The DOI matches its Crossref record; 88 of the 89 references it cites were found in a registry or an index.
Increased Synaptic Dopamine Function in Associative Regions of the Striatum in Schizophrenia
Abstract
CONTEXT: A long-standing version of the dopamine hypothesis of schizophrenia postulates that hyperactivity of dopaminergic transmission at D(2) receptors in the limbic striatum is associated with the illness and that blockade of mesolimbic D(2) receptors is responsible for the antipsychotic action of D(2) receptor antagonists. OBJECTIVE: To localize dopaminergic hyperactivity within the striatum in schizophrenia. DESIGN: Case-control study. SETTING: Inpatient research unit. PARTICIPANTS: Eighteen untreated patients with schizophrenia and 18 healthy control subjects matched for age, sex, ethnicity, parental socioeconomic status, cigarette smoking, and weight. MAIN OUTCOME MEASURES: Percentage change in dopamine D(2) receptor availability in striatal subregions within each subject measured by positron emission tomography with carbon 11-labeled raclopride before and during pharmacologically induced dopamine depletion. RESULTS: In the associative striatum, acute dopamine depletion resulted in a larger increase in D(2) receptor availability in patients with schizophrenia (mean [SD], 15% [7%]) than in control subjects (10% [7%], P = .045), suggesting higher synaptic dopamine concentration. Within the associative striatum, this effect was most pronounced in the precommissural dorsal caudate (15% [8%] in patients vs 9% [8%] in controls, P = .03). No between-group differences were observed in the limbic and sensorimotor striatum. CONCLUSIONS: These findings suggest that schizophrenia is associated with elevated dopamine function in associative regions of the striatum. Because the precommissural dorsal caudate processes information from the dorsolateral prefrontal cortex, this observation also suggests that elevated subcortical dopamine function might adversely affect performance of the dorsolateral prefrontal cortex in schizophrenia. On the other hand, the absence of a group difference in the limbic striatum brings into question the therapeutic relevance of the mesolimbic selectivity of second-generation antipsychotic drugs.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“Synaptic dopamine is also increased in psychosis(50, 51).”
From Aberrant Salience, Information Processing, and Dopaminergic Signaling in People at Clinical High Risk for Psychosis (2020) · cites this paper as [50]
In the citing paper
“In CHR subjects in general, as well as in the subgroup that later become psychotic, the greatest alterations in dopamine synthesis and release capacity have been found in the associative striatum (57-59, 62), paralleling findings in psychotic patients(50, 69).”
From Aberrant Salience, Information Processing, and Dopaminergic Signaling in People at Clinical High Risk for Psychosis (2020) · cites this paper as [50]
In the citing paper
“a PET study found higher synaptic DA concentrations in the ventral striatum in schizophrenia [425].”
From Reward circuitry dysfunction in psychiatric and neurodevelopmental disorders and genetic syndromes: animal models and clinical findings (2012) · cites this paper as [425]
Citations
Cites
The Positive and Negative Syndrome Scale (PANSS) for schizophrenia.
Kay, S. R., Fiszbein, A., & Opler, L. A. (1987) · Schizophrenia Bulletin · doi:10.1093/schbul/13.2.261 · Cited by 21,378
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
Four Factor Index of Social Status
Paschou, R. (1975) · Cited by 6,989
Effectiveness of Antipsychotic Drugs in Patients with Chronic Schizophrenia
Lieberman, J. A., Stroup, T. S., McEvoy, J. P., Swartz, M. S., Rosenheck, R. A., Perkins, D. O., Keefe, R. S. E., Davis, S. M., Davis, C. E., Lebowitz, B. D., et al. (2005) · New England Journal of Medicine · doi:10.1056/nejmoa051688 · Cited by 5,892
