Cited by 669Neuroscience and Neuropharmacology ResearchMemory and Neural MechanismsNeural dynamics and brain function

The DOI matches its Crossref record; 62 of the 62 references it cites were found in a registry or an index.

Hippocampal CA1 interneurons: an in vivo intracellular labeling study

Open access

Sik, A, Penttonen, M, Ylinen, A, Buzsaki, G·1995·The Journal of Neuroscience

DOI 10.1523/jneurosci.15-10-06651.1995PMC PMC6577981

Open this paper in CoChat — free account

Abstract

Fast spiking interneurons in the CA1 area of the dorsal hippocampus were recorded from and filled with biocytin in anesthetized rats. The full extent of their dendrites and axonal arborizations as well as their calcium binding protein content were examined. Based on the spatial extent of axon collaterals, local circuit cells (basket and O- LM neurons) and long-range cells (bistratified, trilaminar, and backprojection neurons) could be distinguished. Basket cells were immunoreactive for parvalbumin and their axon collaterals were confined to the pyramidal layer. A single basket cell contacted more than 1500 pyramidal neurons and 60 other parvalbumin-positive interneurons. Commissural stimulation directly discharged basket cells, followed by an early and late IPSPs, indicating interneuronal inhibition of basket cells. The dendrites of another local circuit neuron (O-LM) were confined to stratum oriens and it had a small but high-density axonal terminal field in stratum lacunosum-moleculare. The fastest firing cell of all interneurons was a calbindin-immunoreactive bistratified neuron with axonal targets in stratum oriens and radiatum. Two neurons with their cell bodies in the alveus innervated the CA3 region (backprojection cells), in addition to rich axon collaterals in the CA1 region. The trilaminar interneuron had axon collaterals in strata radiatum, oriens and pyramidale with its dendrites confined to stratum oriens. Commissural stimulation evoked an early EPSP-IPSP-late depolarizing potential sequence in this cell. All interneurons formed symmetric synapses with their targets at the electron microscopic level. These findings indicate that interneurons with distinct axonal targets have differential functions in shaping the physiological patterns of the CA1 network.

Integrity signals

Registry

Crossref · 10.1523/jneurosci.15-10-06651.1995

Cites

62 of 62 references verified0 citation errors · 0 not checkable

Statistics

Recomputing p-values needs the paper’s full text.

Claims the paper makes

We couldn’t retrieve this paper’s full text, so its claims and self-check weren’t run. The registry and citation checks still apply.

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?

The Intrinsic Electrophysiological Properties of Mammalian Neurons: Insights into Central Nervous System Function
Llinás, R. R. (1988) · Science · doi:10.1126/science.3059497 · Cited by 2,285
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
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
Sharp wave-associated high-frequency oscillation (200 Hz) in the intact hippocampus: network and intracellular mechanisms
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
Self-citation
The metabotropic glutamate receptor (mGluRlα) is concentrated at perisynaptic membrane of neuronal subpopulations as detected by immunogold reaction
Baude, A., Nusser, Z., Roberts, J. D. B., Mulvihill, E., Jeffrey Mcllhinney, R. A., & Somogyi, P. (1993) · Neuron · doi:10.1016/0896-6273(93)90086-7 · Cited by 927
Neuronal Networks of the Hippocampus
Traub, R. D., & Miles, R. (1991) · doi:10.1017/cbo9780511895401 · Cited by 802
The hippocampal CA3 network: An in vivo intracellular labeling study
Li, X. ‐., Somogyi, P., Ylinen, A., & Buzsáki, G. (1994) · The Journal of Comparative Neurology · doi:10.1002/cne.903390204 · Cited by 751
Self-citation
Parvalbumin in Most γ-Aminobutyric Acid-Containing Neurons of the Rat Cerebral Cortex
Celio, M. R. (1986) · Science · doi:10.1126/science.3945815 · Cited by 740
Calcium‐binding protein (calbindin‐D 28k ) and parvalbumin immunocytochemistry: Localization in the rat hippocampus with specific reference to the selective vulnerability of hippocampal neurons to seizure activity
Sloviter, R. S. (1989) · The Journal of Comparative Neurology · doi:10.1002/cne.902800203 · Cited by 686
Feed‐forward dendritic inhibition in rat hippocampal pyramidal cells studied in vitro
Alger, B. E., & Nicoll, R. A. (1982) · The Journal of Physiology · doi:10.1113/jphysiol.1982.sp014255 · Cited by 528

