The DOI matches its Crossref record; 33 of the 33 references it cites were found in a registry or an index.
Routing of spike series by dynamic circuits in the hippocampus
Abstract
Recurrent inhibitory loops are simple neuronal circuits found in the central nervous system, yet little is known about the physiological rules governing their activity. Here we use simultaneous somatic and dendritic recordings in rat hippocampal slices to show that during a series of action potentials in pyramidal cells recurrent inhibition rapidly shifts from their soma to the apical dendrites. Two distinct inhibitory circuits are sequentially recruited to produce this shift: one, time-locked with submillisecond precision to the onset of the action potential series, transiently inhibits the somatic and perisomatic regions of pyramidal cells; the other, activated in proportion to the rate of action potentials in the series, durably inhibits the distal apical dendrites. These two operating modes result from the synergy between pre- and postsynaptic properties of excitatory synapses onto recurrent inhibitory neurons with distinct projection patterns. Thus, the onset of a series of action potentials and the rate of action potentials in the series are selectively captured and transformed into different spatial patterns of recurrent inhibition.
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In the citing paper
“excitatory inputs onto Sst INs, apparently regardless of subtypes, are strongly facilitating”
From GABAergic Interneurons in the Neocortex: From Cellular Properties to Circuits (2016) · cites this paper as Pouille and Scanziani, 2004
In the citing paper
“Indeed, the restriction of horizontally oriented O-LM soma and spiny dendrites within s.o. and the alveus dictates that the dominant source of excitatory recruitment is from CA1 pyramidal cell collaterals while the preferential axonal targeting to s.l.m. then distributes inhibition back to the distal apical dendritic tufts of CA1 pyramidal cells to gate excitatory input from the entorhinal cortex”
From Hippocampal GABAergic Inhibitory Interneurons (2017) · cites this paper as [923]
In the citing paper
“Trains of action potentials from CA1 pyramidal cells drive excitation onto two populations of interneurons termed “onset transient” and “late persistent” interneurons (923).”
From Hippocampal GABAergic Inhibitory Interneurons (2017) · cites this paper as [923]
In the citing paper
“Pouille and Scanziani (923) provided the first demonstration that recurrent inhibition onto CA1 pyramidal cells occurs via a dynamic rerouting of inhibitory drive that commences via perisomatic inhibitory input followed by a delayed primarily dendritic inhibition.”
From Hippocampal GABAergic Inhibitory Interneurons (2017) · cites this paper as [923]
Citations
Cites
Interneurons of the hippocampus
Freund, T. F., & Buzsáki, G. (1998) · Hippocampus · doi:10.1002/(sici)1098-1063(1996)6:4 · Cited by 3,478
Theoretical Neuroscience: Computational and Mathematical Modeling of Neural Systems
Dayan, P., & Abbott, L. F. (2001) · Cited by 3,153
Spikes: Exploring the Neural Code
Rieke, F. M., Warland, D., van Steveninck, R. R. D. R., & Bialek, W. (1996) · Medical Entomology and Zoology · Cited by 2,844
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 2,643
Brain-state- and cell-type-specific firing of hippocampal interneurons in vivo
Klausberger, T., Magill, P. J., Márton, L. F., Roberts, J. D. B., Cobden, P. M., Buzsáki, G., & Somogyi, P. (2003) · Nature · doi:10.1038/nature01374 · Cited by 1,345
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
