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A Memory Retrieval-Extinction Procedure to Prevent Drug Craving and Relapse
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Disrupting Drug Memories: In drug recovery programs, conditioned responses to drug cues can be inhibited by extinction protocols. However, extinguished behavioral responses can return after renewed exposure to the drug itself, or to drug-associated paraphernalia, and sometimes these responses reemerge spontaneously. Attempts have been made to disrupt cue-memory reconsolidation or to strengthen extinction learning, but these efforts have often relied on pharmacological agents that either are not approved for human use or cause problematic side effects. Xue et al. (p. 241 ; see the Perspective by Milton and Everitt ) have tried to circumvent the limitations of pharmacological approaches in daily retrieval trials conducted in rats within the short timeframe of the “reconsolidation window” before the extinction sessions reduced drug-induced reinstatement, spontaneous recovery, and renewal of drug seeking. When translated to heroin-addicted humans, similar retrieval trials before extinction sessions impaired cue-induced heroin craving up to 6 months later. This retrieval-extinction procedure is thus a promising non-pharmacological treatment for addiction.
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“while cue-induced responses (e.g. craving, approach tendencies evoked by drug paraphernalia) can be reduced by similar reconsolidation-update manipulations as those used in phobias [153,154].”
From Multiple memory systems, multiple time points: How science can inform treatment to control the expression of unwanted emotional memories (2018) · cites this paper as [153]
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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
Effects of an expanding-spaced vs massed exposure schedule on fear reduction and return of fear
Rowe, M. K., & Craske, M. G. (1998) · Behaviour Research and Therapy · doi:10.1016/s0005-7967(97)10016-x · Cited by 1,782
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
Neural Mechanisms of Extinction Learning and Retrieval
Quirk, G. J., & Mueller, D. (2008) · Neuropsychopharmacology · doi:10.1038/sj.npp.1301555 · Cited by 1,645
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
Self-citationA role for lateral hypothalamic orexin neurons in reward seeking
Harris, G. C., Wimmer, M., & Aston-Jones, G. (2005) · Nature · doi:10.1038/nature04071 · Cited by 1,311
Stewart, J., de Wit, H., & Eikelboom, R. (1984) · Psychological Review · doi:10.1037/0033-295x.91.2.251 · Cited by 1,261
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
Extinction-Reconsolidation Boundaries: Key to Persistent Attenuation of Fear Memories
Monfils, M.-H., Cowansage, K. K., Klann, E., & LeDoux, J. E. (2009) · Science · doi:10.1126/science.1167975 · Cited by 960
Reinstatement of cocaine-reinforced responding in the rat
de Wit, H., & Stewart, J. (1981) · Psychopharmacology · doi:10.1007/bf00432175 · Cited by 928
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Research works printed but not linked: 1
- C. P. O’Brien R. N. Ehrman J. W. Ternes in Behavioral Analysis of Drug Dependence S. Goldberg I. Stolerman Eds. (Academic Press Orlando FL 1986) pp. 329–356.
