Cited by 224Cannabis and Cannabinoid ResearchNeuroscience and Neuropharmacology ResearchNeural dynamics and brain function

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Distinct timing in the activity of cannabinoid-sensitive and cannabinoid-insensitive basket cells

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Glickfeld, Lindsey L, Scanziani, Massimo·2006·Nature Neuroscience

DOI 10.1038/nn1688PMC PMC3509385

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Abstract

Cannabinoids are powerful modulators of inhibition, yet the precise spike timing of cannabinoid receptor (CB1R)-expressing inhibitory neurons in relation to other neurons in the circuit is poorly understood. Here we found that the spike timing of CB1R-expressing basket cells, a major target for cannabinoids in the rat hippocampus, was distinct from the other main group of basket cells, the CB1R-negative. Despite receiving the same afferent inputs, the synaptic and biophysical properties of the two cell types were tuned to detect different features of activity. CB1R-negative basket cells responded reliably and immediately to subtle and repetitive excitation. In contrast, CB1R-positive basket cells responded later and did not follow repetitive activity, but were better suited to integrate the consecutive excitation of independent afferents. This temporal separation in the activity of the two basket cell types generated distinct epochs of somatic inhibition that were differentially affected by endocannabinoids.

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Freund, T. F., & Buzsáki, G. (1998) · Hippocampus · doi:10.1002/(sici)1098-1063(1996)6:4 · Cited by 3,478
Endogenous cannabinoids mediate retrograde signalling at hippocampal synapses
Wilson, R. I., & Nicoll, R. A. (2001) · Nature · doi:10.1038/35069076 · Cited by 1,607
Synchronization of neuronal activity in hippocampus by individual GABAergic interneurons
Cobb, S. R., Buhl, E. H., Halasy, K., Paulsen, O., & Somogyi, P. (1995) · Nature · doi:10.1038/378075a0 · Cited by 1,498
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
Presynaptically Located CB1 Cannabinoid Receptors Regulate GABA Release from Axon Terminals of Specific Hippocampal Interneurons
Katona, I., Sperlágh, B., Sı́k, A., Käfalvi, A., Vizi, E. S., Mackie, K., & Freund, T. F. (1999) · The Journal of Neuroscience · doi:10.1523/jneurosci.19-11-04544.1999 · Cited by 1,218
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-citation
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 1,031
Differences between somatic and dendritic inhibition in the hippocampus
Miles, R., Tóth, K., Gulyás, A. I., Hájos, N., & Freund, T. F. (1996) · Neuron · doi:10.1016/s0896-6273(00)80101-4 · Cited by 942
The effects of cannabinoids on the brain
Ameri, A. (1999) · Progress in Neurobiology · doi:10.1016/s0301-0082(98)00087-2 · Cited by 825
Hippocampal CA1 interneurons: an in vivo intracellular labeling study
Sik, A., Penttonen, M., Ylinen, A., & Buzsaki, G. (1995) · The Journal of Neuroscience · doi:10.1523/jneurosci.15-10-06651.1995 · Cited by 669

