The DOI matches its Crossref record; 94 of the 97 references it cites were found in a registry or an index.
The addicted synapse: mechanisms of synaptic and structural plasticity in nucleus accumbens
Open accessAbstract
Addictive drugs cause persistent restructuring of several neuronal cell types in the limbic regions of brain thought to be responsible for long-term behavioral plasticity driving addiction. Although these structural changes are well documented in nucleus accumbens medium spiny neurons, little is known regarding the underlying molecular mechanisms. Additionally, it remains unclear whether structural plasticity and its synaptic concomitants drive addictive behaviors or whether they reflect homeostatic compensations to the drug not related to addiction per se. Here, we discuss recent paradoxical data, which either support or oppose the hypothesis that drug-induced changes in dendritic spines drive addictive behavior. We define areas where future investigation can provide a more detailed picture of drug-induced synaptic reorganization, including ultrastructural, electrophysiological and behavioral studies.
Overview
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
Cites
Statistics
Verification
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?
The source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“According to this model there are distinguishable associative and nonassociative components of addiction, and the molecular mechanisms and neural substrates underlying these processes may overlap with those involved in canonical forms of memory (Anagnostaras and Robinson, 1996; Anagnostaras et al., 2002; Russo et al., 2010).”
From Proteasome phosphorylation regulates cocaine-induced sensitization (2018) · cites this paper as Russo et al., 2010
Experimental — accuracy not yet measured
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Long-Term Potentiation--A Decade of Progress?
Malenka, R. C., & Nicoll, A. R. A. (1999) · Science · doi:10.1126/science.285.5435.1870 · Cited by 2,729
Self-citationStructural basis of long-term potentiation in single dendritic spines
Matsuzaki, M., Honkura, N., Ellis-Davies, G. C. R., & Kasai, H. (2004) · Nature · doi:10.1038/nature02617 · Cited by 2,483
Ikemoto, S. (2007) · Brain Research Reviews · doi:10.1016/j.brainresrev.2007.05.004 · Cited by 1,477
Carlezon, W. A., Duman, R. S., & Nestler, E. J. (2005) · Trends in Neurosciences · doi:10.1016/j.tins.2005.06.005 · Cited by 1,382
Self-citationChanging subunit composition of heteromeric NMDA receptors during development of rat cortex
Sheng, M., Cummings, J., Roldan, L. A., Jan, Y. N., & Jan, L. Y. (1994) · Nature · doi:10.1038/368144a0 · Cited by 1,377
A translational profiling approach for the molecular characterization of CNS cell types
Heiman, M., Schaefer, A., Gong, S., Peterson, J. D., Day, M., Ramsey, K. E., Suárez-Fariñas, M., Schwarz, C., Stephan, D. A., Surmeier, D. J., et al. (2008) · Cell · doi:10.1016/j.cell.2008.10.028 · Cited by 1,134
Transient and persistent dendritic spines in the neocortex in vivo
Holtmaat, A. J. G. D., Trachtenberg, J. T., Wilbrecht, L., Shepherd, G. M., Zhang, X., Knott, G. W., & Svoboda, K. (2005) · Neuron · doi:10.1016/j.neuron.2005.01.003 · Cited by 1,131
Structural plasticity associated with exposure to drugs of abuse
Robinson, T. E., & Kolb, B. E. (2004) · Neuropharmacology · doi:10.1016/j.neuropharm.2004.06.025 · Cited by 1,130
Molecular mechanisms of drug addiction
Nestler, E. J. (2004) · Neuropharmacology · doi:10.1016/j.neuropharm.2004.06.031 · Cited by 1,108
Self-citationHarris, K. M., Jensen, F. E., & Tsao, B. (1992) · Journal of Neuroscience · doi:10.1523/jneurosci.12-07-02685.1992 · Cited by 1,036
Flagged first, then by citations
3 of the 97 references couldn’t be matched to a known paper.