Four Factor Index of Social Status [1975]
Hollingshead, A. B. (1975) · Cited by 5,151
Dopamine Receptor Binding Predicts Clinical and Pharmacological Potencies of Antischizophrenic Drugs
Creese, I., Burt, D. R., & Snyder, S. H. (1976) · Science · doi:10.1126/science.3854 · Cited by 2,220
Functional anatomy of the basal ganglia. I. The cortico-basal ganglia-thalamo-cortical loop
Parent, A., & Hazrati, L.-N. (1995) · Brain Research Reviews · doi:10.1016/0165-0173(94)00007-c · Cited by 2,161
Dopamine in schizophrenia: a review and reconceptualization
Davis, K. L., Kahn, R. S., Ko, G., & Davidson, M. (1991) · American Journal of Psychiatry · doi:10.1176/ajp.148.11.1474 · Cited by 2,051
Physiologic Dysfunction of Dorsolateral Prefrontal Cortex in Schizophrenia
Weinberger, D. R. (1986) · Archives of General Psychiatry · doi:10.1001/archpsyc.1986.01800020020004 · Cited by 2,025
Negative v Positive Schizophrenia
Andreasen, N. C. (1982) · Archives of General Psychiatry · doi:10.1001/archpsyc.1982.04290070025006 · Cited by 2,008
Cited by
Sorted by citations
Items 501–565 of 565
The alpha2C-adrenoceptor as a neuropsychiatric drug tar-get - PET studies in human subjects
Lehto, J. (2015) · UTUPub (University of Turku)
Prefrontaal dopamine en werkgeheugen bij schizofrenie
van de Giessen, E. (2015) · Neuropraxis · doi:10.1007/s12474-015-0101-4
Banasikowski, T. J. (2012) · QSpace (Queen's University Library)
Imaging of Neurochemical Transmission in the Central Nervous System
Deuitch, L., & Narendran, R. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-418677-4.00019-1
Neto, A. F. R. (2016) · TDX (Tesis Doctorals en Xarxa)
Molecular Imaging in Schizophrenia
Howes, O. D. (2012) · Neuromethods · doi:10.1007/7657_2012_57
Kasanova, Z., Hernaus, D., Vaessen, T., van Amelsvoort, T., Winz, O., Heinzel, A., Pruessner, J. C., Mottaghy, F. M., Collip, D., & Myin‐Germeys, I. (2016) · PLoS ONE · doi:10.18154/rwth-conv-212412
[Treatment of furunculosis and pseudofurunculosis in children].
Karimov, K. R. (1991) · PubMed
RODENT MODELS OF SCHIZOPHRENIA-LIKE SYMPTOMS INCREASE POLYDIPSIA
Hawken, E. R. (2012) · QSpace (Queen's University Library)
The role of basal ganglia circuitry in motivation
Poyraz, F. C. (2016) · doi:10.7916/d89z94qz
Screening of a Histone Methyltransferase Inhibitor in Animal Models of Psychiatric Illness
Kosowan, J. (2014) · TSpace (University of Toronto)
Clinical imaging in drug development
Matthews, P. M. (2013) · Elsevier eBooks · doi:10.1016/b978-0-7020-4299-7.00018-4
Santis, M. D. (2018) · Research Online (University of Wollongong)
Hedges, D., Farrer, T. J., Bigler, E. D., & Hopkins, R. O. (2019) · Springer eBooks · doi:10.1007/978-3-030-14260-5_4
Avram, M., Brandl, F., Knolle, F., Cabello, J., Leucht, C., Scherr, M., Mustafa, M., Koutsouleris, N., Leucht, S., Ziegler, S. I., et al. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/847178
A via das quinureninas e suas implicações na esquizofrenia
Cunha, S. F., Bachur, T. P. R., & Aragão, G. F. (2020) · Revista de Ciências Médicas e Biológicas · doi:10.9771/cmbio.v1i1.33570 · Cited by 1
Graf, I., Willeit, M., Kasper, S. F., & Praschak-Rieder, N. (2020) · Springer eBooks · doi:10.1007/978-3-030-53176-8_6 · Cited by 1
Extrastriatal dopamine D2/3 receptors in schizophrenia
Tuppurainen, H. (2011) · UEF eRepo (University of Eastern Finland)
Xiu, M. H., Guan, X., Kosten, T. R., & Zhang, X. (2021) · SSRN Electronic Journal · doi:10.2139/ssrn.3915670
Cavichioli, A. M. (2022) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/d.17.2022.tde-06052022-144555
Neurodevelopmental Mechanisms for Psychotic Disorders
Gamo, N. J., Sakurai, T., Jaaro-Peled, H., & Sawa, A. (2017) · Oxford University Press eBooks · doi:10.1093/med/9780190681425.003.0019
Psychiatric Disorders in Animal Models of Schizophrenia
Wąsik, A. (2021) · Springer eBooks · doi:10.1007/978-3-030-71519-9_241-1
