Place-Selective Firing of CA1 Pyramidal Cells during Sharp Wave/Ripple Network Patterns in Exploratory Behavior
Open accessAbstract
We observed sharp wave/ripples (SWR) during exploration within brief (<2.4 s) interruptions of or during theta oscillations. CA1 network responses of SWRs occurring during exploration (eSWR) and SWRs detected in waking immobility or sleep were similar. However, neuronal activity during eSWR was location dependent, and eSWR-related firing was stronger inside the place field than outside. The eSPW-related firing increase was stronger than the baseline increase inside compared to outside, suggesting a "supralinear" summation of eSWR and place-selective inputs. Pairs of cells with similar place fields and/or correlated firing during exploration showed stronger coactivation during eSWRs and subsequent sleep-SWRs. Sequential activation of place cells was not required for the reactivation of waking co-firing patterns; cell pairs with symmetrical cross-correlations still showed reactivated waking co-firing patterns during sleep-SWRs. We suggest that place-selective firing during eSWRs facilitates initial associations between cells with similar place fields that enable place-related ensemble patterns to recur during subsequent sleep-SWRs.
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Signs of assembly reactivation occur in the hippocampus and several other regions of the brain during sleep after exploration.
“These studies uniformly confirmed that signs of assembly reactivation occur in the hippocampus and several other regions of the brain also during sleep after exploration (870, 871, 985).”
From About Sleep's Role in Memory (2013) · cites this paper as [870]
The Discussion (page unavailable) reports reactivation of waking co-firing patterns during sleep, supporting the hippocampal part of the claim. The paper’s account concerns CA1 activity; the passages do not establish assembly reactivation in several other brain regions. (LLM, conf=0.88)
Experimental — accuracy not yet measuredNeuron assemblies linked to place fields that were longer or more frequently explored during waking showed stronger reactivation during succeeding sleep.
“Neuron assemblies linked to place fields that were longer or more frequently explored during waking showed stronger reactivation during succeeding sleep (870, 871).”
From About Sleep's Role in Memory (2013) · cites this paper as [870]
The Results section reports stronger co-firing during sleep after exploration for cells with overlapping place fields, supporting place-related reactivation. It does not link stronger reactivation to place fields being explored for longer or more frequently during waking; the comparison is between overlapping and nonoverlapping fields. Page numbers are not available in our copy. (LLM, conf=0.86)
Experimental — accuracy not yet measuredWake reactivations occur conjointly with SW-Rs that are observed at somewhat lower rates during wakefulness than during SWS.
“They also occur conjointly with SW-Rs that are observed at somewhat lower rates during wakefulness than during SWS (159,191,870).”
From About Sleep's Role in Memory (2013) · cites this paper as [870]
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Cites
(1978) · UA Campus Repository (The University of Arizona) · Cited by 8,010 · see citing works
The hippocampus as a spatial map. Preliminary evidence from unit activity in the freely-moving rat
O'Keefe, J., & Dostrovsky, J. (1971) · Brain Research · doi:10.1016/0006-8993(71)90358-1 · Cited by 6,151 · see citing works
The hippocampus as a cognitive map
Passingham, R. E. (1979) · Neuroscience · doi:10.1016/0306-4522(79)90015-0 · Cited by 5,128 · see citing works
Bi, G.-Q., & Poo, M.-M. (1998) · The Journal of Neuroscience · doi:10.1523/jneurosci.18-24-10464.1998 · Cited by 4,744 · see citing works
Spectrum estimation and harmonic analysis
Thomson, D. J. (1982) · Proceedings of the IEEE · doi:10.1109/proc.1982.12433 · Cited by 4,411 · see citing works
Regulation of Synaptic Efficacy by Coincidence of Postsynaptic APs and EPSPs
Markram, H., Lübke, J., Frotscher, M., & Sakmann, B. (1997) · Science · doi:10.1126/science.275.5297.213 · Cited by 3,832 · see citing works
Theta oscillations in the hippocampus
Buzsáki, G. (2002) · Neuron · doi:10.1016/s0896-6273(02)00586-x · Cited by 3,332 · see citing works
The Medial Temporal Lobe Memory System
Squire, L. R., & Zola-Morgan, S. (1991) · Science · doi:10.1126/science.1896849 · Cited by 3,282 · see citing works
Reactivation of hippocampal ensemble memories during sleep
Wilson, M. A., & McNaughton, B. L. (1994) · Science · doi:10.1126/science.8036517 · Cited by 3,118 · see citing works
Hippocampal electrical activity and voluntary movement in the rat
Vanderwolf, C. H. (1969) · Electroencephalography and Clinical Neurophysiology · doi:10.1016/0013-4694(69)90092-3 · Cited by 1,928 · see citing works