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Buzsáki, G., & Wang, X.-J. (2012) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-062111-150444 · Cited by 2,796
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
GABAergic Interneurons in the Neocortex: From Cellular Properties to Circuits
Tremblay, R., Lee, S., & Rudy, B. (2016) · Neuron · doi:10.1016/j.neuron.2016.06.033 · Cited by 2,033
“They have been studied in the hippocampus and neocortex, where their properties have been contrasted with those of PV FS basket cells (Freund and Katona, 2007; Glickfeld and Scanziani, 2006; Klausberger et al., 2005).”
How Inhibition Shapes Cortical Activity
Isaacson, J. S., & Scanziani, M. (2011) · Neuron · doi:10.1016/j.neuron.2011.09.027 · Cited by 1,678
Self-citation
Inhibition of inhibition in visual cortex: the logic of connections between molecularly distinct interneurons
Pfeffer, C. K., Xue, M., He, M., Huang, Z. J., & Scanziani, M. (2013) · Nature Neuroscience · doi:10.1038/nn.3446 · Cited by 1,353
Self-citation
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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
Dendritic Excitability and Synaptic Plasticity
Sjöström, P. J., Rancz, E. A., Roth, A., & Häusser, M. (2008) · Physiological Reviews · doi:10.1152/physrev.00016.2007 · Cited by 740
Perisomatic Inhibition
Freund, T. F., & Katona, I. (2007) · Neuron · doi:10.1016/j.neuron.2007.09.012 · Cited by 656
Instantaneous Modulation of Gamma Oscillation Frequency by Balancing Excitation with Inhibition
Atallah, B. V., & Scanziani, M. (2009) · Neuron · doi:10.1016/j.neuron.2009.04.027 · Cited by 614
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Nanodomain coupling between Ca2+ channels and sensors of exocytosis at fast mammalian synapses
Eggermann, E., Bucurenciu, I., Goswami, S. P., & Jonas, P. (2012) · Nature Reviews Neuroscience · doi:10.1038/nrn3125 · Cited by 500
Long-term synaptic plasticity in hippocampal interneurons
Kullmann, D. M., & Lamsa, K. P. (2007) · Nature Reviews Neuroscience · doi:10.1038/nrn2207 · Cited by 340
Oxytocin enhances hippocampal spike transmission by modulating fast-spiking interneurons
Owen, S. F., Tuncdemir, S. N., Bader, P. L., Tirko, N. N., Fishell, G., & Tsien, R. W. (2013) · Nature · doi:10.1038/nature12330 · Cited by 339
The organization of two new cortical interneuronal circuits
Jiang, X., Wang, G., Lee, A. J., Stornetta, R. L., & Zhu, J. J. (2013) · Nature Neuroscience · doi:10.1038/nn.3305 · Cited by 338
Input normalization by global feedforward inhibition expands cortical dynamic range
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Self-citation
Behavior-dependent specialization of identified hippocampal interneurons
Lapray, D., Lasztóczi, B., Lagler, M., Viney, T. J., Katona, L., Valenti, O., Hartwich, K., Borhegyi, Z., Somogyi, P., & Klausberger, T. (2012) · Nature Neuroscience · doi:10.1038/nn.3176 · Cited by 267
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 274
Parvalbumin-Containing Fast-Spiking Basket Cells Generate the Field Potential Oscillations Induced by Cholinergic Receptor Activation in the Hippocampus
Gulyás, A. I., Szabo, G. G., Ulbert, I., Holderith, N. B., Monyer, H., Erdélyi, F., Szabó, G., Freund, T. F., & Hájos, N. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.4104-10.2010 · Cited by 257
Interneurons hyperpolarize pyramidal cells along their entire somatodendritic axis
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Cell-Type-Specific Circuit Connectivity of Hippocampal CA1 Revealed through Cre-Dependent Rabies Tracing
Sun, Y., Nguyen, A. Q., Nguyen, J. P., Le, L., Saur, D., Choi, J., Callaway, E. M., & Xu, X. (2014) · Cell Reports · doi:10.1016/j.celrep.2014.02.030 · Cited by 218
Tasks for inhibitory interneurons in intact brain circuits
Roux, L., & Buzsáki, G. (2015) · Neuropharmacology · doi:10.1016/j.neuropharm.2014.09.011 · Cited by 218
Stringent Specificity in the Construction of a GABAergic Presynaptic Inhibitory Circuit
Betley, J. N., Wright, C. V. E., Kawaguchi, Y., Erdélyi, F., Szabó, G., Jessell, T. M., & Kaltschmidt, J. A. (2009) · Cell · doi:10.1016/j.cell.2009.08.027 · Cited by 224
