The DOI matches its Crossref record; 161 of the 161 references it cites were found in a registry or an index.
Learning to forget: manipulating extinction and reconsolidation processes to treat addiction
Open accessAbstract
Finding effective long-lasting treatments for drug addiction has been an elusive goal. Consequently, researchers are beginning to investigate novel treatment strategies including manipulations of drug-associated memories. When environmental stimuli (cues) become associated with drug use, they become powerful motivators of continued drug use and relapse after abstinence. Reducing the strength of these cue-drug memories could decrease the number of factors that induce craving and relapse to aid in the treatment of addiction. Enhancing the consolidation of extinction learning and/or disrupting cue-drug memory reconsolidation are two strategies that have been proposed to reduce the strength of cues in motivating drug-seeking and drug-taking behavior. Here, we review the latest basic and clinical research elucidating the mechanisms underlying consolidation of extinction and reconsolidation of cue-drug memories in the hopes of developing pharmacological tools that exploit these signaling systems to treat addiction.
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 check wasn’t confident either way, so it gives no verdict — never disputed.
In the citing paper
“Research supports that CBT is effective for a wide range of individuals who are trying to quit smoking, including PTSD patients,63 people living with HIV,66 individuals with mental illness,67 low socioeconomic smokers,57 adults with chronic pain,68 overweight and disadvantaged smokers,61 and youth.65”
From Are smoking cessation treatments associated with suicidality risk? An overview (2016) · cites this paper as [63]
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
Fear memories require protein synthesis in the amygdala for reconsolidation after retrieval
Nader, K., Schafe, G. E., & Le Doux, J. E. (2000) · Nature · doi:10.1038/35021052 · Cited by 2,706
NEURAL MECHANISMS OF ADDICTION: The Role of Reward-Related Learning and Memory
Hyman, S. E., Malenka, R. C., & Nestler, E. J. (2006) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.29.051605.113009 · Cited by 2,647
Context and Behavioral Processes in Extinction: Table 1.
Bouton, M. E. (2004) · Learning & Memory · doi:10.1101/lm.78804 · Cited by 1,808
The Neurobiology of Consolidations, Or, How Stable is the Engram?
Dudai, Y. (2004) · Annual Review of Psychology · doi:10.1146/annurev.psych.55.090902.142050 · Cited by 1,671
Context, ambiguity, and unlearning: sources of relapse after behavioral extinction
Bouton, M. E. (2002) · Biological Psychiatry · doi:10.1016/s0006-3223(02)01546-9 · Cited by 1,662
Meta‐analysis of cue‐reactivity in addiction research
Carter, B. L., & Tiffany, S. T. (1999) · Addiction · doi:10.1046/j.1360-0443.1999.9433273.x · Cited by 1,638 · cited 3×
“Environmental stimuli (cues) that are repeatedly associated with a drug are known to promote compulsive drug taking and craving and are a primary trigger of relapse (Carter and Tiffany 1999; Shalev et al. 2002; See 2002).”
