The DOI matches its Crossref record; 63 of the 65 references it cites were found in a registry or an index.
Astrocyte-Neuron Lactate Transport Is Required for Long-Term Memory Formation
Open accessAbstract
We report that, in the rat hippocampus, learning leads to a significant increase in extracellular lactate levels that derive from glycogen, an energy reserve selectively localized in astrocytes. Astrocytic glycogen breakdown and lactate release are essential for long-term but not short-term memory formation, and for the maintenance of long-term potentiation (LTP) of synaptic strength elicited in vivo. Disrupting the expression of the astrocytic lactate transporters monocarboxylate transporter 4 (MCT4) or MCT1 causes amnesia, which, like LTP impairment, is rescued by L-lactate but not equicaloric glucose. Disrupting the expression of the neuronal lactate transporter MCT2 also leads to amnesia that is unaffected by either L-lactate or glucose, suggesting that lactate import into neurons is necessary for long-term memory. Glycogenolysis and astrocytic lactate transporters are also critical for the induction of molecular changes required for memory formation, including the induction of phospho-CREB, Arc, and phospho-cofilin. We conclude that astrocyte-neuron lactate transport is required for long-term memory formation.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
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?
The source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“Increased levels of lactate have also been shown to be correlated with neuronal network activity, as the astrocyte-neuron lactate shuttle is known to regulate neuronal activity.31”
From ApoE4-dependent lysosomal cholesterol accumulation impairs mitochondrial homeostasis and oxidative phosphorylation in human astrocytes (2023) · cites this paper as [31]
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“Increased levels of lactate have also been shown to be correlated with neuronal network activity, as the astrocyte-neuron lactate shuttle is known to regulate neuronal activity.31”
From ApoE4-dependent lysosomal cholesterol accumulation impairs mitochondrial homeostasis and oxidative phosphorylation in human astrocytes (2023) · cites this paper as [31]
Experimental — accuracy not yet measuredThe cited source says what the claim attributes to it.
In the citing paper
“Conversely, metabolic state may, in turn, influence the properties of neuronal computation19, suggesting a bidirectional interaction between energy metabolism and information processing.”
From Energy paradox in REM sleep: balancing supply and consumption in brain metabolism (2026) · cites this paper as [19]
In the citing paper
“Another astrocyte-derived molecule, L-lactate, plays a key role in LTP at hippocampal CA1 synapses 37 .”
From Astrocyte function from information processing to cognition and cognitive impairment (2019) · cites this paper as [37]
In the citing paper
“A first study identified a necessary role for L-lactate in long-term episodic memory by pharmacological inhibition of its production in astrocytes 37 .”
From Astrocyte function from information processing to cognition and cognitive impairment (2019) · cites this paper as [37]
In the citing paper
“The fact that L-lactate cannot be substituted in this function by equicaloric glucose 37 hints, however, at additional non-metabolic functions for this molecule.”
From Astrocyte function from information processing to cognition and cognitive impairment (2019) · cites this paper as [37]
In the citing paper
“blocking neuronal oxidative utilization of lactate affects neuronal survival and even memory formation (Suzuki et al., 2011; Lee et al., 2012).”
From Metabolic reprogramming during neuronal differentiation from aerobic glycolysis to neuronal oxidative phosphorylation (2016) · cites this paper as Suzuki et al., 2011
In the citing paper
“If an ANLS operates at rest, it could also explain why chronic disruption of MCT, LDH, or glycogenolysis in astrocytes can affect neuronal function (Suzuki et al., 2011; Zhang et al., 2016; Mazuel et al., 2017); these and similar results showing that MCT and lactate transport contribute to neuronal health and function provide evidence for some critical biological role for lactate uptake, but do”
From Fueling thought: Management of glycolysis and oxidative phosphorylation in neuronal metabolism (2018) · cites this paper as Suzuki et al., 2011
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
The molecular biology of memory storage: a dialogue between genes and synapses
Kandel, E. R. (2001) · Science · doi:10.1126/science.1067020 · Cited by 3,917
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 1×
“…Fédérale de Lausanne (EPFL) and Center for Psychiatric Neuroscience, University of Lausanne-CHUV, Lausanne, Switzerland 6These authors contributed equally to this work *Correspondence: cristina.alberini@mssm.edu (C.M.A.), pierre.magistretti@epfl.ch (P.J.M.) DOI 10.1016/j.cell.2011.02.018”
InfluentialSelf-citationTranscriptional regulation by the phosphorylation-dependent factor CREB
Mayr, B., & Montminy, M. (2001) · Nature Reviews Molecular Cell Biology · doi:10.1038/35085068 · Cited by 2,587
Learning induces long-term potentiation in the hippocampus
Whitlock, J. R., Heynen, A. J., Shuler, M. G., & Bear, M. F. (2006) · Science · doi:10.1126/science.1128134 · Cited by 1,913
Tripartite synapses: astrocytes process and control synaptic information
Perea, G., Navarrete, M., & Araque, A. (2009) · Trends in Neurosciences · doi:10.1016/j.tins.2009.05.001 · Cited by 1,820
The Neurobiology of Consolidations, Or, How Stable is the Engram?
