Acetylcholine contributes through muscarinic receptors to attentional modulation in V1
Open accessAbstract
Attention exerts a strong influence over neuronal processing in cortical areas. It selectively increases firing rates and affects tuning properties, including changing receptive field locations and sizes. Although these effects are well studied, their cellular mechanisms are poorly understood. To study the cellular mechanisms, we combined iontophoretic pharmacological analysis of cholinergic receptors with single cell recordings in V1 while rhesus macaque monkeys (Macaca mulatta) performed a task that demanded top-down spatial attention. Attending to the receptive field of the V1 neuron under study caused an increase in firing rates. Here we show that this attentional modulation was enhanced by low doses of acetylcholine. Furthermore, applying the muscarinic antagonist scopolamine reduced attentional modulation, whereas the nicotinic antagonist mecamylamine had no systematic effect. These results demonstrate that muscarinic cholinergic mechanisms play a central part in mediating the effects of attention in V1.
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In primates, locally applied ACh enhances the attentional modulation of neuronal activity in the primary visual cortex.
“In primates, locally applied ACh enhances the attentional modulation of neuronal activity in the primary visual cortex, while the muscarinic antagonist scopolamine reduces the effects of attention (Herrero et al., 2008).”
From Acetylcholine as a Neuromodulator: Cholinergic Signaling Shapes Nervous System Function and Behavior (2012) · cites this paper as Herrero et al., 2008
In primates, the muscarinic antagonist scopolamine reduces the effects of attention.
“while the muscarinic antagonist scopolamine reduces the effects of attention (Herrero et al., 2008).”
From Acetylcholine as a Neuromodulator: Cholinergic Signaling Shapes Nervous System Function and Behavior (2012) · cites this paper as Herrero et al., 2008
In the primary visual cortex, blockade of muscarinic but not nicotinic AChRs impairs the attentional modulation of V1 neurons.
“Herrero et al. demonstrated that in the primary visual cortex, blockade of muscarinic but not nicotinic AChRs impaired the attentional modulation of V1 neurons (Herrero et al, 2008; see also Deco and Thiele, 2009).”
From Modes and models of forebrain cholinergic neuromodulation of cognition (2011) · cites this paper as Herrero et al, 2008
Activation of muscarinic ACh receptors, but not nicotinic ACh receptors, may in part mediate attentional modulation of neural response gain in non-human-primate cortex.
“Other work in non-human-primate cortex suggests that activation of muscarinic ACh receptors (mAChRs), but not nAChRs, may in part mediate the attentional modulation of neural response gain174.”
From Mechanisms underlying gain modulation in the cortex (2020) · cites this paper as [174]
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Control of goal-directed and stimulus-driven attention in the brain
Corbetta, M., & Shulman, G. L. (2002) · Nature Reviews Neuroscience · doi:10.1038/nrn755 · Cited by 12,881 · see citing works
Modulation of Oscillatory Neuronal Synchronization by Selective Visual Attention
Fries, P., Reynolds, J. H., Rorie, A. E., & Desimone, R. (2001) · Science · doi:10.1126/science.1055465 · Cited by 2,786 · see citing works
Uncertainty, Neuromodulation, and Attention
Yu, A. J., & Dayan, P. (2005) · Neuron · doi:10.1016/j.neuron.2005.04.026 · Cited by 1,774 · see citing works
Self-citationNeural mechanisms of spatial selective attention in areas V1, V2, and V4 of macaque visual cortex
Luck, S. J., Chelazzi, L., Hillyard, S. A., & Desimone, R. (1997) · Journal of Neurophysiology · doi:10.1152/jn.1997.77.1.24 · Cited by 1,615 · see citing works
Competitive Mechanisms Subserve Attention in Macaque Areas V2 and V4
Reynolds, J. H., Chelazzi, L., & Desimone, R. (1999) · The Journal of Neuroscience · doi:10.1523/jneurosci.19-05-01736.1999 · Cited by 1,236 · see citing works
Selective gating of visual signals by microstimulation of frontal cortex
Moore, T., & Armstrong, K. M. (2003) · Nature · doi:10.1038/nature01341 · Cited by 1,156 · see citing works
Attentional modulation of visual motion processing in cortical areas MT and MST
Treue, S., & Maunsell, J. H. R. (1996) · Nature · doi:10.1038/382539a0 · Cited by 1,025 · see citing works
Attention Increases Sensitivity of V4 Neurons
Reynolds, J. H., Pasternak, T., & Desimone, R. (2000) · Neuron · doi:10.1016/s0896-6273(00)81206-4 · Cited by 1,017 · see citing works
Increased Attention Enhances Both Behavioral and Neuronal Performance
