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NMDA receptors and memory encoding
Abstract
It is humbling to think that 30 years have passed since the paper by Collingridge, Kehl and McLennan showing that one of Jeff Watkins most interesting compounds, R-2-amino-5-phosphonopentanoate (d-AP5), blocked the induction of long-term potentiation in vitro at synapses from area CA3 of the hippocampus to CA1 without apparent effect on baseline synaptic transmission (Collingridge et al., 1983). This dissociation was one of the key triggers for an explosion of interest in glutamate receptors, and much has been discovered since that collectively contributes to our contemporary understanding of glutamatergic synapses - their biophysics and subunit composition, of the agonists and antagonists acting on them, and their diverse functions in different networks of the brain and spinal cord. It can be fairly said that Collingridge et al.'s (1983) observation was the stimulus that has led, on the one hand, to structural biological work at the atomic scale describing the key features of NMDA receptors that enables their coincidence function to happen; and, on the other, to work with whole animals investigating the contributions that calcium signalling via this receptor can have on rhythmical activities controlled by spinal circuits, memory encoding in the hippocampus (the topic of this article), visual cortical plasticity, sensitization in pain, and other functions. In this article, I lay out how my then interest in long-term potentiation (LTP) as a model of memory enabled me to recognise the importance of Collingridge et al.'s discovery - and how I and my colleagues endeavoured to take things forward in the area of learning and memory. This is in some respects a personal story, and I tell it as such. The idea that NMDA receptor activation is essential for memory encoding, though not for storage, took time to develop and to be accepted. Along the way, there have been confusions, challenges, and surprises surrounding the idea that activation of NMDA receptors can trigger memory. Some of these are described and how they have been addressed and resolved. Last, I touch on some new directions of interest with respect to the functional role of the NMDA receptor in cognition. This article is part of the Special Issue entitled 'Glutamate Receptor-Dependent Synaptic Plasticity'.
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“Enhanced glutamatergic NMDA-mediated transmission may improve memory consolidation (136) but in excess may be neurotoxic (137).”
From A brain-centric model of suicidal behavior (2020) · cites this paper as [136]
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Cites
Neural networks and physical systems with emergent collective computational abilities.
Hopfield, J. J. (1982) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.79.8.2554 · Cited by 19,270
Place navigation impaired in rats with hippocampal lesions
Morris, R. G. M., Garrud, P., Rawlins, J. N. P., & O'Keefe, J. (1982) · Nature · doi:10.1038/297681a0 · Cited by 6,340
Self-citation“Neural” computation of decisions in optimization problems
Hopfield, J. J., & Tank, D. W. (1985) · Biological Cybernetics · doi:10.1007/bf00339943 · Cited by 6,037
Magnesium gates glutamate-activated channels in mouse central neurones
Nowak, L. M., Bregestovski, P. D., Ascher, P., Herbet, A., & Prochiantz, A. (1984) · Nature · doi:10.1038/307462a0 · Cited by 4,116
Morris, R. G. M., Anderson, E., Lynch, G. S., & Baudry, M. (1986) · Nature · doi:10.1038/319774a0 · Cited by 3,640
