Cited by 302Neurotransmitter Receptor Influence on BehaviorNeural and Behavioral Psychology StudiesSubstance Abuse Treatment and Outcomes

The DOI matches its Crossref record; 50 of the 50 references it cites were found in a registry or an index.

Expectation Enhances the Regional Brain Metabolic and the Reinforcing Effects of Stimulants in Cocaine Abusers

Open access

Volkow, Nora D., Wang, Gene-Jack, Ma, Yemin, Fowler, Joanna S., Zhu, Wei, Maynard, Laurence, Telang, Frank, Vaska, Paul, Ding, Yu-Shin, Wong, Christopher, Swanson, James M.·2003·The Journal of Neuroscience

DOI 10.1523/jneurosci.23-36-11461.2003PMC PMC6740524

Open this paper in CoChat — free account Open PDF

Abstract

The reinforcing effects of drugs of abuse result from the complex interaction between pharmacological effects and conditioned responses. Here we evaluate how expectation affects the response to the stimulant drug methylphenidate in 25 cocaine abusers. The effects of methylphenidate (0.5 mg/kg, i.v.) on brain glucose metabolism (measured by [18 F]deoxyglucose-positron emission tomography) and on its reinforcing effects (self-reports of drug effects) were evaluated in four conditions: (1) expecting placebo and receiving placebo; (2) expecting placebo and receiving methylphenidate; (3) expecting methylphenidate and receiving methylphenidate; (4) expecting methylphenidate and receiving placebo. Methylphenidate increased brain glucose metabolism, and the largest changes were in cerebellum, occipital cortex, and thalamus. The increases in metabolism were ∼50% larger when methylphenidate was expected than when it was not, and these differences were significant in cerebellum (vermis) and thalamus. In contrast, unexpected methylphenidate induced greater increases in left lateral orbitofrontal cortex than when it was expected. Methylphenidate-induced increases in self-reports of “high” were also ∼50% greater when subjects expected to receive it than when they did not and were significantly correlated with the metabolic increases in thalamus but not in cerebellum. These findings provide evidence that expectation amplifies the effects of methylphenidate in brain and its reinforcing effects. They also suggest that the thalamus, a region involved with conditioned responses, may mediate the enhancement of the reinforcing effects of methylphenidate by expectation and that the orbitofrontal cortex mediates the response to unexpected reinforcement. The enhanced cerebellar activation with expectation may reflect conditioned responses that are not linked to conscious responses.

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

Integrity signals

Registry

Crossref · 10.1523/jneurosci.23-36-11461.2003

Cites

50 of 50 references verified0 citation errors · 0 not checkable

Statistics

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

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?

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Statistical parametric maps in functional imaging: A general linear approach
Friston, K. J., Holmes, A. P., Worsley, K. J., Poline, J. ‐., Frith, C. D., & Frackowiak, R. S. J. (1994) · Human Brain Mapping · doi:10.1002/hbm.460020402 · Cited by 9,688
The Jackknife, the Bootstrap and Other Resampling Plans
Efron, B. (1982) · Society for Industrial and Applied Mathematics eBooks · doi:10.1137/1.9781611970319 · Cited by 8,120
The neural basis of drug craving: An incentive-sensitization theory of addiction
Robinson, T. (1993) · Brain Research Reviews · doi:10.1016/0165-0173(93)90013-p · Cited by 7,346
THE [ 14 C]DEOXYGLUCOSE METHOD FOR THE MEASUREMENT OF LOCAL CEREBRAL GLUCOSE UTILIZATION: THEORY, PROCEDURE, AND NORMAL VALUES IN THE CONSCIOUS AND ANESTHETIZED ALBINO RAT 1
Sokoloff, L., Reivich, M., Kennedy, C., Rosiers, M. H. D., Patlak, C. S., Pettigrew, K. D., Sakurada, O., & Shinohara, M. (1977) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.1977.tb10649.x · Cited by 6,000
Drugs abused by humans preferentially increase synaptic dopamine concentrations in the mesolimbic system of freely moving rats.
Di Chiara, G., & Imperato, A. (1988) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.85.14.5274 · Cited by 4,733
The jackknife-a review
Miller, R. G. (1974) · Biometrika · doi:10.1093/biomet/61.1.1 · Cited by 1,391
NOTES ON BIAS IN ESTIMATION
Quenouille, M. H. (1956) · Biometrika · doi:10.1093/biomet/43.3-4.353 · Cited by 1,305
Acute effects of cocaine on human brain activity and emotion
Breiter, H. C., Gollub, R. L., Weisskoff, R. M., Kennedy, D. N., Makris, N., Berke, J. D., Goodman, J. M., Kantor, H. L., Gastfriend, D. R., Riorden, J. P., et al. (1997) · Neuron · doi:10.1016/s0896-6273(00)80374-8 · Cited by 1,270
Expectation and Dopamine Release: Mechanism of the Placebo Effect in Parkinson's Disease
de la Fuente‐Fernández, R., Ruth, T. J., Sossi, V., Schulzer, M., Calne, D. B., & Stoessl, A. J. (2001) · Science · doi:10.1126/science.1060937 · Cited by 991
Reward processing in primate orbitofrontal cortex and basal ganglia
Schultz, W. (2000) · Cerebral Cortex · doi:10.1093/cercor/10.3.272 · Cited by 942

