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Mechanisms of Sleep-Dependent Consolidation of Cortical Plasticity
Open accessAbstract
Sleep is thought to consolidate changes in synaptic strength, but the underlying mechanisms are unknown. We investigated the cellular events involved in this process during ocular dominance plasticity (ODP)-a canonical form of in vivo cortical plasticity triggered by monocular deprivation (MD) and consolidated by sleep via undetermined, activity-dependent mechanisms. We find that sleep consolidates ODP primarily by strengthening cortical responses to nondeprived eye stimulation. Consolidation is inhibited by reversible, intracortical antagonism of NMDA receptors (NMDARs) or cAMP-dependent protein kinase (PKA) during post-MD sleep. Consolidation is also associated with sleep-dependent increases in the activity of remodeling neurons and in the phosphorylation of proteins required for potentiation of glutamatergic synapses. These findings demonstrate that synaptic strengthening via NMDAR and PKA activity is a key step in sleep-dependent consolidation of ODP.
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“Conversely, the GABA A agonist muscimol and also zolpidem impaired sleep-dependent plastic changes in the visual cortex in a developmental model of synaptic plasticity in cats [i.e., ocular dominance plasticity (ODP); see sect.VIIA3 for details] (48,411,1059), suggesting that GABA plays a critical role for plastic processes occurring during sleep.”
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“Of the GABA A agonistic substances zaleplon, eszopiclone, zolpidem, and triazolam, only zolpidem impaired sleep-dependent ODP, although all substances distinctly reduced REM sleep and increased non-REM sleep (48,1059).”
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“These sleep-dependent changes are prevented by blocking NMDA receptors or cAMP-dependent protein kinase (PKA) during sleep after monocular experience (48)”
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“Sleep-dependent ODP is prevented by blocking glutamatergic NMDA receptors or cAMP-dependent protein kinase (PKA) during sleep after monocular deprivation (48).”
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“The beneficial effect of sleep on consolidation of ODP mainly leads to a strengthening of the cortical responses to stimulation of the nondeprived eye (48).”
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“ODP was impaired following application of the atypical hypnotic trazodone, probably acting via blocking 5-HT 2c receptors during sleep (48).”
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“Work in the visual cortex also shows that sleep affects memory consolidation,80–82”
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Citations
Cites
Memory - A century of consolidation
McGaugh, J. L. (2000) · Science · doi:10.1126/science.287.5451.248 · Cited by 4,250
Reactivation of hippocampal ensemble memories during sleep
Wilson, M. A., & McNaughton, B. L. (1994) · Science · doi:10.1126/science.8036517 · Cited by 3,118
The period of susceptibility to the physiological effects of unilateral eye closure in kittens
Hubel, D. H., & Wiesel, T. N. (1970) · The Journal of Physiology · doi:10.1113/jphysiol.1970.sp009022 · Cited by 3,030
Sleep function and synaptic homeostasis
Tononi, G., & Cirelli, C. (2006) · Sleep Medicine Reviews · doi:10.1016/j.smrv.2005.05.002 · Cited by 2,151
Long-Term Potentiation and Memory
Lynch, M. A. (2004) · Physiological Reviews · doi:10.1152/physrev.00014.2003 · Cited by 2,074
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
Coordinated memory replay in the visual cortex and hippocampus during sleep
Ji, D., & Wilson, M. A. (2007) · Nature Neuroscience · doi:10.1038/nn1825 · Cited by 1,669
Regulation of distinct AMPA receptor phosphorylation sites during bidirectional synaptic plasticity
Lee, H.-K., Barbarosie, M., Kameyama, K., Bear, M. F., & Huganir, R. L. (2000) · Nature · doi:10.1038/35016089 · Cited by 1,116
Sleep-Dependent Learning and Memory Consolidation
Walker, M. P., & Stickgold, R. (2004) · Neuron · doi:10.1016/j.neuron.2004.08.031 · Cited by 1,113 · cited 1×
“, 2006) and that consolidation can occur during sleep (Frank and Benington, 2006; Walker and Stickgold, 2004).”
