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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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Burst activity of ventral tegmental dopamine neurons is elicited by sensory stimuli in the awake cat
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Human substantia nigra neurons encode unexpected financial rewards
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“Thus, endogenous stimulation of VR1 could be implicated in motivation and reward mechanisms linked to the dopaminergic system (Schultz, 1986; Mirenowicz and Schultz, 1996).”
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“In particular, mesostriatal dopaminergic neurons signal reward-predicting stimuli and receipt of unpredicted rewards by brief bursts of high-frequency neuron activity (Schultz, 1986, 2002).”
InfluentialFunctional imaging of the human dopaminergic midbrain
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“…trained in an operant task detect some dopaminergic VTA neurons that encode discrepancies between a predicted outcome, such as a juice reward normally delivered following a conditioned stimulus, and the reward’s actual occurrence (Schultz 1986; Romo and Schultz 1990; Schultz et al. 1993).”
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“Durations of 1 ms represent the typical cutoff between DA and slow-firing non-DA cells under these recording conditions in both rats and monkeys (Schultz, 1986; Romo and Schultz, 1990; Ljungberg et al., 1992; Hyland et al., 2002).”
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“These neurons seem to essentially capture the properties of the δ-signal in TD learning (Miller et al. 1981; Schultz 1986; Mirenowicz and Schultz 1994; Hollerman and Schultz 1998 for reviews see Schultz 1998; Schultz and Dickinson 2000; Schultz 2002, but see Redgrave et al. 1999).”
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“Left: In this model, phasic DA release is proposed to occur as a result of a behaviorally relevant stimulus causing DA cells to emit a burst of spikes (Schultz 1986).”
Dopamine Signaling in Dorsal Versus Ventral Striatum: The Dynamic Role of Cholinergic Interneurons
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“The switch in firing mode of mesostriatal DA neurons, from low to higher firing frequencies, is thought to encode information about the prediction and receipt of reward or behaviorally salient stimuli (Schultz, 1986, 2002; Morris et al., 2004; Matsumoto and Hikosaka, 2009).”
BackgroundCortical regulation of subcortical dopamine systems and its possible relevance to schizophrenia
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“However, once the behavioral act is acquired, the DA system no longer responds to the learned stimulus event (Schultz, 1986; Schultz and Romo, 1990).”
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Tonically discharging neurons of monkey striatum respond to preparatory and rewarding stimuli
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“Using methods described previously (Schultz 1986), extracellular activity was recorded with moveable microelectrodes from single neurons in the left striatum of two Macaca fascicularis monkeys during contralateral performance of a delayed go-nogo task.”
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“Dopamine (DA) neurons arising from the ventral tegmental area (VTA) and substantia nigra pars compacta (SNc) contribute during the formation of rewarded behaviors (Bayer and Glimcher, 2005; Schultz, 1986, 1998).”
BackgroundActivity of dopamine neurons in the behaving primate
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Self-citationAltered Dopamine Release and Uptake Kinetics in Mice Lacking D2Receptors
Schmitz, Y., Schmauss, C., & Sulzer, D. L. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-18-08002.2002 · Cited by 176
“The time course of maximal autoinhibition appears to be suitable to enhance the DA signal in response to " meaningful " burst firing (Schultz, 1986), as opposed to baseline firing of substantia nigra neurons.”
BackgroundSummerfield, C., & Tsetsos, K. (2012) · Frontiers in Neuroscience · doi:10.3389/fnins.2012.00070 · Cited by 167
“…such as the dopaminergic midbrain or orbitofrontal cortex (OFC), where neurons respond directly to the reinforcing properties of food or money (Schultz, 1986; Critchley and Rolls, 1996; O’Doherty et al., 2001), and on the structures such as the striatum or anterior cortex, where neuronal…”
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
“Although the DA neurons that project to the prefrontal cortex may have higher discharge rates (Chiodo et al., 1984; Lammel et al., 2008), many midbrain DA neurons often exhibit similar overall firing properties (Schultz, 1986; Clark and Chiodo, 1988; Gariano et al., 1989; Robinson et al., 2004).”
