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Responses of midbrain dopamine neurons to behavioral trigger stimuli in the monkey
Abstract
Destruction of the midbrain dopamine (DA) system in Parkinsonian man and experimental animals leads to deficits in initiation of behavior, motor performance, and cognitive mechanisms. We have investigated the extracellular impulse activity of single midbrain DA neurons in unlesioned monkeys performing in a controlled behavioral task that was designed to paradigmatically test behavioral reactivity. Animals were trained to execute natural forelimb reaching movements for food reward in response to a trigger stimulus. Presumptive DA neurons were histologically located in the pars compacta of substantia nigra and in neighboring areas A8 and A10. They spontaneously discharged polyphasic impulses of relatively long duration (1.4-3.6 ms) and at low frequencies (0.5-8.5/s). Systemic injections of low doses of the DA autoreceptor agonist apomorphine (0.05-0.2 mg/kg) depressed the activity of virtually all thus tested DA neurons. In following established criteria, these characteristics strongly suggest the DAergic nature of the recorded neurons. The majority of midbrain DA neurons (70 of 128) responded to the behavioral trigger stimulus of the task with a short burst of impulses. Latencies ranged from 39 to 105 ms (median 65 ms) for onset and from 65 to 165 ms (median 95 ms) for peak of responses. Responses occurred before arm movement and at the time of or before onset of electromyographic (EMG) activity in prime mover muscles. Responses were time-locked to the stimulus and not to the onset of movement or EMG. Responses remained present in most neurons but were reduced when vision of the behavioral trigger stimulus was prevented while maintaining the associated acoustic signals. In another variation of the task, most neurons also responded to a stimulus that was physically identical to the behavioral trigger but to which the animal made no movement. The activity of a few DA neurons (11 of 128) was reduced following presentation of the behavioral trigger stimulus, with latencies comparable to those of activations. The activity of many DA neurons was increased (40 of 128) or reduced (22 of 128) during execution of the forelimb reaching movement. These changes were of a slow and moderate nature, and were minor compared with responses to the behavioral trigger stimulus. About half of movement-related neurons also responded to the behavioral trigger. The activity of a few DA neurons was increased (11 to 128) or reduced (1 to 128) when the food reward reached the mouth. These changes did not occur with spontaneous mouth movements. About half of these neurons also responded to the behavioral trigger.(ABSTRACT TRUNCATED AT 400 WORDS)
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“various subsets of dopamine neurons (1–44%) show slow, sluggish and diverse changes in the seconds time range that are inconsistently related to various aspects of behavioural task engagement and reactivity with stimulus-triggered or self-initiated arm or mouth movements11,12,14,18”
From Dopamine reward prediction-error signalling: A two-component response (2016) · cites this paper as [12]
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Items 301–390 of 390
Integrating information at single synaptic connections.
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McBride, S. D., & Hemmings, A. (2004) · BSAP Occasional Publication · doi:10.1017/s0263967x00041227 · Cited by 5
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Studer, A., Sundström, E., Jonsson, G., et al. (1988) · Neuropharmacology · doi:10.1016/0028-3908(88)90120-7 · Cited by 5
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“, 2017), we found a mixture of external events and goal-directed actions predicting the neural signal of VTA DA neurons consistent with task-related modulation in DA firing rates described in monkeys while performing a forelimb reaching task (Schultz, 1986).”
BackgroundKim, J., Gilbert, E. T., Arndt, K. C., Huang, H., Oleniacz, P. W., Jiang, S., Kimbrough, I. F., Sontheimer, H. W., English, D. F., & Jia, X. (2024) · Biosensors and Bioelectronics · doi:10.1016/j.bios.2024.116696 · Cited by 4
Striatal Acetylcholine Control of Reward-Related Dopamine Signalling
Cragg, S. J., Exley, R. A., & Clements, M. A. (2005) · Springer eBooks · doi:10.1007/0-387-28066-9_9 · Cited by 5
“due to salient primary rewards or conditioned reward predictions ( Schultz, 1986 ).”
