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Control of the repetitive discharge of rat CA 1 pyramidal neurones in vitro.
Open accessAbstract
Experiments using intracellular recording techniques were performed on rat hippocampal neurones in vitro, to study the discharge properties of these cells. When CA 1 pyramidal cells were excited by injecting long depolarizing current pulses (approximately 600‐800 ms), they responded with an initial rapid action potential discharge which slowed, or accommodated, and then stopped after 200‐300 ms. The train of action potentials was followed by a hyperpolarization which was due primarily to calcium‐activated potassium conductance (GK(Ca]. The amplitude of this hyperpolarization increased with an increasing number of action potentials in the initial discharge. Blocking the calcium‐activated potassium conductance, by injecting EGTA into the cell, by bathing the cell in cadmium, a calcium channel blocker, or by bathing the cell in calcium‐free medium, reduced the after‐hyperpolarization (a.h.p.) and accommodation such that the frequency of action potential discharge increased and the duration of this discharge was prolonged. Blocking the calcium‐activated potassium conductance had a greater effect on discharge frequency later in the action potential train, as late interspike intervals were shortened more than early ones by the application of cadmium or of calcium‐free medium. This was presumably because the calcium‐activated potassium conductance was more developed later in the train. Accommodation was not completely abolished in the absence of calcium and presence of cadmium, suggesting that other factors, in addition to calcium‐activated potassium conductance, contributed to this process. This remaining accommodation was reduced by low doses of carbachol, suggesting that the M‐current also plays a role in accommodation. We conclude that accommodation of the action potential discharge of hippocampal pyramidal cells may be regulated by at least two potassium currents: the calcium‐activated potassium current and the M‐current. Both of these currents are turned on during excitation of the neurone and act in an inhibitory manner on that neurone to limit further action potential discharge.
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Cites
Voltage-clamp analysis of muscarinic excitation in hippocampal neurons
Halliwell, J. V., & Adams, P. R. (1982) · Brain Research · doi:10.1016/0006-8993(82)90954-4 · Cited by 1,046
CALCIUM-DEPENDENT POTASSIUM ACTIVATION IN NERVOUS TISSUES
Meech, R. W. (1978) · Annual Review of Biophysics and Bioengineering · doi:10.1146/annurev.bb.07.060178.000245 · Cited by 754
Prediction of repetitive firing behaviour from voltage clamp data on an isolated neurone soma
Connor, J. A., & Stevens, C. F. (1971) · The Journal of Physiology · doi:10.1113/jphysiol.1971.sp009366 · Cited by 735
Noradrenaline blocks accommodation of pyramidal cell discharge in the hippocampus
Madison, D. V., & Nicoll, R. A. (1982) · Nature · doi:10.1038/299636a0 · Cited by 581
Self-citationA calcium-activated hyperpolarization follows repetitive firing in hippocampal neurons
Hotson, J. R., & Prince, D. A. (1980) · Journal of Neurophysiology · doi:10.1152/jn.1980.43.2.409 · Cited by 569
