Cited by 434Neuroscience and Neuropharmacology ResearchNeural dynamics and brain functionMemory and Neural Mechanisms

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Routing of spike series by dynamic circuits in the hippocampus

Pouille, Frédéric, Scanziani, Massimo·2004·Nature

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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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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-citation
Total number and distribution of inhibitory and excitatory synapses on hippocampal CA1 pyramidal cells
Megı́as, M., Emri, Z., Freund, T. F., & Gulyás, A. I. (2001) · Neuroscience · doi:10.1016/s0306-4522(00)00496-6 · Cited by 950
Salient features of synaptic organisation in the cerebral cortex1Published on the World Wide Web on 3 March 1998.1
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
Patch-clamp recordings from the soma and dendrites of neurons in brain slices using infrared video microscopy
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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Authors: Pouille, F., & Scanziani, M.
Affiliations: University of California San Diego (US)
Corresponding author: Scanziani, Massimo
ORCID: Scanziani, Massimo
Venue: Nature
Publisher: Springer Science and Business Media LLC
Published: 2004-05-30
Volume: 429
Issue: 6993
Pages: 717-723
ISSN: 0028-0836 (ISSN-L)
1476-4687
DOI: 10.1038/nature02615
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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Routing of spike series by dynamic circuits in the hippocampus

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