The Neurobiology of Cocaine Addiction

Molecular basis of long-term plasticity underlying addiction

Nestler, E. J. (2001) · Nature reviews. Neuroscience · doi:10.1038/35053570 · Cited by 1,857 · see citing works

Incentive-sensitization and addiction

Robinson, T. E., & Berridge, K. C. (2001) · Addiction · doi:10.1046/j.1360-0443.2001.9611038.x · Cited by 1,435 · see citing works

Addiction and the brain: The neurobiology of compulsion and its persistence

Hyman, S. E., & Malenka, R. C. (2001) · Nature reviews. Neuroscience · doi:10.1038/35094560 · Cited by 1,297 · see citing works

Neuroscience of addiction

Koob, G. F., Sanna, P. P., & Bloom, F. E. (1998) · Neuron · doi:10.1016/s0896-6273(00)80557-7 · Cited by 1,026 · see citing works

The addicted human brain: insights from imaging studies

Volkow, N. D., Fowler, J. S., & Wang, G.-J. (2003) · Journal of Clinical Investigation · doi:10.1172/jci18533 · Cited by 916 · see citing works

ΔFosB: A sustained molecular switch for addiction

Nestler, E. J., Barrot, M., & Self, D. W. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.191352698 · Cited by 640 · cited 3× · see citing works

Regulation of gene expression and cocaine reward by CREB and ΔFosB

McClung, C. A., & Nestler, E. J. (2003) · Nature Neuroscience · doi:10.1038/nn1143 · Cited by 625 · see citing works

Brain circuitry and the reinstatement of cocaine-seeking behavior

Kalivas, P., & McFarland, K. (2003) · Psychopharmacology · doi:10.1007/s00213-003-1393-2 · Cited by 613 · see citing works

ΔFosB: a molecular switch for long-term adaptation in the brain

McClung, C. A., Ulery, P. G., Perrotti, L. I., Zachariou, V., Berton, O., & Nestler, E. J. (2004) · Molecular Brain Research · doi:10.1016/j.molbrainres.2004.05.014 · Cited by 398 · see citing works

The Addicted Brain

Nestler, E. J., & Malenka, R. C. (2004) · Scientific American · doi:10.1038/scientificamerican0304-78 · Cited by 172 · see citing works

Research Advances in the Understanding and Treatment of Addiction

O’Brien, C. P. (2003) · American Journal on Addictions · doi:10.1111/j.1521-0391.2003.tb00555.x · Cited by 75 · see citing works

Probability and predictors of transition from first use to dependence on nicotine, alcohol, cannabis, and cocaine: Results of the National Epidemiologic Survey on Alcohol and Related Conditions (NESARC)

Lopez‐Quintero, C., Cobos, J. P. D. L., Hasin, D. S., Okuda, M., Wang, S., Grant, B. F., & Blanco, C. (2010) · Drug and Alcohol Dependence · doi:10.1016/j.drugalcdep.2010.11.004 · Cited by 702 · see citing works

Epigenetic regulation of brain region-specific microglia clearance activity

Ayata, P., Badimon, A., Strasburger, H. J., Duff, M. K., Montgomery, S. E., Loh, Y.-H. E., Ebert, A., Pimenova, A. A., Ramirez, B. R., Chan, A. T., et al. (2018) · Nature Neuroscience · doi:10.1038/s41593-018-0192-3 · Cited by 460 · see citing works

Neurobiology of addiction

Goodman, A. (2007) · Biochemical Pharmacology · doi:10.1016/j.bcp.2007.07.030 · Cited by 412 · see citing works

Targeting voltage-gated calcium channels in neurological and psychiatric diseases

Zamponi, G. W. (2015) · Nature Reviews Drug Discovery · doi:10.1038/nrd.2015.5 · Cited by 371 · see citing works

Voices from within: gut microbes and the CNS

Forsythe, P., & Kunze, W. A. (2013) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-012-1028-z · Cited by 336 · see citing works

The Cardiovascular Effects of Cocaine

Havakuk, O., Rezkalla, S. H., & Kloner, R. A. (2017) · Journal of the American College of Cardiology · doi:10.1016/j.jacc.2017.05.014 · Cited by 243 · see citing works