The reinstatement model of drug relapse: history, methodology and major findings
Shaham, Y., Shalev, U., Lu, L., de Wit, H., & Stewart, J. (2003) · Psychopharmacology · doi:10.1007/s00213-002-1224-x · Cited by 1,615
Jentsch, J. D., & Taylor, J. R. (1999) · Psychopharmacology · doi:10.1007/pl00005483 · Cited by 1,545
Self-citationTzschentke, T. M. (2007) · Addiction Biology · doi:10.1111/j.1369-1600.2007.00070.x · Cited by 1,336
Preventing the return of fear in humans using reconsolidation update mechanisms
Schiller, D., Monfils, M.-H., Raio, C. M., Johnson, D. C., LeDoux, J. E., & Phelps, E. A. (2010) · Nature · doi:10.1038/nature08637 · Cited by 1,248
Cited by
Sorted by citations
Bossert, J. M., Marchant, N. J., Calu, D. J., & Shaham, Y. (2013) · Psychopharmacology · doi:10.1007/s00213-013-3120-y · Cited by 453
Everitt, B. J. (2014) · European Journal of Neuroscience · doi:10.1111/ejn.12644 · Cited by 318
Drug-Induced Conditioned Place Preference and Its Practical Use in Substance Use Disorder Research
McKendrick, G., & Graziane, N. (2020) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2020.582147 · Cited by 218
Reconsolidation of memory: A decade of debate
Besnard, A., Caboche, J., & Laroche, S. (2012) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2012.07.002 · Cited by 187
Kredlow, M. A., Unger, L. D., & Otto, M. W. (2016) · Psychological Bulletin · doi:10.1037/bul0000034 · Cited by 130
Ketamine can reduce harmful drinking by pharmacologically rewriting drinking memories
Das, R. K., Gale, G., Walsh, K., Hennessy, V. E., Iskandar, G., Mordecai, L. A., Brandner, B., Kindt, M., Curran, H. V., & Kamboj, S. K. (2019) · Nature Communications · doi:10.1038/s41467-019-13162-w · Cited by 122
Lattal, K. M., & Wood, M. A. (2013) · Nature Neuroscience · doi:10.1038/nn.3302 · Cited by 116
Castilla‐Ortega, E., Serrano, A., Blanco, E., Araos, P. F., Suárez, J., Pavón, F. J., de Fonseca, F. R., & Santín, L. J. (2016) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2016.03.030 · Cited by 104
Saladin, M. E., Gray, K. M., McRae‐Clark, A. L., LaRowe, S. D., Yeatts, S. D., Baker, N. L., Hartwell, K. J., & Brady, K. T. (2013) · Psychopharmacology · doi:10.1007/s00213-013-3039-3 · Cited by 101
Xue, Y.-X., Deng, J., Chen, Y., Zhang, L., Wu, P., Huang, G.-D., Luo, Y., Bao, Y., Wang, Y., Shaham, Y., et al. (2017) · JAMA Psychiatry · doi:10.1001/jamapsychiatry.2016.3907 · Cited by 94
Barker, J. M., Taylor, J. R., Vries, T. J. D., & Peters, J. (2014) · Brain Research · doi:10.1016/j.brainres.2014.10.058 · Cited by 87
Self-citationAddiction: a drug-induced disorder of memory reconsolidation
Tronson, N. C., & Taylor, J. R. (2013) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2013.01.022 · Cited by 85
Self-citationModeling cocaine relapse in rodents: Behavioral considerations and circuit mechanisms
Farrell, M. R., Schoch, H., & Mahler, S. V. (2018) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2018.01.002 · Cited by 90
Li, X., Hartwell, K. J., Henderson, S., Badran, B. W., Brady, K. T., & George, M. S. (2020) · Brain stimulation · doi:10.1016/j.brs.2020.06.007 · Cited by 76
The role of progesterone in memory: An overview of three decades
Barros, L. A., Tufik, S. B., & Andersen, M. L. (2014) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2014.11.015 · Cited by 91