Self-citationVoltage-dependent block by Mg2+ of NMDA responses in spinal cord neurones
Mayer, M. L., Westbrook, G. L., & Guthrie, P. B. (1984) · Nature · doi:10.1038/309261a0 · Cited by 2,941
Simple memory: a theory for archicortex
Marr, D. (1971) · Philosophical Transactions of the Royal Society of London. B, Biological Sciences · doi:10.1098/rstb.1971.0078 · Cited by 2,771
Collingridge, G. L., Kehl, S. J., & McLennan, H. (1983) · The Journal of Physiology · doi:10.1113/jphysiol.1983.sp014478 · Cited by 2,413
Amit, D. J. (1989) · Cambridge University Press eBooks · doi:10.1017/cbo9780511623257 · Cited by 2,261
Schizophrenia genes, gene expression, and neuropathology: on the matter of their convergence
Harrison, P. J., & Weinberger, D. R. (2005) · Molecular Psychiatry · doi:10.1038/sj.mp.4001558 · Cited by 2,020
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Brier, M. R., Day, G. S., Snyder, A. Z., Tanenbaum, A., & Ances, B. M. (2016) · Journal of Neurology · doi:10.1007/s00415-016-8083-6 · Cited by 28
Malikowska‐Racia, N., Podkowa, A., & Sałat, K. (2018) · Neurotoxicity Research · doi:10.1007/s12640-018-9901-7 · Cited by 29
Remembering Mechanosensitivity of NMDA Receptors
Johnson, L. R., Battle, A. R., & Martinac, B. (2019) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2019.00533 · Cited by 27
García, F., Lobos, P., Ponce, A., Cataldo, K., Meza, D., Farías, P., Estay, C., Oyarzun-Ampuero, F. A., Herrera‐Molina, R., Paula-Lima, A. C., et al. (2020) · Marine Drugs · doi:10.3390/md18060335 · Cited by 27
An ancient conserved role for prion protein in learning and memory
Leighton, P. L. A., Nadolski, N. J., Morrill, A., Hamilton, T. J., & Allison, W. T. (2018) · Biology Open · doi:10.1242/bio.025734 · Cited by 27
Li, J., Guo, M., Liu, Y., Wu, G., Miao, L., Zhang, J., Zuo, Z., & Li, Y. (2019) · Toxicological Sciences · doi:10.1093/toxsci/kfz135 · Cited by 27
Tokairin, Y., Konno, H., Noireau, A., West, C., Moriwaki, H., Soloshonok, V. A., Nicolas, C., & Gillaizeau, I. (2021) · Organic Chemistry Frontiers · doi:10.1039/d1qo00159k · Cited by 26
Kouvaros, S., & Papatheodoropoulos, C. (2017) · Neuroscience · doi:10.1016/j.neuroscience.2017.03.050 · Cited by 27
Ballesteros, J. J., Buschler, A., Köhr, G., & Manahan‐Vaughan, D. (2016) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2016.00033 · Cited by 25
Kazemi, M., Sahraei, H., Aliyari, H., Tekieh, E., Saberi, M., Tavacoli, H., Meftahi, G. H., Ghanaati, H., Salehi, M., & Hajnasrollah, M. (2018) · Basic and Clinical Neuroscience Journal · doi:10.29252/nirp.bcn.9.3.167 · Cited by 25
Long-term plasticity in identified hippocampal GABAergic interneurons in the CA1 area in vivo
Lau, P., Katona, L., Sághy, P., Newton, K., Somogyi, P., & Lamsa, K. P. (2016) · Brain Structure and Function · doi:10.1007/s00429-016-1309-7 · Cited by 26
Roles and Transcriptional Responses of Inhibitory Neurons in Learning and Memory
Giorgi, C., & Marinelli, S. (2021) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2021.689952 · Cited by 24
Kim, W., & Kwak, I. (2022) · Fish & Shellfish Immunology · doi:10.1016/j.fsi.2022.02.014 · Cited by 25
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Cappelletti, P., Piubelli, L., Murtas, G., Caldinelli, L., Valentino, M., Molla, G., Pollegioni, L., & Sacchi, S. (2015) · Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics · doi:10.1016/j.bbapap.2015.02.005 · Cited by 24
Lunardi, P. S., Sachser, R. M., Sierra, R. O., Pedraza, L. K., Medina, C., de la Fuente, V., Romano, A. G., Quillfeldt, J. A., & Alvares, L. D. O. (2017) · Molecular Neurobiology · doi:10.1007/s12035-016-0361-x · Cited by 28