BackgroundReplay and Time Compression of Recurring Spike Sequences in the Hippocampus
Nádasdy, Z., Hirase, H., Czurkó, A., Csicsvari, J., & Buzsáki, G. (1999) · The Journal of Neuroscience · doi:10.1523/jneurosci.19-21-09497.1999 · Cited by 932 · cited 2×
“, 2000; Pavlides and Winson, 1989; Wilson and McNaughton, 1994), which may provide sufficient neuronal depolarization to activate NMDARs (Nadasky et al., 1999).”
Background
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Diekelmann, S., & Born, J. (2010) · Nature Reviews Neuroscience · doi:10.1038/nrn2762 · Cited by 3,760
Rasch, B., & Born, J. (2013) · Physiological Reviews · doi:10.1152/physrev.00032.2012 · Cited by 2,783
“The beneficial effect of sleep on consolidation of ODP mainly leads to a strengthening of the cortical responses to stimulation of the nondeprived eye (48).”
BackgroundInfluentialTononi, G., & Cirelli, C. (2014) · Neuron · doi:10.1016/j.neuron.2013.12.025 · Cited by 2,356
Control of sleep and wakefulness
Brown, R. E., Basheer, R., McKenna, J. T., Strecker, R. E., & McCarley, R. W. (2012) · Physiological Reviews · doi:10.1152/physrev.00032.2011 · Cited by 1,477
Cortical firing and sleep homeostasis
Vyazovskiy, V. V., Olcese, U., Lazimy, Y. M., Faraguna, U., Esser, S. K., Williams, J. C., Cirelli, C., & Tononi, G. (2009) · Neuron · doi:10.1016/j.neuron.2009.08.024 · Cited by 740
Squire, L. R., Genzel, L., Wixted, J. T., & Morris, R. G. (2015) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a021766 · Cited by 700
The Restless Engram: Consolidations Never End
Dudai, Y. (2012) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-062111-150500 · Cited by 644
Sleep promotes branch-specific formation of dendritic spines after learning
Yang, G., Lai, C. S. W., Cichon, J., Ma, L., Li, W., & Gan, W.-B. (2014) · Science · doi:10.1126/science.1249098 · Cited by 616
Sleep viewed as a state of adaptive inactivity
Siegel, J. M. (2009) · Nature Reviews Neuroscience · doi:10.1038/nrn2697 · Cited by 468
Sleep function: Toward elucidating an enigma
Krueger, J. M., Frank, M. G., Wisor, J. P., & Roy, S. (2016) · Sleep Medicine Reviews · doi:10.1016/j.smrv.2015.08.005 · Cited by 440
Sleep Deprivation and Circadian Disruption
McEwen, B. S., & Karatsoreos, I. N. (2015) · Sleep Medicine Clinics · doi:10.1016/j.jsmc.2014.11.007 · Cited by 338
Raven, F., Van der Zee, E. A., Meerlo, P., & Havekes, R. (2018) · Sleep Medicine Reviews · doi:10.1016/j.smrv.2017.05.002 · Cited by 331
Stowell, R. D., Sipe, G. O., Dawes, R. P., Batchelor, H. N., Lordy, K. A., Whitelaw, B. S., Stoessel, M. B., Bidlack, J. M., Brown, E., Sur, M., et al. (2019) · Nature Neuroscience · doi:10.1038/s41593-019-0514-0 · Cited by 321
Neuronal Firing Rate Homeostasis Is Inhibited by Sleep and Promoted by Wake
Hengen, K. B., Pacheco, A. T., McGregor, J. N., Hooser, S. D. V., & Turrigiano, G. G. (2016) · Cell · doi:10.1016/j.cell.2016.01.046 · Cited by 302
Sleep Oscillations in the Thalamocortical System Induce Long-Term Neuronal Plasticity
Chauvette, S., Seigneur, J., & Timofeev, I. (2012) · Neuron · doi:10.1016/j.neuron.2012.08.034 · Cited by 304
Schmidt, M. H. (2014) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2014.08.001 · Cited by 291
EEG sleep slow-wave activity as a mirror of cortical maturation
