Theta Phase Segregation of Input-Specific Gamma Patterns in Entorhinal-Hippocampal Networks
Open accessAbstract
Precisely how rhythms support neuronal communication remains obscure. We investigated interregional coordination of gamma oscillations using high-density electrophysiological recordings in the rat hippocampus and entorhinal cortex. We found that 30-80 Hz gamma dominated CA1 local field potentials (LFPs) on the descending phase of CA1 theta waves during navigation, with 60-120 Hz gamma at the theta peak. These signals corresponded to CA3 and entorhinal input, respectively. Above 50 Hz, interregional phase-synchronization of principal cell spikes occurred mostly for LFPs in the axonal target domain. CA1 pyramidal cells were phase-locked mainly to fast gamma (>100 Hz) LFP patterns restricted to CA1, which were strongest at the theta trough. While theta phase coordination of spiking across entorhinal-hippocampal regions depended on memory demands, LFP gamma patterns below 100 Hz in the hippocampus were consistently layer specific and largely reflected afferent activity. Gamma synchronization as a mechanism for interregional communication thus rapidly loses efficacy at higher frequencies.
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
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?
Fast gamma oscillations have previously been described in rodents.
“but have previously been described in rodents37.”
From Local hippocampal fast gamma rhythms precede brain-wide hyperemic patterns during spontaneous rodent REM sleep (2018) · cites this paper as [37]
Hippocampal theta and gamma rhythms were confirmed by phase inversion across recording sites in successive hippocampal layers, time-frequency decomposition, and phase-amplitude cross-frequency coupling.
“Hippocampal theta and gamma rhythms were confirmed by phase inversion across recording sites in successive hippocampal layers, time-frequency decomposition, and phase-amplitude cross-frequency coupling37,38.”
From Local hippocampal fast gamma rhythms precede brain-wide hyperemic patterns during spontaneous rodent REM sleep (2018) · cites this paper as [37]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
(1978) · UA Campus Repository (The University of Arizona) · Cited by 8,010 · 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
A mechanism for cognitive dynamics: neuronal communication through neuronal coherence.
Fries, P. (2005) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2005.08.011 · Cited by 4,284 · see citing works
The origin of extracellular fields and currents — EEG, ECoG, LFP and spikes
Buzsáki, G., Anastassiou, C. A., & Koch, C. (2012) · Nature Reviews Neuroscience · doi:10.1038/nrn3241 · Cited by 4,225 · see citing works
Self-citationFrequency Dependence of Signal Power and Spatial Reach of the Local Field Potential
Leski, S., Lindén, H., Tetzlaff, T., Pettersen, K. H., & Einevoll, G. T. (2013) · PubMed Central · doi:10.18154/rwth-conv-084442 · Cited by 3,662 · see citing works
Interneurons of the hippocampus
Freund, T. F., & Buzsáki, G. (1998) · Hippocampus · doi:10.1002/(sici)1098-1063(1996)6:4 · Cited by 3,423 · see citing works
Self-citationTheta oscillations in the hippocampus
Buzsáki, G. (2002) · Neuron · doi:10.1016/s0896-6273(02)00586-x · Cited by 3,332 · see citing works
Self-citationMechanisms of Gamma Oscillations
Buzsáki, G., & Wang, X.-J. (2012) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-062111-150444 · Cited by 2,796 · see citing works
Self-citationHigh Gamma Power Is Phase-Locked to Theta Oscillations in Human Neocortex
Canolty, R. T., Edwards, E., Dalal, S. S., Soltani, M., Nagarajan, S. S., Kirsch, H. E., Berger, M. S., Barbaro, N. M., & Knight, R. T. (2006) · Science · doi:10.1126/science.1128115 · Cited by 2,650 · see citing works
Phase relationship between hippocampal place units and the EEG theta rhythm
O'Keefe, J. M., & Recce, M. L. (1993) · Hippocampus · doi:10.1002/hipo.450030307 · Cited by 2,561 · see citing works
The three-dimensional organization of the hippocampal formation: A review of anatomical data
Amaral, D. G., & Witter, M. P. (1989) · Neuroscience · doi:10.1016/0306-4522(89)90424-7 · Cited by 2,180 · see citing works