Early Phase in the Development of Cannabidiol as a Treatment for Addiction: Opioid Relapse Takes Initial Center Stage

Hurd, Y. L., Yoon, M. J., Manini, A. F., Hernandez, S. H., Olmedo, R., Östman, M., & Jutras‐Aswad, D. (2015) · Neurotherapeutics · doi:10.1007/s13311-015-0373-7 · Cited by 167 · see citing works

Regulation of dopamine transporter function by protein‐protein interactions: new discoveries and methodological challenges

Eriksen, J., Jørgensen, T. N., & Gether, U. (2010) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2010.06599.x · Cited by 141 · see citing works

G protein-coupled receptor kinases as regulators of dopamine receptor functions

Gurevich, E. V., Gainetdinov, R. R., & Gurevich, V. V. (2016) · Pharmacological Research · doi:10.1016/j.phrs.2016.05.010 · Cited by 139 · see citing works

Adolescent drug exposure: A review of evidence for the development of persistent changes in brain function

Salmanzadeh, H., Ahmadi‐Soleimani, S. M., Pachenari, N., Azadi, M., Halliwell, R. F., Rubino, T., & Azizi, H. (2020) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2020.01.007 · Cited by 146 · see citing works

Borderline personality disorder: a dysregulation of the endogenous opioid system?

Bandelow, B., Schmahl, C., Falkai, P., & Wedekind, D. (2010) · Psychological Review · doi:10.1037/a0018095 · Cited by 135 · see citing works

Glutamate-Mediated Excitotoxicity in the Pathogenesis and Treatment of Neurodevelopmental and Adult Mental Disorders

Nicosia, N., Giovenzana, M., Misztak, P., Mingardi, J., & Musazzi, L. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25126521 · Cited by 135 · see citing works

Attomole quantification and global profile of RNA modifications: Epitranscriptome of human neural stem cells

Basanta‐Sanchez, M., Temple, S., Ansari, S. A., D'Amico, A., & Agris, P. F. (2015) · Nucleic Acids Research · doi:10.1093/nar/gkv971 · Cited by 117 · see citing works

In vitro modeling of the human dopaminergic system using spatially arranged ventral midbrain–striatum–cortex assembloids

Reumann, D., Krauditsch, C., Novatchkova, M., Sozzi, E., Wong, S. N., Zabolocki, M., Priouret, M., Doleschall, B., Ritzau‐Reid, K. I., Piber, M., et al. (2023) · Nature Methods · doi:10.1038/s41592-023-02080-x · Cited by 113 · see citing works

Dopamine D1 Receptors, Regulation of Gene Expression in the Brain, and Neurodegeneration

Cadet, J. L., Jayanthi, S., McCoy, M. T., Beauvais, G., & Cai, N. S. (2010) · CNS & Neurological Disorders - Drug Targets · doi:10.2174/187152710793361496 · Cited by 109 · see citing works

Nicotine-induced behavioral sensitization is associated with extracellular dopamine release and expression of c-Fos in the striatum and nucleus accumbens of the rat

Shim, I., Javaid, J. I., Wirtshafter, D., Jang, S.-Y., Shin, K.-H., Lee, H., Chung, Y.-C., & Chun, B. (2001) · Behavioural Brain Research · doi:10.1016/s0166-4328(01)00161-9 · Cited by 102 · see citing works

Inhibition of aldehyde dehydrogenase-2 suppresses cocaine seeking by generating THP, a cocaine use–dependent inhibitor of dopamine synthesis

Yao, L., Fan, P., Arolfo, M. P., Jiang, Z., Olive, M. F., Zablocki, J. A., Sun, H.-L., Chu, N., Lee, J., Kim, H., et al. (2010) · Nature Medicine · doi:10.1038/nm.2200 · Cited by 99 · see citing works

ΔFosB in the nucleus accumbens is critical for reinforcing effects of sexual reward

Pitchers, K. K., Frohmader, K. S., Vialou, V., Mouzon, E., Nestler, E. J., Lehman, M. N., & Coolen, L. M. (2010) · Genes Brain & Behavior · doi:10.1111/j.1601-183x.2010.00621.x · Cited by 87 · see citing works