Cited by
Sorted by citations
Items 201–300 of 512
Jiao, D., Liu, Y., Long, J.-D., Du, J., Ju, Y., Zan, G., Liu, J.-G., & Zhao, M. (2016) · Neuroscience · doi:10.1016/j.neuroscience.2016.02.001 · Cited by 24
Chen, Y., Zhang, L., Li, Y., Meng, S., Gong, Y.-M., Lü, L., Xue, Y.-X., & Shi, J. (2019) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2019.00157 · Cited by 25
Self-citationLiu, P., Zhang, J., Li, M., & Sui, N. (2016) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2016.00050 · Cited by 24
Active suppression prevents the return of threat memory in humans
Wang, Y., Zhu, Z., Hu, J., Schiller, D., & Li, J. (2021) · Communications Biology · doi:10.1038/s42003-021-02120-2 · Cited by 30
The Mechanisms and Boundary Conditions of Drug Memory Reconsolidation
Chen, L., He, Y., Wang, Y., He, Z., Leng, Q., Huang, S., Wu, F., Feng, X., & Yan, J. (2021) · Frontiers in Neuroscience · doi:10.3389/fnins.2021.717956 · Cited by 23
The evidence for and against reactivation-induced memory updating in humans and nonhuman animals
Jardine, K. H., Huff, A. E., Wideman, C. E., McGraw, S. D., & Winters, B. D. (2022) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2022.104598 · Cited by 32
Monsey, M. S., Sanchez, H., & Taylor, J. R. (2016) · Neuropsychopharmacology · doi:10.1038/npp.2016.117 · Cited by 24
Helfer, P., & Shultz, T. R. (2018) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1006147 · Cited by 24
Recent developments in the behavioural and pharmacological enhancement of extinction of drug seeking
Chesworth, R., & Corbit, L. H. (2015) · Addiction Biology · doi:10.1111/adb.12337 · Cited by 25
Post-retrieval extinction in adolescence prevents return of juvenile fearPreprint
Jones, C. E., & Monfils, M. (2016) · Learning & Memory · doi:10.1101/lm.043281.116 · Cited by 25
The ethics of research in compulsory drug detention centres in Asia
Pearshouse, R., & Amon, J. J. (2012) · Journal of the International AIDS Society · doi:10.7448/ias.15.2.18491 · Cited by 23
The role of PKMζ in the maintenance of long-term memory: a review
Patel, H., & Zamani, R. (2021) · Reviews in the Neurosciences · doi:10.1515/revneuro-2020-0105 · Cited by 23
Su, S., Deng, J., Yuan, K., Gong, Y.-M., Zhang, Y., Li, H., Cao, K.-X., Huang, X., Lin, X., Wu, P., et al. (2021) · iScience · doi:10.1016/j.isci.2021.103614 · Cited by 26
Self-citationYan, Y., Newman, A. H., & Xu, M. (2014) · Neuroscience · doi:10.1016/j.neuroscience.2014.08.008 · Cited by 24
Rindal, E. J., DeFranco, R., Rich, P. R., & Zaragoza, M. S. (2016) · Journal of Experimental Psychology Learning Memory and Cognition · doi:10.1037/xlm0000265 · Cited by 23
Prospects for reconsolidation-focused treatments of substance use and anxiety-related disorders
Paulus, D. J., Kamboj, S. K., Das, R., & Saladin, M. E. (2019) · Current Opinion in Psychology · doi:10.1016/j.copsyc.2019.03.001 · Cited by 23
Retrieval-Extinction and Relapse Prevention: Rewriting Maladaptive Drug Memories?
Kuijer, E. J., Ferragud, A., & Milton, A. L. (2020) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2020.00023 · Cited by 24
Ecker, B., Ticic, R., & Hulley, L. (2013) · The Neuropsychotherapist · doi:10.12744/tnpt(1)082-099 · Cited by 24
Role 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
Self-citationGale, 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
Reichelt, A. C., & Lee, J. L. C. (2012) · Psychopharmacology · doi:10.1007/s00213-012-2934-3 · Cited by 24
Boyuan, Z., Chen, Y., Cheng, K., Xueyong, S., & Liu, S. (2014) · Evidence-based Complementary and Alternative Medicine · doi:10.1155/2014/313549 · Cited by 21
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
Duncan, J. R. (2012) · ISRN Neurology · doi:10.5402/2012/972607 · Cited by 22
Conditioned Contribution of Peripheral Cocaine Actions to Cocaine Reward and Cocaine-Seeking
Wang, B., You, Z., Oleson, E. B., Cheer, J. F., Myal, S. E., & Wise, R. A. (2013) · Neuropsychopharmacology · doi:10.1038/npp.2013.75 · Cited by 22
AMPK 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
Self-citationZhang, L., Meng, S., Chen, W., Chen, Y., Huang, E., Zhang, G., Liang, Y., Ding, Z., Xue, Y.-X., Chen, Y., et al. (2021) · Frontiers in Pharmacology · doi:10.3389/fphar.2021.705813 · Cited by 19
Self-citationVermes, J. S., Ayres, R., Goés, A. S., Real, N. D., Araújo, Á. C., Schiller, D., Neto, F. L., & Corchs, F. (2020) · Journal of Affective Disorders · doi:10.1016/j.jad.2020.06.052 · Cited by 24
Milton, A. L., & Everitt, B. J. (2012) · Science · doi:10.1126/science.1221691 · Cited by 21
Baharlouei, N., Sarihi, A., Moradi, M., Zarrabian, S., & Haghparast, A. (2018) · Behavioural Pharmacology · doi:10.1097/fbp.0000000000000375 · Cited by 21
Jorgensen, E. T., Gonzalez, A. E., Harkness, J. H., Hegarty, D. M., Thakar, A., Burchi, D. J., Aadland, J. A., Aicher, S. A., Sorg, B. A., & Brown, T. E. (2020) · Addiction Biology · doi:10.1111/adb.12947 · Cited by 20
A Case for Translation From the Clinic to the Laboratory
Kredlow, M. A., de Voogd, L. D., & Phelps, E. A. (2022) · Perspectives on Psychological Science · doi:10.1177/17456916211039852 · Cited by 25
Heinbockel, H., Wagner, A. D., & Schwabe, L. (2024) · Science Advances · doi:10.1126/sciadv.adm7504 · Cited by 21
Addictive behaviors: Why and how impaired mental time matters?
