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Rapid Erasure of Long-Term Memory Associations in the Cortex by an Inhibitor of PKMζ
Abstract
Little is known about the neuronal mechanisms that subserve long-term memory persistence in the brain. The components of the remodeled synaptic machinery, and how they sustain the new synaptic or cellwide configuration over time, are yet to be elucidated. In the rat cortex, long-term associative memories vanished rapidly after local application of an inhibitor of the protein kinase C isoform, protein kinase M zeta (PKMζ). The effect was observed for at least several weeks after encoding and may be irreversible. In the neocortex, which is assumed to be the repository of multiple types of long-term memory, persistence of memory is thus dependent on ongoing activity of a protein kinase long after that memory is considered to have consolidated into a long-term stable form.
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“Positive feedback loops that maintain key kinases and other molecules in persistently active states at strengthened synapses may also contribute to such long-term memory storage75–79.”
From The right time to learn: Mechanisms and optimization of spaced learning (2016) · cites this paper as [77]
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Cites
REMEMBERING: A STUDY IN EXPERIMENTAL AND SOCIAL PSYCHOLOGY
Bartlett, F. C., & Burt, C. (1933) · British Journal of Educational Psychology · doi:10.1111/j.2044-8279.1933.tb02913.x · Cited by 7,475
Bartlett, F. C., & Kintsch, W. (1995) · Cambridge University Press eBooks · doi:10.1017/cbo9780511759185 · Cited by 2,408
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
Self-citationSchemas and Memory Consolidation.
Tse, D., Langston, R. F., Kakeyama, M., Bethus, I., Spooner, P. A., Wood, E. R., Witter, M. P., & Morris, R. G. M. (2007) · Science · doi:10.1126/science.1135935 · Cited by 1,244
Storage of spatial information by the maintenance mechanism of LTP
Pastalkova, E., Serrano, P., Pinkhasova, D., Wallace, E., Fenton, A. A., & Sacktor, T. C. (2006) · Science · doi:10.1126/science.1128657 · Cited by 848
Self-citationNader, K. (2003) · Trends in Neurosciences · doi:10.1016/s0166-2236(02)00042-5 · Cited by 763
Stability of retrieved memory: Inverse correlation with trace dominance
Eisenberg, M., Kobilo, T., Berman, D. E., & Dudai, Y. (2003) · Science · doi:10.1126/science.1086881 · Cited by 518
Self-citationRites of Passage of the Engram
Dudai, Y., & Eisenberg, M. (2004) · Neuron · doi:10.1016/j.neuron.2004.09.003 · Cited by 478
Self-citationBerman, D. E., & Dudai, Y. (2001) · Science · doi:10.1126/science.1058165 · Cited by 472
Self-citationProtein kinase Mζ is necessary and sufficient for LTP maintenance
Ling, D. S. F., Benardo, L. S., Serrano, P. A., Blace, N., Kelly, M. T., Crary, J. F., & Sacktor, T. C. (2002) · Nature Neuroscience · doi:10.1038/nn829 · Cited by 419
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Translational control of long-lasting synaptic plasticity and memory
Costa-Mattioli, M., Sossin, W. S., Klann, E., & Sonenberg, N. (2009) · Neuron · doi:10.1016/j.neuron.2008.10.055 · Cited by 944
The Restless Engram: Consolidations Never End
Dudai, Y. (2012) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-062111-150500 · Cited by 644
Self-citationThe Cell Biology of Synaptic Plasticity
Ho, V. M., Lee, J.-A., & Martin, K. C. (2011) · Science · doi:10.1126/science.1209236 · Cited by 573
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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., et al. (2012) · Science · doi:10.1126/science.1215070 · Cited by 511
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Crawley, J. N. (2008) · Neuron · doi:10.1016/j.neuron.2008.03.001 · Cited by 439
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Sacktor, T. C. (2011) · Nature Reviews Neuroscience · doi:10.1038/nrn2949 · Cited by 431
Self-citationEarly Tagging of Cortical Networks Is Required for the Formation of Enduring Associative Memory
Lesburguères, E., Gobbo, O. L., Alaux‐Cantin, S., Hambücken, A., Trifilieff, P., & Bontempi, B. (2011) · Science · doi:10.1126/science.1196164 · Cited by 412
Is plasticity of synapses the mechanism of long-term memory storage?