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
Self-citationPharmacological inhibition of the M‐current
Adams, P. R., Brown, D. A., & Constanti, A. (1982) · The Journal of Physiology · doi:10.1113/jphysiol.1982.sp014411 · Cited by 431
Alger, B. E., & Nicoll, R. A. (1980) · Science · doi:10.1126/science.7444438 · Cited by 421
Self-citationHaas, H. L., & Konnerth, A. (1983) · Nature · doi:10.1038/302432a0 · Cited by 414
Acetylcholine Mediates a Slow Synaptic Potential in Hippocampal Pyramidal Cells
Cole, A. E., & Nicoll, R. A. (1983) · Science · doi:10.1126/science.6612345 · Cited by 374
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Popescu, I. R., Le, K. Q., Palenzuela, R., Voglewede, R., & Mostany, R. (2017) · Scientific Reports · doi:10.1038/s41598-017-14971-z · Cited by 5
The Role of Acetylcholine in Barrel Cortex
Juliano, S. L., & Jacobs, S. E. (1995) · Cerebral cortex · doi:10.1007/978-1-4757-9616-2_10 · Cited by 6
Calcium Currents in Mammalian Central Neurones
Brown, D. A., Docherty, R. J., Gähwiler, B. H., & Halliwell, J. V. (1985) · Bayer-Symposium · doi:10.1007/978-3-642-70499-4_5 · Cited by 6
Hegemann, R. U., & Abraham, W. C. (2021) · Journal of Neurophysiology · doi:10.1152/jn.00514.2020 · Cited by 5
de Nobel, J., Martens, S. S. M., Briaire, J. J., Bäck, T., Kononova, A. V., & Frijns, J. H. M. (2024) · Hearing Research · doi:10.1016/j.heares.2024.109011 · Cited by 5
Pillai, A. G., Henckens, M. J. A. G., Fernández, G., & Joëls, M. (2014) · PLoS ONE · doi:10.1371/journal.pone.0099208 · Cited by 5
Hatch, R. J., Berecki, G., Jancovski, N., Li, M., Rollo, B., Jafar‐Nejad, P., Rigo, F., Kaila, K., Reid, C. A., & Petrou, S. (2023) · Journal of Neuroscience · doi:10.1523/jneurosci.1387-22.2022 · Cited by 5
Ruiz, A. J. (2011) · Advances in experimental medicine and biology · doi:10.1007/978-1-4419-9557-5_6 · Cited by 5
Propagating waves in visual cortex: A large scale model of turtlevisual cortex
Nenadić, Z., Ghosh, B. K., & Ulinski, P. S. (2002) · Mathematical and Computer Modelling · doi:10.1016/s0895-7177(02)00045-6 · Cited by 5
Ambros‐Ingerson, J., Grover, L. M., & Holmes, W. R. (2008) · Neural Computation · doi:10.1162/neco.2007.07-07-564 · Cited by 5
Urdapilleta, E. (2016) · Europhysics Letters (EPL) · doi:10.1209/0295-5075/115/68002 · Cited by 5
Urdapilleta, E. (2016) · Americanae (AECID Library) · Cited by 5
Synchrony upon repetition: One or multiple neural mechanisms?
Weiner, K. S., & Kalanit Grill-spector, A. (2012) · Cognitive Neuroscience · doi:10.1080/17588928.2012.689973 · Cited by 5
Yi, G., Wang, J., Wei, X., Deng, B., Li, H., & Che, Y. (2016) · Communications in Nonlinear Science and Numerical Simulation · doi:10.1016/j.cnsns.2016.11.011 · Cited by 4
Zitricky, F., & Ježek, K. (2019) · Scientific Reports · doi:10.1038/s41598-019-47842-w · Cited by 4
Chang, L., Wang, J., Deng, B., Wei, X., & Li, H. (2011) · Neurocomputing · doi:10.1016/j.neucom.2011.11.015 · Cited by 3
Morphological heterogeneity of non-pyramidal neurons in the CA1 region of the rat hippocampus
Han, Z. (1996) · Neuroscience Research · doi:10.1016/0168-0102(96)01024-3 · Cited by 5
A neuroholographic model of memory: Theta rhythms, facilitation, and calcium channels.
