The DOI matches its Crossref record; 72 of the 72 references it cites were found in a registry or an index.
Modulatory functions of neurotransmitters in the striatum: ACh/dopamine/NMDA interactions
Abstract
The striatum is viewed as a structure performing fast neurotransmitter-mediated operations through somatotopically organized projections to medium-size spiny neurons. This view is contrasted with another view that depicts the striatum as a site of diffuse modulatory influences mediated by cholinergic interneurons and by dopamine and N-methyl-D-aspartate receptors. These two operational and organizational modes both contribute, through their mutual interaction, to the function of basal ganglia. Detailed knowledge of the neural mechanisms by which such interactions take place and are expressed into behaviour, can provide new insight into the physiopathology and new clues for therapy of disorders of basal ganglia.
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“The striatum is thought to be a region of broad modulatory effects mediated by cholinergic interneurons, dopa mine, and N-methyl-D-aspartate (NMDA) receptors (Chiara et al., 1994).”
From Predictive coding in neuropsychiatric disorders: a systematic transdiagnostic review. (2025) · cites this paper as Chiara et al., 1994
Citations
Cites
Parallel organization of functionally segregated circuits linking basal ganglia and cortex
Alexander, G. E., DeLong, M. R., & Strick, P. L. (1986) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.09.030186.002041 · Cited by 8,527
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
Seeman, P. M. (1980) · Pharmacological Reviews · doi:10.1016/s0031-6997(25)06839-5 · Cited by 1,888
Neurotransmitters and neuromodulators in the basal ganglia
Graybiel, A. M. (1990) · Trends in Neurosciences · doi:10.1016/0166-2236(90)90104-i · Cited by 1,576
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
Hulme, E. C., Birdsall, N. J. M., & Buckley, N. J. (1990) · The Annual Review of Pharmacology and Toxicology · doi:10.1146/annurev.pa.30.040190.003221 · Cited by 1,366
The mysterious motor function of the basal ganglia
MARSDEN, C. D. (1982) · Neurology · doi:10.1212/wnl.32.5.514 · Cited by 924
SCH 23390, a potential benzazepine antipsychotic with unique interactions on dopaminergic systems.
Iorio, L. C., Barnett, A., Leitz, F. H., Houser, V. P., & Korduba, C. A. (1983) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1016/s0022-3565(25)21599-3 · Cited by 896
Research works printed but not linked: 17
- Kitai, 1993, Adv. Neurol., 60, 40
- Herrling, 1992, Arzneimit. Forsch. Drug Res., 42, 202
- Morelli, 1992, J. Pharmacol. Exp. Ther., 260, 402
- Meredithy, 1990, Neurology, 296, 204
- Kimura, 1984, 81, 4998
- Maura, 1988, J. Pharmacol. Exp. Ther., 247, 680
- Jarvie, 1993, Adv. Neurol., 60, 325
- Iorio, 1983, J. Pharmacol. Exp. Ther., 226, 462
- Damsma, 1991, J. Pharmacol. Exp. Ther., 259, 1064
- Imperato, 1993, J. Pharmacol. Exp. Ther., 366, 557
- Meller, 1987, Mol. Pharmacol., 31, 592
- Seeman, 1981, Pharmacol. Rev., 32, 229
- Le Moine, 1990, 87, 230
- Le Moine, 1991, 88, 4205
- Di Chiara G.; Morelli M. Basal Ganglia IV, Proc. IVth Meeting Int. Basal Ganglia Society Percheron G.; McKenzie J.S. Plenum Press (in press.)