Two-stage model of memory trace formation: A role for “noisy” brain states
Buzsáki, G. (1989) · Neuroscience · doi:10.1016/0306-4522(89)90423-5 · Cited by 1,709 · see citing works
Gamma (40-100 Hz) oscillation in the hippocampus of the behaving rat
Bragin, A., Jando, G., Nadasdy, Z., Hetke, J., Wise, K., & Buzsaki, G. (1995) · The Journal of Neuroscience · doi:10.1523/jneurosci.15-01-00047.1995 · Cited by 1,527 · see citing works
Cellular bases of hippocampal EEG in the behaving rat
Buzsáki, G., Leung Lai-Wo, S., & Vanderwolf, C. H. (1983) · Brain Research Reviews · doi:10.1016/0165-0173(83)90037-1 · Cited by 1,397 · see citing works
A Synaptically Controlled, Associative Signal for Hebbian Plasticity in Hippocampal Neurons
Magee, J. C., & Johnston, D. (1997) · Science · doi:10.1126/science.275.5297.209 · Cited by 1,303 · see citing works
Memory of sequential experience in the hippocampus during slow wave sleep
Lee, A. K., & Wilson, M. A. (2002) · Neuron · doi:10.1016/s0896-6273(02)01096-6 · Cited by 1,296 · see citing works
High-frequency network oscillation in the hippocampus
Buzsáki, G., Horváth, Z., Urioste, R., Hetke, J. F., & Wise, K. D. (1992) · Science · doi:10.1126/science.1589772 · Cited by 1,223 · see citing works
Replay of neuronal firing sequences in rat hippocampus during sleep following spatial experience
Skaggs, W. E., & McNaughton, B. L. (1996) · Science · doi:10.1126/science.271.5257.1870 · Cited by 1,173 · see citing works
Temporally structured replay of awake hippocampal ensemble activity during rapid eye movement sleep
Louie, K., & Wilson, M. A. (2001) · Neuron · doi:10.1016/s0896-6273(01)00186-6 · Cited by 1,148 · see citing works
Ylinen, A., Bragin, A., Nadasdy, Z., Jando, G., Szabo, I., Sik, A., & Buzsaki, G. (1995) · The Journal of Neuroscience · doi:10.1523/jneurosci.15-01-00030.1995 · Cited by 1,092 · see citing works
Analysis of Dynamic Brain Imaging Data
Mitra, P. P., & Pesaran, B. (1999) · Biophysical Journal · doi:10.1016/s0006-3495(99)77236-x · Cited by 1,044 · see citing works
Mechanisms of Gamma Oscillations in the Hippocampus of the Behaving Rat
Csicsvari, J., Jamieson, B. G., Wise, K. D., & Buzsáki, G. (2003) · Neuron · doi:10.1016/s0896-6273(02)01169-8 · Cited by 990 · see citing works
Self-citationOscillatory coupling of hippocampal pyramidal cells and interneurons in the behaving rat
Csicsvari, J., Hirase, H., Czurkó, A., Mamiya, A., & Buzsáki, G. (1999) · The Journal of Neuroscience · doi:10.1523/jneurosci.19-01-00274.1999 · Cited by 966 · see citing works
Self-citationDendritic spines as basic functional units of neuronal integration
Yuste, R., & Denk, W. (1995) · Nature · doi:10.1038/375682a0 · Cited by 950 · see citing works
The Hippocampo-Neocortical Dialogue
Buzsáki, G. (1996) · Cerebral Cortex · doi:10.1093/cercor/6.2.81 · Cited by 938 · see citing works
Replay 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 · see citing works
Self-citationHippocampal sharp waves: Their origin and significance
Buzsáki, G. (1986) · Brain Research · doi:10.1016/0006-8993(86)91483-6 · Cited by 925 · see citing works
Analysis of Dynamic Brain Imaging Data
Mitra, P. P., & Pesaran, B. (1998) · Cold Spring Harbor Laboratory Institutional Repository (Cold Spring Harbor Laboratory) · Cited by 898 · see citing works
Cholinergic induction of network oscillations at 40 Hz in the hippocampus in vitro
Fisahn, A., Pike, F. G., Buhl, E. H., & Paulsen, O. (1998) · Nature · doi:10.1038/28179 · Cited by 884 · see citing works
Organization of cell assemblies in the hippocampus
Harris, K. D., Csicsvari, J., Hirase, H., Dragoi, G., & Buzsáki, G. (2003) · Nature · doi:10.1038/nature01834 · Cited by 869 · see citing works
Self-citationNeuromodulation: acetylcholine and memory consolidation
Hasselmo, M. E. (1999) · Trends in Cognitive Sciences · doi:10.1016/s1364-6613(99)01365-0 · Cited by 809 · see citing works
Kudrimoti, H. S., Barnes, C. A., & McNaughton, B. L. (1999) · The Journal of Neuroscience · doi:10.1523/jneurosci.19-10-04090.1999 · Cited by 753 · see citing works
The global record of memory in hippocampal neuronal activity
Wood, E. R., Dudchenko, P. A., & Eichenbaum, H. (1999) · Nature · doi:10.1038/17605 · Cited by 707 · see citing works
Electrical coupling underlies high-frequency oscillations in the hippocampus in vitro
Draguhn, A., Traub, R. D., Schmitz, D., & Jefferys, J. G. R. (1998) · Nature · doi:10.1038/28184 · Cited by 703 · see citing works
Role of experience and oscillations in transforming a rate code into a temporal code
Mehta, M. R., Lee, A. K., & Wilson, M. A. (2002) · Nature · doi:10.1038/nature00807 · Cited by 630 · see citing works
Reliability and State Dependence of Pyramidal Cell–Interneuron Synapses in the Hippocampus
Csicsvari, J., Hirase, H., Czurko, A., & Buzsáki, G. (1998) · Neuron · doi:10.1016/s0896-6273(00)80525-5 · Cited by 606 · see citing works