Ataniya, R., Koike, K., & Inamoto, A. (2022) · Research Square · doi:10.21203/rs.3.rs-1699376/v1
Psychiatric Disorders in Animal Models of Schizophrenia
Wąsik, A. (2022) · Springer eBooks · doi:10.1007/978-3-031-15080-7_241
On the bumpy road of psychotic disorders
van Hooijdonk, C. F. M. (2023) · Research Publications (Maastricht University) · doi:10.26481/dis.20231201ch
Zawadzki, J. A., Girard, T. A., Samsom, J., Foussias, G., Siddiqui, I., Lerch, J. P., Grady, C. L., & Wong, A. H. C. (2024) · Psychiatry Research Neuroimaging · doi:10.1016/j.pscychresns.2024.111826
A Rare Syndrome in Adolescents: Capgras Syndrome and Its Psychopharmacological Treatment
Özbek, T. C., & Özbek, M. M. (2024) · European Journal of Therapeutics · doi:10.58600/eurjther2140
Boiko, A. S., Paderina, D. Z., Викторовна, М. Е., Kornetova, E. G., Bokhan, N. A., & Ivanova, S. А. (2024) · Neurochemical Journal · doi:10.1134/s1819712424010045
Lower density of calretinin‐immunopositive neurons in the putamen of subjects with schizophrenia
Kelmer, P., Hoppa, P., Frank, E., Tyler, T., & Adorján, I. (2024) · Journal of Anatomy · doi:10.1111/joa.14180
From Circuits to Drug Targets: The Promise of Opto- and Chemogenetics for Drug Discovery
Kätzel, D. (2024) · Royal Society of Chemistry eBooks · doi:10.1039/9781837672059-00185 · Cited by 1
The Birth of Our Free Imagination
Tse, P. U. (2024) · Oxford University Press eBooks · doi:10.1093/oso/9780198901181.003.0002
Tse, P. U. (2024) · Oxford University Press eBooks · doi:10.1093/oso/9780198901181.003.0001
Tse, P. U. (2024) · Oxford University Press eBooks · doi:10.1093/oso/9780198901181.002.0003
Tse, P. U. (2024) · Oxford University Press eBooks · doi:10.1093/oso/9780198901181.002.0004
The Birth of Good and Evil in Our Free Imaginations
Tse, P. U. (2024) · Oxford University Press eBooks · doi:10.1093/oso/9780198901181.003.0003
Tse, P. U. (2024) · Oxford University Press eBooks · doi:10.1093/oso/9780198901181.002.0005
Translational Models for Psychosis
Corlett, P. R. (2025) · Oxford University Press eBooks · doi:10.1093/med/9780197640654.003.0017
Tubiolo, P. N., Williams, J. C., Gil, R. B., Cassidy, C., Haubold, N. K., Patel, Y., Abeykoon, S. K., Zheng, Z. J., Pham, D. T., Ojeil, N., et al. (2025) · medRxiv · doi:10.1101/2025.03.31.25324962 · Cited by 1
Self-citationHigh-Affinity State of Dopamine D2/3 Receptors in Schizophrenia: A Dual-Radioligand Approach
Kodaka, F. (2025) · Neuromethods · doi:10.1007/978-1-0716-4494-2_8
Dopamine dysfunction in psychosis
McCutcheon, R. A., & Zauchenberger, C.-Z. (2025) · Handbook of behavioral neuroscience · doi:10.1016/b978-0-443-29867-7.00035-9
GOFF, D. C. (2025) · Journal of Clinical Psychopharmacology · doi:10.1097/jcp.0000000000002029
Bedwell, S. A. (2025) · Cambridge University Press eBooks · doi:10.1017/9781009407946.012
Reyes-Madrigal, F., León-Ortíz, P., Wengler, K., Bachmann, H. P., Singletary, N. M., Ortuño, M., Mao, X., Rivera-Chávez, L. F., Malacara, M., Shungu, D. C., et al. (2025) · Biological Psychiatry Cognitive Neuroscience and Neuroimaging · doi:10.1016/j.bpsc.2025.10.019
Santis, M. D. (2012) · Research Online (University of Wollongong)
Lang, X., Xue, M., Zang, X., Wu, F., 修梅红, & Zhang, X. (2024) · Figshare · doi:10.6084/m9.figshare.26601814
Purves-Tyson, T. D., Brown, A. M., Weissleder, C., Rothmond, D. A., & Shannon-Weickert, C. (2021) · Figshare · doi:10.6084/m9.figshare.14853387
Kirenskaya, A. V., Novototsky-Vlasov, V. Y., Kibitov, A. O., Merkulova, T. V., Tkachenko, A. A., & Storozheva, Z. I. (2026) · Molecular Biology Reports · doi:10.1007/s11033-025-11419-w
Quantitative susceptibility mapping of deep brain nuclei in 22q11.2 deletion syndrome
Muñoz, N., Saborit, M. G., Cuiza, A., Tepper, Á., Núñez, J. V., Ramírez-Mahaluf, J. P., Barbagelata, D., Aguirre, J. M., Maldonado, M. E., Ornstein, C., et al. (2026) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2025.1652700
