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Impaired Action Potential Initiation in GABAergic Interneurons Causes Hyperexcitable Networks in an Epileptic Mouse Model Carrying a Human NaV1.1 Mutation
Open accessAbstract
Mutations in SCN1A and other ion channel genes can cause different epileptic phenotypes, but the precise mechanisms underlying the development of hyperexcitable networks are largely unknown. Here, we present a multisystem analysis of an SCN1A mouse model carrying the Na V 1.1-R1648H mutation, which causes febrile seizures and epilepsy in humans. We found a ubiquitous hypoexcitability of interneurons in thalamus, cortex, and hippocampus, without detectable changes in excitatory neurons. Interestingly, somatic Na+channels in interneurons and persistent Na+currents were not significantly changed. Instead, the key mechanism of interneuron dysfunction was a deficit of action potential initiation at the axon initial segment that was identified by analyzing action potential firing. This deficit increased with the duration of firing periods, suggesting that increased slow inactivation, as recorded for recombinant mutated channels, could play an important role. The deficit in interneuron firing caused reduced action potential-driven inhibition of excitatory neurons as revealed by less frequent spontaneous but not miniature IPSCs. Multiple approaches indicated increased spontaneous thalamocortical and hippocampal network activity in mutant mice, as follows: (1) more synchronous and higher-frequency firing was recorded in primary neuronal cultures plated on multielectrode arrays; (2) thalamocortical slices examined by field potential recordings revealed spontaneous activities and pathological high-frequency oscillations; and (3) multineuron Ca 2+imaging in hippocampal slices showed increased spontaneous neuronal activity. Thus, an interneuron-specific generalized defect in action potential initiation causes multisystem disinhibition and network hyperexcitability, which can well explain the occurrence of seizures in the studied mouse model and in patients carrying this mutation.
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“Scn1a is a gene that encodes Nav1.1, a sodium channel necessary for PV cell firing (Ogiwara et al., 2007; Hedrich et al., 2014).”
From The Perineuronal ‘Safety’ Net? Perineuronal Net Abnormalities in Neurological Disorders (2018) · cites this paper as Hedrich et al., 2014
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“Recent studies demonstrate that reduced PV cell spike output may contribute to seizures in mice with genetic knock-in of mutated human Scn1a, which results in subtle changes in Nav1.1 functionality (Ogiwara et al., 2007; Hedrich et al., 2014).”
From The Perineuronal ‘Safety’ Net? Perineuronal Net Abnormalities in Neurological Disorders (2018) · cites this paper as Hedrich et al., 2014
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Cites
Shrestha, S., & Offer, S. M. (2016) · Medical Epigenetics · doi:10.1159/000444713 · Cited by 8,951
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
De Novo Mutations in the Sodium-Channel Gene SCN1A Cause Severe Myoclonic Epilepsy of Infancy
Claes, L., Del-Favero, J., Ceulemans, B., Lagae, L., Van Broeckhoven, C., & De Jonghe, P. (2001) · The American Journal of Human Genetics · doi:10.1086/320609 · Cited by 1,292
Tamamaki, N., Yanagawa, Y., Tomioka, R., Miyazaki, J., Obata, K., & Kaneko, T. (2003) · The Journal of Comparative Neurology · doi:10.1002/cne.10905 · Cited by 1,277
Yu, F. H., Mantegazza, M., Westenbroek, R. E., Robbins, C. A., Kalume, F., Burton, K. A., Spain, W. J., McKnight, G. S., Scheuer, T., & Catterall, W. A. (2006) · Nature Neuroscience · doi:10.1038/nn1754 · Cited by 1,173
Self-citationMutations of SCN1A, encoding a neuronal sodium channel, in two families with GEFS+2
Escayg, A., MacDonald, B. T., Meisler, M. H., Baulac, S., Huberfeld, G., An-Gourfinkel, I., Brice, A., LeGuern, E., Moulard, B., Chaigne, D., et al. (2000) · Nature Genetics · doi:10.1038/74159 · Cited by 996
Self-citationOgiwara, I., Miyamoto, H., Morita, N., Atapour, N., Mazaki, E., Inoue, I., Takeuchi, T., Itohara, S., Yanagawa, Y., Obata, K., et al. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.5270-06.2007 · Cited by 879
