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Dopamine neurons of the monkey midbrain: contingencies of responses to active touch during self-initiated arm movements
Abstract
1. Previous studies have shown that midbrain dopamine (DA) neurons in monkeys respond to external stimuli that are used to initiate behavioral reactions. In the present study, we investigated to what extent changes in neuronal activity would occur when behavioral acts are generated internally or whether they would depend solely on external stimuli. 2. Monkeys performed self-initiated arm movements from a resting key into a covered, food-containing box at a self-chosen moment and without external preparatory or triggering signals. In a second task, the arm movement was triggered by rapid opening of the door of the food box. This stimulus was either audible and visible or only audible to the animal. Impulses of DA neurons were recorded with movable microelectrodes from the pars compacta of substantia nigra (area A9) and areas A8 and A10 and were discriminated from those of other neurons by their long duration (1.5-5.0 ms) and low spontaneous frequency (0.5-8.5 imp/s). 3. The activity of 12% of 104 DA neurons increased slowly and moderately up to 1,500 ms before the onset of individual self-initiated arm movements. Median increases amounted to 91% over background discharge rate. A further 16% of DA neurons were activated together with the onset of muscle activity and during the movement. 4. During self-initiated movements, a nonhabituating, phasic burst of impulses occurred when the monkey's hand touched a morsel of food inside the box. This response was seen in 84% of 154 neurons on the contralateral side, with median onset latency of 65 ms and duration of 160 ms. A comparable percentage of neurons responded to ipsilateral touch with similar latency and duration. 5. The touch response during self-initiated movements was absent, both on the contra- and ipsilateral sides, when the animal's hand touched the bare wire normally holding the food, when touching nonfood objects, or during tactile exploration of the empty interior of the food box. Thus responses appeared to be related to the appetitive properties of the object being touched rather than the object itself. 6. In the task employing stimulus-triggered movements, 77% of 86 DA neurons discharged a burst of impulses in response to door opening but entirely failed to respond to the touch of food in the box. The response to door opening in this task was similar to the touch response during self-initiated movements in the same neurons in terms of latency, duration, and magnitude.(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 [14]
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Schultz, W. (1992) · Seminars in Neuroscience · doi:10.1016/1044-5765(92)90011-p · Cited by 178
Self-citationMetabolic hormones, dopamine circuits, and feeding
Narayanan, N. S., Guarnieri, D. J., & Dileone, R. (2009) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2009.10.004 · Cited by 182
“Dopaminergic neurons increase in firing rate when an animal touches food [78;79] and when liquid reward is administered to the animal outside of a behavioral context [77].”
BackgroundControls of tonic and phasic dopamine transmission in the dorsal and ventral striatum
Zhang, L., Doyon, W. M., Clark, J. J., Phillips, P. E. M., & Dani, J. A. (2009) · Molecular Pharmacology · doi:10.1124/mol.109.056317 · Cited by 161
“Conversely, the relative stability of dorsolateral striatal DA release in response to changes in firing rate is consistent with the hypothesis that DA release in the dorsal striatum enables the initiation of cognitive and motor responses but does not necessarily correlate with the induction of movement (Romo and Schul…”
ResultHaloperidol Impairs Learning and Error-related Negativity in Humans
Zirnheld, P. J., Carroll, C. A., Kieffaber, P. D., O’Donnell, B. F., Shekhar, A., & Hetrick, W. P. (2004) · Journal of Cognitive Neuroscience · doi:10.1162/0898929041502779 · Cited by 171
“…error signal used in animal learning (Schultz et al., 1997; Schultz, 1996; Schultz et al., 1993; Mirenowicz & Schultz, 1994; Ljungberg et al., 1992; Romo & Schultz, 1990; Schultz, 1986), (2) the evidence linking dopamine to learning (Rammsayer, 1999; Kumari et al., 1997; Dobkin & Hanlon, 1993;…”
BackgroundEfficient coding and the neural representation of value
Louie, K., & Glimcher, P. W. (2012) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2012.06496.x · Cited by 171
Neural circuits and topographic organization of the basal ganglia and related regions
Nakano, K. (2000) · Brain and Development · doi:10.1016/s0387-7604(00)00139-x · Cited by 164
“[106] Romo R, Schultz W.”
BackgroundInfluentialSchultz, W., Stauffer, W. R., & Lak, A. (2017) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2017.03.013 · Cited by 171
“Similar activations occur when these movements occur spontaneously (12%) in a design that addressed the most impaired movement type in Parkinsonism [52].”
Self-citationFloresco, S., Yang, C. R., Phillips, A. G., & Blaha, C. D. (1998) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.1998.00133.x · Cited by 163
“In primates, presentation of different foods and sweet solutions, or visual and auditory stimuli paired previously with reward results in brief, phasic firing of DA neurons in the VTA (Romo & Schultz, 1990; Schultz & Romo, 1990; Ljungberget al., 1992).”