Dudai, Y. (2004) · Annual Review of Psychology · doi:10.1146/annurev.psych.55.090902.142050 · Cited by 1,671
Long-term potentiation depends on release of d-serine from astrocytes
Henneberger, C., Papouin, T., Oliet, S. H. R., & Rusakov, D. A. (2010) · Nature · doi:10.1038/nature08673 · Cited by 1,389
Magistretti, P. J., Pellerin, L., Rothman, D. L., & Shulman, R. G. (1999) · Science · doi:10.1126/science.283.5401.496 · Cited by 1,170
Self-citationMetabolic coupling between glia and neurons
Tsacopoulos, M., & Magistretti, P. (1996) · The Journal of Neuroscience · doi:10.1523/jneurosci.16-03-00877.1996 · Cited by 1,006
Self-citationTranscription Factors in Long-Term Memory and Synaptic Plasticity
Alberini, C. M. (2009) · Physiological Reviews · doi:10.1152/physrev.00017.2008 · Cited by 991
Self-citation
Flagged first, then by citations
2 of the 65 references couldn’t be matched to a known paper.
Cited by
Sorted by citations
Items 801–900 of 1,003
Astrocytic transporters in Alzheimer's disease
Ugbode, C., Hu, Y., Whalley, B., Peers, C., Rattray, M., & Dallas, M. L. (2017) · Biochemical Journal · doi:10.1042/bcj20160505 · Cited by 25
Jin, C., Gao, L., Li, Y., Wu, S., Lu, X., Yang, J., & Cai, Y. (2017) · Experimental Brain Research · doi:10.1007/s00221-017-5102-5 · Cited by 25
Stores, Channels, Glue, and Trees: Active Glial and Active Dendritic Physiology
Ashhad, S., & Narayanan, R. (2018) · Molecular Neurobiology · doi:10.1007/s12035-018-1223-5 · Cited by 25
Metabolic reprogramming and astrocytes polarization following ischemic stroke
Lu, W., & Wen, J. (2025) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2025.01.002 · Cited by 27
Mitochondrial Ca2+ efflux controls neuronal metabolism and long-term memory across species
Vishwanath, A. A., Comyn, T., Mira, R. G., Brossier, C., Pascual-Caro, C., Faour, M., Boumendil, K., Chintaluri, C., Ramon‐Duaso, C., Fan, R., et al. (2026) · Nature Metabolism · doi:10.1038/s42255-026-01451-w · Cited by 28
Small neutral molecular carriers for selective carboxylate transport
Haynes, C. J. E., Berry, S. N., Garric, J., Herniman, J., Hiscock, J. R., Kirby, I. L., Light, M. E., Perkes, G., & Gale, P. A. (2012) · Chemical Communications · doi:10.1039/c2cc37468d · Cited by 24
Hertz, L., Chen, Y., & Song, D. (2016) · Neurochemical Research · doi:10.1007/s11064-016-1828-x · Cited by 25
Origins of Brain Insulin and Its Function
Nakabeppu, Y. (2019) · Advances in experimental medicine and biology · doi:10.1007/978-981-13-3540-2_1 · Cited by 23
Aging is not equal across memory systems
Gardner, R. S., Newman, L. A., Mohler, E. G., Tunur, T., Gold, P. E., & Korol, D. L. (2020) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2020.107232 · Cited by 24
Xu, J., Zheng, Y., Lv, S., Kang, J., Yu, Y., Hou, K., Li, Y., & Chi, G. (2020) · Neuroscience · doi:10.1016/j.neuroscience.2020.06.041 · Cited by 24