Harvey, P. D., Bowie, C. R., McDonald, S., & Podhorná, J. (2020) · Clinical Drug Investigation · doi:10.1007/s40261-020-00893-8 · Cited by 24
Rivi, V., Benatti, C., Actis, P., Tascedda, F., & Blom, J. M. C. (2022) · Neuroendocrinology · doi:10.1159/000527489 · Cited by 23
NMDA or 5-HT receptor antagonists impair memory reconsolidation and induce various types of amnesia
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Kalweit, A. N., Amanpour-Gharaei, B., Colitti-Klausnitzer, J., & Manahan‐Vaughan, D. (2017) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2017.00036 · Cited by 22
Houck, D. R., Sindelar, L., Sanabria, C. R., Stanworth, S. H., Krueger, M., Suh, M., & Madsen, T. M. (2018) · Clinical and Translational Science · doi:10.1111/cts.12584 · Cited by 22
Gao, J., Zhou, N., Wu, Y., Lu, M., Wang, Q., Xia, C., Zhou, M., & Xu, Y. (2021) · Journal of Translational Medicine · doi:10.1186/s12967-021-03032-9 · Cited by 21
Ketamine enhances novel object recognition memory reconsolidation via the BDNF/TrkB pathway in mice
Fan, J., Tang, Z.-H., Wang, S., Lei, S., Zhang, B., & Tian, S. (2021) · Physiology & Behavior · doi:10.1016/j.physbeh.2021.113626 · Cited by 22
Molecular mechanisms of forgetting
Moreno, A. (2020) · European Journal of Neuroscience · doi:10.1111/ejn.14839 · Cited by 20
Radiske, A., González, M. C., Nôga, D. A., Rossato, J. I., Bevilaqua, L. R., & Cammarota, M. (2021) · Scientific Reports · doi:10.1038/s41598-020-80674-7 · Cited by 22
Perineuronal Net Receptor PTPσ Regulates Retention of Memories
Lesnikova, A., Casarotto, P., Moliner, R., Fred, S. M., Biojone, C., & Castrén, E. (2021) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2021.672475 · Cited by 21
Duque, D., Ayala, Y. A., & Malmierca, M. S. (2015) · Cell and Tissue Research · doi:10.1007/s00441-015-2134-7 · Cited by 22
Acute and chronic excitotoxicity in ischemic stroke and late-onset Alzheimer’s disease
Yu, S. P., Choi, E., Jiang, M. Q., & Wei, L. (2024) · Neural Regeneration Research · doi:10.4103/nrr.nrr-d-24-00398 · Cited by 21
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Escamilla, S., Sáez‐Valero, J., & Cuchillo‐Ibáñez, I. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms251810220 · Cited by 22
Gadd45α modulates aversive learning through post‐transcriptional regulation of memory‐related mRNAs
Rey, A. A., Karaulanov, E., Sharopov, S., Arab, K., Schäfer, A., Gierl, M. S., Guggenhuber, S., Brandes, C., Pennella, L., Gruhn, W. H., et al. (2019) · EMBO Reports · doi:10.15252/embr.201846022 · Cited by 20
Kapolowicz, M. R., & Thompson, L. T. (2016) · Hearing Research · doi:10.1016/j.heares.2016.09.010 · Cited by 20
Thacker, J. S., Xu, Y., Tang, C., Tupling, A. R., Staines, R. W., & Mielke, J. G. (2019) · Neuroscience · doi:10.1016/j.neuroscience.2019.05.051 · Cited by 21
Skřenková, K., Song, J., Kortus, Š., Kolcheva, M., Netolický, J., Hemelíková, K., Kaniaková, M., Krausová, B. H., Kucera, T., Korábečný, J., et al. (2020) · Scientific Reports · doi:10.1038/s41598-020-75646-w · Cited by 20
Bartsch, J., von Cramon, M., Gruber, D., Heinemann, U., & Behr, J. (2021) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2021.658465 · Cited by 21
Mammillary body regulates state-dependent fear by alternating cortical oscillations
Jiang, J., Wang, G., Luo, W., Xie, H. B., & Guan, J. (2018) · Scientific Reports · doi:10.1038/s41598-018-31622-z · Cited by 20
