The DOI matches its Crossref record; 35 of the 35 references it cites were found in a registry or an index.
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.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The text we found for this paper looks like another document, so the self-check wasn’t run.
Citations
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
Self-citation
Cited by
Sorted by citations
Items 101–200 of 744
Giocomo, L. M., & Hasselmo, M. E. (2007) · Molecular Neurobiology · doi:10.1007/s12035-007-0032-z · Cited by 165
Faber, E. S. L., Callister, R., & Sah, P. (2001) · Journal of Neurophysiology · doi:10.1152/jn.2001.85.2.714 · Cited by 165
Lacaille, J., & Williams, S. (1990) · Neuroscience · doi:10.1016/0306-4522(90)90431-3 · Cited by 160
Learning to learn – Intrinsic plasticity as a metaplasticity mechanism for memory formation
Sehgal, M., Song, C., Ehlers, V. L., & Moyer, J. R. (2013) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2013.07.008 · Cited by 161
Yue, C., & Yaari, Y. (2006) · Journal of Neurophysiology · doi:10.1152/jn.01333.2005 · Cited by 156
Jensen, M. S., & Yaari, Y. (1988) · Annals of Neurology · doi:10.1002/ana.410240502 · Cited by 155
Contrasting Effects of the Persistent Na+ Current on Neuronal Excitability and Spike Timing
Vervaeke, K., Hu, H., Graham, L. J., & Storm, J. F. (2006) · Neuron · doi:10.1016/j.neuron.2005.12.022 · Cited by 152
Prescott, S. A., Ratté, S., Koninck, Y. D., & B, T. J. S. A. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.1388-06.2006 · Cited by 150
Hatch, R. J., Yan, W., Xia, D., & Götz, J. (2017) · Acta Neuropathologica · doi:10.1007/s00401-017-1674-1 · Cited by 156
M1 and M4 Receptors Modulate Hippocampal Pyramidal Neurons
Dasari, S., & Gulledge, A. T. (2010) · Journal of Neurophysiology · doi:10.1152/jn.00686.2010 · Cited by 145
Recapitulation and Reversal of Schizophrenia-Related Phenotypes in Setd1a-Deficient Mice
Mukai, J., Cannavò, E., Crabtree, G. W., Sun, Z., Diamantopoulou, A., Thakur, P., Chang, C., Cai, Y., Lomvardas, S., Takata, A., et al. (2019) · Neuron · doi:10.1016/j.neuron.2019.09.014 · Cited by 146
Increased Excitability of Aged Rabbit CA1 Neurons after Trace Eyeblink Conditioning
Moyer, J. R., Power, J., Thompson, L. T., & Disterhoft, J. F. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-14-05476.2000 · Cited by 143
Meeter, M., Murre, J. M. J., & Talamini, L. M. (2004) · Hippocampus · doi:10.1002/hipo.10214 · Cited by 146
Lübke, J. H. R., Frotscher, M., & Spruston, N. (1998) · Journal of Neurophysiology · doi:10.1152/jn.1998.79.3.1518 · Cited by 139
Vervaeke, K., Gu, N., Agdestein, C., Hu, H., & Storm, J. F. (2006) · The Journal of Physiology · doi:10.1113/jphysiol.2006.111336 · Cited by 135
Spike-Rate Coding and Spike-Time Coding Are Affected Oppositely by Different Adaptation Mechanisms
Prescott, S. A., & B, T. J. S. A. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.1792-08.2008 · Cited by 145
Chapter 11 Chapter Membrane currents in hippocampal neurons
Brown, D. A., Gähwiler, B. H., Griffith, W. H., & Halliwell, J. V. (1990) · Progress in brain research · doi:10.1016/s0079-6123(08)61247-9 · Cited by 137
Lamas, J. A., Selyanko, A. A., & Brown, D. A. (1997) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.1997.tb01637.x · Cited by 135
Slow and fast transient potassium currents in cultured rat hippocampal cells.
Ficker, E. K., & Heinemann, U. (1992) · The Journal of Physiology · doi:10.1113/jphysiol.1992.sp018932 · Cited by 133
Adenosine actions on CA1 pyramidal neurones in rat hippocampal slices.