Couty, P., Yung, S., Dulapt, I., Berger, L., Santoro, A., Hardt, L., Petitbon, A., Ducrocq, F., Walle, R., Catanese, J., et al. (2026) · Neuropsychopharmacology · doi:10.1038/s41386-026-02400-7
Goutaudier, R. (2022) · theses.fr (ABES) · doi:10.70675/6619b466z54bfz41e3z8a90zf0967825d579
The design of multi-target ligands and their role in schizophrenia therapy: an update
Gagić, Ž., Popović-Nikolić, M. R., Čarapić, M., Zukic, S., Oljačić, S., & Nikolić, K. (2026) · Expert Opinion on Drug Discovery · doi:10.1080/17460441.2026.2669617
Avanesyan, H., Parsadanyan, M. A., Shahinyan, M. A., Багдасарович, Л. А., Mikaelyan, M. S., Grigoryan, S. V., & Vardevanyan, P. O. (2025) · Neurophysiology · doi:10.1007/s11062-026-10001-9
Efeitos do estresse gerado pelo isolamento social e pela discriminação na saúde mental
Ferigato, E. (2026) · Vértices · doi:10.19180/1809-2667.v28n22026.23544
SwapIII: Clarifying the role of D2 receptor occupancy in psychosis and movement disorders
Shakir, M., van Harten, P. N., Hoogendoorn, A. W., Willems, A. E., Stout, T. L. L., & Tenback, D. E. (2026) · Psychiatry Research Communications · doi:10.1016/j.psycom.2026.100266
Levitt, J. J., Zhang, F., Vangel, M. G., Nestor, P. G., Yogesh Rathi, A., Karayumak, S. C., Kubicki, M. R., Pasternak, O., Coleman, M. J., Lewandowski, K. E., et al. (2026) · Molecular Psychiatry · doi:10.1038/s41380-026-03719-9 · Cited by 1
Navaneethan, B., Costa, P. A., Debs, S. R., Gavljak, I., Conn, I., Penklis, A. G., Weickert, C. S., & Purves-Tyson, T. D. (2026) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2026.111933
Two Coordinates for Dopamine in the Basal Ganglia
Horváth, S., & Mirnics, K. (2026) · NeuroSci · doi:10.3390/neurosci7050104
Transdiagnostic mechanisms underlying non-affective psychosis: A role for hippocampal networks?
Kaplan, C., Perepezko, K., Pontone, G. M., & Bakker, A. (2026) · American Journal of Geriatric Psychiatry · doi:10.1016/j.jagp.2026.10.010
Nader, G., Azizi, N., Qian, J., Sivapatham, S., Ducharme, M., Simpson, A. I. F., Graff, A., Fischer, C., Gerretsen, P., Strafella, A. P., et al. (2026) · Journal of Neural Transmission · doi:10.1007/s00702-026-03258-1
Metadata
- Authors
- Kegeles, L. S., Abi-Dargham, A., Frankle, W. G., Gil, R., Cooper, T. B., Slifstein, M., Hwang, D.-R., Huang, Y., Haber, S. N., & Laruelle, M.
- Affiliations
- Columbia University Irving Medical Center (US)
- ORCID
- Venue
- Archives of General Psychiatry
- Publisher
- American Medical Association (AMA)
- Published
- 2010-03-01
- Volume
- 67
- Issue
- 3
- Pages
- 231
- ISSN
- 0003-990X (ISSN-L)
- OpenAlex
- W1999984108
- Cited by
- 565
- References
- 89
- Citations by year
- 2026: 17 · 2025: 26 · 2024: 33 · 2023: 25 · 2022: 42 · 2021: 23 · 2020: 32 · 2019: 42 · 2018: 32 · 2017: 38 · 2016: 45 · 2015: 41 · 2014: 47 · 2013: 32 · 2012: 47
- FWCI
- 25.78
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Archives of General Psychiatry (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institute of Mental Health (K02MH01603-01, K02MH001603, R01MH054192)
- Topics
- Health Sciences › Medicine › Psychiatry and Mental health › Schizophrenia research and treatment
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
- Health Sciences › Medicine › Clinical Neurology › Parkinson's Disease Mechanisms and Treatments
- Keywords
- schizophrenia, synaptic dopamine, associative striatum, dorsal caudate, dopamine depletion, mesolimbic dopamine system, dopamine hypothesis of schizophrenia, atypical antipsychotics, dorsolateral prefrontal cortex, positron emission tomography, raclopride
- MeSH terms
- Adult, Brain Mapping, Carbon Radioisotopes, Caudate Nucleus, Corpus Striatum, Dopamine, Female, Humans, Image Processing, Computer-Assisted, Male, Synaptic Transmission, Putamen, Schizophrenia, Synapses, Case-Control Studies, Prefrontal Cortex, Receptors, Dopamine D2, alpha-Methyltyrosine, Raclopride, Positron-Emission Tomography
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review