Müller-Thomsen, L., Borgmann, D., Morcinek, K., Schröder, S. L., Dengler, B., Moser, N., Neumaier, F., Schneider, T., Schröder, H., & Huggenberger, S. (2020) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2020.03.007 · Cited by 19
Chen, G., Li, T., Xiao, J., Wang, J., Shang, Q., Qian, H., Qiao, C., Zhang, P., Chen, T., & Liu, X. (2020) · Neurochemical Research · doi:10.1007/s11064-020-02966-8 · Cited by 19
Serine Racemase Deletion Affects the Excitatory/Inhibitory Balance of the Hippocampal CA1 Network
Ploux, E., Bouët, V., Radzishevsky, I. S., Wolosker, H., Fréret, T., & Billard, J. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21249447 · Cited by 19
Aroniadou‐Anderjaska, V., Pidoplichko, V. I., Figueiredo, T. H., & Braga, M. F. M. (2018) · Neuroscience · doi:10.1016/j.neuroscience.2018.01.021 · Cited by 20
Santora, V. J., Almos, T. A., Barido, R., Basinger, J., Bellows, C. L., Bookser, B. C., Breitenbucher, J. G., Broadbent, N., Cabebe, C., Chai, C.-K., et al. (2018) · Journal of Medicinal Chemistry · doi:10.1021/acs.jmedchem.8b00372 · Cited by 18
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Demeter, I., Nagy, K., Farkas, T., Kis, Z., Kocsis, K., Knapp, L., Gellért, L., Fülöp, F., Vécsei, L., & Toldi, J. (2013) · Neuroscience Letters · doi:10.1016/j.neulet.2013.08.028 · Cited by 18
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Bauminger, H., & Gaisler‐Salomon, I. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23158617 · Cited by 16
The effect of hippocampal NMDA receptor blockade by MK-801 on cued fear extinction
Zhang, B., Li, C., & Wang, X. (2017) · Behavioural Brain Research · doi:10.1016/j.bbr.2017.05.067 · Cited by 17
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Zalcman, G., Federman, N., Fiszbein, A., de la Fuente, V., Ameneiro, L., Schor, I. E., & Romano, A. G. (2018) · Molecular Neurobiology · doi:10.1007/s12035-018-1144-3 · Cited by 18
Long-Term Synaptic Plasticity in Rat Barrel Cortex
Han, Y. N., Huang, M.-D., Sun, M.-L., Duan, S., & Yu, Y. (2014) · Cerebral Cortex · doi:10.1093/cercor/bhu071 · Cited by 16
de Oliveira, D. R., Zamberlam, C. R., Rêgo, G. M., Cavalheiro, A. J., Cerutti, J. M., & Cerutti, S. M. (2016) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2015.00345 · Cited by 16
Klima, S., Brüll, M., Spreng, A., Suciu, I., Falt, T., Schwamborn, J. C., Waldmann, T., Karreman, C., & Leist, M. (2021) · Archives of Toxicology · doi:10.1007/s00204-021-03024-0 · Cited by 16
Yan, J., Wang, Y., Hellwig, A., & Bading, H. (2024) · Cell Reports Medicine · doi:10.1016/j.xcrm.2024.101413 · Cited by 16
Elkader, H. A. E. A., & Al‐Shami, A. S. (2024) · Aquatic Toxicology · doi:10.1016/j.aquatox.2024.106971 · Cited by 16
NMDAR PAMs: Multiple Chemotypes for Multiple Binding Sites
Goldsmith, P. J. (2019) · Current Topics in Medicinal Chemistry · doi:10.2174/1568026619666191011095341 · Cited by 16
Ashabi, G., Sadat‐Shirazi, M., Khalifeh, S., Elhampour, L., & Zarrindast, M. (2017) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2017.01.020 · Cited by 16
Liu, Y.-P., Ding, M., Zhang, X., Liu, Y., Xuan, J., Xing, J., Xia, X., Yao, J., & Wang, B. (2019) · BMC Medical Genetics · doi:10.1186/s12881-019-0757-3 · Cited by 16
Schmidt, R. W., & Thompson, M. L. (2016) · Mental Health Clinician · doi:10.9740/mhc.2016.11.266 · Cited by 14
Mitra, S., Munni, Y. A., Dash, R., Sultana, A., & Moon, I. S. (2022) · Phytotherapy Research · doi:10.1002/ptr.7466 · Cited by 15
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González, M. C., Villar, M. E., Igaz, L. M., Viola, H., & Medina, J. H. (2015) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2015.10.007 · Cited by 16
