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Prolonged Disynaptic Inhibition in the Cortex Mediated by Slow, Non-α7 Nicotinic Excitation of a Specific Subset of Cortical Interneurons
Open accessAbstract
Cholinergic activation of nicotinic receptors in the cortex plays a critical role in arousal, attention, and learning. Here we demonstrate that cholinergic axons from the basal forebrain of mice excite a specific subset of cortical interneurons via a remarkably slow, non-α7 nicotinic receptor-mediated conductance. In turn, these inhibitory cells generate a delayed and prolonged wave of disynaptic inhibition in neighboring cortical neurons, altering the spatiotemporal pattern of inhibition in cortical circuits.
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“Anatomical, pharmacological and optogenetic evidence support this view (Acsady et al., 1993; Arroyo et al., 2012; Choi and Callaway, 2011; Ferezou et al., 2002; Lee et al., 2010).”
From GABAergic Interneurons in the Neocortex: From Cellular Properties to Circuits (2016) · cites this paper as Arroyo et al., 2012
Experimental — accuracy not yet measuredThe check wasn’t confident either way, so it gives no verdict — never disputed.
In the citing paper
“Expression of high levels of voltage-gated K+ channels with a depolarized activation voltage and fast deactivation rates of the Kv3 subfamily; channels specialized for rapid repolarization with little interference during the inter-spike interval.”
From GABAergic Interneurons in the Neocortex: From Cellular Properties to Circuits (2016) · cites this paper as [10]
Experimental — accuracy not yet measuredThe check wasn’t confident either way, so it gives no verdict — never disputed.
In the citing paper
“Kv3 channels also contribute to the generation of a large and fast AHP that facilitates the recovery of Na+ channels from inactivation9–11.”
From GABAergic Interneurons in the Neocortex: From Cellular Properties to Circuits (2016) · cites this paper as [10]
Experimental — accuracy not yet measuredIn the citing paper
“The fast inhibition is at least partially mediated by the actions of both nAChRs and mAChRs that increase the excitability and firing rates of dendrite-targeting GABAergic interneurons (Arroyo et al., 2012; Couey et al., 2007; Fanselow et al., 2008; Ferezou et al., 2002; Gulledge et al., 2007; Kawaguchi and Kubota, 1997).”
From Acetylcholine as a Neuromodulator: Cholinergic Signaling Shapes Nervous System Function and Behavior (2012) · cites this paper as Arroyo et al., 2012
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Cites
The distinct modes of vision offered by feedforward and recurrent processing
Lamme, V. A. F., & Roelfsema, P. R. (2000) · Trends in Neurosciences · doi:10.1016/s0166-2236(00)01657-x · Cited by 2,338 · cited 1×
“Moreover we propose that, given the delayed kinetics of the IPSC barrage, sensory activation of the BF will preferentially impact long latency intracortical activity over the initial feedforward sensory response (Lamme and Roelfsema, 2000).”