Cited by
Sorted by citations
Items 301–400 of 654
Neuroadaptations and TGF-β signaling: emerging role in models of neuropsychiatric disorders
Mitra, S., Werner, C. T., & Dietz, D. (2021) · Molecular Psychiatry · doi:10.1038/s41380-021-01186-y · Cited by 29
Self-citationCalarco, C. A., Fox, M. E., Terheyden, S. V., Turner, M. D., Alipio, J. B., Chandra, R., & Lobo, M. K. (2021) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2021.737389 · Cited by 27
Roberts, A. J., Casal, L., Huitrón‐Reséndiz, S., Thompson, T., & Tarantino, L. M. (2018) · Psychopharmacology · doi:10.1007/s00213-018-4834-7 · Cited by 26
Modeling drug exposure in rodents using e-cigarettes and other electronic nicotine delivery systems
Miliano, C., Scott, E. R., Murdaugh, L. B., Gnatowski, E. R., Faunce, C. L., Anderson, M. S., Reyes, M. M., Gregus, A. M., & Buczynski, M. W. (2019) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2019.108458 · Cited by 26
Mango, D., & Ledonne, A. (2023) · Cells · doi:10.3390/cells12121588 · Cited by 25
Li, S., Lo, Y., Tseng, H.-Y., Lin, S.-H., Kuo, C., Chen, T.-C., Chang, C.-W., Liang, Y., Lin, Y.-C., Wang, C.-Y., et al. (2023) · Neurobiology of Stress · doi:10.1016/j.ynstr.2023.100566 · Cited by 29
Intravenous morphine self-administration alters accumbal microRNA profiles in the mouse brain
Im, H., Moon, C., & Kim, J. (2018) · Neural Regeneration Research · doi:10.4103/1673-5374.224374 · Cited by 25
Pharmacotherapeutic management of co-morbid alcohol and opioid use
Hood, L. E., Leyrer‐Jackson, J. M., & Olive, M. F. (2020) · Expert Opinion on Pharmacotherapy · doi:10.1080/14656566.2020.1732349 · Cited by 25
Gramage, E., Martín, Y. B., Ramanah, P., Pérez‐García, C., & Herradón, G. (2011) · Neuroscience · doi:10.1016/j.neuroscience.2011.06.014 · Cited by 24
Coccurello, R., Oliverio, A., & Mele, A. (2012) · Neuropsychopharmacology · doi:10.1038/npp.2011.296 · Cited by 24
Operant behavior to obtain palatable food modifies ERK activity in the brain reward circuit
Guegan, T., Cutando, L., Gangarossa, G., Santini, E., Fisone, G., Martínez, A., Valjent, E., Maldonado, R. J., & Martín, M. (2012) · European Neuropsychopharmacology · doi:10.1016/j.euroneuro.2012.04.009 · Cited by 25
Negrete‐Díaz, J. V., Shumilov, K., Real, M. A., Medina-Luque, J., Valderrama‐Carvajal, A., Flores, G., Moreno, A. R., & Rivera, A. (2019) · Neuropharmacology · doi:10.1016/j.neuropharm.2019.01.024 · Cited by 24
Liu, Z.-Q., Gu, X.-H., Yang, Y.-J., Yin, X.-P., Xu, L.-J., & Wang, W. (2016) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2016.02.002 · Cited by 23
Acute ketamine-induced neuroplasticity
Tedesco, V., Ravagnani, C., Bertoglio, D., & Chiamulera, C. (2013) · Neuroreport · doi:10.1097/wnr.0b013e32836131ad · Cited by 23
Becker, J. A. J., Pellissier, L. P., Corde, Y., Laboute, T., Léauté, A., Gandía, J., & Merrer, J. L. (2020) · Neuropsychopharmacology · doi:10.1038/s41386-020-00927-x · Cited by 21
Claussen, C. M., Chong, S. L., & Dafny, N. (2014) · Physiology & Behavior · doi:10.1016/j.physbeh.2014.02.024 · Cited by 23