Abraham, W. C., Jones, O. D., & Glanzman, D. L. (2019) · npj Science of Learning · doi:10.1038/s41539-019-0048-y · Cited by 398
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Restivo, L., Vetere, G., Bontempi, B., & Ammassari‐Teule, M. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.0966-09.2009 · Cited by 350
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Davis, R. L., & Zhong, Y. (2017) · Neuron · doi:10.1016/j.neuron.2017.05.039 · Cited by 341
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Volk, L. J., Bachman, J. L., Johnson, R., Yu, Y., & Huganir, R. L. (2013) · Nature · doi:10.1038/nature11802 · Cited by 310
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Migues, P. V., Hardt, O., Wu, D. C., Gamache, K., Sacktor, T. C., Wang, Y. T., & Nader, K. (2010) · Nature Neuroscience · doi:10.1038/nn.2531 · Cited by 283
Self-citationMcCutcheon, J. E., & Marinelli, M. (2009) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2009.06648.x · Cited by 299
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Sacco, T., & Sacchetti, B. (2010) · Science · doi:10.1126/science.1183165 · Cited by 272
Yao, Y., Kelly, M. T., Sajikumar, S., Serrano, P. A., Tian, D., Bergold, P. J., Frey, J. U., & Sacktor, T. C. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.0223-08.2008 · Cited by 272
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Lee, A. M., Kanter, B. R., Wang, D., Lim, J. P., Zou, M. E., Qiu, C., McMahon, T., Dadgar, J., Fischbach-Weiss, S., & Messing, R. O. (2013) · Nature · doi:10.1038/nature11803 · Cited by 259
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Rizzo, F. R., Musella, A., Vito, F. D., Fresegna, D., Bullitta, S., Vanni, V., Guadalupi, L., Bassi, M. S., Buttari, F., Mandolesi, G., et al. (2018) · Neural Plasticity · doi:10.1155/2018/8430123 · Cited by 221
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Sacktor, T. C. (2008) · Progress in Brain Research · doi:10.1016/s0079-6123(07)00002-7 · Cited by 208
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Wu-Zhang, A. X., & Newton, A. C. (2013) · Biochemical Journal · doi:10.1042/bj20130220 · Cited by 200
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Kotaleski, J. H., & Blackwell, K. T. (2010) · Nature reviews. Neuroscience · doi:10.1038/nrn2807 · Cited by 195
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Torregrossa, M. M., & Taylor, J. R. (2013) · Psychopharmacology · doi:10.1007/s00213-012-2750-9 · Cited by 172
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Shema, R., Haramati, S., Ron, S., Hazvi, S., Chen, A., Sacktor, T. C., & Dudai, Y. (2011) · Science · doi:10.1126/science.1200215 · Cited by 181
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Geuter, S., Koban, L., & Wager, T. D. (2017) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-072116-031132 · Cited by 174
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Chen, S., Cai, D., Pearce, K. C., Sun, P. Y., Roberts, A. C., & Glanzman, D. L. (2014) · eLife · doi:10.7554/elife.03896 · Cited by 154
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Ka, M., Condorelli, G., Woodgett, J. R., & Kim, W.-Y. (2014) · Development · doi:10.1242/dev.108282 · Cited by 125
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Rahn, E. J., Karlsson, M. G., & Sweatt, J. D. (2013) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2013.06.008 · Cited by 113
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Huentelman, M. J., Stephan, D. A., Talboom, J. S., Corneveaux, J. J., Reiman, D., Gerber, J. D., Barnes, C. A., Alexander, G. E., Reiman, E. M., & Bimonte‐Nelson, H. A. (2009) · Behavioral Neuroscience · doi:10.1037/a0014260 · Cited by 107
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Li, Y.-Q., Xue, Y.-X., He, Y., Li, F., Xue, L., Xu, C., Sacktor, T. C., Shaham, Y., & Lü, L. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.5884-10.2011 · Cited by 104
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Bekinschtein, P., Katche, C., Slipczuk, L. N., Gonzalez, C., Dorman, G. S., Cammarota, M., Izquierdo, I., & Medina, J. H. (2010) · Neurotoxicity Research · doi:10.1007/s12640-010-9155-5 · Cited by 87