Spitzer, H., Desimone, R., & Moran, J. (1988) · Science · doi:10.1126/science.3353728 · Cited by 815 · see citing works
Object-based attention in the primary visual cortex of the macaque monkey
Roelfsema, P. R., Lamme, V. A. F., & Spekreijse, H. (1998) · Nature · doi:10.1038/26475 · Cited by 814 · see citing works
D1 receptors in prefrontal cells and circuits
Goldman-Rakic, P. (2000) · Brain Research Reviews · doi:10.1016/s0165-0173(99)00045-4 · Cited by 807 · see citing works
Sarter, M., Hasselmo, M. E., Bruno, J. P., & Givens, B. (2005) · Brain Research Reviews · doi:10.1016/j.brainresrev.2004.08.006 · Cited by 667 · see citing works
Prefrontal Acetylcholine Release Controls Cue Detection on Multiple Timescales
Parikh, V., Kozak, R., Martinez, V., & Sarter, M. (2007) · Neuron · doi:10.1016/j.neuron.2007.08.025 · Cited by 623 · see citing works
Gain Modulation by Nicotine in Macaque V1
Disney, A. A., Aoki, C., & Hawken, M. J. (2007) · Neuron · doi:10.1016/j.neuron.2007.09.034 · Cited by 331 · see citing works
Dynamic shifts of visual receptive fields in cortical area MT by spatial attention
Womelsdorf, T., Anton-Erxleben, K., Pieper, F., & Treue, S. (2006) · Nature Neuroscience · doi:10.1038/nn1748 · Cited by 317 · see citing works
McGaughy, J., Dalley, J. W., Morrison, C. H., Everitt, B. J., & Robbins, T. W. (2002) · The Journal of Neuroscience · doi:10.1523/jneurosci.22-05-01905.2002 · Cited by 311 · see citing works
Chemistry of the mind: Neurochemical modulation of prefrontal cortical function
Robbins, T. W. (2005) · Journal of Comparative Neurology · doi:10.1002/cne.20717 · Cited by 292 · see citing works
The afferent connections of the substantia innominata in the monkey,Macaca fascicularis
Russchen, F. T., Amaral, D., & Price, J. L. (1985) · The Journal of Comparative Neurology · doi:10.1002/cne.902420102 · Cited by 270 · see citing works
Attention Modulates the Responses of Simple Cells in Monkey Primary Visual Cortex
McAdams, C. J., & Reid, R. C. (2005) · The Journal of Neuroscience · doi:10.1523/jneurosci.2904-05.2005 · Cited by 203 · see citing works
Local Infusion of Scopolamine Into Intraparietal Cortex Slows Covert Orienting in Rhesus Monkeys
Davidson, M. C., & Marrocco, R. T. (2000) · Journal of Neurophysiology · doi:10.1152/jn.2000.83.3.1536 · Cited by 188 · see citing works
Witte, E. A., Davidson, M. C., & Marrocco, R. T. (1997) · Psychopharmacology · doi:10.1007/s002130050352 · Cited by 187 · see citing works
Thiel, C. M., Zilles, K., & Fink, G. R. (2005) · Neuropsychopharmacology · doi:10.1038/sj.npp.1300633 · Cited by 182 · see citing works
Functional Characterization of Intrinsic Cholinergic Interneurons in the Cortex
von Engelhardt, J., Eliava, M., Meyer, A. H., Rozov, A., & Monyer, H. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.4647-06.2007 · Cited by 177 · see citing works
Attention alters spatial integration in macaque V1 in an eccentricity-dependent manner
Roberts, M. J., Delicato, L. S., Herrero, J. L., Gieselmann, M. A., & Thiele, A. (2007) · Nature Neuroscience · doi:10.1038/nn1967 · Cited by 133 · see citing works
Self-citationPrefrontal cortical modulation of acetylcholine release in posterior parietal cortex
Nelson, C. L., Sarter, M., & Bruno, J. P. (2005) · Neuroscience · doi:10.1016/j.neuroscience.2004.12.007 · Cited by 128 · see citing works
Selective Effects of Cholinergic Modulation on Task Performance during Selective Attention
Furey, M. L., Pietrini, P., Haxby, J. V., & Drevets, W. C. (2008) · Neuropsychopharmacology · doi:10.1038/sj.npp.1301461 · Cited by 107 · see citing works
Disney, A. A., Domakonda, K. V., & Aoki, C. (2006) · The Journal of Comparative Neurology · doi:10.1002/cne.21096 · Cited by 99 · see citing works
Cholinergic modulation, visual function and Alzheimer's dementia
Nobili, L., & Sannita, W. G. (1997) · Vision Research · doi:10.1016/s0042-6989(97)00076-x · Cited by 78 · see citing works
Modality- and region-specific acetylcholine release in the rat neocortex
Fournier, G. N., Semba, K., & Rasmusson, D. D. (2004) · Neuroscience · doi:10.1016/j.neuroscience.2004.04.002 · Cited by 73 · see citing works
Thiele, A., Delicato, L. S., Roberts, M. J., & Gieselmann, M. A. (2006) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2006.05.032 · Cited by 68 · see citing works
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Modulation of visual responses by behavioral state in mouse visual cortex
Niell, C. M., & Stryker, M. P. (2010) · Neuron · doi:10.1016/j.neuron.2010.01.033 · Cited by 1,483 · see citing works
“, 2007), and the potential role of acetylcholine in modulating cortical responsiveness (Goard and Dan, 2009; Hasselmo and Giocomo, 2006; Herrero et al., 2008; Weinberger, 2007).”
