PET Measures of Amphetamine-Induced Dopamine Release in Ventral versus Dorsal Striatum

Drevets, W

doi:10.1016/s0893-133x(99)00079-2

Cited by 123Neurotransmitter Receptor Influence on BehaviorSchizophrenia research and treatmentParkinson's Disease Mechanisms and Treatments

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PET Measures of Amphetamine-Induced Dopamine Release in Ventral versus Dorsal Striatum

Drevets, W·1999·Neuropsychopharmacology

DOI 10.1016/s0893-133x(99)00079-2

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Abstract

Regional differences in dextroamphetamine (AMPH)-induced dopamine (DA) release in the baboon striatum were assessed using positron emission tomographic (PET) measures of [11C]raclopride specific binding to DA D2/D3 receptors acquired before and after AMPH administration. The magnitude of the reduction in [11C]raclopride binding, following AMPH administration, was two-fold greater in the anteroventral striatum (comprised of ventral caudate, anteroventral putamen, and nucleus accumbens) than the dorsal striatum (dorsal caudate). A simulation study demonstrated that any potential biases due to resolution (partial volume) and alignment effects were significantly smaller than the magnitude of the observed results. These regional differences in the sensitivity of AMPH are compatible with microdialysis evidence in rats indicating that the magnitude of DA release in response to AMPH concentrations in the range tested is greater in ventral than dorsal striatal regions. Post hoc tests involving measures in other striatal regions showed that the baseline DA D2/D3 binding was highest and the correlation between AMPH dose and change in [11C]raclopride binding most significant in the putamen.

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Ventral Striatal Dopamine Release in Response to Smoking a Regular vs a Denicotinized Cigarette
Brody, A. L., Mandelkern, M. A., Olmstead, R. E., Allen-Martinez, Z., Scheibal, D., Abrams, A. L., Costello, M. R., Farahi, J., Saxena, S., Monterosso, J., et al. (2009) · Neuropsychopharmacology · doi:10.1038/npp.2008.87 · Cited by 183
Dopamine transport function is elevated in cocaine users
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Dopamine D2 receptor availability is linked to hippocampal–caudate functional connectivity and episodic memory
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In vivo vulnerability to competition by endogenous dopamine: Comparison of the D2 receptor agonist radiotracer (–)‐N‐[11C]propyl‐norapomorphine ([11C]NPA) with the D2 receptor antagonist radiotracer [11C]‐raclopride
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Within-Subject Comparison of [ 11 C]-( + )-PHNO and [ 11 C]raclopride Sensitivity to Acute Amphetamine Challenge in Healthy Humans
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Therapeutic doses of amphetamine or methylphenidate differentially increase synaptic and extracellular dopamine
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Anticonvulsants for cocaine dependence
Minozzi, S., Cinquini, M., Amato, L., Davoli, M., Farrell, M., Pani, P. P., & Vecchi, S. (2015) · Cochrane Database of Systematic Reviews · doi:10.1002/14651858.cd006754.pub4 · Cited by 131