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Hardt, O., Migues, P. V., Hastings, M., Wong, J., & Nader, K. (2010) · Hippocampus · doi:10.1002/hipo.20708 · Cited by 79
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Liao, S. M., & Sandberg, A. (2008) · Neuroethics · doi:10.1007/s12152-008-9009-5 · Cited by 84
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Bougie, J. K., Lim, T., Farah, C. A., Manjunath, V., Nagakura, I., Ferraro, G. B., & Sossin, W. S. (2009) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2009.06045.x · Cited by 74
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Ren, Z.-Y., Liu, M.-M., Xue, Y.-X., Ding, Z.-B., Xue, L.-F., Zhai, S.-D., & Lu, L. (2013) · Neuropsychopharmacology · doi:10.1038/npp.2012.243 · Cited by 73
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Mastushita-Sakai, T., White‐Grindley, E., Samuelson, J., Seidel, C. W., & Si, K. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1004433107 · Cited by 72
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Kukushkin, N. V., & Carew, T. J. (2017) · Neuron · doi:10.1016/j.neuron.2017.05.029 · Cited by 72
He, Y., Xue, Y.-X., Wang, J., Fang, Q., Liu, J., Xue, L., & Lü, L. (2011) · Neuropsychopharmacology · doi:10.1038/npp.2011.63 · Cited by 67
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Cao, X., Wang, H., Mei, B., An, S., Yin, L., Wang, L. P., & Tsien, J. Z. (2008) · Neuron · doi:10.1016/j.neuron.2008.08.027 · Cited by 69
Irmady, K., Hale, C. R., Qadri, R., Fak, J. J., Simelane, S., Carroll, T., Przedborski, S., & Darnell, R. B. (2023) · Nature Communications · doi:10.1038/s41467-023-39652-6 · Cited by 63
Madroñal, N., Gruart, A., Sacktor, T. C., & Delgado-Garcia, J. M. (2010) · PLoS ONE · doi:10.1371/journal.pone.0010400 · Cited by 63
Self-citationPersistent increased PKMζ in long-term and remote spatial memory
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Tabatadze, N., Tomas, C., McGonigal, R., Lin, B., Schook, A. C., & Routtenberg, A. (2011) · Hippocampus · doi:10.1002/hipo.20991 · Cited by 61
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Inoue, A., Sawatari, E., Hisamoto, N., Kitazono, T., Teramoto, T., Fujiwara, M., Matsumoto, K., & Ishihara, T. (2013) · Cell Reports · doi:10.1016/j.celrep.2013.02.019 · Cited by 59
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Parsons, R. G., & Davis, M. (2011) · Nature Neuroscience · doi:10.1038/nn.2745 · Cited by 57
Villareal, G., Li, Q., Cai, D., Fink, A. E., Lim, T., Bougie, J. K., Sossin, W. S., & Glanzman, D. L. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.4149-08.2009 · Cited by 57
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Chen, G., Wang, L. P., & Tsien, J. Z. (2009) · PLoS ONE · doi:10.1371/journal.pone.0008256 · Cited by 56
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Kim, J., Song, B., Hong, I., Kim, J., Lee, J. L. C., Park, S., Eom, J. Y., Lee, C. J., Lee, S., & Choi, S. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.0940-10.2010 · Cited by 56
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Metadata
- Authors
- Shema, R., Sacktor, T. C., & Dudai, Y.
- Affiliations
- SUNY Downstate Health Sciences University (US)
- Corresponding author
- Dudai, Yadin
- Venue
- Science
- Published
- 2007-08-17
- Volume
- 317
- Issue
- 5840
- Pages
- 951-953
- ISSN
- 0036-8075 (ISSN-L)
- 1095-9203
- OpenAlex
- W2099036181
- Cited by
- 353
- References
- 32
- Citations by year
- 2026: 6 · 2025: 1 · 2024: 5 · 2023: 10 · 2022: 5 · 2021: 8 · 2020: 9 · 2019: 13 · 2018: 15 · 2017: 24 · 2016: 18 · 2015: 26 · 2014: 20 · 2013: 36 · 2012: 30
- FWCI
- 14.49
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Science (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institute of Mental Health (MH 57068, R01MH53576, R01MH053576)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory Processes and Influences
- Keywords
- long-term memory, memory persistence, PKMzeta, protein kinase C, memory erasure, neocortex, synaptic plasticity, memory consolidation
- MeSH terms
- Animals, Conditioning, Psychological, Enzyme Inhibitors, Hippocampus, Male, Memory, Oligopeptides, Protein Kinase C, Taste, Time Factors, Rats, Wistar, Neocortex, Rats
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