Gavriel, Y., Rabinovich-Nikitin, I., Ezra, A., Barbiro, B., & Solomon, B. (2020) · Journal of Alzheimer s Disease · doi:10.3233/jad-200506 · Cited by 27
Alternative Targets to Fight Alzheimer’s Disease: Focus on Astrocytes
Valenza, M., Facchinetti, R., Menegoni, G., Steardo, L., & Scuderi, C. (2021) · Biomolecules · doi:10.3390/biom11040600 · Cited by 25
So, K., Li, A., Liang, Y., Zhang, L., Luo, X., Wu, L.-L., Chen, Z.-W., Wei, G.-H., Zhang, K., Du, Z.-A., et al. (2021) · Neural Regeneration Research · doi:10.4103/1673-5374.325012 · Cited by 27
Zhang, M., Wang, Y., Bai, Y., Dai, L., & Guo, H. (2022) · Frontiers in Neurology · doi:10.3389/fneur.2022.781063 · Cited by 26
Antipsychotics impair regulation of glucose metabolism by central glucose
Castellani, L. N., Pereira, S., Kowalchuk, C., Asgariroozbehani, R., Singh, R., Wu, S., Hamel, L., Alganem, K., Ryan, W. G., Zhang, X., et al. (2022) · Molecular Psychiatry · doi:10.1038/s41380-022-01798-y · Cited by 24
Wu, Y., Hu, H., Liu, W., Zhao, Y. F., Xie, F., Sun, Z., Zhang, L., Dong, H., Wang, X. B., & Qian, L. (2024) · Brain Sciences · doi:10.3390/brainsci14040327 · Cited by 24
Baud, M. O., Parafita, J., Nguyen, A., Magistretti, P. J., & Petit, J. (2016) · Journal of Sleep Research · doi:10.1111/jsr.12419 · Cited by 24
Self-citationImaging brain aerobic glycolysis as a marker of synaptic plasticity
Magistretti, P. J. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1607423113 · Cited by 23
Self-citationMathieu, 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 24
Heterogeneity and function of hippocampal macroglia
Seifert, G., & Steinhäuser, C. (2017) · Cell and Tissue Research · doi:10.1007/s00441-017-2746-1 · Cited by 25
Taufique, S. K. T., Prabhat, A., & Kumar, V. (2018) · Journal of Experimental Zoology Part A Ecological and Integrative Physiology · doi:10.1002/jez.2238 · Cited by 26
Glucose metabolism impairment in major depressive disorder
Meng, F., Wang, J., Wang, L., & Zou, W. (2025) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2025.111191 · Cited by 26
Han, H., Wu, Y., Mi, R., Zhang, C., Guan, F., Lu, X., Zhang, G., Meng, Z., Chen, L., & Zhang, M. (2025) · BMC Medicine · doi:10.1186/s12916-025-04168-x · Cited by 27
Implications of Gliotransmission for the Pharmacotherapy of CNS Disorders
Rossi, D., Martorana, F., & Brambilla, L. (2011) · CNS Drugs · doi:10.2165/11593090-000000000-00000 · Cited by 24
Luo, F., Zhang, J., Burke, K., Romito‐DiGiacomo, R. R., Miller, R. H., & Yang, Y. (2018) · Experimental Neurology · doi:10.1016/j.expneurol.2018.05.001 · Cited by 23
Analysis of Metabolic Alterations Related to Pathogenic Process of Diabetic Encephalopathy Rats
Dong, M., Ren, M., Li, C., Zhang, X., Yang, C., Zhao, L., & Gao, H. (2019) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2018.00527 · Cited by 23
The Mechanism of Downregulated Interstitial Fluid Drainage Following Neuronal Excitation
