, J.-R., & Hwang, P. (2014) · Frontiers in Zoology · doi:10.1186/s12983-014-0053-1 · Cited by 44
Livingston, N. R., Calsolaro, V., Hinz, R., Nowell, J., Raza, S., Gentleman, S., Tyacke, R. J., Myers, J., Venkataraman, A. V., Perneczky, R., et al. (2022) · Molecular Psychiatry · doi:10.1038/s41380-021-01429-y · Cited by 44
Immunomodulatory Role of CB2 Receptors in Emotional and Cognitive Disorders
Morcuende, Á., García‐Gutiérrez, M. S., Tambaro, S., Nieto, E. O., Manzanares, J., & Femenía, T. (2022) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2022.866052 · Cited by 45
The Role of Bioenergetics in Neurodegeneration
Strope, T. A., Birky, C. J., & Wilkins, H. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23169212 · Cited by 44
Johnson, R. J., Tolan, D. R., Bredesen, D. E., Nagel, M. A., Sánchez‐Lozada, L. G., Fini, M. A., Burtis, S., Lanaspa, M. A., & Perlmutter, D. (2023) · American Journal of Clinical Nutrition · doi:10.1016/j.ajcnut.2023.01.002 · Cited by 49
The Impact of Metabolic Rewiring in Glioblastoma: The Immune Landscape and Therapeutic Strategies
Vijayanathan, Y., & Ho, I. A. W. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26020669 · Cited by 47
Ultrasensitive detection of 3D cerebral microvascular network dynamics in vivo
Pan, Y., You, J., Volkow, N. D., Park, K., & Du, C. (2014) · NeuroImage · doi:10.1016/j.neuroimage.2014.08.051 · Cited by 44
Concepts for regulation of axon integrity by enwrapping glia
Beirowski, B. (2013) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2013.00256 · Cited by 47
Herwerth, M., Kalluri, S. R., Srivastava, R., Kleele, T., Kenet, S., Illés, Z., Merkler, D., Bennett, J. L., Misgeld, T., & Hemmer, B. (2016) · Annals of Neurology · doi:10.1002/ana.24630 · Cited by 44
Gerkau, N. J., Rakers, C., Petzold, G. C., & Rose, C. R. (2017) · Journal of Neuroscience Research · doi:10.1002/jnr.23995 · Cited by 44
A trade-off between cognitive and physical performance, with relative preservation of brain function
Longman, D. P., Stock, J. T., & Wells, J. C. K. (2017) · Scientific Reports · doi:10.1038/s41598-017-14186-2 · Cited by 46
An Update on Stiripentol Mechanisms of Action: A Narrative Review
Bacq, A., Depaulis, A., Castagné, V., Guern, M. L., Wirrell, E. C., & Verleye, M. (2024) · Advances in Therapy · doi:10.1007/s12325-024-02813-0 · Cited by 43
Shen, Y., Zhang, G., Wei, C., Zhao, P., Wang, Y., Li, M., & Sun, L. (2024) · Neural Regeneration Research · doi:10.4103/nrr.nrr-d-23-01343 · Cited by 44
Modern Perspective of Lactate Metabolism
Vavricka, J., Brož, P., Follprecht, D., Novák, J., & Kroužecký, A. (2024) · Physiological Research · doi:10.33549/physiolres.935331 · Cited by 50
Loría, F., & Díaz‐Nido, J. (2014) · Neurobiology of Disease · doi:10.1016/j.nbd.2014.12.017 · Cited by 41
Stuntz, E., Gong, Y., Sood, D., Liaudanskaya, V., Pouli, D., Quinn, K. P., Alonzo, C., Liu, Z., Kaplan, D. L., & Georgakoudi, I. (2017) · Scientific Reports · doi:10.1038/s41598-017-01015-9 · Cited by 43
Mitochondrial Dynamics and Hypothalamic Regulation of Metabolism
Jin, S., & Diano, S. (2018) · Endocrinology · doi:10.1210/en.2018-00667 · Cited by 45
A Mesenchymal stem cell line (B10) increases angiogenesis in a rat MCAO model
Sheikh, A. M., Yano, S., Mitaki, S., Haque, M. A., Yamaguchi, S., & Nagai, A. (2018) · Experimental Neurology · doi:10.1016/j.expneurol.2018.10.001 · Cited by 43
Equine Neonatal Encephalopathy
Toribio, R. E. (2019) · Veterinary Clinics of North America Equine Practice · doi:10.1016/j.cveq.2019.03.004 · Cited by 43