Show all 48 references

Research works printed but not linked: 6

2001, J Nucl Med, 42, 535
Dirckx, SG, Risinger RC, Ross TJ, Li Z, Li SJ, Stein EA 2003 Comparing iv methylphenidate and cocaine in the human brain using fMRI. 9th International Conference on Functional Mapping of the Human Brain, New York, June.
1997, Arch Ital Biol, 135, 369
1995, Cereb Cortex, 2, 95
1999, Life Sci, 65, 7
1992, Radiology, 186, 59

Sorted by citations

Items 101–200 of 302

Cannabis Abusers Show Hypofrontality and Blunted Brain Responses to a Stimulant Challenge in Females but not in Males
Wiers, C. E., Kojori, E. S., Wong, C., Abi‐Dargham, A., Demiral, Ş. B., Tomasi, D. G., Wang, G., & Volkow, N. D. (2016) · Neuropsychopharmacology · doi:10.1038/npp.2016.67 · Cited by 64
Self-citation
The nicotinic acetylcholine receptor partial agonist varenicline and the treatment of drug dependence: A review
Crunelle, C. L., Miller, M. L., Booij, J., & van den Brink, W. (2009) · European Neuropsychopharmacology · doi:10.1016/j.euroneuro.2009.11.001 · Cited by 66
Placebo and nocebo effect: a mini-review.
Požgain, I., Požgain, Z., & Degmečić, D. (2014) · PubMed · Cited by 63
Animal models of binge drinking, current challenges to improve face validity
Jeanblanc, J., Rolland, B., Gierski, F., Martinetti, M. P., & Naassïla, M. (2018) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2018.05.002 · Cited by 62
A Systematic Review of Obesity and Binge Eating Associated Impairment of the Cognitive Inhibition System
Saruco, E., & Pleger, B. (2021) · Frontiers in Nutrition · doi:10.3389/fnut.2021.609012 · Cited by 63
Episodic Memories and Their Relevance for Psychoactive Drug Use and Addiction
Müller, C. P. (2013) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2013.00034 · Cited by 62
Placebo and Endogenous Mechanisms of Analgesia
Benedetti, F. (2007) · Springer eBooks · doi:10.1007/978-3-540-33823-9_14 · Cited by 59
The cerebellum on cocaine: plasticity and metaplasticity
Vazquez-Sanroman, D. B., Leto, K., Cerezo, M., Carbo‐Gas, M., Sanchis‐Segura, C., Carulli, D., Rossi, F., & Miquel, M. (2015) · Addiction Biology · doi:10.1111/adb.12223 · Cited by 59
Selective dopamine D4 receptor agonist (A-412997) improves cognitive performance and stimulates motor activity without influencing reward-related behaviour in rat
Woolley, M. L., Waters, K. A., Reavill, C., Bull, S., Lacroix, L. P., Martyn, A., Hutcheson, D. M., Valerio, E., Bate, S. T., Jones, D. N. C., et al. (2008) · Behavioural Pharmacology · doi:10.1097/fbp.0b013e32831c3b06 · Cited by 58
Placebo response in clinical trials with schizophrenia patients
Kinon, B. J., Potts, A. J., & Watson, S. B. (2011) · Current Opinion in Psychiatry · doi:10.1097/yco.0b013e32834381b0 · Cited by 58
Expectation Modulates Human Brain Responses to Acute Cocaine: A Functional Magnetic Resonance Imaging Study
Kufahl, P. R., Li, Z., Risinger, R. C., Rainey, C. J., Piacentine, L. B., Wu, G., Bloom, A. S., Zheng, Y., & Li, S. (2007) · Biological Psychiatry · doi:10.1016/j.biopsych.2007.03.021 · Cited by 57
Experimental designs and brain mapping approaches for studying the placebo analgesic effect
Colloca, L., Benedetti, F., & Porro, C. (2008) · European Journal of Applied Physiology · doi:10.1007/s00421-007-0593-6 · Cited by 53
The Effect of Treatment History on Therapeutic Outcome: Psychological and Neurobiological Underpinnings
Kessner, S. S., Forkmann, K., Ritter, C., Wiech, K., Ploner, M., & Bingel, U. (2014) · PLoS ONE · doi:10.1371/journal.pone.0109014 · Cited by 59
8.3 Imaging Dopamine’s Role in Drug Abuse and Addiction
Volkow, N. D., Fowler, J. S., Wang, G., Telang, F., & Baler, R. (2009) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780195373035.003.0028 · Cited by 58
Self-citation
Placebo-Induced Improvements: How Therapeutic Rituals Affect the Patient's Brain
Benedetti, F. (2012) · Journal of Acupuncture and Meridian Studies · doi:10.1016/j.jams.2012.03.001 · Cited by 61
An fMRI investigation of the impact of withdrawal on regional brain activity during nicotine anticipation
Gloria, R., Angelos, L., Schaefer, H. S., Davis, J. M., Majeskie, M. R., Richmond, B. S., Curtin, J. J., Davidson, R. J., & Baker, T. B. (2009) · Psychophysiology · doi:10.1111/j.1469-8986.2009.00823.x · Cited by 53