Self-citationMegı́as, M., Emri, Z., Freund, T. F., & Gulyás, A. I. (2001) · Neuroscience · doi:10.1016/s0306-4522(00)00496-6 · Cited by 950
Somogyi, P., Tamás, G., Luján, R., & Buhl, E. H. (1998) · Brain Research Reviews · doi:10.1016/s0165-0173(97)00061-1 · Cited by 876
Activity-Dependent Action Potential Invasion and Calcium Influx into Hippocampal CA1 Dendrites
Spruston, N., Schiller, Y., Stuart, G. J., & Sakmann, B. J. (1995) · Science · doi:10.1126/science.7716524 · Cited by 839
Stuart, G. J., Dodt, H., & Sakmann, B. J. (1993) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/bf00374949 · Cited by 800
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Items 101–200 of 425
Local Feedback Inhibition Tightly Controls Rapid Formation of Hippocampal Place Fields
Rolotti, S. V., Ahmed, M. S., Szoboszlay, M., Geiller, T., Negrean, A., Blockus, H., Gonzalez, K. C., Sparks, F. T., Canales, A. S. S., Tuttman, A. L., et al. (2021) · Neuron · doi:10.1016/j.neuron.2021.12.003 · Cited by 115
Stratum oriens horizontal interneurone diversity and hippocampal network dynamics
Maccaferri, G. (2004) · The Journal of Physiology · doi:10.1113/jphysiol.2004.077081 · Cited by 114
Lawrence, J. J., Statland, J. M., Grinspan, Z. M., & McBain, C. J. (2006) · The Journal of Physiology · doi:10.1113/jphysiol.2005.100875 · Cited by 109
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Berger, T. K., Silberberg, G., Perin, R., & Markram, H. (2010) · PLoS Biology · doi:10.1371/journal.pbio.1000473 · Cited by 112
Synaptic and circuit mechanisms promoting broadband transmission of olfactory stimulus dynamics
Nagel, K. I., Hong, E. J., & Wilson, R. I. (2014) · Nature Neuroscience · doi:10.1038/nn.3895 · Cited by 108
Suzuki, N., & Bekkers, J. M. (2009) · The Journal of Comparative Neurology · doi:10.1002/cne.22295 · Cited by 107
Neocortical Interneurons: From Diversity, Strength
Moore, C. I., Carlén, M., Knoblich, U., & Cardin, J. A. (2010) · Cell · doi:10.1016/j.cell.2010.07.005 · Cited by 113
Carlson, G. C., Talbot, K., Halene, T. B., Gandal, M. J., Kazi, H. A., Schlosser, L., Phung, Q. H., Gur, R. E., Arnold, S. E., & Siegel, S. J. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1109625108 · Cited by 103
Obermayer, J., Heistek, T. S., Kerkhofs, A., Goriounova, N. A., Kroon, T., Baayen, J. C., Idema, S., Testa-Silva, G., Couey, J. J., & Mansvelder, H. D. (2018) · Nature Communications · doi:10.1038/s41467-018-06628-w · Cited by 114
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Chiovini, B., Turi, G. F., Katona, G., Kaszás, A., Pálfi, D., Maák, P. A., Szalay, G., Szabó, M. F., Szabó, G., Szadai, Z., et al. (2014) · Neuron · doi:10.1016/j.neuron.2014.04.004 · Cited by 101
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Karpova, A. Y., Tervo, D. G. R., Gray, N. W., & Svoboda, K. (2005) · Neuron · doi:10.1016/j.neuron.2005.11.015 · Cited by 100
Rubinstein, M., Westenbroek, R. E., Yu, F. H., Jones, C. J., Scheuer, T., & Catterall, W. A. (2014) · Neurobiology of Disease · doi:10.1016/j.nbd.2014.09.017 · Cited by 97
Motor Cortex Broadly Engages Excitatory and Inhibitory Neurons in Somatosensory Barrel Cortex
Kinnischtzke, A. K., Simons, D. J., & Fanselow, E. E. (2013) · Cerebral Cortex · doi:10.1093/cercor/bht085 · Cited by 105
Quantal Size Is Independent of the Release Probability at Hippocampal Excitatory Synapses
Biró, Á. A., Holderith, N. B., & Nusser, Z. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.3688-04.2005 · Cited by 102
Dendritic inhibition mediated by O-LM and bistratified interneurons in the hippocampus
