Cited by 272Neuroscience and Neuropharmacology ResearchNeural dynamics and brain functionMemory and Neural Mechanisms

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Plasticity of intrinsic neuronal excitability

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Debanne, Dominique, Inglebert, Yanis, Russier, Michaël·2019·Current Opinion in Neurobiology

DOI 10.1016/j.conb.2018.09.001

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Abstract

Long-term synaptic modification is not the exclusive mode of memory storage, and persistent regulation of voltage-gated ion channels also participates in memory formation. Intrinsic plasticity is expressed in virtually all neuronal types including principal cells and interneurons. Activation of synaptic glutamate receptors initiates long-lasting changes in neuronal excitability at presynaptic and postsynaptic side. As synaptic plasticity, intrinsic plasticity is bi-directional and expresses a certain level of input-specificity or cell-specificity. We discuss here the nature of the learning rules shared by intrinsic and synaptic plasticity and the impact of intrinsic plasticity on temporal processing.

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Synchronized oscillations in interneuron networks driven by metabotropic glutamate receptor activation
Whittington, M. A., Traub, R. D., & Jefferys, J. G. R. (1995) · Nature · doi:10.1038/373612a0 · Cited by 1,613
Variability, compensation and homeostasis in neuron and network function
Marder, E., & Goaillard, J.-M. (2006) · Nature Reviews Neuroscience · doi:10.1038/nrn1949 · Cited by 1,212
The Spike-Timing Dependence of Plasticity
Feldman, D. E. (2012) · Neuron · doi:10.1016/j.neuron.2012.08.001 · Cited by 1,071
The other side of the engram: experience-driven changes in neuronal intrinsic excitability
Zhang, W., & Linden, D. J. (2003) · Nature reviews. Neuroscience · doi:10.1038/nrn1248 · Cited by 889
Time cells in the hippocampus: a new dimension for mapping memories
Eichenbaum, H. (2014) · Nature Reviews Neuroscience · doi:10.1038/nrn3827 · Cited by 843
Plasticity in the intrinsic excitability of cortical pyramidal neurons
Desai, N. S., Rutherford, L. C., & Turrigiano, G. G. (1999) · Nature Neuroscience · doi:10.1038/9165 · Cited by 806
Graded persistent activity in entorhinal cortex neurons
Egorov, A. V., Hamam, B. N., Fransén, E., Hasselmo, M. E., & Alonso, A. A. (2002) · Nature · doi:10.1038/nature01171 · Cited by 769
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
Compartmentalized dendritic plasticity and input feature storage in neurons
Losonczy, A., Makara, J. K., & Magee, J. C. (2008) · Nature · doi:10.1038/nature06725 · Cited by 598

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Authors: Debanne, D., Inglebert, Y., & Russier, M.
Affiliations: Inserm (FR)
Corresponding author: Debanne, Dominique
ORCID: Debanne, Dominique
Inglebert, Yanis
Russier, Michaël
Venue: Current Opinion in Neurobiology
Publisher: Elsevier BV
Published: 2019-02
Volume: 54
Pages: 73-82
ISSN: 0959-4388 (ISSN-L)
DOI: 10.1016/j.conb.2018.09.001
OpenAlex: W2891094463
Cited by: 272
References: 84
Citations by year: 2026: 35 · 2025: 56 · 2024: 38 · 2023: 37 · 2022: 31 · 2021: 36 · 2020: 20 · 2019: 18
FWCI: 2.43
Type: journal article
Language: en
Open access: bronze
doi.org
Licence: www.elsevier.com/tdm/userlicense/1.0/ (tdm)
www.elsevier.com/legal/tdmrep-license (tdm)
Locations: Current Opinion in Neurobiology (publishedVersion)
PubMed (publishedVersion)
HAL (submittedVersion, cc-by)
Funders: INSERM, CNRS, AMU, FRM (FDT2170437059, DVS20131228768)
ANR NEUC 2014 (ANR-14-NEUC-0004)
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: intrinsic plasticity, neuronal excitability, voltage-gated ion channels, synaptic plasticity, memory formation, glutamate receptors, learning rules, temporal processing, interneurons, principal cells
MeSH terms: Action Potentials, Animals, Brain, Humans, Learning, Neuronal Plasticity, Neurons

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Plasticity of intrinsic neuronal excitability

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