Postsynaptic origin of CB1‐dependent tonic inhibition of GABA release at cholecystokinin‐positive basket cell to pyramidal cell synapses in the CA1 region of the rat hippocampus
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The Diversity of Cortical Inhibitory Synapses
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Alternating sources of perisomatic inhibition during behavior
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Chen, K., Neu, A. D., Howard, A. L., Földy, C., Echegoyen, J. C., Hilgenberg, L. G. W., Smith, M. J., Mackie, K., & Soltész, I. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.3966-06.2007 · Cited by 157
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Reduction in endocannabinoid tone is a homeostatic mechanism for specific inhibitory synapses
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Bidirectional perisomatic inhibitory plasticity of a Fos neuronal network
Yap, E.-L., Pettit, N. L., Davis, C. P., Nagy, M. A., Harmin, D. A., Golden, E., Dağliyan, O., Lin, C., Rudolph, S., Sharma, N., et al. (2020) · Nature · doi:10.1038/s41586-020-3031-0 · Cited by 154
Fast-Spiking Interneurons Supply Feedforward Control of Bursting, Calcium, and Plasticity for Efficient Learning
Owen, S. F., Berke, J. D., & Kreitzer, A. C. (2018) · Cell · doi:10.1016/j.cell.2018.01.005 · Cited by 158
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Pan, B., Hillard, C. J., & Liu, Q.-S. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.4033-07.2008 · Cited by 142
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Cellular architecture of the mouse hippocampus: A quantitative aspect of chemically defined GABAergic neurons with stereology
Jinno, S., & Kosaka, T. (2006) · Neuroscience Research · doi:10.1016/j.neures.2006.07.007 · Cited by 145
Cortical basket cell dysfunction in schizophrenia
Curley, A. A., & Lewis, D. A. (2012) · The Journal of Physiology · doi:10.1113/jphysiol.2011.224659 · Cited by 136
Basket cell dichotomy in microcircuit function
Armstrong, C., & Soltész, I. (2011) · The Journal of Physiology · doi:10.1113/jphysiol.2011.223669 · Cited by 141
Synaptic Cross Talk between Perisomatic-Targeting Interneuron Classes Expressing Cholecystokinin and Parvalbumin in Hippocampus
Karson, M. A., Tang, A.-H., Milner, T. A., & Alger, B. E. (2009) · The Journal of Neuroscience · doi:10.1523/jneurosci.5264-08.2009 · Cited by 135
All-optical physiology resolves a synaptic basis for behavioral timescale plasticity
Fan, L. Z., Kim, D. K., Jennings, J. H., Tian, H., Wang, P. Y., Ramakrishnan, C., Randles, S., Sun, Y., Thadhani, E., Kim, Y. S., et al. (2023) · Cell · doi:10.1016/j.cell.2022.12.035 · Cited by 136
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
Functional characteristics of parvalbumin‐ and cholecystokinin‐expressing basket cells
Bartos, M., & Elgueta, C. (2012) · The Journal of Physiology · doi:10.1113/jphysiol.2011.226175 · Cited by 127
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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
Selective populations of hippocampal interneurons express ErbB4 and their number and distribution is altered in ErbB4 knockout mice
Neddens, J., & Buonanno, A. (2009) · Hippocampus · doi:10.1002/hipo.20675 · Cited by 126
Cell type–specific gating of perisomatic inhibition by cholecystokinin
Földy, C., Lee, S. Y., Szabadics, J., Neu, A. D., & Soltész, I. (2007) · Nature Neuroscience · doi:10.1038/nn1952 · Cited by 121
Synaptic Properties of SOM- and CCK-Expressing Cells in Dentate Gyrus Interneuron Networks
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Direct excitation of parvalbumin‐positive interneurons by M 1 muscarinic acetylcholine receptors: roles in cellular excitability, inhibitory transmission and cognition
Yi, F., Ball, J., Stoll, K., Satpute, V. C., Mitchell, S., Pauli, J. L., Holloway, B. B., Johnston, A. D., Nathanson, N. M., Deisseroth, K. A., et al. (2014) · The Journal of Physiology · doi:10.1113/jphysiol.2014.275453 · Cited by 124
Interneuron activity controls endocannabinoid-mediated presynaptic plasticity through calcineurin
Heifets, B. D., Chevaleyre, V., & Castillo, P. E. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0711880105 · Cited by 116