Buchmann, A., Ringli, M., Kurth, S., Schaerer, M., Geiger, A., Jenni, O. G., & Huber, R. (2011) · Cerebral Cortex · doi:10.1093/cercor/bhq129 · Cited by 273
Sparsification of neuronal activity in the visual cortex at eye-opening
Rochefort, N. L., Garaschuk, O., Milos, R., Narushima, M., Marandi, N., Pichler, B., Kovalchuk, Y., & Konnerth, A. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0907660106 · Cited by 291
Genzel, L., Kroes, M. C. W., Dresler, M., & Battaglia, F. P. (2013) · Trends in Neurosciences · doi:10.1016/j.tins.2013.10.002 · Cited by 285
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Turrigiano, G. G. (2017) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2016.0258 · Cited by 251
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Joiner, W. J. (2016) · Current Biology · doi:10.1016/j.cub.2016.08.068 · Cited by 232
Form and function of sleep spindles across the lifespan
Clawson, B. C., Durkin, J., & Aton, S. J. (2016) · Neural Plasticity · doi:10.1155/2016/6936381 · Cited by 178
Nardone, R., Höller, Y., Brigo, F., Seidl, M., Christova, M., Bergmann, J., Golaszewski, S. M., & Trinka, E. (2013) · Brain Research · doi:10.1016/j.brainres.2012.12.034 · Cited by 182
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Poe, G. R., Walsh, C. M., & Bjorness, T. E. (2010) · Progress in brain research · doi:10.1016/b978-0-444-53702-7.00001-4 · Cited by 183
Synaptic plasticity in sleep: learning, homeostasis and disease
Wang, G., Grone, B., Colas, D., Appelbaum, L., & Mourrain, P. (2011) · Trends in Neurosciences · doi:10.1016/j.tins.2011.07.005 · Cited by 172
Circadian clocks: genes, sleep, and cognition
Kyriacou, C. P., & Hastings, M. H. (2010) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2010.03.007 · Cited by 179
Rapid eye movement sleep promotes cortical plasticity in the developing brain
Dumoulin Bridi, M. C., Aton, S. J., Seibt, J., Renouard, L., Coleman, T., & Frank, M. G. (2015) · Science Advances · doi:10.1126/sciadv.1500105 · Cited by 157
Protein Synthesis during Sleep Consolidates Cortical Plasticity In Vivo
Seibt, J., Dumoulin, M. C., Aton, S. J., Coleman, T., Watson, A., Naidoo, N., & Frank, M. G. (2012) · Current Biology · doi:10.1016/j.cub.2012.02.016 · Cited by 162
Self-citationGómez, R. L., & Edgin, J. O. (2015) · Developmental Cognitive Neuroscience · doi:10.1016/j.dcn.2015.08.009 · Cited by 171
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Aguilar, J., Humanes-Valera, D., Alonso‐Calviño, E., Yagüe, J. G., Moxon, K. A., Oliviero, A., & Foffani, G. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.0379-10.2010 · Cited by 151
REM sleep promotes experience-dependent dendritic spine elimination in the mouse cortex
Zhou, Y., Lai, C. S. W., Bai, Y., Li, W., Zhao, R., Yang, G., Frank, M. G., & Gan, W. (2020) · Nature Communications · doi:10.1038/s41467-020-18592-5 · Cited by 139
Dual function of thalamic low-vigilance state oscillations: rhythm-regulation and plasticity
Crunelli, V., Lörincz, M. L., Connelly, W. M., David, F., Hughes, S. W., Lambert, R. C., Leresche, N., & Errington, A. C. (2018) · Nature reviews. Neuroscience · doi:10.1038/nrn.2017.151 · Cited by 131
Krueger, J. M., Rector, D. M., & Churchill, L. (2007) · Sleep Medicine Clinics · doi:10.1016/j.jsmc.2007.03.003 · Cited by 128
Linking Network Activity to Synaptic Plasticity during Sleep: Hypotheses and Recent Data