Corbetta, M., Miezin, F. M., Dobmeyer, S., Shulman, G. L., & Petersen, S. (1991) · Journal of Neuroscience · doi:10.1523/jneurosci.11-08-02383.1991 · Cited by 1,590
Three groups of interneurons account for nearly 100% of neocortical GABAergic neurons
Rudy, B., Fishell, G., Lee, S., & Hjerling‐Leffler, J. (2011) · Developmental Neurobiology · doi:10.1002/dneu.20853 · Cited by 1,420
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
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
Nicotinic Acetylcholine Receptors and Nicotinic Cholinergic Mechanisms of the Central Nervous System
Dani, J. A., & Bertrand, D. (2007) · Annual Review of Pharmacology and Toxicology · doi:10.1146/annurev.pharmtox.47.120505.105214 · Cited by 1,197
Steinlein, O. K., Mulley, J. C., Propping, P., Wallace, R. H., Phillips, H. A., Sutherland, G. R., Scheffer, I. E., & Berkovic, S. F. (1995) · Nature Genetics · doi:10.1038/ng1095-201 · Cited by 1,134
Gong, S., Doughty, M., Harbaugh, C. R., Cummins, A., Hatten, M. E., Heintz, N., & Gerfen, C. R. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.2707-07.2007 · Cited by 977
A disinhibitory microcircuit for associative fear learning in the auditory cortex
Letzkus, J. J., Wolff, S. B. E., Meyer, E. M. M., Tovote, P., Courtin, J., Herry, C., & Lüthi, A. (2011) · Nature · doi:10.1038/nature10674 · Cited by 840 · cited 3×
“…acetylcholine receptors (nAChRs) have been shown to play an important role in attention (Howe et al., 2010; Guillem et al., 2011) and learning (Letzkus et al., 2011), and gain of function mutations in a non- 7 receptor subunit has been linked to a heritable form of epilepsy (Steinlein et al.,…”
InfluentialRye, D. B., Wainer, B. H., Mesulam, M.-M., Mufson, E. J., & Saper, C. B. (1984) · Neuroscience · doi:10.1016/0306-4522(84)90083-6 · Cited by 743
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GABAergic Interneurons in the Neocortex: From Cellular Properties to Circuits
Tremblay, R., Lee, S., & Rudy, B. (2016) · Neuron · doi:10.1016/j.neuron.2016.06.033 · Cited by 2,033
Acetylcholine as a Neuromodulator: Cholinergic Signaling Shapes Nervous System Function and Behavior
Picciotto, M. R., Higley, M. J., & Mineur, Y. S. (2012) · Neuron · doi:10.1016/j.neuron.2012.08.036 · Cited by 1,404
Cortical interneurons that specialize in disinhibitory control
Pi, H.-J., Hangya, B., Kvitsiani, D., Sanders, J. I., Huang, Z. J., & Kepecs, A. (2013) · Nature · doi:10.1038/nature12676 · Cited by 1,136
A Cortical Circuit for Gain Control by Behavioral State
Fu, Y., Tucciarone, J. M., Espinosa, J. S., Sheng, N., Darcy, D. P., Nicoll, R. A., Huang, Z. J., & Stryker, M. P. (2014) · Cell · doi:10.1016/j.cell.2014.01.050 · Cited by 937
“No fast nAChR component like that shown in layer I inhibitory neurons (Letzkus et al., 2011) was evident; our findings showed instead a response with slow kinetics resembling what has been found in ChATpositive bipolar neurons (Arroyo et al., 2012).”
BackgroundResultInfluentialCorticostriatal connectivity and its role in disease
Shepherd, G. M. G. (2013) · Nature Reviews Neuroscience · doi:10.1038/nrn3469 · Cited by 824
Balancing Plasticity/Stability Across Brain Development
Takesian, A. E., & Hensch, T. K. (2013) · Progress in Brain Research · doi:10.1016/b978-0-444-63327-9.00001-1 · Cited by 667
Inhibition dominates sensory responses in the awake cortex
Haider, B., Häusser, M., & Carandini, M. (2012) · Nature · doi:10.1038/nature11665 · Cited by 547
Pakan, J. M., Lowe, S. C., Dylda, E., Keemink, S. W., Currie, S. P., Coutts, C. A., & Rochefort, N. L. (2016) · eLife · doi:10.7554/elife.14985 · Cited by 282
“Previous work has demonstrated cholinergic facilitation of cortical inhibitory neurons (Kawaguchi, 1997; Xiang et al., 1998; Arroyo et al., 2012; Alitto and Dan, 2012), including SST neurons (Kawaguchi, 1997; Fanselow et al., 2008; Xu et al., 2013; Chen et al., 2015).”