Li, Y., Han, H., Shi, K., Cui, D., Yang, J., Alberts, I., Yuan, L., Zhao, G., Wang, R., Cai, X., et al. (2020) · Aging and Disease · doi:10.14336/ad.2020.0224 · Cited by 23
Yu, X., Zhang, R., Wei, C., Gao, Y., Yu, Y., Wang, L., Jiang, J., Zhang, X., Li, J., & Chen, X. (2021) · Animal Cells and Systems · doi:10.1080/19768354.2021.1915379 · Cited by 23
Stephan, J. S., & Sleiman, S. F. (2021) · Frontiers in Neurology · doi:10.3389/fneur.2021.600365 · Cited by 25
Wdfy3 regulates glycophagy, mitophagy, and synaptic plasticity
Napoli, E., Panoutsopoulos, A. A., Kysar, P. E., Satriya, N., Sterling, K., Shibata, B., Imai, D. M., Ruskin, D. N., Zarbalis, K. S., & Giulivi, C. (2021) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1177/0271678x211027384 · Cited by 24
Amyloid-β42 stimulated hippocampal lactate release is coupled to glutamate uptake
Hascup, E., Sime, L. N., Peck, M. R., & Hascup, K. (2021) · Scientific Reports · doi:10.1038/s41598-022-06637-2 · Cited by 20
Differential role of neuronal glucose and PFKFB3 in memory formation during development
Cruz, E., Bessières, B., Magistretti, P. J., & Alberini, C. M. (2022) · Glia · doi:10.1002/glia.24248 · Cited by 24
Self-citationExercise‐induced modulation of neuroinflammation in ageing
Barad, Z., Augusto, J., & Kelly, Á. M. (2022) · The Journal of Physiology · doi:10.1113/jp282894 · Cited by 27
Mitochondrial Ca2+ handling as a cell signaling hub: lessons from astrocyte function
Cabral‐Costa, J. V., & Kowaltowski, A. J. (2023) · Essays in Biochemistry · doi:10.1042/ebc20220094 · Cited by 25
Vints, W. A. J., Gökçe, E., Langeard, A., Павлова, Ю., Çevik, Ö. S., Ziaaldini, M. M., Todri, J., Lena, O., Sakkas, G. K., Jak, S., et al. (2023) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2023.1213057 · Cited by 29
Han, S., Jiang, B., Ren, J., Gao, F., Wen, J., Zhou, T., Wang, L., & Wei, X. (2023) · Anesthesiology · doi:10.1097/aln.0000000000004756 · Cited by 23
Monocarboxylate transporter and lactate metabolism
Kitaoka, Y., Hoshino, D., & Hatta, H. (2012) · The Journal of Physical Fitness and Sports Medicine · doi:10.7600/jpfsm.1.247 · Cited by 23
Lavoie, S., Allaman, I., Petit, J.-M., Kim, Q., & Magistretti, P. J. (2011) · PLoS ONE · doi:10.1371/journal.pone.0022875 · Cited by 23
Self-citationThe Role of Circulating Amino Acids in the Hypothalamic Regulation of Liver Glucose Metabolism
Arrieta‐Cruz, I., & Juárez, R. G. (2016) · Advances in Nutrition · doi:10.3945/an.115.011171 · Cited by 25
Agus, M., Boges, D. J., Gagnon, N., Magistretti, P. J., Hadwiger, M., & Calì, C. (2018) · Computers & Graphics · doi:10.1016/j.cag.2018.04.007 · Cited by 25
Self-citationDeciphering the star codings: astrocyte manipulation alters mouse behavior
Park, K., & Lee, S. J. (2020) · Experimental & Molecular Medicine · doi:10.1038/s12276-020-0468-z · Cited by 26
Tripathi, S. J., Chakraborty, S., Srikumar, B. N., Raju, T. R., & Rao, B. S. S. (2018) · Molecular Neurobiology · doi:10.1007/s12035-018-1057-1 · Cited by 24
