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Antipsychotic Drugs: Direct Correlation Between Clinical Potency and Presynaptic Action on Dopamine Neurons
Abstract
Neuroleptic (antipsychotic) drugs inhibited the electrically stimulated release of [3 H]dopamine from rat striatal slices. The concentrations for 50 percent inhibition (ranging from 11.5 nanomolar for spiroperidol to 800 nanomolar for thioridazine) correlated closely with the average daily dosages of 25 neuroleptic drugs used clinically for schizophrenia. The correlation includes butyrophenones, phenothiazines, reserpine, pimozide, clozapine, and (+)-butaclamol. Clinically inactive isomers [trans-thiothixene,trans-flupenthixol, and (-)-butaclamol] required 20 to 1000 times higher concentrations than the active isomers to inhibit release. Compared to the inhibition of [3 H]dopamine release, much higher neuroleptic concentrations were needed to inhibit the electrically stimulated release of other neurotransmitters—[3 H]acetylcholine, [3 H]GABA (γ-aminobutyric acid). The neuroleptic drugs may block the presynaptic coupling between impulse and neurosecretion.
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“The DA hypothesis of schizophrenia suggests that excess DA transmission may be pro-psychotic, and originally gained support from pharmacological evidence that drugs that decrease DA activity (for example,, the phenothiazine neuroleptics) are antipsychotic, whereas drugs that promote DA activity (for example,, amphetamines) are psychotomimetic [76,357].”
From Reward circuitry dysfunction in psychiatric and neurodevelopmental disorders and genetic syndromes: animal models and clinical findings (2012) · cites this paper as [76]
In the citing paper
“the medications that have proven successful for treating schizophrenia/psychosis are drugs that primarily antagonize D2 receptors [76,358]”
From Reward circuitry dysfunction in psychiatric and neurodevelopmental disorders and genetic syndromes: animal models and clinical findings (2012) · cites this paper as [76]
Citations
Cites
The Membrane Actions of Anesthetics and Tranquilizers
Seeman, P. M. (1972) · Pharmacological Reviews · doi:10.1016/s0031-6997(25)06931-5 · Cited by 2,241
Self-citationCarlsson, A., & Lindqvist, M. (1963) · Acta Pharmacologica et Toxicologica · doi:10.1111/j.1600-0773.1963.tb01730.x · Cited by 2,156
DOPAMINERGIC NEURONS: EFFECT OF ANTIPSYCHOTIC DRUGS AND AMPHETAMINE ON SINGLE CELL ACTIVITY
Bunney, B. S., Walters, J. R., Roth, R. H., & Aghajanian, G. K. (1973) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1016/s0022-3565(25)29539-8 · Cited by 1,283
Receptor activity and turnover of dopamine and noradrenaline after neuroleptics
Andén, N., Butcher, S. G., CORRODI, H., Fuxé, K., & Ungerstedt, U. (1970) · European Journal of Pharmacology · doi:10.1016/0014-2999(70)90006-3 · Cited by 1,026
Drugs, Neurotransmitters, and Schizophrenia
Snyder, S. H., Banerjee, S. P., Yamamura, H. I., & Greenberg, D. A. (1974) · Science · doi:10.1126/science.184.4143.1243 · Cited by 834
The significance of dopamine-receptor blockade for the mechanism of action of neuroleptic drugs.
Jm, V. R. (1966) · PubMed · Cited by 508
Clement‐Cormier, Y. C., Kebabian, J. W., Petzold, G. L., & Greengard, P. (1974) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.71.4.1113 · Cited by 452
Evidence for a receptor-mediated feedback control of striatal tyrosine hydroxylase activity
Kehr, W., Carlsson, A., Lindqvist, M., Magnusson, T., & Atack, C. (1972) · Journal of Pharmacy and Pharmacology · doi:10.1111/j.2042-7158.1972.tb09104.x · Cited by 417
Janssen, P. A., Cj, N., & Schellekens, K. H. L. (1965) · PubMed · Cited by 348
Antipsychotic drug actions: a clue to the neuropathology of schizophrenia?
Matthysse, S. (1973) · PubMed · Cited by 338
Flagged first, then by citations
Research works printed but not linked: 9
- Aghajanian, G. K., Frontiers in Neurology and Neuroscience Research: 4 (1974).
- FARNEBO, L. O., ACTA PHYSIOLOGICA SCANDINAVICA 371: 19 (1971).
- FARNEBO, L. O., ACTA PHYSIOLOGICA SCANDINAVICA 371: 35 (1971).
- Munkvad, I., The Neuroleptics. Modern Problems in Pharmacopsychiatrv 5: 44 (1970).
- RITCHIE, J.M., ON ACTIVE STRUCTURE OF LOCAL ANESTHETICS, JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS 133: 241 (1961).