Self-citationIndependent rate and temporal coding in hippocampal pyramidal cells
Huxter, J. R., Burgess, N., & O'Keefe, J. M. (2003) · Nature · doi:10.1038/nature02058 · Cited by 594 · see citing works
Ensemble Patterns of Hippocampal CA3-CA1 Neurons during Sharp Wave–Associated Population Events
Csicsvari, J. L., Hirase, H., Mamiya, A., & Buzsáki, G. (2000) · Neuron · doi:10.1016/s0896-6273(00)00135-5 · Cited by 503 · see citing works
Self-citationVoltage clamp analysis of cholinergic action in the hippocampus
Madison, D. V., Lancaster, B., & Nicoll, R. A. (1987) · Journal of Neuroscience · doi:10.1523/jneurosci.07-03-00733.1987 · Cited by 503 · see citing works
Experience-Dependent Asymmetric Shape of Hippocampal Receptive Fields
Mehta, M. R., Quirk, M. C., & Wilson, M. A. (2000) · Neuron · doi:10.1016/s0896-6273(00)81072-7 · Cited by 488 · see citing works
Hasselmo, M., & Schnell, E. (1994) · The Journal of Neuroscience · doi:10.1523/jneurosci.14-06-03898.1994 · Cited by 466 · see citing works
Madison, D. V., & Nicoll, R. A. (1986) · The Journal of Physiology · doi:10.1113/jphysiol.1986.sp016006 · Cited by 391 · see citing works
Temporal Interaction between Single Spikes and Complex Spike Bursts in Hippocampal Pyramidal Cells
Harris, K. D., Hirase, H., Leinekugel, X., Henze, D. A., & Buzsáki, G. (2001) · Neuron · doi:10.1016/s0896-6273(01)00447-0 · Cited by 388 · see citing works
tFast Network Oscillations in the Hippocampal CA1 Region of the Behaving Rat
Csicsvari, T., Hirase, H., Czurkó, A., Mamiya, A., & Buzsáki, G. (1999) · Journal of Neuroscience · doi:10.1523/jneurosci.19-16-j0001.1999 · Cited by 353 · see citing works
Maier, N., Nimmrich, V., & Draguhn, A. (2003) · The Journal of Physiology · doi:10.1113/jphysiol.2003.044602 · Cited by 335 · see citing works
Sustained activation of hippocampal pyramidal cells by ‘space clamping’ in a running wheel
Czurkó, A., Hirase, H., Csicsvari, J. L., & Buzsáki, G. (1999) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.1999.00446.x · Cited by 326 · see citing works
Self-citationMann, E. O., Suckling, J. M., Hájos, N., Greenfield, S. A., & Paulsen, O. (2005) · Neuron · doi:10.1016/j.neuron.2004.12.016 · Cited by 318 · see citing works
Dendritic Spikes Are Enhanced by Cooperative Network Activity in the Intact Hippocampus
Kamondi, A., Acsády, L., & Buzsáki, G. (1998) · Journal of Neuroscience · doi:10.1523/jneurosci.18-10-03919.1998 · Cited by 252 · see citing works
Dutar, P., & Nicoll, R. A. (1988) · Journal of Neuroscience · doi:10.1523/jneurosci.08-11-04214.1988 · Cited by 251 · see citing works
Traub, R. D., & Bibbig, A. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-06-02086.2000 · Cited by 250 · see citing works
NMDA Receptor Antagonism Blocks Experience-Dependent Expansion of Hippocampal “Place Fields”
Ekstrom, A. D., Meltzer, J., McNaughton, B. L., & Barnes, C. A. (2001) · Neuron · doi:10.1016/s0896-6273(01)00401-9 · Cited by 245 · see citing works
Presynaptic inhibitory action of acetylcholine in area CA1 of the hippocampus
Hounsgaard, J. (1978) · Experimental Neurology · doi:10.1016/0014-4886(78)90284-4 · Cited by 221 · see citing works
Luddites must not block progress in genetics
Wood, D. (1999) · Nature · doi:10.1038/16564 · Cited by 208 · see citing works
Hirase, H., Leinekugel, X., Czurkó, A., Csicsvari, J., & Buzsáki, G. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.161274398 · Cited by 173 · see citing works
Self-citationNimmrich, V., Maier, N., Schmitz, D., & Draguhn, A. (2005) · The Journal of Physiology · doi:10.1113/jphysiol.2004.079558 · Cited by 128 · see citing works
Hebbian modification of a hippocampal population pattern in the rat
King, C., Henze, D. A., Leinekugel, X., & Buzsáki, G. (1999) · The Journal of Physiology · doi:10.1111/j.1469-7793.1999.00159.x · Cited by 122 · see citing works
Williams, S. R., & Stuart, G. J. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-22-08238.2000 · Cited by 113 · see citing works
Long‐term potentiation is impaired in rat hippocampal slices that produce spontaneous sharp waves
Colgin, L. L., Kubota, D., Jia, Y., Rex, C. S., & LYNCH, G. S. (2004) · The Journal of Physiology · doi:10.1113/jphysiol.2004.068080 · Cited by 112 · see citing works
Interaction between spike waveform classification and temporal sequence detection
Quirk, M. C., & Wilson, M. A. (1999) · Journal of Neuroscience Methods · doi:10.1016/s0165-0270(99)00124-7 · Cited by 99 · see citing works
Linear to Supralinear Summation of AMPA-Mediated EPSPs in Neocortical Pyramidal Neurons
Nettleton, J. S., & Spain, W. J. (2000) · Journal of Neurophysiology · doi:10.1152/jn.2000.83.6.3310 · Cited by 71 · see citing works
Spontaneous EEG spikes in the normal hippocampus II. Relations to synchronous burst discharges
Suzuki, S. S., & Smith, G. K. (1988) · Electroencephalography and Clinical Neurophysiology · doi:10.1016/0013-4694(88)90165-4 · Cited by 63 · see citing works