Itzhak, Y., Ergui, I., & Young, J. I. (2014) · Molecular Psychiatry · doi:10.1038/mp.2014.7 · Cited by 72
Linking Social Cognition to Learning and Memory
Leblanc, H., & Ramirez, S. (2020) · The Journal of Neuroscience · doi:10.1523/jneurosci.1280-20.2020 · Cited by 69
A randomized clinical trial of cue exposure treatment through virtual reality for smoking cessation
Pericot‐Valverde, I., Secades‐Villa, R., & Gutiérrez‐Maldonado, J. (2018) · Journal of Substance Abuse Treatment · doi:10.1016/j.jsat.2018.10.003 · Cited by 67
Reconsolidation and psychopathology: Moving towards reconsolidation-based treatments
Dunbar, A. B., & Taylor, J. R. (2016) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2016.11.005 · Cited by 70
Self-citationEpigenetic Mechanisms in Drug Relapse
Werner, C. T., Altshuler, R. D., Shaham, Y., & Li, X. (2020) · Biological Psychiatry · doi:10.1016/j.biopsych.2020.08.005 · Cited by 61
Xue, Y.-X., Chen, Y., Zhang, L., Zhang, L.-Q., Huang, G.-D., Sun, S.-C., Deng, J., Luo, Y., Bao, Y., Wu, P., et al. (2017) · Biological Psychiatry · doi:10.1016/j.biopsych.2017.04.017 · Cited by 58
Park, C.-B., Choi, J., Park, S. M., Lee, J., Jung, H. Y., Seol, J.-M., Hwang, J. Y., Gwak, A. R., & Kwon, J. S. (2014) · Cyberpsychology Behavior and Social Networking · doi:10.1089/cyber.2013.0253 · Cited by 56
Martínez-Rivera, F. J., Rodríguez-Romaguera, J., Lloret-Torres, M. E., Monte, F. H. D., Quirk, G. J., & Barreto-Estrada, J. L. (2016) · Biological Psychiatry · doi:10.1016/j.biopsych.2016.05.015 · Cited by 56
Circuits that encode and guide alcohol-associated preference
Scaplen, K. M., Talay, M., Salamon, S., Nuñez, K. M., Waterman, A. G., Gang, S., Song, S. L., Barnea, G., & Kaun, K. R. (2020) · eLife · doi:10.7554/elife.48730 · Cited by 61
Plasticity at Thalamo-amygdala Synapses Regulates Cocaine-Cue Memory Formation and Extinction
Rich, M. T., Huang, Y. H., & Torregrossa, M. M. (2019) · Cell Reports · doi:10.1016/j.celrep.2018.12.105 · Cited by 53
Self-citationSynaptic Cytoskeletal Plasticity in the Prefrontal Cortex Following Psychostimulant Exposure
DePoy, L. M., & Gourley, S. L. (2015) · Traffic · doi:10.1111/tra.12295 · Cited by 52
Degoulet, M., Stelly, C. E., Ahn, K.-C., & Morikawa, H. (2015) · Molecular Psychiatry · doi:10.1038/mp.2015.84 · Cited by 50
The Promises and Pitfalls of Retrieval-Extinction Procedures in Preventing Relapse to Drug Seeking
Hutton-Bedbrook, K., & McNally, G. P. (2013) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2013.00014 · Cited by 49
“Chasing the first high”: memory sampling in drug choice
Bornstein, A. M., & Pickard, H. (2020) · Neuropsychopharmacology · doi:10.1038/s41386-019-0594-2 · Cited by 49
Rich, M. T., Abbott, T. B., Chung, L., Gulcicek, E. E., Stone, K. L., Colangelo, C. M., Lam, T. T., Nairn, A. C., Taylor, J. R., & Torregrossa, M. M. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.1108-16.2016 · Cited by 47
Self-citationSchramm, M. W. J., Everitt, B. J., & Milton, A. L. (2015) · Neuropsychopharmacology · doi:10.1038/npp.2015.248 · Cited by 44
Neuroscience of learning and memory for addiction medicine
Torregrossa, M. M., & Taylor, J. R. (2015) · Progress in brain research · doi:10.1016/bs.pbr.2015.07.006 · Cited by 43