Editorial: All 3 Types of Glial Cells Are Important for Memory Formation
Hertz, L., & Chen, Y. (2016) · Frontiers in Integrative Neuroscience · doi:10.3389/fnint.2016.00031 · Cited by 23
Cuautle, D. G., Donna, S., Cieri, M. B., Villarreal, A., & Ramos, A. J. (2024) · Journal of Neurochemistry · doi:10.1111/jnc.16164 · Cited by 23
PRDM16-DT is a novel lncRNA that regulates astrocyte function in Alzheimer’s disease
Schröder, S., Fuchs, U., Gisa, V., Peña, T., Krüger, D. M., Hempel, N., Burkhardt, S., Salinas, G., Schütz, A., Delalle, I., et al. (2024) · Acta Neuropathologica · doi:10.1007/s00401-024-02787-x · Cited by 27
Metabolomics in Parkinson’s Disease and Correlation with Disease State
Ostrakhovitch, E. A., Ono, K., & Yamasaki, T. R. (2025) · Metabolites · doi:10.3390/metabo15030208 · Cited by 24
Putative Receptors Underpinning l-Lactate Signalling in Locus Coeruleus
Mosienko, V., Rasooli-Nejad, S. M. A., Kishi, K., Both, M. D. D., Jane, D. E., Huentelman, M. J., Kasparov, S., & Teschemacher, A. G. (2018) · Neuroglia · doi:10.3390/neuroglia1020025 · Cited by 24
Astroglial FMRP modulates synaptic signaling and behavior phenotypes in FXS mouse model
Jin, S., Higashimori, H., Schin, C., Orrego, A. T., Men, Y., Chiang, M. S. R., Jarvis, R., Cox, D., Feig, L. A., & Yang, Y. (2020) · Glia · doi:10.1002/glia.23915 · Cited by 22
MCT4 Promotes Tumor Malignancy in F98 Glioma Cells
Reuss, A. M., Groos, D., Ghoochani, A., Buchfelder, M., & Savaskan, N. E. (2021) · Journal of Oncology · doi:10.1155/2021/6655529 · Cited by 22
Buscemi, L., Blochet, C., Magistretti, P. J., & Hirt, L. (2021) · Frontiers in Physiology · doi:10.3389/fphys.2021.689239 · Cited by 24
Self-citationGlial Cells Response in Stroke
Jadhav, P., Karande, M., Sarkar, A., Sahu, S., Sarmah, D., Datta, A., Chaudhary, A., Kalia, K., Sharma, A., Wang, X., et al. (2022) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-021-01183-3 · Cited by 25
Frame, A. K., Robinson, J. W., Mahmoudzadeh, N. H., Tennessen, J. M., Simon, A. F., & Cumming, R. C. (2023) · Aging · doi:10.18632/aging.204565 · Cited by 22
Glial modulation of the parallel memory formation
Kanaya, T., Ito, R., Morizawa, Y. M., Sasaki, D., Yamao, H., Ishikane, H., Hiraoka, Y., Tanaka, K., & Matsui, K. (2023) · Glia · doi:10.1002/glia.24431 · Cited by 22
Kelsall, I. R., Voß, M., Munro, S., Cuthbertson, D. J., & Cohen, P. T. W. (2011) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2011.07345.x · Cited by 23
Gibbs, M. E., & Hertz, L. (2014) · Frontiers in Pharmacology · doi:10.3389/fphar.2014.00054 · Cited by 22
Dynamics of Hippocampal Protein Expression During Long-term Spatial Memory Formation
Borovok, N., Nesher, E., Levin, Y., Reichenstein, M., Pinhasov, A., & Michaelevski, I. (2015) · Molecular & Cellular Proteomics · doi:10.1074/mcp.m115.051318 · Cited by 22
In vivo and in vitro effects of vortioxetine on molecules associated with neuroplasticity