- SEEMAN, P, FEDERATION PROCEEDINGS 33: 246 (1974).
- SOTELO, C, ULTRASTRUCTURAL IDENTIFICATION OF NIGRAL DOPAMINERGIC CELLS IN RAT, JOURNAL DE PHARMACOLOGIE 5: 55 (1974).
- STAWARZ, R.J., SIGNIFICANCE OF INCREASE OF HOMOVANILLIC-ACID (HVA) CAUSED BY ANTIPSYCHOTICS IN CORPUS STRIATUM AND LIMBIC FOREBRAIN, FEDERATION PROCEEDINGS 33: 246 (1974).
- ZIVKOVIC, B, SPECIFIC ACTIVATION OF STRIATAL TYROSINE-HYDROXYLASE (TH) BY NEUROLEPTICS, FEDERATION PROCEEDINGS 33: 536 (1974).
Cited by
Sorted by citations
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Response : Dopamine Receptors and Average Clinical Doses
Creese, I., Burt, D. R., & Snyder, S. H. (1976) · Science · doi:10.1126/science.194.4264.546 · Cited by 71
Pre-clinical Pharmacology of Atypical Antipsychotic Drugs: A Selective Review
Meltzer, H. Y. (1996) · The British Journal of Psychiatry · doi:10.1192/s0007125000298280 · Cited by 71
“Clozapine, the prototypical atypical antipsychotic drug, also satisfies both criteria (Seeman & Lee, 1975; Chiodo & Bunney, 1985).”
BackgroundTreatment of Gilles de la Tourette syndrome with pimozide
Shapiro, A. K., Shapiro, E., & Eisenkraft, G. J. (1983) · American Journal of Psychiatry · doi:10.1176/ajp.140.9.1183 · Cited by 71
Data-Driven Taxonomy for Antipsychotic Medication: A New Classification System
McCutcheon, R. A., Harrison, P. J., Howes, O. D., McGuire, P. K., Taylor, D. M., & Pillinger, T. (2023) · Biological Psychiatry · doi:10.1016/j.biopsych.2023.04.004 · Cited by 70
Kumamoto, N., Matsuzaki, S., Inoue, K., Hattori, T., Shimizu, S., Hashimoto, R., Yamatodani, A., Katayama, T., & Tohyama, M. (2006) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2006.04.163 · Cited by 70
Soden, M. E., Jones, G. L., Sanford, C. A., Chung, A. S., Güler, A. D., Chavkin, C., Luján, R., & Zweifel, L. S. (2013) · Neuron · doi:10.1016/j.neuron.2013.07.044 · Cited by 74
“Indeed, dopamine has been linked to psychosis since the discovery of dopamine receptors as a central target of antipsychotics (Seeman and Lee, 1975; Creese et al., 1976).”
BackgroundAssociation study of GSK3 gene polymorphisms with schizophrenia and clozapine response
de Souza, R. P., Romano‐Silva, M. A., Lieberman, J. A., Meltzer, H. Y., Wong, A. H. C., & Kennedy, J. L. (2008) · Psychopharmacology · doi:10.1007/s00213-008-1193-9 · Cited by 71
“All antipsychotics bind to dopamine D2 receptors with an affinity inversely proportional to the clinically effective dose (Seeman and Lee 1975).”
BackgroundThe antipsychotic potential of muscarinic allosteric modulation
Bridges, T. M., Lebois, E. P., Hopkins, C. R., Wood, M. R., Jones, C. K., Conn, P. J., & Lindsley, C. W. (2010) · Drug News & Perspectives · doi:10.1358/dnp.2010.23.4.1416977 · Cited by 68
Haloperidol versus low-potency first-generation antipsychotic drugs for schizophrenia
Tardy, M., Huhn, M., Kissling, W., Engel, R. R., & Leucht, S. (2014) · Cochrane Database of Systematic Reviews · doi:10.1002/14651858.cd009268.pub2 · Cited by 70
Clark, S. D., & Abi‐Dargham, A. (2019) · Biological Psychiatry · doi:10.1016/j.biopsych.2019.05.012 · Cited by 68
Stimulated Lymphocytes in Schizophrenia
Hirata-Hibi, M. (1982) · Archives of General Psychiatry · doi:10.1001/archpsyc.1982.04290010058011 · Cited by 68
Schizophrenic psychology, associative learning and the role of forebrain dopamine
Miller, R. (1976) · Medical Hypotheses · doi:10.1016/0306-9877(76)90040-2 · Cited by 67
D2 receptor regulation of synaptic burst firing in prefrontal cortical pyramidal neurons
Wang, Y., & Goldman‐Rakic, P. S. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0400954101 · Cited by 67
Emerging drugs for schizophrenia
Agid, O., Kapur, S., & Remington, G. J. (2008) · Expert Opinion on Emerging Drugs · doi:10.1517/14728214.13.3.479 · Cited by 68
“The finding of CPZ’s antipsychotic activity was serendipitous, and over the next decade it was established that it was very likely the blockade of dopamine (DA), in particular the D 2 receptors, that accounted for this effect [5,6] .”