Parkes, S. L., Ferreira, G., & Coutureau, É. (2015) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2015.12.005 · Cited by 14
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Leiva, R., Phillips, M. B., Turcu, A. L., Gratacòs‐Batlle, E., León-García, L., Sureda, F. X., Soto, D., Johnson, J. W., & Vázquez, S. (2018) · ACS Chemical Neuroscience · doi:10.1021/acschemneuro.8b00154 · Cited by 14
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Viejo, L., Rubio‐Alarcón, M., Arribas, R. L., Moreno-Castro, M., Pérez-Marín, R., Braun-Cornejo, M., Estrada, M., & Rı́os, C. D. L. (2021) · Molecules · doi:10.3390/molecules26154473 · Cited by 14
Grochowska, K. M., Bär, J., Gomes, G. M., Kreutz, M. R., & Karpova, A. (2021) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2021.787494 · Cited by 14
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Park, S., Kim, J. I., Cho, N., Oh, S. W., Park, J., Yoo, I. D., Gil, H., & Lee, S. M. (2020) · Journal of Clinical Medicine · doi:10.3390/jcm9041213 · Cited by 13
van den Buuse, M., Biel, D., & Radscheit, K. (2017) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2017.02.009 · Cited by 13
Nachtigall, E. G., Myskiw, J. D. C., Izquierdo, I., & Furini, C. R. G. (2023) · Psychopharmacology · doi:10.1007/s00213-023-06463-y · Cited by 14
Krolik, A., Diamandakis, D., Zych, A. D., Stafiej, A., & Salińska, E. (2020) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2020.107209 · Cited by 12
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Kagan, D., Rivi, V., Benatti, C., Tascedda, F., Blom, J. M. C., & Lukowiak, K. D. (2023) · Journal of Experimental Biology · doi:10.1242/jeb.245566 · Cited by 13
Yan, J., & Bading, H. (2023) · Pharmaceuticals · doi:10.3390/ph16081085 · Cited by 12
Meneses, A. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-408139-0.00002-x · Cited by 12
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Murtas, G., Caldinelli, L., Cappelletti, P., Sacchi, S., & Pollegioni, L. (2017) · Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics · doi:10.1016/j.bbapap.2017.12.007 · Cited by 12
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Saber-Ayad, M. M., Hammoudeh, S. M., Radwan, H. M., Manzoor, S., Jabbar, H. A., Wardeh, R., Ashraf, A., Habib, P. T., Alsamman, A. M., & Hamoudi, R. (2020) · Journal of Advanced Research · doi:10.1016/j.jare.2020.05.020 · Cited by 11
Discovery of GluN2A subtype-selective N-methyl-d-aspartate (NMDA) receptor ligands
Jiang, L., Liu, N., Zhao, F., Huang, B., Kang, D., Zhan, P., & Liu, X. (2024) · Acta Pharmaceutica Sinica B · doi:10.1016/j.apsb.2024.01.004 · Cited by 11
Different components of conditioned food aversion memory
Nikitin, V. P., Solntseva, S. V., Kozyrev, S. A., Nikitin, P. V., & Shevelkin, A. V. (2016) · Brain Research · doi:10.1016/j.brainres.2016.03.017 · Cited by 11
Association of CaMK2A and MeCP2 signaling pathways with cognitive ability in adolescents
Lee, L., Su, M., Huang, H.-Y., Cho, Y., Yeh, T., & Chang, C. (2021) · Molecular Brain · doi:10.1186/s13041-021-00858-8 · Cited by 11
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Borges, A. C., Broersen, K., Leandro, P., & Fernandes, T. G. (2022) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2021.787242 · Cited by 14
Munni, Y. A., Dash, R., Choi, H. J., Mitra, S., Hannan, M. A., Mazumder, K., Timalsina, B., & Moon, I. S. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241713386 · Cited by 11