Long-Term Test–Retest Reliability of Striatal and Extrastriatal Dopamine D 2/3 Receptor Binding: Study with [ 11 C]Raclopride and High-Resolution PET
Alakurtti, K., Johansson, J. J., Joutsa, J., Laine, M., Bäckman, L., Nyberg, L. H., & Rinne, J. O. (2015) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.2015.53 · Cited by 125
Antipsychotic medications for cocaine dependence
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A Review of Neurotransmitters Sensing Methods for Neuro-Engineering Research
Niyonambaza, S. D., Kumar, P., Xing, P., Mathault, J., Koninck, P. D., Boisselier, É., Boukadoum, M., & Miled, A. (2019) · Applied Sciences · doi:10.3390/app9214719 · Cited by 121
Dopamine Type-1 Receptor Binding in Major Depressive Disorder Assessed Using Positron Emission Tomography and [11C]NNC-112
Cannon, D. M., Klaver, J. M., Peck, S. A., Rallis, D., Erickson, K., & Drevets, W. C. (2008) · Neuropsychopharmacology · doi:10.1038/npp.2008.194 · Cited by 119
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A positron emission tomography study of nigro-striatal dopaminergic mechanisms underlying attention: implications for ADHD and its treatment
del Campo, N., Fryer, T. D., Hong, Y. T., Smith, R., Brichard, L., Acosta-Cabronero, J., Chamberlain, S. R., Tait, R., Izquierdo, D., Regenthal, R., et al. (2013) · Brain · doi:10.1093/brain/awt263 · Cited by 113
Brain region binding of the D2/3 agonist [11C]‐(+)‐PHNO and the D2/3 antagonist [11C]raclopride in healthy humans
Graff‐Guerrero, A., Willeit, M., Ginovart, N., Mamo, D. C., Mizrahi, R., Rusjan, P., Vitcu, I., Seeman, P. M., Wilson, A. A., & Kapur, S. (2007) · Human Brain Mapping · doi:10.1002/hbm.20392 · Cited by 107
Dopamine agonists for the treatment of cocaine dependence
Minozzi, S., Amato, L., Pani, P. P., Solimini, R., Vecchi, S., Crescenzo, F. D., Zuccaro, P., & Davoli, M. (2015) · Cochrane Database of Systematic Reviews · doi:10.1002/14651858.cd003352.pub4 · Cited by 108
Are there volumetric brain differences associated with the use of cocaine and amphetamine-type stimulants?
Mackey, S., & Paulus, M. P. (2012) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2012.12.003 · Cited by 106
Central Nervous System Monoamine Correlates of Social Dominance in Cynomolgus Monkeys (Macaca fascicularis)
Kaplan, J. (2002) · Neuropsychopharmacology · doi:10.1016/s0893-133x(01)00344-x · Cited by 106
L-Dopa Modulates Functional Connectivity in Striatal Cognitive and Motor Networks: A Double-Blind Placebo-Controlled Study
Kelly, A., de Zubicaray, G. I., Martino, A. D., Copland, D. A., Reiss, P., Klein, D., Castellanos, F. X., Milham, M., & McMahon, K. (2009) · NeuroImage · doi:10.1016/s1053-8119(09)70601-9 · Cited by 100
Antidepressants for cocaine dependence and problematic cocaine use
Pani, P. P., Trogu, E., Vecchi, S., & Amato, L. (2011) · Cochrane Database of Systematic Reviews · doi:10.1002/14651858.cd002950.pub3 · Cited by 105
The effect of nicotine on striatal dopamine release in man: A [11C]raclopride PET study
Montgomery, A. J., Lingford-Hughes, A. R., Egerton, A., Nutt, D., & Grasby, P. M. (2007) · Synapse · doi:10.1002/syn.20419 · Cited by 93
NMDA antagonist effects on striatal dopamine release: Positron emission tomography studies in humans