BackgroundDopamine Receptors and Average Clinical Doses
Meltzer, H. Y. (1976) · Science · doi:10.1126/science.9693 · Cited by 67
A human D1 dopamine receptor gene is located on chromosome 5 at q35.1 and identifies an EcoRI RFLP.
Grandy, D. K., Zhou, Q., Allen, L., Litt, R., Magenis, R. E., Civelli, O., & Litt, M. (1990) · PubMed · Cited by 67
Analysis of the D4 Dopamine Receptor Gene Variant in an Italian Schizophrenia Kindred
Macciardi, F. M. (1994) · Archives of General Psychiatry · doi:10.1001/archpsyc.1994.03950040032004 · Cited by 67
Acute effects of neuroleptics on brain self-stimulation thresholds in rats
Schaefer, G. J., & Michael, R. P. (1980) · Psychopharmacology · doi:10.1007/bf00427589 · Cited by 67
Presynaptic Regulation of Dopamine Transmission in Schizophrenia
Lyon, G. J., Abi‐Dargham, A., Moore, H. M., Lieberman, J. A., Javitch, J. A., & Sulzer, D. (2009) · Schizophrenia Bulletin · doi:10.1093/schbul/sbp010 · Cited by 71
Blockade of [11C](+)-PHNO binding in human subjects by the dopamine D3 receptor antagonist ABT-925
Graff‐Guerrero, A., Redden, L., Abi‐Saab, W., Katz, D. A., Houle, S., Barsoum, P., Bhathena, A., Palaparthy, R., Saltarelli, M. D., & Kapur, S. (2009) · The International Journal of Neuropsychopharmacology · doi:10.1017/s1461145709990642 · Cited by 66
“Dysregulation of the dopaminergic system is implicated in several pathological conditions, including schizophrenia (Seeman & Lee, 1975), Parkinson’s disease (Cotzias, 1968), depression (Bunney et al. 1971) and drug addiction (Di Chiara & Imperato, 1988).”
BackgroundReimann, W., Zumstein, A., Jackisch, R., Starke, K., & Hertting, G. (1979) · Naunyn-Schmiedeberg s Archives of Pharmacology · doi:10.1007/bf00515593 · Cited by 66
Targeting Serotonin 5-HT2A Receptors to Better Treat Schizophrenia: Rationale and Current Approaches
Kantrowitz, J. T. (2020) · CNS Drugs · doi:10.1007/s40263-020-00752-2 · Cited by 68
Dysfunctional Striatal Systems in Treatment-Resistant Schizophrenia
White, T. P., Wigton, R. L., Joyce, D. W., Collier, T., Fornito, A., & Shergill, S. S. (2015) · Neuropsychopharmacology · doi:10.1038/npp.2015.277 · Cited by 64
“Current medication for schizophrenia principally targets the striatum (Seeman and Lee, 1975); and clinical potency is predicted by its binding to and blockade of the dopamine D2 receptor (Creese et al, 1976).”
BackgroundAntipsychotics Activate mTORC1-Dependent Translation to Enhance Neuronal Morphological Complexity
Bowling, H. L., Zhang, G., Bhattacharya, A., Pérez-Cuesta, L. M., Deinhardt, K., Hoeffer, C. A., Neubert, T. A., Gan, W., Klann, E., & Chao, M. V. (2014) · Science Signaling · doi:10.1126/scisignal.2004331 · Cited by 64
“We chose a concentration of 20 nM on the basis of its binding affinity and clinical potency profile in human patients (20), and confirmed that this concentration was effective at stimulating phosphorylation of Akt in mouse primary striatal neurons (fig.”
BackgroundChun, S., Du, F., Westmoreland, J. J., Han, S. B., Wang, Y., Eddins, D. M., Bayazitov, I. T., Devaraju, P., Yu, J., Lagarde, M. M. M., et al. (2016) · Nature Medicine · doi:10.1038/nm.4240 · Cited by 65
Neurochemistry and Child Psychiatry
Cohen, D. J., & Young, J. G. (1977) · Journal of the American Academy of Child Psychiatry · doi:10.1016/s0002-7138(09)61596-x · Cited by 63
Tarumi, R., Tsugawa, S., Noda, Y., Plitman, E., Honda, S., Matsushita, K., Chavez, S., Sawada, K., Wada, M., Matsui, M., et al. (2019) · Neuropsychopharmacology · doi:10.1038/s41386-019-0589-z · Cited by 56
“The clinical effects of these drugs have provided the basis for the dopamine hypothesis of schizophrenia [4], which posits that aberrant dopaminergic function is implicated in the pathophysiology of schizophrenia [5].”
