The DOI matches its Crossref record; 76 of the 76 references it cites were found in a registry or an index.
Prefrontal Acetylcholine Release Controls Cue Detection on Multiple Timescales
Open accessAbstract
Cholinergic neurons originating from the basal forebrain innervate the entire cortical mantle. Choline-sensitive microelectrodes were used to measure the synaptic release of cortical acetylcholine (ACh) at a subsecond resolution in rats performing a task involving the detection of cues. Cues that were detected, defined behaviorally, evoked transient increases in cholinergic activity (at the scale of seconds) in the medial prefrontal cortex (mPFC), but not in a nonassociational control region (motor cortex). In trials involving missed cues, cholinergic transients were not observed. Cholinergic deafferentation of the mPFC, but not motor cortex, impaired cue detection. Furthermore, decreases and increases in precue cholinergic activity predicted subsequent cue detection or misses, respectively. Finally, cue-evoked cholinergic transients were superimposed over slower (at the timescale of minutes) changes in cholinergic activity. Cortical cholinergic neurotransmission is regulated on multiple timescales to mediate the detection of behaviorally significant cues and to support cognitive performance.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“nicotine can stimulate the firing of both POMC neurons that signal satiety, and neuropeptide Y (NPY) neurons that stimulate food seeking (Parikh et al. 2007(Parikh et al. , 2008)).”
From Mechanisms of Nicotine Addiction (2021) · cites this paper as Parikh et al. 2007
In the citing paper
“mice lacking the β2, but not the α7, subunit show impaired performance in an attentional task (Parikh et al. 2007(Parikh et al. , 2008)).”
From Mechanisms of Nicotine Addiction (2021) · cites this paper as Parikh et al. 2007
In the citing paper
“rapid acetylcholine transients in the mPFC are correlated with attention to brief cues”
From Mechanisms of Nicotine Addiction (2021) · cites this paper as Parikh et al. 2007
In the citing paper
“in a slice preparation, the effects of nicotine on firing of POMC neurons persist longer than firing of NPY neurons (Parikh et al. 2007(Parikh et al. , 2008))”
From Mechanisms of Nicotine Addiction (2021) · cites this paper as Parikh et al. 2007
In the citing paper
“Furthermore, the timing of the peak amplitude varied with the duration of the interval between cue and reward, with peak times at about 1.5 s after cue presentation recorded in animals trained on shortest cue-reward intervals (2±1 s; see Parikh et al, 2007).”
From Modes and models of forebrain cholinergic neuromodulation of cognition (2011) · cites this paper as Parikh et al, 2007
In the citing paper
“In the mPFC, cues that were detected evoked transient increases in cholinergic activity (Figure 1).”
From Modes and models of forebrain cholinergic neuromodulation of cognition (2011) · cites this paper as Parikh et al, 2007
In the citing paper
“Recordings from such trials as well as from several control procedures indicated that the presence or absence of reward and reward-related behavior did not contribute to the generation of cholinergic transients.”
From Modes and models of forebrain cholinergic neuromodulation of cognition (2011) · cites this paper as Parikh et al, 2007
In the citing paper
“This results in an excitatory feedback process that drives the large transient increase in acetylcholine seen with cue detection (Parikh et al, 2007), as shown in Figure 3B.”
From Modes and models of forebrain cholinergic neuromodulation of cognition (2011) · cites this paper as Parikh et al, 2007
In the citing paper
“This transition from encoding to retrieval could be mediated by changes in cholinergic neurotransmission on a time scale of the sort demonstrated with amperometry in the neocortex (Parikh et al., 2007).”
From Modes and models of forebrain cholinergic neuromodulation of cognition (2011) · cites this paper as Parikh et al., 2007
Citations
Cites
A Coefficient of Agreement for Nominal Scales
Cohen, J. (1960) · Educational and Psychological Measurement · doi:10.1177/001316446002000104 · Cited by 42,398
Aston-Jones, G., & Cohen, J. D. (2005) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.28.061604.135709 · Cited by 4,472
Attention and the detection of signals.