Abdelkarim, D., Zhao, Y., Turner, M. P., Sivakolundu, D. K., Lu, H., & Bart Rypma, A. (2019) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2019.09.005 · Cited by 47
Neuronal lactate levels depend on glia‐derived lactate during high brain activity in Drosophila
González‐Gutiérrez, A., Ibacache, A., Esparza, A., Barros, L. F., & Sierralta, J. A. (2019) · Glia · doi:10.1002/glia.23772 · Cited by 49
Rajkumar, R., Brambilla, C. R., Veselinović, T., Bierbrier, J. L., Wyss, C., Ramkiran, S., Orth, L., Lang, M., Kops, E. R., Mauler, J., et al. (2021) · Translational Psychiatry · doi:10.1038/s41398-020-01160-2 · Cited by 44
Huo, M., Wang, Z., Fu, W., Lu, T., Li, W., Zhou, Z., Chen, Y., Wei, J., & Abliz, Z. (2021) · Journal of Proteome Research · doi:10.1021/acs.jproteome.1c00179 · Cited by 43
Mitochondria in Early Forebrain Development: From Neurulation to Mid-Corticogenesis
Fame, R. M., & Lehtinen, M. K. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.780207 · Cited by 47
Wan, J., Zhou, S., Mea, H. J., Guo, Y., Ku, H., & Urbina, B. (2022) · Chemical Reviews · doi:10.1021/acs.chemrev.1c00480 · Cited by 45
Advantages and drawbacks of dexamethasone in glioblastoma multiforme
Afshari, A. R., Sanati, M., Aminyavari, S., Shakeri, F., Bibak, B., Keshavarzi, Z., Soukhtanloo, M., Jalili‐Nik, M., Sadeghi, M. M., Mollazadeh, H., et al. (2022) · Critical Reviews in Oncology/Hematology · doi:10.1016/j.critrevonc.2022.103625 · Cited by 43
Kleinkauf‐Rocha, J., Bobermin, L. D., Machado, P. D. M., Gonçalves, C., Gottfried, C., & Quincozes‐Santos, A. (2012) · International Journal of Developmental Neuroscience · doi:10.1016/j.ijdevneu.2012.12.006 · Cited by 44
Cabello-Rivera, D., Sarmiento‐Soto, H., López‐Barneo, J., & Muñoz-Cabello, A. M. (2019) · Frontiers in Neuroscience · doi:10.3389/fnins.2019.00664 · Cited by 42
The gut microbiota‐astrocyte axis: Implications for type 2 diabetic cognitive dysfunction
Li, Z.-H., Jiang, Y., Long, C., Peng, Q., & Yue, R. (2023) · CNS Neuroscience & Therapeutics · doi:10.1111/cns.14077 · Cited by 41
Colucci, A. C. M., Tassinari, I. D., Loss, E. D. S., & de Fraga, L. S. (2023) · Neuroscience · doi:10.1016/j.neuroscience.2023.06.022 · Cited by 46
Vestergaard, M. B., & Larsson, H. B. W. (2017) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1177/0271678x17737909 · Cited by 42
Zika Virus and the Metabolism of Neuronal Cells
Rothan, H. A., Fang, S., Mahesh, M., & Byrareddy, S. N. (2018) · Molecular Neurobiology · doi:10.1007/s12035-018-1263-x · Cited by 42
Souza, A. D. O., Lima, C. A. C., Catalão, C. H. R., Santos-Júnior, N. N., dos Santos, J. F., Rocha, M. J. A., & Alberici, L. C. (2018) · NeuroToxicology · doi:10.1016/j.neuro.2018.11.013 · Cited by 39
Neurobiological findings underlying depressive behavior in Parkinson’s disease: A review
Mendonça, I. P., Duarte-Silva, E. P., Chaves-Filho, A. J. M., Andrade‐da‐Costa, B. L. D. S., & Peixoto, C. A. (2020) · International Immunopharmacology · doi:10.1016/j.intimp.2020.106434 · Cited by 42
Tang, M., & Monani, U. R. (2021) · Neuroscience Insights · doi:10.1177/26331055211011507 · Cited by 44
Astrocyte Molecular Clock Function in the Nucleus Accumbens Is Important for Reward-Related Behavior
Becker‐Krail, D. D., Ketchesin, K. D., Burns, J. N., Zong, W., Hildebrand, M. A., DePoy, L. M., Vadnie, C. A., Tseng, G. C., Logan, R. W., Huang, Y. H., et al. (2022) · Biological Psychiatry · doi:10.1016/j.biopsych.2022.02.007 · Cited by 44
Appraising the Role of Astrocytes as Suppliers of Neuronal Glutathione Precursors
Pérez‐Sala, D., & Pajares, M. A. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24098059 · Cited by 42
