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Role for dopamine in the behavioral functions of the prefrontal corticostriatal system: implications for mental disorders and psychotropic drug action
Abstract
We have discussed the role of dopamine in modulating the interactions between cortical and striatal regions that are involved in behavioral regulation. The evidence reviewed seems to suggest that dopamine acts, overall, to promote stimulus-induced responding for conditioned or reward-related stimuli by integrative actions at multiple forebrain sites. It is thus not surprising that dopaminergic dysfunction has been implicated in a number of neuropsychiatric disorders that involve abnormal cognitive and affective function. Future studies aimed at pinpointing the precise anatomical sites of action and molecular mechanisms involved in dopaminergic transmission within the corticolimbic circuit are critical for trying to disentangle the cellular mechanisms by which dopamine exerts its actions. Moreover, the afferent control of dopamine neurons from brainstem and forebrain sites need to be fully explored in order to begin to understand what mechanisms are involved in regulating the dopaminergic response to stimuli with incentive value. Finally, the post-synaptic consequences of prolonged and supranormal dopaminergic activation need to be investigated in order to understand what persistent neuroadaptations result from chronic activation of this neuromodulatory system (e.g. in drug addiction). Answers to these sorts of questions will undoubtedly provide important insights into the nature of dopaminergic function in the animal and human brain.
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Cocaine produces excessive dopamine signalling in the PFC, which weakens PFC function, including the ability to resist taking drugs.
“For example, drugs of abuse such as cocaine produce excessive dopamine signalling in the PFC, which weakens PFC function150, including the ability to resist taking drugs.”
From Stress signalling pathways that impair prefrontal cortex structure and function (2009) · cites this paper as [150]
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Metadata
- Authors
- Jentsch, J. D., Roth, R. H., & Taylor, J. R.
- Affiliations
- University of Pittsburgh (US)
- Yale University (US)
- Corresponding author
- Jentsch, J.David
- Venue
- Progress in Brain Research
- Publisher
- Elsevier
- Published
- 2000
- Volume
- 126
- Pages
- 433-453
- ISSN
- 0079-6123 (ISSN-L)
- OpenAlex
- W1488942925
- Cited by
- 99
- References
- 15
- Citations by year
- 2025: 3 · 2024: 1 · 2023: 1 · 2022: 3 · 2021: 4 · 2020: 1 · 2019: 1 · 2018: 1 · 2017: 3 · 2015: 1 · 2014: 3 · 2013: 1 · 2012: 2
- FWCI
- 3.65
- Type
- book chapter
- Language
- en
- Open access
- closed
- Locations
- Progress in 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 › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Keywords
- dopamine, striatum, behavioral regulation, reward, conditioned responding, neuropsychiatric disorders, psychotropic drugs, dopaminergic dysfunction, corticolimbic circuits, dopamine signaling, drug addiction, neural adaptation, incentive value
- MeSH terms
- Amphetamines, Amygdala, Central Nervous System Stimulants, Animals, Haplorhini, Behavior, Mental Disorders, Brain Mapping, Cognition, Corpus Striatum, Depression, Dopamine, Emotions, Humans, Learning, Limbic System, Mammals, Memory, Neural Pathways, Nucleus Accumbens, Phencyclidine, Psychotropic Drugs, Reward, Schizophrenia, Prefrontal Cortex, Receptors, Neurotransmitter, Neurotransmitter Agents, Dopamine Agonists, Substance-Related Disorders
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