Posner, M. I., Snyder, C. R., & Davidson, B. J. (1980) · Journal of Experimental Psychology: General · doi:10.1037/0096-3445.109.2.160 · Cited by 3,778
Gorillas in our midst: sustained inattentional blindness for dynamic events
Simons, D. J., & Chabris, C. F. (1999) · Perception · doi:10.1068/p281059 · Cited by 3,181
Large-scale neurocognitive networks and distributed processing for attention, language, and memory
Mesulam, M. (1990) · Annals of Neurology · doi:10.1002/ana.410280502 · Cited by 2,684
Berridge, C. W., & Waterhouse, B. D. (2003) · Brain Research Reviews · doi:10.1016/s0165-0173(03)00143-7 · Cited by 2,529
The neural bases of momentary lapses in attention
Weissman, D. H., Roberts, K. C., Visscher, K. M., & Woldorff, M. G. (2006) · Nature Neuroscience · doi:10.1038/nn1727 · Cited by 1,566
CENTRAL CHOLINERGIC SYSTEMS AND COGNITION
Everitt, B. J., & Robbins, T. W. (1997) · Annual Review of Psychology · doi:10.1146/annurev.psych.48.1.649 · Cited by 1,348
Cortical Map Reorganization Enabled by Nucleus Basalis Activity
Kilgard, M. P., & Merzenich, M. M. (1998) · Science · doi:10.1126/science.279.5357.1714 · Cited by 1,197
Posner, M. I., & Dehaene, S. (1994) · Trends in Neurosciences · doi:10.1016/0166-2236(94)90078-7 · Cited by 897
Flagged first, then by citations
Cited by
Sorted by citations
Items 301–400 of 624
Birtalan, E., Bánhidi, A., Sanders, J. I., Balázsfi, D., & Hangya, B. (2020) · Scientific Reports · doi:10.1038/s41598-020-79290-2 · Cited by 29
Basal Forebrain Cholinergic Neurons Selectively Drive Coordinated Motor Learning in Mice
Li, Y., & Hollis, E. (2021) · Journal of Neuroscience · doi:10.1523/jneurosci.1152-21.2021 · Cited by 23
Cholinergic activity reflects reward expectations and predicts behavioral responses
Hegedüs, P., Sviatkó, K., Király, B., Martínez‐Bellver, S., & Hangya, B. (2022) · iScience · doi:10.1016/j.isci.2022.105814 · Cited by 28
Aracri, P., Amadeo, A., Pasini, M. E., Fascio, U., & Becchetti, A. (2013) · Synapse · doi:10.1002/syn.21655 · Cited by 27
Kim, K., Bohnen, N. I., Müller, M. L. T. M., & Lustig, C. (2018) · NeuroImage · doi:10.1016/j.neuroimage.2018.01.021 · Cited by 27
Hassani, S. A., Lendor, S., Boyacı, E., Pawliszyn, J. B., & Womelsdorf, T. (2019) · Journal of Neurophysiology · doi:10.1152/jn.00321.2019 · Cited by 26
Parsa, P. V., D’Souza, R. D., & Vijayaraghavan, S. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1424406112 · Cited by 26
Galvin, V. C., Arnsten, A. F. T., & Wang, M. (2018) · Frontiers in Neural Circuits · doi:10.3389/fncir.2018.00067 · Cited by 25
Galanthamine plus estradiol treatment enhances cognitive performance in aged ovariectomized rats
Gibbs, R. B., Chipman, A. M., Hammond, R., & Nelson, D. A. (2011) · Hormones and Behavior · doi:10.1016/j.yhbeh.2011.08.010 · Cited by 25
Cholinergic Contributions to Supramodal Attentional Processes in Rats
Ljubojevic, V., Luu, P., & Rosa, E. D. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.1024-13.2014 · Cited by 26
Cholinergic circuit control of postnatal neurogenesis
Asrican, B., Páez, P., Erb, J., & Kuo, C. T. (2016) · Neurogenesis · doi:10.1080/23262133.2015.1127310 · Cited by 25
Kucinski, A. J., de Jong, I. E. M., & Sarter, M. F. (2016) · European Journal of Neuroscience · doi:10.1111/ejn.13354 · Cited by 25
Self-citationDisney, A. A., McKinney, C., Grissom, L., Lu, X., & Reynolds, J. H. (2015) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2015.07.009 · Cited by 25
Zhou, W., Gao, X., & Picciotto, M. R. (2015) · eNeuro · doi:10.1523/eneuro.0052-14.2015 · Cited by 24
Stress Regulation of Sustained Attention and the Cholinergic Attention System
Eck, S. R., Xu, S., Telenson, A. M., Duggan, M. R., Cole, R. D., Wicks, B., Bergmann, J., Lefebo, H., Shore, M. E., Shepard, K. A., et al. (2020) · Biological Psychiatry · doi:10.1016/j.biopsych.2020.04.013 · Cited by 26
Self-citationNoftz, W. A., Beebe, N. L., Mellott, J. G., & Schofield, B. R. (2020) · Frontiers in Neural Circuits · doi:10.3389/fncir.2020.00043 · Cited by 25
Contribution of the basal forebrain to corticocortical network interactions
Gombkötő, P., Gielow, M. R., Varsanyi, P., Chavez, C. M., & Záborszky, L. (2021) · Brain Structure and Function · doi:10.1007/s00429-021-02290-z · Cited by 23
Is the role of sleep in memory consolidation overrated?