Noël, X., Jaafari, N., & Bechara, A. (2017) · Progress in brain research · doi:10.1016/bs.pbr.2017.07.011 · Cited by 22
Cross-species approaches to cognitive neuroplasticity research
Mishra, J., & Gazzaley, A. H. (2015) · NeuroImage · doi:10.1016/j.neuroimage.2015.09.002 · Cited by 23
The Computational Nature of Memory ModificationPreprint
Gershman, S. J., Monfils, M., Norman, K. A., & Niv, Y. (2016) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/036442 · Cited by 21
Disrupting astrocyte-neuron lactate transport prevents cocaine seeking after prolonged withdrawal
Chen, W., Zhang, Y., Liang, J., Zhang, Z., Zhang, L., Huang, E., Zhang, G., Lü, L., Han, Y., & Shi, J. (2023) · Science Advances · doi:10.1126/sciadv.adi4462 · Cited by 19
Self-citationEpigenetic modification of PKMζ rescues aging-related cognitive impairment
Chen, C., Meng, S., Xue, Y.-X., Han, Y., Sun, C., Deng, J., Chen, N., Bao, Y., Zhang, F., Cao, L., et al. (2016) · Scientific Reports · doi:10.1038/srep22096 · Cited by 19
Self-citationUsing model systems to understand errant plasticity mechanisms in psychiatric disorders
Averbeck, B. B., & Chafee, M. V. (2016) · Nature Neuroscience · doi:10.1038/nn.4413 · Cited by 18
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
Yuan, K., Cao, L., Xue, Y., Luo, Y., Liu, X., Kong, F., Tabarak, S., Liao, F., Meng, S., Han, Y., et al. (2019) · Addiction Biology · doi:10.1111/adb.12793 · Cited by 19
Self-citationExton-McGuinness, M. T. J., Drame, M. L., Flavell, C. R., & Lee, J. L. C. (2019) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2019.00242 · Cited by 19
Wu, P., Ding, Z., Meng, S., Shen, H., Sun, S.-C., Luo, Y., Liu, J., Lü, L., Zhu, W., & Shi, J. (2014) · Psychopharmacology · doi:10.1007/s00213-014-3462-0 · Cited by 19
Self-citationShumake, J., & Monfils, M. H. (2015) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2015.00355 · Cited by 18
Disruption of relapse to alcohol seeking by aversive counterconditioning following memory retrieval
Goltseker, K., Handrus, H., & Barak, S. (2020) · Addiction Biology · doi:10.1111/adb.12935 · Cited by 18
Sodium butyrate modulates a methamphetamine‐induced conditioned place preference
Zhu, J., Zhao, N., Chen, Y., Zhu, L., Zhong, Q., Liu, J., & Chen, T. (2016) · Journal of Neuroscience Research · doi:10.1002/jnr.23835 · Cited by 18
Ucha, M., Roura‐Martínez, D., Ambrosio, E., & Higuera‐Matas, A. (2020) · Journal of Psychopharmacology · doi:10.1177/0269881120944159 · Cited by 20
Barak, S., & Goltseker, K. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22084090 · Cited by 19
Unconscious learning of likes and dislikes is persistent, resilient, and reconsolidates
Pine, A., Mendelsohn, A., & Dudai, Y. (2014) · Frontiers in Psychology · doi:10.3389/fpsyg.2014.01051 · Cited by 19
Lancaster, C. L., Monfils, M., & Telch, M. J. (2020) · Behaviour Research and Therapy · doi:10.1016/j.brat.2020.103730 · Cited by 18
Deng, J., Shi, L., Yuan, K., Yao, P., Chen, S., Que, J., Gong, Y.-M., Bao, Y., Shi, J., Han, Y., et al. (2020) · Translational Psychiatry · doi:10.1038/s41398-020-01023-w · Cited by 18
Self-citationMonsey, M. S., Ruiz, S. G., & Taylor, J. R. (2020) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2019.00281 · Cited by 17