Self-citationD’Souza, M. S. (2019) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2019.00509 · Cited by 50
Renewal of conditioned responding to food cues in rats: Sex differences and relevance of estradiol
Anderson, L. C., & Petrovich, G. D. (2015) · Physiology & Behavior · doi:10.1016/j.physbeh.2015.07.035 · Cited by 40
Molecular and circuit mechanisms regulating cocaine memory
Bender, B. N., & Torregrossa, M. M. (2020) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-020-03498-8 · Cited by 39
Self-citationDesplats, P. (2014) · Advances in neurobiology · doi:10.1007/978-1-4939-1372-5_16 · Cited by 37
Torregrossa, M. M., Gordon, J., & Taylor, J. R. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.0489-13.2013 · Cited by 35
Self-citationDunbar, A. B., & Taylor, J. R. (2017) · Neuropsychopharmacology · doi:10.1038/npp.2017.27 · Cited by 35
Self-citationDrug memory reconsolidation: from molecular mechanisms to the clinical context
Milton, A. L. (2023) · Translational Psychiatry · doi:10.1038/s41398-023-02666-1 · Cited by 35
Sheynin, J., Moustafa, A. A., Beck, K. D., Servatius, R. J., Casbolt, P., Haber, P., Elsayed, M., Hogarth, L., & Myers, C. E. (2016) · The Journal of Clinical Psychiatry · doi:10.4088/jcp.14m09284 · Cited by 32
Das, R., Freeman, T. P., & Kamboj, S. K. (2012) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2012.11.018 · Cited by 29
Endocannabinoids underlie reconsolidation of hedonic memories in Wistar rats
de Carvalho, C. R., Pamplona, F. A., Cruz, J. S., & Takahashi, R. N. (2013) · Psychopharmacology · doi:10.1007/s00213-013-3331-2 · Cited by 31
Sun, K., Mu, Q., Chang, H., Zhang, C., Wang, Y., Rong, S., Liu, S., Zuo, D., He, Z., Wan, D., et al. (2020) · Frontiers in Pharmacology · doi:10.3389/fphar.2020.00743 · Cited by 29
Silent Synapses in Cocaine-Associated Memory and Beyond
Wright, W. J., & Dong, Y. (2021) · Journal of Neuroscience · doi:10.1523/jneurosci.1559-21.2021 · Cited by 31
Yousuf, H., Smies, C. W., Hafenbreidel, M., Tuscher, J. J., Fortress, A. M., Frick, K. M., & Mueller, D. T. (2019) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2019.00168 · Cited by 29
Liu, W., Chen, X., Wen, Y., Winkler, M. H., Paul, P., He, Y., Wang, L., Chen, H., & Li, Y. (2020) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2020.00322 · Cited by 29
Werner, C. T., Milovanovic, M., Christian, D., Loweth, J. A., & Wolf, M. E. (2015) · Neuropsychopharmacology · doi:10.1038/npp.2015.156 · Cited by 28
Pharmacological Disruption of Maladaptive Memory
Taylor, J. R., & Torregrossa, M. M. (2015) · Handbook of experimental pharmacology · doi:10.1007/978-3-319-16522-6_13 · Cited by 27
Self-citationFuture perspectives of emerging novel drug targets and immunotherapies to control drug addiction
Malik, J. A., & Agrewala, J. N. (2023) · International Immunopharmacology · doi:10.1016/j.intimp.2023.110210 · Cited by 32
Rich, M. T., & Torregrossa, M. M. (2018) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2017.09.003 · Cited by 27
Self-citation17β-Estradiol is necessary for extinction of cocaine seeking in female ratsPreprint
Twining, R. C., Tuscher, J. J., Doncheck, E. M., Frick, K. M., & Mueller, D. T. (2013) · Learning & Memory · doi:10.1101/lm.030304.113 · Cited by 27
Psychostimulant-Induced Adaptations in Nucleus Accumbens Glutamatergic TransmissionPreprint