Dastgheib, M., Kulanayagam, A., & Dringenberg, H. C. (2022) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2022.104799 · Cited by 27
In vivo cholinergic modulation of the cellular properties of medial entorhinal cortex neurons
Tsuno, Y., Schultheiss, N. W., & Hasselmo, M. E. (2013) · The Journal of Physiology · doi:10.1113/jphysiol.2012.250431 · Cited by 27
Lemercier, C. E., Schulz, S., Heidmann, K. E., Kovács, R., & Gerevich, Z. (2016) · Frontiers in Pharmacology · doi:10.3389/fphar.2015.00297 · Cited by 23
Cortical acetylcholine dynamics are predicted by cholinergic axon activity and behavior state
Neyhart, E., Zhou, N., Munn, B., Law, R., Smith, C. L., Mridha, Z., Blanco, F. A., Li, G., Li, Y., Hu, M., et al. (2024) · Cell Reports · doi:10.1016/j.celrep.2024.114808 · Cited by 23
Basal Forebrain Mediates Motivational Recruitment of Attention by Reward-Associated Cues
Tashakori-Sabzevar, F., & Ward, R. D. (2018) · Frontiers in Neuroscience · doi:10.3389/fnins.2018.00786 · Cited by 23
Increased cortical excitability but stable effective connectivity index during attentional lapses
Cardone, P., Egroo, M. V., Chylinski, D., Narbutas, J., Gaggioni, G., & Vandewalle, G. (2020) · SLEEP · doi:10.1093/sleep/zsaa284 · Cited by 22
Baxter, M. G., & Bucci, D. J. (2013) · Behavioral Neuroscience · doi:10.1037/a0033781 · Cited by 22
Spectral Processing in Auditory Cortex
Schreiner, C. E., Froemke, R. C., & Atencio, C. A. (2010) · Springer eBooks · doi:10.1007/978-1-4419-0074-6_13 · Cited by 24
Serotonergic Suppression of Mouse Prefrontal Circuits Implicated in Task Attention
Tian, M. K., Schmidt, E. F., & Lambe, E. K. (2016) · eNeuro · doi:10.1523/eneuro.0269-16.2016 · Cited by 26
Smith, S. K., Lugo‐Morales, L. Z., Tang, C., Gosrani, S. P., Lee, C. A., Roberts, J. G., Morton, S. W., McCarty, G. S., Khan, S. A., & Sombers, L. A. (2018) · ChemPhysChem · doi:10.1002/cphc.201701235 · Cited by 24
Apamin Improves Prefrontal Nicotinic Impairment in Mouse Model of Alzheimer’s Disease
Proulx, É., Power, S. K., Oliver, D. K., Sargin, D., McLaurin, J., & Lambe, E. K. (2019) · Cerebral Cortex · doi:10.1093/cercor/bhz107 · Cited by 23
Thomsen, M. S., Hay‐Schmidt, A., Hansen, H. H., & Mikkelsen, J. D. (2010) · Cerebral Cortex · doi:10.1093/cercor/bhp283 · Cited by 23
Cholinergic Overstimulation Attenuates Rule Selectivity in Macaque Prefrontal Cortex
Major, A. J., Vijayraghavan, S., & Everling, S. (2017) · Journal of Neuroscience · doi:10.1523/jneurosci.3198-17.2017 · Cited by 22
Acetylcholine Mediates Dynamic Switching Between Information Coding Schemes in Neuronal Networks
Roach, J. P., Eniwaye, B. P., Booth, V., Sander, L. M., & Żochowski, M. (2019) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2019.00064 · Cited by 22
Kanamaru, T., Fujii, H., & Aihara, K. (2013) · PLoS ONE · doi:10.1371/journal.pone.0053854 · Cited by 23
Scopolamine impairs auditory delayed matching-to-sample performance in monkeys
Plakke, B., Ng, C.-W., & Poremba, A. (2008) · Neuroscience Letters · doi:10.1016/j.neulet.2008.04.015 · Cited by 24