Cocaine craving and attentional bias in cocaine-dependent schizophrenic patients

Copersino, M. L., Serper, M. R., Vadhan, N. P., Goldberg, B. R., Richarme, D., Chou, J. C.-Y., Stitzer, M. L., & Cancro, R. (2004) · Psychiatry Research · doi:10.1016/j.psychres.2004.07.006 · Cited by 85 · see citing works

The effects of Beta-Endorphin: state change modification

Veening, J. G., & Barendregt, H. P. (2015) · Fluids and Barriers of the CNS · doi:10.1186/2045-8118-12-3 · Cited by 84 · see citing works

Fos After Single and Repeated Self-Administration of Cocaine and Saline in the Rat: Emphasis on the Basal Forebrain and Recalibration of Expression

Zahm, D. S., Becker, M. L., Freiman, A. J., Strauch, S., DeGarmo, B., Geisler, S., Meredith, G. E., & Marinelli, M. (2009) · Neuropsychopharmacology · doi:10.1038/npp.2009.149 · Cited by 81 · see citing works

DARK Classics in Chemical Neuroscience: Cocaine

Drake, L. R., & Scott, P. J. H. (2018) · ACS Chemical Neuroscience · doi:10.1021/acschemneuro.8b00117 · Cited by 80 · see citing works

Discovery of Drugs to Treat Cocaine Dependence: Behavioral and Neurochemical Effects of Atypical Dopamine Transport Inhibitors

Tanda, G., Newman, A. H., & Katz, J. L. (2009) · Advances in pharmacology · doi:10.1016/s1054-3589(08)57007-4 · Cited by 77 · see citing works

Drug addiction: from bench to bedside

Cheron, J., & Kerchove d’Exaerde, A. D. (2021) · Translational Psychiatry · doi:10.1038/s41398-021-01542-0 · Cited by 75 · see citing works

Biosynthesis and synthetic biology of psychoactive natural products

Jamieson, C. S., Misa, J., Tang, Y., & Billingsley, J. M. (2021) · Chemical Society Reviews · doi:10.1039/d1cs00065a · Cited by 71 · see citing works

Cocaine elicits autophagic cytotoxicity via a nitric oxide-GAPDH signaling cascade

Guha, P., Harraz, M. M., & Snyder, S. H. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1524860113 · Cited by 70 · see citing works

From controlled to compulsive drug-taking: The role of the habenula in addiction

Mathis, V., & Kenny, P. J. (2018) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2018.06.018 · Cited by 71 · see citing works

Cocaine Induces Inflammatory Gut Milieu by Compromising the Mucosal Barrier Integrity and Altering the Gut Microbiota Colonization

Chivero, E. T., Ahmad, R., Thangaraj, A., Periyasamy, P., Kumar, B., Kroeger, E., Feng, D., Guo, M., Roy, S., Dhawan, P., et al. (2019) · Scientific Reports · doi:10.1038/s41598-019-48428-2 · Cited by 70 · see citing works

Activation of Dopamine D1-D2 Receptor Complex Attenuates Cocaine Reward and Reinstatement of Cocaine-Seeking through Inhibition of DARPP-32, ERK, and ΔFosB

Hasbi, A., Perreault, M. L., Shen, M. Y. F., Fan, T., Nguyen, T., Alijaniaram, M., Banasikowski, T. J., Grace, A. A., O’Dowd, B. F., Fletcher, P. J., et al. (2018) · Frontiers in Pharmacology · doi:10.3389/fphar.2017.00924 · Cited by 65 · see citing works

Effects of nicotine on homeostatic and hedonic components of food intake

Stojakovic, A., Espinosa, E. V. P., Farhad, O. T., & Lutfy, K. (2017) · Journal of Endocrinology · doi:10.1530/joe-17-0166 · Cited by 65 · see citing works

The Cambridge Handbook of Substance and Behavioral Addictions

Sussman, S. Y. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108632591 · Cited by 63 · see citing works

Volume transmission of beta-endorphin via the cerebrospinal fluid; a review

Veening, J., Gerrits, P., & Barendregt, H. (2012) · Fluids and Barriers of the CNS · doi:10.1186/2045-8118-9-16 · Cited by 61 · see citing works