Striatal dopamine D2 receptor availability predicts the thalamic and medial prefrontal responses to reward in cocaine abusers three years later
Asensio, S., Romero, M. J., Romero, F. J., Wong, C., Nelly Alia-klein, A., Tomasi, D. G., Wang, G., Telang, F., Volkow, N. D., & Goldstein, R. Z. (2009) · Synapse · doi:10.1002/syn.20741 · Cited by 53
Self-citation
Subtyping patients with heroin addiction at treatment entry: factor derived from the Self-Report Symptom Inventory (SCL-90)
Maremmani, I., Pani, P. P., Pacini, M., Bizzarri, J. V., Trogu, E., Maremmani, A. G. I., Gerra, G., Perugi, G., & Dell’Osso, L. (2010) · Annals of General Psychiatry · doi:10.1186/1744-859x-9-15 · Cited by 55
Mirtazapine Alters Cue-Associated Methamphetamine Seeking in Rats
Graves, S. M., & Napier, T. C. (2010) · Biological Psychiatry · doi:10.1016/j.biopsych.2010.09.032 · Cited by 51
The sweetest pill to swallow: How patient neurobiology can be harnessed to maximise placebo effects
Jubb, J., & Bensing, J. M. (2013) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2013.09.006 · Cited by 52
Reciprocal responsiveness of nucleus accumbens shell and core dopamine to food- and drug-conditioned stimuli
Bassareo, V., Musio, P., & Chiara, G. D. (2010) · Psychopharmacology · doi:10.1007/s00213-010-2072-8 · Cited by 52
Enhanced midbrain response at 6‐month follow‐up in cocaine addiction, association with reduced drug‐related choice
Moeller, S. J., Tomasi, D. G., Woicik, P. A., Maloney, T., Alia‐Klein, N., Honorio, J., Telang, F., Wang, G., Wang, R., Sinha, R., et al. (2012) · Addiction Biology · doi:10.1111/j.1369-1600.2012.00440.x · Cited by 51
Self-citation
Mirtazapine, and mirtazapine-like compounds as possible pharmacotherapy for substance abuse disorders: Evidence from the bench and the bedside
Graves, S. M., Rafeyan, R., Watts, J., & Napier, T. C. (2012) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2012.08.013 · Cited by 49
Differential cocaine-induced modulation of glutamate and dopamine transporters after contingent and non-contingent administration
Miguéns, M., Crespo, J. A., Olmo, N. D., Higuera‐Matas, A., Montoya, G. L., Garcı́a-Lecumberri, C., & Ambrosio, E. (2008) · Neuropharmacology · doi:10.1016/j.neuropharm.2008.06.042 · Cited by 49
Acute effects of sublingual buprenorphine on brain responses to heroin-related cues in early-abstinent heroin addicts: an uncontrolled trial
Mei, W., Zhang, J. X., & Xiao, Z. (2010) · Neuroscience · doi:10.1016/j.neuroscience.2010.07.033 · Cited by 49
Expectancy effects on serotonin and dopamine transporters during SSRI treatment of social anxiety disorder: a randomized clinical trial
Hjorth, O. R., Frick, A., Gingnell, M., Hoppe, J. M., Faria, V., Hultberg, S., Alaie, I., Månsson, K. N. T., Rosén, J., Reis, M., et al. (2021) · Translational Psychiatry · doi:10.1038/s41398-021-01682-3 · Cited by 46
Patterns of Brain Activation Associated With Contextual Conditioning to Methamphetamine in Mice.
Rhodes, J. S., Ryabinin, A. E., & Crabbe, J. C. (2005) · Behavioral Neuroscience · doi:10.1037/0735-7044.119.3.759 · Cited by 49
Involving the cerebellum in cocaine-induced memory: pattern of cFos expression in mice trained to acquire conditioned preference for cocaine
Carbo‐Gas, M., Vazquez-Sanroman, D. B., Aguirre-Manzo, L., Coria‐Ávila, G. A., Manzo, J., Sanchis‐Segura, C., & Miquel, M. (2013) · Addiction Biology · doi:10.1111/adb.12042 · Cited by 45
Predominance of D2 Receptors in Mediating Dopamine's Effects in Brain Metabolism: Effects of Alcoholism
Volkow, N. D., Tomasi, D. G., Wang, G., Telang, F., Fowler, J. S., Logan, J., Maynard, L. J., & Wong, C. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.5261-12.2013 · Cited by 42
Self-citation
Putative therapeutic targets for symptom subtypes of adult ADHD: D4 receptor agonism and COMT inhibition improve attention and response inhibition in a novel translational animal model
Tomlinson, A., Grayson, B., Marsh, S., Hayward, A., Marshall, K. M., & Neill, J. C. (2014) · European Neuropsychopharmacology · doi:10.1016/j.euroneuro.2014.11.016 · Cited by 42
Double dissociating effects of sensory stimulation and cocaine on serotonin activity in the occipital and temporal cortices