BackgroundMcOmish, C. E., Burrows, E. L., Howard, M. L., & Hannan, A. J. (2008) · Hippocampus · doi:10.1002/hipo.20443 · Cited by 60
“…physiological basis is highlighted by the multitude of pathways that have been implicated in pathogenesis including those involving dopaminergic (Seeman and Lee, 1975; Creese et al., 1976), serotonergic (Scarr et al., 2001; Lopez-Figueroa et al., 2004), muscarinic (Bennett et al., 1979;…”
Another view of the history of antipsychotic drug discovery and development
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Subcortical Dopamine and Cognition in Schizophrenia: Looking Beyond Psychosis in Preclinical Models
Conn, K., Burne, T. H. J., & Kesby, J. P. (2020) · Frontiers in Neuroscience · doi:10.3389/fnins.2020.00542 · Cited by 66
Imaging extrastriatal dopamine D(2) receptor occupancy by endogenous dopamine in healthy humans.
Fujita, M., Verhoeff, N., Varrone, A., Zoghbi, S., Baldwin, R., Jatlow, P., Anderson, G. M., Seibyl, J., & Innis, R. B. (2000) · European Journal of Pharmacology · doi:10.1016/s0014-2999(99)00817-1 · Cited by 68
Shi, S., Leites, C., He, D., Schwartz, D., Moy, W., Shi, J., & Duan, J. (2014) · Journal of Biological Chemistry · doi:10.1074/jbc.m113.535203 · Cited by 61
History of the dopamine hypothesis of antipsychotic action
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Abboud, R., Noronha, C., & Diwadkar, V. A. (2017) · European Psychiatry · doi:10.1016/j.eurpsy.2017.04.004 · Cited by 65
Bertolino, A., & Blasi, G. (2009) · Neuroscience · doi:10.1016/j.neuroscience.2009.04.038 · Cited by 63
Glutamatergic antipsychotic drugs: a new dawn in the treatment of schizophrenia?
Stone, J. M. (2011) · Therapeutic Advances in Psychopharmacology · doi:10.1177/2045125311400779 · Cited by 60
“For more than 50 years, the only effective antipsychotic drugs available have been dopamine D2 receptor antagonists [Kapur and Mamo, 2003], with their clinical potency directly corresponding to their affinity at D2 receptors [Seeman and Lee, 1975].”
BackgroundAntipsychotic drug treatment alters expression of mRNAs encoding lipid metabolism-related proteins
Thomas, E. A., George, R. C., Danielson, P. E., Nelson, P. A., Warren, A. J., Lo, D. D., & Sutcliffe, J. G. (2003) · Molecular Psychiatry · doi:10.1038/sj.mp.4001425 · Cited by 60
Brain insulin action in schizophrenia: Something borrowed and something new
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Central nervous system effects of haloperidol on THC in healthy male volunteers
Liem-Moolenaar, M., Beek, E. T. T., de Kam, M. L., Franson, K. L., Kahn, R. S., Hijman, R., Touw, D. J., & van Gerven, J. (2010) · Journal of Psychopharmacology · doi:10.1177/0269881109358200 · Cited by 59
“Since psychotic symptoms have consistently been related to increased dopamine function in the striatum (Angrist and Van Kammen, 1984; Seeman and Lee, 1975), elevated striatal dopamine release after 9-tetrahydrocannabinol (THC) use may explain how cannabis contributes to the development and pathophysiology of schizophr…”
BackgroundBossong, M. G., Jansma, J. M., Bhattacharyya, S., & Ramsey, N. F. (2014) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2013.11.017 · Cited by 62
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Correlation between antiavoidance activities of antipsychotic drugs in rats and daily clinical doses
Kuribara, H., & Tadokoro, S. (1981) · Pharmacology Biochemistry and Behavior · doi:10.1016/0091-3057(81)90241-0 · Cited by 59
Brain mitochondrial nitric oxide synthase: in vitro and in vivo inhibition by chlorpromazine
Lores‐Arnaiz, S., D’Amico, G., Czerniczyniec, A., Bustamante, J., & Boveris, A. (2004) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2004.07.012 · Cited by 58