Cocaine'omics: Genome‐wide and transcriptome‐wide analyses provide biological insight into cocaine use and dependence

Huggett, S. B., & Stallings, M. C. (2019) · Addiction Biology · doi:10.1111/adb.12719 · Cited by 53 · see citing works

Dopamine inhibits GABAA currents in ventral tegmental area dopamine neurons via activation of presynaptic G-protein coupled inwardly-rectifying potassium channels

Michaeli, A., & Yaka, R. (2009) · Neuroscience · doi:10.1016/j.neuroscience.2009.11.045 · Cited by 58 · see citing works

Persistent effects of obesity: A neuroplasticity hypothesis

Matikainen‐Ankney, B. A., & Kravitz, A. V. (2018) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.13665 · Cited by 56 · see citing works

Convergent pharmacological mechanisms in impulsivity and addiction: insights from rodent models

Jupp, B., & Dalley, J. W. (2014) · British Journal of Pharmacology · doi:10.1111/bph.12787 · Cited by 56 · see citing works

Effects of cocaine and withdrawal on the mouse nucleus accumbens transcriptome

Eipper-Mains, J. E., Kiraly, D. D., Duff, M. O., Horowitz, M., McManus, C. J., Eipper, B. A., Graveley, B. R., & Mains, R. E. (2012) · Genes Brain & Behavior · doi:10.1111/j.1601-183x.2012.00873.x · Cited by 51 · see citing works

Changes in microRNA expression profile in hippocampus during the acquisition and extinction of cocaine-induced conditioned place preference in rats

Chen, C., Liu, H., & Guan, X. (2013) · Journal of Biomedical Science · doi:10.1186/1423-0127-20-96 · Cited by 56 · see citing works

Differential regulation of ionotropic glutamate receptor subunits following cocaine self-administration

Hemby, S. E., Horman, B. M., & Tang, W. (2005) · Brain Research · doi:10.1016/j.brainres.2005.09.051 · Cited by 56 · see citing works

Dysregulation of cannabinoid CB1 receptor and associated signaling networks in brains of cocaine addicts and cocaine-treated rodents

Álvaro-Bartolomé, M., & Garcı́a-Sevilla, J. A. (2013) · Neuroscience · doi:10.1016/j.neuroscience.2013.05.035 · Cited by 54 · see citing works

Structural plasticity of the brain to psychostimulant use

Nyberg, F. (2014) · Neuropharmacology · doi:10.1016/j.neuropharm.2014.07.004 · Cited by 49 · see citing works

Addiction and the kynurenine pathway: A new dancing couple?

Morales‐Puerto, N., Giménez‐Gómez, P., Pérez‐Hernández, M., Abuin-Martínez, C., de Biedma‐Elduayen, L. G., Vidal, R., Gutiérrez‐López, M. D., O’Shea, E., & Colado, M. I. (2021) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2021.107807 · Cited by 52 · see citing works

Behavioral Economic Considerations of Novel Addictions and Nonaddictive Behavior: Research and Analytic Methods

Reed, D. D., Naudé, G. P., Gelino, B. W., & Amlung, M. T. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108632591.011 · Cited by 48 · see citing works

Exposure to a diet high in fat attenuates dendritic spine density in the medial prefrontal cortex

Dingess, P. M., Darling, R. A., Dolence, E. K., Culver, B. W., & Brown, T. E. (2016) · Brain Structure and Function · doi:10.1007/s00429-016-1208-y · Cited by 49 · see citing works

CRHCeA→VTA inputs inhibit the positive ensembles to induce negative effect of opiate withdrawal

Jiang, C., Yang, X., He, G., Wang, Z., Wang, Z., Xu, W., Ma, L., Ma, L., & Wang, F. (2021) · Molecular Psychiatry · doi:10.1038/s41380-021-01321-9 · Cited by 47 · see citing works

The Resurrection of Phenotypic Drug Discovery

Childers, W. E., Elokely, K. M., & Abou-Gharbia, M. A. (2020) · ACS Medicinal Chemistry Letters · doi:10.1021/acsmedchemlett.0c00006 · Cited by 45 · see citing works