ller, C. M. ⁄., & Remy, S. (2014) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2014.00023 · Cited by 103
Spencer, K. (2009) · Frontiers in Human Neuroscience · doi:10.3389/neuro.09.033.2009 · Cited by 102
Goldin, M., Epsztein, J., Jorquera, I., Represa, A., Ben-Ari, Y., Crépel, V., & Cossart, R. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.1237-07.2007 · Cited by 93
The Role of the GABAergic System in Diseases of the Central Nervous System
Zhang, W., Xiong, B., Zhang, L.-Q., Huang, X., Yuan, X., Tian, Y., & Tian, X. (2021) · Neuroscience · doi:10.1016/j.neuroscience.2021.06.037 · Cited by 97
Target-cell-specific short-term plasticity in local circuits
Blackman, A. V., Abrahamsson, T., Costa, R. P., Lalanne, T., & Sjöström, P. J. (2013) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2013.00011 · Cited by 100
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Feller, M. B., & Scanziani, M. (2005) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2005.01.012 · Cited by 92
Self-citationMarinelli, S., Pacioni, S., Bisogno, T., Marzo, V. D., Prince, D. A., Huguenard, J. R., & Bacci, A. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.0847-08.2008 · Cited by 92
Target-Dependent Feedforward Inhibition Mediated by Short-Term Synaptic Plasticity in the Cerebellum
Bao, J., Reim, K., & Sakaba, T. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.0276-10.2010 · Cited by 100
Szabo, G. G., Holderith, N. B., Gulyás, A. I., Freund, T. F., & Hájos, N. (2010) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2010.07292.x · Cited by 94
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 89
Park, K., Lee, J., Jang, H. J., Richards, B. A., Kohl, M. M., & Kwag, J. (2020) · BMC Biology · doi:10.1186/s12915-019-0732-7 · Cited by 87
Elfant, D., Pál, B. Z., Emptage, N., & Capogna, M. (2008) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2007.06001.x · Cited by 82
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Cornford, J. H., Mercier, M. S., Leite, M., Magloire, V., Häusser, M., & Kullmann, D. M. (2019) · eLife · doi:10.7554/elife.49872 · Cited by 84
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Palmer, L. M., Murayama, M., & Larkum, M. E. (2012) · Frontiers in Neural Circuits · doi:10.3389/fncir.2012.00026 · Cited by 88
Hu, H., Ma, Y., & Agmon, A. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.4881-10.2011 · Cited by 81
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Inagaki, H., Chen, S., Daie, K., Finkelstein, A., Fontolan, L., Romani, S., & Svoboda, K. (2022) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-092021-121730 · Cited by 77
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Aponte, Y., Bischofberger, J., & Jónás, P. (2008) · The Journal of Physiology · doi:10.1113/jphysiol.2007.147298 · Cited by 81
Traub, R. D., Pais, I., Bibbig, A., LeBeau, F. E. N., Buhl, E. H., Garner, H., Monyer, H., & Whittington, M. A. (2005) · Journal of Neurophysiology · doi:10.1152/jn.00069.2005 · Cited by 82
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Brown, J. T., Davies, C. H., & Randall, A. D. (2007) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2007.05544.x · Cited by 77
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Beierlein, M., & Regehr, W. G. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.0958-06.2006 · Cited by 76
Synapse-specific inhibitory control of hippocampal feedback inhibitory circuit
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Kerr, A. M., Reisinger, E., & Jonas, P. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0800621105 · Cited by 75