BackgroundNeuronal activity in the monkey striatum during the initiation of movements
Schultz, W., & Romo, R. (1988) · Experimental Brain Research · doi:10.1007/bf00247503 · Cited by 171
“Although lesions of the nigrostriatal dopamine system lead to severe akinesia (Poirier 1960; Schultz et al. 1985), we found that dopamine neurons showed no comparable premovement activation in either of the tasks used presently (Romo and Schultz 1986, and unpublished) while responding well to trigger stimuli ( Schultz…”
BackgroundSelf-citationHaloperidol 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
“have helped explain how the firing rate of dopamine neurons is coded within the midbrain (Schultz et al., 1997; Schultz, 1996; Mirenowicz & Schultz, 1994; Schultz, Apicella, & Ljungberg, 1993; Ljungberg, Apicella, & Schultz, 1992; Romo & Schultz, 1990; Schultz, 1986).”
BackgroundInfluentialWICKENS, J. R., BUDD, C. S., HYLAND, B. I., & ARBUTHNOTT, G. W. (2007) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1390.016 · Cited by 165
Schultz, W., Stauffer, W. R., & Lak, A. (2017) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2017.03.013 · Cited by 171
“During large arm reaching movements toward food boxes, which engage a large proportion of arm and eye muscles in monkeys, select subpopulations of dopamine neurones are activated (31–44%) or depressed (15–17%) [50,51] (Figure 2a,b), sometimes distinguishing between contraand ipsilateral reaching [50].”
Self-citationRichardson, N. R., & Gratton, A. P. (1996) · Journal of Neuroscience · doi:10.1523/jneurosci.16-24-08160.1996 · Cited by 160
“The biphasic, time-locked changes in NAcc DA transmission suggested by our data, 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 a…”
BackgroundResultDopamine neurons encoding long-term memory of object value for habitual behavior
Kim, H. F., Ghazizadeh, A., & Hikosaka, O. (2015) · Cell · doi:10.1016/j.cell.2015.10.063 · Cited by 157
“These features are similar to those used previously to characterize DA neurons in the monkey SNc (Schultz, 1986 ), suggesting that both update-and sustain-type neurons were dopaminergic.”
InfluentialStocchi, F. (2002) · Brain · doi:10.1093/brain/awf214 · Cited by 158
Vargo, J. M., & Marshall, J. F. (1996) · Synapse · doi:10.1002/(sici)1098-2396(199604)22:4 · Cited by 24
Salamone, J. D. (1996) · Journal of Neuroscience Methods · doi:10.1016/0165-0270(95)00125-5 · Cited by 156
Romo, R., & Schultz, W. (1987) · Experimental Brain Research · doi:10.1007/bf00247297 · Cited by 155
“Dopamine neurons in the substantia nigra of monkeys respond to trigger stimuli for behavioral reactions ( Schultz 1986b ).”
BackgroundSelf-citationPeoples, L. L., & West, M. O. (1996) · Journal of Neuroscience · doi:10.1523/jneurosci.16-10-03459.1996 · Cited by 150
Neuronal Activity in Substantia Nigra Pars Reticulata during Target Selection
Basso, M. A., & Wurtz, R. H. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-05-01883.2002 · Cited by 140
“Identification of the substantia nigra through the thalamus was described originally by Schultz (1986).”
Nicotine Dependence, Midbrain Dopamine Systems and Psychiatric Disorders
Nisell, M., Nomikos, G. G., & Svensson, T. H. (1995) · Pharmacology & Toxicology · doi:10.1111/j.1600-0773.1995.tb00123.x · Cited by 143
Neurobiological factors in personality and depression
Depue, R. A. (1995) · European Journal of Personality · doi:10.1002/per.2410090509 · Cited by 145
Kiyatkin, E. A., & Gratton, A. P. (1994) · Brain Research · doi:10.1016/0006-8993(94)90231-3 · Cited by 143
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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