Show all 62 references

Sorted by citations

Items 101–200 of 662

GABAergic basket cells expressing cholecystokinin contain vesicular glutamate transporter type 3 (VGLUT3) in their synaptic terminals in hippocampus and isocortex of the rat
Somogyi, J., Baude, A., Omori, Y., Shimizu, H., Mestikawy, S. E., Fukaya, M., Shigemoto, R., Watanabe, M., & Somogyi, P. (2004) · European Journal of Neuroscience · doi:10.1111/j.0953-816x.2003.03091.x · Cited by 207
Postsynaptic targets of somatostatin-immunoreactive interneurons in the rat hippocampus
Katona, I., Acsády, L., & Freund, T. F. (1999) · Neuroscience · doi:10.1016/s0306-4522(98)00302-9 · Cited by 210
Simulation of Gamma Rhythms in Networks of Interneurons and Pyramidal Cells
Traub, R. D., Jefferys, J. G. R., & Whittington, M. A. (1997) · Journal of Computational Neuroscience · doi:10.1023/a:1008839312043 · Cited by 207
The 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 212
How simple is the organization of the olfactory glomerulus?: the heterogeneity of so-called periglomerular cells
Kosaka, K., Toida, K., Aika, Y., & Kosaka, T. (1998) · Neuroscience Research · doi:10.1016/s0168-0102(98)00002-9 · Cited by 202
Facilitating pyramid to horizontal oriens‐alveus interneurone inputs: dual intracellular recordings in slices of rat hippocampus
Ali, A. B., & Thomson, A. M. (1998) · The Journal of Physiology · doi:10.1111/j.1469-7793.1998.185bu.x · Cited by 202
Dendritic 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
On the Mechanism of the γ → β Frequency Shift in Neuronal Oscillations Induced in Rat Hippocampal Slices by Tetanic Stimulation
Traub, R. D., Whittington, M. A., Buhl, E. H., Jefferys, J. G. R., & Faulkner, H. J. (1999) · Journal of Neuroscience · doi:10.1523/jneurosci.19-03-01088.1999 · Cited by 202
The rhythmicity of cells of the medial septum/diagonal band of Broca in the awake freely moving rat: relationships with behaviour and hippocampal theta
King, C., Recce, M. L., & O'Keefe, J. M. (1998) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.1998.00026.x · Cited by 197
Parvalbumin interneuron vulnerability and brain disorders
Ruden, J. B., Dugan, L. L., & Konradi, C. (2021) · Neuropsychopharmacology · doi:10.1038/s41386-020-0778-9 · Cited by 194
Physiologically realistic formation of autoassociative memory in networks with theta/gamma oscillations: role of fast NMDA channels.Preprint
Jensen, O. B., Idiart, M. A., & Lisman, J. E. (1996) · Learning & Memory · doi:10.1101/lm.3.2-3.243 · Cited by 192
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 200
On the formation of gamma-coherent cell assemblies by oriens lacunosum-moleculare interneurons in the hippocampus
Tort, A. B. L., Rotstein, H. G., Dugladze, T., Gloveli, T., & Kopell, N. J. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0705708104 · Cited by 192
Amygdalocortical Circuitry in Schizophrenia: From Circuits to Molecules
Benes, F. M. (2009) · Neuropsychopharmacology · doi:10.1038/npp.2009.116 · Cited by 192
Gamma-frequency oscillations: a neuronal population phenomenon, regulated by synaptic and intrinsic cellular processes, and inducing synaptic plasticity
Traub, R. D., Spruston, N., Soltész, I., Konnerth, A., Whittington, M. A., & Jefferys, J. G. R. (1998) · Progress in Neurobiology · doi:10.1016/s0301-0082(98)00020-3 · Cited by 190
Unitary IPSPs evoked by interneurons at the stratum radiatum‐stratum lacunosum‐moleculare border in the CA1 area of the rat hippocampus in vitro
Vida, I., Halasy, K., Szinyei, C., Somogyi, P., & Buhl, E. H. (1998) · The Journal of Physiology · doi:10.1111/j.1469-7793.1998.755bv.x · Cited by 190
Interneurons in the Hippocampal Dentate Gyrus: an In Vivo intracellular Study