Greene, R. W., & Haas, H. L. (1985) · The Journal of Physiology · doi:10.1113/jphysiol.1985.sp015788 · Cited by 127
SK channels and the varieties of slow after‐hyperpolarizations in neurons
Vogalis, F., Storm, J. F., & Lancaster, B. (2003) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2003.03040.x · Cited by 122
Higgs, M. H., Slee, S. J., & Spain, W. J. (2006) · The Journal of Neuroscience · doi:10.1523/jneurosci.1792-06.2006 · Cited by 124
Bumps, Breathers, and Waves in a Neural Network with Spike Frequency Adaptation
Coombes, S., & Owen, M. R. (2005) · Physical Review Letters · doi:10.1103/physrevlett.94.148102 · Cited by 124
Alterations in intrinsic neuronal excitability during normal aging
Disterhoft, J. F., & Oh, M. M. (2007) · Aging Cell · doi:10.1111/j.1474-9726.2007.00297.x · Cited by 128
A Cellular Correlate of Learning-induced Metaplasticity in the Hippocampus
Zelcer, I., Cohen, H., Richter‐Levin, G., Lebiosn, T., Grossberger, T., & Barkai, E. (2005) · Cerebral Cortex · doi:10.1093/cercor/bhi125 · Cited by 123
Tzingounis, A. V., Kobayashi, M., Takamatsu, K., & Nicoll, R. A. (2007) · Neuron · doi:10.1016/j.neuron.2007.01.011 · Cited by 120
Self-citationCorticosteroid receptor-dependent modulation of calcium currents in rat hippocampal CA1 neurons
Karst, H., Wadman, W. J., & Joëls, M. (1994) · Brain Research · doi:10.1016/0006-8993(94)91069-3 · Cited by 119
Brown, D. A. (1988) · Springer eBooks · doi:10.1007/978-1-4615-7302-9_2 · Cited by 120
Balanced excitation and inhibition are required for high-capacity, noise-robust neuronal selectivity
Rubin, R., Abbott, L. F., & Sompolinsky, H. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1705841114 · Cited by 127
Long-Lasting Cholinergic Modulation Underlies Rule Learning in Rats
Saar, D., Grossman, Y. R., & Barkai, E. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-04-01385.2001 · Cited by 118
Metabotropic Regulation of Intrinsic Excitability by Synaptic Activation of Kainate Receptors
Melyan, Z., Lancaster, B., & Wheal, H. V. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.5356-03.2004 · Cited by 117
Long-term potentiation: studies in the hippocampal slice
Sarvey, J. M., Burgard, E. C., & Decker, G. (1989) · Journal of Neuroscience Methods · doi:10.1016/0165-0270(89)90016-2 · Cited by 118
Physiological heterogeneity of nonpyramidal cells in rat hippocampal CA1 region
Kawaguchi, Y., & Hama, K. (1988) · Experimental Brain Research · doi:10.1007/bf00250594 · Cited by 116
Temporal considerations for stimulating spiral ganglion neurons with cochlear implants.
Boulet, J., White, M., & Bruce, I. C. (2016) · Journal of the Association for Research in Otolaryngology · doi:10.1007/s10162-015-0545-5 · Cited by 114
van Dongen, P. A. M., Grillner, S. E., & Hökfelt, T. G. M. (1986) · Brain Research · doi:10.1016/0006-8993(86)91310-7 · Cited by 115
Long‐term modifications in intrinsic neuronal properties and rule learning in rats
Saar, D., & Barkai, E. (2003) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.2003.02699.x · Cited by 114
Multiple mechanisms of spike-frequency adaptation in motoneurones
Powers, R. K., Sawczuk, A., Musick, J. R., & Binder, M. D. (1999) · Journal of Physiology-Paris · doi:10.1016/s0928-4257(99)80141-7 · Cited by 114
Small Conductance Ca2+-activated K+ Channels and Calmodulin
Lee, C. W., Ngo‐Anh, T. J., Bruening‐Wright, A., Maylie, J., & Adelman, J. P. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m302091200 · Cited by 114
Subthreshold Membrane-Potential Resonances Shape Spike-Train Patterns in the Entorhinal Cortex
