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Emotional learning selectively and retroactively strengthens memories for related events
Open accessAbstract
Neurobiological models of long-term memory propose a mechanism by which initially weak memories are strengthened through subsequent activation that engages common neural pathways minutes to hours later. This synaptic tag-and-capture model has been hypothesized to explain how inconsequential information is selectively consolidated following salient experiences. Behavioural evidence for tag-and-capture is provided by rodent studies in which weak early memories are strengthened by future behavioural training. Whether a process of behavioural tagging occurs in humans to transform weak episodic memories into stable long-term memories is unknown. Here we show, in humans, that information is selectively consolidated if conceptually related information, putatively represented in a common neural substrate, is made salient through an emotional learning experience. Memory for neutral objects was selectively enhanced if other objects from the same category were paired with shock. Retroactive enhancements as a result of emotional learning were observed following a period of consolidation, but were not observed in an immediate memory test or for items strongly encoded before fear conditioning. These findings provide new evidence for a generalized retroactive memory enhancement, whereby inconsequential information can be retroactively credited as relevant, and therefore selectively remembered, if conceptually related information acquires salience in the future.
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“Moreover, the present VR setup allowed us to project the same 3D virtual scenes during the encoding and retrieval sessions, providing us arguably with a level of experimental control that is comparable to examinations of classical word/picture-based recognition paradigms [99–102], which are typically used to study memory.”
From First-person view of one’s body in immersive virtual reality: Influence on episodic memory (2019) · cites this paper as [100]
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Cites
Lakens, D. (2013) · Frontiers in Psychology · doi:10.3389/fpsyg.2013.00863 · Cited by 10,303
THE AMYGDALA MODULATES THE CONSOLIDATION OF MEMORIES OF EMOTIONALLY AROUSING EXPERIENCES
McGaugh, J. L. (2004) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.27.070203.144157 · Cited by 2,296
Cognitive neuroscience of emotional memory
LaBar, K. S., & Cabeza, R. (2006) · Nature Reviews Neuroscience · doi:10.1038/nrn1825 · Cited by 1,834
Synaptic tagging and long-term potentiation
Frey, U., & Morris, R. G. M. (1997) · Nature · doi:10.1038/385533a0 · Cited by 1,736
The Representation of Object Concepts in the Brain
Martin, A. D. (2006) · Annual Review of Psychology · doi:10.1146/annurev.psych.57.102904.190143 · Cited by 1,631
Mechanisms of emotional arousal and lasting declarative memory.
Cahill, L., & McGaugh, J. L. (1998) · Trends in Neurosciences · doi:10.1016/s0166-2236(97)01214-9 · Cited by 1,575
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
Sleep-dependent memory triage: evolving generalization through selective processing
Stickgold, R., & Walker, M. P. (2013) · Nature Neuroscience · doi:10.1038/nn.3303 · Cited by 755
Integrating Memories in the Human Brain: Hippocampal-Midbrain Encoding of Overlapping Events
Daphna Shohamy, A., & Wagner, A. D. (2008) · Neuron · doi:10.1016/j.neuron.2008.09.023 · Cited by 525
Paired-associate learning as a function of arousal and interpolated interval.