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Tobler, P. N., & Kobayashi, S. (2009) · Elsevier eBooks · doi:10.1016/b978-0-12-374620-7.00002-9 · Cited by 4
VTA Dopamine Neurons Multiplex External with Internal Representations of Goal-Directed ActionPreprint
Kremer, Y., Flakowski, J., Rohner, C., & Lüscher, C. (2018) · SSRN Electronic Journal · doi:10.2139/ssrn.3249465 · Cited by 4
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Aldridge, J. W., & Berridge, K. C. (2002) · Advances in behavioral biology · doi:10.1007/978-1-4615-0715-4_7 · Cited by 3
Shapovalova, K. B., & Kamkina, Y. V. (2009) · Neuroscience and Behavioral Physiology · doi:10.1007/s11055-009-9228-1 · Cited by 3
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Self-citationShinba, T., Andow, Y., Shinozaki, T., Ozawa, N., & Yamamoto, K.-I. (1998) · Brain Research · doi:10.1016/s0006-8993(97)01254-7 · Cited by 3
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“As this association solidifies, it becomes less sensitive to changes (Bayley et al., 2005; Schultz, 1986).”
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“However, we specifically discuss the strength modulation in terms of reward mechanisms, in which the basal ganglia has been implicated [32], [33].”
McClure, S. M., & D’Ardenne, K. (2009) · Elsevier eBooks · doi:10.1016/b978-0-12-374620-7.00010-8 · Cited by 5
Ivlieva, N. Y., Timofeeva, N. O., & Ivliev, D. A. (2014) · The Journal of Cognitive Science · Cited by 2
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Dudhabhate, B. B., & Costa, K. M. (2026) · Frontiers in Computational Neuroscience · doi:10.3389/fncom.2026.1825622 · Cited by 2
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Doncheck, E. M., Clarke, R. E., Gordon, A. G., et al. (2026) · Nature Protocols · doi:10.1038/s41596-026-01406-1 · Cited by 1
Najafi, F. (2014) · ScholarlyCommons (University of Pennsylvania) · Cited by 1
Сашков, В. А., Джандарова, Т. И., & Сельверова, Н. Б. (2007) · Neuroscience and Behavioral Physiology · doi:10.1007/s11055-007-0061-0 · Cited by 1
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Poh, J.-H., & Adcock, R. A. (2024) · Elsevier eBooks · doi:10.1016/b978-0-443-15754-7.00049-3 · Cited by 1
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Tobler, P. N. (2009) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780195373035.003.0022 · Cited by 3
Miller, E. M. (2014) · UKnowledge (University of Kentucky) · Cited by 1
Alosaimi, F., Dominguez-Paredes, D., Knoben, R., et al. (2022) · SSRN Electronic Journal · doi:10.2139/ssrn.4191017 · Cited by 1
“Although a few studies have linked the activity of dopaminergic neurons to a particular behavior [26,27], the activity of dopaminergic neurons was somewhat related to the speed of the animal [24].”
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Exley, R. A., Clements, M. A., & Cragg, S. J. (2009) · Advances in behavioral biology · doi:10.1007/978-1-4419-0340-2_25 · Cited by 1
“the presentation of primary reward, a conditioned reinforcer or reward predictor ( Schultz 1986; Hyland et al. 2002; Bayer and Glimcher 2005).”
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Wood, J. T. (2015) · D-Scholarship@Pitt (University of Pittsburgh)
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Hutchison, W. D., Dostrovsky, J. O., & Lozano, A. M. (2003) · Handbook of clinical neurophysiology · doi:10.1016/s1567-4231(09)70157-1
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Sullivan, M. A. (2008)
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Mathé, J. M. (1998) · Figshare
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Guthrie, M. (2006) · ERA
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Lissek, S. (2004) · Dokumentenrepositorium der RUB (Ruhr University Bochum)
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van der Ham, E. (2007)
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Gluck, M. A. (2008) · Defense Technical Information Center (DTIC)
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Caffrey, M. K. (2013) · Digital Repository Service (Northeastern University) · doi:10.17760/d20003119
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Holmes, L. J. (2010) · Open Collections · doi:10.14288/1.0098090
Byrom, N., & Murphy, R. A. (2016) · Wiley eBooks · doi:10.1002/9781118650813.ch3
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Ngolab, J. (2015) · The Journal of the American Medical Association (JAMA) Network (American Medical Association) · doi:10.13028/m2730b
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Poyraz, F. C. (2016) · doi:10.7916/d89z94qz
Parlikar, R. U., Dinakaran, D., Bose, A., Rao, N. P., & Venkatasubramanian, G. (2017) · Journal of the Indian Institute of Science · doi:10.1007/s41745-017-0058-9
Hurtado-Zavala, J. I. (2017) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-6067
“This system comprises dopaminergic inputs from the ventral tegmental area (VTA) to both the nucleus accumbens and the prefrontal cortex (Bonci et al., 2003; Chiara and Imperato, 1988; Maeda and Mogenson, 1982; Marinelli et al., 2004; Schultz, 1986).”