The Normalization Model of Attention
Reynolds, J. H., & Heeger, D. J. (2009) · Neuron · doi:10.1016/j.neuron.2009.01.002 · Cited by 1,457 · see citing works
Attention, uncertainty, and free-energy
Feldman, H., & Friston, K. J. (2010) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2010.00215 · Cited by 1,365 · see citing works
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 · see citing works
Modes and models of forebrain cholinergic neuromodulation of cognition
Hasselmo, M. E., & Sarter, M. (2011) · Neuropsychopharmacology · doi:10.1038/npp.2010.104 · Cited by 733 · see citing works
Cellular mechanisms of brain state-dependent gain modulation in visual cortex
Polack, P.-O., Friedman, J., & Golshani, P. (2013) · Nature Neuroscience · doi:10.1038/nn.3464 · Cited by 628 · see citing works
Action understanding and active inference
Friston, K., Mattout, J., & Kilner, J. (2011) · Biological Cybernetics · doi:10.1007/s00422-011-0424-z · Cited by 665 · see citing works
Fast modulation of visual perception by basal forebrain cholinergic neurons
Pinto, L., Goard, M. J., Estandian, D., Xu, M., Kwan, A. C., Lee, S.-H., Harrison, T. C., Feng, G., & Dan, Y. (2013) · Nature Neuroscience · doi:10.1038/nn.3552 · Cited by 529 · see citing works
Brain plasticity through the life span: Learning to learn and action video games
Bavelier, D., Green, C. S., Pouget, A., & Schrater, P. (2012) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-060909-152832 · Cited by 541 · see citing works
Neural mechanisms of selective visual attention.
Moore, T., & Zirnsak, M. (2017) · Annual Review of Psychology · doi:10.1146/annurev-psych-122414-033400 · Cited by 471 · see citing works
Plasticity of Cortical Excitatory-Inhibitory Balance
Froemke, R. C. (2015) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-071714-034002 · Cited by 458 · see citing works
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Baluch, F., & Itti, L. (2011) · Trends in Neurosciences · doi:10.1016/j.tins.2011.02.003 · Cited by 437 · see citing works
Toward a neurobiology of delusions
Corlett, P. R., Taylor, J. R., Wang, X.-J., Fletcher, P. C., & Krystal, J. H. (2010) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2010.06.007 · Cited by 394 · see citing works
Central Cholinergic Neurons Are Rapidly Recruited by Reinforcement Feedback
Hangya, B., Ranade, S. P., Lorenc, M., & Kepecs, A. (2015) · Cell · doi:10.1016/j.cell.2015.07.057 · Cited by 399 · see citing works
From drugs to deprivation: A Bayesian framework for understanding models of psychosis
Corlett, P. R., Frith, C. D., & Fletcher, P. C. (2009) · Psychopharmacology · doi:10.1007/s00213-009-1561-0 · Cited by 367 · see citing works
“Increased levels of acetylcholine alter the strengths of the connections in primary visual cortex and the biophysical state of sensory neurons, which may then allow spatially specific glutamatergic feedback to enhance the processing of specific incoming information ( Herrero et al. 2008 ), with a view to learning more…”
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Morishita, H., Miwa, J. M., Heintz, N., & Hensch, T. K. (2010) · Science · doi:10.1126/science.1195320 · Cited by 365 · see citing works
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Noudoost, B., & Moore, T. (2011) · Nature · doi:10.1038/nature09995 · Cited by 324 · see citing works
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Thiele, A., & Bellgrove, M. A. (2018) · Neuron · doi:10.1016/j.neuron.2018.01.008 · Cited by 350 · see citing works
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Ferguson, K. A., & Cardin, J. A. (2020) · Nature Reviews Neuroscience · doi:10.1038/s41583-019-0253-y · Cited by 327 · see citing works
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Parr, T., & Friston, K. J. (2017) · Journal of The Royal Society Interface · doi:10.1098/rsif.2017.0376 · Cited by 252 · see citing works
Runyan, C. A., Schummers, J., Van Wart, A., Kuhlman, S. J., Wilson, N. R., Huang, Z. J., & Sur, M. (2010) · Neuron · doi:10.1016/j.neuron.2010.08.006 · Cited by 244 · see citing works