Wright, W. J., & Dong, Y. (2020) · Cold Spring Harbor Perspectives in Medicine · doi:10.1101/cshperspect.a039255 · Cited by 29
Ruglass, L. M., López‐Castro, T., Cheref, S., Papini, S., & Hien, D. A. (2014) · Current Psychiatry Reports · doi:10.1007/s11920-014-0505-5 · Cited by 28
Cross-talk between the epigenome and neural circuits in drug addiction
Mews, P., & Calipari, E. S. (2017) · Progress in brain research · doi:10.1016/bs.pbr.2017.08.012 · Cited by 25
Skelly, M. J., Ariwodola, O. J., & Weiner, J. L. (2016) · Neuropharmacology · doi:10.1016/j.neuropharm.2016.10.003 · Cited by 24
Rich, M. T., Huang, Y. H., & Torregrossa, M. M. (2020) · The Journal of Neuroscience · doi:10.1523/jneurosci.0453-19.2019 · Cited by 25
Self-citationBailey, C. P., & Husbands, S. M. (2014) · Expert Opinion on Drug Discovery · doi:10.1517/17460441.2014.964203 · Cited by 25
Montesinos, J., Castilla‐Ortega, E., Sánchez‐Marín, L., Montagud‐Romero, S., Araos, P. F., Pedraz, M., Porras-Perales, Ó., García‐Marchena, N., Serrano, A., Suárez, J., et al. (2019) · Neuropharmacology · doi:10.1016/j.neuropharm.2019.107840 · Cited by 24
Theis (2016) · doi:10.1016/j.cnur.2016.01.007 · Cited by 24
Rossato, J. I., Köhler, C. A., Radiske, A., Bevilaqua, L. R., & Cammarota, M. (2015) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2015.09.001 · Cited by 22
Yu, Y., Chang, C., & Gean, P. (2013) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2013.04.004 · Cited by 25
Spontaneous recovery of reward memory through active forgetting of extinction memory
Yang, Q., Zhou, J. W., Wang, L., Hu, W., Zhong, Y., & Li, Q. (2023) · Current Biology · doi:10.1016/j.cub.2023.01.022 · Cited by 24
Monsey, M. S., Sanchez, H., & Taylor, J. R. (2016) · Neuropsychopharmacology · doi:10.1038/npp.2016.117 · Cited by 24
Self-citationThe Paradoxical Effect of Deep Brain Stimulation on Memory
Kai, T. S. Z., Man-Lung, F., Koh, J., Ying-Shing, C., & Lim, L. W. (2020) · Aging and Disease · doi:10.14336/ad.2019.0511 · Cited by 26
Dunbar, A. B., & Taylor, J. R. (2016) · Learning & Memory · doi:10.1101/lm.042838.116 · Cited by 26
Self-citationRole of prefrontal cortex in the extinction of drug memories
Zhang, W., Cao, K.-X., Ding, Z., Yang, J., Pan, B., & Xue, Y.-X. (2018) · Psychopharmacology · doi:10.1007/s00213-018-5069-3 · Cited by 24
Gale, G., Walsh, K., Hennessy, V. E., Stemerding, L., Ni, K. S., Thomas, E., Kamboj, S. K., & Das, R. (2020) · Psychological Medicine · doi:10.1017/s0033291720001531 · Cited by 22
The metabotropic glutamate 5 receptor is necessary for extinction of cocaine‐associated cues
Perry, C. J., Reed, F. M., Zbukvic, I., Kim, J. H., & Lawrence, A. J. (2016) · British Journal of Pharmacology · doi:10.1111/bph.13437 · Cited by 23
Das, R., Gale, G., Hennessy, V. E., & Kamboj, S. K. (2018) · Journal of Visualized Experiments · doi:10.3791/56097 · Cited by 24
Briggs, S. B., Blouin, A. M., Young, E. J., Rumbaugh, G., & Miller, C. A. (2017) · Learning & Memory · doi:10.1101/lm.043976.116 · Cited by 21
Eskandari, K., Fattahi, M., Riahi, E., Khosrowabadi, R., & Haghparast, A. (2023) · Life Sciences · doi:10.1016/j.lfs.2023.121503 · Cited by 19
Pildervasser, J. V. N., Abrahao, K. P., & Formigoni, M. L. O. D. S. (2014) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2014.00267 · Cited by 19