Müller, C. P., Silva, M. A. D. S., & Huston, J. P. (2006) · Neuropharmacology · doi:10.1016/j.neuropharm.2006.10.002 · Cited by 41
Repeated cocaine exposure decreases dopamine D2‐like receptor modulation of Ca2+homeostasis in rat nucleus accumbens neurons
Perez, M. F., Ford, K. A., Goussakov, I., Stutzmann, G. E., & Hu, X. (2011) · Synapse · doi:10.1002/syn.20831 · Cited by 40
Children's and parents' perspectives on open‐label use of placebos in the treatment of ADHD
Sandler, A., Glesne, C., & Geller, G. (2007) · Child Care Health and Development · doi:10.1111/j.1365-2214.2007.00743.x · Cited by 40
Negative dimension in psychiatry. Amotivational syndrome as a paradigm of negative symptoms in substance abuse
Rovai, L., Maremmani, A. G. I., Pacini, M., Pani, P. P., Rugani, F., Lamanna, F., Schiavi, E., Mautone, S., Dell’Osso, L., & Maremmani, I. (2013) · Rivista di psichiatria · doi:10.1708/1228.13610 · Cited by 42
Cocaine withdrawal and neuro-adaptations in ion channel function
Hu, X. (2007) · Molecular Neurobiology · doi:10.1007/bf02700626 · Cited by 39
Pain Experience is Somatotopically Organized and Overlaps with Pain Anticipation in the Human Cerebellum
Welman, F. H. S. M., Smit, A. E., Jongen, J. L. M., Tibboel, D., van der Geest, J. N., & Holstege, J. C. (2018) · The Cerebellum · doi:10.1007/s12311-018-0930-9 · Cited by 38
Cerebellar neurotransmission in attention-deficit/hyperactivity disorder: Does dopamine neurotransmission occur in the cerebellar vermis?
Glaser, P. E. A., Surgener, S. P., Grondin, R., Gash, C. R., Palmer, M., Castellanos, F. X., & Gerhardt, G. A. (2006) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2005.09.019 · Cited by 37
Substituted Cathinone Products
Gunderson, E. W., Kirkpatrick, M. G., Willing, L. M., & Holstege, C. P. (2013) · Journal of Addiction Medicine · doi:10.1097/adm.0b013e31829084b7 · Cited by 35
Investigation of the neuroanatomical substrates of reward seeking following protracted abstinence in mice
Madsen, H. B., Brown, R. M., Short, J. L., & Lawrence, A. J. (2012) · The Journal of Physiology · doi:10.1113/jphysiol.2011.225219 · Cited by 36
Relationship of cortisol levels and genetic polymorphisms to antidepressant response to placebo and fluoxetine in patients with major depressive disorder: a prospective study
Ventura-Juncá, R., Symon, A., López, P., Fiedler, J. L., Rojas, G., Heskia, C., Lara, P., Marín, F., Viviana Guajardo, T., Araya, A. V., et al. (2014) · BMC Psychiatry · doi:10.1186/s12888-014-0220-0 · Cited by 34
Belief about Nicotine Modulates Subjective Craving and Insula Activity in Deprived Smokers
Gu, X., Lohrenz, T. M., Salas, R., Baldwin, P. R., Soltani, A., Kirk, U., Cinciripini, P. M., & Montague, P. R. (2016) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2016.00126 · Cited by 33
Can the Chronic Administration of the Combination of Buprenorphine and Naloxone Block Dopaminergic Activity Causing Anti-reward and Relapse Potential?
Blum, K., Chen, T. J. H., Bailey, J., Bowirrat, A., Femino, J., Chen, A. L., Simpatico, T. A., Morse, S. A., Giordano, J., Damle, U. J., et al. (2011) · Molecular Neurobiology · doi:10.1007/s12035-011-8206-0 · Cited by 35
Human brain imaging and substance abuse
Lingford-Hughes, A. R. (2004) · Current Opinion in Pharmacology · doi:10.1016/j.coph.2004.10.002 · Cited by 35
Naltrexone moderates the relationship between cue-induced craving and subjective response to methamphetamine in individuals with methamphetamine use disorder
Roche, D. J. O., Worley, M. J., Courtney, K. E., Bujarski, S., London, E. D., SHOPTAW, S. J., & Ray, L. A. (2017) · Psychopharmacology · doi:10.1007/s00213-017-4607-8 · Cited by 32
Substance abuse disorders
Reid, A. G., Lingford-Hughes, A. R., Cancela, L. M., & Kalivas, P. W. (2012) · Handbook of clinical neurology · doi:10.1016/b978-0-444-52002-9.00024-3 · Cited by 35
Placebo and Nocebo Effects: An Introduction to Psychological and Biological Mechanisms
Kong, J., & Benedetti, F. (2014) · Handbook of experimental pharmacology · doi:10.1007/978-3-662-44519-8_1 · Cited by 34
Investigating expectation and reward in human opioid addiction with [ 11 C ]raclopride PET