BackgroundThalamic control of layer 1 circuits in prefrontal cortex
Cruikshank, S. J., Ahmed, O. J., Stevens, T. R., Patrick, S. L., Gonzalez, A. N., Elmaleh, M., & Connors, B. W. (2012) · The Journal of Neuroscience · doi:10.1523/jneurosci.3231-12.2012 · Cited by 212
An acetylcholine-activated microcircuit drives temporal dynamics of cortical activity
Chen, N., Sugihara, H., & Sur, M. (2015) · Nature Neuroscience · doi:10.1038/nn.4002 · Cited by 210
Corelease of acetylcholine and GABA from cholinergic forebrain neurons
Saunders, A., Granger, A. J., & Sabatini, B. L. (2015) · eLife · doi:10.7554/elife.06412 · Cited by 200
Nelson, A., & MOONEY, R. D. (2016) · Neuron · doi:10.1016/j.neuron.2016.03.031 · Cited by 192
Nicotine reverses hypofrontality in animal models of addiction and schizophrenia
Koukouli, F., Rooy, M., Tziotis, D., Sailor, K. A., O’Neill, H. C., Levenga, J., Witte, M., Nilges, M., Changeux, J., Hoeffer, C. A., et al. (2017) · Nature Medicine · doi:10.1038/nm.4274 · Cited by 191
Layer- and Cell Type-Specific Modulation of Excitatory Neuronal Activity in the Neocortex
Radnikow, G., & Feldmeyer, D. (2018) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2018.00001 · Cited by 185
Neuromodulation by acetylcholine: examples from schizophrenia and depression
Higley, M. J., & Picciotto, M. R. (2014) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2014.06.004 · Cited by 184
A transcriptomic axis predicts state modulation of cortical interneurons
Bugeon, S., Duffield, J. A. M., Dipoppa, M., Ritoux, A., Prankerd, I., Nicoloutsopoulos, D., Orme, D., Shinn, M., Peng, H., Forrest, H., et al. (2022) · Nature · doi:10.1038/s41586-022-04915-7 · Cited by 185
Layer 6 Corticothalamic Neurons Activate a Cortical Output Layer, Layer 5a
Kim, J., Matney, C. J., Blankenship, A. G., Hestrin, S., & Brown, S. P. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.1325-14.2014 · Cited by 170
Self-citationFan, L. Z., Kheifets, S., Böhm, U. L., Wu, H., Piatkevich, K. D., Xie, M. E., Parot, V., Ha, Y., Evans, K. E., Boyden, E. S., et al. (2020) · Cell · doi:10.1016/j.cell.2020.01.001 · Cited by 160
Cell-type-specific modulation of neocortical activity by basal forebrain input
Alitto, H. J., & Dan, Y. (2013) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2012.00079 · Cited by 156
Bloem, B., Poorthuis, R. B., & Mansvelder, H. D. (2014) · Frontiers in Neural Circuits · doi:10.3389/fncir.2014.00017 · Cited by 163
Therapeutic Potential of α7 Nicotinic Acetylcholine Receptors
Bertrand, D., Lee, C., Flood, D. G., Marger, F., & Donnelly‐Roberts, D. L. (2015) · Pharmacological Reviews · doi:10.1124/pr.113.008581 · Cited by 142
Bloem, B., Schoppink, L., Rotaru, D. C., Faiz, A., Hendriks, P., Mansvelder, H. D., van de Berg, W. D. J., & Wouterlood, F. G. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.3011-14.2014 · Cited by 143
Cholinergic modulation of spatial learning, memory and navigation
Solari, N., & Hangya, B. (2018) · European Journal of Neuroscience · doi:10.1111/ejn.14089 · Cited by 146
Importance of the nicotinic acetylcholine receptor system in the prefrontal cortex
Wallace, T. L., & Bertrand, D. (2013) · Biochemical Pharmacology · doi:10.1016/j.bcp.2013.04.001 · Cited by 133
Cellular, Synaptic and Network Effects of Acetylcholine in the Neocortex
Colangelo, C., Shichkova, P., Keller, D. X., Markram, H., & Ramaswamy, S. (2019) · Frontiers in Neural Circuits · doi:10.3389/fncir.2019.00024 · Cited by 143
Spatiotemporal specificity in cholinergic control of neocortical function
Muñoz, W., & Rudy, B. (2014) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2014.02.015 · Cited by 124
A Dendritic Substrate for the Cholinergic Control of Neocortical Output Neurons