Sik, A., Penttonen, M., & Buzsáki, G. (1997) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.1997.tb01634.x · Cited by 189
Self-citation
Nucleus Reuniens Thalami Modulates Activity in Hippocampal Field CA1 through Excitatory and Inhibitory Mechanisms
der Weel, M. J. D.-V., Lopes, F. H. D. S., & Witter, M. P. (1997) · Journal of Neuroscience · doi:10.1523/jneurosci.17-14-05640.1997 · Cited by 189
Synaptic effects of identified interneurons innervating both interneurons and pyramidal cells in the rat hippocampus
Cobb, S. R., Halasy, K., Vida, I., Nyı́ri, G., Tamás, G., Buhl, E. H., & Somogyi, P. (1997) · Neuroscience · doi:10.1016/s0306-4522(97)00055-9 · Cited by 188
Microcircuits in action – from CPGs to neocortex
Grillner, S. E., Markram, H., Schutter, E. D., Silberberg, G., & LeBeau, F. E. N. (2005) · Trends in Neurosciences · doi:10.1016/j.tins.2005.08.003 · Cited by 192
Correlated morphological and neurochemical features identify different subsets of vasoactive intestinal polypeptide-immunoreactive interneurons in rat hippocampus
Acsády, L., Arabadzisz, D., & Freund, T. F. (1996) · Neuroscience · doi:10.1016/0306-4522(95)00610-9 · Cited by 187
Differential Modulation of CA1 and Dentate Gyrus Interneurons During Exploration of Novel Environments
Nitz, D. A., & McNaughton, B. L. (2004) · Journal of Neurophysiology · doi:10.1152/jn.00614.2003 · Cited by 191
Interneurons are the local targets of hippocampal inhibitory cells which project to the medial septum
Gulyás, A. I., Hájos, N., Katona, I., & Freund, T. F. (2003) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.2003.02630.x · Cited by 181
Hippocampal Interneurons Express a Novel Form of Synaptic Plasticity
McMahon, L. L., & Kauer, J. A. (1997) · Neuron · doi:10.1016/s0896-6273(00)80269-x · Cited by 182
Calretinin-immunoreactive local circuit neurons in area 17 of the cynomolgus monkey,Macaca fascicularis
Meskenaïte, V. (1997) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19970303)379:1 · Cited by 180
CA1 pyramidal to basket and bistratified cell EPSPs: dual intracellular recordings in rat hippocampal slices
Ali, A. B., Deuchars, J., Pawelzik, H., & Thomson, A. M. (1998) · The Journal of Physiology · doi:10.1111/j.1469-7793.1998.201bu.x · Cited by 181
Parvalbumin, calbindin, or calretinin in cortically projecting and GABAergic, cholinergic, or glutamatergic basal forebrain neurons of the rat
Gritti, I., Manns, I. D., Mainville, L., & Jones, B. E. (2003) · The Journal of Comparative Neurology · doi:10.1002/cne.10505 · Cited by 178
Cholinergic Excitation of Septohippocampal GABA But Not Cholinergic Neurons: Implications for Learning and Memory
Wu, M., Shanabrough, M., Léránth, C., & Alreja, M. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-10-03900.2000 · Cited by 171
Pioneer GABA Cells Comprise a Subpopulation of Hub Neurons in the Developing Hippocampus
Picardo, M. A., Guigue, P., Bonifazi, P., Batista-Brito, R., Allene, C., Ribas, A., Fishell, G., Baude, A., & Cossart, R. (2011) · Neuron · doi:10.1016/j.neuron.2011.06.018 · Cited by 167
The development of hippocampal interneurons in rodents
Danglot, L., Triller, A., & Marty, S. (2006) · Hippocampus · doi:10.1002/hipo.20225 · Cited by 167
The Synaptic Basis of GABAA,slow
Banks, M. I., Li, T.-B., & Pearce, R. A. (1998) · Journal of Neuroscience · doi:10.1523/jneurosci.18-04-01305.1998 · Cited by 168
Asynchronous States and the Emergence of Synchrony in Large Networks of Interacting Excitatory and Inhibitory Neurons
Hansel, D., & Mato, G. (2003) · Neural Computation · doi:10.1162/089976603321043685 · Cited by 160
Temporal redistribution of inhibition over neuronal subcellular domains underlies state-dependent rhythmic change of excitability in the hippocampus
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 160