Neuro-Vulnerability in Energy Metabolism Regulation: A Comprehensive Narrative Review
Clemente‐Suárez, V. J., Beltrán-Velasco, A. I., Redondo-Flórez, L., Martín-Rodríguez, A., Sepulveda, R. A. Y., & Tornero-Aguilera, J. F. (2023) · Nutrients · doi:10.3390/nu15143106 · Cited by 46
Gogna, T., Housden, B. E., & Houldsworth, A. (2024) · Antioxidants · doi:10.3390/antiox13091138 · Cited by 47
Xiong, J., Ge, X., Pan, D., Zhu, Y., Zhou, Y., Gao, Y., Wang, H., Wang, X., Gu, Y., Wu, Y., et al. (2025) · Cell Death and Differentiation · doi:10.1038/s41418-025-01467-x · Cited by 41
Gliopreventive effects of guanosine against glucose deprivation in vitro
Quincozes-Santos, A., Bobermin, L., de Souza, D. G., Bellaver, B., Gonçalves, C., & Souza, D. O. (2013) · Purinergic Signalling Purinergic Signalling · doi:10.1007/s11302-013-9377-0 · Cited by 38
Koivisto, H., Leinonen, H., Puurula, M., Hafez, H. S., Alquicer, G., Stridh, M. H., Waagepetersen, H. S., Tiainen, M., Soininen, P., Zilberter, Y., et al. (2016) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2016.00041 · Cited by 41
Hopiavuori, B. R., Deák, F., Wilkerson, J. L., Brush, R. S., Rocha-Hopiavuori, N. A., Hopiavuori, A. R., Ozan, K. G., Sullivan, M. T., Wren, J. D., Georgescu, C., et al. (2017) · Molecular Neurobiology · doi:10.1007/s12035-017-0824-8 · Cited by 42
Investigating the energy crisis in Alzheimer disease using transcriptome study
Dharshini, S. A. P., Taguchi, Y., & Gromiha, M. M. (2019) · Scientific Reports · doi:10.1038/s41598-019-54782-y · Cited by 40
Sivalingam, K., Cirino, T. J., McLaughlin, J. P., & Samikkannu, T. (2020) · Molecular Neurobiology · doi:10.1007/s12035-020-02131-w · Cited by 40
Gould, R. W., Gage, H. D., & Nader, M. A. (2012) · Biological Psychiatry · doi:10.1016/j.biopsych.2012.05.001 · Cited by 41
Jaber, S. M., Bordt, E. A., Bhatt, N. M., Lewis, D. M., Gerecht, S., Fiskum, G., & Polster, B. M. (2018) · Neurochemistry International · doi:10.1016/j.neuint.2017.09.003 · Cited by 40
Mitochondria-Targeted Therapeutics for Alzheimer's Disease: The Good, the Bad, the Potential
Mi, Y., Qi, G., Brinton, R. D., & Yin, F. (2021) · Antioxidants & Redox Signaling · doi:10.1089/ars.2020.8070 · Cited by 43
de Melo, A. D., Freire, V. A. F., Diogo, Í. L., Santos, H. D. L., Barbosa, L. A., & Carvalho‐Tavares, J. (2023) · Antioxidants · doi:10.3390/antiox12071397 · Cited by 40
Decoding metabolic signatures in Alzheimer’s disease: a mitochondrial perspective
Bano, D., Ehninger, D., & Bagetta, G. (2023) · Cell Death Discovery · doi:10.1038/s41420-023-01732-3 · Cited by 41
Shen, Y., Zhao, M., Zhao, P., Meng, L., Zhang, Y., Zhang, G., Taishi, Y., & Sun, L. (2024) · Frontiers in Pharmacology · doi:10.3389/fphar.2024.1408462 · Cited by 45
Regulation of Mct1 by cAMP-dependent internalization in rat brain endothelial cells
Smith, J. P., Uhernik, A. L., Li, L., Liu, Z., & Drewes, L. R. (2012) · Brain Research · doi:10.1016/j.brainres.2012.08.026 · Cited by 40
Mitochondrial matrix pH as a decisive factor in neurometabolic imaging
Schaefer, P. M., Hilpert, D. C., Niederschweiberer, M. A., Neuhauser, L., Kalinina, S., Calzia, E., Rueck, A. C., von Einem, B., & Arnim, C. A. F. V. (2017) · Neurophotonics · doi:10.1117/1.nph.4.4.045004 · Cited by 40
Ishii, T., Warabi, E., & Mann, G. E. (2018) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2018.01.026 · Cited by 44
Cholesterol sulfate alters astrocyte metabolism and provides protection against oxidative stress