Palma, J., Grossberg, S., & Massimiliano Versace, A. (2012) · Frontiers in Computational Neuroscience · doi:10.3389/fncom.2012.00042 · Cited by 21
Betts, G., Hynes, T. J., & Winstanley, C. A. (2021) · Journal of Psychopharmacology · doi:10.1177/0269881120972421 · Cited by 25
Ostlund, S. B., Kosheleff, A. R., & Maidment, N. T. (2013) · Neuropsychopharmacology · doi:10.1038/npp.2013.348 · Cited by 24
Herrera, B., Sajad, A., Woodman, G. F., Schall, J. D., & Riera, J. J. (2020) · Journal of Neuroscience · doi:10.1523/jneurosci.0221-20.2020 · Cited by 20
α7 nicotinic acetylcholine receptor in memory processing
Pastor, V. E., & Medina, J. H. (2023) · European Journal of Neuroscience · doi:10.1111/ejn.15913 · Cited by 24
Grupe, M., Paolone, G., Jensen, A. A., Sandager‐Nielsen, K., Sarter, M. F., & Grunnet, M. (2013) · Biochemical Pharmacology · doi:10.1016/j.bcp.2013.09.005 · Cited by 21
Self-citationCholine‐mediated modulation of hippocampal sharp wave–ripple complexesin vitro
Fischer, V., Both, M., Draguhn, A., & Egorov, A. V. (2014) · Journal of Neurochemistry · doi:10.1111/jnc.12693 · Cited by 21
Potential roles of cholinergic modulation in the neural coding of location and movement speed
Dannenberg, H., Hinman, J. R., & Hasselmo, M. E. (2016) · Journal of Physiology-Paris · doi:10.1016/j.jphysparis.2016.09.002 · Cited by 22
Hersman, S., Cushman, J. D., Lemelson, N., Wassum, K. M., Lotfipour, S., & Fanselow, M. S. (2017) · Scientific Reports · doi:10.1038/s41598-017-02542-1 · Cited by 21
Recollection-related increases in functional connectivity across the healthy adult lifespan
King, D. R., de Chastelaine, M., & Rugg, M. D. (2017) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2017.09.026 · Cited by 19
Endogenous Acetylcholine and Its Modulation of Cortical Microcircuits to Enhance Cognition
Venkatesan, S., Jeoung, H., Chen, T., Power, S. K., Liu, Y., & Lambe, E. K. (2020) · Current topics in behavioral neurosciences · doi:10.1007/7854_2020_138 · Cited by 21
Lammers‐Lietz, F., Mobascher, A., Musso, F., Shah, N. J., Warbrick, T., Záborszky, L., & Winterer, G. (2015) · Brain and Behavior · doi:10.1002/brb3.421 · Cited by 20
Make a Left Turn: Cortico‐Striatal Circuitry Mediating the Attentional Control of Complex Movements
Sarter, M. F., Avila, C., Kucinski, A. J., & Donovan, E. (2021) · Movement Disorders · doi:10.1002/mds.28532 · Cited by 23
Self-citationAbbondanza, A., Urushadze, A., Alves-Barboza, A. R., & Janíčková, H. (2024) · Pharmacological Research · doi:10.1016/j.phrs.2024.107190 · Cited by 20
Spiking activity in the visual thalamus is coupled to pupil dynamics across temporal scales
Crombie, D., Spacek, M. A., Leibold, C., & Busse, L. (2024) · PLoS Biology · doi:10.1371/journal.pbio.3002614 · Cited by 24
Blockade of muscarinic receptors impairs the retrieval of well-trained memory
Soma, S., Suematsu, N., & Shimegi, S. (2014) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2014.00063 · Cited by 20
Electrochemical techniques for subsecond neurotransmitter detection in live rodents.