The role of fibroblast growth factor 2 in drug addiction
Even‐Chen, O., & Barak, S. (2018) · European Journal of Neuroscience · doi:10.1111/ejn.14133 · Cited by 26
Mutation of MeCP2 alters transcriptional regulation of select immediate-early genes
Su, D., Cha, Y. M., & West, A. E. (2012) · Epigenetics · doi:10.4161/epi.7.2.18907 · Cited by 24
Epigenetic Regulation of Circadian Clocks and Its Involvement in Drug Addiction
Saad, L., Zwiller, J., Kalsbeek, A., & Anglard, P. (2021) · Genes · doi:10.3390/genes12081263 · Cited by 24
Cuesta, S., Batuecas, J., Severin, M. J., Funes, A., Rosso, S. B., & Pacchioni, A. M. (2016) · Journal of Neurochemistry · doi:10.1111/jnc.13863 · Cited by 23
Ceglia, I., Lee, K.-W., Cahill, M. E., Graves, S. M., Dietz, D., Surmeier, D. J., Nestler, E. J., Nairn, A. C., Greengard, P., & Kim, Y. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1621185114 · Cited by 21
Self-citationE3 Ubiquitin-Protein Ligase SMURF1 in the Nucleus Accumbens Mediates Cocaine Seeking
Werner, C. T., Viswanathan, R., Martin, J. A., Gobira, P. H., Mitra, S., Thomas, S. A., Wang, Z.-J., Liu, J., Stewart, A. F., Neve, R. L., et al. (2018) · Biological Psychiatry · doi:10.1016/j.biopsych.2018.07.013 · Cited by 22
Self-citationAMPK signaling in the nucleus accumbens core mediates cue-induced reinstatement of cocaine seeking
Gao, X., Yuan, K., Cao, L., Yan, W., Luo, Y., Jian, M., Liu, J., Fang, Q., Wang, J., Han, Y., et al. (2017) · Scientific Reports · doi:10.1038/s41598-017-01043-5 · Cited by 22
Vollmer, K. M., Doncheck, E. M., Grant, R. I., Winston, K. T., Romanova, E. V., Bowen, C. W., Siegler, P. N., Green, L. M., Bobadilla, A., Trujillo‐Pisanty, I., et al. (2021) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2021.744715 · Cited by 22
Fan, X., Li, D., Lichti, C. F., & Green, T. A. (2013) · PLoS ONE · doi:10.1371/journal.pone.0073689 · Cited by 21
Biever, A., Boubaker-Vitre, J., Cutando, L., Gracia‐Rubio, I., Costa‐Mattioli, M., Puighermanal, E., & Valjent, E. (2017) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2016.00165 · Cited by 23
Mouri, A., Noda, Y., Niwa, M., Matsumoto, Y., Mamiya, T., Nitta, A., Yamada, K., Furukawa, S., Iwamura, T., & Nabeshima, T. (2017) · Behavioural Brain Research · doi:10.1016/j.bbr.2017.04.052 · Cited by 21
Hamida, S. B., Laguesse, S., Morisot, N., Park, J., Phuamluong, K., Berger, A. L., Park, K. D., & Dorit Ron, A. (2018) · Addiction Biology · doi:10.1111/adb.12653 · Cited by 21
Glutamate delta-1 receptor regulates cocaine-induced plasticity in the nucleus accumbens
Liu, J., Gandhi, P. J., Pavuluri, R., Shelkar, G. P., & Dravid, S. M. (2018) · Translational Psychiatry · doi:10.1038/s41398-018-0273-9 · Cited by 25
Molecular Plasticity of the Nucleus Accumbens Revisited—Astrocytic Waves Shall Rise
Kardos, J., Dobolyi, Á., Szabó, Z. M., Simon, Á., Lourmet, G. S., Palkovits, M., & Héja, L. (2019) · Molecular Neurobiology · doi:10.1007/s12035-019-1641-z · Cited by 22
Boissoneault, J., Stennett, B., & Robinson, M. E. (2019) · Drug and Alcohol Dependence · doi:10.1016/j.drugalcdep.2019.107811 · Cited by 20
