The DOI matches its Crossref record; 75 of the 76 references it cites were found in a registry or an index.
Kv3 channels: voltage-gated K+ channels designed for high-frequency repetitive firing
Abstract
Analysis of the Kv3 subfamily of K(+) channel subunits has lead to the discovery of a new class of neuronal voltage-gated K(+) channels characterized by positively shifted voltage dependencies and very fast deactivation rates. These properties are adaptations that allow these channels to produce currents that can specifically enable fast repolarization of action potentials without compromising spike initiation or height. The short spike duration and the rapid deactivation of the Kv3 currents after spike repolarization maximize the quick recovery of resting conditions after an action potential. Several neurons in the mammalian CNS have incorporated into their repertoire of voltage-dependent conductances a relatively large number of Kv3 channels to enable repetitive firing at high frequencies - an ability that crucially depends on the special properties of Kv3 channels and their impact on excitability.
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In the citing paper
“One set of co-expressed genes encoded proteins that enable fast and persistent action potentials, including the Kcnc1–3 (Kv3.1), Kcna1 (Kv1.1) and Scn8a (Nav1.6) channels”
From Molecular diversity and specializations among the cells of the adult mouse brain (2018) · cites this paper as Rudy and McBain, 2001
In the citing paper
“Early attempts to match expression patterns of recent cloned channel transcripts with biophysical properties measured by whole cell recording techniques in in vitro slices did, however, yield some modest successes, particularly with channels formed by the Kv3 family of voltage-gated potassium channels (967) as discussed below.”
From Hippocampal GABAergic Inhibitory Interneurons (2017) · cites this paper as [967]
In the citing paper
“Delayed rectifier channels assembled from Kv3 subunits are instrumental components in conferring high-frequency action potential firing in numerous hippocampal and cortical interneuron subtypes (304, 967, 1187).”
From Hippocampal GABAergic Inhibitory Interneurons (2017) · cites this paper as [967]
In the citing paper
“This optimism was short lived as it became apparent that few channels expressed in recombinant systems perfectly matched the biophysical properties of native channels (967).”
From Hippocampal GABAergic Inhibitory Interneurons (2017) · cites this paper as [967]
In the citing paper
“Importantly, the rapid activation kinetics enforces a narrow temporal window that minimizes Na+ channel inactivation, and the consequent deep hyperpolarization serves to deinactivate other voltage-gated channels ensuring a high fraction are available for activation during trains of action potentials (967).”
From Hippocampal GABAergic Inhibitory Interneurons (2017) · cites this paper as [967]
In the citing paper
“Their rapid activation ensures efficient spike repolarization, and their rapid deactivation allows minimal K+ current accumulation during the interspike interval that would interfere with generation of subsequent action potentials.”
From Hippocampal GABAergic Inhibitory Interneurons (2017) · cites this paper as [967]
In the citing paper
“Dendritic Kv3 currents act to accelerate the decay time course of excitatory postsynaptic potentials (EPSPs), imposing a narrow window for temporal integration (504, 967), and minimize the impact of clustered excitatory input to favor distributed synaptic inputs (504).”
From Hippocampal GABAergic Inhibitory Interneurons (2017) · cites this paper as [967]
Citations
Cites
Interneurons of the hippocampus
Freund, T. F., & Buzsáki, G. (1998) · Hippocampus · doi:10.1002/(sici)1098-1063(1996)6:4 · Cited by 3,478
Comparative electrophysiology of pyramidal and sparsely spiny stellate neurons of the neocortex
McCormick, D. A., Connors, B. W., Lighthall, J. W., & Prince, D. A. (1985) · Journal of Neurophysiology · doi:10.1152/jn.1985.54.4.782 · Cited by 1,935
Intrinsic firing patterns of diverse neocortical neurons
Connors, B. W., & Gutnick, M. J. (1990) · Trends in Neurosciences · doi:10.1016/0166-2236(90)90185-d · Cited by 1,440
GABAergic cell subtypes and their synaptic connections in rat frontal cortex
Kawaguchi, Y. (1997) · Cerebral Cortex · doi:10.1093/cercor/7.6.476 · Cited by 1,416
Molecular Diversity of K+ Channels
COETZEE, W. A., AMARILLO, Y., CHIU, J., CHOW, A., LAU, D., McCORMACK, T., MORENA, H., NADAL, M. S., OZAITA, A., POUNTNEY, D., et al. (1999) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1999.tb11293.x · Cited by 1,095
Self-citationGray, C. M., & McCormick, D. A. (1996) · Science · doi:10.1126/science.274.5284.109 · Cited by 911
Grissmer, S., Nguyen, A. N., Aiyar, J., Hanson, D. C., Mather, R. J., Gutman, G. A., Karmilowicz, M. J., Auperin, D. D., & Chandy, K. G. (1994) · Molecular Pharmacology · doi:10.1016/s0026-895x(25)10594-4 · Cited by 777
McBain, C. J., & Fisahn, A. (2001) · Nature Reviews Neuroscience · doi:10.1038/35049047 · Cited by 581
Self-citationModulation of ION Channels by Protein Phosphorylation and Dephosphorylation