Landfield, P. W., & Thibault, O. (2001) · American Psychological Association eBooks · doi:10.1037/10413-015 · Cited by 3
Cholinergic modulation of hippocampal epileptic activity in vitro
Yaari, Y., & Jensen, M. S. (1989) · Proceedings of the Fourth International Symposium on Polarization Phenomena in Nuclear Reactions · doi:10.1007/978-3-0348-9138-7_15 · Cited by 4
Postsynaptic Actions of Acetylcholine in the Mammalian Brain in Vitro
McCormick, D. A., & Prince, D. A. (1988) · Springer eBooks · doi:10.1007/978-1-4613-0925-3_18 · Cited by 4
Influence of cholinesterase inhibitors on cortical slow-wave activity in aging nonhuman primate
Fitten, L. J., Perryman, K. M., O’Neill, J., & Halgren, E. (1994) · Pharmacology Biochemistry and Behavior · doi:10.1016/0091-3057(94)90483-9 · Cited by 4
Factors affecting phase synchronization in integrate-and-fire oscillators
Troyer, T. W. (2006) · Journal of Computational Neuroscience · doi:10.1007/s10827-006-6174-6 · Cited by 4
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Characterizing optogenetically mediated rebound effects in anaesthetized mouse primary visual cortex
Shapiro, J. T., Michaud, N. M., & Crowder, N. A. (2025) · The Journal of Physiology · doi:10.1113/jp287265 · Cited by 3
Rominto, A. M., Montarolo, F., Berrino, L., Loddo, M., Bertolotto, A., Tempia, F., & Hoxha, E. (2025) · Scientific Reports · doi:10.1038/s41598-025-22321-7 · Cited by 4
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Ji, Z., Chu, T., Dong, X., Yu, C., Bush, D., Burgess, N., & Wu, S. (2026) · Nature Communications · doi:10.1038/s41467-025-68042-3 · Cited by 12
Gaudreau, S. F., & Bui, T. V. (2026) · The Journal of Physiology · doi:10.1113/jp290012 · Cited by 3
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Wilmerding, L. K., Yazdanbakhsh, A., & Hasselmo, M. E. (2022) · Cell Reports Methods · doi:10.1016/j.crmeth.2022.100208 · Cited by 4
Awasthi, R., Chandra, N., & Barkai, E. (2022) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2022.934838 · Cited by 3
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Muellerleile, J., Vnencak, M., Sethi, M. V. A., Jungenitz, T., Schwarzacher, S. W., & Jedlička, P. (2023) · eNeuro · doi:10.1523/eneuro.0471-22.2023 · Cited by 3
Wang, J., Deng, B., Wang, J., Xiang, L., Gao, T., Yu, H., & Liu, C. (2024) · Communications in Nonlinear Science and Numerical Simulation · doi:10.1016/j.cnsns.2024.108164 · Cited by 3
Modulatory Influences on the Hippocampus and Entorhinal Cortex
Gupta, K., & Hasselmo, M. E. (2014) · Springer eBooks · doi:10.1007/978-3-7091-1292-2_7 · Cited by 3
Functions of the Persistent Na+ Current in Cortical Neurons Revealed by Dynamic Clamp
Storm, J. F., Vervaeke, K., Hu, H., & Graham, L. J. (2009) · Springer eBooks · doi:10.1007/978-0-387-89279-5_8 · Cited by 3
Tell me something interesting: Context dependent adaptation in somatosensory cortex
Davies, L. A., Garcia‐Lazaro, J. A., Schnupp, J. W. H., Wennekers, T., & Denham, S. L. (2011) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2011.12.003 · Cited by 3
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Mavritsaki, E., Allen, H. A., & Humphreys, G. W. (2009) · Lecture notes in computer science · doi:10.1007/978-3-642-00582-4_10 · Cited by 3
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Conn, P. J. (1990) · doi:10.1007/978-1-349-11922-6_4 · Cited by 3
Ma, X., Miraucourt, L. S., Qiu, H., Sharif‐Naeini, R., & Khadra, A. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.03.05.531043 · Cited by 3
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Neurotransmitter Interactions and Responsivity to Cholinomimetic Agents
Haroutunian, V. H., Santucci, A., & Davis, K. L. (1992) · Birkhäuser Boston eBooks · doi:10.1007/978-1-4615-9843-5_8 · Cited by 3