Williams, S. R., & Fletcher, L. N. (2018) · Neuron · doi:10.1016/j.neuron.2018.11.035 · Cited by 128
Impact of Basal Forebrain Cholinergic Inputs on Basolateral Amygdala Neurons
Ünal, Ç. T., Paré, D., & Záborszky, L. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.2706-14.2015 · Cited by 124
Chrna2-Martinotti cells synchronize layer 5 type A pyramidal cells via rebound excitation
Hilscher, M. M., Leão, R. N., Edwards, S. J., Leão, K. E., & Kullander, K. (2017) · PLoS Biology · doi:10.1371/journal.pbio.2001392 · Cited by 118
Lin, S., Brown, R. E., Shuler, M. G. H., Petersen, C. C. H., & Kepecs, Á. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.2590-15.2015 · Cited by 115
Normalization and the Cholinergic Microcircuit: A Unified Basis for Attention
Schmitz, T. W., & Duncan, J. (2018) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2018.02.011 · Cited by 119
The Cortical States of Wakefulness
Poulet, J. F. A., & Crochet, S. (2019) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2018.00064 · Cited by 126
Lecrux, C., & Hamel, É. (2016) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2015.0350 · Cited by 126
Cotransmission of acetylcholine and GABA
Granger, A. J., Mulder, N., Saunders, A. B., & Sabatini, B. L. (2015) · Neuropharmacology · doi:10.1016/j.neuropharm.2015.07.031 · Cited by 101
Obermayer, J., Heistek, T. S., Kerkhofs, A., Goriounova, N. A., Kroon, T., Baayen, J. C., Idema, S., Testa-Silva, G., Couey, J. J., & Mansvelder, H. D. (2018) · Nature Communications · doi:10.1038/s41467-018-06628-w · Cited by 114
Borden, P. M., Zhang, P., Shivange, A. V., Marvin, J. S., Cichon, J., Dan, C., Podgorski, K., Figueiredo, A. M. P. D., Novák, O., Tanimoto, M., et al. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.02.07.939504 · Cited by 98
Obermayer, J., Verhoog, M. B., Luchicchi, A., & Mansvelder, H. D. (2017) · Frontiers in Neural Circuits · doi:10.3389/fncir.2017.00100 · Cited by 106
Layer-specific cholinergic control of human and mouse cortical synaptic plasticity
Verhoog, M. B., Obermayer, J., Kortleven, C., Wilbers, R., Wester, J., Baayen, J. C., de Kock, C. P. J., Meredith, R. M., & Mansvelder, H. D. (2016) · Nature Communications · doi:10.1038/ncomms12826 · Cited by 104
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Urban-Ciecko, J., Jouhanneau, J.-S., Myal, S. E., Poulet, J. F. A., & Barth, A. L. (2018) · Neuron · doi:10.1016/j.neuron.2018.01.037 · Cited by 93
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Hangya, B., Pi, H.-J., Kvitsiani, D., Ranade, S., & Kepecs, Á. (2014) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2014.01.007 · Cited by 91
Zhang, G., Sun, W., Zingg, B., Shen, L., He, J., Xiong, Y., Tao, H. W., & Zhang, L. I. (2017) · Neuron · doi:10.1016/j.neuron.2017.12.010 · Cited by 95
Cell-type-specific nicotinic input disinhibits mouse barrel cortex during active sensing
Gasselin, C., Hohl, B., Vernet, A., Crochet, S., & Petersen, C. C. H. (2021) · Neuron · doi:10.1016/j.neuron.2020.12.018 · Cited by 90
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Brombas, A., Fletcher, L. N., & Williams, S. R. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.4470-13.2014 · Cited by 90
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Hedrick, T. P., & Waters, J. (2015) · Journal of Neurophysiology · doi:10.1152/jn.00716.2014 · Cited by 92
Obermayer, J., Luchicchi, A., Heistek, T. S., de Kloet, S. F., Terra, H., Bruinsma, B., Mnie-Filali, O., Kortleven, C., Galakhova, A. A., Khalil, A. J., et al. (2019) · Nature Communications · doi:10.1038/s41467-019-13244-9 · Cited by 83
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Bennett, C., Arroyo, S., Berns, D. S., & Hestrin, S. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.3565-12.2012 · Cited by 80