Kegeles, L., Martinez, D., Kochan, L., Hwang, D., Huang, Y., Mawlawi, O., Suckow, R., Heertum, R. V. V., & Laruelle, M. (2002) · Synapse · doi:10.1002/syn.10010 · Cited by 106
Lateralization and Gender Differences in the Dopaminergic Response to Unpredictable Reward in the Human Ventral Striatum
Martin-Soelch, C., Szczepanik, J., Nugent, A., Barhaghi, K., Rallis, D., Herscovitch, P., Carson, R. E., & Drevets, W. C. (2011) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2011.07642.x · Cited by 92
Self-citation
Heterogeneity in Dopamine Neuron Synaptic Actions Across the Striatum and Its Relevance for Schizophrenia
Chuhma, N., Mingote, S., Kalmbach, A., Yetnikoff, L., & Rayport, S. (2016) · Biological Psychiatry · doi:10.1016/j.biopsych.2016.07.002 · Cited by 93
D-Amphetamine Boosts Language Learning Independent of its Cardiovascular and Motor Arousing Effects
Breitenstein, C., Wailke, S., Bushuven, S., Kamping, S., Zwitserlood, P., Ringelstein, E. B., & Knecht, S. (2004) · Neuropsychopharmacology · doi:10.1038/sj.npp.1300464 · Cited by 80
Antidepressants for cocaine dependence
de Lima, M. S., Farrell, M., Reisser, A. A. L., & Soares, B. G. (2003) · Cochrane Database of Systematic Reviews · doi:10.1002/14651858.cd002950 · Cited by 80
Retracted
Dopamine antagonist modulation of amphetamine response as detected using pharmacological MRI
Dixon, A. L., Prior, M. J. W., Morris, P. M., Shah, Y. B., Joseph, M. H., & Young, A. M. J. (2004) · Neuropharmacology · doi:10.1016/j.neuropharm.2004.10.006 · Cited by 77
Dopamine mediation of positive reinforcing effects of amphetamine in stimulant naı̈ve healthy volunteers: results from a large cohort
Abi‐Dargham, A., Kegeles, L. S., Martínez, D., Innis, R. B., & Laruelle, M. A. (2003) · European Neuropsychopharmacology · doi:10.1016/j.euroneuro.2003.08.007 · Cited by 72
Effects of acute nicotine on hemodynamics and binding of [11C]raclopride to dopamine D2,3 receptors in pig brain
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Effect of amphetamine on [18F]fallypride in vivo binding to D2 receptors in striatal and extrastriatal regions of the primate brain: Single bolus and bolus plus constant infusion studies
Slifstein, M., Narendran, R., Hwang, D., Sudo, Y., Talbot, P., Huang, Y., & Laruelle, M. (2004) · Synapse · doi:10.1002/syn.20062 · Cited by 73
Effect of Simple Motor Performance on Regional Dopamine Release in the Striatum in Parkinson Disease Patients and Healthy Subjects: A Positron Emission Tomography Study
Ouchi, Y., Yoshikawa, E., Futatsubashi, M., Okada, H., Torizuka, T., & Sakamoto, M. (2002) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1097/00004647-200206000-00013 · Cited by 65
Nicotine-Induced Dopamine Release in Primates Measured with [11C]Raclopride PET
Marenco, S., Carson, R. E., Berman, K. F., Herscovitch, P., & Weinberger, D. R. (2003) · Neuropsychopharmacology · doi:10.1038/sj.npp.1300287 · Cited by 62
Multiplexed Monitoring of Neurochemicals via Electrografting-Enabled Site-Selective Functionalization of Aptamers on Field-Effect Transistors
Gao, Z. J., Wu, G., Song, Y., Li, H., Zhang, Y., Schneider, M. J., Qiang, Y., Kaszas, J., Weng, Z., Sun, H., et al. (2022) · Analytical Chemistry · doi:10.1021/acs.analchem.1c05531 · Cited by 60
What Is the Functional Significance of Hippocampal Pathology in Schizophrenia?