Hascup, K. N., & Hascup, E. R. (2014) · PubMed · Cited by 19
A network model of behavioural performance in a rule learning task
Hasselmo, M. E., & Stern, C. E. (2018) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2017.0275 · Cited by 20
Lü, Y., Sarter, M. F., Żochowski, M., & Booth, V. (2020) · European Journal of Neuroscience · doi:10.1111/ejn.14744 · Cited by 20
Self-citationHussein, A., Tielemans, A., Baxter, M. G., Benson, D. L., & Huntley, G. W. (2022) · Experimental Neurology · doi:10.1016/j.expneurol.2022.114145 · Cited by 19
Cholinergic Mechanisms in Gastrointestinal Neoplasia
Moura, N. S., Schledwitz, A., Alizadeh, M. A., Kodan, A., Njei, L., & Raufman, J. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25105316 · Cited by 20
Nicotine Acts on Cholinergic Signaling Mechanisms to Directly Modulate Choroid Plexus Function
Lallai, V., Grimes, N. P., Fowler, J. P., Sequeira, P. A., Cartagena, P. M., Limón, A., Coutts, M., Monuki, E. S., Bunney, W. E., Demuro, A., et al. (2019) · eNeuro · doi:10.1523/eneuro.0051-19.2019 · Cited by 19
Azimi, M., Oemisch, M., & Womelsdorf, T. (2019) · Psychopharmacology · doi:10.1007/s00213-019-05430-w · Cited by 19
Theta-gamma coupling emerges from spatially heterogeneous cholinergic neuromodulation
Yang, Y., Gritton, H. J., Sarter, M. F., Aton, S. J., Booth, V., & Żochowski, M. (2021) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1009235 · Cited by 19
Self-citationSaravanan, V., Arabali, D., Jochems, A., Cui, A., Gootjes-Dreesbach, L., Cutsuridis, V., & Yoshida, M. (2015) · Hippocampus · doi:10.1002/hipo.22429 · Cited by 18
Basal forebrain dynamics during nonassociative and associative olfactory learning
Devore, S., Pender-Morris, N., Dean, O. R., Smith, D. M., & Linster, C. (2015) · Journal of Neurophysiology · doi:10.1152/jn.00572.2015 · Cited by 19
Computational model of visual hallucination in dementia with Lewy bodies
Tsukada, H., Fujii, H., Aihara, K., & Tsuda, I. (2015) · Neural Networks · doi:10.1016/j.neunet.2014.09.001 · Cited by 17
Hoffmann, L. C., Cicchese, J. J., & Berry, S. D. (2015) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2015.00050 · Cited by 20
Melamine Disrupts Acetylcholine-Mediated Neural Information Flow in the Hippocampal CA3–CA1 Pathway
Sun, W., Liu, P., Tang, C., & An, L. (2021) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2021.594907 · Cited by 18
Cell-specific modulation of plasticity and cortical state by cholinergic inputs to the visual cortex
杉原, 弘., Chen, N., & Sur, M. (2016) · Journal of Physiology-Paris · doi:10.1016/j.jphysparis.2016.11.004 · Cited by 18
Nagasaka, K., Watanabe, Y., & Takashima, I. (2017) · Brain stimulation · doi:10.1016/j.brs.2017.06.008 · Cited by 18
Takahashi, S., Ohmiya, M., Honda, S., & Ni, K. (2018) · PLoS ONE · doi:10.1371/journal.pone.0207750 · Cited by 18
Baker, K. L., Bolger, F. B., Doran, M. M., & Lowry, J. P. (2018) · Electroanalysis · doi:10.1002/elan.201800642 · Cited by 17
The Basal Forebrain Modulates Neuronal Response in an Active Olfactory Discrimination Task
Nunez-Parra, A., Rio, C. A. C.-D., Huntsman, M. M., & Restrepo, D. (2020) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2020.00141 · Cited by 17
Kipp, B. T., Nunes, P. T., Galaj, E., Hitchcock, B., Nasra, T., Poynor, K. R., Heide, S., Reitz, N. L., & Savage, L. M. (2021) · Neuroscience · doi:10.1016/j.neuroscience.2021.08.014 · Cited by 18
Eickhoff, S., Franzen, L., Korda, A. I., Rogg, H. V., Trulley, V.-N., Borgwardt, S., & Avram, M. (2022) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2022.909961 · Cited by 17