The role of inhibitory circuits in hippocampal memory processing
Topolnik, L., & Tamboli, S. (2022) · Nature reviews. Neuroscience · doi:10.1038/s41583-022-00599-0 · Cited by 165
Kainic acid‐induced recurrent mossy fiber innervation of dentate gyrus inhibitory interneurons: Possible anatomical substrate of granule cell hyperinhibition in chronically epileptic rats
Sloviter, R. S., Zappone, C. A., Harvey, B. D., & Frotscher, M. (2005) · The Journal of Comparative Neurology · doi:10.1002/cne.20850 · Cited by 163
Large-Scale 3D Two-Photon Imaging of Molecularly Identified CA1 Interneuron Dynamics in Behaving Mice
Geiller, T., Vancura, B., Terada, S., Troullinou, E., Chavlis, S., Tsagkatakis, G., Tsakalides, P., Ócsai, K., Poirazi, P., Rózsa, B. J., et al. (2020) · Neuron · doi:10.1016/j.neuron.2020.09.013 · Cited by 158
Termination of Epileptic Afterdischarge in the Hippocampus
Bragin, A., Penttonen, M., & Buzsáki, G. (1997) · Journal of Neuroscience · doi:10.1523/jneurosci.17-07-02567.1997 · Cited by 153
Self-citation
Theta/gamma networks with slow NMDA channels learn sequences and encode episodic memory: role of NMDA channels in recall.Preprint
Jensen, O. B., & Lisman, J. E. (1996) · Learning & Memory · doi:10.1101/lm.3.2-3.264 · Cited by 155
Neurogliaform cells in cortical circuits
Overstreet-Wadiche, L., & McBain, C. J. (2015) · Nature Reviews Neuroscience · doi:10.1038/nrn3969 · Cited by 152
Neuronal fast oscillations as a target site for psychoactive drugs
Whittington, M. A. (2000) · Pharmacology & Therapeutics · doi:10.1016/s0163-7258(00)00038-3 · Cited by 151
Firing rate and theta‐phase coding by hippocampal pyramidal neurons during ‘space clamping’
Hirase, H., Czurkó, A., Csicsvari, J., & Buzsáki, G. (1999) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.1999.00853.x · Cited by 148
Estrogen receptor‐beta colocalizes extensively with parvalbumin‐labeled inhibitory neurons in the cortex, amygdala, basal forebrain, and hippocampal formation of intact and ovariectomized adult rats
Blurton-Jones, M. M., & Tuszynski, M. H. (2002) · The Journal of Comparative Neurology · doi:10.1002/cne.10393 · Cited by 148
Cholinergic Induction of Theta-Frequency Oscillations in Hippocampal Inhibitory Interneurons and Pacing of Pyramidal Cell Firing
Chapman, C. A., & Lacaille, J.-C. (1999) · The Journal of Neuroscience · doi:10.1523/jneurosci.19-19-08637.1999 · Cited by 144
Cholecystokinin-immunopositive basket and Schaffer collateral-associated interneurones target different domains of pyramidal cells in the CA1 area of the rat hippocampus
Cope, D. W., Maccaferri, G., Márton, L. F., Roberts, J. D. B., Cobden, P. M., & Somogyi, P. (2002) · Neuroscience · doi:10.1016/s0306-4522(01)00440-7 · Cited by 144
Mode shifting between storage and recall based on novelty detection in oscillating hippocampal circuits
Meeter, M., Murre, J. M. J., & Talamini, L. M. (2004) · Hippocampus · doi:10.1002/hipo.10214 · Cited by 146
Cortistatin Is Expressed in a Distinct Subset of Cortical Interneurons
de Lecea, L., del Rı́o, J. A., Criado, J. R., Alcántara, S., Morales, M., Danielson, P. E., Henriksen, S. J., Soriano, E., & Sutcliffe, J. G. (1997) · Journal of Neuroscience · doi:10.1523/jneurosci.17-15-05868.1997 · Cited by 143
Hippocampal GABAergic interneurons and memory
Tzilivaki, A., Tukker, J. J., Maier, N., Poirazi, P., Sammons, R. P., & Schmitz, D. (2023) · Neuron · doi:10.1016/j.neuron.2023.06.016 · Cited by 154
Different Balance of Excitation and Inhibition in Forward and Feedback Circuits of Rat Visual Cortex
Shao, Z., & Burkhalter, A. (1996) · Journal of Neuroscience · doi:10.1523/jneurosci.16-22-07353.1996 · Cited by 145
Differential Expression of Group I Metabotropic Glutamate Receptors in Functionally Distinct Hippocampal Interneurons