Self-citationSun, Y.-G., Pita‐Almenar, J. D., Wu, C., Renger, J. J., Uebele, V. N., Lu, H., & Beierlein, M. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.3177-12.2013 · Cited by 79
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Kang, J. I., Huppé‐Gourgues, F., & Vaucher, E. (2014) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2014.00172 · Cited by 75
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Pakan, J. M. P., Francioni, V., & Rochefort, N. L. (2018) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2018.04.020 · Cited by 75
Ren, C., Peng, K., Yang, R., Liu, W., Liu, C., & Komiyama, T. (2022) · Neuron · doi:10.1016/j.neuron.2022.04.031 · Cited by 79
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Gentet, L. J. (2012) · Frontiers in Neural Circuits · doi:10.3389/fncir.2012.00052 · Cited by 83
Antagonism of the 5-HT 6 receptor – Preclinical rationale for the treatment of Alzheimer's disease
de Jong, I. E. M., & Mørk, A. (2017) · Neuropharmacology · doi:10.1016/j.neuropharm.2017.07.010 · Cited by 80
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Poorthuis, R. B., Muhammad, K., Wang, M., Verhoog, M. B., Junek, S., Wrana, A., Mansvelder, H. D., & Letzkus, J. J. (2018) · Cell Reports · doi:10.1016/j.celrep.2018.03.111 · Cited by 73
Mesik, L., Ma, W., Li, L., Ibrahim, L. A., Huang, Z. J., Zhang, L. I., & Tao, H. W. (2015) · Frontiers in Neural Circuits · doi:10.3389/fncir.2015.00022 · Cited by 74
Luchicchi, A., Bloem, B., Viaña, J. N. M., Mansvelder, H. D., & Role, L. W. (2014) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2014.00024 · Cited by 74
Target selectivity of septal cholinergic neurons in the medial and lateral entorhinal cortex
Desikan, S., Koser, D. E., Neitz, A., & Monyer, H. (2018) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1716531115 · Cited by 72
Yiannakas, A., & Rosenblum, K. (2017) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2017.00335 · Cited by 72
Helboe, L., Egebjerg, J., & de Jong, I. E. M. (2015) · Neuroscience · doi:10.1016/j.neuroscience.2015.09.064 · Cited by 70
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Self-citationPoorthuis, R. B., Enke, L., & Letzkus, J. J. (2014) · The Journal of Physiology · doi:10.1113/jphysiol.2014.273862 · Cited by 66
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Beierlein, M. (2014) · The Journal of Physiology · doi:10.1113/jphysiol.2014.277376 · Cited by 61
Wester, J. C., & McBain, C. J. (2014) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2014.07.007 · Cited by 50
Hay, Y. A., Lambolez, B., & Tricoire, L. (2015) · Cerebral Cortex · doi:10.1093/cercor/bhv085 · Cited by 51
Demars, M. P., & Morishita, H. (2014) · Molecular Brain · doi:10.1186/s13041-014-0075-9 · Cited by 54
Poorthuis, R. B., & Mansvelder, H. D. (2013) · Biochemical Pharmacology · doi:10.1016/j.bcp.2013.07.003 · Cited by 54
Dasgupta, R., Seibt, F., & Beierlein, M. (2018) · The Journal of Neuroscience · doi:10.1523/jneurosci.0566-18.2018 · Cited by 47
Soma, S., Shimegi, S., Suematsu, N., Tamura, H., & Sato, H. (2013) · PLoS ONE · doi:10.1371/journal.pone.0068430 · Cited by 46
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Sur, M., Nagakura, I., Chen, N., & 杉原, 弘. (2013) · Progress in brain research · doi:10.1016/b978-0-444-63327-9.00002-3 · Cited by 44
Proenneke, A., Witte, M., Möck, M., & Staiger, J. F. (2019) · Cerebral Cortex · doi:10.1093/cercor/bhz102 · Cited by 50
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Wietek, J., & Prigge, M. (2016) · Methods in molecular biology · doi:10.1007/978-1-4939-3512-3_10 · Cited by 40
Estakhr, J., Abazari, D., Frisby, K., McIntosh, J. M., & Nashmi, R. (2017) · Current Biology · doi:10.1016/j.cub.2017.05.084 · Cited by 40