Watson, B. J., Taylor, L. G., Reid, A. G., Wilson, S. J., Stokes, P. R. A., Brooks, D. J., Myers, J. F., Turkheimer, F., Nutt, D., & Lingford-Hughes, A. R. (2013) · Addiction Biology · doi:10.1111/adb.12073 · Cited by 34
Neuroimaging and drug taking in primates
Murnane, K. S., & Howell, L. L. (2011) · Psychopharmacology · doi:10.1007/s00213-011-2222-7 · Cited by 33
Cerebellar Lingula Size and Experiential Risk Factors Associated with High Levels of Alcohol and Drug Use in Young Adults
Anderson, C. M., Rabi, K., Lukas, S. E., & Teicher, M. H. (2009) · The Cerebellum · doi:10.1007/s12311-009-0141-5 · Cited by 32
Betel quid dependence is associated with functional connectivity changes of the anterior cingulate cortex: a resting-state fMRI study
Liu, T., Li, J., Zhao, Z., Zhong, Y., Zhang, Z., Xu, Q., Yang, G., Lu, G., Pan, S., & Chen, F. (2016) · Journal of Translational Medicine · doi:10.1186/s12967-016-0784-1 · Cited by 33
Regional homogeneity changes between heroin relapse and non-relapse patients under methadone maintenance treatment: a resting-state fMRI study
Chang, H., Li, W., Li, Q., Chen, J., Zhu, J., Ye, J., Liu, J., Li, Z., Li, Y., Shi, M., et al. (2016) · BMC Neurology · doi:10.1186/s12883-016-0659-3 · Cited by 30
Altered Spontaneous Brain Activity in Betel Quid Dependence
Liu, T., Li, J., Zhao, Z., Yang, G., Pan, M.-J., Li, C., Pan, S.-Y., & Chen, F. (2016) · Medicine · doi:10.1097/md.0000000000002638 · Cited by 28
Traditional and Innovative Experimental and Clinical Trial Designs and Their Advantages and Pitfalls
Weimer, K., & Enck, P. (2014) · Handbook of experimental pharmacology · doi:10.1007/978-3-662-44519-8_14 · Cited by 29
Enhancing Placebo Effects in Somatic Symptoms Through Oxytocin
Skvortsova, A., Veldhuijzen, D. S., van Middendorp, H., den Bergh, O. V., & Evers, A. W. M. (2018) · Psychosomatic Medicine · doi:10.1097/psy.0000000000000571 · Cited by 28
Cerebellar hallmarks of conditioned preference for cocaine
Carbo‐Gas, M., Vazquez-Sanroman, D. B., Gil‐Miravet, I., Heras-Chanes, J. D. L., Coria‐Ávila, G. A., Manzo, J. G., Sanchis‐Segura, C., & Miquel, M. (2014) · Physiology & Behavior · doi:10.1016/j.physbeh.2014.04.044 · Cited by 27
ToF‐SIMS imaging of lipids and lipid related compounds in Drosophila brain
Phan, N. T. N., Fletcher, J. S., Sjövall, P., & Ewing, A. G. (2014) · Surface and Interface Analysis · doi:10.1002/sia.5547 · Cited by 26
Neuroimaging as a tool to investigate how cognitive factors influence analgesic drug outcomes
Bingel, U., Tracey, I., & Wiech, K. (2012) · Neuroscience Letters · doi:10.1016/j.neulet.2012.04.043 · Cited by 27
Dysbalance of cortical inhibition and excitation in abstinent cocaine-dependent patients
Gjini, K., Ziemann, U., Napier, T. C., & Boutros, N. N. (2011) · Journal of Psychiatric Research · doi:10.1016/j.jpsychires.2011.10.006 · Cited by 26
Expectancy Modulation of Opioid Neurotransmission
Peciña, M., & Zubieta, J.-K. (2018) · International review of neurobiology · doi:10.1016/bs.irn.2018.02.003 · Cited by 27
Basal Ganglia Activity in Pathological Gambling: A Fluorodeoxyglucose-Positron Emission Tomography Study
Pallanti, S., Haznedar, M. M., Hollander, E., LiCalzi, E. M., Bernardi, S., Newmark, R. E., & Buchsbaum, M. S. (2010) · Neuropsychobiology · doi:10.1159/000317286 · Cited by 25
Cortical activation during cocaine use and extinction in rhesus monkeys
Howell, L. L., Votaw, J. R., Goodman, M. M., & Lindsey, K. P. (2009) · Psychopharmacology · doi:10.1007/s00213-009-1720-3 · Cited by 25
Expectation effects on brain dopamine responses to methylphenidate in cocaine use disorder
Wang, G., Wiers, C. E., Shumay, E., Tomasi, D. G., Yuan, K., Wong, C., Logan, J., Fowler, J. S., & Volkow, N. D. (2019) · Translational Psychiatry · doi:10.1038/s41398-019-0421-x · Cited by 24
Self-citation
Role of placebo effects in pain and neuropsychiatric disorders
Belcher, A. M., Ferré, S., Martinez, P. E., & Colloca, L. (2017) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2017.06.003 · Cited by 25
Correlates of C-reactive protein with neural reward circuitry in adolescents with psychiatric symptoms
Liu, Q., Ely, B. A., Simkovic, S. J., Tao, A., Wolchok, R. E., Alonso, C. M., & Gabbay, V. (2020) · Brain Behavior & Immunity - Health · doi:10.1016/j.bbih.2020.100153 · Cited by 23