BackgroundRichardson, N. R., & Gratton, A. P. (1996) · Journal of Neuroscience · doi:10.1523/jneurosci.16-24-08160.1996 · Cited by 160
“…although unexpected, are nonetheless congruent with electrophysiological evidence that similar changes in VTA DA cell activity are associated with food reinforcement (Schultz, 1986; Nishino et al., 1987; Romo and Schultz, 1990; Schultz and Romo, 1990; Ljungberg et al., 1992; Schultz et al., 1993).”
ResultWenzel, J. M., & Cheer, J. F. (2017) · Neuropsychopharmacology · doi:10.1038/npp.2017.126 · Cited by 161
Prediction error, ketamine and psychosis: An updated model
Corlett, P. R., Honey, G. D., & Fletcher, P. C. (2016) · Journal of Psychopharmacology · doi:10.1177/0269881116650087 · Cited by 142
Peoples, L. L., & West, M. O. (1996) · Journal of Neuroscience · doi:10.1523/jneurosci.16-10-03459.1996 · Cited by 150
“…striatum (VS), and NAcc neurons of moderately trained monkeys were activated during prereward incentive-related events (Nishino et al., 1987; Romo and Schultz, 1990; Apicella et al., 1992; Ljungberg et al., 1992; Schultz et al., 1992) (for related findings in rats, see Carelli and…”
BackgroundThe role of the basal ganglia in motor control: contributions from PET
Brooks, D. J. (1995) · Journal of the Neurological Sciences · doi:10.1016/0022-510x(94)00206-4 · Cited by 150
Learning from Action: Reconsidering Movement Signaling in Midbrain Dopamine Neuron Activity
Coddington, L. T., & Dudman, J. T. (2019) · Neuron · doi:10.1016/j.neuron.2019.08.036 · Cited by 150
Distinct Tonic and Phasic Anticipatory Activity in Lateral Habenula and Dopamine Neurons
Bromberg-Martin, E. S., Matsumoto, M., & Hikosaka, O. (2010) · Neuron · doi:10.1016/j.neuron.2010.06.016 · Cited by 164
“Early reports suggested that some dopamine neurons have small changes in tonic activity in anticipation of arm movements to obtain food rewards (Romo and Schultz, 1990) or delivery of probabilistic rewards (Fiorillo et al., 2003), but these changes have not always been reported in later studies…”
BackgroundResultBeyond reward prediction errors: the role of dopamine in movement kinematics
Barter, J. W., Li, S., Lu, D., Bartholomew, R. A., Rossi, M. A., Shoemaker, C. T., Salas-Meza, D., Gaidis, E., & Yin, H. H. (2015) · Frontiers in Integrative Neuroscience · doi:10.3389/fnint.2015.00039 · Cited by 146
“…Durham, NC 27708, USA hy43@duke.edu Received: 12 April 2015 Accepted: 06 May 2015 Published: 27 May 2015 Citation: Barter JW, Li S, Lu D, Bartholomew RA, Rossi MA, Shoemaker CT, Salas-Meza D, Gaidis E and Yin HH (2015) Beyond reward prediction errors: the role of dopamine in movement kinematics.”
BackgroundInfluentialThe Origins of Oxidant Stress in Parkinson's Disease and Therapeutic Strategies
Surmeier, D. J., Guzmán, J. N., Sánchez-Padilla, J., & Goldberg, J. A. (2010) · Antioxidants and Redox Signaling · doi:10.1089/ars.2010.3521 · Cited by 142
“This pacemaking activity is believed to be important to maintaining ambient DA levels in regions that are innervated by these neurons, particularly the striatum (102).”
Kiyatkin, E. A., & Gratton, A. P. (1994) · Brain Research · doi:10.1016/0006-8993(94)90231-3 · Cited by 143
Metadata
- Authors
- Romo, R., & Schultz, W.
- Affiliations
- University of Fribourg (CH)
- ORCID
- Romo, R.
- Venue
- Journal of Neurophysiology
- Publisher
- American Physiological Society
- Published
- 1990-03-01
- Volume
- 63
- Issue
- 3
- Pages
- 592-606
- ISSN
- 0022-3077 (ISSN-L)
- 1522-1598
- OpenAlex
- W2129717318
- Cited by
- 353
- References
- 0
- Citations by year
- 2026: 3 · 2025: 5 · 2024: 5 · 2023: 4 · 2022: 7 · 2021: 7 · 2020: 8 · 2019: 11 · 2018: 12 · 2017: 15 · 2016: 18 · 2015: 16 · 2014: 11 · 2013: 10 · 2012: 13
- FWCI
- 3.21
- 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
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural and Behavioral Psychology Studies
- Keywords
- dopaminergic neurons, midbrain, substantia nigra pars compacta, active touch, anticipatory activity, single-unit recording, ipsilateral and contralateral responses
- MeSH terms
- Action Potentials, Animals, Arm, Dopamine, Female, Macaca, Macaca fascicularis, Male, Muscles, Psychomotor Performance, Substantia Nigra, Touch
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