Cocaine-induced adaptations in metabotropic inhibitory signaling in the mesocorticolimbic system

Hearing, M. C., Zink, A. N., & Wickman, K. D. (2012) · Reviews in the Neurosciences · doi:10.1515/revneuro-2012-0045 · Cited by 47 · see citing works

Disruption of a dopamine receptor complex amplifies the actions of cocaine

Perreault, M. L., Hasbi, A., Shen, M. Y. F., Fan, T., Navarro, G., Fletcher, P. J., Franco, R., Lanciego, J. L., & George, S. R. (2016) · European Neuropsychopharmacology · doi:10.1016/j.euroneuro.2016.07.008 · Cited by 47 · see citing works

Immediate-Early Genes Modulation by Antipsychotics: Translational Implications for a Putative Gateway to Drug-Induced Long-Term Brain Changes

de Bartolomeis, A., Buonaguro, E. F., Latte, G., Rossi, R., Marmo, F., Iasevoli, F., & Tomasetti, C. (2017) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2017.00240 · Cited by 44 · see citing works

The Prevention and Treatment of Gambling Disorders: Some Art, Some Science

Derevensky, J. L. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108632591.024 · Cited by 45 · see citing works

Considering the Overlap and Nonoverlap of Compulsivity, Impulsivity, and Addiction

Blum, A. W., & Grant, J. E. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108632591.038 · Cited by 44 · see citing works

Neurobiological Foundations of Behavioral Addictions

Vaccaro, A. G., & Potenza, M. N. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108632591.016 · Cited by 45 · see citing works

Neurobiology of Substance Addictions

Christie, N. C., & Bechara, A. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108632591.015 · Cited by 44 · see citing works

Sensitization of Incentive Salience and the Transition to Addiction

Warlow, S. M., Baumgartner, H. M., Freeland, C. M., Naffziger, E. E., Olney, J. J., Berridge, K. C., & Robinson, M. J. F. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108632591.006 · Cited by 45 · see citing works

HIV-1 proteins dysregulate motivational processes and dopamine circuitry

Bertrand, S. J., Mactutus, C. F., Harrod, S. B., Moran, L. M., & Booze, R. M. (2018) · Scientific Reports · doi:10.1038/s41598-018-25109-0 · Cited by 40 · see citing works

Mindfulness-Based Interventions Applied to Addiction Treatments

Kechter, A., & Black, D. S. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108632591.040 · Cited by 43 · see citing works

Multiple Memory Systems, Addiction, and Health Habits: New Routes for Translational Science

Stacy, A. W., Pike, J. R., & Lee, A. Y. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108632591.017 · Cited by 43 · see citing works

Tanning as an Addiction: The State of the Research and Implications for Intervention

Miller, K. A., & Mays, D. M. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108632591.037 · Cited by 43 · see citing works

Food versus Eating Addictions

Schulte, E. M., Schiestl, E. T., & Gearhardt, A. N. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108632591.035 · Cited by 43 · see citing works

How Does the Brain Implement Adaptive Decision Making to Eat?

Compan, V., Walsh, B. T., Kaye, W. H., & Geliebter, A. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.2602-15.2015 · Cited by 43 · see citing works

Behavioral Economics and Addictive Disorders

Jarmolowicz, D. P., & Schneider, T. D. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108632591.005 · Cited by 42 · see citing works

Prevention and Treatment of Compulsive Buying Disorder

Galimov, A., & Black, D. W. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108632591.027 · Cited by 42 · see citing works

Precision Behavioral Management (PBM): A Novel Genetically Guided Therapy to Combat Reward Deficiency Syndrome (RDS) Relevant to the Opiate Crisis

Blum, K., Roy, A. K., Podesta, A., Modestino, E. J., Steinberg, B., Gondré-Lewis, M. C., Baron, D. A., Thanos, P. K., Lott, L., Badgaiyan, S., et al. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108632591.031 · Cited by 42 · see citing works

Prevention and Treatment of “Food Addiction”

Davis, C., & Mason, A. E. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108632591.023 · Cited by 42 · see citing works

Human Neurobiological Approaches to Hedonically Motivated Behaviors

Burger, K. S., Shearrer, G. E., & Sadler, J. R. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108632591.009 · Cited by 42 · see citing works