Puentes-Mestril, C., & Aton, S. J. (2017) · Frontiers in Neural Circuits · doi:10.3389/fncir.2017.00061 · Cited by 130
Sleep promotes cortical response potentiation following visual experience
Aton, S. J., Suresh, A., Broussard, C., & Frank, M. G. (2014) · SLEEP · doi:10.5665/sleep.3830 · Cited by 122
Self-citationHippocampal memory consolidation during sleep: a comparison of mammals and birds
Rattenborg, N. C., Martínez-González, D., Roth, T. C., & Витальевич, П. В. (2010) · Biological reviews/Biological reviews of the Cambridge Philosophical Society · doi:10.1111/j.1469-185x.2010.00165.x · Cited by 128
Slow Wave Sleep Is a Promising Intervention Target for Alzheimer’s Disease
Lee, Y. F., Gerashchenko, D., Timofeev, I., Bacskai, B. J., & Kastanenka, K. V. (2020) · Frontiers in Neuroscience · doi:10.3389/fnins.2020.00705 · Cited by 127
Aton, S. J., Broussard, C., Dumoulin, M., Seibt, J., Watson, A., Coleman, T., & Frank, M. G. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1208093110 · Cited by 113
Sleep, clocks, and synaptic plasticity
Frank, M. G., & Cantera, R. (2014) · Trends in Neurosciences · doi:10.1016/j.tins.2014.06.005 · Cited by 125
Hollway, J. A., & Aman, M. G. (2011) · Research in Developmental Disabilities · doi:10.1016/j.ridd.2010.12.035 · Cited by 119
Sleep slow oscillation and plasticity
Timofeev, I., & Chauvette, S. (2017) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2017.03.019 · Cited by 121
Primed to Sleep: The Dynamics of Synaptic Plasticity Across Brain States
Seibt, J., & Frank, M. G. (2019) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2019.00002 · Cited by 120
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Carracedo, L. M., Kjeldsen, H., Cunnington, L. G., Jenkins, A., Schofield, I. S., Cunningham, M. O., Davies, C. H., Traub, R. D., & Whittington, M. A. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.0735-13.2013 · Cited by 114
Sleep function: current questions and new approaches
Vassalli, A., & Dijk, D. (2009) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2009.06767.x · Cited by 110
Frank, M. G., & Heller, H. C. (2018) · Handbook of experimental pharmacology · doi:10.1007/164_2018_140 · Cited by 121
Sleep, synaptic connectivity, and hippocampal memory during early development
Huber, R., & Jan Born, A. (2014) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2013.12.005 · Cited by 113
Sleep, plasticity, and sensory neurodevelopment
Blumberg, M. S., Dooley, J. C., & Tiriac, A. (2022) · Neuron · doi:10.1016/j.neuron.2022.08.005 · Cited by 93
How rhythms of the sleeping brain tune memory and synaptic plasticity
Puentes-Mestril, C., Roach, J. P., Niethard, N., Żochowski, M., & Aton, S. J. (2019) · SLEEP · doi:10.1093/sleep/zsz095 · Cited by 97
Gómez, R. L., & Edgin, J. O. (2015) · Child Development Perspectives · doi:10.1111/cdep.12130 · Cited by 93
Sleep: a synchrony of cell activity‐driven small network states
Krueger, J. M., Huang, Y. H., Rector, D. M., & Buysse, D. J. (2013) · European Journal of Neuroscience · doi:10.1111/ejn.12238 · Cited by 98
Plasticity during sleep is linked to specific regulation of cortical circuit activity
Niethard, N., Burgalossi, A., & Born, J. (2017) · Frontiers in Neural Circuits · doi:10.3389/fncir.2017.00065 · Cited by 89
Erasing Synapses in Sleep: Is It Time to Be SHY?