The functional role of cross-frequency coupling
Canolty, R. T., & Knight, R. T. (2010) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2010.09.001 · Cited by 2,101 · see citing works
Synaptic mechanisms of synchronized gamma oscillations in inhibitory interneuron networks
Bartos, M., Vida, I., & Jonas, P. (2007) · Nature Reviews Neuroscience · doi:10.1038/nrn2044 · Cited by 2,070 · see citing works
Neuronal Diversity and Temporal Dynamics: The Unity of Hippocampal Circuit Operations
Klausberger, T., & Somogyi, P. (2008) · Science · doi:10.1126/science.1149381 · Cited by 2,050 · see citing works
Neuronal gamma-band synchronization as a fundamental process in cortical computation
Fries, P. (2009) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.051508.135603 · Cited by 1,713 · see citing works
Synchronization of cortical activity and its putative role in information processing and learning
Singer, W. (1993) · Annual Review of Physiology · doi:10.1146/annurev.ph.55.030193.002025 · Cited by 1,685 · see citing works
How Inhibition Shapes Cortical Activity
Isaacson, J. S., & Scanziani, M. (2011) · Neuron · doi:10.1016/j.neuron.2011.09.027 · Cited by 1,678 · see citing works
The role of phase synchronization in memory processes
Fell, J., & Axmacher, N. (2011) · Nature Reviews Neuroscience · doi:10.1038/nrn2979 · Cited by 1,620 · see citing works
Lisman, J. E., & Jensen, O. (2013) · Neuron · doi:10.1016/j.neuron.2013.03.007 · Cited by 1,609 · 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
Frequency of gamma oscillations routes flow of information in the hippocampus
Colgin, L. L., Denninger, T., Fyhn, M., Hafting, T., Bonnevie, T., Jensen, O. B., Moser, M., & Moser, E. I. (2009) · Nature · doi:10.1038/nature08573 · Cited by 1,425 · 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
Self-citationMeasuring Phase-Amplitude Coupling Between Neuronal Oscillations of Different Frequencies
Tort, A. B. L., Komorowski, R. W., Eichenbaum, H., & Kopell, N. (2010) · Journal of Neurophysiology · doi:10.1152/jn.00106.2010 · Cited by 1,365 · see citing works
Internally Generated Cell Assembly Sequences in the Rat Hippocampus
Pastalkova, E., Itskov, V., Amarasingham, A., & Buzsáki, G. (2008) · Science · doi:10.1126/science.1159775 · Cited by 1,301 · see citing works
High-frequency, long-range coupling between prefrontal and visual cortex during attention
Gregoriou, G. G., Gotts, S. J., Zhou, H., & Desimone, R. (2009) · Science · doi:10.1126/science.1171402 · Cited by 1,194 · see citing works
Enforcement of Temporal Fidelity in Pyramidal Cells by Somatic Feed-Forward Inhibition
Pouille, F., & Scanziani, M. (2001) · Science · doi:10.1126/science.1060342 · Cited by 1,097 · see citing works
Gamma rhythms and beta rhythms have different synchronization properties
Kopell, N., Ermentrout, G. B., Whittington, M. A., & Traub, R. D. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.97.4.1867 · Cited by 1,072 · see citing works
Entrainment of Neocortical Neurons and Gamma Oscillations by the Hippocampal Theta Rhythm
Sirota, A., Montgomery, S., Fujisawa, S., Isomura, Y., Zugaro, M., & Buzsáki, G. (2008) · Neuron · doi:10.1016/j.neuron.2008.09.014 · Cited by 1,015 · see citing works
Self-citationDifferent Origins of Gamma Rhythm and High-Gamma Activity in Macaque Visual Cortex
Ray, S., & Maunsell, J. H. R. (2011) · PLoS Biology · doi:10.1371/journal.pbio.1000610 · Cited by 1,012 · see citing works
Wood, E. R., Dudchenko, P. A., Robitsek, R. J., & Eichenbaum, H. (2000) · Neuron · doi:10.1016/s0896-6273(00)00071-4 · Cited by 992 · 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-citationTheta-gamma coupling increases during the learning of item-context associations
Tort, A. B. L., Komorowski, R. W., Manns, J. R., Kopell, N. J., & Eichenbaum, H. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0911331106 · Cited by 919 · see citing works
Functional organization of the extrinsic and intrinsic circuitry of the parahippocampal region
Witter, M. P., Groenewegen, H. J., Lopes, F. H. D. S., & Lohman, A. H. M. (1989) · Progress in Neurobiology · doi:10.1016/0301-0082(89)90009-9 · Cited by 918 · see citing works