Cocaine produces conditioned place aversion in mice with a cocaine‐insensitive dopamine transporter
O’Neill, B., Tilley, M. R., & Gu, H. H. (2012) · Genes Brain & Behavior · doi:10.1111/j.1601-183x.2012.00872.x · Cited by 21
Mice lacking the galanin gene show decreased sensitivity to nicotine conditioned place preference
Neugebauer, N. M., Henehan, R. M., Hales, C. A., & Picciotto, M. R. (2010) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2010.12.015 · Cited by 20
Dias, C., Wang, Y. T., & Phillips, A. G. (2012) · Behavioural Brain Research · doi:10.1016/j.bbr.2012.05.026 · Cited by 21
Ieong, H. F.-H., & Yuan, Z. (2018) · Neurophotonics · doi:10.1117/1.nph.5.2.025011 · Cited by 20
Cocaine activates Rac1 to control structural and behavioral plasticity in caudate putamen
Li, J., Zhang, L., Chen, Z., Xie, M., Huang, L. H., Xue, J., Liu, Y., Liu, N., Guo, F., Zheng, Y., et al. (2015) · Neurobiology of Disease · doi:10.1016/j.nbd.2014.12.031 · Cited by 19
Ferrario, C. R., Goussakov, I. V., Stutzmann, G. E., & Wolf, M. E. (2012) · PLoS ONE · doi:10.1371/journal.pone.0040898 · Cited by 23
Constitutive Knockout of Kalirin-7 Leads to Increased Rates of Cocaine Self-Administration
Kiraly, D. D., Nemirovsky, N. E., LaRese, T. P., Tomek, S. E., Yahn, S. L., Olive, M. F., Eipper, B. A., & Mains, R. E. (2013) · Molecular Pharmacology · doi:10.1124/mol.113.087106 · Cited by 19
Sex-Dependent Ketamine Addiction-Like Behavior Profile Following Exposure to Chronic Mild Stress
Wright, K. N., Hagarty, D. P., Strong, C. E., Schoepfer, K. J., & Kabbaj, M. (2019) · Chronic Stress · doi:10.1177/2470547019832613 · Cited by 20
Jing, M., Ding, X., Han, X., Zhao, T.-Y., Luo, M., Wu, N., Li, J., & Song, R. (2022) · Acta Pharmacologica Sinica · doi:10.1038/s41401-022-00866-x · Cited by 18
Inhibition of PKC disrupts addiction-related memory
Howell, K., Monk, B., Carmack, S. A., Mrowczynski, O., Clark, R. E., & Anagnostaras, S. (2014) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2014.00070 · Cited by 19
Δ JunD overexpression in the nucleus accumbens prevents sexual reward in female Syrian hamsters
Been, L. E., Hedges, V. L., Vialou, V., Nestler, E. J., & Meisel, R. L. (2013) · Genes Brain & Behavior · doi:10.1111/gbb.12060 · Cited by 19
Self-citationDopamine receptor signaling in the forebrain
Savica, R., & Benarroch, E. E. (2014) · Neurology · doi:10.1212/wnl.0000000000000719 · Cited by 19
Hu, L., Jing, X., Cui, C., Xing, G., & Zhu, B. (2012) · Addiction Biology · doi:10.1111/adb.12010 · Cited by 19
Structural Plasticity on the SpiNNaker Many-Core Neuromorphic System
Bogdan, P., Rowley, A. G. D., Rhodes, O., & Furber, S. B. (2018) · Frontiers in Neuroscience · doi:10.3389/fnins.2018.00434 · Cited by 23
AAV Delivery of shRNA Against TRPC6 in Mouse Hippocampus Impairs Cognitive Function
Xie, R., Wang, Z., Liu, T., Xiao, R., Lv, K., Wu, C. F., Luo, Y., Cai, Y., & Fan, X. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.688655 · Cited by 19