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Eggermann, E., Kremer, Y., Crochet, S., & Petersen, C. C. H. (2014) · Cell Reports · doi:10.1016/j.celrep.2014.11.005 · Cited by 234 · see citing works
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Barron, H. C., Auksztulewicz, R., & Friston, K. (2020) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2020.101821 · Cited by 220 · see citing works
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Self, M. W., Kooijmans, R. N., Supèr, H., Lamme, V. A., & Roelfsema, P. R. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1119527109 · Cited by 184 · see citing works
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Záborszky, L., Gombkoto, P., Varsanyi, P., Gielow, M. R., Poe, G., Role, L. W., Ananth, M., Rajebhosale, P., Talmage, D. A., Hasselmo, M. E., et al. (2018) · The Journal of Neuroscience · doi:10.1523/jneurosci.1676-18.2018 · Cited by 202 · see citing works
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“ACh has been shown to facilitate attentionrelated activity through muscarinic receptors in macaque V1 [33].”
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Yildiz, I. B., von Kriegstein, K., & Kiebel, S. J. (2013) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1003219 · Cited by 55 · see citing works
Vijayraghavan, S., Major, A. J., & Everling, S. (2018) · Neuron · doi:10.1016/j.neuron.2018.05.027 · Cited by 51 · see citing works
Dasgupta, R., Seibt, F., & Beierlein, M. (2018) · The Journal of Neuroscience · doi:10.1523/jneurosci.0566-18.2018 · Cited by 47 · see citing works
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Bentley, P., Driver, J., & Dolan, R. J. (2009) · Brain · doi:10.1093/brain/awp176 · Cited by 41 · see citing works
Disney, A. A., & Reynolds, J. H. (2014) · Journal of Comparative Neurology · doi:10.1002/cne.23456 · Cited by 40 · see citing works
“…investigators that cortical cholinergic modulation underlies attention (Arnold et al., 2002; Deco and Thiele, 2011; Hasselmo and McGaughy, 2004; Herrero et al., 2008; Himmelheber et al., 2000; McGaughy and Sarter, 1998; Sarter et al., 2005), and it has also been argued that changes in…”
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- Authors
- Herrero, J. L., Roberts, M. J., Delicato, L. S., Gieselmann, M. A., Dayan, P., & Thiele, A.
- Affiliations
- Newcastle University (GB)
- Gatsby Computational Neuroscience Unit (GB)
- Corresponding author
- Thiele, A.
- Venue
- Nature
- Published
- 2008-07-16
- Volume
- 454
- Issue
- 7208
- Pages
- 1110-1114
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- PMC
- PMC2666819
- OpenAlex
- W2162056177
- Cited by
- 459
- References
- 30
- Citations by year
- 2026: 14 · 2025: 23 · 2024: 26 · 2023: 20 · 2022: 18 · 2021: 34 · 2020: 24 · 2019: 20 · 2018: 30 · 2017: 34 · 2016: 20 · 2015: 28 · 2014: 29 · 2013: 33 · 2012: 30
- FWCI
- 12.92
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- RePEc: Research Papers in Economics (submittedVersion)
- UCL Discovery (University College London) (submittedVersion)
- MPG.PuRe (Max Planck Society) (submittedVersion)
- Sunderland Repository (University of Sunderland) (submittedVersion)
- Newcastle University ePrints (Newcastle Univesity)
- Funders
- Wellcome Trust (070380)
- Biotechnology and Biological Sciences Research Council (BB/F021399/1, BBS/B/09325)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Visual perception and processing mechanisms
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Nicotinic Acetylcholine Receptors Study
- Keywords
- acetylcholine, muscarinic receptors, nicotinic acetylcholine receptors, primary visual cortex, attentional modulation, cholinergic modulation, scopolamine, mecamylamine, rhesus monkeys, neuronal firing rate
- MeSH terms
- Acetylcholine, Animals, Attention, Macaca mulatta, Magnetic Resonance Imaging, Male, Mecamylamine, Receptors, Cholinergic, Receptors, Muscarinic, Scopolamine, Cholinergic Antagonists, Muscarinic Antagonists, Nicotinic Antagonists
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