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BackgroundSmirnitskaya, I. A. (2020) · Studies in computational intelligence · doi:10.1007/978-3-030-60577-3_17
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(1997) · Advances in psychology · doi:10.1016/s0166-4115(97)80114-8
Faculty Opinions recommendation of Dissociable dopamine dynamics for learning and motivation.
Schultz, W. (2019) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.735805842.793565162
Self-citationFaculty Opinions recommendation of Dissociable dopamine dynamics for learning and motivation.
Wolfer, D. P. (2019) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.735805842.793561663
Frank, M. J. (2010) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.7340957.7601055
Faculty Opinions recommendation of Dissociable dopamine dynamics for learning and motivation.
Vanderschuren, L. J. M. J. (2019) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.735805842.793563122
(2019) · Elsevier eBooks · doi:10.1016/b978-0-12-817443-2.00025-2
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Fountoulakis, K. N. (2022) · Springer eBooks · doi:10.1007/978-3-031-10351-3_7
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Montgomery, E. B., & Darbin, O. (2023) · Elsevier eBooks · doi:10.1016/b978-0-443-21699-2.00014-3
Balaban, P. M., & Grigoryan, G. A. (2024) · Успехи физиологических наук · doi:10.31857/s0301179824020063
Kagiampaki, Z., Zhou, X., Lamothe‐Molina, P. J., & Patriarchi, T. (2024) · Current Opinion in Behavioral Sciences · doi:10.1016/j.cobeha.2024.101460 · Cited by 1
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Jovanoski, K. D., & Waddell, S. (2025) · Handbook of behavioral neuroscience · doi:10.1016/b978-0-443-29867-7.00025-6 · Cited by 1
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Roeper, J., Liss, B., Khaliq, Z., & Canavier, C. C. (2025) · Handbook of behavioral neuroscience · doi:10.1016/b978-0-443-29867-7.00003-7
Graf, E. N. (2012) · e-Publications@Marquette (Marquette University)
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Berland, C. (2018) · theses.fr (ABES) · doi:10.70675/3a1dc076z7d5az413czbc66z525614a40de5
“Indeed, dopaminergic neurons fire simultaneously when a likeable stimulus is provided (Schultz, 1986).”
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Canchy, L. (2020) · theses.fr (ABES) · doi:10.70675/343233aaz22bez4109za45bz4a1f2c63ee4f
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Ramírez-Armenta, K., Feng, C., Martinez, A., Andrade, J. E., Quach, J., Paredes, N., Sias, A. C., Griffin, N. K., Sharpe, M. J., & Wassum, K. M. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.06.21.733629
“We found that reward-predictive cues trigger dopamine release in the BLA, consistent with the activity of midbrain dopamine neurons 23-25 and prior evidence that reward cues come to evoke BLA dopamine release with learning 16, 46 .”
Zahm (1996) · doi:10.1002/(sici)1096-9861(19960108)364:2
Metadata
- Authors
- Schultz, W.
- Corresponding author
- Schultz, W.
- ORCID
- Schultz, W.
- Venue
- Journal of Neurophysiology
- Publisher
- American Physiological Society
- Published
- 1986-11-01
- Volume
- 56
- Issue
- 5
- Pages
- 1439-1461
- ISSN
- 0022-3077 (ISSN-L)
- 1522-1598
- OpenAlex
- W1831076810
- Cited by
- 390
- References
- 0
- Citations by year
- 2026: 4 · 2025: 9 · 2024: 10 · 2023: 8 · 2022: 9 · 2021: 8 · 2020: 12 · 2019: 14 · 2018: 15 · 2017: 18 · 2016: 15 · 2015: 14 · 2014: 8 · 2013: 12 · 2012: 8
- FWCI
- 1.96
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Journal of Neurophysiology (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
- Life Sciences › Neuroscience › Cognitive Neuroscience › Motor Control and Adaptation
- Health Sciences › Medicine › Clinical Neurology › Parkinson's Disease Mechanisms and Treatments
- Keywords
- midbrain dopaminergic neurons, substantia nigra pars compacta, behavioral reactivity, apomorphine, dopamine autoreceptors, food reward, single-unit activity, Parkinson's disease, monkeys
- MeSH terms
- Animals, Conditioning, Psychological, Dopamine, Female, Macaca fascicularis, Mesencephalon, Neurons, Reward
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