Hay, Y. A., Andjelić, S., Badr, S., & Lambolez, B. (2014) · Brain Structure and Function · doi:10.1007/s00429-014-0869-7 · Cited by 39
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Neske, G. T., & Connors, B. W. (2016) · Frontiers in Neural Circuits · doi:10.3389/fncir.2016.00052 · Cited by 39
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Pita‐Almenar, J. D., Yu, D., Lu, H., & Beierlein, M. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.2321-14.2014 · Cited by 36
Gaykema, R. P. A., Nguyen, X.-M. T., Boehret, J. M., Lambeth, P. S., Joy-Gaba, J., Warthen, D. M., & Scott, M. M. (2014) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2014.00060 · Cited by 36
Kimura, R., Safari, M.-S., Mirnajafi‐Zadeh, J., Kimura, R., Ebina, T., Yanagawa, Y., Sohya, K., & Tsumoto, T. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.0863-14.2014 · Cited by 32
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Terry, A. V., Callahan, P. M., & Bertrand, D. (2014) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.114.219881 · Cited by 30
Rodríguez-García, G., & Miranda, M. I. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.2340-15.2016 · Cited by 30
Coronel‐Oliveros, C., Cofré, R., & Orio, P. (2021) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1008737 · Cited by 29
Bell, L. A., Bell, K. A., & McQuiston, A. R. (2015) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2015.00115 · Cited by 29
Campbell, M. G., & Giocomo, L. M. (2018) · Journal of Neurophysiology · doi:10.1152/jn.00686.2017 · Cited by 29
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Bugeon, S., Duffield, J. A. M., Dipoppa, M., Ritoux, A., Prankerd, I., Nicoloutsopoulos, D., Orme, D., Shinn, M., Peng, H., Forrest, H., et al. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.10.24.465600 · Cited by 24
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Sun, Y.-G., Rupprecht, V., Zhou, L., Dasgupta, R., Seibt, F., & Beierlein, M. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.0409-16.2016 · Cited by 23
Zhong, P., Cao, Q., & Yan, Z. (2022) · Cerebral Cortex · doi:10.1093/cercor/bhac036 · Cited by 22
Aracri, P., Meneghini, S., Coatti, A., Amadeo, A., & Becchetti, A. (2016) · Neuroscience · doi:10.1016/j.neuroscience.2016.10.045 · Cited by 22
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Metadata
- Authors
- Arroyo, S., Bennett, C., Aziz, D., Brown, S. P., & Hestrin, S.
- Affiliations
- University of Arizona (US)
- Stanford Medicine (US)
- Johns Hopkins University (US)
- Venue
- The Journal of Neuroscience
- Publisher
- Society for Neuroscience
- Published
- 2012-03-14
- Volume
- 32
- Issue
- 11
- Pages
- 3859-3864
- ISSN
- 0270-6474 (ISSN-L)
- 1529-2401
- PMC
- PMC3320796
- OpenAlex
- W2002108201
- Cited by
- 138
- References
- 33
- Citations by year
- 2026: 1 · 2025: 4 · 2024: 2 · 2023: 4 · 2022: 7 · 2021: 7 · 2020: 8 · 2019: 8 · 2018: 14 · 2017: 9 · 2016: 12 · 2015: 19 · 2014: 27 · 2013: 10 · 2012: 6
- FWCI
- 7.98
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Journal of Neuroscience (publishedVersion, cc-by-nc-sa)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Eye Institute (R01EY012114)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Nicotinic Acetylcholine Receptors Study
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
- Keywords
- disynaptic inhibition, nicotinic acetylcholine receptors, cortical interneurons, cholinergic stimulation, basal forebrain, cholinergic axons, cortical circuits
- MeSH terms
- Action Potentials, Animals, Axons, Cerebral Cortex, Female, Interneurons, Male, Mice, Transgenic, Neural Inhibition, Reaction Time, Receptors, Nicotinic, Synapses, Time Factors, Mice, Cholinergic Neurons, alpha7 Nicotinic Acetylcholine Receptor
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