Zamberlam, C. R., Vendrasco, N. C., de Oliveira, D. R., Gaiardo, R. B., & Cerutti, S. M. (2016) · Physiology & Behavior · doi:10.1016/j.physbeh.2016.06.036 · Cited by 19
DNMT3a in the hippocampal CA1 is crucial in the acquisition of morphine self‐administration in rats
Zhang, J., Jiang, F., Zheng, W., Duan, Y., Jin, S., Shen, F., Liang, J., Li, M., & Sui, N. (2019) · Addiction Biology · doi:10.1111/adb.12730 · Cited by 18
Transforming experiences: Neurobiology of memory updating/editing
Osorio‐Gómez, D., Miranda, M. I., Guzmán-Ramos, K. R., & Bermúdez‐Rattoni, F. (2023) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2023.1103770 · Cited by 20
Childs, J. E., Kim, S., Driskill, C. M., Hsiu, E., & Kroener, S. (2019) · Brain stimulation · doi:10.1016/j.brs.2019.07.001 · Cited by 19
Soravia, L. M., Moggi, F., & de Quervain, D. J. ‐. (2021) · Translational Psychiatry · doi:10.1038/s41398-020-01180-y · Cited by 19
Extinction and renewal of cue-elicited reward-seeking
Bezzina, L., Lee, J. C., Lovibond, P. F., & Colagiuri, B. (2016) · Behaviour Research and Therapy · doi:10.1016/j.brat.2016.09.009 · Cited by 18
Eternal sunshine of the neuromodulated mind: Altering fear memories through neuromodulation
Tan, S. Z. K., Sheng, V., Chan, Y., & Lim, L. W. (2019) · Experimental Neurology · doi:10.1016/j.expneurol.2019.01.004 · Cited by 18
Monsey, M. S., Ruiz, S. G., & Taylor, J. R. (2020) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2019.00281 · Cited by 17
Self-citationTargeting drug memory reconsolidation: a neural analysis
Taujanskaitė, U., Cahill, E., & Milton, A. L. (2020) · Current Opinion in Pharmacology · doi:10.1016/j.coph.2020.08.007 · Cited by 16
Zhu, H., Zhou, Y., Liu, Z., Chen, X., Li, Y., Liu, X., & Ma, L. (2017) · The International Journal of Neuropsychopharmacology · doi:10.1093/ijnp/pyx104 · Cited by 17
Mañas-Padilla, M. C., Gil‐Rodríguez, S., Sampedro-Piquero, P., Ávila-Gámiz, F., de Fonseca, F. R., Santín, L., & Castilla-Ortega, E. (2020) · Addiction Biology · doi:10.1111/adb.12886 · Cited by 14
Huang, S., Liu, X., Li, Z., Si, Y., Yang, L., Deng, J., Luo, Y., Xue, Y.-X., & Lü, L. (2024) · Neuroscience Bulletin · doi:10.1007/s12264-024-01294-z · Cited by 15
Phosphoproteomic analysis of cocaine memory extinction and reconsolidation in the nucleus accumbens
Torregrossa, M. M., MacDonald, M. L., Stone, K. L., Lam, T. T., Nairn, A. C., & Taylor, J. R. (2018) · Psychopharmacology · doi:10.1007/s00213-018-5071-9 · Cited by 14
Self-citationMartínez-Rivera, F. J., Martinez, N. A., Martínez, M., Ayala-Pagán, R. N., Silva, W. I., & Barreto-Estrada, J. L. (2019) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2019.107031 · Cited by 13
Bui, U. T. D., & Milton, A. L. (2023) · Neuroscience · doi:10.1016/j.neuroscience.2023.03.013 · Cited by 13
Naloxone effects on extinction of ethanol- and cocaine-induced conditioned place preference in mice
Font, L., Houck, C. A., & Cunningham, C. L. (2017) · Psychopharmacology · doi:10.1007/s00213-017-4672-z · Cited by 13
The effects of Pavlovian cue extinction and ceftriaxone on cocaine relapse after abstinence
Bechard, A. R., & Knackstedt, L. A. (2019) · Drug and Alcohol Dependence · doi:10.1016/j.drugalcdep.2019.01.005 · Cited by 13
