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Muscarinic Modulation of Striatal Function and Circuitry
Abstract
Striatal cholinergic interneurons are pivotal modulators of the striatal circuitry involved in action selection and decision making. Although nicotinic receptors are important transducers of acetylcholine release in the striatum, muscarinic receptors are more pervasive and have been more thoroughly studied. In this review, the effects of muscarinic receptor signaling on the principal cell types in the striatum and its canonical circuits will be discussed, highlighting new insights into their role in synaptic integration and plasticity. These studies, and those that have identified new circuit elements driven by activation of nicotinic receptors, make it clear that temporally patterned activity in cholinergic interneurons must play an important role in determining the effects on striatal circuitry. These effects could be critical to the response to salient environmental stimuli that serve to direct behavior.
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“Additionally, it is clear that cholinergic interneurons and their regulation of muscarinic receptor signaling are also critical components in striatum-dependent decision making (see, e.g. (Goldberg et al., 2012)).”
From Acetylcholine as a Neuromodulator: Cholinergic Signaling Shapes Nervous System Function and Behavior (2012) · cites this paper as Goldberg et al., 2012
Citations
Cites
International Union of Pharmacology: Approaches to the Nomenclature of Voltage-Gated Ion Channels
Catterall, W. A., Chandy, K. G., Clapham, D. E., Gutman, G. A., Hofmann, F., Harmar, A. J., Abernethy, D. R., & Spedding, M. (2003) · Pharmacological Reviews · doi:10.1124/pr.55.4.5 · Cited by 7,126
The functional anatomy of basal ganglia disorders
Albin, R. L., Young, A. B., & Penney, J. B. (1989) · Trends in Neurosciences · doi:10.1016/0166-2236(89)90074-x · Cited by 5,353
The Synaptic Organization of the Brain
(2004) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780195159561.001.1 · Cited by 3,574
D 1 and D 2 Dopamine Receptor-regulated Gene Expression of Striatonigral and Striatopallidal Neurons
Gerfen, C. R., Engber, T. M., Mahan, L. C., Susel, Z., Chase, T. N., Monsma, F. J., & Sibley, D. R. (1990) · Science · doi:10.1126/science.2147780 · Cited by 2,967
THE BASAL GANGLIA: FOCUSED SELECTION AND INHIBITION OF COMPETING MOTOR PROGRAMS
Mink, J. W. (1996) · Progress in Neurobiology · doi:10.1016/s0301-0082(96)00042-1 · Cited by 2,478
Activity-dependent scaling of quantal amplitude in neocortical neurons
Turrigiano, G. G., Leslie, K. R., Desai, N. S., Rutherford, L. C., & Nelson, S. B. (1998) · Nature · doi:10.1038/36103 · Cited by 2,226
Handbook of Experimental Pharmacology.
Meakin, J. W. (1971) · Archives of Internal Medicine · doi:10.1001/archinte.1971.00310230151026 · Cited by 1,959
International Union of Pharmacology. XVII. Classification of Muscarinic Acetylcholine Receptors
Caulfield, M. P., & Birdsall, N. J. M. (1998) · Pharmacological Reviews · doi:10.1016/s0031-6997(24)01362-0 · Cited by 1,474
The neostriatal mosaic: multiple levels of compartmental organization
Gerfen, C. R. (1992) · Trends in Neurosciences · doi:10.1016/0166-2236(92)90355-c · Cited by 1,471
Dichotomous dopaminergic control of striatal synaptic plasticity
Shen, W., Flajolet, M., Greengard, P., & Surmeier, D. J. (2008) · Science · doi:10.1126/science.1160575 · Cited by 1,190
Self-citation
Research works printed but not linked: 2
- Arbuthnott GW, MacLeod NK, Rutherfod A (1985) The rate cortico-striatal pathway in vitro. J Physiol 367:102p
- Wooten GF (1990) Parkinsonism. In: Pearlman AL, Collins RC (eds) Neurobiology of disease. Oxford University Press, New York, pp 454–468
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Maurice, N., Liberge, M., Jaouen, F., Ztaou, S., Hanini, M., Camon, J., Deisseroth, K. A., Amalric, M., Goff, L. K., & Beurrier, C. (2015) · Cell Reports · doi:10.1016/j.celrep.2015.09.034 · Cited by 125