Crowley, J. J., Fioravante, D., & Regehr, W. G. (2009) · Neuron · doi:10.1016/j.neuron.2009.09.004 · Cited by 74
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Differential Activity-Dependent, Homeostatic Plasticity of Two Neocortical Inhibitory Circuits
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Schwabe, L., Ichida, J. M., Shushruth, S., Mangapathy, P., & Angelucci, A. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2010.01.032 · Cited by 72
Stachniak, T. J., Sylwestrak, E., Scheiffele, P., Hall, B. J., & Ghosh, A. (2019) · Journal of Neuroscience · doi:10.1523/jneurosci.2276-18.2019 · Cited by 72
Beierlein, M., Fioravante, D., & Regehr, W. G. (2007) · Neuron · doi:10.1016/j.neuron.2007.06.002 · Cited by 78
Cortical Circuits of Callosal GABAergic Neurons
Rock, C., Zurita, H., Lebby, S., Wilson, C. J., & Apicella, A. J. (2017) · Cerebral Cortex · doi:10.1093/cercor/bhx025 · Cited by 73
Shaping inhibition: activity dependent structural plasticity of GABAergic synapses
Flores, C. E., & Méndez, P. (2014) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2014.00327 · Cited by 74
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Zhang, W., & Buckmaster, P. S. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.6199-08.2009 · Cited by 75
Short-term ionic plasticity at GABAergic synapses
Raimondo, J. V., Markram, H., & Akerman, C. J. (2012) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2012.00005 · Cited by 71
Neocortical calretinin neurons in primates: increase in proportion and microcircuitry structure
aja, D. D. ⁄., Hladnik, A., Bičanić, I., Baković, M., & Petanjek, Z. (2014) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2014.00103 · Cited by 73
Guyonneau, R., VanRullen, R., & Thorpe, S. J. (2004) · Journal of Physiology-Paris · doi:10.1016/j.jphysparis.2005.09.004 · Cited by 69
Hertäg, L., & Sprekeler, H. (2019) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1006999 · Cited by 75
All Optical Interface for Parallel, Remote, and Spatiotemporal Control of Neuronal Activity
Wang, S., Szobota, S., Wang, Y., Volgraf, M., Liu, Z., Sun, C., Trauner, D. H., Isacoff, E. Y., & Zhang, X. (2007) · Nano Letters · doi:10.1021/nl072783t · Cited by 68
Active Dendritic Conductances Dynamically Regulate GABA Release from Thalamic Interneurons
Acuna, C., Brenowitz, S. D., & Regehr, W. G. (2008) · Neuron · doi:10.1016/j.neuron.2007.12.022 · Cited by 70
The contribution of synaptic location to inhibitory gain control in pyramidal cells
Pouille, F., Watkinson, O., Scanziani, M., & Trevelyan, A. J. (2013) · Physiological Reports · doi:10.1002/phy2.67 · Cited by 65
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Piskorowski, R. A., & Chevaleyre, V. (2011) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-011-0769-4 · Cited by 72
Space matters: local and global dendritic Ca2+ compartmentalization in cortical interneurons
Goldberg, J. H., & Yuste, R. (2005) · Trends in Neurosciences · doi:10.1016/j.tins.2005.01.005 · Cited by 65
Creating diverse synapses from the same molecules
Nusser, Z. (2018) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2018.01.001 · Cited by 71
Interneuron Types and Their Circuits in the Basolateral Amygdala
Hájos, N. (2021) · Frontiers in Neural Circuits · doi:10.3389/fncir.2021.687257 · Cited by 66
Roux, N. L., Cabezas, C., Böhm, U. L., & Poncer, J. C. (2013) · The Journal of Physiology · doi:10.1113/jphysiol.2012.245852 · Cited by 58
Assortment of GABAergic Plasticity in the Cortical Interneuron Melting Pot
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Data‐driven integration of hippocampal CA1 synaptic physiology in silico