van Hooft, J. A., Giuffrida, R., Blatow, M., & Monyer, H. (2000) · The Journal of Neuroscience · doi:10.1523/jneurosci.20-10-03544.2000 · Cited by 141
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
Nonsynaptic Chemical Transmission Through Nicotinic Acetylcholine Receptors
Lendvai, B., & Vizi, E. S. (2008) · Physiological Reviews · doi:10.1152/physrev.00040.2006 · Cited by 142
Metabotropic Glutamate Receptor 8-Expressing Nerve Terminals Target Subsets of GABAergic Neurons in the Hippocampus
Ferraguti, F., Klausberger, T., Cobden, P., Baude, A., Roberts, J. D. B., Szucs, P., Kinoshita, A., Shigemoto, R., Somogyi, P., & Dalezios, Y. (2005) · The Journal of Neuroscience · doi:10.1523/jneurosci.2547-05.2005 · Cited by 137
Local synaptic connections of basal forebrain neurons
Záborszky, L., & Duque, A. (2000) · Behavioural Brain Research · doi:10.1016/s0166-4328(00)00255-2 · Cited by 135
Inhibitory control of hippocampal inhibitory neurons
Chamberland, S., & Topolnik, L. (2012) · Frontiers in Neuroscience · doi:10.3389/fnins.2012.00165 · Cited by 134
Interactions between Distinct GABAA Circuits in Hippocampus
Banks, M. I., White, J. A., & Pearce, R. A. (2000) · Neuron · doi:10.1016/s0896-6273(00)80907-1 · Cited by 134
Cell type dependence and variability in the short‐term plasticity of EPSCs in identified mouse hippocampal interneurones
Losonczy, A., Zhang, L., Shigemoto, R., Somogyi, P., & Nusser, Z. (2002) · The Journal of Physiology · doi:10.1113/jphysiol.2002.020024 · Cited by 133
Long-Term Potentiation in Distinct Subtypes of Hippocampal Nonpyramidal Neurons
Maccaferri, G., & McBain, C. J. (1996) · The Journal of Neuroscience · doi:10.1523/jneurosci.16-17-05334.1996 · Cited by 133
Interneuron loss reduces dendritic inhibition and GABA release in hippocampus of aged rats
Stanley, E. M., Fadel, J. R., & Mott, D. D. (2011) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2010.12.014 · Cited by 135
Mu opioid receptors are in discrete hippocampal interneuron subpopulations
Drake, C. T., & Milner, T. A. (2002) · Hippocampus · doi:10.1002/hipo.1107 · Cited by 132
Synaptic Communication among Hippocampal Interneurons: Properties of Spontaneous IPSCs in Morphologically Identified Cells
Hájos, N., & Mody, I. (1997) · The Journal of Neuroscience · doi:10.1523/jneurosci.17-21-08427.1997 · Cited by 131
Inhibitory Control of LTP and LTD: Stability of Synapse Strength
Steele, P. M., & Mauk, M. D. (1999) · Journal of Neurophysiology · doi:10.1152/jn.1999.81.4.1559 · Cited by 129
The Specific Role of cGMP in Hippocampal LTPPreprint
Son, H., Lü, Y.-F., Zhuo, M., Arancio, O., Kandel, E. R., & Hawkins, R. D. (1998) · Learning & Memory · doi:10.1101/lm.5.3.231 · Cited by 128
Immunocytochemical localization of nuclear estrogen receptors and progestin receptors within the rat dorsal raphe nucleus
Alves, S. E., Weiland, N. G., Hayashi, S., & McEwen, B. S. (1998) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19980216)391:3 · Cited by 140
Self-citation
Existence and Stability of Persistent States in Large Neuronal Networks
Hansel, D., & Mato, G. (2001) · Physical Review Letters · doi:10.1103/physrevlett.86.4175 · Cited by 125
Gating, modulation and subunit composition of voltage‐gated K+ channels in dendritic inhibitory interneurones of rat hippocampus
Lien, C., Martina, M., Schultz, J. H., Ehmke, H., & Jonas, P. (2002) · The Journal of Physiology · doi:10.1113/jphysiol.2001.013066 · Cited by 124
Immunolocalization of metabotropic glutamate receptor 1α (mGluR1α) in distinct classes of interneuron in the CA1 region of the rat hippocampus
Ferraguti, F., Cobden, P., Pollard, M., Cope, D., Shigemoto, R., Watanabe, M., & Somogyi, P. (2004) · Hippocampus · doi:10.1002/hipo.10163 · Cited by 124