Xanomeline restores endogenous nicotinic acetylcholine receptor signaling in mouse prefrontal cortex
Power, S. K., Venkatesan, S., & Lambe, E. K. (2023) · Neuropsychopharmacology · doi:10.1038/s41386-023-01531-5 · Cited by 17
Thiele, A. (2009) · Nature Neuroscience · doi:10.1038/nn1109-1359 · Cited by 17
Vu, M. T., Du, G., Bayliss, D. A., & Horner, R. L. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.1445-15.2015 · Cited by 17
Proulx, É., Suri, D., Heximer, S. P., Vaidya, V. A., & Lambe, E. K. (2013) · Biological Psychiatry · doi:10.1016/j.biopsych.2013.10.017 · Cited by 18
In cerebro unveiling unconscious mechanisms during reading
Lévy, J. (2010) · Max Planck Digital Library · Cited by 17
Kanamaru, T., & Aihara, K. (2019) · PLoS ONE · doi:10.1371/journal.pone.0223592 · Cited by 18
Dopamine influences attentional rate modulation in Macaque posterior parietal cortex
van Kempen, J., Brandt, C., Distler, C., Bellgrove, M. A., & Thiele, A. (2022) · Scientific Reports · doi:10.1038/s41598-022-10634-w · Cited by 16
Verhoog, M. B., & Mansvelder, H. D. (2011) · Neural Plasticity · doi:10.1155/2011/870763 · Cited by 16
Bogachouk, A. P., Storozheva, Z. I., Solovjeva, O. A., Sherstnev, V. V., Zolotarev, Y. A., Азев, В. Н., Rodionov, I. L., Surina, E. A., & Lipkin, V. M. (2015) · Journal of Psychopharmacology · doi:10.1177/0269881115616393 · Cited by 16
Potential Mechanisms Underlying Intercortical Signal Regulation via Cholinergic Neuromodulators
Lee, J. H., Whittington, M. A., & Kopell, N. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.0629-15.2015 · Cited by 16
Kang, L., Tian, M. K., Bailey, C. D. C., & Lambe, E. K. (2015) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2015.00398 · Cited by 15
Yegla, B., & Parikh, V. (2014) · Neuroscience · doi:10.1016/j.neuroscience.2013.12.042 · Cited by 16
Self-citationKehr, J., Hu, X.-J., Yoshitake, T., Wang, F.-H., Osborne, P. G., Stenfors, C., & Ögren, S. O. (2010) · European Neuropsychopharmacology · doi:10.1016/j.euroneuro.2010.03.003 · Cited by 16
Reduced spiking in entorhinal cortex during the delay period of a cued spatial response taskPreprint
Gupta, K., Keller, L. A., & Hasselmo, M. E. (2012) · Learning & Memory · doi:10.1101/lm.025866.112 · Cited by 14
Vijayraghavan, S., & Everling, S. (2021) · Frontiers in Neural Circuits · doi:10.3389/fncir.2021.648624 · Cited by 19
Schneider, K. K., Schote, A. B., Meyer, J., Markett, S. A., Reuter, M., & Frings, C. (2015) · Behavioural Brain Research · doi:10.1016/j.bbr.2015.01.041 · Cited by 16
Involvement of Nicotinic Receptors in Working Memory Function
Galvin, V. C., Arnsten, A. F. T., & Wang, M. (2020) · Current topics in behavioral neurosciences · doi:10.1007/7854_2020_142 · Cited by 18
Cholinergic modulation of sensory processing in awake mouse cortex
Jiménez-Martín, J., Потапов, Д. О., Potapov, K., Knöpfel, T., & Empson, R. M. (2021) · Scientific Reports · doi:10.1038/s41598-021-96696-8 · Cited by 18
Hall, B. J., Abreu‐Villaça, Y., Cauley, M. C., Junaid, S., White, H., Kiany, A., & Levin, E. D. (2017) · Neuropharmacology · doi:10.1016/j.neuropharm.2017.01.019 · Cited by 16
Tsolias, A., & Medalla, M. (2022) · Frontiers in Neural Circuits · doi:10.3389/fncir.2021.795325 · Cited by 13
Temporal dynamics of cholinergic activity in the septo-hippocampal system
Kopsick, J. D., Hartzell, K., Lazaro, H., Nambiar, P., Hasselmo, M. E., & Dannenberg, H. (2022) · Frontiers in Neural Circuits · doi:10.3389/fncir.2022.957441 · Cited by 14