Frank, M. G. (2012) · Neural Plasticity · doi:10.1155/2012/264378 · Cited by 117
Durkin, J., Suresh, A. K., Colbath, J., Broussard, C., Wu, J., Żochowski, M., & Aton, S. J. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1710613114 · Cited by 90
Neuroligin-1 links neuronal activity to sleep-wake regulation
Helou, J. E., Bélanger-Nelson, E., Freyburger, M., Dorsaz, S., Curie, T., Spada, F. L., Gaudreault, P., Beaumont, É., Pouliot, P., Lesage, F., et al. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1221381110 · Cited by 97
Selbach, O., Bohla, C., Barbara, A. B., Doreulee, N., Eriksson, K. S., Sergeeva, O. A., & Haas, H. L. (2009) · Acta Physiologica · doi:10.1111/j.1748-1716.2009.02021.x · Cited by 88
Gorgoni, M., D’Atri, A., Lauri, G., Rossini, P. M., Ferlazzo, F., & Gennaro, L. D. (2013) · Neural Plasticity · doi:10.1155/2013/103949 · Cited by 95
Delorme, J. E., Wang, L., Kuhn, F. R., Kodoth, V., Ma, J., Martinez, J. D., Raven, F., Toth, B. A., Balendran, V., Vega-Medina, A., et al. (2021) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2019318118 · Cited by 82
CA1 hippocampal network activity changes during sleep-dependent memory consolidation
Ognjanovski, N., Maruyama, D., Lashner, N., Zochowski, M., & Aton, S. J. (2014) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2014.00061 · Cited by 81
Hippocampal Network Oscillations Rescue Memory Consolidation Deficits Caused by Sleep Loss
Ognjanovski, N., Broussard, C., Żochowski, M., & Aton, S. J. (2018) · Cerebral Cortex · doi:10.1093/cercor/bhy174 · Cited by 84
Feld, G. B., & Jan Born, A. (2019) · Neuropsychopharmacology · doi:10.1038/s41386-019-0490-9 · Cited by 84
Adolescent sleep and the foundations of prefrontal cortical development and dysfunction
Anastasiades, P. G., de Vivo, L., Bellesi, M., & Jones, M. W. (2022) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2022.102338 · Cited by 89
Sleep Deprivation Impairs Consolidation of Cued Fear Memory in Rats
Kumar, T., & Jha, S. K. (2012) · PLoS ONE · doi:10.1371/journal.pone.0047042 · Cited by 80
Sleep and Synaptic Plasticity in the Developing and Adult Brain
Frank, M. G. (2014) · Current topics in behavioral neurosciences · doi:10.1007/7854_2014_305 · Cited by 80
Sleep and homeostatic control of plasticity
Lanza, G., DelRosso, L. M., & Ferri, R. (2022) · Handbook of clinical neurology · doi:10.1016/b978-0-12-819410-2.00004-7 · Cited by 78
Sleep and protein synthesis-dependent synaptic plasticity: impacts of sleep loss and stress
Grønli, J., Soule, J. D., & Bramham, C. R. (2014) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2013.00224 · Cited by 79
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Bhat, A., Pires, A. S., Tan, V. X., Chidambaram, S. B., & Guillemin, G. J. (2020) · International Journal of Tryptophan Research · doi:10.1177/1178646920970902 · Cited by 81
Durkin, J., & Aton, S. J. (2016) · Sleep · doi:10.5665/sleep.5338 · Cited by 68
Self-citationMussig, L., Richlitzki, A., Rössler, R., Eisenhardt, D., Menzel, R., & Leboulle, G. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.5543-09.2010 · Cited by 72
Slow Wave Activity During Sleep: Functional and Therapeutic Implications
Greene, R. W., & Frank, M. G. (2010) · The Neuroscientist · doi:10.1177/1073858410377064 · Cited by 72
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Sleep Regulates Incubation of Cocaine Craving
Chen, B., Wang, Y., Liu, X., Liu, Z., Dong, Y., & Huang, Y. H. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.1065-15.2015 · Cited by 70
Experience-dependent homeostatic synaptic plasticity in neocortex
Whitt, J. L., Petrus, E., & Lee, H. (2013) · Neuropharmacology · doi:10.1016/j.neuropharm.2013.02.016 · Cited by 70
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BLUMBERG, M. S. (2010) · Frontiers in Neurology · doi:10.3389/fneur.2010.00140 · Cited by 68