Martínez-Maldonado, A., Barba, R. J., Sión, A., Centeno, I. D., Castillo-Parra, G., Prieto-Montalvo, J., & Rubio, G. (2019) · International Journal of Psychophysiology · doi:10.1016/j.ijpsycho.2019.10.004 · Cited by 14
Xie, X., Chen, R., Huang, Y., Wang, X., & Wang, J. (2025) · Neuropharmacology · doi:10.1016/j.neuropharm.2025.110646 · Cited by 12
Franco‐García, A., Fernández-Gómez, F.-J., Gómez‐Murcia, V., Hidalgo, J. M., Núñez, C., & Milanés, M. V. (2022) · Biomedicines · doi:10.3390/biomedicines10030588 · Cited by 12
The emerging neuroscience of appetitive and drug cue extinction in humans
Konova, A. B., & Goldstein, R. Z. (2018) · Psychopharmacology · doi:10.1007/s00213-018-5098-y · Cited by 15
Zhu, C., Hong, T., Li, H., Jiang, S., Guo, B., Wang, L., Ding, J., Gao, C., Sun, Y., Sun, T., et al. (2021) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2021.711750 · Cited by 11
Qian, H., Wang, J., Shang, Q., Xiao, J., Chen, G., Gao, B., Liang, M., Li, T., & Liu, X. (2020) · Neuroscience Letters · doi:10.1016/j.neulet.2020.134817 · Cited by 11
Fuchs, R. A., Higginbotham, J. A., & Hansen, E. J. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-812202-0.00002-6 · Cited by 11
Rezapour, T., Aupperle, R. L., Paulus, M. P., & Ekhtiari, H. (2019) · Elsevier eBooks · doi:10.1016/b978-0-12-815298-0.00029-0 · Cited by 10
The Efficacy of Lidocaine in Disrupting Cocaine Cue-Induced Memory Reconsolidation
Becker, J. E., Price, J. L., Leonard, D., Surís, A., Kandil, E. S., Shaw, M. A., Kroener, S., Brown, E. S., & Adinoff, B. H. (2020) · Drug and Alcohol Dependence · doi:10.1016/j.drugalcdep.2020.108062 · Cited by 10
Smaga, I., Wydra, K., Suder, A., Frankowska, M., Sanak, M., Caffino, L., Fumagalli, F., & Filip, M. (2021) · Neurotoxicity Research · doi:10.1007/s12640-021-00350-0 · Cited by 10
Lloret-Torres, M. E., Ayala-Pagán, R. N., Martínez-Rivera, F. J., Bonilla-Rullán, P., & Barreto-Estrada, J. L. (2022) · IBRO Neuroscience Reports · doi:10.1016/j.ibneur.2022.10.007 · Cited by 9
Metadata
- Authors
- Torregrossa, M. M., & Taylor, J. R.
- Affiliations
- Yale University (US)
- Corresponding author
- Torregrossa, Mary M.
- Venue
- Psychopharmacology
- Published
- 2012-05-26
- Volume
- 226
- Issue
- 4
- Pages
- 659-672
- ISSN
- 0033-3158 (ISSN-L)
- 1432-2072
- PMC
- PMC3466391
- OpenAlex
- W2043662856
- Cited by
- 172
- References
- 157
- Citations by year
- 2026: 7 · 2025: 9 · 2024: 12 · 2023: 11 · 2022: 5 · 2021: 13 · 2020: 23 · 2019: 18 · 2018: 11 · 2017: 8 · 2016: 17 · 2015: 12 · 2014: 13 · 2013: 11 · 2012: 2
- FWCI
- 0.96
- Type
- journal article
- Language
- en
- Open access
- green
- europepmc.org
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Psychopharmacology (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institute on Drug Abuse (K01DA031745, P20DA027844, R01DA011717, R01DA015222)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory Processes and Influences
- Keywords
- drug addiction, extinction learning, memory reconsolidation, relapse, craving, memory consolidation, pharmacological treatment of addiction, drug-seeking behavior
- MeSH terms
- Animals, Cues, Extinction, Psychological, Humans, Memory, Motivation, Time Factors, Behavior, Addictive, Substance-Related Disorders, Secondary Prevention
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