- Di Chiara, 1993, Adv. Neurol., 60, 102
- Riederer, 1993, Adv. Neurol., 60, 626
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Items 401–467 of 467
Clinical syndromes of neurotransmitter system dysfunction in severe brain injury
Александрова, Е. В., Zaytsev, O. S., & Aa, P. (2015) · S S Korsakov Journal of Neurology and Psychiatry · doi:10.17116/jnevro20151157140-46 · Cited by 5
He, N., Mao, L., Sturich, A. W., Jin, D.-Z., & Wang, J. Q. (2018) · Brain Research · doi:10.1016/j.brainres.2018.03.019 · Cited by 5
Functional organization of the dorsal striatum : comparison to the hippocampal system
Devan, B. D. (1997) · Library and Archives Canada (Government of Canada) · doi:10.82308/2143 · Cited by 5
Tanabe, M., Hashimoto, M., & Ono, H. (2008) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2008.06.013 · Cited by 4
Авдеева, Н. В., Sa, S., Povetkin, S. V., Жернакова, Н. И., & Сернов, Л. Н. (2018) · University proceedings Volga region Medical sciences · doi:10.21685/2072-3032-2018-3-18 · Cited by 4
Drugs of Abuse and Striatal Gene Expression
McGinty, J. F., & Wang, J. Q. (1997) · Advances in pharmacology · doi:10.1016/s1054-3589(08)60920-5 · Cited by 4
Case Report: Delusional Jealousy Following Right-Sided Cerebral Infarct
Wong, A. H. C., & Meier, H. (1997) · Neurocase · doi:10.1080/13554799708411978 · Cited by 4
The biochemistry of Tourette's Syndrome
Chokka, P. R., Baker, G. B., Bornstein, R. A., & de Groot, C. M. (1995) · Metabolic Brain Disease · doi:10.1007/bf01991859 · Cited by 4
Okada, F., Ito, A., Horikawa, T., Tokumitsu, Y., & Nomura, Y. (1996) · Neurochemistry International · doi:10.1016/0197-0186(95)00074-7 · Cited by 4
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Wess, J. (2007) · Wiley eBooks · doi:10.1002/9780470101001.hcn005 · Cited by 4
Cholinergic modulation of reinforcement learning and prefrontal value computations under uncertaintyPreprint
Kurtenbach, H., Froböse, M. I., Ort, E., Bahners, B. H., Butz, M., Schnitzler, A., Hirschmann, J., & Jocham, G. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.09.20.614105 · Cited by 4
Histaminergic H 2 receptor ligands modulate acetylcholine release in the ventral striatum
Philippu, A., Tran, M. H., & Prast, H. (1999) · Inflammation Research · doi:10.1007/s000110050402 · Cited by 3
Koekkoek, L. L., Unmehopa, U. A., Eggels, L., Kool, T., Lamuadni, K., Diepenbroek, C., Mul, J. D., Serlie, M. J. M., & la Fleur, S. E. (2020) · Physiology & Behavior · doi:10.1016/j.physbeh.2020.112936 · Cited by 3
von der Kammer, H., Mayhaus, M., Albrecht, C., Andresen, B., Klaudiny, J., Demiralay, C., & Nitsch, R. M. (2000) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2000.tb06939.x · Cited by 3
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Tien, L., Fan, L.-W., Ma, T., Loh, H. H., & Ho, I. K. (2005) · The Journal of Toxicological Sciences · doi:10.2131/jts.30.43 · Cited by 3
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Davidowa, H., Wetzel, K., & Vierig, G. (1997) · Peptides · doi:10.1016/s0196-9781(97)00054-5 · Cited by 3
Pontine reticular formation is involved in catalepsy produced by cholinergic drugs
Elazar, Z., Ganchrow, D., & Paz, M. (1997) · Naunyn-Schmiedeberg s Archives of Pharmacology · doi:10.1007/pl00005037 · Cited by 3
Schröeder, H., Schröeder, U., & Sabel, B. A. (1997) · Pharmacology Biochemistry and Behavior · doi:10.1016/s0091-3057(97)00026-9 · Cited by 3
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Авдеева, Н. В. (2019) · Pharmacy & Pharmacology · doi:10.19163/2307-9266-2019-7-2-84-89 · Cited by 2
del Pilar, E. (2012) · Cited by 2