Prah, J., Winters, A., Chaudhari, K., Hersh, J., Liu, R., & Yang, S. (2019) · Brain Research · doi:10.1016/j.brainres.2019.146378 · Cited by 40
D’Antoni, S., Lidia de, B. A. R. I., Valenti, D., Borro, M., Bonaccorso, C. M., Simmaco, M., Vacca, R. A., & Catania, M. V. (2019) · Biological Chemistry · doi:10.1515/hsz-2019-0221 · Cited by 42
Shi, Y., Li, Y., Wang, Y., Xu, Z., Fu, H., & Zheng, G. (2020) · Frontiers in Pharmacology · doi:10.3389/fphar.2020.00285 · Cited by 40
Tassinari, I. D., Andrade, M. K. G., da Rosa, L. A., Hoff, M. L. M., Nunes, R. R., Vogt, É. L., Fabres, R. B., Sanches, E. F., Netto, C. A., Paz, A. H. D. R., et al. (2020) · Neuroscience · doi:10.1016/j.neuroscience.2020.09.006 · Cited by 43
Assessment of astrocytes as a mediator of memory and learning in rodents
Akther, S., & Hirase, H. (2021) · Glia · doi:10.1002/glia.24099 · Cited by 38
Glia-Driven Brain Circuit Refinement Is Altered by Early-Life Adversity: Behavioral Outcomes
Milbocker, K. A., Campbell, T. S., Collins, N. J., Kim, S., Smith, E. A., Roth, T. L., & Klintsova, A. Y. (2021) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2021.786234 · Cited by 46
Rupprecht, A., Sittner, D., Тихоновна, С. А., Hilse, K. E., Goyn, J., Moldzio, R., Seiler, A. E. M., Bräuer, A. U., & Pohl, E. E. (2014) · PLoS ONE · doi:10.1371/journal.pone.0088474 · Cited by 41
Akter, M., Ma, H., Hasan, M., Karim, A., Zhu, X., Zhang, L. N., & Li, Y. (2023) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2023.1117146 · Cited by 40
Wang, H., Liu, S., Sun, Y., Chen, C., Hu, Z., Li, Q., Long, J., Yan, Q., Liang, J., Lin, Y., et al. (2024) · Ageing Research Reviews · doi:10.1016/j.arr.2024.102472 · Cited by 39
Larrea, D., Tamucci, K. A., Kabra, K., VELASCO, K. R., Yun, T. D., Pera, M., Montesinos, J., Agrawal, R. R., Paradas, C., Smerdon, J. W., et al. (2025) · Nature Communications · doi:10.1038/s41467-024-51578-1 · Cited by 46
Wiśniewski, J. R., Gizak, A., & Rakus, D. (2015) · Journal of Proteome Research · doi:10.1021/acs.jproteome.5b00276 · Cited by 38
Zheng, H. X., Zheng, Y., Wang, D., Cai, A., Lin, Q., Zhao, L., Chen, M., Deng, M., Ye, X., & Gao, H. (2016) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1177/0271678x15626154 · Cited by 39
Resveratrol modulates GSH system in C6 astroglial cells through heme oxygenase 1 pathway
Arús, B. A., de Souza, D. G., Bellaver, B., Souza, D. O., Gonçalves, C., Quincozes‐Santos, A., & Bobermin, L. D. (2017) · Molecular and Cellular Biochemistry · doi:10.1007/s11010-016-2917-5 · Cited by 40
Metabolic pathways as possible therapeutic targets for progressive multiple sclerosis
LeVine, S., Heidker, R. M., & Emerson, M. R. (2017) · Neural Regeneration Research · doi:10.4103/1673-5374.213542 · Cited by 39
Conflicting Roles of Connexin43 in Tumor Invasion and Growth in the Central Nervous System
Uzu, M., Sin, W. C., Shimizu, A., & Sato, H. (2018) · International Journal of Molecular Sciences · doi:10.3390/ijms19041159 · Cited by 39
Molecular Bases of Alzheimer’s Disease and Neurodegeneration: The Role of Neuroglia
Luca, A., Calandra, C., & Luca, M. (2018) · Aging and Disease · doi:10.14336/ad.2018.0201 · Cited by 42
Li, C., Wei, Q., Gu, X., Chen, Y., Chen, X., Cao, B., Ou, R., & Shang, H. (2019) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2019.00114 · Cited by 39
Blood-brain barrier and innate immunity in the pathogenesis of Alzheimer's disease
Šimić, G., Španić, E., Horvat, L. L., & Hof, P. R. (2019) · Progress in molecular biology and translational science · doi:10.1016/bs.pmbts.2019.06.003 · Cited by 40
CYP1B1: A key regulator of redox homeostasis.