Kleinsmith, L. J., & Kaplan, S. (1963) · Journal of Experimental Psychology · doi:10.1037/h0040288 · Cited by 495
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Green, D. M., Moeck, E. K., & Takarangi, M. K. T. (2024) · Consciousness and Cognition · doi:10.1016/j.concog.2024.103695
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Britt, N., Chau, J., & Sun, H. (2024) · Research Square · doi:10.21203/rs.3.rs-5010340/v1
Mechanisms of systems consolidation and their behavioral consequence
Tompary, A., & Murty, V. P. (2024) · Elsevier eBooks · doi:10.1016/b978-0-443-15754-7.00054-7
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Ivanova, A., Ivashkin, D., Toropova, K. A., Ivashkina, O. I., & Anokhin, K. V. (2024) · Scientific School Dynamics of Complex Networks and their Applications (DCNA) · doi:10.1109/dcna63495.2024.10718502
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LaBar, K. S. (2025) · Cambridge University Press eBooks · doi:10.1017/9781009342919.021
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Timing of reward cues alters the interaction between reward and interest on memory over time
Hu, Z., & Yang, J. (2025) · npj Science of Learning · doi:10.1038/s41539-025-00374-7
Diversifying Description Phase Techniques During DebriefingPreprint
Serrat‐Antolí, N., Martínez, S. O., Camps, A., & González-Fernández, A. (2026) · Research Square · doi:10.21203/rs.3.rs-8462808/v1
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Söylemez, S., & Kapucu, A. (2026) · Research Square · doi:10.21203/rs.3.rs-8501007/v1
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Huang, R., CHEN, Z., Zou, F., Ali, A., Jain, S., & Clewett, D. (2026) · SSRN Electronic Journal · doi:10.2139/ssrn.6400626
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Zhang, Q., Li, Z., Zhao, H., & Liang, J. (2026) · BMC Nursing · doi:10.1186/s12912-026-04452-y
A disynaptic pathway linking the cerebellum to the hippocampus
Zenelaj, X. (2024) · theses.fr (ABES) · doi:10.70675/94d94e26z34bez4c6bz880az1e3421294c0a
Nie, A., Deng, C., Yin, H. M., & Ding, X. (2026) · Quarterly Journal of Experimental Psychology · doi:10.1177/17470218261444325
Bączkowski, B. M., Sakaki, M., Kalbe, F., Murayama, K., & Schwabe, L. (2026) · Psychonomic Bulletin & Review · doi:10.3758/s13423-026-02924-5
Disgust learning and memory generalization across category exemplars and learning contexts
Söylemez, S., & Kapucu, A. (2026) · Motivation and Emotion · doi:10.1007/s11031-026-10260-3
Effects of threat intensity on sensory preconditioning
Ouyang, L., Cooper, S. E., & Dunsmoor, J. E. (2026) · Biological Psychology · doi:10.1016/j.biopsycho.2026.109351
Self-citationDifferential Modulation of Retroactive Emotional Learning on Concrete and Abstract Word Processing
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Metadata
- Authors
- Dunsmoor, J. E., Murty, V. P., Davachi, L., & Phelps, E. A.
- Affiliations
- New York University (US)
- Nathan Kline Institute for Psychiatric Research (US)
- Corresponding author
- Davachi, Lila
- Phelps, Elizabeth A.
- Venue
- Nature
- Published
- 2015-01-21
- Volume
- 520
- Issue
- 7547
- Pages
- 345-348
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- PMC
- PMC4432479
- OpenAlex
- W2067886794
- Cited by
- 332
- References
- 26
- Citations by year
- 2026: 15 · 2025: 18 · 2024: 46 · 2023: 28 · 2022: 19 · 2021: 26 · 2020: 32 · 2019: 45 · 2018: 31 · 2017: 29 · 2016: 27 · 2015: 15
- FWCI
- 20.21
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- RePEc: Research Papers in Economics (submittedVersion)
- Funders
- National Institutes of Health
- National Institute of Mental Health (R01MH074692, R01 MH047692, R01MH097085, T32MH019524)
- National Institute on Drug Abuse (F31 DA036361, F32DA036361)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory Processes and Influences
- Life Sciences › Neuroscience › Cognitive Neuroscience › Sleep and Wakefulness Research
- Keywords
- retrograde amnesia, emotional learning, fear conditioning, episodic memory consolidation, memory reconsolidation, synaptic tagging and capture
- MeSH terms
- Conditioning, Classical, Emotions, Fear, Female, Humans, Male, Memory, Short-Term, Models, Neurological, Neural Pathways, Photic Stimulation, Mental Recall, Time Factors, Recognition, Psychology, Young Adult, Memory, Long-Term, Memory, Episodic
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