Potentials evoked by alvear tract in hippocampal CA1 region of rats. II. Spatial field analysis
Leung, S. W. (1979) · Journal of Neurophysiology · doi:10.1152/jn.1979.42.6.1571 · Cited by 62 · see citing works
Lee, A. K., & Wilson, M. A. (2004) · Journal of Neurophysiology · doi:10.1152/jn.01030.2003 · Cited by 40 · see citing works
Jarosiewicz, B., & Skaggs, W. E. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.5650-03.2004 · Cited by 30 · see citing works
Benardo, L. S. (1993) · Neuroscience · doi:10.1016/0306-4522(93)90280-s · Cited by 23 · see citing works
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- [47]47. Nimmrich, V. ∙ Maier, N. ∙ Schmitz, D. ... Induced sharp wave-ripple complexes in the absence of synaptic inhibition J. Physiol. 2005; 563:663-670 Crossref Scopus (78) PubMed Google Scholar
Cited by
Sorted by citations
Rasch, B., & Born, J. (2013) · Physiological Reviews · doi:10.1152/physrev.00032.2012 · Cited by 2,783 · see citing works
Place Cells, Grid Cells, and the Brain's Spatial Representation System
Moser, E. I., Kropff, E., & Moser, M.-B. (2008) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.31.061307.090723 · Cited by 1,934 · see citing works
Hippocampal sharp wave-ripple: A cognitive biomarker for episodic memory and planning
Buzsáki, G. (2015) · Hippocampus · doi:10.1002/hipo.22488 · Cited by 1,759 · see citing works
Neural ensembles in CA3 transiently encode paths forward of the animal at a decision point
Johnson, A., & Redish, A. D. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.3761-07.2007 · Cited by 1,003 · see citing works
Hippocampal replay in the awake state: a potential substrate for memory consolidation and retrieval
Carr, M. F., Jadhav, S. P., & Frank, L. M. (2011) · Nature Neuroscience · doi:10.1038/nn.2732 · Cited by 958 · see citing works
Awake hippocampal sharp-wave ripples support spatial memory
Jadhav, S. P., Kemere, C., German, P. W., & Frank, L. M. (2012) · Science · doi:10.1126/science.1217230 · Cited by 924 · see citing works
Hippocampal GABAergic Inhibitory Interneurons
Pelkey, K. A., Chittajallu, R., Craig, M. T., Tricoire, L., Wester, J. C., & McBain, C. J. (2017) · Physiological Reviews · doi:10.1152/physrev.00007.2017 · Cited by 889 · see citing works
The reorganization and reactivation of hippocampal maps predict spatial memory performance
Dupret, D., O'Neill, J., Pleydell-Bouverie, B., & Csicsvari, J. (2010) · Nature Neuroscience · doi:10.1038/nn.2599 · Cited by 769 · see citing works
Self-citationAwake replay of remote experiences in the hippocampus
Karlsson, M. P., & Frank, L. M. (2009) · Nature Neuroscience · doi:10.1038/nn.2344 · Cited by 769 · see citing works
Hippocampal replay is not a simple function of experience
Gupta, A. S., van der Meer, M. A. A., Touretzky, D. S., & Redish, A. D. (2010) · Neuron · doi:10.1016/j.neuron.2010.01.034 · Cited by 733 · see citing works
Preplay of future place cell sequences by hippocampal cellular assemblies
Dragoi, G., & Tonegawa, S. (2011) · Nature · doi:10.1038/nature09633 · Cited by 716 · see citing works
Neuromodulation of Brain States
Lee, S., & Dan, Y. (2012) · Neuron · doi:10.1016/j.neuron.2012.09.012 · Cited by 666 · see citing works
Compartmentalized dendritic plasticity and input feature storage in neurons
Losonczy, A., Makara, J. K., & Magee, J. C. (2008) · Nature · doi:10.1038/nature06725 · Cited by 598 · see citing works
Place Cells, Grid Cells, and MemoryPreprint
Moser, M., Rowland, D. C., & Moser, E. I. (2015) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a021808 · Cited by 539 · see citing works
Conjunctive input processing drives feature selectivity in hippocampal CA1 neurons
Bittner, K. C., Grienberger, C., Vaidya, S. P., Milstein, A. D., Macklin, J. J., Suh, J., Tonegawa, S., & Magee, J. C. (2015) · Nature Neuroscience · doi:10.1038/nn.4062 · Cited by 540 · see citing works
Play it again: reactivation of waking experience and memory
O’Neill, J., Pleydell-Bouverie, B., Dupret, D., & Csicsvari, J. L. (2010) · Trends in Neurosciences · doi:10.1016/j.tins.2010.01.006 · Cited by 448 · see citing works
Self-citationThe hippocampal sharp wave-ripple in memory retrieval for immediate use and consolidation
Joo, H. R., & Frank, L. M. (2018) · Nature Reviews Neuroscience · doi:10.1038/s41583-018-0077-1 · Cited by 430 · see citing works
Rewarded Outcomes Enhance Reactivation of Experience in the Hippocampus
Singer, A. C., & Frank, L. M. (2009) · Neuron · doi:10.1016/j.neuron.2009.11.016 · Cited by 385 · see citing works
Ripples in the medial temporal lobe are relevant for human memory consolidation
Axmacher, N., Elger, C. E., & Fell, J. (2008) · Brain · doi:10.1093/brain/awn103 · Cited by 372 · see citing works
Buzsáki, G. (2019) · doi:10.1093/oso/9780190905385.001.0001 · Cited by 358 · see citing works
A clustered plasticity model of long-term memory engrams.