Kugathasan, P., Waller, J. A., Westrich, L., Abdourahman, A., Tamm, J. A., Pehrson, A. L., Dale, E., Gulinello, M. E., Sánchez, C., & Li, Y. (2016) · Journal of Psychopharmacology · doi:10.1177/0269881116667710 · Cited by 22
Bai, Q., Song, D., Gu, L., Verkhratsky, A., & Peng, L. (2017) · Psychopharmacology · doi:10.1007/s00213-017-4547-3 · Cited by 22
McGuire, J. L., DePasquale, E. A. K., Watanabe, M., Anwar, F. N., Ngwenya, L. B., Atluri, G., Romick‐Rosendale, L. E., McCullumsmith, R. E., & Evanson, N. K. (2018) · Molecular Neurobiology · doi:10.1007/s12035-018-1276-5 · Cited by 22
Antiamnesic effects of tofisopam against scopolamine-induced cognitive impairments in rats
Üçel, U. İ., Can, Ö. D., Özkay, Ü. D., & Ulupınar, E. (2020) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2020.172858 · Cited by 22
Jesmin, S., Shima, T., Soya, M., Takahashi, K., Koki, O., Ogura, K., Koizumi, H., & Soya, H. (2021) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00326.2021 · Cited by 22
Dienel, G. A., Rothman, D. L., & Mangia, S. (2025) · Journal of Neurochemistry · doi:10.1111/jnc.70111 · Cited by 21
Ding, R., Tan, Y., Du, A., Wen, G., Ren, X., Yao, H., Ren, W., Liu, H., Wang, X., Yu, H. Q., et al. (2020) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2020.00060 · Cited by 21
Lack of Astrocytic Glycogen Alters Synaptic Plasticity but Not Seizure Susceptibility
Durán, J., Brewer, M. K., Hervera, A., Gruart, A., del Rı́o, J. A., Delgado-Garcia, J. M., & Guinovart, J. J. (2020) · Molecular Neurobiology · doi:10.1007/s12035-020-02055-5 · Cited by 21
Song, Y., Liu, Z., Zhu, X., Hao, C., Hao, W., Wu, S., Yang, J., Lu, X., & Jin, C. (2022) · Biochemical Pharmacology · doi:10.1016/j.bcp.2022.115140 · Cited by 21
The Memory Orchestra: Contribution of Astrocytes
Chen, Y., Jin, S., Yang, J., & Gao, T. (2023) · Neuroscience Bulletin · doi:10.1007/s12264-023-01024-x · Cited by 24
Lactate: a prospective target for therapeutic intervention in psychiatric disease
Cai, Y., Guo, H., Han, T., & Wang, H. (2023) · Neural Regeneration Research · doi:10.4103/1673-5374.387969 · Cited by 23
Olfactory bulb astrocytes link social transmission of stress to cognitive adaptation in male mice
Gómez-Sotres, P., Skupio, U., Tor, T. D., Julio‐Kalajzić, F., Cannich, A., Gisquet, D., Río, I. B., Drago, F., Puente, N., Grandes, P., et al. (2024) · Nature Communications · doi:10.1038/s41467-024-51416-4 · Cited by 21
Newman, L. A., Scavuzzo, C. J., Gold, P. E., & Korol, D. L. (2016) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2016.12.001 · Cited by 21
Rao, R., Nashawaty, M., Fatima, S., Ennis, K., & Tkáč, I. (2018) · NMR in Biomedicine · doi:10.1002/nbm.3910 · Cited by 21
Wang, Y., Peng, Y., Zhang, C., & Zhou, X. (2021) · Neuroscience Letters · doi:10.1016/j.neulet.2021.136205 · Cited by 26
FGF-2 induces neuronal death through upregulation of system xc-.