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Dresler, M., Spoormaker, V. I., Beitinger, P., Czisch, M., Kimura, M., Steiger, A., & Holsboer, F. (2014) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2013.10.012 · Cited by 63
Ribeiro, S. T. G. (2011) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s00424-011-1031-5 · Cited by 65
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Xu, Y., Schneider, A. M., Weßel, R., & Hengen, K. B. (2024) · Nature Neuroscience · doi:10.1038/s41593-023-01536-9 · Cited by 62
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Cirelli, C. (2017) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2017.03.016 · Cited by 64
Spindle activity orchestrates plasticity during development and sleep
Lindemann, C., Ahlbeck, J., Bitzenhofer, S. H., & Hanganu-Opatz, I. L. (2016) · Neural Plasticity · doi:10.1155/2016/5787423 · Cited by 59
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Frank, M. G. (2011) · Progress in brain research · doi:10.1016/b978-0-444-53839-0.00014-4 · Cited by 57
Picchioni, D., Reith, R. M., Nadel, J., & Smith, C. B. (2014) · Brain Sciences · doi:10.3390/brainsci4010150 · Cited by 56
Feld, G. B., Lange, T., Gais, S., & Jan Born, A. (2013) · Neuropsychopharmacology · doi:10.1038/npp.2013.179 · Cited by 56
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Hanlon, E. C., Vyazovskiy, V. V., Faraguna, U., Tononi, G., & Cirelli, C. (2011) · Current Topics in Medicinal Chemistry · doi:10.2174/156802611797470312 · Cited by 59
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Bridi, M., Aton, S. J., Watson, A. J. R., Renouard, L., Coleman, T., & Frank, M. G. (2013) · Cerebral Cortex · doi:10.1093/cercor/bht250 · Cited by 51
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Pocivavsek, A., Baratta, A. M., Mong, J. A., & Viechweg, S. S. (2017) · SLEEP · doi:10.1093/sleep/zsx141 · Cited by 50
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Weiss, J. T., & Donlea, J. M. (2022) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2021.777799 · Cited by 49
Schmidt, M. H., Swang, T. W., Hamilton, I. M., & Best, J. A. (2017) · PLoS ONE · doi:10.1371/journal.pone.0185746 · Cited by 52
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Metadata
- Authors
- Aton, S. J., Seibt, J., Dumoulin, M., Jha, S. K., Steinmetz, N., Coleman, T., Naidoo, N., & Frank, M. G.
- Affiliations
- University of Pennsylvania (US)
- Jawaharlal Nehru University (IN)
- Corresponding author
- Frank, Marcos G.
- Venue
- Neuron
- Publisher
- Elsevier BV
- Published
- 2009-02
- Volume
- 61
- Issue
- 3
- Pages
- 454-466
- ISSN
- 0896-6273 (ISSN-L)
- PMC
- PMC2665998
- OpenAlex
- W2161849272
- Cited by
- 244
- References
- 58
- Citations by year
- 2026: 5 · 2025: 12 · 2024: 12 · 2023: 9 · 2022: 17 · 2021: 11 · 2020: 14 · 2019: 16 · 2018: 16 · 2017: 20 · 2016: 13 · 2015: 12 · 2014: 18 · 2013: 21 · 2012: 15
- FWCI
- 7.58
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Neuron (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Surrey Research Insight Open Access (The University of Surrey) (submittedVersion)
- UCL Discovery (University College London) (submittedVersion)
- Funders
- National Eye Institute (F32EY006831, R01EY019022, F32EY017766)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Sleep and Wakefulness Research
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Keywords
- ocular dominance plasticity, monocular deprivation, NMDA receptor, protein kinase A, synaptic plasticity, glutamatergic synapses, synaptic potentiation, cortical plasticity, protein phosphorylation
- MeSH terms
- Animals, Cats, Cerebral Cortex, Enzyme Inhibitors, Learning, Synaptic Transmission, Neuronal Plasticity, Phosphorylation, Photic Stimulation, Sensory Deprivation, Sleep, Synapses, Receptors, N-Methyl-D-Aspartate, Cyclic AMP-Dependent Protein Kinases, Excitatory Amino Acid Antagonists, Glutamic Acid
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