Hasselmo, M. E., Bodelón, C., & Wyble, B. P. (2002) · Neural Computation · doi:10.1162/089976602317318965 · Cited by 875 · see citing works
Modelling and analysis of local field potentials for studying the function of cortical circuits
Einevoll, G. T., Kayser, C., Logothetis, N. K., & Panzeri, S. (2013) · Nature Reviews Neuroscience · doi:10.1038/nrn3599 · Cited by 857 · see citing works
Brunel, N., & Wang, X. (2003) · Journal of Neurophysiology · doi:10.1152/jn.01095.2002 · Cited by 854 · see citing works
Cross-Frequency Phase–Phase Coupling between Theta and Gamma Oscillations in the Hippocampus
Belluscio, M. A., Mizuseki, K., Schmidt, R., Kempter, R., & Buzsáki, G. (2012) · The Journal of Neuroscience · doi:10.1523/jneurosci.4122-11.2012 · Cited by 784 · see citing works
Self-citationAction potential initiation and backpropagation in neurons of the mammalian CNS
Stuart, G., Spruston, N., Sakmann, B., & Häusser, M. (1997) · Trends in Neurosciences · doi:10.1016/s0166-2236(96)10075-8 · Cited by 768 · see citing works
Attentional stimulus selection through selective synchronization between monkey visual areas
Bosman, C. A., Schoffelen, J.-M., Brunet, N., Oostenveld, R., Bastos, A. M., Womelsdorf, T., Rubehn, B., Stieglitz, T., De Weerd, P., & Fries, P. (2012) · Neuron · doi:10.1016/j.neuron.2012.06.037 · Cited by 720 · see citing works
Mizuseki, K., Sirota, A., Pastalkova, E., & Buzsáki, G. (2009) · Neuron · doi:10.1016/j.neuron.2009.08.037 · Cited by 718 · see citing works
Self-citationNicholson, C., & Freeman, J. A. (1975) · Journal of Neurophysiology · doi:10.1152/jn.1975.38.2.356 · Cited by 699 · see citing works
Major Dissociation Between Medial and Lateral Entorhinal Input to Dorsal Hippocampus
Hargreaves, E. L., Rao, G., Lee, I., & Knierim, J. J. (2005) · Science · doi:10.1126/science.1110449 · Cited by 685 · see citing works
Dendritic spikes as a mechanism for cooperative long-term potentiation
Golding, N. L., Staff, N. P., & Spruston, N. (2002) · Nature · doi:10.1038/nature00854 · Cited by 623 · see citing works
Untangling cross-frequency coupling in neuroscience
Aru, J., Aru, J., Priesemann, V., Wibral, M., Lana, L., Pipa, G., Singer, W., & Vicente, R. (2014) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2014.08.002 · Cited by 612 · see citing works
Shadlen, M. N., & Movshon, J. A. (1999) · Neuron · doi:10.1016/s0896-6273(00)80822-3 · Cited by 606 · 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-citationEnsemble 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-citationHippocampal CA1 pyramidal cells form functionally distinct sublayers
Mizuseki, K., Diba, K., Pastalkova, E., & Buzsáki, G. (2011) · Nature Neuroscience · doi:10.1038/nn.2894 · Cited by 453 · see citing works
Self-citationFeed-forward inhibition in the hippocampal formation
BUZSAKI, G. (1984) · Progress in Neurobiology · doi:10.1016/0301-0082(84)90023-6 · Cited by 453 · see citing works
Pyramidal Cell-Interneuron Interactions Underlie Hippocampal Ripple Oscillations
Stark, E., Roux, L., Eichler, R., Senzai, Y., Royer, S., & Buzsáki, G. (2014) · Neuron · doi:10.1016/j.neuron.2014.06.023 · Cited by 441 · see citing works
Self-citationCoordination of entorhinal–hippocampal ensemble activity during associative learning
Igarashi, K. M., Lu, L., Colgin, L. L., Moser, M., & Moser, E. I. (2014) · Nature · doi:10.1038/nature13162 · Cited by 435 · see citing works
Gamma oscillations dynamically couple hippocampal CA3 and CA1 regions during memory task performance
Montgomery, S. M., & Buzsáki, G. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0701826104 · Cited by 431 · see citing works
Self-citationDifferences in Gamma Frequencies across Visual Cortex Restrict Their Possible Use in Computation
Ray, S., & Maunsell, J. H. R. (2010) · Neuron · doi:10.1016/j.neuron.2010.08.004 · Cited by 424 · see citing works
Spike Transmission and Synchrony Detection in Networks of GABAergic Interneurons
Galarreta, M., & Hestrin, S. (2001) · Science · doi:10.1126/science.1061395 · Cited by 389 · see citing works
Theta and gamma coordination of hippocampal networks during waking and rapid eye movement sleep.