Falero-Perez, J., Song, Y., Sorenson, C. M., & Sheibani, N. (2018) · PubMed · Cited by 39
Wang, Y., Shang, Y., Mishra, A., Bacon, E., Yin, F., & Brinton, R. (2020) · Scientific Reports · doi:10.1038/s41598-020-65402-5 · Cited by 42
The Dichotomous Role of Inflammation in the CNS: A Mitochondrial Point of View
Vezzani, B., Carinci, M., Patergnani, S., Pasquin, M., Guarino, A., Aziz, N., Pinton, P., Simonato, M., & Giorgi, C. (2020) · Biomolecules · doi:10.3390/biom10101437 · Cited by 40
Glucocorticoids, metabolism and brain activity
Jaszczyk, A., & Juszczak, G. R. (2021) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2021.03.007 · Cited by 45
A high‐fat diet changes astrocytic metabolism to promote synaptic plasticity and behavior
Popov, A., Brazhe, N. A., Fedotova, A., Tiaglik, A. B., Bychkov, M. L., Morozova, K. I., Brazhe, A., Aronov, D. A., Lyukmanova, E. N., Lazareva, N. B., et al. (2022) · Acta Physiologica · doi:10.1111/apha.13847 · Cited by 39
Astrocytes of the early postnatal brain
Felix, L., Stephan, J., & Rose, C. R. (2020) · European Journal of Neuroscience · doi:10.1111/ejn.14780 · Cited by 40
Resident immune responses to spinal cord injury: role of astrocytes and microglia
Brockie, S. T., Zhou, C., & Fehlings, M. G. (2023) · Neural Regeneration Research · doi:10.4103/1673-5374.389630 · Cited by 41
Metabolic Dysfunction of Astrocyte: An Initiating Factor in Beta-amyloid Pathology?
Yan, L., Xiao, M., Chen, R., & Cai, Z. (2013) · PubMed · Cited by 39
Tramutola, A., Arena, A., Cini, C., Butterfield, D. A., & Barone, E. (2016) · Expert Review of Neurotherapeutics · doi:10.1080/14737175.2017.1246183 · Cited by 40
Higher physiological vulnerability to hypoxic exposure with advancing age in the human brain
Vestergaard, M. B., Jensen, M. L., Arngrim, N., Lindberg, U., & Larsson, H. B. W. (2018) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1177/0271678x18818291 · Cited by 38
Glia-derived extracellular vesicles in parkinson’s disease.