Feedback Models for Gambling Control: The Use and Efficacy of Online Responsible Gambling Tools

Griffiths, M. D. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108632591.034 · Cited by 42 · see citing works

How machine learning is used to study addiction in digital healthcare: A systematic review

Chhetri, B., Goyal, L. M., & Mittal, M. (2023) · International Journal of Information Management Data Insights · doi:10.1016/j.jjimei.2023.100175 · Cited by 42 · see citing works

Adolescent Cocaine Exposure Causes Enduring Macroscale Changes in Mouse Brain Structure

Wheeler, A. L., Lerch, J. P., Chakravarty, M. M., Friedel, M., Sled, J. G., Fletcher, P. J., Josselyn, S. A., & Frankland, P. W. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.3830-12.2013 · Cited by 44 · see citing works

The Neurochemistry of Tourette Syndrome

Singer, H. S. (2013) · Oxford University Press eBooks · doi:10.1093/med/9780199796267.003.0013 · Cited by 41 · see citing works

Selective inhibition of M 5 muscarinic acetylcholine receptors attenuates cocaine self‐administration in rats

Gunter, B. W., Gould, R. W., Bubser, M., McGowan, K. M., Lindsley, C. W., & Jones, C. K. (2017) · Addiction Biology · doi:10.1111/adb.12567 · Cited by 39 · see citing works

Animal Models of Drug Addiction

Belin‐Rauscent, A., & Belin, D. (2012) · InTech eBooks · doi:10.5772/52079 · Cited by 39 · see citing works

Possible role of a dysregulation of the endogenous opioid system in antisocial personality disorder

Bandelow, B., & Wedekind, D. (2015) · Human Psychopharmacology Clinical and Experimental · doi:10.1002/hup.2497 · Cited by 36 · see citing works

Selective Enhancement of Dopamine Release in the Ventral Pallidum of Methamphetamine-Sensitized Mice

Stout, K. A., Dunn, A. R., Lohr, K. M., Alter, S. P., Cliburn, R. A., Guillot, T. S., & Miller, G. W. (2016) · ACS Chemical Neuroscience · doi:10.1021/acschemneuro.6b00131 · Cited by 36 · see citing works

Diminished Role of Dopamine D1-Receptor Signaling with the Development of an Addicted Phenotype in Rats

Ramôa, C. P., Doyle, S. E., Lycas, M. D., Chernau, A. K., & Lynch, W. J. (2013) · Biological Psychiatry · doi:10.1016/j.biopsych.2013.09.028 · Cited by 36 · see citing works

Cognitive and neuroanatomical impairments associated with chronic exposure to levamisole-contaminated cocaine

Vonmoos, M., Hirsiger, S., Preller, K. H., Hulka, L. M., Allemann, D., Herdener, M., Baumgartner, M. R., & Quednow, B. B. (2018) · Translational Psychiatry · doi:10.1038/s41398-018-0279-3 · Cited by 35 · see citing works

The ubiquitin-proteasome system and learning-dependent synaptic plasticity – A 10 year update

Patrick, M. B., Omar, N., Werner, C. T., Mitra, S., & Jarome, T. J. (2023) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2023.105280 · Cited by 35 · see citing works

Cocaine-mediated circadian reprogramming in the striatum through dopamine D2R and PPARγ activation

Brami‐Cherrier, K., Lewis, R. G., Cervantes, M., Liu, Y., Tognini, P., Baldi, P., Sassone‐Corsi, P., & Borrelli, E. (2020) · Nature Communications · doi:10.1038/s41467-020-18200-6 · Cited by 34 · see citing works

Behavioural, biochemical and molecular changes induced by chronic crack-cocaine inhalation in mice: The role of dopaminergic and endocannabinoid systems in the prefrontal cortex

Areal, L. B., Rodrigues, L. C. M., Andrich, F., de Moraes, L. S., Cicilini, M. A., Mendonça, J. B., Pelição, F. S., Nakamura-Palacios, E. M., Martins-Silva, C., & Pires, R. G. W. (2015) · Behavioural Brain Research · doi:10.1016/j.bbr.2015.04.036 · Cited by 34 · see citing works