Engel, T. A., Schimansky-Geier, L., Herz, A. V. M., Schreiber, S., & Erchova, I. A. (2008) · Journal of Neurophysiology · doi:10.1152/jn.01282.2007 · Cited by 114
Dopamine decreases the calcium-activated afterhyperpolarization in hippocampal CA1 pyramidal cells
Malenka, R. C., & Nicoll, R. A. (1986) · Brain Research · doi:10.1016/0006-8993(86)90773-0 · Cited by 114
Self-citationMidtgaard, J. (1992) · The Journal of Physiology · doi:10.1113/jphysiol.1992.sp019381 · Cited by 113
Gotts, S. J., & Plaut, D. C. (2002) · Cognitive Affective & Behavioral Neuroscience · doi:10.3758/cabn.2.3.187 · Cited by 116
Lopez-Garcia, J. A., & King, A. E. (1994) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.1994.tb00594.x · Cited by 111
Haug, T. M., & Storm, J. F. (2000) · Journal of Neurophysiology · doi:10.1152/jn.2000.83.4.2071 · Cited by 110
Calcium‐Activated Potassium Currents In Mammalian Neurons
Sah, P., & Davies, P. (2000) · Clinical and Experimental Pharmacology and Physiology · doi:10.1046/j.1440-1681.2000.03317.x · Cited by 109
Benda, J., Maler, L., & Longtin, A. (2010) · Journal of Neurophysiology · doi:10.1152/jn.00240.2010 · Cited by 109
Schwindt, P. C., Spain, W. J., & Crill, W. E. (1992) · Neuroscience · doi:10.1016/0306-4522(92)90166-y · Cited by 109
Fisahn, A., Heinemann, S. F., & McBain, C. J. (2004) · The Journal of Physiology · doi:10.1113/jphysiol.2004.077412 · Cited by 108
Mensi, S., Naud, R., Pozzorini, C., Avermann, M., Petersen, C. C. H., & Wulfram Gerstner, B. (2011) · Journal of Neurophysiology · doi:10.1152/jn.00408.2011 · Cited by 112
Crook, S. M., Ermentrout, B., & Bower, J. M. (1998) · Neural Computation · doi:10.1162/089976698300017511 · Cited by 108
A Sodium-Pump-Mediated Afterhyperpolarization in Pyramidal Neurons
Gulledge, A. T., Dasari, S., Onoue, K., Stephens, E. K., Hasse, J. M., & Avesar, D. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.0220-13.2013 · Cited by 105
Weinreich, D. M., & Wonderlin, W. F. (1987) · The Journal of Physiology · doi:10.1113/jphysiol.1987.sp016878 · Cited by 106
Kilpatrick, Z. P., & Bressloff, P. C. (2009) · Physica D Nonlinear Phenomena · doi:10.1016/j.physd.2009.06.003 · Cited by 105
Takakusaki, K., Shiroyama, T., & Kitai, S. T. (1997) · Neuroscience · doi:10.1016/s0306-4522(97)00019-5 · Cited by 105
Heterogeneity of rat corticospinal neurons
Tseng, G., & Prince, D. A. (1993) · The Journal of Comparative Neurology · doi:10.1002/cne.903350107 · Cited by 105
Bowden, S. E. H., Fletcher, S., Loane, D. J., & Marrion, N. V. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-20-j0006.2001 · Cited by 103
Nathan, P. J., Watson, J. M., Jesper, L., Davies, C. H., Peters, G., Dodds, C. M., Swirski, B., Lawrence, P., Bentley, G., O’Neill, B. V., et al. (2012) · The International Journal of Neuropsychopharmacology · doi:10.1017/s1461145712000752 · Cited by 100
Kaczorowski, C. C., & Disterhoft, J. F. (2009) · Learning & Memory · doi:10.1101/lm.1365609 · Cited by 101
Baraban, S. C., & Schwartzkroin, P. A. (1995) · Epilepsy Research · doi:10.1016/0920-1211(95)00045-3 · Cited by 102
A Na+‐activated K+ current in cultured brain stem neurones from chicks.
Dryer, S. E., Fujii, J. T., & Martin, A. R. (1989) · The Journal of Physiology · doi:10.1113/jphysiol.1989.sp017533 · Cited by 101
The calcium-activated slow AHP: cutting through the Gordian knot
Andrade, R., Foehring, R. C., & Tzingounis, A. V. (2012) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2012.00047 · Cited by 106
Muscarinic responses of rat basolateral amygdaloid neurons recorded in vitro.