Marchetti, B., Leggio, L., L’Episcopo, F., Vivarelli, S., Tirolo, C., Paternò, G., Giachino, C., Caniglia, S., Serapide, M. F., & Iraci, N. (2020) · Journal of Clinical Medicine · doi:10.3390/jcm9061941 · Cited by 38
Drp1 is required for AgRP neuronal activity and feeding
Jin, S., Yoon, N. A., Liu, Z.-W., Song, J. E., Horvath, T. L., Kim, J. D., & Diano, S. (2021) · eLife · doi:10.7554/elife.64351 · Cited by 39
Mitochondria: new players in homeostatic regulation of firing rate set points
Ruggiero, A., Katsenelson, M., & Slutsky, I. (2021) · Trends in Neurosciences · doi:10.1016/j.tins.2021.03.002 · Cited by 37
Astrocyte Gliotransmission in the Regulation of Systemic Metabolism
Murat, C. D. B., & García‐Cáceres, C. (2021) · Metabolites · doi:10.3390/metabo11110732 · Cited by 38
Sweet Taste Receptor Signaling Network: Possible Implication for Cognitive Functioning
Welcome, M. O., Mastorakis, N. E., & Pereverzev, V. A. (2015) · Neurology Research International · doi:10.1155/2015/606479 · Cited by 39
Astrocytes and Microglia in Stress-Induced Neuroinflammation: The African Perspective
Olude, M. A., Mouihate, A., Mustapha, O. A., Farina, C., Quintana, F. J., & Olopade, J. O. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.795089 · Cited by 37
Sun, J., Osenberg, S., Irwin, A., Ma, L.-H., Lee, N., Xiang, Y., Li, F., Wan, Y.-W., Park, I.-H., Maletic-Savatic, M., et al. (2023) · Cell Reports · doi:10.1016/j.celrep.2022.111942 · Cited by 37
Borbor, M., Yin, D., Brockmeier, U., Wang, C., Doeckel, M., Pillath‐Eilers, M., Kaltwasser, B., Hermann, D. M., & Dzyubenko, E. (2023) · Glia · doi:10.1002/glia.24357 · Cited by 39
Martin, C. J. (2014) · Frontiers in Neuroscience · doi:10.3389/fnins.2014.00211 · Cited by 39
Mathieu, C., Dupret, J., & Rodrigues‐Lima, F. (2016) · FEBS Journal · doi:10.1111/febs.13937 · Cited by 37
Reprogramming energetic metabolism in Alzheimer's disease
Vallée, A., Lecarpentier, Y., Guillevin, R., & Vallée, J.-N. (2017) · Life Sciences · doi:10.1016/j.lfs.2017.10.033 · Cited by 38
Datta, S., & Chakrabarti, N. (2018) · Neurochemistry International · doi:10.1016/j.neuint.2018.04.007 · Cited by 37
Mai, N., Miller‐Rhodes, K., Knowlden, S. A., & Halterman, M. W. (2019) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1177/0271678x19835552 · Cited by 40
Nanomaterial-Based Approaches for Neural Regeneration
Teleanu, R. I., Gherasim, O., Gherasim, T. G., Grumezescu, V., Grumezescu, A. M., & Teleanu, D. M. (2019) · Pharmaceutics · doi:10.3390/pharmaceutics11060266 · Cited by 37
Chumarina, M., Russ, K., Azevedo, C., Heuer, A., Pihl, M., Collin, A., Frostner, E. Å., Elmér, E., Hyttel, P., Cappelletti, G., et al. (2019) · Acta Neuropathologica Communications · doi:10.1186/s40478-019-0863-7 · Cited by 38
Qi, G., Mi, Y., & Yin, F. (2020) · Frontiers in Physiology · doi:10.3389/fphys.2019.01531 · Cited by 38
Metadata
- Authors
- Bélanger, M., Allaman, I., & Magistretti, P. J.
- Affiliations
- École Polytechnique Fédérale de Lausanne (CH)
- Centre Hospitalier Universitaire Vaudois (CH)
- Corresponding author
- Magistretti, Pierre J.
- Venue
- Cell Metabolism
- Publisher
- Elsevier BV
- Published
- 2011-12
- Volume
- 14
- Issue
- 6
- Pages
- 724-738
- ISSN
- 1550-4131 (ISSN-L)
- OpenAlex
- W2016927879
- Cited by
- 2,313
- References
- 135
- Citations by year
- 2026: 169 · 2025: 194 · 2024: 206 · 2023: 207 · 2022: 197 · 2021: 218 · 2020: 203 · 2019: 175 · 2018: 159 · 2017: 152 · 2016: 137 · 2015: 111 · 2014: 76 · 2013: 73 · 2012: 31
- FWCI
- 5.48
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Cell Metabolism (publishedVersion)
- PubMed (publishedVersion)
- Infoscience (Ecole Polytechnique Fédérale de Lausanne) (submittedVersion)
- Infoscience (Ecole Polytechnique Fédérale de Lausanne) (submittedVersion, cc-by-nc-nd)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Biochemistry › Amino Acid Enzymes and Metabolism
- Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
- Keywords
- brain energy metabolism, astrocytes, neurons, neuroenergetics, glial cells, energy storage, neuronal activity
- MeSH terms
- Astrocytes, Brain, Energy Metabolism, Glycogen, Models, Biological, Neurons, Regional Blood Flow, Oxidative Stress, Lactic Acid
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review