McKendrick, G., McDevitt, D. S., Shafeek, P., Cottrill, A. R., & Graziane, N. (2022) · Frontiers in Neuroscience · doi:10.3389/fnins.2022.972658 · Cited by 17
Retrieval-extinction of drug memory requires AMPA receptor trafficking
Lv, X., Zhang, J., & Yuan, T. (2022) · Science Advances · doi:10.1126/sciadv.add6642 · Cited by 16
Benvenuti, F., Colombo, D., Soverchia, L., Cannella, N., Domi, E., & Ciccocioppo, R. (2023) · Psychopharmacology · doi:10.1007/s00213-023-06384-w · Cited by 18
Bergeria, C. L., Gipson, C. D., Smith, K. E., Stoops, W. W., & Strickland, J. C. (2024) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2024.105618 · Cited by 17
Krawczyk, M. C., Millan, J., Blake, M. G., Feld, M., & Boccia, M. M. (2019) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2019.00095 · Cited by 16
Rafei, P., Rezapour, T., Bickel, W. K., & Ekhtiari, H. (2021) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2021.692645 · Cited by 17
Buffalari, D. M., Feltenstein, M. W., & See, R. E. (2013) · Psychopharmacology · doi:10.1007/s00213-013-3156-z · Cited by 16
How Mindfulness Training May Help to Reduce Vulnerability for Recurrent Depression
Barnhofer, T., Huntenburg, J. M., Lifshitz, M., Wild, J., Antonova, E., & Margulies, D. S. (2015) · Clinical Psychological Science · doi:10.1177/2167702615595036 · Cited by 18
Of mice and mental health: facilitating dialogue and seeing further
Milton, A. L., & Holmes, E. A. (2018) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2017.0022 · Cited by 16
Zhao, S., Li, Y., Li, M., Wang, R., Bi, Y., Zhang, Y., Lu, X., Yu, D., Yang, L., & Yuan, K. (2018) · Brain Imaging and Behavior · doi:10.1007/s11682-018-9911-3 · Cited by 16
Shen, X., Hui, R., Luo, Y., Yu, H., Feng, S., Xie, B., Bi, H., Galaj, E., Cong, B., Ma, C., et al. (2020) · Frontiers in Pharmacology · doi:10.3389/fphar.2020.00476 · Cited by 15
Self-citationA Hierarchical Instrumental Decision Theory of Nicotine Dependence
Hogarth, L., & Troisi, J. (2015) · Current topics in behavioral neurosciences · doi:10.1007/978-3-319-13665-3_7 · Cited by 16
Yue, J.-L., Yuan, K., Bao, Y., Meng, S., Shi, L., Fang, Q., Guo, X.-J., Cao, L., Sun, Y., Lu, T., et al. (2022) · EBioMedicine · doi:10.1016/j.ebiom.2022.104283 · Cited by 15
Self-citationManipulating critical memory periods to treat psychiatry disorders
Deng, J., Lin, X., Zheng, Y., Su, S., Liu, X., Yuan, K., Shi, L., Bao, Y., & Lü, L. (2023) · 中国科学通报:英文版 · doi:10.1016/j.scib.2023.08.050 · Cited by 15
Self-citationLactate release from astrocytes to neurons contributes to cocaine memory formation
Boury‐Jamot, B., Halfon, O., Magistretti, P. J., & Boutrel, B. (2016) · BioEssays · doi:10.1002/bies.201600118 · Cited by 16
"Abra a felicidade"? Implicações para o vício alimentar
Sawaya, A. L., & Filgueiras, A. R. (2013) · Estudos Avançados · doi:10.1590/s0103-40142013000200005 · Cited by 17
A virtual reality study on postretrieval extinction of smoking memory reconsolidation in smokers
Zandonai, T., Benvegnù, G., Tommasi, F., Ferrandi, E., Libener, E., Ferraro, S., Maris, B., & Chiamulera, C. (2021) · Journal of Substance Abuse Treatment · doi:10.1016/j.jsat.2021.108317 · Cited by 14
Is Reconsolidation a General Property of Memory?