Liang, M., Zhu, L., Wang, R., Su, H., Ma, D., Wang, H., & Chen, T. (2022) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2022.892757 · Cited by 18
Quantitative Mapping of Cocaine-Induced ΔFosB Expression in the Striatum of Male and Female Rats
Sato, S. M., Wissman, A. M., McCollum, A. F., & Woolley, C. S. (2011) · PLoS ONE · doi:10.1371/journal.pone.0021783 · Cited by 19
Inflexible ethanol intake: A putative link with the Lrrk2 pathway
Silva, D. A. D. S. E., Ribeiro, A. F., Damasceno, S., Rocha, C. S., de Matos, A. H. B., Boerngen-Lacerda, R., Correia, D., & Godard, A. L. B. (2016) · Behavioural Brain Research · doi:10.1016/j.bbr.2016.07.001 · Cited by 18
Miller, M. B., Yan, Y., Machida, K., Kiraly, D. D., Levy, A. D., Wu, Y. I., Lam, T. T., Abbott, T., Koleske, A. J., Eipper, B. A., et al. (2017) · ACS Chemical Neuroscience · doi:10.1021/acschemneuro.7b00076 · Cited by 18
Assessing the Role of Long Noncoding RNA in Nucleus Accumbens in Subjects With Alcohol Dependence
McMichael, G. O., Drake, J., Vornholt, E., Cresswell, K. G., Williamson, V. S., Chatzinakos, C., Mamdani, M., Hariharan, S., Kendler, K. S., Miles, M. F., et al. (2020) · Alcoholism Clinical and Experimental Research · doi:10.1111/acer.14479 · Cited by 19
FGF2 is an endogenous regulator of alcohol reward and consumption
Even‐Chen, O., Herburg, L., Kefalakes, E., Urshansky, N., Grothe, C., & Barak, S. (2021) · Addiction Biology · doi:10.1111/adb.13115 · Cited by 18
Frolov, A., Reyes-Vasquez, C., & Dafny, N. (2014) · Journal of Neurophysiology · doi:10.1152/jn.00633.2013 · Cited by 18
Gao, Y., Peng, S., Wen, Q., Zheng, C., Lin, J., Tan, Y., Ma, Y., Luo, Y., Xue, Y.-X., Wu, P., et al. (2014) · International Journal of Neuropsychopharmacology · doi:10.1017/s1461145714000650 · Cited by 18
Sex-specific role of the 5-HT2A receptor in psilocybin-induced extinction of opioid reward
Jaster, A. M., Hadlock, T. M., Buzzi, B., Maltman, J. L., Silva, G. M., Saha, S., Köşeli, E., Pondelick, A. M., Thakur, N., Zhang, X., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-64887-w · Cited by 19
Addiction-induced plasticity in underlying neural circuits
Kourosh‐Arami, M., Komaki, A., & Gholami, M. (2022) · Neurological Sciences · doi:10.1007/s10072-021-05778-y · Cited by 20
Opioid Dependence and NMDA Receptors
Glass, M. J. (2011) · ILAR Journal · doi:10.1093/ilar.52.3.342 · Cited by 17
Ruegsegger, G. N., Toedebusch, R. G., Childs, T. E., Grigsby, K. B., & Booth, F. W. (2016) · The Journal of Physiology · doi:10.1113/jp272489 · Cited by 17
Ehlinger, D. G., Burke, J. C., McDonald, C. G., Smith, R. F., & Bergstrom, H. C. (2017) · Neuroscience · doi:10.1016/j.neuroscience.2017.05.036 · Cited by 18
Gross, K. S., Moore, K. M., Meisel, R. L., & Mermelstein, P. G. (2018) · Frontiers in Neuroscience · doi:10.3389/fnins.2018.00855 · Cited by 17
Solecki, W., Wilczkowski, M., Pradel, K., Karwowska, K., Kiełbiński, M., Drwiȩga, G., Zajda, K., Błasiak, T., Sołtys, Z., Rajfur, Z., et al. (2019) · Addiction Biology · doi:10.1111/adb.12826 · Cited by 17