Govindarajan, A., Kelleher, R. J., & Tonegawa, S. (2006) · Nature reviews. Neuroscience · doi:10.1038/nrn1937 · Cited by 355 · see citing works
Long-term synaptic plasticity in hippocampal interneurons
Kullmann, D. M., & Lamsa, K. P. (2007) · Nature Reviews Neuroscience · doi:10.1038/nrn2207 · Cited by 340 · see citing works
Hippocampal ripples and memory consolidation
Girardeau, G., & Zugaro, M. (2011) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2011.02.005 · Cited by 330 · see citing works
The role of sleep in declarative memory consolidation: passive, permissive, active or none?
Ellenbogen, J. M., Payne, J. D., & Stickgold, R. (2006) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2006.10.006 · Cited by 326 · see citing works
Reactivation of experience-dependent cell assembly patterns in the hippocampus
O'Neill, J., Senior, T. J., Allen, K., Huxter, J. R., & Csicsvari, J. (2008) · Nature Neuroscience · doi:10.1038/nn2037 · Cited by 318 · see citing works
Self-citationSullivan, D. W., Csicsvari, J. L., Mizuseki, K., Montgomery, S. M., Diba, K., & Buzsáki, G. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.0294-11.2011 · Cited by 292 · see citing works
Self-citationNew Experiences Enhance Coordinated Neural Activity in the Hippocampus
Cheng, S., & Frank, L. M. (2008) · Neuron · doi:10.1016/j.neuron.2007.11.035 · Cited by 286 · see citing works
Sustained increase in hippocampal sharp-wave ripple activity during slow-wave sleep after learning
Eschenko, O., Ramadan, W., Mölle, M., Born, J., & Sara, S. J. (2008) · Learning & Memory · doi:10.1101/lm.726008 · Cited by 277 · see citing works
Foffani, G., Uzcategui, Y. G., Gal, B., & de la Prida, L. M. (2007) · Neuron · doi:10.1016/j.neuron.2007.07.040 · Cited by 275 · see citing works
Transient Slow Gamma Synchrony Underlies Hippocampal Memory Replay
Carr, M. F., Karlsson, M. P., & Frank, L. M. (2012) · Neuron · doi:10.1016/j.neuron.2012.06.014 · Cited by 255 · see citing works
Determinants of different deep and superficial CA1 pyramidal cell dynamics during sharp-wave ripples
Valero, M., Cid, E., Averkin, R. G., Aguilar, J., Sánchez-Aguilera, A., Viney, T. J., Gómez-Domínguez, D., Bellistri, E., & de la Prida, L. M. (2015) · Nature Neuroscience · doi:10.1038/nn.4074 · Cited by 259 · see citing works
Fuentealba, P., Begum, R., Capogna, M., Jinno, S., Márton, L. F., Csicsvari, J., Thomson, A., Somogyi, P., & Klausberger, T. (2008) · Neuron · doi:10.1016/j.neuron.2008.01.034 · Cited by 255 · see citing works
Self-citationHigh frequency oscillations in the intact brain
Buzsáki, G., & Lopes, F. H. D. S. (2012) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2012.02.004 · Cited by 247 · see citing works
Jadhav, S. P., Rothschild, G., Roumis, D. K., & Frank, L. M. (2016) · Neuron · doi:10.1016/j.neuron.2016.02.010 · Cited by 250 · see citing works
Goal-Related Activity in Hippocampal Place Cells
Hok, V., Lenck‐Santini, P., Roux, S., Save, É., Muller, R. U., & Poucet, B. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.2864-06.2007 · Cited by 232 · see citing works
Role of Hippocampal CA2 Region in Triggering Sharp-Wave Ripples
Oliva, A., Fernández‐Ruiz, A., Buzsáki, G., & Berényi, A. (2016) · Neuron · doi:10.1016/j.neuron.2016.08.008 · Cited by 217 · see citing works
Decoupling through Synchrony in Neuronal Circuits with Propagation Delays
Lubenov, E. V., & Siapas, A. G. (2008) · Neuron · doi:10.1016/j.neuron.2008.01.036 · Cited by 196 · see citing works
Dendritic spikes induce single-burst long-term potentiation
Remy, S., & Spruston, N. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0707919104 · Cited by 179 · see citing works
Memory trace replay: The shaping of memory consolidation by neuromodulation
Atherton, L. A., Dupret, D., & Mellor, J. R. (2015) · Trends in Neurosciences · doi:10.1016/j.tins.2015.07.004 · Cited by 180 · see citing works
English, D. F., Peyrache, A., Stark, E., Roux, L., Vallentin, D., Long, M. A., & Buzsáki, G. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.2600-14.2014 · Cited by 176 · see citing works
The content of hippocampal “replay”
Pfeiffer, B. E. (2017) · Hippocampus · doi:10.1002/hipo.22824 · Cited by 172 · see citing works
Superficial layers of the medial entorhinal cortex replay independently of the hippocampus
O’Neill, J., Boccara, C. N., Stella, F., Schoenenberger, P., & Csicsvari, J. (2017) · Science · doi:10.1126/science.aag2787 · Cited by 177 · see citing works