Ecker, A., Romani, A., Sáray, S., Káli, S., Migliore, M., Falck, J. E., Lange, S., Mercer, A., Thomson, A. M., Muller, E. B., et al. (2020) · Hippocampus · doi:10.1002/hipo.23220 · Cited by 55
CA1 pyramidal cell diversity is rooted in the time of neurogenesis
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Neuropeptide F regulates courtship in Drosophila through a male-specific neuronal circuit
Liu, W., Ganguly, A., Huang, J., Wang, Y., Ni, J. D., Gurav, A. S., Aguilar, M. A., & Montell, C. (2019) · eLife · doi:10.7554/elife.49574 · Cited by 58
Barbero‐Castillo, A., Mateos‐Aparicio, P., Porta, L. D., Camassa, A., Perez-Mendez, L., & Sanchez-Vives, M. V. (2021) · Journal of Neuroscience · doi:10.1523/jneurosci.1837-20.2021 · Cited by 53
Parrish, R. R., Codadu, N. K., Scott, C. M., & Trevelyan, A. J. (2019) · The Journal of Physiology · doi:10.1113/jp277749 · Cited by 55
Éltes, T., Kirizs, T., Nusser, Z., & Holderith, N. B. (2017) · Journal of Neuroscience · doi:10.1523/jneurosci.2024-16.2017 · Cited by 53
TRPV1 regulates excitatory innervation of OLM neurons in the hippocampus
Hurtado-Zavala, J. I., Ramachandran, B., Ahmed, S., Halder, R., Bolleyer, C., Awasthi, A., Stahlberg, M. A., Wagener, R. J., Anderson, K., Drenan, R. M., et al. (2017) · Nature Communications · doi:10.1038/ncomms15878 · Cited by 52
Hippocampal hyperactivity in a rat model of Alzheimer’s disease
Sosulina, L., Mittag, M., Geis, H., Hoffmann, K., Klyubin, I. V., Qi, Y., Steffen, J., Friedrichs, D., Henneberg, N., Fuhrmann, F., et al. (2021) · Journal of Neurochemistry · doi:10.1111/jnc.15323 · Cited by 55
Stella, F., & Treves, A. (2011) · Neural Plasticity · doi:10.1155/2011/683961 · Cited by 59
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
Aldahabi, M., Balint, F., Holderith, N., Lorincz, A., Reva, M., & Nusser, Z. (2022) · Neuron · doi:10.1016/j.neuron.2022.09.035 · Cited by 50
Bartos, M., Alle, H., & Vida, I. (2010) · Neuropharmacology · doi:10.1016/j.neuropharm.2010.12.017 · Cited by 53
Luo, X. M., Guet-McCreight, A., Villette, V., Francavilla, R., Marino, B., Chamberland, S., Skinner, F. K., & Topolnik, L. (2019) · Cerebral Cortex · doi:10.1093/cercor/bhz334 · Cited by 52
González‐Burgos, G., Kroener, S., Seamans, J. K., Lewis, D. A., & Barrionuevo, G. (2005) · Journal of Neurophysiology · doi:10.1152/jn.00698.2005 · Cited by 51
Understanding the molecular diversity of synapses
van Oostrum, M., & Schuman, E. M. (2025) · Nature Reviews Neuroscience · doi:10.1038/s41583-024-00888-w · Cited by 49
Francioni, V., & Harnett, M. T. (2021) · Neuroscience · doi:10.1016/j.neuroscience.2021.05.038 · Cited by 50
A Diversity of Synaptic Filters Are Created by Temporal Summation of Excitation and Inhibition
George, A. A., Lyons-Warren, A. M., Ma, X., & Carlson, B. A. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.1424-11.2011 · Cited by 50
Bartley, A. F., & Dobrunz, L. E. (2015) · European Journal of Neuroscience · doi:10.1111/ejn.12898 · Cited by 49
Palacios-Filardo, J., Udakis, M., Brown, G. A., Tehan, B. G., Congreve, M., Nathan, P. J., Brown, A., & Mellor, J. R. (2021) · Nature Communications · doi:10.1038/s41467-021-25280-5 · Cited by 51
Synapse‐specific expression of calcium‐permeable AMPA receptors in neocortical layer 5
Lalanne, T., Oyrer, J., Mancino, A. S., Gregor, E., Chung, A. J., Huynh, L., Burwell, S., Maheux, J., Farrant, M., & Sjöström, P. J. (2015) · The Journal of Physiology · doi:10.1113/jp271394 · Cited by 49
Structured inhibitory activity dynamics in new virtual environments