Montgomery, S. M., Sirota, A., & Buzsaki, G. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.1227-08.2008 · Cited by 371 · see citing works
Impaired Spatial Representation in CA1 after Lesion of Direct Input from Entorhinal Cortex
Brun, V. H., Leutgeb, S., Wu, H., Schwarcz, R. M., Witter, M. P., Moser, E. I., & Moser, M. (2008) · Neuron · doi:10.1016/j.neuron.2007.11.034 · Cited by 364 · see citing works
OLM interneurons differentially modulate CA3 and entorhinal inputs to hippocampal CA1 neurons
Leão, R. N., Mikulovic, S., Leão, K. E., Munguba, H., Gezelius, H., Enjin, A., Patra, K., Eriksson, A., Loew, L. M., Tort, A. B. L., et al. (2012) · Nature Neuroscience · doi:10.1038/nn.3235 · Cited by 359 · see citing works
Successful Execution of Working Memory Linked to Synchronized High-Frequency Gamma Oscillations
Yamamoto, J., Suh, J., Takeuchi, D., & Tonegawa, S. (2014) · Cell · doi:10.1016/j.cell.2014.04.009 · Cited by 350 · see citing works
Vertes, R. P., Hoover, W. B., Szigeti‐Buck, K., & Léránth, C. (2007) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2006.12.002 · Cited by 345 · see citing works
Experience-dependent phase-reversal of hippocampal neuron firing during REM sleep
Poe, G. R., Nitz, D. A., McNaughton, B. L., & Barnes, C. A. (2000) · Brain Research · doi:10.1016/s0006-8993(99)02310-0 · Cited by 318 · see citing works
Pathway Interactions and Synaptic Plasticity in the Dendritic Tuft Regions of CA1 Pyramidal Neurons
Takahashi, H., & Magee, J. C. (2009) · Neuron · doi:10.1016/j.neuron.2009.03.007 · Cited by 312 · see citing works
Jarsky, T., Roxin, A., Kath, W. L., & Spruston, N. (2005) · Nature Neuroscience · doi:10.1038/nn1599 · Cited by 301 · see citing works
Large-scale, high-density (up to 512 channels) recording of local circuits in behaving animals
Berényi, A., Somogyvári, Z., Nagy, A. J., Roux, L., Long, J. D., Fujisawa, S., Stark, E., Leonardo, A. M., Harris, T. D., & Buzsáki, G. (2013) · Journal of Neurophysiology · doi:10.1152/jn.00785.2013 · Cited by 299 · 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-citationYeckel, M. F., & Berger, T. W. (1990) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.87.15.5832 · Cited by 286 · see citing works
Brankačk, J., Stewart, M., & Fox, S. E. (1993) · Brain Research · doi:10.1016/0006-8993(93)90043-m · Cited by 279 · see citing works
Spatial Representation along the Proximodistal Axis of CA1
Henriksen, E. J., Colgin, L. L., Barnes, C. A., Witter, M. P., Moser, M., & Moser, E. I. (2010) · Neuron · doi:10.1016/j.neuron.2010.08.042 · Cited by 260 · see citing works
Naber, P. A., da Silva, F. H. L., & Witter, M. P. (2001) · Hippocampus · doi:10.1002/hipo.1028 · Cited by 258 · 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
Varga, C., Golshani, P., & Soltesz, I. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1210929109 · Cited by 253 · see citing works
Buzsáki, G., Czopf, J., Kondákor, I., & Kellényi, L. (1986) · Brain Research · doi:10.1016/0006-8993(86)90729-8 · Cited by 250 · see citing works
Self-citationInterneurons hyperpolarize pyramidal cells along their entire somatodendritic axis
Glickfeld, L. L., Roberts, J. D. B., Somogyi, P., & Scanziani, M. (2008) · Nature Neuroscience · doi:10.1038/nn.2230 · Cited by 238 · see citing works
Mechanisms of Inhibition within the Telencephalon: “Where the Wild Things Are”