Relation of Plasma Prolactin to Clinical Response in Schizophrenic Patients
GRUEN, P. H. (1978) · Archives of General Psychiatry · doi:10.1001/archpsyc.1978.01770340072008 · Cited by 58
Cocaine cue-induced dopamine release in the human prefrontal cortex
Milella, M. S., Fotros, A., Gravel, P., Casey, K. F., Larcher, K., Verhaeghe, J. A. J., Cox, S. M. L., Reader, A. J., Dagher, A., Benkelfat, C., et al. (2016) · Journal of Psychiatry and Neuroscience · doi:10.1503/jpn.150207 · Cited by 56
Striosomes control dopamine via dual pathways paralleling canonical basal ganglia circuits
Lazaridis, I., Crittenden, J. R., Ahn, G., Hirokane, K., Wickersham, I. R., Yoshida, T., Mahar, A., Skara, V., Loftus, J., Parvataneni, K., et al. (2024) · Current Biology · doi:10.1016/j.cub.2024.09.070 · Cited by 58
Cho, H. P., García-Barrantes, P. M., Brogan, J. T., Hopkins, C. R., Niswender, C. M., Rodriguez, A. L., Venable, D. F., Morrison, R. D., Bubser, M., Daniels, J. S., et al. (2014) · ACS Chemical Biology · doi:10.1021/cb500560h · Cited by 58
Narayan, S., Kass, K. E., & Thomas, E. A. (2006) · Journal of Neuroscience Research · doi:10.1002/jnr.21161 · Cited by 56
“The typical antipsychotics, including haloperidol, chlorpromazine, and fluphenazine, are primarily dopamine D2 receptor antagonists (Seeman and Lee, 1975; Creese et al., 1976), whereas the \atypical" antipsychotics, such as clozapine, risperidone, quetiapine, and olanzapine, are antagonists at…”
BackgroundCitrome, L., Stensbøl, T. B., & Maeda, K. (2015) · Expert Review of Neurotherapeutics · doi:10.1586/14737175.2015.1086269 · Cited by 63
“Postsynaptic dopamine (D2) receptor antagonism has been shown to be responsible for the antipsychotic effect of most antipsychotics [4]; however, full D2 blockade is often accompanied by hyperprolactinemia and motor side effects leading to EPS [5,6].”
BackgroundDopamine receptor antagonist thioridazine inhibits tumor growth in a murine breast cancer model
Yin, T., He, S., Shen, G., Ye, T., Guo, F., & Wang, Y. (2015) · Molecular Medicine Reports · doi:10.3892/mmr.2015.3967 · Cited by 55
“Thioridazine is a well established anti‑psychotic and ‑anxiety agent which acts through DR1‑5 (15).”
BackgroundParada, M. A., Hernandez, L., de Parada, M. P., Rada, P. V., & Murzi, E. (1997) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1016/s0022-3565(24)36626-1 · Cited by 55
“…of the relative impact of neuroleptics on cholinergic systems is important because these drugs are dopamine receptor blockers (Creese et al., 1976; Seeman and Lee, 1975; Snyder et al., 1975), some postsynaptic DA receptors are located on cholinergic neurons (Dawson et al., 1988; Le Moine et al.,…”
BackgroundPoulos, C. X., & Hinson, R. E. (1982) · Science · doi:10.1126/science.6889765 · Cited by 55
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Olsen, R. W., LAMAR, E. E., & BAYLESS, J. D. (1977) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.1977.tb07748.x · Cited by 55
Monoamines and Aversively Motivated Behaviors
Peters, D. A., Anisman, H., & Pappas, B. A. (1978) · Springer eBooks · doi:10.1007/978-1-4684-2394-5_5 · Cited by 55
Developmental vitamin D deficiency alters MK-801-induced behaviours in adult offspring
Kesby, J. P., O’Loan, J., Alexander, S., Deng, C., Huang, X., McGrath, J. J., Eyles, D. W., & Burne, T. H. J. (2011) · Psychopharmacology · doi:10.1007/s00213-011-2492-0 · Cited by 54
“This understanding is based on the correlation between clinical doses of antipsychotic drugs and their potency to block dopamine 2 receptors and ameliorate symptoms (Seeman and Lee 1975).”