Washburn, M. S., & Moises, H. C. (1992) · The Journal of Physiology · doi:10.1113/jphysiol.1992.sp019078 · Cited by 99
Kawaguchi, Y., & Hama, K. (1987) · Brain Research · doi:10.1016/0006-8993(87)90700-1 · Cited by 99
Effects of histamine on hippocampal pyramidal cells of the rat in vitro
Haas, H. L., & Greene, R. W. (1986) · Experimental Brain Research · doi:10.1007/bf00237408 · Cited by 99
IKCa Channels Are a Critical Determinant of the Slow AHP in CA1 Pyramidal Neurons
King, B., Rizwan, A. P., Asmara, H., Heath, N. C., Engbers, J. D. T., Dykstra, S., Bartoletti, T. M., Hameed, S., Zamponi, G. W., & Turner, R. W. (2015) · Cell Reports · doi:10.1016/j.celrep.2015.03.026 · Cited by 98
Kaczorowski, C. C., Sametsky, E. A., Shah, S., Vassar, R. J., & Disterhoft, J. F. (2009) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2009.09.003 · Cited by 96
Ashwood, T., Lancaster, B., & Wheal, H. V. (1986) · Experimental Brain Research · doi:10.1007/bf00237415 · Cited by 98
CRF Facilitates Calcium Release from Intracellular Stores in Midbrain Dopamine Neurons
Riegel, A. C., & Williams, J. T. (2008) · Neuron · doi:10.1016/j.neuron.2007.12.029 · Cited by 97
Chacron, M. J., Pakdaman, K., & Longtin, A. (2003) · Neural Computation · doi:10.1162/089976603762552915 · Cited by 97
Modeling sharp wave‐ripple complexes through a CA3‐CA1 network model with chemical synapses
Taxidis, J., Coombes, S., Mason, R., & Owen, M. R. (2011) · Hippocampus · doi:10.1002/hipo.20930 · Cited by 97
Fang, X., Jiang, S., Wang, J., Bai, Y., Kim, C. S., Blake, D., Weintraub, N. L., Lei, Y., & Lu, X.-Y. (2021) · Molecular Psychiatry · doi:10.1038/s41380-020-01004-x · Cited by 95
The septo-hippocampal projection: a model cholinergic pathway
Nicoll, R. A. (1985) · Trends in Neurosciences · doi:10.1016/0166-2236(85)90190-0 · Cited by 95
Self-citationYoshida, M., & Hasselmo, M. E. (2009) · The Journal of Neuroscience · doi:10.1523/jneurosci.5154-08.2009 · Cited by 94
Ashe, J. H., McKenna, T. M., & Weinberger, N. M. (1989) · Synapse · doi:10.1002/syn.890040106 · Cited by 94
APP Family Regulates Neuronal Excitability and Synaptic Plasticity but Not Neuronal Survival
Lee, S. H., Kang, J., Ho, A., Watanabe, H., Bolshakov, V. Y., & Shen, J. (2020) · Neuron · doi:10.1016/j.neuron.2020.08.011 · Cited by 97
McBain, C. J., Boden, P., & Hill, R. G. (1989) · Journal of Neuroscience Methods · doi:10.1016/0165-0270(89)90051-4 · Cited by 93
Wallén, P., Robertson, B., Cangiano, L., Löw, P., Bhattacharjee, A., Kaczmarek, L. K., & Grillner, S. E. (2007) · The Journal of Physiology · doi:10.1113/jphysiol.2007.138156 · Cited by 92
Sah, P., & Clements, J. D. (1999) · Journal of Neuroscience · doi:10.1523/jneurosci.19-10-03657.1999 · Cited by 91
Biophysical alterations of hippocampal pyramidal neurons in learning, ageing and Alzheimer's disease
Disterhoft, J. F., Wu, W., & Ohno, M. (2004) · Ageing Research Reviews · doi:10.1016/j.arr.2004.07.001 · Cited by 90
Groten, C. J., & MacVicar, B. A. (2022) · Communications Biology · doi:10.1038/s42003-022-03848-1 · Cited by 93
Weiss, C., Preston, A. R., Oh, M. M., Schwarz, R. D., Welty, D. F., & Disterhoft, J. F. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-02-00783.2000 · Cited by 89
Contribution of Outward Currents to Spike-Frequency Adaptation in Hypoglossal Motoneurons of the Rat