Levitan, I. B. (1994) · Annual Review of Physiology · doi:10.1146/annurev.ph.56.030194.001205 · Cited by 531
Erisir, A., Lau, D., Rudy, B., & Leonard, C. S. (1999) · Journal of Neurophysiology · doi:10.1152/jn.1999.82.5.2476 · Cited by 458
Self-citation
Research works printed but not linked: 4
- Freund, 1996, Interneurons in the hippocampus, Hippocampus, 6, 345
- Ozaita, 2000, Role of alternatively-spliced C-termini in the subcellular localization of Kv3 potassium channels in neurons, Soc. Neurosci. Abstr., 26, 1636
- Vega-Saenz de Miera, 1994, Modulation of Kv3.3 K+ channels by oxidation and phosphorylation, Soc. Neurosci. Abstr., 20, 725
- Macica, 2000, Knockout of the Kv3.1 gene impairs high frequency firing in auditory neurons, Soc. Neurosci. Abstr., 26, 1705
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Boda, E., Hoxha, E., Pini, A., Montarolo, F., & Tempia, F. (2011) · Journal of Molecular Neuroscience · doi:10.1007/s12031-011-9648-6 · Cited by 43
Holst, G. L., Stoy, W. A., Yang, B., Kolb, I., Kodandaramaiah, S. B., Li, L., Knoblich, U., Zeng, H., Haider, B., Boyden, E. S., et al. (2019) · Journal of Neurophysiology · doi:10.1152/jn.00738.2018 · Cited by 40
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Hirai, S., Miwa, H., Tanaka, T., Toriumi, K., Kunii, Y., Shimbo, H., Sakamoto, T., Hino, M., Izumi, R., Nagaoka, A., et al. (2021) · Science Advances · doi:10.1126/sciadv.abl6077 · Cited by 42
Wang, S., Wang, J., Luo, R., Cui, W.-Y., & Wang, H. (2008) · Clinical and Experimental Pharmacology and Physiology · doi:10.1111/j.1440-1681.2008.04964.x · Cited by 42
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Peng, I., & Wu, C. (2006) · Journal of Neurophysiology · doi:10.1152/jn.01012.2006 · Cited by 40
Lovell, P. V., Carleton, J. B., & Mello, C. V. (2013) · BMC Genomics · doi:10.1186/1471-2164-14-470 · Cited by 46
Smith, K. M., Fagel, D. M., Stevens, H. E., Rabenstein, R. L., Maragnoli, M. E., Ohkubo, Y., Picciotto, M. R., Schwartz, M. L., & Vaccarino, F. M. (2007) · Biological Psychiatry · doi:10.1016/j.biopsych.2007.09.020 · Cited by 39
Chen, W., Luo, B., Gao, N., Li, H., Wang, H., Li, L., Cui, W., Zhang, L., Sun, D., Liu, F., et al. (2021) · Journal of Clinical Investigation · doi:10.1172/jci136956 · Cited by 39
Ichinohe, N., Watakabe, A., Miyashita, T., Yamamori, T., Hashikawa, T., & Rockland, K. S. (2004) · Neuroscience · doi:10.1016/j.neuroscience.2004.08.005 · Cited by 39
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Poirier, K., Viot, G., Lombardi, L., Jauny, C., Billuart, P., & Bienvenu, T. (2017) · European Journal of Human Genetics · doi:10.1038/ejhg.2017.3 · Cited by 39
Liu, P. W., Blair, N. T., & Bean, B. P. (2017) · Journal of Neuroscience · doi:10.1523/jneurosci.1703-17.2017 · Cited by 39
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Henderson, Z., Lu, C., Janzsó, G., Matto, N., McKinley, C. E., Yanagawa, Y., & Halasy, K. (2010) · Neuroscience · doi:10.1016/j.neuroscience.2010.01.020 · Cited by 39
Vitellaro‐Zuccarello, L., Bosisio, P., Mazzetti, S., Monti, C., & Biasi, S. D. (2006) · Cell and Tissue Research · doi:10.1007/s00441-006-0289-y · Cited by 40
Chen, C., Wang, L., Rong, X., Wang, W., & Wang, X. (2014) · Acta Pharmaceutica Sinica B · doi:10.1016/j.apsb.2014.12.004 · Cited by 39
Soares, D., Goldrick, I., Lemon, R., Kraskov, A., Greensmith, L., & Kalmár, B. (2017) · The Journal of Comparative Neurology · doi:10.1002/cne.24192 · Cited by 40
Constantinople, C. M., Disney, A. A., Maffie, J. K., Rudy, B., & Hawken, M. J. (2009) · The Journal of Comparative Neurology · doi:10.1002/cne.22111 · Cited by 38
Self-citation
Metadata
- Authors
- Rudy, B., & McBain, C. J.
- Affiliations
- New York University (US)
- Eunice Kennedy Shriver National Institute of Child Health and Human Development (US)
- Corresponding author
- Rudy, Bernardo
- McBain, Chris J.
- Venue
- Trends in Neurosciences
- Publisher
- Elsevier BV
- Published
- 2001-09
- Volume
- 24
- Issue
- 9
- Pages
- 517-526
- ISSN
- 0166-2236 (ISSN-L)
- OpenAlex
- W2034132958
- Cited by
- 781
- References
- 76
- Citations by year
- 2026: 36 · 2025: 27 · 2024: 45 · 2023: 27 · 2022: 36 · 2021: 33 · 2020: 39 · 2019: 32 · 2018: 32 · 2017: 34 · 2016: 20 · 2015: 26 · 2014: 23 · 2013: 30 · 2012: 32
- FWCI
- 1.84
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Trends in Neurosciences (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institutes of Health (1r01ns035215-01a1, 5r01ns030989-22)
- National Institute of Neurological Disorders and Stroke (NS-30989, NS-35215)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Ion channel regulation and function
- Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Cardiac electrophysiology and arrhythmias
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Keywords
- voltage-gated potassium channels, action potential repolarization, repetitive firing, neuronal excitability, spike initiation, central nervous system neurons
- MeSH terms
- Action Potentials, Animals, Brain, Humans, Neurons, Potassium Channels, Potassium Channels, Voltage-Gated, Shaw Potassium Channels
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