Vannemreddy, P. S. S. V., & Slavin, K. V. (2019) · Neurology India · doi:10.4103/0028-3886.271239 · Cited by 17
Mutti, V., Bono, F., Tomasoni, Z., Bontempi, L., Guglielmi, A., Bolognin, S., Schwamborn, J. C., Missale, C., & Fiorentini, C. (2022) · Molecular Neurobiology · doi:10.1007/s12035-022-02748-z · Cited by 17
Strong, C. E., Wright, K. N., & Kabbaj, M. (2019) · eNeuro · doi:10.1523/eneuro.0221-19.2019 · Cited by 16
Gancarz, A. M., Schroeder, G. L., Panganiban, C. H., Adank, D. N., Humby, M. S., Kausch, M. A., Clark, S. D., & Dietz, D. (2013) · PLoS ONE · doi:10.1371/journal.pone.0083834 · Cited by 16
Self-citationMorphine Regulated Synaptic Networks Revealed by Integrated Proteomics and Network Analysis
Stockton, S. D., Gomes, I., Liu, T., Chandrakala, M. V., Hipólito, L., Jones, M. R., Ma’ayan, A., Morón, J. A., Li, H., & Devi, L. A. (2015) · Molecular & Cellular Proteomics · doi:10.1074/mcp.m115.047977 · Cited by 16
Werner, C. T., Murray, C. H., Reimers, J. M., Chauhan, N. M., Woo, K., Molla, H. M., Loweth, J. A., & Wolf, M. E. (2016) · Neuropharmacology · doi:10.1016/j.neuropharm.2016.12.014 · Cited by 15
Drastichová, Z., Hejnová, L., Trubacova, R., & Novotný, J. (2021) · Life · doi:10.3390/life11070683 · Cited by 16
Dopamine D4 Receptor Is a Regulator of Morphine-Induced Plasticity in the Rat Dorsal Striatum
Rivera, A., Suárez‐Boomgaard, D., Miguélez, C., Valderrama‐Carvajal, A., Baufreton, J., Shumilov, K., Taupignon, A., Gago, B., & Real, M. A. (2021) · Cells · doi:10.3390/cells11010031 · Cited by 17
Fish oil treatment reduces chronic alcohol exposure induced synaptic changes
Shi, Z., Xie, Y., Ren, H., He, B., Wang, M., Wan, J., Yuan, T., Yao, X., & Su, H. (2018) · Addiction Biology · doi:10.1111/adb.12623 · Cited by 18
Fu, Y., & Depue, R. A. (2019) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2019.09.026 · Cited by 18
Human genetic variants disrupt RGS14 nuclear shuttling and regulation of LTP in hippocampal neurons
Squires, K. E., Gerber, K. J., Tillman, M. C., Lustberg, D. J., Montañez‐Miranda, C., Zhao, M., Ramineni, S., Scharer, C. D., Saha, R. N., Shu, F., et al. (2020) · Journal of Biological Chemistry · doi:10.1074/jbc.ra120.016009 · Cited by 15
Zhornitsky, S., Oliva, H. N. P., Jayne, L. A., Allsop, A. S., Kaye, A. P., Potenza, M. N., & Angarita, G. A. (2023) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2023.1197890 · Cited by 15
Advanced Fluorescence Protein-Based Synapse-Detectors
Lee, H., Oh, W. C., Seong, J., & Kim, J. (2016) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2016.00016 · Cited by 15
Diolistic Labeling and Analysis of Dendritic Spines
Olive, M. F., Franco, A. P. D., & Gipson, C. D. (2017) · Methods in molecular biology · doi:10.1007/978-1-4939-7571-6_14 · Cited by 15
Becker‐Krail, D. D., Parekh, P. K., Ketchesin, K. D., Yamaguchi, S., Yoshino, J., Hildebrand, M. A., Dunham, B., Ganapathiraju, M. K., Logan, R. W., & McClung, C. A. (2022) · European Journal of Neuroscience · doi:10.1111/ejn.15596 · Cited by 15