Fishell, G., & Rudy, B. (2011) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-061010-113717 · Cited by 233 · see citing works
Cell-Type-Specific Synchronization of Neural Activity in FEF with V4 during Attention
Gregoriou, G. G., Gotts, S. J., & Desimone, R. (2012) · Neuron · doi:10.1016/j.neuron.2011.12.019 · Cited by 229 · see citing works
Slow and Fast Gamma Rhythms Coordinate Different Spatial Coding Modes in Hippocampal Place Cells
Bieri, K. W., Bobbitt, K. N., & Colgin, L. L. (2014) · Neuron · doi:10.1016/j.neuron.2014.03.013 · Cited by 221 · see citing works
Factors mediating powerful voltage attenuation along CA1 pyramidal neuron dendrites
Golding, N. L., Mickus, T. J., Katz, Y., Kath, W. L., & Spruston, N. (2005) · The Journal of Physiology · doi:10.1113/jphysiol.2005.086793 · Cited by 216 · see citing works
Activity dynamics and behavioral correlates of CA3 and CA1 hippocampal pyramidal neurons
Mizuseki, K., Royer, S., Diba, K., & Buzsáki, G. (2012) · Hippocampus · doi:10.1002/hipo.22002 · Cited by 216 · see citing works
Self-citationThe Spiking Component of Oscillatory Extracellular Potentials in the Rat Hippocampus
Schomburg, E. W., Anastassiou, C. A., Buzsáki, G., & Koch, C. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.0656-12.2012 · Cited by 205 · see citing works
Self-citationDendritic Mechanisms Underlying Rapid Synaptic Activation of Fast-Spiking Hippocampal Interneurons
Hu, H., Martina, M., & Jonas, P. (2010) · Science · doi:10.1126/science.1177876 · Cited by 202 · see citing works
Removal of Spurious Correlations Between Spikes and Local Field Potentials
Zanos, T. P., Mineault, P., & Pack, C. C. (2010) · Journal of Neurophysiology · doi:10.1152/jn.00642.2010 · Cited by 192 · see citing works
Dudman, J. T., Tsay, D., & Siegelbaum, S. A. (2007) · Neuron · doi:10.1016/j.neuron.2007.10.020 · Cited by 192 · see citing works
Behavior-Dependent Coordination of Multiple Theta Dipoles in the Hippocampus
Montgomery, S. M., Betancur, M. I., & Buzsáki, G. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.4339-08.2009 · Cited by 190 · see citing works
Self-citationDirect cortical input modulates plasticity and spiking in CA1 pyramidal neurons
Remondes, M., & Schuman, E. M. (2002) · Nature · doi:10.1038/416736a · Cited by 189 · see citing works
Gamma and the Coordination of Spiking Activity in Early Visual Cortex
Jia, X., Tanabe, S., & Kohn, A. (2013) · Neuron · doi:10.1016/j.neuron.2012.12.036 · Cited by 176 · see citing works
Layer-Specific GABAergic Control of Distinct Gamma Oscillations in the CA1 Hippocampus
Lasztóczi, B., & Klausberger, T. (2014) · Neuron · doi:10.1016/j.neuron.2014.01.021 · Cited by 170 · see citing works
Exploring the role of context‐dependent hippocampal activity in spatial alternation behavior
Ainge, J. A., van der Meer, M. A. A., Langston, R. F., & Wood, E. R. (2007) · Hippocampus · doi:10.1002/hipo.20301 · Cited by 169 · see citing works
Temporal synchrony and gamma-to-theta power conversion in the dendrites of CA1 pyramidal neurons
Vaidya, S. P., & Johnston, D. (2013) · Nature Neuroscience · doi:10.1038/nn.3562 · Cited by 158 · see citing works
Hippocampal CA1 spiking during encoding and retrieval: Relation to theta phase
Manns, J. R., Zilli, E. A., Ong, K. C., Hasselmo, M. E., & Eichenbaum, H. (2006) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2006.05.007 · Cited by 139 · see citing works
Diba, K., & Buzsáki, G. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.3824-08.2008 · Cited by 138 · see citing works