Liu, X., Albano, R., & Lobner, D. (2014) · Brain Research · doi:10.1016/j.brainres.2013.12.018 · Cited by 22
Ceylan, H. İ., Silva, A. F., Ramírez‐Campillo, R., & Murawska‐Ciałowicz, E. (2024) · Biology · doi:10.3390/biology13050323 · Cited by 28
Metabolic reprogramming of astrocytes: Emerging roles of lactate
Liu, Z., Guo, Y., Zhang, Y., Gao, Y., & Ning, B. (2024) · Neural Regeneration Research · doi:10.4103/nrr.nrr-d-24-00776 · Cited by 22
Angamo, E. A., Haq, R. U., Rösner, J., Gabriel, S., Gerevich, Z., Heinemann, U., & Kovács, R. (2017) · International Journal of Molecular Sciences · doi:10.3390/ijms18091835 · Cited by 20
Regional Distribution of Glycogen in the Mouse Brain Visualized by Immunohistochemistry
Oe, Y., Akther, S., & Hirase, H. (2019) · Advances in neurobiology · doi:10.1007/978-3-030-27480-1_5 · Cited by 21
Astrocytic Calcium Dynamics Along the Pain Pathway
Cho, J., & Huh, Y. (2020) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2020.594216 · Cited by 22
Adult Hippocampal Neurogenesis: One Lactate to Rule Them All
Nicola, R., & Okun, E. (2021) · NeuroMolecular Medicine · doi:10.1007/s12017-021-08658-y · Cited by 21
Pan, S., Pan, Y., Tang, Y., Zuo, N., Zhang, Y., Jia, K., & Kong, L. (2021) · Journal of Neurochemistry · doi:10.1111/jnc.15489 · Cited by 21
Moretti, R. L., Dias, E. N., Kiel, S. G., Augusto, M. C. M., Rodrigues, P., Sampaio, A. C., de Medeiros, L. I. P., Martins, M. D. F. M., Suffredini, I. B., Cardoso, C. V., et al. (2021) · Research in Veterinary Science · doi:10.1016/j.rvsc.2021.09.009 · Cited by 23
Magistretti, P. J., & Allaman, I. (2022) · Springer eBooks · doi:10.1007/978-3-030-88832-9_56 · Cited by 20
Self-citationTian, Q., Li, J., Wu, B., Wang, J., Xiao, Q., Tian, N., Yi, L., Luo, M., Li, Z., Pang, Y., et al. (2023) · The FASEB Journal · doi:10.1096/fj.202301173rrr · Cited by 20
Forgetfulness during aging: An integrated biology
Gold, P. E., & Korol, D. L. (2014) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2014.03.005 · Cited by 20
Synaptic Plasticity and the Warburg Effect
Magistretti, P. J. (2014) · Cell Metabolism · doi:10.1016/j.cmet.2013.12.012 · Cited by 20
Self-citationSanguinetti, E., Liistro, T., Mainardi, M., Pardini, S., Salvadori, P. A., Vannucci, A., Burchielli, S., & Iozzo, P. (2016) · Diabetologia · doi:10.1007/s00125-015-3848-5 · Cited by 22
Pharmacological Tools to Study the Role of Astrocytes in Neural Network Functions
Peña‐Ortega, F., Rivera‐Angulo, A., & Lorea-Hernández, J. J. (2016) · Advances in experimental medicine and biology · doi:10.1007/978-3-319-40764-7_3 · Cited by 23
Fibre sub‐type specific conduction reveals metabolic function in mouse sciatic nerve
Rich, L. R., & Brown, A. M. (2018) · The Journal of Physiology · doi:10.1113/jp275680 · Cited by 25
Glial Cells in the Genesis and Regulation of Circadian Rhythms
Chi-Castañeda, D., & Ortega, A. (2018) · Frontiers in Physiology · doi:10.3389/fphys.2018.00088 · Cited by 21
Lindberg, D. M., Ho, A. M., Peyton, L., & Choi, D. (2019) · Alcoholism Clinical and Experimental Research · doi:10.1111/acer.14137 · Cited by 20
The Structure and the Regulation of Glycogen Phosphorylases in Brain
Mathieu, C., Dupret, J., & Rodrigues‐Lima, F. (2019) · Advances in neurobiology · doi:10.1007/978-3-030-27480-1_4 · Cited by 20
Structure and Regulation of Glycogen Synthase in the Brain
Pederson, B. A. (2019) · Advances in neurobiology · doi:10.1007/978-3-030-27480-1_3 · Cited by 22
Duda, P., Wójtowicz, T., Janczara, J., Krowarsch, D., Czyrek, A. A., Gizak, A., & Rakus, D. (2020) · Cells · doi:10.3390/cells9061375 · Cited by 20
Matsui, T., Soya, S., Kawanaka, K., & Soya, H. (2015) · Neurochemical Research · doi:10.1007/s11064-015-1594-1 · Cited by 20