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
Ultrastructural study of gap junctions between dendrites of parvalbumin-containing GABAergic neurons in various neocortical areas of the adult rat
Fukuda, T., & Kosaka, T. (2003) · Neuroscience · doi:10.1016/s0306-4522(03)00328-2 · Cited by 128
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
Hippocampal Pyramidal Cell–Interneuron Spike Transmission Is Frequency Dependent and Responsible for Place Modulation of Interneuron Discharge
Marshall, L., Henze, D. A., Hirase, H., Leinekugel, X., Dragoi, G., & Buzsáki, G. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-02-j0001.2002 · Cited by 118
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
Visual and motor connectivity and the distribution of calcium-binding proteins in macaque frontal eye field: Implications for saccade target selection
Pouget, P. (2009) · Frontiers in Neuroanatomy · doi:10.3389/neuro.05.002.2009 · Cited by 124
Immunocytochemical characterization of hippocamposeptal projecting GABAergic nonprincipal neurons in the mouse brain: a retrograde labeling study
Jinno, S., & Kosaka, T. (2002) · Brain Research · doi:10.1016/s0006-8993(02)02804-4 · Cited by 117
The generation of rhythms within a cortical region: Analysis of a neural mass model
Ursino, M., Cona, F., & Zavaglia, M. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2009.12.084 · Cited by 119
Excitatory gaba input directly drives seizure-like rhythmic synchronization in mature hippocampal CA1 pyramidal cells
Fujiwara‐Tsukamoto, Y., Isomura, Y., Nambu, A., & Takada, M. (2003) · Neuroscience · doi:10.1016/s0306-4522(03)00102-7 · Cited by 117
Hippocampal Formation
Cappaert, N. L. M., van Strien, N. M., & Witter, M. P. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-374245-2.00020-6 · Cited by 120
Neuronal Substrates of Sleep and Epilepsy
Steriade, M. (2001) · Cambridge University Press eBooks · doi:10.1017/cbo9780511541711 · Cited by 118
Extracellular levels of serotonin and GABA in the hippocampus after chronic mild stress in rats. A microdialysis study in an animal model of depression
Grønli, J., Fiske, E., Murison, R. C. C., Bjorvatn, B., Sørensen, E., Ursin, R., & Portas, C. M. (2007) · Behavioural Brain Research · doi:10.1016/j.bbr.2007.03.018 · Cited by 116
A Reorganized GABAergic Circuit in a Model of Epilepsy: Evidence from Optogenetic Labeling and Stimulation of Somatostatin Interneurons
Peng, Z., Zhang, N., Wei, W., Huang, C. S., Cetina, Y., Otis, T. S., & Houser, C. R. (2013) · The Journal of Neuroscience · doi:10.1523/jneurosci.2045-13.2013 · Cited by 114
Characterization of Neurons in the CA2 Subfield of the Adult Rat Hippocampus
Mercer, A., Trigg, H. L., & Thomson, A. M. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.1829-07.2007 · Cited by 113
Epileptic afterdischarge in the hippocampal–entorhinal system: current source density and unit studies
Bragin, A., Csicsvari, J. L., Penttonen, M., & Buzsáki, G. (1997) · Neuroscience · doi:10.1016/s0306-4522(96)00446-0 · Cited by 114
Self-citation
SCN1A mutations in Dravet syndrome: Impact of interneuron dysfunction on neural networks and cognitive outcome
Bender, A. C., Morse, R. P., Scott, R. C., Holmes, G. L., & Lenck‐Santini, P. (2012) · Epilepsy & Behavior · doi:10.1016/j.yebeh.2011.11.022 · Cited by 115
Long-Term Activity-Dependent Plasticity of Action Potential Propagation Delay and Amplitude in Cortical Networks
Bakkum, D. J., Chao, Z. C., & Potter, S. M. (2008) · PLoS ONE · doi:10.1371/journal.pone.0002088 · Cited by 114
Lack of thyroid hormone receptor α1 is associated with selective alterations in behavior and hippocampal circuits