The Role of the Cerebellum in Learning to Predict Reward: Evidence from Cerebellar Ataxia
Nicholas, J., Amlang, C. J., Lin, C.-Y. R., Montaser‐Kouhsari, L., Desai, N. A., Pan, M., Kuo, S., & Daphna Shohamy, A. (2023) · The Cerebellum · doi:10.1007/s12311-023-01633-2 · Cited by 23
Structural and Functional Alterations in Betel-Quid Chewers: A Systematic Review of Neuroimaging Findings
Sariah, A., Liu, Z., Pu, W., Liu, H., Xue, Z., & Huang, X. (2019) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2019.00016 · Cited by 23
Update on pathological gambling
Grant, J. E., Williams, K. A., & Kim, S. W. (2006) · Current Psychiatry Reports · doi:10.1007/s11920-006-0081-4 · Cited by 22
Induced beliefs about a fictive energy drink influences 200‐m sprint performance†
Marcos, R. D. L. V., Alberti, S., Barquín, R. R., Soós, I., & Szabó, A. (2017) · European Journal of Sport Science · doi:10.1080/17461391.2017.1339735 · Cited by 27
Differential Sensitivity of A2A and Especially D2 Receptor Trafficking to Cocaine Compared with Lipid Rafts in Cotransfected CHO Cell Lines. Novel Actions of Cocaine Independent of the DA Transporter
Genedani, S., Carone, C., Guidolin, D., Filaferro, M., Marcellino, D. J., Fuxé, K., & Agnati, L. F. (2010) · Journal of Molecular Neuroscience · doi:10.1007/s12031-010-9328-y · Cited by 21
The atypical antidepressant mirtazapine attenuates expression of morphine-induced place preference and motor sensitization
Graves, S. M., Persons, A. L., Riddle, J. L., & Napier, T. C. (2012) · Brain Research · doi:10.1016/j.brainres.2012.07.007 · Cited by 21
Effects of perceived cocaine availability on subjective and objective responses to the drug
Yamamoto, R. T., Karlsgodt, K. H., Rott, D., Lukas, S. E., & Elman, I. (2007) · Substance Abuse Treatment Prevention and Policy · doi:10.1186/1747-597x-2-30 · Cited by 21
Open-label dose-extending placebos for opioid use disorder: a protocol for a randomised controlled clinical trial with methadone treatment
Belcher, A. M., Cole, T. O., Greenblatt, A. D., Hoag, S. W., Epstein, D. H., Wagner, M. A., Billing, A. S., Massey, E. C., Hamilton, K. R., Kozak, Z., et al. (2019) · BMJ Open · doi:10.1136/bmjopen-2018-026604 · Cited by 20
Altered Long- and Short-Range Functional Connectivity in Patients with Betel Quid Dependence: A Resting-State Functional MRI Study
Liu, T., Li, J., Zhang, Z., Xu, Q., Lu, G., Huang, S., Pan, M., & Chen, F. (2016) · Cellular Physiology and Biochemistry · doi:10.1159/000453212 · Cited by 19
The Role of Expectation in the Therapeutic Outcomes of Alcohol and Drug Addiction Treatments
Spagnolo, P. A., Colloca, L., & Heilig, M. A. (2015) · Alcohol and Alcoholism · doi:10.1093/alcalc/agv015 · Cited by 19
Understanding the Role of Substance Expectancies in Addiction
Metrik, J., & Rohsenow, D. J. (2013) · Wiley eBooks · doi:10.1002/9781118384404.ch17 · Cited by 19
For Placebo Effects in Medicine, Seeing Is Believing
Gollub, R. L., & Kong, J. (2011) · Science Translational Medicine · doi:10.1126/scitranslmed.3002120 · Cited by 18
Better than nothing: A historical account of placebos and placebo effects from modern to contemporary medicine
Annoni, M. (2020) · International review of neurobiology · doi:10.1016/bs.irn.2020.03.028 · Cited by 18
Verslaving, een chronisch recidiverende hersenziekte
van den Brink, W. (2005) · Verslaving · doi:10.1007/bf03075325 · Cited by 17
Cocaine induces the expression of homer 1b/c, homer 3a/b, and hsp 27 proteins in rat cerebellum
Dietrich, J., Arpin‐Bott, M., Kao, D., Dirrig‐Grosch, S., Aunis, D., & Zwiller, J. (2007) · Synapse · doi:10.1002/syn.20412 · Cited by 16
Efficacy of Buprenorphine/Naloxone Rapidly Dissolving Sublingual Tablets (BNX-RDT) After Switching From BNX Sublingual Film
Gunderson, E. W., & Sumner, M. (2016) · Journal of Addiction Medicine · doi:10.1097/adm.0000000000000201 · Cited by 15
Baseline Substance Use Interferes with Maintenance of HIV Medication Adherence Skills
Dale, S. K., Traeger, L. N., O’Cleirigh, C. M., Bedoya, C. A., Pinkston, M. M., Wilner, J. G., Stein, M. D., & Safren, S. A. (2016) · AIDS Patient Care and STDs · doi:10.1089/apc.2015.0340 · Cited by 15
Social Isolation Blunted the Response of Mesocortical Dopaminergic Neurons to Chronic Ethanol Voluntary Intake
