Cited by 289Neurotransmitter Receptor Influence on BehaviorNeuroscience and Neuropharmacology ResearchSchizophrenia research and treatment

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Synaptic Regulation of Mesocorticolimbic Dopamine Neurons

White, F J·1996·Annual Review of Neuroscience

DOI 10.1146/annurev.ne.19.030196.002201

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Abstract

The mesocorticolimbic dopamine system is thought to be involved in psychosis and drug addiction. Many intrinsic membrane properties and synaptic regulators have been identified and characterized in the midbrain ventral tegmental dopamine neurons that give rise to this system. Other neuronal properties remain subject to considerable debate. The present review brings together a large literature regarding neurophysiological studies of the synaptic mechanisms thought to regulate the activity of ventral tegmental dopamine neurons. This work is placed within the context of the behavioral responsiveness of midbrain dopamine neurons and the alterations produced in these neurons by repeated treatment with and withdrawal from antipsychotic drugs and drugs of abuse.

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EVIDENCE FOR THE EXISTENCE OF MONOAMINE-CONTAINING NEURONS IN THE CENTRAL NERVOUS SYSTEM. I. DEMONSTRATION OF MONOAMINES IN THE CELL BODIES OF BRAIN STEM NEURONS.
Dahlstroem, A., & Fuxé, K. (1964) · PubMed · Cited by 5,133
Stereotaxic mapping of the monoamine pathways in the rat brain
Ungerstedt, U. (1971) · Acta Physiologica Scandinavica · doi:10.1111/j.1365-201x.1971.tb10998.x · Cited by 3,819
International Union of Pharmacology classification of receptors for 5-hydroxytryptamine (Serotonin).
Hoyer, D., Clarke, D. E., Fozard, J. R., Hartig, P. R., Martin, G. R., Mylecharane, E. J., Saxena, P. R., & Humphrey, P. P. A. (1994) · Pharmacological Reviews · doi:10.1016/s0031-6997(25)06783-3 · Cited by 3,025
Dopamine transmission in the initiation and expression of drug- and stress-induced sensitization of motor activity.
Kalivas, P., & Stewart, J. (1991) · Brain research. Brain research reviews · doi:10.1016/0165-0173(91)90007-u · Cited by 2,087
Drugs of abuse: anatomy, pharmacology and function of reward pathways
Koob, G. F. (1992) · Trends in Pharmacological Sciences · doi:10.1016/0165-6147(92)90060-j · Cited by 2,070
Opioids excite dopamine neurons by hyperpolarization of local interneurons
Johnson, S., & North, R. (1992) · The Journal of Neuroscience · doi:10.1523/jneurosci.12-02-00483.1992 · Cited by 1,637
The control of firing pattern in nigral dopamine neurons: burst firing
Grace, A., & Bunney, B. (1984) · Journal of Neuroscience · doi:10.1523/jneurosci.04-11-02877.1984 · Cited by 1,346
Intracellular and extracellular electrophysiology of nigral dopaminergic neurons—1. Identification and characterization
Grace, A. A., & Bunney, B. S. (1983) · Neuroscience · doi:10.1016/0306-4522(83)90135-5 · Cited by 937
Typical and atypical neuroleptics: differential effects of chronic administration on the activity of A9 and A10 midbrain dopaminergic neurons
Chiodo, L. A., & Bunney, B. (1983) · Journal of Neuroscience · doi:10.1523/jneurosci.03-08-01607.1983 · Cited by 680
Nonlinear relationship between impulse flow and dopamine released by rat midbrain dopaminergic neurons as studied by in vivo electrochemistry
Gonon, F. G. (1988) · Neuroscience · doi:10.1016/0306-4522(88)90307-7 · Cited by 676

Show all 95 references

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Authors: White, F. J.
Corresponding author: White, F J
ORCID: White, F J
Venue: Annual Review of Neuroscience
Publisher: Annual Reviews
Published: 1996-03
Volume: 19
Issue: 1
Pages: 405-436
ISSN: 0147-006X (ISSN-L)
1545-4126
DOI: 10.1146/annurev.ne.19.030196.002201
OpenAlex: W2175469462
Cited by: 289
References: 95
Citations by year: 2026: 1 · 2025: 1 · 2024: 2 · 2022: 3 · 2021: 3 · 2020: 2 · 2019: 1 · 2018: 2 · 2017: 8 · 2016: 6 · 2015: 9 · 2014: 7 · 2013: 1 · 2012: 12
FWCI: 6.59
Type: journal article
Language: en
Open access: closed
Locations: Annual Review of Neuroscience (publishedVersion)
PubMed (publishedVersion)
Funders: National Institutes of Health (5k02da000207-04, 5r01mh040832-06)
U.S. Public Health Service
National Institute of Mental Health (MH-40832)
National Institute on Drug Abuse (DA-04093, DA00207)
Topics: Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
Health Sciences › Medicine › Psychiatry and Mental health › Schizophrenia research and treatment
Keywords: mesocorticolimbic dopamine system, ventral tegmental area, dopaminergic neurons, synaptic regulation, intrinsic membrane properties, psychosis, drug addiction, antipsychotic drugs, drug withdrawal, behavioral responsiveness, midbrain dopaminergic neurons
MeSH terms: Afferent Pathways, Animals, Dopamine, gamma-Aminobutyric Acid, Homeostasis, Humans, Limbic System, Mesencephalon, Neurons, Norepinephrine, Receptors, Dopamine, Serotonin, Substance Withdrawal Syndrome, Synapses, Tegmentum Mesencephali, Antipsychotic Agents, Excitatory Amino Acids, Substance-Related Disorders

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Synaptic Regulation of Mesocorticolimbic Dopamine Neurons

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