Goldman, M. B., & Mitchell, C. P. (2004) · Schizophrenia Bulletin · doi:10.1093/oxfordjournals.schbul.a007086 · Cited by 60
Rising taurine and ethanol concentrations in nucleus accumbens interact to produce dopamine release after ethanol administration
Ericson, M., Chau, P., Clarke, R. B. C., Adermark, L., & Söderpalm, B. (2010) · Addiction Biology · doi:10.1111/j.1369-1600.2010.00245.x · Cited by 59
Analyses of [18F]altanserin bolus injection PET data. II: Consideration of radiolabeled metabolites in humans
Price, J. C., Lopresti, B. J., MELTZER, C. C., Smith, G. S., Mason, N. S., Huang, Y. H., Holt, D. P., Gunn, R. N., & Mathis, C. A. (2001) · Synapse · doi:10.1002/syn.1055 · Cited by 59
Effect of endogenous dopamine on extrastriatal [11C]FLB 457 binding measured by PET
Okauchi, T., Suhara, T., Maeda, J., Kawabe, K., Obayashi, S., & Suzuki, K. (2001) · Synapse · doi:10.1002/syn.1063 · Cited by 58
Extrastriatal D2 and striatal D2 receptors in depressive illness: Pilot PET studies using [11C]FLB 457 and [11C]raclopride
Montgomery, A. J., Stokes, P. R. A., Kitamura, Y., & Grasby, P. M. (2007) · Journal of Affective Disorders · doi:10.1016/j.jad.2006.11.010 · Cited by 58
Dopamine Synthesis Capacity is Associated with D2/3 Receptor Binding but Not Dopamine Release
Berry, A. S., Shah, V. D., Furman, D. J., White, R. L., Baker, S., O'Neil, J., Janabi, M., D'Esposito, M., & Jagust, W. (2017) · Neuropsychopharmacology · doi:10.1038/npp.2017.180 · Cited by 55
Anticonvulsants for cocaine dependence
Minozzi, S., Amato, L., Davoli, M., Farrell, M., Reisser, A. A. L., Pani, P. P., de Lima, M. S., Soares, B. G., & Vecchi, S. (2008) · Cochrane Database of Systematic Reviews · doi:10.1002/14651858.cd006754.pub2 · Cited by 56
Retracted
Amphetamine induced dopamine release increases anxiety in individuals recovered from anorexia nervosa
Bailer, U., Narendran, R., Frankle, W., Himes, M. L., Duvvuri, V., Mathis, C., & Kaye, W. (2011) · International Journal of Eating Disorders · doi:10.1002/eat.20937 · Cited by 54
Abnormal Striatal Circuitry and Intensified Novelty Seeking among Adolescents Who Abuse Methamphetamine and Cannabis
Churchwell, J. C., Carey, P. D., Ferrett, H. L., Stein, D. J., & Yurgelun-Todd, D. A. (2012) · Developmental Neuroscience · doi:10.1159/000337724 · Cited by 52
Excited Delirium and Sudden Death: A Syndromal Disorder at the Extreme End of the Neuropsychiatric Continuum
Mash, D. C. (2016) · Frontiers in Physiology · doi:10.3389/fphys.2016.00435 · Cited by 53
Imaging Neurotransmitter Release by Drugs of Abuse
Martínez, D., & Narendran, R. (2009) · Current topics in behavioral neurosciences · doi:10.1007/7854_2009_34 · Cited by 50
The relationship between childhood trauma, dopamine release and dexamphetamine-induced positive psychotic symptoms: a [11C]-(+)-PHNO PET study
Dahoun, T., Nour, M. M., McCutcheon, R. A., Adams, R. A., Bloomfield, M., & Howes, O. D. (2019) · Translational Psychiatry · doi:10.1038/s41398-019-0627-y · Cited by 45
Measuring Dopamine Synaptic Transmission with Molecular Imaging and Pharmacological Challenges: The State of the Art
Laruelle, M. A. (2012) · Neuromethods · doi:10.1007/7657_2012_45 · Cited by 43
A Single Neurotoxic Dose of Methamphetamine Induces a Long-Lasting Depressive-Like Behaviour in Mice
Silva, C., Neves, A. F., Dias, A. I., de Freitas, H. J. F., Mendes, S. M., Pita, I. R., Viana, S., de Oliveira, P. A., Cunha, R. A., Ribeiro, C., et al. (2013) · Neurotoxicity Research · doi:10.1007/s12640-013-9423-2 · Cited by 43
Dopamine agonists for the treatment of cocaine dependence
Amato, L., Minozzi, S., Pani, P. P., Solimini, R., Vecchi, S., Zuccaro, P., & Davoli, M. (2011) · Cochrane Database of Systematic Reviews · doi:10.1002/14651858.cd003352.pub3 · Cited by 43
Cue-Induced Dopamine Release Predicts Cocaine Preference: Positron Emission Tomography Studies in Freely Moving Rodents