Damuka, N., Martin, T. J., Bansode, A. H., Krizan, I. M., Martin, C. W., Miller, M. D., Whitlow, C. T., Nader, M. A., & Sai, K. K. S. (2022) · Frontiers in Medicine · doi:10.3389/fmed.2022.817274 · Cited by 15
Inhibition of Protein Kinase Mζ (PKMζ) in the Mesolimbic System Alters Cocaine Sensitization in Rats
Vélez-Hernández, M. E., Vázquez‐Torres, R., Velásquez-Martínez, M. C., Jiménez, L. M., Báez, F., Sacktor, T. C., & Jiménez‐Rivera, C. A. (2013) · Journal of Drug and Alcohol Research · doi:10.4303/jdar/235669 · Cited by 14
Han, M., & Friedman, A. K. (2011) · Neuropharmacology · doi:10.1016/j.neuropharm.2011.09.009 · Cited by 15
Risk and Resilience: The Role of Brain-derived Neurotrophic Factor in Alcohol Use Disorder
Ceballos, N. A., & Sharma, S. (2016) · AIMS neuroscience · doi:10.3934/neuroscience.2016.4.398 · Cited by 14
Selective effects of Δ9-tetrahydrocannabinol on medium spiny neurons in the striatum
Fernández-Cabrera, M. R., Higuera‐Matas, A., Fernaud-Espinosa, I., DeFelipe, J., Ambrosio, E., & Miguéns, M. (2018) · PLoS ONE · doi:10.1371/journal.pone.0200950 · Cited by 12
Selvas, A., Coria, S. M., Kastanauskaite, A., Fernaud-Espinosa, I., DeFelipe, J., Ambrosio, E., & Miguéns, M. (2015) · Addiction Biology · doi:10.1111/adb.12294 · Cited by 14
Promoter Methylation and BDNF and DAT1 Gene Expression Profiles in Patients with Drug Addiction
Kordi-Tamandani, D. M., Tajoddini, S., & Salimi, F. (2015) · Pathobiology · doi:10.1159/000430465 · Cited by 14
Leyrer‐Jackson, J. M., Olive, M. F., & Gipson, C. D. (2019) · Methods in molecular biology · doi:10.1007/978-1-4939-9077-1_9 · Cited by 14
The Role of Epigenetics in Addiction: Clinical Overview and Recent Updates
Beayno, A., Hayek, S. E., Noufi, P. E., Tarabay, Y., & Shamseddeen, W. A. (2019) · Methods in molecular biology · doi:10.1007/978-1-4939-9554-7_35 · Cited by 13
Schoenrock, S. A., Gagnon, L. H., Olson, A., Leonardo, M. R., Philip, V. M., He, H., Reinholdt, L. G., Rizzo, S. J. S., Jentsch, D., Chesler, E. J., et al. (2022) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2022.886524 · Cited by 13
Neurogenetics of acute and chronic opiate opioid abstinence treating symptoms and the cause
Blum, K. (2017) · Frontiers in bioscience · doi:10.2741/4544 · Cited by 15
Treasure, J. L., & Eid, L. (2019) · Current Opinion in Psychiatry · doi:10.1097/yco.0000000000000550 · Cited by 15
Chen, Z.-G., Wang, Y.-J., Chen, R.-S., Geng, F., Gan, C., Wang, W., Liu, X., Zhou, H., He, L., Hu, G., et al. (2019) · Molecular Psychiatry · doi:10.1038/s41380-019-0533-y · Cited by 14
Hájos, N., Holderith, N. B., Németh, B., Papp, O. I., Szabo, G. G., Zemankovics, R., Freund, T. F., & Haller, J. (2011) · Phytotherapy Research · doi:10.1002/ptr.3556 · Cited by 13
The α1 Antagonist Doxazosin Alters the Behavioral Effects of Cocaine in Rats
Haile, C. N., Hao, Y., O'Malley, P. W., Newton, T. F., & Kosten, T. A. (2012) · Brain Sciences · doi:10.3390/brainsci2040619 · Cited by 13
Koob, G. F., Kandel, D. B., Baler, R., & Volkow, N. D. (2015) · Wiley eBooks · doi:10.1002/9781118753378.ch22 · Cited by 14