Self-citationThe morphoelectrotonic transform: a graphical approach to dendritic function
Zador, A. M., Agmon-Snir, H., & Segev, I. (1995) · Journal of Neuroscience · doi:10.1523/jneurosci.15-03-01669.1995 · Cited by 135 · see citing works
Stimulus repetition modulates gamma-band synchronization in primate visual cortex
Brunet, N. M., Bosman, C. A., Vinck, M., Roberts, M., Oostenveld, R., Desimone, R., De Weerd, P., & Fries, P. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1309714111 · Cited by 130 · see citing works
On High-Frequency Field Oscillations (>100 Hz) and the Spectral Leakage of Spiking Activity
Scheffer-Teixeira, R., Belchior, H., Leão, R. N., Ribeiro, S. T. G., & Tort, A. B. L. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.4217-12.2013 · Cited by 128 · see citing works
Basu, J., Srinivas, K. V., Cheung, S. K., Taniguchi, H., Huang, Z. J., & Siegelbaum, S. A. (2013) · Neuron · doi:10.1016/j.neuron.2013.07.001 · Cited by 122 · see citing works
Cabral, H., Vinck, M. A., Fouquet, C., Pennartz, C. M. A., Rondi‐Reig, L., & Battaglia, F. P. (2014) · Neuron · doi:10.1016/j.neuron.2013.11.010 · Cited by 114 · see citing works
Akam, T. E., & Kullmann, D. M. (2012) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1002760 · Cited by 93 · cited 1× · see citing works
“…interregional communication (Singer, 1993; Fries, 2005), this hypothesis remains hotly debated (Shadlen and Movshon, 1999; Kopell et al., 2000; Fries, 2009; Ray and Maunsell, 2010; Fell and Axmacher, 2011; Bosman et al., 2012; Akam and Kullmann, 2012; Jia et al., 2013; Srinath and Ray, 2014).”
BackgroundFernández‐Ruiz, A., Makarov, V. A., Benito, N., & Herreras, Ó. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.4499-11.2012 · Cited by 81 · see citing works
Self-citationZemankovics, R., Veres, J. M., Oren, I., & Hájos, N. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.3680-12.2013 · Cited by 74 · see citing works
Environmental novelty elicits a later theta phase of firing in CA1 but not subiculum
Lever, C., Burton, S., Jeewajee, A., Wills, T. J., Cacucci, F., Burgess, N., & O'Keefe, J. M. (2009) · Hippocampus · doi:10.1002/hipo.20671 · Cited by 73 · see citing works
Patterned Activity in Stratum Lacunosum Moleculare Inhibits CA1 Pyramidal Neuron Firing
Dvorak-Carbone, H., & Schuman, E. M. (1999) · Journal of Neurophysiology · doi:10.1152/jn.1999.82.6.3213 · Cited by 71 · see citing works
Stewart, M., Quirk, G., Barry, M. K., & Fox, S. E. (1992) · Experimental Brain Research · doi:10.1007/bf00229252 · Cited by 70 · see citing works
Effect of amplitude correlations on coherence in the local field potential
Srinath, R., & Ray, S. (2014) · Journal of Neurophysiology · doi:10.1152/jn.00851.2013 · Cited by 60 · see citing works
Benito, N., Fernández‐Ruiz, A., Makarov, V. A., et al. (2013) · Cerebral Cortex · doi:10.1093/cercor/bht022 · Cited by 58 · see citing works
Self-citationLong-Term Depression of Temporoammonic-CA1 Hippocampal Synaptic Transmission
Dvorak-Carbone, H., & Schuman, E. M. (1999) · Journal of Neurophysiology · doi:10.1152/jn.1999.81.3.1036 · Cited by 52 · see citing works
Mizuseki, K., Diba, K., Pastalkova, E., Teeters, J., Sirota, A., & Buzsáki, G. (2014) · F1000Research · doi:10.12688/f1000research.3895.1 · Cited by 50 · see citing works