Zhang, L., Peng, Z., Bian, W., Zhu, P., Tang, B., Liao, W., & Su, T. (2021) · Molecular Neurobiology · doi:10.1007/s12035-020-02229-1 · Cited by 2
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Ladenbauer, J., Augustin, M., & Obermayer, K. (2016) · Understanding complex systems · doi:10.1007/978-3-319-28028-8_23 · Cited by 2
Sinha, N., Heckman, C. J., & Yang, Y. (2020) · Journal of Theoretical Biology · doi:10.1016/j.jtbi.2020.110509 · Cited by 2
Special Features of the Hippocampal Formation with Respect to Seizure Conditions
Haas, H. L. (1987) · Springer eBooks · doi:10.1007/978-3-642-71103-9_6 · Cited by 2
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Wheal, H. V. (1990) · Springer eBooks · doi:10.1007/978-3-7091-9104-0_2 · Cited by 2
Berner, J. E., & Woody, C. D. (1991) · Biological Cybernetics · doi:10.1007/bf00196455 · Cited by 2
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Batueva, I. V., Buchanan, J. T., Vesselkin, N. P., Suderevskaya, E. I., & Tsvetkov, E. (2002) · Neuroscience and Behavioral Physiology · doi:10.1023/a:1012960711757 · Cited by 2
Distinct Regulation of History-dependent Responses by Two Cortical Interneuron PopulationsPreprint
Phillips, E. A. K., Schreiner, C. E., & Hasenstaub, A. R. (2017) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/129593 · Cited by 2
Bhatnagar, S., Corbett, B. F., Urban, K. R., Luz, S., Arner, J., & Yan, J. (2022) · Research Square · doi:10.21203/rs.3.rs-1501873/v1 · Cited by 2
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McCleney, Z., & Kilpatrick, Z. P. (2016) · Journal of Mathematical Biology · doi:10.1007/s00285-016-0984-6 · Cited by 1
Bressloff, P. C. (2013) · Lecture notes on mathematical modelling in the life sciences · doi:10.1007/978-1-4614-8866-8_4 · Cited by 1
Kilpatrick, Z. P. (2012) · doi:10.26053/0h-et4r-fqg0 · Cited by 1
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Sehgal, M., Zhou, M., Cai, D. J., Lavi, A., Huang, S., & Silva, A. J. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-809324-5.21123-1 · Cited by 1
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Moyse, L. B., & Berry, H. (2024) · Journal of Theoretical Biology · doi:10.1016/j.jtbi.2024.111818 · Cited by 2
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Klement, G. (2007) · Figshare · Cited by 1
Lytvynenko, S. V. (2011) · Neurophysiology · doi:10.1007/s11062-011-9175-7 · Cited by 1
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King, B. (2015) · Libraries and Cultural Resources (University of Calgary) · doi:10.5072/prism/27131 · Cited by 1
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Ziehm, U. (2013) · doi:10.18452/16947 · Cited by 1
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Lee, J. H., Wang, X., & Bendor, D. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/661751 · Cited by 1
Fisch, K. (2011) · Elektronische Hochschulschriften der LMU München (Ludwig-Maximilians-Universität München) · doi:10.5282/edoc.13511 · Cited by 1
Guntu, V. (2020) · MOspace Institutional Repository (University of Missouri) · doi:10.32469/10355/88874 · Cited by 1
Bargas, J., Galarraga, E., & Surmeier, D. J. (1993) · Research notes in neural computing · doi:10.1007/978-3-642-78102-5_1 · Cited by 1
Gating Domain of Calcium‐Activated Potassium Channel with Calcium and Calmodulin
Schumacher, M. A. (2004) · Encyclopedia of Inorganic and Bioinorganic Chemistry · doi:10.1002/9781119951438.eibc0506
Segerstråle, M. (2011) · Työväentutkimus Vuosikirja
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Janahmadi, M., Farajnia, S., Ghasemi, Z., & Rastqar, A. (2011) · InTech eBooks · doi:10.5772/23636