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Initial loss but later excess of GABAergic synapses with dentate granule cells in a rat model of temporal lobe epilepsy
Thind, K. K., Yamawaki, R. M., Phanwar, I., Zhang, G., Wen, X., & Buckmaster, P. S. (2009) · The Journal of Comparative Neurology · doi:10.1002/cne.22235 · Cited by 111
Cannabinoids and the Brain
Köfalvi, A. (2007) · Springer eBooks · doi:10.1007/978-0-387-74349-3 · Cited by 110
Input-Output Features of Anatomically Identified CA3 Neurons during Hippocampal Sharp Wave/Ripple Oscillation In Vitro
Hájos, N., Karlócai, M. R., Nemeth, B., Ulbert, I., Monyer, H., Szabó, G., Erdélyi, F., Freund, T. F., & Gulyás, A. I. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.5729-12.2013 · Cited by 118
Inhibitory neurons in the anterior piriform cortex of the mouse: Classification using molecular markers
Suzuki, N., & Bekkers, J. M. (2009) · The Journal of Comparative Neurology · doi:10.1002/cne.22295 · Cited by 107
Interneuron networks in the hippocampus
Kullmann, D. M. (2011) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2011.05.006 · Cited by 119
Cholinergic modulation of synaptic integration and dendritic excitability in the striatum
Oldenburg, I. A., & Ding, J. (2011) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2011.04.004 · Cited by 103
Postsynaptic diacylglycerol lipase α mediates retrograde endocannabinoid suppression of inhibition in mouse prefrontal cortex
Yoshino, H., Miyamae, T., Hansen, G. M., Zambrowicz, B., Flynn, M., Pedicord, D. L., Blat, Y., Westphal, R. S., Zaczek, R. C., Lewis, D. A., et al. (2011) · The Journal of Physiology · doi:10.1113/jphysiol.2011.212225 · Cited by 102
M3 Muscarinic Acetylcholine Receptor Expression Confers Differential Cholinergic Modulation to Neurochemically Distinct Hippocampal Basket Cell Subtypes
Cea-del Rio, C. A., Lawrence, J. J., Tricoire, L., Erdelyi, F., Szabo, G., & McBain, C. J. (2010) · The Journal of Neuroscience · doi:10.1523/jneurosci.5040-09.2010 · Cited by 99
Dendritic Spikes Induce Ripples in Parvalbumin Interneurons during Hippocampal Sharp Waves
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
Functional Specificity of Mossy Fiber Innervation of GABAergic Cells in the Hippocampus
Szabadics, J., & Soltész, I. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.5390-08.2009 · Cited by 98
Persistent inhibitory circuit defects and disrupted social behaviour following in utero exogenous cannabinoid exposure
Vargish, G. A., Pelkey, K. A., Yuan, X., Chittajallu, R., Collins, D., Fang, C., & McBain, C. J. (2017) · Molecular Psychiatry · doi:10.1038/mp.2016.17 · Cited by 93
Role of Ionotropic Glutamate Receptors in Long-Term Potentiation in Rat Hippocampal CA1 Oriens-Lacunosum Moleculare Interneurons
Oren, I., Nissen, W., Kullmann, D. M., Somogyi, P., & Lamsa, K. P. (2009) · The Journal of Neuroscience · doi:10.1523/jneurosci.3251-08.2009 · Cited by 93
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
Distinct synaptic properties of perisomatic inhibitory cell types and their different modulation by cholinergic receptor activation in the CA3 region of the mouse hippocampus
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
Distinct Dendritic Arborization andIn VivoFiring Patterns of Parvalbumin-Expressing Basket Cells in the Hippocampal Area CA3
Tukker, J. J., Lasztóczi, B., Katona, L., Roberts, J. D. B., Pissadaki, E. K., Dalezios, Y., Márton, L. F., Zhang, L., Klausberger, T., & Somogyi, P. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.5052-12.2013 · Cited by 95
Complementary Modulation of Somatic Inhibition by Opioids and Cannabinoids
Glickfeld, L. L., Atallah, B. V., & Scanziani, M. (2008) · The Journal of Neuroscience · doi:10.1523/jneurosci.4700-07.2008 · Cited by 88
Self-citation
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Manseau, F., Marinelli, S., Méndez, P., Schwaller, B., Prince, D. A., Huguenard, J. R., & Bacci, A. (2010) · PLoS Biology · doi:10.1371/journal.pbio.1000492 · Cited by 89
Cholecystokinin: A multi‐functional molecular switch of neuronal circuits
Lee, S. Y., & Soltész, I. (2010) · Developmental Neurobiology · doi:10.1002/dneu.20815 · Cited by 84