Papadeas, S. T., & Breese, G. R. (2022) · Springer eBooks · doi:10.1007/978-3-031-15080-7_59 · Cited by 2
M1 Muscarinic Receptor Stimulation Decreases Aspartate Release in the Rat Neostriatum
Expósito, I., Sanz‐Barbero, B., & Mora, F. (1997) · Neurochemical Research · doi:10.1023/a:1021906529055 · Cited by 2
Fuqua, J. L. (2010) · UKnowledge (University of Kentucky) · Cited by 2
Neurobiological Issues in Tourette’s Syndrome
Singer, H. S., & Minzer, K. (2004) · Neurological disease and therapy · doi:10.1201/b14236-15 · Cited by 2
Muscarinic acetylcholine receptor knockout mice: Phenotypical analysis and clinical implications
(2002) · Pharmacochemistry library · doi:10.1016/s0165-7208(02)80012-5 · Cited by 2
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Marcotte, E. R., & Mishra, R. K. (2003) · Humana Press eBooks · doi:10.1385/0-89603-490-9:139 · Cited by 2
Nicotinic Involvement in Cognitive Function of Rats
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Zonuzirad, M. (2024) · Springer eBooks · doi:10.1007/978-981-97-7433-3_3 · Cited by 2
Glutamatergic Receptors in Parkinson’s Disease
Sampedro, A., Tarragón, E., Yuste, J. E., Ros‐Bernal, F., Ortiz, V., Campuzano, C. M., Gómez, A., Ros, C. M. B., Fernández‐Villalba, E., & Herrero, M. T. (2014) · Springer eBooks · doi:10.1007/978-1-4614-5836-4_154 · Cited by 1
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Ramos, A. C., Dieckmann, L. H. J., & Galduróz, J. C. F. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-803750-8.00066-x · Cited by 1
Non-Dopaminergic Approaches to the Treatment of Parkinson’s Disease
Brotchie, J. M., Maneuf, Y. P., Hughes, N., Duty, S., & Crossman, A. R. (1994) · Advances in behavioral biology · doi:10.1007/978-1-4613-0485-2_57 · Cited by 1
de Barioglio, S. R., & Brito, M. I. (1996) · Peptides · doi:10.1016/s0196-9781(96)00229-x · Cited by 1
Protection Against Nigrostriatal Dopamine Cell Death by Pedunculopontine Tegmental Nucleus Lesions
Takada, M., Matsumura, M., Kojima, J., Yamaji, Y., Inase, M., Tokuno, H., Nambu, A., & Imai, H. (2002) · Advances in behavioral biology · doi:10.1007/978-1-4615-0715-4_8 · Cited by 1
Cholinergic modulation of neuronal responses to cholecystokinin in anesthetized rats
Davidowa, H., Wetzel, K., & Vierig, G. (1998) · Brain Research Bulletin · doi:10.1016/s0361-9230(98)00036-7 · Cited by 1
Cowen, S. L. (2007) · UA Campus Repository (The University of Arizona) · Cited by 1
Changes of Glutamatergic Control of Striatal Acetylcholine Release in Experimental Parkinsonism
Mela, F., Marti, M., Bianchi, C., & Morari, M. (2005) · Springer eBooks · doi:10.1007/0-387-28066-9_10 · Cited by 1
Pesticides and pesticide combinations on brain neurochemistry
Aguilar, C. (2004) · VTechWorks (Virginia Tech) · Cited by 1
Zhou, H., Shi, H., Li, X., Zhang, J., Sui, X. Y., Zhao, Z., Nie, Z., Wang, Y., Li, J., & Wang, L. (2021) · Research Square · doi:10.21203/rs.3.rs-290339/v1 · Cited by 1
Kornhuber, J., Wiltfang, J., & Streifler, M. (1999) · Springer eBooks · doi:10.1007/978-3-7091-6400-6_31 · Cited by 1
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Fox, S. H., & Brotchie, J. M. (2011) · Parkinson s Disease · doi:10.1002/9781444397970.ch38 · Cited by 1
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Raedler, T. J., & Freedman, R. (2009) · Springer eBooks · doi:10.1007/978-0-387-30410-6_2 · Cited by 1
Andersson, D. R. (2009) · Gothenburg University Publications Electronic Archive (Gothenburg University)
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Shapovalova, K. B., & Tikhomirova, P. L. (2011) · Neuroscience and Behavioral Physiology · doi:10.1007/s11055-011-9490-x
[Drug-craving animal models and mechanisms].