de Bartolomeis, A., Manchia, M., Marmo, F., Vellucci, L., Iasevoli, F., & Barone, A. (2020) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2020.00369 · Cited by 54
“This hypothesis holds that hyperactivity of dopamine transmission is responsible for positive symptoms (1) and it was formulated in the 1960s, after the discovery of antipsychotic action of chlorpromazine (33), and further endorsed by the correlation between clinical response to antipsychotic drugs and their potency t…”
BackgroundGarcı́a, C., Oyola, R., Piñero, L. E., Arce, R., Silva, J., & Sánchez, V. (2005) · The Journal of Physical Chemistry A · doi:10.1021/jp044530j · Cited by 54
Laruelle, M. A., Jaskiw, G. E., Lipska, B. K., Kolachana, B. S., Casanova, M. F., Kleinman, J. E., & Weinberger, D. R. (1992) · Brain Research · doi:10.1016/0006-8993(92)90421-5 · Cited by 54
Approaches to Brain Amines in Psychiatric Patients: A Reevaluation of Cerebrospinal Fluid Studies
Post, R. M., & Goodwin, F. K. (1978) · Springer eBooks · doi:10.1007/978-1-4684-3189-6_3 · Cited by 54
Uehara, T., Sumiyoshi, T., Seo, T., Matsuoka, T., Itoh, H., Suzuki, M., & Kurachi, M. (2010) · Brain Research · doi:10.1016/j.brainres.2010.07.013 · Cited by 53
Dopamine Transmission in the Schizophrenic Brain
Laruelle, M. A. (2003) · Wiley eBooks · doi:10.1002/9780470987353.ch20 · Cited by 53
Neuropathological changes in the substantia nigra in schizophrenia but not depression
Williams, M. R., Galvin, K., OSullivan, B., Macdonald, C., Ching, E. W.-K., Turkheimer, F., Howes, O. D., Pearce, R. K. B., Hirsch, S. R., & Maier, M. (2013) · European Archives of Psychiatry and Clinical Neuroscience · doi:10.1007/s00406-013-0479-z · Cited by 52
“The clinical effectiveness of antipsychotic dopamine receptor affinity correlates with clinical effectiveness [60], and antipsychotic treatment in SZ cases gave expected binding in D2-rich regions such as the caudate and putamen, and D3 receptor occupancy was higher in the globus”
BackgroundPalmer, A. A., Brown, A. S., Keegan, D. A., Siska, L. D., Susser, E., Rotrosen, J., & Butler, P. D. (2008) · Brain Research · doi:10.1016/j.brainres.2008.07.089 · Cited by 51
Simpson, E. H., Winiger, V., Biezonski, D. K., Haq, I., Kandel, E. R., & Kellendonk, C. (2013) · Biological Psychiatry · doi:10.1016/j.biopsych.2013.11.023 · Cited by 51
“Schwartz JC, Diaz J, Pilon C, Sokoloff P (2000): Possible implications of the dopamine D(3) receptor in schizophrenia and in antipsychotic drug actions.”
Neurosurgery for schizophrenia: an update on pathophysiology and a novel therapeutic target
Mikell, C. B., Sinha, S. R., & Sheth, S. A. (2015) · Journal of neurosurgery · doi:10.3171/2015.4.jns15120 · Cited by 53
Ranganath, A., & Jacob, S. N. (2015) · The Neuroscientist · doi:10.1177/1073858415602850 · Cited by 52
“The strongest evidence for the involvement of dopamine in schizophrenia comes from early studies that identified D2Rs as the main target of antipsychotic drugs used to treat positive symptoms (Seeman and Lee 1975).”
BackgroundBobo, W. V., & Shelton, R. C. (2010) · Expert Review of Neurotherapeutics · doi:10.1586/ern.10.143 · Cited by 50
Probing cortical dopamine function in schizophrenia: what can D1 receptors tell us?
Abi‐Dargham, A. (2003) · Europe PMC (PubMed Central) · Cited by 52
Miller, R. J. (1987) · Psychopharmacology · doi:10.1007/bf00176470 · Cited by 50
“Therapeutic potency ( Seeman and Lee 1975; Wyatt 1976; Seeman 1977; Rotrosen et al. 1978; Stanley et al. 1980; Martindale 1982) is expressed as gmole/day.”
BackgroundBlockade of morphine-withdrawal body shakes by haloperidol
Lal, H., & Numan, R. (1976) · Life Sciences · doi:10.1016/0024-3205(76)90020-5 · Cited by 50
Ether-a-go-go Related Gene Potassium Channels: What's All the Buzz About?
Shepard, D. S., Canavier, C. C., & Levitan, E. S. (2006) · Schizophrenia Bulletin · doi:10.1093/schbul/sbm106 · Cited by 49
Schizophrenia: Dopamine β-Hydroxylase Activity and Treatment Response
Sternberg, D. E., VanKammen, D. P., Lerner, P., & Bunney, W. E. (1982) · Science · doi:10.1126/science.6124036 · Cited by 49
Varty, G. B., Hodgson, R. A., Pond, A. J., Grzelak, M. E., Parker, E. M., & Hunter, J. C. (2008) · Psychopharmacology · doi:10.1007/s00213-008-1214-8 · Cited by 48
“Pharmacological blockade of DA D2 receptors produces therapeutic effects in schizophrenic patients and is a central mechanism underlying the beneficial effects of established antipsychotic drugs ( Seeman and Lee 1975 ).”