Zelinka, E. S., Brevig, J. K., McDonald, J., & Jin, R. (2010) · Journal of ExtraCorporeal Technology · doi:10.1051/ject/201042045 · Cited by 11
Lee, N. J., Song, J. M., Cho, H.-J., Sung, Y. M., Lee, T., Chung, A., Hong, S., Cifelli, J. L., Rubinshtein, M., Habib, L. K., et al. (2015) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2015.12.007 · Cited by 11
de Sousa, T. R., Correia, D. T., & Novais, F. (2021) · CNS & Neurological Disorders - Drug Targets · doi:10.2174/1871527320666210902164235 · Cited by 10
Role of Hippocampal Wnt Signaling Pathways on Contextual Fear Memory Reconsolidation
Nachtigall, E. G., de Freitas, J. D. R., Myskiw, J. D. C., & Furini, C. R. G. (2023) · Neuroscience · doi:10.1016/j.neuroscience.2023.05.028 · Cited by 9
Ketchum, M. J., Weyand, T. G., Weed, P. F., & Winsauer, P. J. (2015) · Hippocampus · doi:10.1002/hipo.22545 · Cited by 10
Pinzón-Parra, C. A., Coatl-Cuaya, H., Díaz, A., Guevara, J., Moreno, A. R., & Flores, G. (2021) · Journal of Chemical Neuroanatomy · doi:10.1016/j.jchemneu.2021.102054 · Cited by 10
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Wang, W., Duclot, F., Groveman, B. R., Carrier, N., Qiao, H., Fang, X., Wang, H., Xin, W., Jiang, X., Salter, M. W., et al. (2018) · PLoS ONE · doi:10.1371/journal.pone.0195095 · Cited by 11
Ross, A. P., Barnett, N., Faulkner, A. D., Hannapel, R., & Parent, M. B. (2018) · Behavioural Brain Research · doi:10.1016/j.bbr.2018.07.031 · Cited by 9
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Sahota, A., Nadappuram, B. P., Kwan, Z., Lesept, F., Howden, J. H., Claxton, S., Kittler, J. T., Devine, M. J., Edel, J. B., & Ivanov, A. P. (2025) · ACS Nano · doi:10.1021/acsnano.5c02056 · Cited by 9
Тиунова, А. А., Bezryadnov, D. V., Gaeva, D. R., Solodovnikov, V. S., & Анохин, К. В. (2020) · Behavioural Brain Research · doi:10.1016/j.bbr.2020.112695 · Cited by 9
Hippocampus NMDA receptors selectively mediate latent extinction of place learning
Goodman, J., Gabriele, A., & Packard, M. G. (2016) · Hippocampus · doi:10.1002/hipo.22594 · Cited by 11
Тиунова, А. А., Komissarova, N. V., Bezryadnov, D. V., & Анохин, К. В. (2016) · Bulletin of Experimental Biology and Medicine · doi:10.1007/s10517-016-3529-5 · Cited by 9
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Amiri, S., Azadmanesh, K., Shasaltaneh, M. D., Mayahi, V., & Naghdi, N. (2019) · Iranian Biomedical Journal · doi:10.29252/ibj.24.2.64 · Cited by 8
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Metadata
- Authors
- Morris, R. G. M.
- Affiliations
- University of Edinburgh (GB)
- Corresponding author
- Morris, Richard G.M.
- ORCID
- Morris, Richard G.M.
- Venue
- Neuropharmacology
- Publisher
- Elsevier BV
- Published
- 2013-11
- Volume
- 74
- Pages
- 32-40
- ISSN
- 0028-3908 (ISSN-L)
- OpenAlex
- W2027844417
- Cited by
- 295
- References
- 102
- Citations by year
- 2026: 13 · 2025: 17 · 2024: 18 · 2023: 18 · 2022: 17 · 2021: 33 · 2020: 29 · 2019: 20 · 2018: 33 · 2017: 27 · 2016: 31 · 2015: 20 · 2014: 14 · 2013: 4
- FWCI
- 2.34
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Neuropharmacology (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Medical Research Council
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
- Keywords
- NMDA receptor, memory encoding, long-term potentiation, hippocampus, D-AP5, glutamate receptors, synaptic plasticity, learning and memory, calcium signaling, cognitive function
- MeSH terms
- Animals, Hippocampus, Learning, Memory, 2-Amino-5-phosphonovalerate, Receptors, N-Methyl-D-Aspartate, Long-Term Potentiation
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