Guadaño‐Ferraz, A., Benavides‐Piccione, R., Venero, C., Lancha, C., Vennström, B., Sandi, C., DeFelipe, J., & Bernal, J. (2003) · Molecular Psychiatry · doi:10.1038/sj.mp.4001196 · Cited by 111
Muscarinic Receptor Activity Has Multiple Effects on the Resting Membrane Potentials of CA1 Hippocampal Interneurons
McQuiston, A. R., & Madison, D. V. (1999) · Journal of Neuroscience · doi:10.1523/jneurosci.19-14-05693.1999 · Cited by 114
Inhibitory control of GABAergic interneurons in the hippocampus
Freund, T. F., & Gulyás, A. I. (1997) · Canadian Journal of Physiology and Pharmacology · doi:10.1139/y97-033 · Cited by 110
Quantitative analysis of ERα and GAD colocalization in the hippocampus of the adult female rat
Hart, S. A., Patton, J. D., & Woolley, C. S. (2001) · The Journal of Comparative Neurology · doi:10.1002/cne.1376 · Cited by 115
Estrogen up-regulates estrogen receptor α and synaptophysin in slice cultures of rat hippocampus
Rune, G. M., Wehrenberg, U., Prange‐Kiel, J., Zhou, L., Adelmann, G., & Frotscher, M. (2002) · Neuroscience · doi:10.1016/s0306-4522(02)00152-5 · Cited by 107
Cell type‐specific dependence of muscarinic signalling in mouse hippocampal stratum oriens interneurones
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
Quantitative analysis of GABAergic neurons in the mouse hippocampus, with optical disector using confocal laser scanning microscope
Jinno, S., Aika, Y., Fukuda, T., & Kosaka, T. (1998) · Brain Research · doi:10.1016/s0006-8993(98)01075-0 · Cited by 107
Robust gamma oscillations in networks of inhibitory hippocampal interneurons
Tiesinga, P. H. E., & José, J. V. (2000) · Network Computation in Neural Systems · doi:10.1088/0954-898x_11_1_301 · Cited by 112
High level of mGluR7 in the presynaptic active zones of select populations of GABAergic terminals innervating interneurons in the rat hippocampus
Somogyi, P., Dalezios, Y., Luján, R., Roberts, J. D. B., Watanabe, M., & Shigemoto, R. (2003) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.2003.02697.x · Cited by 104
Target selectivity and neurochemical characteristics of VIP-immunoreactive interneurons in the rat dentate gyrus
Hájos, N., Acsády, L., & Freund, T. F. (1996) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.1996.tb01604.x · Cited by 103
Models, structure, function: the transformation of cortical signals in the dentate gyrus
Acsády, L., & Káli, S. (2007) · Progress in brain research · doi:10.1016/s0079-6123(07)63031-3 · Cited by 110
Rat hippocampal GABAergic molecular markers are differentially affected by ageing
Vela, J. M., Gutiérrez, A., Vitórica, J., & Ruano, D. (2003) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.2003.01681.x · Cited by 102
Resonant Synchronization in Heterogeneous Networks of Inhibitory Neurons
Maex, R., & Schutter, E. D. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-33-10503.2003 · Cited by 100
Collagen XIX is expressed by interneurons and contributes to the formation of hippocampal synapses
Su, J., Gorse, K. M., Ramirez, F., & Fox, M. A. (2009) · The Journal of Comparative Neurology · doi:10.1002/cne.22228 · Cited by 101
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
Neurovascular relationships in hippocampal slices: physiological and anatomical studies of mechanisms underlying flow-metabolism coupling in intraparenchymal microvessels
Lovick, T. A., Brown, L. A., & Key, B. J. (1999) · Neuroscience · doi:10.1016/s0306-4522(98)00737-4 · Cited by 99
GABAergic axon terminals at perisomatic and dendritic inhibitory sites show different immunoreactivities against two GAD isoforms, GAD67 and GAD65, in the mouse hippocampus: A digitized quantitative analysis
Fukuda, T., Aika, Y., Heizmann, C. W., & Kosaka, T. (1998) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19980601)395:2 · Cited by 96