Self-citationFernández‐Ruiz, A., & Herreras, Ó. (2013) · Frontiers in Computational Neuroscience · doi:10.3389/fncom.2013.00005 · Cited by 48 · see citing works
Self-citationDistal Dendritic Inputs Control Neuronal Activity by Heterosynaptic Potentiation of Proximal Inputs
Han, E. B., & Heinemann, S. F. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.3219-12.2013 · Cited by 42 · see citing works
Untangling cross-frequency coupling in neurosciencePreprint
Aru, J., Aru, J., Priesemann, V., et al. (2014) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/005926 · Cited by 41 · see citing works
Possible physiological role of the perforant path‐CA1 projection
Buzsáki, G., Penttonen, M., Bragin, A., Nádasdy, Z., & Chrobak, J. J. (1995) · Hippocampus · doi:10.1002/hipo.450050210 · Cited by 40 · see citing works
Self-citationEpisodic memory, semantic memory, and amnesia
Squire, L. R., & Zola, S. M. (1998) · Hippocampus · doi:10.1002/(sici)1098-1063(1998)8:3
Flagged first, then by citations
Cited by
Sorted by citations
Rhythms for cognition: communication through coherence
Fries, P. (2015) · Neuron · doi:10.1016/j.neuron.2015.09.034 · Cited by 2,725 · 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
Self-citationMichalareas, G., Vezoli, J., van Pelt, S., Schoffelen, J.-M., Kennedy, H., & Fries, P. (2016) · Neuron · doi:10.1016/j.neuron.2015.12.018 · Cited by 696 · see citing works
Rhythms of the hippocampal network
Colgin, L. L. (2016) · Nature reviews. Neuroscience · doi:10.1038/nrn.2016.21 · Cited by 654 · see citing works
Long-duration hippocampal sharp wave ripples improve memory
Fernández-Ruiz, A., Oliva, A., Fermino de Oliveira, E., Rocha-Almeida, F., Tingley, D., & Buzsáki, G. (2019) · Science · doi:10.1126/science.aax0758 · Cited by 490 · see citing works
Self-citationRespiration-Entrained Brain Rhythms Are Global but Often Overlooked
Tort, A. B. L., Brankačk, J., & Draguhn, A. (2018) · Trends in Neurosciences · doi:10.1016/j.tins.2018.01.007 · Cited by 335 · see citing works
Gating of hippocampal activity, plasticity, and memory by entorhinal cortex long-range inhibition
Basu, J., Zaremba, J. D., Cheung, S. K., Hitti, F. L., Zemelman, B. V., Losonczy, A., & Siegelbaum, S. A. (2016) · Science · doi:10.1126/science.aaa5694 · Cited by 274 · see citing works
Hippocampal sharp-wave ripples linked to visual episodic recollection in humans
Norman, Y., Yeagle, E. M., Khuvis, S., Harel, M., Mehta, A. D., & Malach, R. (2019) · Science · doi:10.1126/science.aax1030 · Cited by 270 · see citing works
Bezaire, M. J., Raikov, I., Burk, K., Vyas, D., & Soltesz, I. (2016) · eLife · doi:10.7554/elife.18566 · Cited by 198 · see citing works
Functional fission of parvalbumin interneuron classes during fast network events
Varga, C., Oijala, M., Lish, J., Szabo, G. G., Bezaire, M., Marchionni, I., Golshani, P., & Soltesz, I. (2014) · eLife · doi:10.7554/elife.04006 · Cited by 130 · see citing works
Bergel, A., Deffieux, T., Demené, C., Tanter, M., & Cohen, I. (2018) · Nature Communications · doi:10.1038/s41467-018-07752-3 · Cited by 117 · see citing works
Ventral hippocampal OLM cells control type 2 theta oscillations and response to predator odor
Mikulovic, S., Restrepo, C. E., Siwani, S., Bauer, P., Pupe, S., Tort, A. B. L., Kullander, K., & Leão, R. N. (2018) · Nature Communications · doi:10.1038/s41467-018-05907-w · Cited by 114 · see citing works