Self-citationThe Neurobiology of Mammalian Navigation
Poulter, S. L., Hartley, T., & Lever, C. (2018) · Current Biology · doi:10.1016/j.cub.2018.05.050 · Cited by 171 · see citing works
Senior, T. J., Huxter, J. R., Allen, K. L., O'Neill, J., & Csicsvari, J. L. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.4669-07.2008 · Cited by 180 · see citing works
Self-citationLocal Generation and Propagation of Ripples along the Septotemporal Axis of the Hippocampus
Patel, J., Schomburg, E. W., Berényi, A., Fujisawa, S., & Buzsáki, G. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.2036-13.2013 · Cited by 167 · see citing works
Attentive scanning behavior drives one-trial potentiation of hippocampal place fields
Monaco, J. D., Rao, G., Roth, E. D., & Knierim, J. J. (2014) · Nature Neuroscience · doi:10.1038/nn.3687 · Cited by 163 · see citing works
Acetylcholine bidirectionally regulates learning and memory
Huang, Q., Liao, C., Ge, F., Ao, J., & Liu, T. (2022) · Journal of Neurorestoratology · doi:10.1016/j.jnrt.2022.100002 · Cited by 165 · see citing works
Priming of Hippocampal Population Bursts by Individual Perisomatic-Targeting Interneurons
Ellender, T. J., Nissen, W., Colgin, L. L., Mann, E. O., & Paulsen, O. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.3962-09.2010 · Cited by 157 · see citing works
Somogyi, P., Katona, L., Klausberger, T., Lasztóczi, B., & Viney, T. J. (2013) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2012.0518 · Cited by 158 · see citing works
Dynamic Reconfiguration of Hippocampal Interneuron Circuits during Spatial Learning
Dupret, D., O’Neill, J., & Csicsvari, J. (2013) · Neuron · doi:10.1016/j.neuron.2013.01.033 · Cited by 158 · see citing works
Self-citationCsicsvari, J. L., O'Neill, J., Allen, K. L., & Senior, T. J. (2007) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2007.05684.x · Cited by 145 · see citing works
Self-citationPapale, A. E., Zielinski, M. C., Frank, L. M., Jadhav, S. P., & Redish, A. D. (2016) · Neuron · doi:10.1016/j.neuron.2016.10.028 · Cited by 139 · see citing works
Theta Phase Modulates Multiple Layer-Specific Oscillations in the CA1 Region
Scheffer-Teixeira, R., Belchior, H., Caixeta, F. V., Souza, B. C., Ribeiro, S. T. G., & Tort, A. B. L. (2011) · Cerebral Cortex · doi:10.1093/cercor/bhr319 · Cited by 138 · see citing works
Deep Brain Stimulation for Epilepsy
Halpern, C. H., Samadani, U., Litt, B., Jaggi, J. L., & Baltuch, G. H. (2008) · Neurotherapeutics · doi:10.1016/j.nurt.2007.10.065 · Cited by 138 · see citing works
Li, M., Long, C., & Yang, L. (2015) · BioMed Research International · doi:10.1155/2015/810548 · Cited by 137 · see citing works
Reactivation, Replay, and Preplay: How It Might All Fit Together
Buhry, L., Azizi, A. H., & Cheng, S. (2011) · Neural Plasticity · doi:10.1155/2011/203462 · Cited by 134 · see citing works
Sasaki, T., Piatti, V. C., Hwaun, E., Ahmadi, S., Lisman, J. E., Leutgeb, S., & Leutgeb, J. K. (2018) · Nature Neuroscience · doi:10.1038/s41593-017-0061-5 · Cited by 134 · see citing works
McKenzie, S., Robinson, N. T. M., Herrera, L., Churchill, J. C., & Eichenbaum, H. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.0879-13.2013 · Cited by 132 · see citing works
Task Demands Predict a Dynamic Switch in the Content of Awake Hippocampal Replay
Ólafsdóttir, H., Carpenter, F., & Barry, C. (2017) · bioRxiv · doi:10.1016/j.neuron.2017.09.035 · Cited by 94 · see citing works
Jackson, J. C., Johnson, A. C., & Redish, A. D. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.4118-06.2006 · Cited by 128 · see citing works
Valero, M., Averkin, R. G., Fernández‐Lamo, I., Aguilar, J., Lopez‐Pigozzi, D., Brotons‐Mas, J. R., Cid, E., Tamás, G., & de la Prida, L. M. (2017) · Neuron · doi:10.1016/j.neuron.2017.05.032 · Cited by 126 · see citing works
Replay, the default mode network and the cascaded memory systems model
Kaefer, K., Stella, F., McNaughton, B. L., & Battaglia, F. P. (2022) · Nature reviews. Neuroscience · doi:10.1038/s41583-022-00620-6 · Cited by 124 · see citing works
Experience-dependent compartmentalized dendritic plasticity in rat hippocampal CA1 pyramidal neurons
Makara, J. K., Losonczy, A., Wen, Q., & Magee, J. C. (2009) · Nature Neuroscience · doi:10.1038/nn.2428 · Cited by 126 · see citing works
Network dynamics of hippocampal cell‐assemblies resemble multiple spatial maps within single tasks