Kim, G., Kwon, M., Kang, W., & Lee, S. (2021) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2021.643106 · Cited by 16
Effects of retrieval-extinction training on internet gaming disorder
Zhao, Q., Zhang, Y., Wang, M., Ren, J., Chen, Y., Chen, X., Wei, Z., Sun, J., & Zhang, X. (2022) · Journal of Behavioral Addictions · doi:10.1556/2006.2022.00006 · Cited by 14
Dai, Z., Liu, Y., Nie, L.-N., Chen, W., Xu, X., Li, Y., Zhang, J., Shen, F., Sui, N., & Liang, J. (2022) · Neuropsychopharmacology · doi:10.1038/s41386-022-01477-0 · Cited by 15
Li, S., Ma, X., Chen, H., Wang, M., Zheng, Y., Yang, B., Ni, H., Potenza, M. N., & Dong, G. (2024) · Journal of Affective Disorders · doi:10.1016/j.jad.2024.01.048 · Cited by 13
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
Self-citationAcquisition of responding with a remifentanil-associated conditioned reinforcer in the rat
Bertz, J. W., & Woods, J. H. (2013) · Psychopharmacology · doi:10.1007/s00213-013-3102-0 · Cited by 14
Lowry, N., Marsden, J., Clydesdale, B., Eastwood, B., Havelka, E. M., & Goetz, C. (2021) · Addiction · doi:10.1111/add.15405 · Cited by 13
Qian, S., Shi, C., Huang, S., Yang, C., & Luo, Y. (2022) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2022.1002139 · Cited by 14
Self-citationBehavioral Roles of Oxytocin and Vasopressin
Benjamin, C. (2012) · InTech eBooks · doi:10.5772/50422 · Cited by 14
Xie, Y., Zhang, Y., Hu, T., Zhao, Z., Liu, Q., & Li, H. (2022) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2022.932939 · Cited by 14
Crisis, what crisis? Addiction neuroscience and the challenges of translation
McLean, S., & Rose, N. (2020) · Wellcome Open Research · doi:10.12688/wellcomeopenres.16265.1 · Cited by 15
Bui, U. T. D., & Milton, A. L. (2023) · Neuroscience · doi:10.1016/j.neuroscience.2023.03.013 · Cited by 13
Garland, E. L., Recasens, M., Taple, B. J., Donaldson, G. W., & Weisberg, R. B. (2024) · Annals of Medicine · doi:10.1080/07853890.2024.2392870 · Cited by 14
The chains of habits: too strong to be broken by reconsolidation blockade?