Schiffer, W. K., Liebling, C. N. B., Reiszel, C., Hooker, J. M., Brodie, J. D., & Dewey, S. L. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.5221-08.2009 · Cited by 40
Effect of a History of Major Depressive Disorder on Smoking-Induced Dopamine Release
Brody, A. L., Olmstead, R. E., Abrams, A. L., Costello, M. R., Khan, A., Kozman, D. M., Saxena, S., Farahi, J. B., London, E. D., & Mandelkern, M. A. (2009) · Biological Psychiatry · doi:10.1016/j.biopsych.2009.06.011 · Cited by 40
An extended simplified reference tissue model for the quantification of dynamic PET with amphetamine challenge
Zhou, Y., Chen, M., Endres, C. J., Ye, W., Brašić, J. R., Alexander, M., Crabb, A. H., Guilarte, T. R., & Wong, D. F. (2006) · NeuroImage · doi:10.1016/j.neuroimage.2006.06.038 · Cited by 39
Structural covariance networks of striatum subdivision in patients with P arkinson's disease
Chou, K., Lin, W., Lee, P., Tsai, N., Huang, Y., Chen, H.-L., Cheng, K., Chen, P., Wang, H., Lin, T., et al. (2014) · Human Brain Mapping · doi:10.1002/hbm.22724 · Cited by 40
Mapping the amphetamine-evoked changes in [11C]raclopride binding in living rat using small animal PET: modulation by MAO-inhibition
Pedersen, K., Simonsen, M., Østergaard, S. D., Lajord Munk, O., Rosa-Neto, P., Olsen, A. K., Jensen, S. B., Møller, A., & Cumming, P. (2007) · NeuroImage · doi:10.1016/j.neuroimage.2006.11.038 · Cited by 37
MR atlas of the baboon brain for functional neuroimaging
Greer, P. J., Villemagne, V. L., Ruszkiewicz, J., Graves, A. K., MELTZER, C. C., Mathis, C. A., & Price, J. C. (2002) · Brain Research Bulletin · doi:10.1016/s0361-9230(02)00810-9 · Cited by 37
Dextroamphetamine causes a change in regional brain activity in vivo during cognitive tasks: A functional magnetic resonance imaging study of blood oxygen level-dependent response
Willson, M. C., Wilman, A. H., Bell, E. C., Asghar, S. J., & Silverstone, P. H. (2004) · Biological Psychiatry · doi:10.1016/j.biopsych.2004.06.008 · Cited by 36
Increases in amphetamine-like discriminative stimulus effects of the abused inhalant toluene in mice
Bowen, S. E. (2006) · Psychopharmacology · doi:10.1007/s00213-006-0381-8 · Cited by 33
Impairment of acquisition of intravenous cocaine self-administration by RNA-interference of dopamine D1-receptors in the nucleus accumbens shell
Pisanu, A., Lecca, D., Valentini, V., Bahí, A., Dreyer, J., Cacciapaglia, F., Scifo, A., Piras, G., Cadoni, C., & Chiara, G. D. (2014) · Neuropharmacology · doi:10.1016/j.neuropharm.2014.10.018 · Cited by 32
Striatal Dopamine Release in Response to Morphine: A [11C]Raclopride Positron Emission Tomography Study in Healthy Men
Spagnolo, P. A., Kimes, A. S., Schwandt, M. L., Kojori, E. S., Thada, S., Phillips, K. A., Diazgranados, N., Preston, K. L., Herscovitch, P., Tomasi, D. G., et al. (2019) · Biological Psychiatry · doi:10.1016/j.biopsych.2019.03.965 · Cited by 30
Analyses of [18F]altanserin bolus injection PET data. I: Consideration of radiolabeled metabolites in baboons
Price, J. C., Lopresti, B. J., Mason, N. S., Holt, D. P., Huang, Y. H., & Mathis, C. A. (2001) · Synapse · doi:10.1002/syn.1054 · Cited by 29
Mapping the amphetamine-evoked dopamine release in the brain of the Gottingen minipig
Lind, N. M., Olsen, A. K., Moustgaard, A., Jensen, S. B., Jakobsen, S., Hansen, A. K., Arnfred, S. M., Hemmingsen, R. P., Gjedde, A., & Cumming, P. (2005) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2004.08.007 · Cited by 28
Effect of monoamine oxidase inhibition on amphetamine-evoked changes in dopamine receptor availability in the living pig: A dual tracer PET study with [11C]harmine and [11C]raclopride
Jensen, S. B., Olsen, A. K., Pedersen, K., & Cumming, P. (2006) · Synapse · doi:10.1002/syn.20258 · Cited by 27
SIC, an intracerebral beta(+)-range-sensitive probe for radiopharmacology investigations in small laboratory animals: binding studies with (11)C-raclopride.