Authors: Sik, A., Penttonen, M., Ylinen, A., & Buzsaki, G.
Affiliations: Rutgers, The State University of New Jersey (US)
ORCID: Sik, A
Penttonen, M
Venue: The Journal of Neuroscience
Publisher: Society for Neuroscience
Published: 1995-10-01
Volume: 15
Issue: 10
Pages: 6651-6665
ISSN: 0270-6474 (ISSN-L)
1529-2401
DOI: 10.1523/jneurosci.15-10-06651.1995
PMC: PMC6577981
OpenAlex: W1568625389
Cited by: 669
References: 62
Citations by year: 2026: 3 · 2025: 18 · 2024: 10 · 2023: 12 · 2022: 15 · 2021: 11 · 2020: 26 · 2019: 26 · 2018: 23 · 2017: 27 · 2016: 29 · 2015: 18 · 2014: 27 · 2013: 14 · 2012: 23
FWCI: 12.66
Type: journal article
Language: en
Open access: hybrid
doi.org
Licence: cc-by-nc-sa
creativecommons.org/licenses/by-nc-sa/4.0/ (vor, 183 d)
Locations: Journal of Neuroscience (publishedVersion, cc-by-nc-sa)
PubMed Central (publishedVersion)
PubMed (publishedVersion)
Funders: National Institutes of Health
U.S. Public Health Service (34994)
Topics: Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
Keywords: hippocampal CA1, fast-spiking interneurons, basket cells, parvalbumin, calbindin, axon collaterals, dendritic branching, inhibitory postsynaptic potentials, local circuit neurons, synaptic ultrastructure
MeSH terms: Animals, Axons, Electrophysiology, Hippocampus, Interneurons, Intracellular Membranes, Lysine, Microscopy, Electron, Nerve Tissue Proteins, Parvalbumins, Rats, Sprague-Dawley, Rats, Calbindins, S100 Calcium Binding Protein G

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

Hippocampal CA1 interneurons: an in vivo intracellular labeling study

Abstract

Overview

Integrity signals

Verification

Claims the paper makes

Claims other papers make about this one

Citations

Cites

Cited by

Related

Metadata

Record

About these checks