Lallai, V., Manca, L., & Dazzi, L. (2016) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2016.00155 · Cited by 14
PET and SPECT in Drug and Substance Abuse
Mena, J. C., Cuellar, H., Vargas, D., & Riascos, R. (2005) · Topics in Magnetic Resonance Imaging · doi:10.1097/01.rmr.0000192177.01789.c0 · Cited by 14
Oral methylphenidate challenge selectively decreases putaminal T2 in healthy subjects
Silveri, M. M., Anderson, C. M., McNeil, J. F., Diaz, C. I., Lukas, S. E., Mendelson, J. H., Renshaw, P. F., & Kaufman, M. J. (2004) · Drug and Alcohol Dependence · doi:10.1016/j.drugalcdep.2004.04.016 · Cited by 14
Drug use as consumer behavior
Foxall, G. R., & Sigurðsson, V. (2011) · Behavioral and Brain Sciences · doi:10.1017/s0140525x11000707 · Cited by 14
Towards a neuroscience of attention-deficit/hyperactivity disorder: Fractionating the phenotype
Castellanos, F. X., Glaser, P. E. A., & Gerhardt, G. A. (2006) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2005.11.002 · Cited by 13
The effect of placebo on endurance capacity in normal weight children – a randomized trial
Fanti‐Oren, S., Birenbaum‐Carmeli, D., Eliakim, A., Pantanowitz, M., & Nemet, D. (2019) · BMC Pediatrics · doi:10.1186/s12887-019-1394-x · Cited by 13
Sacramental and spiritual use of hallucinogenic drugs
Móró, L., & Noreika, V. (2011) · Behavioral and Brain Sciences · doi:10.1017/s0140525x11000768 · Cited by 13
HMG-CoA synthase 2 drives brain metabolic reprogramming in cocaine exposure
Shao, X., Tang, Y., Long, H., Gu, H., Zhang, J., Deng, P., Zhao, Y., & Cen, X. (2017) · Neuropharmacology · doi:10.1016/j.neuropharm.2017.10.001 · Cited by 13
Abnormal Brain Networks Related to Drug and Nondrug Reward Anticipation and Outcome Processing in Stimulant Use Disorder: A Functional Connectomics Approach
Nestor, L. J., & Ersche, K. D. (2022) · Biological Psychiatry Cognitive Neuroscience and Neuroimaging · doi:10.1016/j.bpsc.2022.08.014 · Cited by 11
Placebo for a single night improves sleep in patients with objective insomnia.
Rogev, E., & Pillar, G. (2013) · PubMed · Cited by 12
The placebo response in conditions other than pain
Colloca, L., Lopiano, L., Benedetti, F., & Lanotte, M. (2005) · Seminars in Pain Medicine · doi:10.1016/j.spmd.2005.02.006 · Cited by 12
Sex-Dependent Alterations of Regional Homogeneity in Cigarette Smokers
Wen, Z., Han, X., Wang, Y., Ding, W., Sun, Y., Kang, Y., Zhou, Y., Lei, H. C., & Lin, F. (2022) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2022.874893 · Cited by 12
Presentation of Smoking-Associated Cues Does Not Elicit Dopamine Release after One-Hour Smoking Abstinence: A [11C]-(+)-PHNO PET Study
Chiuccariello, L., Boileau, I., Guranda, M., Rusjan, P., Wilson, A. A., Zawertailo, L. A., Houle, S., Busto, U. E., & Foll, B. L. (2013) · PLoS ONE · doi:10.1371/journal.pone.0060382 · Cited by 12
Neural underpinnings of expecting alcohol: Placebo alcohol administration alters nucleus accumbens resting state functional connectivity
Kirsch, D. E., Le, V.-H., Kosted, R., Fromme, K., & Lippard, E. (2022) · Behavioural Brain Research · doi:10.1016/j.bbr.2022.114148 · Cited by 10
Cognitive Disruptions in Drug Addiction: A Focus on the Prefrontal Cortex
Goldstein, R. Z., Moeller, S. J., & Volkow, N. D. (2011) · Wiley eBooks · doi:10.1002/9781119998938.ch8 · Cited by 10
Self-citation
Clinical Health Psychology
Weinman, J. A., O’Carroll, R. E., & Petrie, K. J. (2011) · Wiley eBooks · doi:10.1002/9781444395150.ch3 · Cited by 10
Limbic activation to novel versus familiar food cues predicts food preference and alcohol intake
Michaelides, M., Miller, M. L., Subrize, M., Kim, R., Robison, L. S., Hurd, Y. L., Wang, G., Volkow, N. D., & Thanos, P. K. (2013) · Brain Research · doi:10.1016/j.brainres.2013.03.006 · Cited by 9
Self-citation
The Blinded-Dose Purchase Task: assessing hypothetical demand based on cocaine, methamphetamine, and alcohol administration
Berry, M. S., Naudé, G. P., Johnson, P. S., & Johnson, M. W. (2023) · Psychopharmacology · doi:10.1007/s00213-023-06334-6 · Cited by 9
Effect of expectation on pain assessment of lower- and higher-intensity stimuli
Ružić, V., Ivanec, D., & Stanke, K. M. (2016) · Scandinavian Journal of Pain · doi:10.1016/j.sjpain.2016.09.013 · Cited by 10