Zimmer, L., Hassoun, W., Pain, F., Bonnefoi, F., Lanièce, P., Mastrippolito, R., Pinot, L., Pujol, J. F., & Leviel, V. (2002) · PubMed · Cited by 27
No difference in striatal dopamine transporter availability between active smokers, ex-smokers and non-smokers using [123I]FP-CIT (DaTSCAN) and SPECT
Thomsen, G. K., Knudsen, G. M., Jensen, P. S., Ziebell, M., Holst, K. K., Asenbaum, S., Booij, J., Darcourt, J., Dickson, J. C., Ozlem Kapucu, L., et al. (2013) · EJNMMI Research · doi:10.1186/2191-219x-3-39 · Cited by 27
Anticonvulsants for cocaine dependence
Minozzi, S., Amato, L., Davoli, M., Farrell, M., Reisser, A. A. L., Pani, P. P., de Lima, M. S., Soares, B. G., & Vecchi, S. (2015) · Cochrane Database of Systematic Reviews · doi:10.1002/14651858.cd006754.pub3 · Cited by 26
Retracted
Amphetamine challenge decreases yohimbine binding to α2 adrenoceptors in Landrace pig brain
Landau, A. M., Doudet, D. J., & Jakobsen, S. (2012) · Psychopharmacology · doi:10.1007/s00213-011-2632-6 · Cited by 24
Dopamine system: manager of neural pathways
Hong, S. (2013) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2013.00854 · Cited by 24
Sequential H(2)(15)O PET studies in baboons: before and after amphetamine.
Price, J. C., Drevets, W. C., Ruszkiewicz, J., Greer, P. J., Villemagne, V. L., Xu, L., Mazumdar, S., Cantwell, M. N., & Mathis, C. A. (2002) · PubMed · Cited by 24
Self-citation
Limitations of SRTM, Logan graphical method, and equilibrium analysis for measuring transient dopamine release with [(11)C]raclopride PET.
Sullivan, J. M., Kim, S., Cosgrove, K., & Morris, E. D. (2013) · Europe PMC (PubMed Central) · Cited by 22
Brain dopamine responses to ultra-processed milkshakes are highly variable and not significantly related to adiposity in humans
Darcey, V. L., Guo, J., Chi, M., Chung, S. T., Courville, A. B., Gallagher, I., Herscovitch, P., Joseph, P. V., Howard, R., LaNoire, M., et al. (2025) · Cell Metabolism · doi:10.1016/j.cmet.2025.02.002 · Cited by 22
Positron Emission Tomography Studies of Potential Mechanisms Underlying Phencyclidine-Induced Alterations in Striatal Dopamine
Schiffer, W. K., Logan, J., & Dewey, S. L. (2003) · Neuropsychopharmacology · doi:10.1038/sj.npp.1300258 · Cited by 18
In the Loop: Extrastriatal Regulation of Spiny Projection Neurons by GPR52
Spark, D. L., Mao, M., Ma, S., Sarwar, M., Nowell, C. J., Shackleford, D. M., Sexton, P. M., Nithianantharajah, J., Stewart, G. D., & Langmead, C. J. (2020) · ACS Chemical Neuroscience · doi:10.1021/acschemneuro.0c00197 · Cited by 15
Antipsychotic medications for cocaine dependence
Amato, L., Minozzi, S., Pani, P. P., & Davoli, M. (2007) · Cochrane Database of Systematic Reviews · doi:10.1002/14651858.cd006306.pub2 · Cited by 15
Chapter IX Human forebrain dopamine systems: Characterization of the normal brain and in relation to psychiatric disorders
Hurd, Y. L., & Hall, H. (2005) · Handbook of chemical neuroanatomy · doi:10.1016/s0924-8196(05)80013-2 · Cited by 14
Cocaine
Trifilieff, P., & Martínez, D. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-418679-8.00005-8 · Cited by 14
Dopamine and Depression