BackgroundEffects of neuroleptics on release of 3H-dopamine from slices of rat corpus striatum
Dismukes, K., & Mulder, A. H. (1977) · Naunyn-Schmiedeberg s Archives of Pharmacology · doi:10.1007/bf00508806 · Cited by 48
Gene-sex interactions in schizophrenia: focus on dopamine neurotransmission
Godar, S. C., & Bortolato, M. (2014) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2014.00071 · Cited by 46
“…was originally postulated following the discovery that D2 dopamine receptor antagonism was a fundamental pharmacological requisite of antipsychotic drugs, and that the therapeutic efficacy of these agents was correlated with their inhibitory potency (Seeman and Lee, 1975; Creese et al., 1976).”
BackgroundPletscher, A. (1977) · British Journal of Pharmacology · doi:10.1111/j.1476-5381.1977.tb08395.x · Cited by 47
In Vivo Binding of Antipsychotics to D3 and D2 Receptors: A PET Study in Baboons with [11C]-(+)-PHNO
Girgis, R. R., Miyake, N., Xu, X., Easwaramoorthy, B., Castrillon, J., Gunn, R. N., Rabiner, E. A., Abi‐Dargham, A., & Slifstein, M. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2010.04.079 · Cited by 46
Jäger, M., Schmauß, M., Laux, G., Pfeiffer, H., Naber, D., Schmidt, L., Gäebel, W., Klosterkötter, J., Heuser, I., Maier, W., et al. (2009) · European Psychiatry · doi:10.1016/j.eurpsy.2009.02.005 · Cited by 46
Goyette, M.-A., Cusseddu, R., Elkholi, I. E., Abu-Thuraia, A., El-Hachem, N., Haibe‐Kains, B., Gratton, J., & Côté, J. (2019) · Oncotarget · doi:10.18632/oncotarget.26725 · Cited by 47
Gianutsos, G., & Lal, H. (1976) · Life Sciences · doi:10.1016/0024-3205(76)90329-5 · Cited by 46
Do presynaptic auto-receptors control dopamine release?
Raiteri, M., Cervoni, A. M., CARMINE, R. D., & LEVI, G. (1978) · Nature · doi:10.1038/274706a0 · Cited by 46
Ishiwari, K., Betz, A. J., Weber, S. M., Felsted, J., & Salamone, J. D. (2005) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2004.12.006 · Cited by 45
“The therapeutic potencies of antipsychotic drugs directly correlate with their affinities for the D2 receptor (Creese et al., 1976; Seeman and Lee, 1975; Seeman et al., 1976).”
BackgroundOosterhof, C. A., Mansari, M. E., & Blier, P. (2014) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.114.218578 · Cited by 45
“Indeed, D2 receptor antagonism is an effective strategy for treatment of positive symptoms in schizophrenia (Seeman and Lee, 1975; Rao and Remington, 2013).”
BackgroundPsychosis breakthrough on antipsychotic maintenance: results from a nationwide study
Rubio, J. M., Taipale, H., Correll, C. U., Tanskanen, A., Kane, J. M., & Tiihonen, J. (2020) · Psychological Medicine · doi:10.1017/s0033291719001296 · Cited by 45
“This theory assumes that the cumulative exposure to antipsychotics, all of which block the dopamine D2 receptor (Seeman and Lee, 1975), would result in a compensatory upregulation of the D2 receptor (Seeman et al.”
BackgroundKesby, J. P., Cui, X., Burne, T. H. J., & Eyles, D. W. (2013) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2013.00111 · Cited by 45
“Haloperidol is a typical antipsychotic used to treat the positive symptoms of schizophrenia and its antipsychotic potency is directly related to the blockade of DA 2 receptors (Seeman and Lee, 1975; Creese et al., 1976).”
BackgroundInfluentialAliphatic propargylamines: New antiapoptotic drugs
Boulton, A. A., Davis, B. A., Durden, D. A., Dyck, L. E., Juorio, A. V., Li, X., Paterson, I. A., & Yu, P. H. (1997) · Drug Development Research · doi:10.1002/(sici)1098-2299(199711/12)42:3/4 · Cited by 103
Lindsley, C. W., Zhao, Z., Leister, W., O'Brien, J. L., Lemaire, W., Williams, D. L., Chen, T., Chang, R. S. L., Burno, M., Jacobson, M. A., et al. (2006) · ChemMedChem · doi:10.1002/cmdc.200600097 · Cited by 44
Can the supersensitivity of rodents to dopamine be regarded as a model of tardive dyskinesia?
Wolfarth, S., & Ossowska, K. (1989) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/0278-5846(89)90036-5 · Cited by 44
Interaction of chlorpromazine with biological membranes. A photochemical study using spin labels
Leterrier, F., Mendyk, A., & Viret, J. (1976) · Biochemical Pharmacology · doi:10.1016/0006-2952(76)90450-0 · Cited by 44
Biomarkers for Psychiatric Disorders
Turck, C. W. (2009) · Springer eBooks · doi:10.1007/978-0-387-79251-4 · Cited by 42
Managing Negative Symptoms of Schizophrenia: How Far Have We Come?