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Bressloff, P. C. (2013) · Lecture notes on mathematical modelling in the life sciences · doi:10.1007/978-1-4614-8866-8_9
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Malenka, R. C., Madison, D. V., Dutar, P., Andrade, R., & Nicoll, R. A. (1988) · Springer eBooks · doi:10.1007/978-3-642-73160-0_14
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Wang, J., Wang, K., Chang, L., Deng, B., Wei, X., & Li, H. (2013) · Chinese Control and Decision Conference (CCDC) · doi:10.1109/ccdc.2013.6561391
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Bressloff, P. C. (2013) · Lecture notes on mathematical modelling in the life sciences · doi:10.1007/978-1-4614-8866-8_6
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Lindley, M. A., Thomas, M. P., & Horowitz, J. M. (1987) · Computer Methods and Programs in Biomedicine · doi:10.1016/0169-2607(87)90072-1
Adaptation shapes spike train correlations: theory and application to tinnitus
Ocker, G. K., Tzounopoulos, T., & Doiron, B. (2012) · BMC Neuroscience · doi:10.1186/1471-2202-13-s1-p146
Riblet, R., Kaur, A., Kaur, H., & Womble, M. D. (2010) · BIOS · doi:10.1893/011.081.0203
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Adaptation of locust wing stretch receptor firing in dynamic mode
Alaburda, A., Kaminskas, O., & Rukšėnas, O. (2009) · Biologija · doi:10.2478/v10054-009-0013-4
Canales de K+ tipo M y su relación con la canalopatía en la epileptogénesis
Solís, H., & López-Hernández, E. (2011) · Archivos de Neurociencias
Thibault, O., Hadley, R. W., & Landfield, P. W. (2001)
The Auditory Transduction Chain
Fakult, M.-N. (2004)
Locust wing stretch receptor adaptation and recovery from adaptation
Alaburda, A., Buišas, R., Guzulaitis, R., Kaminskas, O., & Rukšėnas, O. (2010) · Biologija · doi:10.2478/v10054-010-0008-1
Ganglion Cells of the Ferret Calcium-Activated Potassium Conductances in Retinal
Robinson, D. W., Chalupa, L. M., Wong, R. C. S., Cloherty, S. L., Ibbotson, M. R., O’Brien, B. J., Trenholm, S., McLaughlin, A. J., Schwab, D. J., Awatramani, G. B., et al. (2015)
The Role of LMO4 in the Regulation of Hippocampal and Amygdalar Synaptic Function
Qin, Z. (2013) · uO Research (University of Ottawa) · doi:10.20381/ruor-2709
Response recovery in the locust auditory pathway
Wirtssohn, S., & Ronacher, B. (2015) · Journal of Neurophysiology · doi:10.1152/jn.00832.2015
Studies on the effects of hemoglobin on synaptic transmission in the hippocampus
Yip, S. (2009) · cIRcle (University of British Columbia) · doi:10.14288/1.0099514
Metadata
- Authors
- Madison, D. V., & Nicoll, R. A.
- ORCID
- Madison, D V
- Venue
- The Journal of Physiology
- Publisher
- Wiley
- Published
- 1984-09
- Volume
- 354
- Issue
- 1
- Pages
- 319-331
- ISSN
- 0022-3751 (ISSN-L)
- 1469-7793
- PMC
- PMC1193414
- OpenAlex
- W2048528277
- Cited by
- 746
- References
- 35
- Citations by year
- 2026: 7 · 2025: 8 · 2024: 6 · 2023: 11 · 2022: 11 · 2021: 10 · 2020: 21 · 2019: 19 · 2018: 12 · 2017: 18 · 2016: 21 · 2015: 15 · 2014: 21 · 2013: 30 · 2012: 30
- FWCI
- 6.39
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- The Journal of Physiology (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Topics
- 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
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
- Keywords
- CA1 pyramidal neurons, hippocampus, accommodation, afterhyperpolarization, calcium-activated potassium current, M-current, carbachol, cadmium, EGTA, interspike intervals, neuronal excitability
- MeSH terms
- Action Potentials, Animals, Cadmium, Calcium, Calcium Channel Blockers, Egtazic Acid, Electric Conductivity, Hippocampus, Membrane Potentials, Neurons, Potassium, Rats, In Vitro Techniques
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