Willner, P. (2002) · Handbook of experimental pharmacology · doi:10.1007/978-3-662-06765-9_12 · Cited by 13
Quantification of receptor–ligand binding potential in sub-striatal domains using probabilistic and template regions of interest
del Campo, N., Tait, R. J., Acosta‐Cabronero, J., Hong, Y. T., Izquierdo‐Garcia, D., Smith, R., Aigbirhio, F. I., Sahakian, B. J., Müller, U., Robbins, T. W., et al. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2010.11.071 · Cited by 12
Measuring amphetamine‐induced dopamine release in humans: A comparative meta‐analysis of [11C]‐raclopride and [11C]‐(+)‐PHNO studies
Caravaggio, F., Porco, N., Kim, J., Torres‐Carmona, E., Brown, E. E., Iwata, Y., Nakajima, S., Gerretsen, P., Remington, G. J., & Graff‐Guerrero, A. (2021) · Synapse · doi:10.1002/syn.22195 · Cited by 12
Plasmonic Sensing Assay for Long-Term Monitoring (PSALM) of Neurotransmitters in Urine
Chen, W., Wang, W., Lin, Q., Grys, D., Niihori, M., Huang, J., Hu, S., de Nijs, B., Scherman, O. A., & Baumberg, J. J. (2022) · ACS Nanoscience Au · doi:10.1021/acsnanoscienceau.2c00048 · Cited by 11
Disulfiram for the treatment of cocaine dependence
Traccis, F., Minozzi, S., Trogu, E., Vacca, R., Vecchi, S., Pani, P. P., & Agabio, R. (2024) · Cochrane Database of Systematic Reviews · doi:10.1002/14651858.cd007024.pub3 · Cited by 14
Subregion-specific effects on striatal neurotransmission and dopamine-signaling by acute and repeated amphetamine exposure
Danielsson, K., Lagström, O., Ericson, M., Söderpalm, B., & Adermark, L. (2021) · Neuropharmacology · doi:10.1016/j.neuropharm.2021.108638 · Cited by 11
A 26.5 pArms Neurotransmitter Front-End With Class-AB Background Subtraction
Ying, D., Rosenberg, J. V., Singh, N. K., & Hall, D. A. (2022) · IEEE Transactions on Biomedical Circuits and Systems · doi:10.1109/tbcas.2022.3194809 · Cited by 10
Rising Taurine and Ethanol Concentrations in Nucleus Accumbens Interact to Produce the Dopamine-Activating Effects of Alcohol
Ericson, M., Chau, P., Adermark, L., & Söderpalm, B. (2013) · Advances in experimental medicine and biology · doi:10.1007/978-1-4614-6130-2_18 · Cited by 10
Anticonvulsants for cocaine dependence
Minozzi, M., Amato, L., Pani, P., Vecchi, S., & Davoli, M. (2007) · Cochrane Database of Systematic Reviews · doi:10.1002/14651858.cd006754 · Cited by 10
Retracted
Altered Functional Connectivity of Striatum Based on the Integrated Connectivity Model in First-Episode Schizophrenia
Zhang, B., Lin, P., Wang, X., Öngür, D., Ji, X., Situ, W., Yao, S., & Wang, X. (2019) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2019.00756 · Cited by 9
Antidepressants for cocaine dependence
de Lima, M. S., Farrell, M., Reisser, A. A. L., & Soares, B. G. (2010) · Cochrane Database of Systematic Reviews · doi:10.1002/14651858.cd002950.pub2 · Cited by 9
Retracted
Understanding and restoring dopaminergic function in fibromyalgia patients using a mindfulness-based psychological intervention: a [18F]-DOPA PET study. Study protocol for the FIBRODOPA study—a randomized controlled trial