Arriaga, M. A., & Han, E. B. (2019) · eLife · doi:10.7554/elife.47611 · Cited by 49
Chapter 14 Long-term synaptic plasticity in hippocampal feedback inhibitory networks
Pelletier, J. G., & Lacaille, J. (2008) · Progress in brain research · doi:10.1016/s0079-6123(07)00014-3 · Cited by 49
Copying and Evolution of Neuronal Topology
Fernando, C., Karishma, K. K., & Szathmáry, E. (2008) · PLoS ONE · doi:10.1371/journal.pone.0003775 · Cited by 47
González‐Burgos, G., Rotaru, D. C., Zaitsev, A. V., Povysheva, N. V., & Lewis, D. A. (2008) · Journal of Neurophysiology · doi:10.1152/jn.91161.2008 · Cited by 49
Lee, C.-T., Kao, M.-H., Hou, W., Wei, Y.-T., Chen, C., & Lien, C. (2016) · Scientific Reports · doi:10.1038/srep36885 · Cited by 46
Polysynaptic subcircuits in the neocortex: spatial and temporal diversity
Silberberg, G. (2008) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2008.08.009 · Cited by 46
Hippocampal microcircuit dynamics probed using optical imaging approaches
Coulter, D. A., Yue, C., Ang, C. W., Weissinger, F., Goldberg, E. M., Hsu, F., Carlson, G. C., & Takano, H. (2011) · The Journal of Physiology · doi:10.1113/jphysiol.2010.202184 · Cited by 47
Rapid Dynamic Changes of Dendritic Inhibition in the Dentate Gyrus by Presynaptic Activity Patterns
Liu, Y., Cheng, J., & Lien, C. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.2566-13.2014 · Cited by 47
Inhibition shapes the organization of hippocampal representations
McKenzie, S. (2017) · Hippocampus · doi:10.1002/hipo.22803 · Cited by 46
Matt, L., Michalakis, S., Hofmann, F. B., Hammelmann, V., Ludwig, A., Biel, M., & Kleppisch, T. (2010) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-010-0446-z · Cited by 44
Strüber, M., Jonas, P., & Bartos, M. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1412996112 · Cited by 43
Differential regulation at functionally divergent release sites along a common axon
Pelkey, K. A., & McBain, C. J. (2007) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2007.04.008 · Cited by 43
Apicella, A. J., & Marchionni, I. (2022) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2022.811484 · Cited by 45
Kim, M.-H., Radaelli, C., Thomsen, E. R., Monet, D., Chartrand, T., Jorstad, N. L., Mahoney, J. T., Taormina, M. J., Long, B., Baker, K. S., et al. (2023) · eLife · doi:10.7554/elife.81863 · Cited by 46
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Metadata
- Authors
- Pouille, F., & Scanziani, M.
- Affiliations
- University of California San Diego (US)
- Corresponding author
- Scanziani, Massimo
- ORCID
- Scanziani, Massimo
- Venue
- Nature
- Published
- 2004-05-30
- Volume
- 429
- Issue
- 6993
- Pages
- 717-723
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- OpenAlex
- W2047403459
- Cited by
- 434
- References
- 33
- Citations by year
- 2026: 6 · 2025: 11 · 2024: 13 · 2023: 24 · 2022: 20 · 2021: 28 · 2020: 14 · 2019: 24 · 2018: 22 · 2017: 12 · 2016: 12 · 2015: 17 · 2014: 23 · 2013: 17 · 2012: 25
- FWCI
- 8.56
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- RePEc: Research Papers in Economics (submittedVersion)
- Funders
- Foundation for the National Institutes of Health
- Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Keywords
- recurrent inhibition, hippocampus, pyramidal neurons, dendritic inhibition, inhibitory interneurons, excitatory synapses, synaptic plasticity, rat hippocampal slices
- MeSH terms
- Action Potentials, Animals, Dendrites, Electrophysiology, Hippocampus, Interneurons, Rats, Wistar, Excitatory Postsynaptic Potentials, Rats, In Vitro Techniques
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