Characterization of the Brain Functional Architecture of Psychostimulant Withdrawal Using Single-Cell Whole-Brain Imaging

Kimbrough, A., Smith, L. C., Kallupi, M., Simpson, S., Collazo, A., & George, O. (2021) · eNeuro · doi:10.1523/eneuro.0208-19.2021 · Cited by 33 · see citing works

Cocaine Self-administration and Extinction Inversely Alter Neuron to Glia Exosomal Dynamics in the Nucleus Accumbens

Jarvis, R., Orrego, A. T., Promes, V., Tu, L., Shi, J., & Yang, Y. (2020) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2019.00581 · Cited by 33 · see citing works

Narrative review on potential role of gut microbiota in certain substance addiction

Qin, C., Hu, J., Wan, Y., Cai, M., Wang, Z., Peng, Z., Liao, Y., Li, D., Yao, P., Liu, L., et al. (2021) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2020.110093 · Cited by 32 · see citing works

Cocaine Destroys Gray Matter Brain Cells and Accelerates Brain Aging

Beheshti, I. (2023) · Biology · doi:10.3390/biology12050752 · Cited by 32 · see citing works

Pharmacogenetics of Addiction Therapy

Nielsen, D. A., Nielsen, E. M., Dasari, T., & Spellicy, C. J. (2014) · Methods in molecular biology · doi:10.1007/978-1-4939-0956-8_15 · Cited by 31 · see citing works

Loss of functional specificity in the dorsal striatum of chronic cocaine users

Hanlon, C. A., Wesley, M. J., & Porrino, L. J. (2009) · Drug and Alcohol Dependence · doi:10.1016/j.drugalcdep.2009.01.005 · Cited by 31 · see citing works

Social rank-associated stress vulnerability predisposes individuals to cocaine attraction

Yanovich, C., Kirby, M. L., Michaelevski, I., Yadid, G., & Pinhasov, A. (2018) · Scientific Reports · doi:10.1038/s41598-018-19816-x · Cited by 31 · see citing works

Cognitive and emotional impairments in adults with attention-deficit/hyperactivity disorder and cocaine use

Wunderli, M. D., Vonmoos, M., Niedecker, S. M., Hulka, L. M., Preller, K. H., Baumgartner, M. R., Kræmer, T., Seifritz, E., Schaub, M. P., Eich‐Höchli, D., et al. (2016) · Drug and Alcohol Dependence · doi:10.1016/j.drugalcdep.2016.03.026 · Cited by 30 · see citing works

Arginine vasopressin gene expression changes within the nucleus accumbens during environment elicited cocaine-conditioned response in rats

Rodríguez-Borrero, E., Rivera-Escalera, F., Candelas, F., Montalvo, J. G., Muñoz-Miranda, W. J., Walker, J. R., & Maldonado-Vlaar, C. S. (2009) · Neuropharmacology · doi:10.1016/j.neuropharm.2009.06.040 · Cited by 30 · see citing works

LORETA Neurofeedback for Addiction and the Possible Neurophysiology of Psychological Processes Influenced: A Case Study and Region of Interest Analysis of LORETA Neurofeedback in Right Anterior Cingulate Cortex

Cannon, R. L., Lubar, J. F., Sokhadze, E. M., & Baldwin, D. R. (2008) · Journal of Neurotherapy · doi:10.1080/10874200802501948 · Cited by 30 · see citing works

Behavioral and neurobiological alterations induced by chronic use of crack cocaine

Rosário, B. D. A., de Nazaré, M. D. F. S., Estadella, D., Ribeiro, D. A., & Viana, M. D. B. (2019) · Reviews in the Neurosciences · doi:10.1515/revneuro-2018-0118 · Cited by 29 · see citing works

Cocaine-related DNA methylation in caudate neurons alters 3D chromatin structure of the IRXA gene cluster

Vaillancourt, K., Yang, J., Chen, G. G., Yerko, V., Théroux, J., Aouabed, Z., López, A. J., Thibeault, K. C., Calipari, E. S., Labonté, B., et al. (2020) · Molecular Psychiatry · doi:10.1038/s41380-020-00909-x · Cited by 29 · see citing works