Jackson, J. C., & Redish, A. D. (2007) · Hippocampus · doi:10.1002/hipo.20359 · Cited by 124 · see citing works
Hippocampal memory consolidation during sleep: a comparison of mammals and birds
Rattenborg, N. C., Martı́nez-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 121 · see citing works
Hippocampal-cortical interaction in decision making
Yu, J. Y., & Frank, L. (2014) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2014.02.002 · Cited by 110 · see citing works
Selection of experience for memory by hippocampal sharp wave ripples
Yang, W., Sun, C., Huszár, R., Hainmueller, T., Kiselev, K., & Buzsáki, G. (2024) · Science · doi:10.1126/science.adk8261 · Cited by 116 · see citing works
Theta-associated high-frequency oscillations (110–160Hz) in the hippocampus and neocortex
Tort, A. B. L., Scheffer-Teixeira, R., Souza, B. C., Draguhn, A., & Brankačk, J. (2012) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2012.09.002 · Cited by 111 · see citing works
Hippocampal reactivation of random trajectories resembling brownian diffusion
Stella, F., Baracskay, P., O’Neill, J., & Csicsvari, J. (2019) · Neuron · doi:10.1016/j.neuron.2019.01.052 · Cited by 107 · see citing works
Self-citationXu, H., Baracskay, P., O’Neill, J., & Csicsvari, J. L. (2018) · Neuron · doi:10.1016/j.neuron.2018.11.015 · Cited by 105 · see citing works
Self-citationBrain Activity Fluctuations Propagate as Waves Traversing the Cortical Hierarchy
Gu, Y., Sainburg, L. E., Kuang, S., Han, F., Williams, J. W., Liu, Y., Zhang, N., Zhang, X., Leopold, D. A., & Liu, X. (2021) · Cerebral Cortex · doi:10.1093/cercor/bhab064 · Cited by 92 · see citing works
Episodic memory—From brain to mind
Ferbinteanu, J., Kennedy, P., & Shapiro, M. L. (2006) · Hippocampus · doi:10.1002/hipo.20204 · Cited by 92 · see citing works
Selection of preconfigured cell assemblies for representation of novel spatial experiences
Dragoi, G., & Tonegawa, S. (2013) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2012.0522 · Cited by 94 · see citing works
Internally generated hippocampal sequences as a vantage point to probe future‐oriented cognition
Pezzulo, G., Kemere, C. T., & van der Meer, M. A. A. (2017) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.13329 · Cited by 93 · see citing works
Modeling sharp wave‐ripple complexes through a CA3‐CA1 network model with chemical synapses
Taxidis, J., Coombes, S., Mason, R., & Owen, M. (2012) · Hippocampus · doi:10.1002/hipo.20930 · Cited by 104 · see citing works
Short‐term plasticity based network model of place cells dynamics
Romani, S., & Tsodyks, M. V. (2014) · Hippocampus · doi:10.1002/hipo.22355 · Cited by 82 · see citing works
Inhibitory Control of Linear and Supralinear Dendritic Excitation in CA1 Pyramidal Neurons
Müller, C., Beck, H., Coulter, D. A., & Remy, S. (2012) · Neuron · doi:10.1016/j.neuron.2012.06.025 · Cited by 87 · see citing works
Activity-Dependent Control of Neuronal Output by Local and Global Dendritic Spike Attenuation
Remy, S., Csicsvari, J. L., & Beck, H. (2009) · Neuron · doi:10.1016/j.neuron.2009.01.032 · Cited by 86 · see citing works
Self-citationHippocampal Sequences During Exploration: Mechanisms and Functions
Drieu, C., & Zugaro, M. (2019) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2019.00232 · Cited by 84 · see citing works
Ripples Make Waves: Binding Structured Activity and Plasticity in Hippocampal Networks
Sadowski, J. H. L. P., Jones, M. W., & Mellor, J. R. (2011) · Neural Plasticity · doi:10.1155/2011/960389 · Cited by 80 · see citing works
Sharp Wave Ripples during Visual Exploration in the Primate Hippocampus
Leonard, T. K., Mikkila, J. M., Eskandar, E., Gerrard, J., Kaping, D., Patel, S. R., Womelsdorf, T., & Hoffman, K. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.0864-15.2015 · Cited by 80 · see citing works
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 78 · see citing works
Rácz, Á., Ponomarenko, A. A., Fuchs, E. C., & Monyer, H. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.5036-08.2009 · Cited by 75 · see citing works
Membrane Potential Dynamics of CA1 Pyramidal Neurons during Hippocampal Ripples in Awake Mice
Hulse, B. K., Moreaux, L. C., Lubenov, E. V., & Siapas, A. G. (2016) · Neuron · doi:10.1016/j.neuron.2016.01.014 · Cited by 73 · see citing works
Memory processes during sleep: beyond the standard consolidation theory
Axmacher, N., Draguhn, A., Elger, C. E., & Fell, J. (2009) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-009-0019-1 · Cited by 73 · see citing works