Kantrowitz, J. T. (2017) · CNS Drugs · doi:10.1007/s40263-017-0428-x · Cited by 46
Lyles-Eggleston, M., Altundaş, R., Xia, J., Sikazwe, D., Fan, P., Yang, Q., Li', S., Zhang, W., Zhu, X., Schmidt, A. W., et al. (2003) · Journal of Medicinal Chemistry · doi:10.1021/jm0301033 · Cited by 43
Schlyer, D. J., Volkow, N. D., Fowler, J. S., Wolf, A. P., Shiue, C., Dewey, S. L., Bendriem, B., Logan, J., Raulli, R. E., HITZEMANN, R. J., et al. (1992) · Synapse · doi:10.1002/syn.890110103 · Cited by 43
Baldessarini, R. J. (1975) · Springer eBooks · doi:10.1007/978-1-4684-3171-1_2 · Cited by 43
Antipsychotic Effects of Pimozide in Schizophrenia
van Kammen, D. P. (1982) · Archives of General Psychiatry · doi:10.1001/archpsyc.1982.04290030011002 · Cited by 43
Banks, P. J., Burroughs, A. C., Barker, G. R. I., Brown, J. T., Warburton, E. C., & Bashir, Z. I. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1512064112 · Cited by 42
Aslostovar, L., Boyd, A. L., Almakadi, M., Collins, T. J., Leong, D. P., Tirona, R. G., Kim, R. B., Julian, J. A., Xenocostas, A., Leber, B. F., et al. (2018) · Blood Advances · doi:10.1182/bloodadvances.2018015677 · Cited by 42
“TDZ has been historically administered as an antipsychotic drug whose properties are mediated through DRD2 antagonism.(37) Previous in vitro assays using patient AML cells suggested that DRDs also mediate TDZ’s selective suppression of human AML, due to a preferential expression pattern in leukemic vs healthy hematopo…”
BackgroundSchizophrenia Exhibits Bi-directional Brain-Wide Alterations in Cortico-Striato-Cerebellar Circuits
Ji, J. L., Diehl, C., Schleifer, C. H., Tamminga, C. A., Keshavan, M. S., Sweeney, J. A., Clementz, B. A., Hill, S. K., Pearlson, G. D., Yang, G., et al. (2018) · Cerebral Cortex · doi:10.1093/cercor/bhy306 · Cited by 44
de Bartolomeis, A., Vellucci, L., Austin, M. C., Simone, G. D., & Barone, A. (2022) · Biomolecules · doi:10.3390/biom12070909 · Cited by 43
“The dopamine hypothesis of schizophrenia has been one of the most enduring assumptions on the origin of the disease, based on the evidence of antipsychotics acting as D2R blockers, and considering the striatal dopamine hyperactivity as responsible for the occurrence of positive symptoms [35,67,68].”
BackgroundPartial agonism and schizophrenia
Bolonna, A., & Kerwin, R. (2005) · British Journal of Psychiatry · doi:10.1192/bjp.186.1.7 · Cited by 46
“The original dopamine hypothesis for schizophrenia was based on the belief that dopamine only innervated subcortical regions, and that these regions were overstimulated by excessive dopamine transmission (Seeman & Lee, 1975; Creese et al, 1976).”
Background
Metadata
- Authors
- Seeman, P., & Lee, T.
- Affiliations
- University of Toronto (CA)
- ORCID
- Venue
- Science
- Published
- 1975-06-20
- Volume
- 188
- Issue
- 4194
- Pages
- 1217-1219
- ISSN
- 0036-8075 (ISSN-L)
- 1095-9203
- OpenAlex
- W2006122360
- Cited by
- 869
- References
- 35
- Citations by year
- 2026: 5 · 2025: 8 · 2024: 13 · 2023: 16 · 2022: 22 · 2021: 13 · 2020: 18 · 2019: 36 · 2018: 21 · 2017: 30 · 2016: 26 · 2015: 28 · 2014: 37 · 2013: 23 · 2012: 32
- FWCI
- 62.55
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Science (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Psychiatry and Mental health › Schizophrenia research and treatment
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Keywords
- antipsychotic drugs, presynaptic dopamine release, striatum, spiperone, thioridazine, butyrophenones, phenothiazines, reserpine, pimozide, clozapine, butaclamol, stereoisomers, acetylcholine release, GABA release, schizophrenia
- MeSH terms
- Acetylcholine, Animals, Corpus Striatum, Dopamine, Dose-Response Relationship, Drug, Electric Stimulation, gamma-Aminobutyric Acid, Haloperidol, Humans, Male, Neurons, Neurosecretion, Schizophrenia, Tranquilizing Agents, Tritium, Rats
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