An acute microglial metabolic response controls metabolism and improves memoryPreprint
Drougard, A., Ma, E. H., Wegert, V., Sheldon, R. D., Panzeri, I., Vatsa, N., Apostle, S., Fagnocchi, L., Schaf, J., Gossens, K., et al. (2023) · eLife · doi:10.7554/elife.87120 · Cited by 19
Disrupting astrocyte-neuron lactate transport prevents cocaine seeking after prolonged withdrawal
Chen, W., Zhang, Y., Liang, J., Zhang, Z., Zhang, L., Huang, E., Zhang, G., Lü, L., Han, Y., & Shi, J. (2023) · Science Advances · doi:10.1126/sciadv.adi4462 · Cited by 19
Nohesara, S., Abdolmaleky, H. M., & Thiagalingam, S. (2024) · Biomedicines · doi:10.3390/biomedicines12020457 · Cited by 19
Pan, X., Zhang, Y., Gan, Y., Zhang, J., Gao, S., Feng, X., Xie, J., Wang, Y., Zhang, X., Wang, P., et al. (2025) · CNS Neuroscience & Therapeutics · doi:10.1111/cns.70231 · Cited by 19
L-Lactate Administration Improved Synaptic Plasticity and Cognition in Early 3xTg-AD Mice
Wang, Y., Zhao, J., & Zhao, L. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26041486 · Cited by 19
Physical Activity and Individual Cognitive Function Parameters: Unique Exercise-Induced Mechanisms
Frith, E., & Loprinzi, P. D. (2018) · Journal of Cognitive-Behavioral Psychotherapy and Research · doi:10.5455/jcbpr.284071 · Cited by 19
Rethinking intellectual disability from neuro- to astro-pathology.
Fernández-Blanco, Á., & Dierssen, M. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21239039 · Cited by 19
Metadata
- Authors
- Suzuki, A., Stern, S. A., Bozdagi, O., Huntley, G. W., Walker, R. H., Magistretti, P. J., & Alberini, C. M.
- Affiliations
- Icahn School of Medicine at Mount Sinai (US)
- James J. Peters VA Medical Center (US)
- Centre Hospitalier Universitaire Vaudois (CH)
- Corresponding author
- Magistretti, Pierre J.
- Alberini, Cristina M.
- ORCID
- Venue
- Cell
- Publisher
- Elsevier BV
- Published
- 2011-03
- Volume
- 144
- Issue
- 5
- Pages
- 810-823
- ISSN
- 0092-8674 (ISSN-L)
- PMC
- PMC3073831
- OpenAlex
- W2001725826
- Cited by
- 1,711
- References
- 65
- Citations by year
- 2026: 157 · 2025: 138 · 2024: 142 · 2023: 145 · 2022: 118 · 2021: 123 · 2020: 119 · 2019: 109 · 2018: 111 · 2017: 88 · 2016: 95 · 2015: 100 · 2014: 78 · 2013: 70 · 2012: 76
- FWCI
- 42.73
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- www.elsevier.com/tdm/userlicense/1.0/ (tdm)
- www.elsevier.com/legal/tdmrep-license (tdm)
- www.elsevier.com/open-access/userlicense/1.0/ (vor, 905 d)
- doi.org/10.15223/policy-017 (stm-asf)
- doi.org/10.15223/policy-037 (stm-asf)
- doi.org/10.15223/policy-012 (stm-asf)
- doi.org/10.15223/policy-029 (stm-asf)
- doi.org/10.15223/policy-004 (stm-asf)
- Locations
- Cell (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- IRIS (submittedVersion)
- Infoscience (Ecole Polytechnique Fédérale de Lausanne) (submittedVersion)
- Infoscience (Ecole Polytechnique Fédérale de Lausanne) (submittedVersion, cc-by-nc-nd)
- SERVAL (Université de Lausanne) (submittedVersion, other-oa)
- Funders
- U.S. Department of Veterans Affairs
- École Polytechnique Fédérale de Lausanne
- National Institutes of Health
- National Institute of Mental Health (R01MH074736, R01MH065635, T32MH087004)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Keywords
- long-term memory, hippocampus, extracellular lactate, MCT4, MCT1, MCT2, long-term potentiation, amnesia, L-lactate, synaptic plasticity, CREB, Arc, cofilin, learning
- MeSH terms
- Monocarboxylate Transport Protein 1, Animals, Arabinose, Astrocytes, Glycogen, Hippocampus, Muscle Proteins, Neurons, Sugar Alcohols, Lactic Acid, Monocarboxylic Acid Transporters, Symporters, Imino Furanoses, Rats, Memory, Long-Term
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