Sharif, F., Tayebi, B., Buzsáki, G., Royer, S., & Fernandez-Ruiz, A. (2021) · Neuron · doi:10.1016/j.neuron.2020.10.034 · Cited by 111 · see citing works
Self-citationHippocampo-cortical circuits for selective memory encoding, routing, and replay
Harvey, R. E., Robinson, H. L., Liu, C., Oliva, A., & Fernandez-Ruiz, A. (2023) · Neuron · doi:10.1016/j.neuron.2023.04.015 · Cited by 101 · see citing works
A cognitive process occurring during sleep is revealed by rapid eye movements
Senzai, Y., & Scanziani, M. (2022) · Science · doi:10.1126/science.abp8852 · Cited by 88 · see citing works
Fast gamma rhythms in the hippocampus promote encoding of novel object-place pairings
Zheng, C., Bieri, K. W., Hwaun, E., & Colgin, L. L. (2016) · eNeuro · doi:10.1523/eneuro.0001-16.2016 · Cited by 79 · see citing works
Radwan, B., Dvorak, D., & Fenton, A. A. (2016) · Neurobiology of Disease · doi:10.1016/j.nbd.2016.01.003 · Cited by 63 · see citing works
Katona, L., Micklem, B., Borhegyi, Z., Swiejkowski, D. A., Valenti, O., Viney, T. J., Kotzadimitriou, D., Klausberger, T., & Somogyi, P. (2017) · Hippocampus · doi:10.1002/hipo.22696 · Cited by 50 · see citing works
Hippocampal Network Dynamics during Rearing Episodes
Barth, A. M., Domonkos, A., Fernandez-Ruiz, A., Freund, T. F., & Varga, V. (2018) · Cell Reports · doi:10.1016/j.celrep.2018.04.021 · Cited by 46 · see citing works
Differential Impact of Acute and Chronic Stress on CA1 Spatial Coding and Gamma Oscillations
Tomar, A., Polygalov, D., & McHugh, T. J. (2021) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2021.710725 · Cited by 21 · see citing works
Kloc, M. L., Chen, Y., Daglian, J. M., Holmes, G. L., Baram, T. Z., & Barry, J. M. (2023) · Hippocampus · doi:10.1002/hipo.23541 · Cited by 21 · see citing works
- Authors
- Schomburg, E. W., Fernández-Ruiz, A., Mizuseki, K., Berényi, A., Anastassiou, C. A., Koch, C., & Buzsáki, G.
- Affiliations
- California Institute of Technology (US)
- Allen Institute for Brain Science (US)
- University of Szeged (HU)
- New York University (US)
- Corresponding author
- Buzsáki, György
- Venue
- Neuron
- Publisher
- Elsevier BV
- Published
- 2014-10
- Volume
- 84
- Issue
- 2
- Pages
- 470-485
- ISSN
- 0896-6273 (ISSN-L)
- PMC
- PMC4253689
- OpenAlex
- W2170430044
- Cited by
- 465
- References
- 110
- Citations by year
- 2026: 22 · 2025: 48 · 2024: 30 · 2023: 40 · 2022: 40 · 2021: 42 · 2020: 42 · 2019: 53 · 2018: 33 · 2017: 34 · 2016: 54 · 2015: 21 · 2014: 3
- FWCI
- 20.82
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Neuron (publishedVersion)
- PubMed (publishedVersion)
- SZTE Publicatio Repozitórium (University of Szeged) (acceptedVersion, other-oa)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- CaltechAUTHORS (California Institute of Technology) (submittedVersion)
- Funders
- National Institute of Mental Health (R01MH054671, R01MH102840, MH54671)
- National Institute of Neurological Disorders and Stroke (NS074015, R01NS034994, R01NS074015, NS-34994)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Keywords
- gamma oscillations, theta oscillations, entorhinal cortex, hippocampus, CA1, CA3, local field potentials, phase synchronization, interregional communication, memory demand, navigation, afferent input
- MeSH terms
- Action Potentials, Animals, Hippocampus, Interneurons, Male, Models, Neurological, Theta Rhythm, Pyramidal Cells, Entorhinal Cortex, Rats, Long-Evans, Gamma Rhythm
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