Cocaethylene: When Cocaine and Alcohol Are Taken Together

Pergolizzi, J. V., Breve, F., Magnusson, P., LeQuang, J. A., & Varrassi, G. (2022) · Cureus · doi:10.7759/cureus.22498 · Cited by 29 · see citing works

Global Approaches to the Role of miRNAs in Drug-Induced Changes in Gene Expression

Eipper-Mains, J. E., Eipper, B. A., & Mains, R. E. (2012) · Frontiers in Genetics · doi:10.3389/fgene.2012.00109 · Cited by 28 · see citing works

Cooccurring Psychiatric and Substance Use Disorders

Robinson, Z. D., & Riggs, P. (2016) · Child and Adolescent Psychiatric Clinics of North America · doi:10.1016/j.chc.2016.05.005 · Cited by 28 · see citing works

Multifunctional Neural Probes Enable Bidirectional Electrical, Optical, and Chemical Recording and Stimulation In Vivo

Driscoll, N., Antonini, M., Cannon, T. M., Maretich, P., Olaitan, G. O., Van, V. D. P., Nagao, K., Sahasrabudhe, A., Paniagua, E. V., Frey, E. J., et al. (2024) · Advanced Materials · doi:10.1002/adma.202408154 · Cited by 29 · see citing works

Modulation and functions of dopamine receptor heteromers in drugs of abuse-induced adaptations

Andrianarivelo, A., Saint‐Jour, E., Walle, R., Trifilieff, P., & Vanhoutte, P. (2018) · Neuropharmacology · doi:10.1016/j.neuropharm.2018.12.003 · Cited by 27 · see citing works

Zwitterionic Polymer Coated and Aptamer Functionalized Flexible Micro-Electrode Arrays for In Vivo Cocaine Sensing and Electrophysiology

Wu, B., Castagnola, E., & Cui, X. T. (2023) · Micromachines · doi:10.3390/mi14020323 · Cited by 26 · see citing works

Lasting Reduction of Cocaine Action in Neostriatum— A Hydrolase Gene Therapy Approach

Gao, Y., & Brimijoin, S. (2009) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.109.152231 · Cited by 26 · see citing works

Binge Cocaine Administration in Adolescent Rats Affects Amygdalar Gene Expression Patterns and Alters Anxiety-Related Behavior in Adulthood

Daws, S. E., Black, Y. D., Naydenov, A. V., Vassoler, F. M., Hanlin, R. P., & Konradi, C. L. (2011) · Biological Psychiatry · doi:10.1016/j.biopsych.2011.03.035 · Cited by 25 · see citing works

Neural mechanisms of reproduction in females as a predisposing factor for drug addiction

Hedges, V. L., Staffend, N. A., & Meisel, R. L. (2010) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2010.02.003 · Cited by 26 · see citing works

Neuronal scaffolding protein spinophilin is integral for cocaine-induced behavioral sensitization and ERK1/2 activation

Areal, L. B., Hamilton, A., Martins-Silva, C., Pires, R. G. W., & Ferguson, S. S. G. (2019) · Molecular Brain · doi:10.1186/s13041-019-0434-7 · Cited by 25 · see citing works

NThe Neurobiology of Cocaine Addiction Cocaine

Nestler, E. J., & Ph., D. (2013)

4 • SCIENCE & PRACTICE PERSPECTIVES—DECEMBER 2005 NThe Neurobiology of Cocaine Addiction

Nestler, E. J., & Ph., D. (2012)

Neurobiology of Drug Addiction & The Treatment of Hard Drug Use Disorder

Sabbineni, A. (2021) · Quality in primary care · doi:10.36648/1479-1072.21.29.67

RevisiónNeurobiología de la cocaíneNeurobiology of cocaine's addiction

Moratalla, R. (2008) · Trastornos Adictivos

Expression of the transcription factor ΔFosB in the brain controls sensitivity to cocaine

Kelz, M. B., Chen, J., Carlezon, W. A., Whisler, K., Gilden, L., Beckmann, A. M., Steffen, C., Zhang, Y.-J., Marotti, L., Self, D. W., et al. (1999) · Nature · doi:10.1038/45790 · Cited by 641 · see citing works