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ORIGINAL ARTICLES Amphetamine-Induced Dopamine Release in Human Ventral Striatum Correlates with Euphoria
Drevets, W. C., Gautier, C. H., Price, J. C., Kupfer, D. J., Kinahan, P. E., Grace, A., Price, J. L., & Mathis, C. A. (2015)
Self-citation
Amphetamine-induced dopamine release in human ventral striatum correlates with euphoria
Drevets, W. C., Gautier, C., Price, J. C., Kupfer, D. J., Kinahan, P. E., Grace, A. A., Price, J. L., & Mathis, C. A. (2001) · Biological Psychiatry · doi:10.1016/s0006-3223(00)01038-6 · Cited by 706
Self-citation
Imaging Human Mesolimbic Dopamine Transmission with Positron Emission Tomography. Part II: Amphetamine-Induced Dopamine Release in the Functional Subdivisions of the Striatum
Martinez, D., Slifstein, M., Broft, A., Mawlawi, O., Hwang, D.-R., Huang, Y., Cooper, T., Kegeles, L., Zarahn, E., Abi-Dargham, A., et al. (2003) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1097/01.wcb.0000048520.34839.1a · Cited by 569
Amphetamine-Induced Dopamine Release Greater in Ventral Than in Dorsal Striatum
Price, J., Drevets, W., Kinahan, P., Lopresti, B., & Mathis, C. (2001) · Elsevier eBooks · doi:10.1016/b978-012285751-5/50035-1 · Cited by 4
Self-citation
Amphetamine-induced dopamine release in rat: Whole-brain spatiotemporal analysis with [ 11 C]raclopride and positron emission tomography
Johansson, J. J., Ericsson, M., Axelsson, J., af Bjerkén, S., Virel, A., & Karalija, N. (2023) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1177/0271678x231210128 · Cited by 2

Authors: Drevets, W.
Affiliations: University of Pittsburgh (US)
Corresponding author: Drevets, W
ORCID: Drevets, W
Venue: Neuropsychopharmacology
Publisher: Springer Science and Business Media LLC
Published: 1999-12
Volume: 21
Issue: 6
Pages: 694-709
ISSN: 0893-133X (ISSN-L)
DOI: 10.1016/s0893-133x(99)00079-2
OpenAlex: W2062446797
Cited by: 122
References: 64
Citations by year: 2025: 2 · 2024: 1 · 2023: 1 · 2022: 4 · 2021: 4 · 2020: 1 · 2019: 5 · 2018: 1 · 2017: 2 · 2016: 5 · 2015: 4 · 2014: 4 · 2013: 9 · 2012: 6
FWCI: 2.39
Type: journal article
Language: en
Open access: closed
Locations: Neuropsychopharmacology (publishedVersion)
PubMed (publishedVersion)
Topics: Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
Health Sciences › Medicine › Psychiatry and Mental health › Schizophrenia research and treatment
Health Sciences › Medicine › Clinical Neurology › Parkinson's Disease Mechanisms and Treatments
Keywords: amphetamine, dopamine release, striatum, ventral striatum, dorsal striatum, [11C]raclopride, D2/D3 receptors, baboons, nucleus accumbens, caudate nucleus, partial volume correction, microdialysis
MeSH terms: Amphetamine, Animals, Carbon Radioisotopes, Caudate Nucleus, Corpus Striatum, Dopamine, Female, Magnetic Resonance Imaging, Male, Nucleus Accumbens, Papio, Putamen, Tomography, Emission-Computed, Receptors, Dopamine D1, Receptors, Dopamine D2, Raclopride, Receptors, Dopamine D3, Rats

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PET Measures of Amphetamine-Induced Dopamine Release in Ventral versus Dorsal Striatum

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