Klug, J. R., Engelhardt, M. D., Cadman, C. N., Li, H., Smith, J. B., Ayala, S., Williams, E., Hoffman, H., & Jin, X. (2018) · eLife · doi:10.7554/elife.35657 · Cited by 127
Corbit, L. H., & Balleine, B. W. (2015) · Current topics in behavioral neurosciences · doi:10.1007/7854_2015_388 · Cited by 118
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Kenny, P. J., Voren, G., & Johnson, P. M. (2013) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2013.04.012 · Cited by 100
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Assous, M., & Tepper, J. M. (2018) · European Journal of Neuroscience · doi:10.1111/ejn.13881 · Cited by 89
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Reynolds, J. N. J., Avvisati, R., Dodson, P. D., Fisher, S. D., Oswald, M. J., Wickens, J. R., & Zhang, Y.-F. (2022) · Nature Communications · doi:10.1038/s41467-022-28950-0 · Cited by 86
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Bertran‐Gonzalez, J., Laurent, V., Chieng, B. C. H., Christie, M. J., & Balleine, B. W. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.1927-13.2013 · Cited by 75
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Adler, A., Katabi, S., Finkes, I., Prut, Y., & Bergman, H. (2013) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2013.00047 · Cited by 41
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Melendez-Zaidi, A. E., Lakshminarasimhah, H., & Surmeier, D. J. (2019) · European Journal of Neuroscience · doi:10.1111/ejn.14528 · Cited by 25
Self-citationOstlund, S. B., Kosheleff, A. R., & Maidment, N. T. (2013) · Neuropsychopharmacology · doi:10.1038/npp.2013.348 · Cited by 24
Blazer, A., Chengappa, K. N. R., Foran, W., Parr, A. C., Kahn, C. E., Luna, B., & Sarpal, D. K. (2022) · Psychopharmacology · doi:10.1007/s00213-022-06138-0 · Cited by 24
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Striatal insights: a cellular and molecular perspective on repetitive behaviors in pathology
Burton, C. L., Longaretti, A., Zlatanovic, A., Gomes, G. M., & Tonini, R. (2024) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2024.1386715 · Cited by 23
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Self-citationMcGuirt, A. F., Lieberman, O. J., Post, M., Pigulevskiy, I., & Sulzer, D. (2021) · Journal of Neuroscience · doi:10.1523/jneurosci.0755-20.2021 · Cited by 17
A tonic nicotinic brake controls spike timing in striatal spiny projection neurons
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Acetylcholine demixes heterogeneous dopamine signals for learning and moving
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Metadata
- Authors
- Goldberg, J. A., Ding, J. B., & Surmeier, D. J.
- Affiliations
- Northwestern University (US)
- Harvard University (US)
- Corresponding author
- Surmeier, D. James
- Venue
- Handbook of Experimental Pharmacology
- Publisher
- Springer Berlin Heidelberg
- Published
- 2011-11-03
- Issue
- 208
- Pages
- 223-241
- ISSN
- 0171-2004 (ISSN-L)
- 1865-0325
- OpenAlex
- W2171464354
- Semantic Scholar
- 15c6ab832bb2759784b39abb97f6cb5d93ea9bbe
- Cited by
- 150
- References
- 160
- Citations by year
- 2026: 7 · 2025: 4 · 2024: 8 · 2023: 7 · 2022: 16 · 2021: 9 · 2020: 14 · 2019: 12 · 2018: 13 · 2017: 10 · 2016: 15 · 2015: 12 · 2014: 10 · 2013: 12 · 2012: 1
- FWCI
- 6.88
- Type
- book chapter
- Language
- en
- Open access
- closed
- Licence
- Locations
- Handbook of experimental pharmacology (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Nicotinic Acetylcholine Receptors Study
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
- Keywords
- muscarinic receptors, striatum, cholinergic interneurons, striatal circuitry, nicotinic acetylcholine receptors, synaptic integration, synaptic plasticity, action selection, decision-making, acetylcholine, salient stimuli
- MeSH terms
- Acetylcholine, Animals, Basal Ganglia, Dystonia, Humans, Interneurons, Neural Pathways, Parkinson Disease, Receptors, Muscarinic, Signal Transduction, Muscarinic Antagonists
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