Tao, K., Chung, M., Watarai, A., Huang, Z., Wang, M., & Okuyama, T. (2022) · Molecular Psychiatry · doi:10.1038/s41380-021-01430-5 · Cited by 74 · see citing works
Sleep and rest facilitate implicit memory in a visual search task
Mednick, S. C., Makovski, T., Cai, D. J., & Jiang, Y. V. (2009) · Vision Research · doi:10.1016/j.visres.2009.04.011 · Cited by 72 · see citing works
Control of recollection by slow gamma dominating mid-frequency gamma in hippocampus CA1
Dvořák, D., Radwan, B., Sparks, F. T., Talbot, Z. N., & Fenton, A. A. (2018) · PLoS Biology · doi:10.1371/journal.pbio.2003354 · Cited by 80 · see citing works
Young, C. K., & Eggermont, J. J. (2009) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2009.06.002 · Cited by 69 · see citing works
El‐Hassar, L., Hagenston, A. M., D’Angelo, L. B., & Yeckel, M. F. (2011) · The Journal of Physiology · doi:10.1113/jphysiol.2011.209783 · Cited by 70 · see citing works
Looking for cognition in the structure within the noise
Johnson, A. C., Fenton, A. A., Kentros, C. G., & Redish, A. D. (2009) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2008.11.005 · Cited by 69 · see citing works
Three brain states in the hippocampus and cortex
Kay, K., & Frank, L. M. (2018) · Hippocampus · doi:10.1002/hipo.22956 · Cited by 63 · see citing works
Stacey, W. C., Lazarewicz, M. T., & Litt, B. (2009) · Journal of Neurophysiology · doi:10.1152/jn.00397.2009 · Cited by 60 · see citing works
HectoSTAR μLED Optoelectrodes for Large‐Scale, High‐Precision In Vivo Opto‐Electrophysiology
Vöröslakos, M., Kim, K., Slager, N., Ko, E., Oh, S., Parizi, S. S., Hendrix, B., Seymour, J. P., Wise, K. D., Buzsáki, G., et al. (2022) · Advanced Science · doi:10.1002/advs.202105414 · Cited by 58 · see citing works
Sharp-Wave Ripples in Primates Are Enhanced near Remembered Visual Objects.
Leonard, T. K., & Hoffman, K. (2017) · Current Biology · doi:10.1016/j.cub.2016.11.027 · Cited by 61 · see citing works
Metabotropic action of postsynaptic kainate receptors triggers hippocampal long-term potentiation
Petrovic, M. M., da Silva, S. V., Clement, J. P., Vyklický, L., Mulle, C., González‐González, I. M., & Henley, J. M. (2017) · Nature Neuroscience · doi:10.1038/nn.4505 · Cited by 59 · see citing works
Sharp wave/ripple network oscillations and learning-associated hippocampal maps
Csicsvari, J. L., & Dupret, D. (2013) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2012.0528 · Cited by 51 · see citing works
Self-citationAlexander, A. S., Rangel, L. M., Tingley, D., & Nitz, D. A. (2018) · Behavioral Neuroscience · doi:10.1037/bne0000254 · Cited by 52 · see citing works
Salib, M., Joshi, A., Katona, L., Howarth, M., Micklem, B. R., Somogyi, P., & Viney, T. J. (2019) · Journal of Neuroscience · doi:10.1523/jneurosci.3024-18.2019 · Cited by 53 · see citing works
The Hippocampal Horizon: Constructing and Segmenting Experience for Episodic Memory
Ross, T. W., & Easton, A. (2021) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2021.11.038 · Cited by 49 · see citing works
- Authors
- O'Neill, J., Senior, T., & Csicsvari, J.
- Affiliations
- University of Oxford (GB)
- Corresponding author
- Csicsvari, Jozsef
- ORCID
- Csicsvari, Jozsef
- Venue
- Neuron
- Publisher
- Elsevier BV
- Published
- 2006-01
- Volume
- 49
- Issue
- 1
- Pages
- 143-155
- ISSN
- 0896-6273 (ISSN-L)
- OpenAlex
- W2129356785
- Cited by
- 281
- References
- 67
- Citations by year
- 2026: 6 · 2025: 16 · 2024: 11 · 2023: 5 · 2022: 11 · 2021: 13 · 2020: 6 · 2019: 28 · 2018: 22 · 2017: 16 · 2016: 10 · 2015: 14 · 2014: 19 · 2013: 17 · 2012: 10
- FWCI
- 8.06
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Neuron (publishedVersion)
- PubMed (publishedVersion)
- ORCA Online Research @Cardiff (Cardiff University) (submittedVersion)
- Funders
- Wellcome Trust
- Medical Research Council
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Keywords
- place cells, CA1 pyramidal neurons, place fields, exploratory behavior, theta oscillations, sleep, memory reactivation, ensemble coding, correlated firing, hippocampus
- MeSH terms
- Action Potentials, Animals, Electrophysiology, Exploratory Behavior, Male, Rats, Inbred Strains, Sleep Stages, Space Perception, Theta Rhythm, Wakefulness, Pyramidal Cells, Rats
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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.
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