Lindeman, S., Fu, X., Reinert, J. K., & Fukunaga, I. (2024) · PLoS Biology · doi:10.1371/journal.pbio.3002536 · Cited by 17
Palma, J., Massimiliano Versace, A., & Grossberg, S. (2011) · Journal of Computational Neuroscience · doi:10.1007/s10827-011-0354-8 · Cited by 14
Cholinergic Control of Information Coding
van Kempen, J., Panzeri, S., & Thiele, A. (2017) · Trends in Neurosciences · doi:10.1016/j.tins.2017.06.006 · Cited by 14
Outcome-Locked Cholinergic Signaling Suppresses Prefrontal Encoding of Stimulus Associations
Tu, G., Halawa, A., Yu, X., Gillman, S., & Takehara‐Nishiuchi, K. (2022) · Journal of Neuroscience · doi:10.1523/jneurosci.1969-21.2022 · Cited by 14
Renard, A., Harrell, E. R., & Bathellier, B. (2022) · Nature Communications · doi:10.1038/s41467-022-31565-0 · Cited by 15
Reduction of falls in a rat model of PD falls by the M1 PAM TAK-071
Kucinski, A. J., & Sarter, M. F. (2021) · Psychopharmacology · doi:10.1007/s00213-021-05822-x · Cited by 13
Self-citationGrossberg, S., Palma, J., & Massimiliano Versace, A. (2016) · Frontiers in Neuroscience · doi:10.3389/fnins.2015.00501 · Cited by 13
Anderson, K., Hoffman, K. M., & Miwa, J. M. (2020) · Neuropharmacology · doi:10.1016/j.neuropharm.2020.108071 · Cited by 13
Cholinergic Reinforcement Signaling Is Impaired by Amyloidosis Prior to Its Synaptic Loss
Allard, S., & Shuler, M. G. H. (2023) · Journal of Neuroscience · doi:10.1523/jneurosci.0967-23.2023 · Cited by 11
M2 receptors are required for spatiotemporal sequence learning in mouse primary visual cortex
Sarkar, S., Martínez, C., Jensen, C. M., & Gavornik, J. P. (2024) · Journal of Neurophysiology · doi:10.1152/jn.00016.2024 · Cited by 12
Metadata
- Authors
- Parikh, V., Kozak, R., Martinez, V., & Sarter, M.
- Affiliations
- University of Michigan (US)
- Corresponding author
- Sarter, Martin
- Venue
- Neuron
- Publisher
- Elsevier BV
- Published
- 2007-10
- Volume
- 56
- Issue
- 1
- Pages
- 141-154
- ISSN
- 0896-6273 (ISSN-L)
- PMC
- PMC2084212
- OpenAlex
- W2101491694
- Cited by
- 623
- References
- 76
- Citations by year
- 2026: 15 · 2025: 25 · 2024: 33 · 2023: 34 · 2022: 28 · 2021: 37 · 2020: 41 · 2019: 28 · 2018: 48 · 2017: 38 · 2016: 32 · 2015: 43 · 2014: 47 · 2013: 44 · 2012: 31
- FWCI
- 9.39
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- www.elsevier.com/tdm/userlicense/1.0/ (tdm)
- www.elsevier.com/legal/tdmrep-license (tdm)
- www.elsevier.com/open-access/userlicense/1.0/ (vor, 2116 d)
- doi.org/10.15223/policy-017 (stm-asf)
- doi.org/10.15223/policy-037 (stm-asf)
- doi.org/10.15223/policy-012 (stm-asf)
- doi.org/10.15223/policy-029 (stm-asf)
- doi.org/10.15223/policy-004 (stm-asf)
- Locations
- Neuron (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institute of Mental Health (1 K02 MH01072, K02MH001072, R03MH073600)
- National Institute of Neurological Disorders and Stroke (R01NS037026, 5 R01 NS37026)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
- Keywords
- acetylcholine release, medial prefrontal cortex, cholinergic neurotransmission, cue detection, cholinergic deafferentation, basal forebrain cholinergic neurons, motor cortex, multiple time scales, cognitive performance, rats
- MeSH terms
- Acetylcholine, Analysis of Variance, Animals, Appetitive Behavior, Behavior, Animal, Cues, Electrochemistry, Food Deprivation, Male, Microelectrodes, Rats, Inbred F344, Reaction Time, Reward, Time Factors, Prefrontal Cortex, Rats
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