Authors: Volkow, N. D., Wang, G.-J., Ma, Y., Fowler, J. S., Zhu, W., Maynard, L., Telang, F., Vaska, P., Ding, Y.-S., Wong, C., & Swanson, J. M.
Affiliations: State University of New York (US)
ORCID: Volkow, Nora D.
Wang, Gene-Jack
Zhu, Wei
Vaska, Paul
Ding, Yu-Shin
Wong, Christopher
Swanson, James M.
Venue: The Journal of Neuroscience
Publisher: Society for Neuroscience
Published: 2003-12-10
Volume: 23
Issue: 36
Pages: 11461-11468
ISSN: 0270-6474 (ISSN-L)
1529-2401
DOI: 10.1523/jneurosci.23-36-11461.2003
PMC: PMC6740524
OpenAlex: W1498104517
Cited by: 302
References: 48
Citations by year: 2025: 1 · 2024: 2 · 2023: 12 · 2022: 9 · 2021: 6 · 2020: 5 · 2019: 14 · 2018: 8 · 2017: 11 · 2016: 20 · 2015: 12 · 2014: 22 · 2013: 20 · 2012: 14
FWCI: 4.75
Type: journal article
Language: en
Open access: hybrid
doi.org
Licence: cc-by-nc-sa
creativecommons.org/licenses/by-nc-sa/4.0/ (vor, 183 d)
Locations: Journal of Neuroscience (publishedVersion, cc-by-nc-sa)
Europe PMC (PubMed Central) (publishedVersion)
PubMed Central (publishedVersion)
PubMed (publishedVersion)
Funders: U.S. Department of Energy
National Institute on Drug Abuse (DA 00280, K20DA000280, DA7092-01)
Biological and Environmental Research
Topics: Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
Life Sciences › Neuroscience › Cognitive Neuroscience › Neural and Behavioral Psychology Studies
Health Sciences › Medicine › Epidemiology › Substance Abuse Treatment and Outcomes
Keywords: expectations, cocaine abusers, methylphenidate, drug reinforcement, conditioned response, brain glucose metabolism, thalamus, cerebellum, orbitofrontal cortex, stimulants
MeSH terms: Adult, Central Nervous System Stimulants, Brain, Conditioning, Psychological, Female, Glucose, Humans, Male, Methylphenidate, Reinforcement, Psychology, Tomography, Emission-Computed, Cocaine-Related Disorders

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

Expectation Enhances the Regional Brain Metabolic and the Reinforcing Effects of Stimulants in Cocaine Abusers

Abstract

Overview

Integrity signals

Verification

Claims the paper makes

Claims other papers make about this one

Self-check

Citations

Cites

Cited by

Related

Metadata

Record

About these checks