Vousden, G. H., & Milton, A. L. (2016) · Current Opinion in Behavioral Sciences · doi:10.1016/j.cobeha.2016.11.010 · Cited by 13
Marsden, J., Goetz, C., Meynen, T., Mitcheson, L., Stillwell, G., Eastwood, B., Strang, J., & Grey, N. (2017) · Contemporary Clinical Trials Communications · doi:10.1016/j.conctc.2017.10.009 · Cited by 14
Tan, X., Liu, X., Liu, E., Liu, M., Mu, S., Hang, Z., Han, W., Wang, T., Zhang, Y., Zhang, J., et al. (2022) · Brain Structure and Function · doi:10.1007/s00429-022-02563-1 · Cited by 13
Enhancing cognition by affecting memory reconsolidation
Merlo, E., Milton, A. L., & Everitt, B. J. (2015) · Current Opinion in Behavioral Sciences · doi:10.1016/j.cobeha.2015.02.003 · Cited by 15
Glucose modulates food‐related salience coding of midbrain neurons in humans
Martin, U., Endres, F. S. J., Kölle, M. A., Adolph, O., Widenhorn‐Müller, K., & Grön, G. (2016) · Human Brain Mapping · doi:10.1002/hbm.23316 · Cited by 13
Marion‐Poll, L., Besnard, A., Longueville, S., Valjent, E., Engmann, O., Caboche, J., Hervé, D., & Girault, J. (2018) · Addiction Biology · doi:10.1111/adb.12600 · Cited by 11
Rey, J. F., Gonzalez-Gonzalez, D., & Redondo, J. (2018) · Behavioral Neuroscience · doi:10.1037/bne0000245 · 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
Rottlerin impairs the formation and maintenance of psychostimulant-supported memory
Liao, T. Y., Tzeng, W.-Y., Wu, H.-H., Cherng, C. G., Wang, C.-Y., Hu, S. S., & Yu, L. (2016) · Psychopharmacology · doi:10.1007/s00213-016-4251-8 · Cited by 14
Rivera, C. C., Price, R., Fortuna, R. P., Li, C., Do, C., Shinkle, J., Ghilotti, M., Shi, X., Kirby, L. G., Smith, G. M., et al. (2025) · Translational Psychiatry · doi:10.1038/s41398-025-03734-4 · Cited by 11
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
Reconsolidation of a post-ingestive nutrient memory requires mTOR in the central amygdala
Yan, Y., Zhang, L., Zhu, T., Deng, S., Ma, B., Lv, H., Shan, X., Cheng, H., Jiang, K., Zhang, T., et al. (2020) · Molecular Psychiatry · doi:10.1038/s41380-020-00874-5 · Cited by 12
Wei, X., Chen, J., Zhu, J., Li, Q., Li, W., & Wang, W. (2021) · Brain Imaging and Behavior · doi:10.1007/s11682-020-00447-8 · Cited by 12
Post, R. M., & Kegan, R. G. (2017) · Psychiatry Research · doi:10.1016/j.psychres.2017.01.034 · Cited by 13
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
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Metadata
- Authors
- Xue, Y.-X., Luo, Y.-X., Wu, P., Shi, H.-S., Xue, L.-F., Chen, C., Zhu, W.-L., Ding, Z.-B., Bao, Y.-P., Shi, J., Epstein, D. H., Shaham, Y., & Lu, L.
- Affiliations
- Peking University (CN)
- National Institute on Drug Dependence, Peking University, Beijing 100191, China.
- National Institutes of Health (US)
- Corresponding author
- Xue, Yan-Xue
- Wu, Ping
- Venue
- Science
- Published
- 2012-04-13
- Volume
- 336
- Issue
- 6078
- Pages
- 241-245
- ISSN
- 0036-8075 (ISSN-L)
- 1095-9203
- PMC
- PMC3695463
- OpenAlex
- W2077594514
- Cited by
- 511
- References
- 62
- Citations by year
- 2026: 21 · 2025: 26 · 2024: 25 · 2023: 23 · 2022: 34 · 2021: 33 · 2020: 34 · 2019: 27 · 2018: 44 · 2017: 36 · 2016: 43 · 2015: 42 · 2014: 46 · 2013: 56 · 2012: 21
- FWCI
- 21.75
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Science (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institutes of Health (Z99 DA999999)
- National Institute on Drug Abuse (ZIADA000434)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Health Sciences › Medicine › Epidemiology › Substance Abuse Treatment and Outcomes
- Keywords
- memory retrieval, extinction, drug craving, relapse prevention, heroin addiction, drug-associated memory, reinstatement, renewal, spontaneous recovery, drug-seeking behavior, cue-induced craving, abstinence, non-pharmacological treatment
- MeSH terms
- Amygdala, Animals, Cocaine, Conditioning, Classical, Conditioning, Operant, Cues, Heroin, Extinction, Psychological, Heroin Dependence, Humans, Male, Memory, Protein Kinase C, Mental Recall, Recurrence, Self Administration, Time Factors, Behavior, Addictive, Rats, Sprague-Dawley, Prefrontal Cortex, Cocaine-Related Disorders, Models, Animal, Rats
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