Cited by 584Neurotransmitter Receptor Influence on BehaviorNeural and Behavioral Psychology StudiesMemory and Neural Mechanisms

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The involvement of nucleus accumbens dopamine in appetitive and aversive motivation

Salamone, John D.·1994·Behavioural Brain Research

DOI 10.1016/0166-4328(94)90153-8

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Abstract

In recent years, considerable emphasis has been placed upon the putative role of nucleus accumbens dopamine systems in appetitive motivation and positive reinforcement. However, considerable evidence indicates that brain dopamine in general, and nucleus accumbens dopamine in particular, is involved in aspects of aversive motivation. Administration of dopamine antagonists or localized interference with nucleus accumbens dopamine systems has been shown to disrupt active avoidance behavior. In addition, accumbens dopamine release and metabolism is activated by a wide variety of stressful conditions. A review of the literature indicates that there are substantial similarities between the characteristics of dopaminergic involvement in appetitive and aversive motivation. There is conflicting evidence about the role of dopamine in emotion, and little evidence to suggest that the profound and consistent changes in instrumental behavior produced by interference with DA systems are due to direct dopaminergic mediation of positive affective responses such as hedonia. It is suggested that nucleus accumbens dopamine is involved in aspects of sensorimotor functions that are involved in both appetitive and aversive motivation.

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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
Cognitive, social, and physiological determinants of emotional state.
Schachter, S., & Singer, J. (1962) · Psychological Review · doi:10.1037/h0046234 · Cited by 6,223
A psychomotor stimulant theory of addiction.
Wise, R. A., & Bozarth, M. A. (1987) · Psychological Review · doi:10.1037/0033-295x.94.4.469 · Cited by 2,747
The pharmacological basis of therapeutics
Frank, A. L. (1981) · Environmental Research · doi:10.1016/0013-9351(81)90176-6 · Cited by 2,738
From motivation to action: Functional interface between the limbic system and the motor system
MOGENSON, G., JONES, D., & YIM, C. (1980) · Progress in Neurobiology · doi:10.1016/0301-0082(80)90018-0 · Cited by 2,331
Nebraska Symposium on Motivation
Wittenborn, J. R. (1959) · The Journal of Nervous and Mental Disease · doi:10.1097/00005053-195907000-00020 · Cited by 1,907
Physiological Role of Pleasure: A stimulus can feel pleasant or unpleasant depending upon its usefulness as determined by internal signals.
Cabanac, M. (1971) · Science · doi:10.1126/science.173.4002.1103 · Cited by 1,521
Adipsia and Aphagia after 6‐Hydroxydopamine Induced Degeneration of the Nigro‐striatal Dopamine System
Ungerstedt, U. (1971) · Acta Physiologica Scandinavica · doi:10.1111/j.1365-201x.1971.tb11001.x · Cited by 1,294
Responses of monkey dopamine neurons to reward and conditioned stimuli during successive steps of learning a delayed response task
Schultz, W., Apicella, P., & Ljungberg, T. (1993) · The Journal of Neuroscience · doi:10.1523/jneurosci.13-03-00900.1993 · Cited by 1,291
The Interaction of Cognitive and Physiological Determinants of Emotional State
Schachter, S. (1964) · Advances in experimental social psychology · doi:10.1016/s0065-2601(08)60048-9 · Cited by 1,186

Show all 238 references

Research works printed but not linked: 2

Janssen, 1965, Is it possible to predict the clinical effects of neuroleptic drugs (major tranquilizers) from animal data?, Arzneim.-Forsch., 15, 104
Louilot, 1993, The response of mesolimbic dopaminergic neurons to the affective value of simulus is regionalized and lateralized, Soc. Neurosci. Abstr., 19, 1827

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Modulation of fear/anxiety responses, but not food intake, following α-adrenoceptor agonist microinjections in the nucleus accumbens shell of free-feeding rats
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GABA receptor subtype antagonists in the nucleus accumbens shell and ventral tegmental area differentially alter feeding responses induced by deprivation, glucoprivation and lipoprivation in rats
Kandov, Y., Israel, Y., Kest, A., Dostova, I., Verasammy, J., Bernal, S. Y., Kasselman, L. J., & Bodnar, R. J. (2006) · Brain Research · doi:10.1016/j.brainres.2006.01.112 · Cited by 17
Dopamine-Glutamate Interactions in Reward-Related Incentive Learning
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Energizing effects of bupropion on effortful behaviors in mice under positive and negative test conditions: modulation of DARPP-32 phosphorylation patterns
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Self-citation
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Authors: Salamone, J. D.
Affiliations: University of Connecticut (US)
Corresponding author: Salamone, John D.
ORCID: Salamone, John D.
Venue: Behavioural Brain Research
Publisher: Elsevier BV
Published: 1994-04
Volume: 61
Issue: 2
Pages: 117-133
ISSN: 0166-4328 (ISSN-L)
DOI: 10.1016/0166-4328(94)90153-8
OpenAlex: W2079322728
Cited by: 584
References: 238
Citations by year: 2026: 4 · 2025: 7 · 2024: 12 · 2023: 9 · 2022: 16 · 2021: 6 · 2020: 7 · 2019: 12 · 2018: 15 · 2017: 15 · 2016: 24 · 2015: 28 · 2014: 22 · 2013: 32 · 2012: 18
FWCI: 1.98
Type: journal article
Language: en
Open access: closed
Licence: www.elsevier.com/tdm/userlicense/1.0/ (tdm)
Locations: Behavioural Brain Research (publishedVersion)
PubMed (publishedVersion)
Topics: Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
Life Sciences › Neuroscience › Cognitive Neuroscience › Neural and Behavioral Psychology Studies
Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
Keywords: nucleus accumbens, dopamine, appetitive motivation, aversive motivation, avoidance behavior, positive reinforcement, stress, dopamine antagonists, hedonia, instrumental behavior, sensorimotor function
MeSH terms: Animals, Appetitive Behavior, Arousal, Avoidance Learning, Dopamine, Motivation, Nucleus Accumbens, Receptors, Dopamine, Reinforcement, Psychology

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The involvement of nucleus accumbens dopamine in appetitive and aversive motivation

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