Sawczuk, A., Powers, R. K., & Binder, M. D. (1997) · Journal of Neurophysiology · doi:10.1152/jn.1997.78.5.2246 · Cited by 88
McLachlan, E. M., & Meckler, R. L. (1989) · The Journal of Physiology · doi:10.1113/jphysiol.1989.sp017714 · Cited by 88
Modulation of Hippocampal Circuits by Muscarinic and Nicotinic Receptors
Dannenberg, H., Young, K., & Hasselmo, M. E. (2017) · Frontiers in Neural Circuits · doi:10.3389/fncir.2017.00102 · Cited by 89
Franceschetti, S., Lavazza, T., Curia, G., Aracri, P., Panzica, F., Sancini, G., AVANZINI, G., & Magistretti, J. (2003) · Journal of Neurophysiology · doi:10.1152/jn.00695.2002 · Cited by 86
Goldstein, P. A., Elsen, F. P., Ying, S., Ferguson, C., Homanics, G. E., & Harrison, N. L. (2002) · Journal of Neurophysiology · doi:10.1152/jn.00885.2001 · Cited by 86
Intracellular Calcium and Control of Burst Generation in Neurons of Guinea‐Pig Neocortex in Vitro
Friedman, A., & Gutnick, M. J. (1989) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.1989.tb00802.x · Cited by 86
Interpretations of Data and Mechanisms for Hippocampal Pyramidal Cell Models
Graham, L. J. (1999) · Cerebral cortex · doi:10.1007/978-1-4615-4903-1_2 · Cited by 87
Tanabe, M., Gähwiler, B. H., & Gerber, U. R. (1998) · Journal of Neurophysiology · doi:10.1152/jn.1998.80.5.2268 · Cited by 85
A threshold sodium current in pyramidal cells in rat hippocampus
French, C. R., & Gage, P. W. (1985) · Neuroscience Letters · doi:10.1016/0304-3940(85)90257-5 · Cited by 85
Inhibitory action of serotonin in CA1 hippocampal neurons In vitro
Ropert, N. (1988) · Neuroscience · doi:10.1016/0306-4522(88)90128-5 · Cited by 83
Nitsch, C., Goping, G., & KLATZO, I. (1989) · Brain Research · doi:10.1016/0006-8993(89)90218-7 · Cited by 83
Muscarinic agonists modulate spontaneous and evoked unit discharge in auditory cortex of cat
McKenna, T. M., Ashe, J. H., Hui, G. K., & Weinberger, N. M. (1988) · Synapse · doi:10.1002/syn.890020109 · Cited by 83
Fisahn, A. (2004) · The Journal of Physiology · doi:10.1113/jphysiol.2004.077388 · Cited by 83
Cholinergic Dysfunction in Temporal Lobe Epilepsy
Friedman, A., Behrens, C., & Heinemann, U. (2007) · Epilepsia · doi:10.1111/j.1528-1167.2007.01300.x · Cited by 82
Intrinsic Firing Dynamics of Vestibular Nucleus Neurons
Sekirnjak, C., & du Lac, S. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-06-02083.2002 · Cited by 81
An Event-Based Neural Network Architecture With an Asynchronous Programmable Synaptic Memory
Moradi, S., & Indiveri, G. (2013) · IEEE Transactions on Biomedical Circuits and Systems · doi:10.1109/tbcas.2013.2255873 · Cited by 79
A non-synaptic mechanism of complex learning: Modulation of intrinsic neuronal excitability
Chandra, N., & Barkai, E. (2017) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2017.11.015 · Cited by 79
Possible role of acetylcholine in regulating spatial novelty effects on theta rhythm and grid cells
Barry, C., Heys, J. G., & Hasselmo, M. E. (2012) · Frontiers in Neural Circuits · doi:10.3389/fncir.2012.00005 · Cited by 81
Cellular defenses against excitotoxic insults
Sapolsky, R. M. (2001) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.2001.00203.x · Cited by 77
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
About these checks
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.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review