Effects of MDMA on neuroplasticity, amyloid burden and phospho-tau expression in APPswe/PS1dE9 mice
Abad, S., Ramon‐Duaso, C., López‐Arnau, R., Folch, J., Pubill, D., Camarasa, J., Camins, A., & Escubedo, E. (2019) · Journal of Psychopharmacology · doi:10.1177/0269881119855987 · Cited by 12
Sayson, L. V., Custodio, R. J. P., Ortiz, D. M., Lee, H. J., Kim, M., Jeong, Y., Lee, Y. S., Kim, H. J., & Cheong, J. H. (2020) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2020.173527 · Cited by 12
Leão, R. M., Cruz, F. C., de Oliveira, P. E. C., Rossetto, D. D. B., Valentini, S. R., Zanelli, C. F., & Planeta, C. S. (2013) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2013.01.007 · Cited by 13
Learning and Memory in Addiction
Carmack, S. A., Koob, G. F., & Anagnostaras, S. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-809324-5.21101-2 · Cited by 13
Social Influences on Nicotine-Related Behaviors
Piña, J. A., Namba, M. D., Leyrer‐Jackson, J. M., Cabrera-Brown, G., & Gipson, C. D. (2018) · International review of neurobiology · doi:10.1016/bs.irn.2018.07.001 · Cited by 15
Activity-Dependent Epigenetic Remodeling in Cocaine Use Disorder
López, A. J., Siciliano, C. A., & Calipari, E. S. (2019) · Handbook of experimental pharmacology · doi:10.1007/164_2019_257 · Cited by 12
Foster, S. L., Lustberg, D. J., Harbin, N. H., Bramlett, S. N., Hepler, J. R., & Weinshenker, D. (2021) · Psychopharmacology · doi:10.1007/s00213-021-05892-x · Cited by 10
Azadi, M., Zare, M., Pachenari, N., Shojaei, A., Semnanian, S., & Azizi, H. (2021) · Neuroscience Letters · doi:10.1016/j.neulet.2021.136111 · Cited by 12
Metadata
- Authors
- Russo, S. J., Dietz, D. M., Dumitriu, D., Morrison, J. H., Malenka, R. C., & Nestler, E. J.
- Affiliations
- Icahn School of Medicine at Mount Sinai (US)
- Stanford Medicine (US)
- Corresponding author
- Russo, Scott J.
- ORCID
- Venue
- Trends in Neurosciences
- Publisher
- Elsevier BV
- Published
- 2010-06
- Volume
- 33
- Issue
- 6
- Pages
- 267-276
- ISSN
- 0166-2236 (ISSN-L)
- PMC
- PMC2891948
- OpenAlex
- W2084967673
- Cited by
- 654
- References
- 97
- Citations by year
- 2026: 10 · 2025: 25 · 2024: 27 · 2023: 25 · 2022: 31 · 2021: 37 · 2020: 35 · 2019: 45 · 2018: 53 · 2017: 57 · 2016: 48 · 2015: 45 · 2014: 49 · 2013: 49 · 2012: 56
- FWCI
- 4.78
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Trends in Neurosciences (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institute on Drug Abuse (F32DA019727, T32DA007290, R01DA014133)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
- Health Sciences › Medicine › Pharmacology (medical) › Treatment of Major Depression
- Keywords
- addiction, nucleus accumbens, synaptic plasticity, structural plasticity, dendritic spines, medium spiny neurons, limbic system, homeostatic compensation, ultrastructure, electrophysiology, behavioral plasticity
- MeSH terms
- Animals, Models, Biological, Neuronal Plasticity, Neurons, Nucleus Accumbens, Illicit Drugs, Synapses, Signal Transduction, Substance-Related Disorders, Dendritic Spines
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