Sakimura, K., Hiranita, T., Miyamoto, M., Nagata, K., & Yamamoto, T. (2005) · Folia Pharmacologica Japonica · doi:10.1254/fpj.126.24
Role of the basal ganglia in conditional associative learning : a multidisciplinary approach
Hadj‐Bouziane, F. (2003) · HAL
Brain muscarinic receptors: lessons from knockout mice
Wess, J. (2006) · CRC Press eBooks · doi:10.1201/b14486-13
deBacker, J. (2012) · QSpace (Queen's University Library)
The effect of vestibular lesions on the hippocampal cholinergic system
Aitken, P. (2017) · Otago University Research Archive (University of Otago)
Targeting muscarinic receptor subtypes as a therapeutic approach in dystonia and Parkinson's disease
Klisko, D. (2017) · Research Portal (King's College London)
Comportamento compulsivo à cocaína e as implicações no sistema colinérgico muscarínico
Spelta, L. E. W. (2017) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/d.9.2017.tde-21112017-155457
Fulcher, C. (2017) · Bradford Scholars (University of Bradford)
Experimental Models and New, Emerging Therapies for Parkinson Disease
Fahn, S., Jankovic, J. J., Hallett, M., & Jenner, P. G. (2007) · Elsevier eBooks · doi:10.1016/b978-0-443-07941-2.50012-7
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Авдеева, Н. В. (2019) · Кубанский научный медицинский вестник · doi:10.25207/1608-6228-2019-26-1-18-27
Terapia génica anti-inflamatoria en el abordaje de la neurodegeneración dopaminérgica motora
Lockhart, E. F. (2020) · El Servicio de Difusión de la Creación Intelectual (National University of La Plata) · doi:10.35537/10915/97168
Seibt, K. J. (2009) · Americanae (AECID Library)
Muscarinic Acetylcholine Receptors
Nathanson, N. M. (2001) · Wiley eBooks · doi:10.1038/npg.els.0000193
Tharavichitkun, J., Arunmanakul, P., Permsuwan, U., Dilokthornsakul, P., Yadee, J., & Sirichanchuen, B. (2023) · Pharmaceutical Sciences Asia · doi:10.29090/psa.2023.04.23.522
Kuru, G., Ünver, H., Üner, E., & Haklar, G. (2026) · Sleep Medicine · doi:10.1016/j.sleep.2026.108949
Amin, E. H. K., Ibrahim, I. H., Khadrawy, Y. A., & Mohammed, H. S. (2026) · Neuropharmacology · doi:10.1016/j.neuropharm.2026.111057
Actions of Dopamine on the Rat Striatal Cholinergic Interneurons
Aosaki, T. (2002) · Advances in behavioral biology · doi:10.1007/978-1-4615-0179-4_49
Metadata
- Authors
- Di Chiara, G., Morelli, M., & Consolo, S.
- Affiliations
- University of Cagliari (IT)
- Mario Negri Institute for Pharmacological Research (IT)
- ORCID
- Morelli, Micaela
- Venue
- Trends in Neurosciences
- Publisher
- Elsevier BV
- Published
- 1994-06
- Volume
- 17
- Issue
- 6
- Pages
- 228-233
- ISSN
- 0166-2236 (ISSN-L)
- OpenAlex
- W1990162104
- Semantic Scholar
- 6620d60a424c6c77bf86292e9bd8b24706c6c57f
- Cited by
- 467
- References
- 72
- Citations by year
- 2026: 2 · 2025: 2 · 2024: 5 · 2023: 1 · 2022: 4 · 2021: 6 · 2020: 8 · 2019: 4 · 2018: 8 · 2017: 11 · 2016: 9 · 2015: 6 · 2014: 7 · 2013: 6 · 2012: 13
- FWCI
- 4.49
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Trends in Neurosciences (publishedVersion)
- PubMed (publishedVersion)
- UNICA IRIS Institutional Research Information System (University of Cagliari) (submittedVersion)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
- Health Sciences › Medicine › Clinical Neurology › Deep Brain Stimulation and Movement Disorders
- Keywords
- striatum, acetylcholine, dopamine, NMDA receptor, cholinergic interneurons, medium spiny neurons, basal ganglia, neurotransmitter interactions, basal ganglia disorders, neuromodulation
- MeSH terms
- Acetylcholine, Animals, Corpus Striatum, Dopamine, Humans, Synaptic Transmission, Receptors, Dopamine, N-Methylaspartate, Neurotransmitter Agents
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