Inhibitory Regulation of Dendritic Activity in vivo
Palmer, L. M., Murayama, M., & Larkum, M. E. (2012) · Frontiers in Neural Circuits · doi:10.3389/fncir.2012.00026 · Cited by 88
Terminal Field and Firing Selectivity of Cholecystokinin-Expressing Interneurons in the Hippocampal CA3 Area
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The role of glutamatergic inputs onto parvalbumin-positive interneurons: relevance for schizophrenia
Rotaru, D. C., Lewis, D. A., & González‐Burgos, G. (2012) · Reviews in the Neurosciences · doi:10.1515/revneuro-2011-0059 · Cited by 81
Relationship of cannabinoid CB1 receptor and cholecystokinin immunoreactivity in monkey dorsolateral prefrontal cortex
Eggan, S. M., Melchitzky, D. S., Sesack, S. R., Fish, K. N., & Lewis, D. A. (2010) · Neuroscience · doi:10.1016/j.neuroscience.2010.06.011 · Cited by 83
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Katona, G., Kaszás, A., Turi, G. F., Hájos, N., Tamás, G., Vizi, E. S., & Rózsa, B. J. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1009270108 · Cited by 79
Control of CA3 Output by Feedforward Inhibition Despite Developmental Changes in the Excitation–Inhibition Balance
Torborg, C. L., Nakashiba, T., Tonegawa, S., & McBain, C. J. (2010) · The Journal of Neuroscience · doi:10.1523/jneurosci.3099-10.2010 · Cited by 76
Synapse-specific inhibitory control of hippocampal feedback inhibitory circuit
Chamberland, S. (2010) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2010.00130 · Cited by 75
Local Control of Postinhibitory Rebound Spiking in CA1 Pyramidal Neuron Dendrites
Ascoli, G. A., Gasparini, S., Medinilla, V., & Migliore, M. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.4066-09.2010 · Cited by 75
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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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Synaptic activation of kainate receptors gates presynaptic CB1 signaling at GABAergic synapses
Lourenço, J., Cannich, A., Carta, M., Coussen, F., Mulle, C., & Marsicano, G. (2010) · Nature Neuroscience · doi:10.1038/nn.2481 · Cited by 69
Quantitative ultrastructural analysis of basket and axo-axonic cell terminals in the mouse hippocampus
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Authors: Glickfeld, L. L., & Scanziani, M.
Affiliations: University of California San Diego (US)
Corresponding author: Scanziani, Massimo
ORCID: Glickfeld, Lindsey L
Scanziani, Massimo
Venue: Nature Neuroscience
Publisher: Springer Science and Business Media LLC
Published: 2006-04-30
Volume: 9
Issue: 6
Pages: 807-815
ISSN: 1097-6256 (ISSN-L)
1546-1726
DOI: 10.1038/nn1688
PMC: PMC3509385
OpenAlex: W2119343718
Cited by: 222
References: 42
Citations by year: 2026: 2 · 2025: 8 · 2024: 6 · 2023: 7 · 2022: 6 · 2021: 7 · 2020: 11 · 2019: 3 · 2018: 8 · 2017: 5 · 2016: 10 · 2015: 7 · 2014: 18 · 2013: 19 · 2012: 13
FWCI: 9.20
Type: journal article
Language: en
Open access: green
www.ncbi.nlm.nih.gov
Licence: www.springer.com/tdm (tdm)
Locations: Nature Neuroscience (publishedVersion)
PubMed (publishedVersion)
PubMed Central (acceptedVersion)
Funders: National Institutes of Health (5t32da007315-11)
National Institute of Mental Health (MH 70058, MH71401, R01MH071401, R01MH070058)
National Institute on Drug Abuse (T32-DA-007315, 5T32DA007315)
Topics: Health Sciences › Medicine › Pharmacology (medical) › Cannabis and Cannabinoid Research
Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
Keywords: CB1 receptor, basket cells, inhibitory interneurons, spike timing, hippocampus, endocannabinoids, somatic inhibition, synaptic integration, afferent input, inhibitory circuits
MeSH terms: Animals, Cannabinoids, Dendrites, Hippocampus, Interneurons, Male, Nerve Net, Neural Inhibition, Neural Pathways, Synaptic Transmission, Organ Culture Techniques, Reaction Time, Synapses, Time Factors, Rats, Wistar, Pyramidal Cells, Patch-Clamp Techniques, Excitatory Postsynaptic Potentials, Receptor, Cannabinoid, CB1, Cell Shape, Rats

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Distinct timing in the activity of cannabinoid-sensitive and cannabinoid-insensitive basket cells

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