Temporal structure in spatially organized neuronal ensembles: a role for interneuronal networks
Buzsáki, G., & Chrobak, J. J. (1995) · Current Opinion in Neurobiology · doi:10.1016/0959-4388(95)80012-3 · Cited by 878
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Dichgans, M., Freilinger, T. M., Eckstein, G., Babini, E., Lorenz‐Depiereux, B., Biskup, S., Ferrari, M. D., Herzog, J., van den Maagdenberg, A. M. J. M., Pusch, M., et al. (2005) · The Lancet · doi:10.1016/s0140-6736(05)66786-4 · Cited by 852
Scheffer, I. E. (1997) · Brain · doi:10.1093/brain/120.3.479 · Cited by 758
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Zerimech, S., Chever, O., Scalmani, P., Pizzamiglio, L., Duprat, F., & Mantegazza, M. (2020) · Neuropharmacology · doi:10.1016/j.neuropharm.2020.107951 · Cited by 19
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Uchino, K., Kawano, H., Tanaka, Y., Adaniya, Y., Asahara, A., Deshimaru, M., Kubota, K., Watanabe, T., Katsurabayashi, S., Iwasaki, K., et al. (2021) · Scientific Reports · doi:10.1038/s41598-021-90224-4 · Cited by 15
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Binini, N., Sancini, G., Villa, C., Magro, R. D., Sansoni, V., Rusconi, R., Mantegazza, M., Grioni, D., Talpo, F., Toselli, M., et al. (2017) · Brain Research · doi:10.1016/j.brainres.2017.09.023 · Cited by 11
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Koch, H., Niturad, C. E., Theiss, S., Bien, C. G., Elger, C. E., Wandinger, K., Vincent, A. C., Malter, M. P., Körtvélyessy, P., Lerche, H., et al. (2019) · Scientific Reports · doi:10.1038/s41598-019-41849-z · Cited by 9
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Xu, C., Zhang, Y., Gozal, D., & Carney, P. R. (2021) · Journal of Central Nervous System Disease · doi:10.1177/11795735211048045 · Cited by 8
Bayraktar, E., Liu, Y., Sonnenberg, L., Hedrich, U. B. S., Sara, Y., Eltokhi, A., Lyu, H., Lerche, H., Wuttke, T. V., & Lauxmann, S. (2022) · British Journal of Pharmacology · doi:10.1111/bph.15981 · Cited by 8
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Metadata
- Authors
- Hedrich, U. B. S., Liautard, C., Kirschenbaum, D., Pofahl, M., Lavigne, J., Liu, Y., Theiss, S., Slotta, J., Escayg, A., Dihné, M., Beck, H., Mantegazza, M., & Lerche, H.
- Affiliations
- Hertie Institute for Clinical Brain Research (DE)
- Centre National de la Recherche Scientifique (FR)
- University of Bonn (DE)
- Heinrich Heine University Düsseldorf (DE)
- Emory University (US)
- ORCID
- Venue
- The Journal of Neuroscience
- Publisher
- Society for Neuroscience
- Published
- 2014-11-05
- Volume
- 34
- Issue
- 45
- Pages
- 14874-14889
- ISSN
- 0270-6474 (ISSN-L)
- 1529-2401
- PMC
- PMC4220023
- OpenAlex
- W1964533239
- Cited by
- 164
- References
- 70
- Citations by year
- 2026: 9 · 2025: 10 · 2024: 15 · 2023: 16 · 2022: 19 · 2021: 20 · 2020: 9 · 2019: 21 · 2018: 13 · 2017: 16 · 2016: 9 · 2015: 6 · 2014: 1
- FWCI
- 8.14
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Journal of Neuroscience (publishedVersion, cc-by-nc-sa)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- DZNE Pub (submittedVersion)
- Journal of Neuroscience Nursing
- Funders
- Danish Cancer Society Research Center
- European Commission
- Deutsche Forschungsgemeinschaft (SFB1089)
- National Institutes of Health
- National Institute of Neurological Disorders and Stroke (R01NS072221)
- Topics
- Health Sciences › Medicine › Clinical Neurology › Epilepsy research and treatment
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Ion channel regulation and function
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Keywords
- SCN1A, Nav1.1, GABAergic interneurons, action potential generation, axon initial segment, slow inactivation, disinhibition, network hyperexcitability, febrile seizures, epilepsy, thalamocortical network, hippocampal network activity, inhibitory postsynaptic currents, sodium channel mutations
- MeSH terms
- Action Potentials, Animals, Axons, Brain, Calcium, Cells, Cultured, Epilepsy, Humans, Interneurons, Mice, Inbred C57BL, Mutation, Nerve Net, Mice, Inhibitory Postsynaptic Potentials, GABAergic Neurons, NAV1.1 Voltage-Gated Sodium Channel
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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.
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