Co-activation of the amygdala, hippocampus and inferior frontal gyrus during autobiographical memory retrieval
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Functional MRI was used to investigate the role of medial temporal lobe and inferior frontal lobe regions in autobiographical recall. Prior to scanning, participants generated cue words for 50 autobiographical memories and rated their phenomenological properties using our autobiographical memory questionnaire (AMQ). During scanning, the cue words were presented and participants pressed a button when they retrieved the associated memory. The autobiographical retrieval task was interleaved in an event-related design with a semantic retrieval task (category generation). Region-of-interest analyses showed greater activation of the amygdala, hippocampus, and right inferior frontal gyrus during autobiographical retrieval relative to semantic retrieval. In addition, the left inferior frontal gyrus showed a more prolonged duration of activation in the semantic retrieval condition. A targeted correlational analysis revealed pronounced functional connectivity among the amygdala, hippocampus, and right inferior frontal gyrus during autobiographical retrieval but not during semantic retrieval. These results support theories of autobiographical memory that hypothesize co-activation of frontotemporal areas during recollection of episodes from the personal past.
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Most prior laboratory-based EM studies used cue words or images to trigger memory retrieval and mental time travel to the past in a controlled fashion.
“Most prior laboratory-based EM studies used cue words or images to trigger memory retrieval and mental time travel to the past in a controlled fashion [5,6,12,31,60,80,87,103–105].”
From First-person view of one’s body in immersive virtual reality: Influence on episodic memory (2019) · cites this paper as [60]
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Spreng, R. N., Mar, R. A., & Kim, A. S. N. (2009) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.2008.21029 · Cited by 2,143 · see citing works
Cognitive neuroscience of emotional memory
LaBar, K. S., & Cabeza, R. (2006) · Nature Reviews Neuroscience · doi:10.1038/nrn1825 · Cited by 1,834 · see citing works
Self-citationPrefrontal-Subcortical Pathways Mediating Successful Emotion Regulation
Wager, T. D., Davidson, M. L., Hughes, B. L., Lindquist, M. A., & Ochsner, K. N. (2008) · Neuron · doi:10.1016/j.neuron.2008.09.006 · Cited by 1,761 · see citing works
“Kim et al., for example, found amygdala increases when participants increased positive emotional responses (Kim and Hamann, 2007), and studies of autobiographical memory retrieval have found co-activation of amygdala and vlPFC (Greenberg et al., 2005; Maguire and Frith, 2003).”
Functional neuroimaging of autobiographical memory
Cabeza, R., & St Jacques, P. (2007) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2007.02.005 · Cited by 736 · see citing works
Self-citationThe role of the hippocampus in flexible cognition and social behavior
Rubin, R. D., Watson, P. D., Duff, M. C., & Cohen, N. J. (2014) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2014.00742 · Cited by 489 · see citing works
Roozendaal, B., & McGaugh, J. L. (2011) · Behavioral Neuroscience · doi:10.1037/a0026187 · Cited by 445 · see citing works
The inferior parietal lobule and temporoparietal junction: A network perspective
Igelström, K. M., & Graziano, M. S. A. (2017) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2017.01.001 · Cited by 367 · see citing works
Daselaar, S. M., Rice, H. J., Greenberg, D. L., Cabeza, R., LaBar, K. S., & Rubin, D. C. (2008) · Cerebral Cortex · doi:10.1093/cercor/bhm048 · Cited by 341 · see citing works
Self-citationAbnormal Amygdala Resting-State Functional Connectivity in Adolescent Depression
Cullen, K. R., Westlund, M. K., Klimes-Dougan, B., Mueller, B. A., Houri, A., Eberly, L. E., & Lim, K. O. (2014) · JAMA Psychiatry · doi:10.1001/jamapsychiatry.2014.1087 · Cited by 324 · see citing works
Neural substrates of the self‐memory system: New insights from a meta‐analysis
Martinelli, P., Sperduti, M., & Piolino, P. (2013) · Human Brain Mapping · doi:10.1002/hbm.22008 · Cited by 281 · see citing works
rTMS to the right inferior parietal lobule disrupts self-other discrimination
Uddin, L. Q., Molnar-Szakacs, I., Zaidel, E., & Iacoboni, M. (2006) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nsl003 · Cited by 267 · see citing works
Task and Content Modulate Amygdala-Hippocampal Connectivity in Emotional Retrieval
Smith, A. P. R., Stephan, K. E., Rugg, M. D., & Dolan, R. J. (2006) · Neuron · doi:10.1016/j.neuron.2005.12.025 · Cited by 252 · see citing works
Carhart-Harris, R. L., Leech, R., Williams, T. M., Erritzoe, D., Abbasi, N., Bargiotas, T., Hobden, P., Sharp, D. J., Evans, J., Feilding, A., et al. (2012) · British Journal of Psychiatry · doi:10.1192/bjp.bp.111.103309 · Cited by 237 · see citing works
How personal experience modulates the neural circuitry of memories of September 11
Sharot, T., Martorella, E. A., Delgado, M. R., & Phelps, E. A. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0609230103 · Cited by 200 · see citing works
The effect of shame and shame memories on paranoid ideation and social anxiety
Matos, M., Pinto‐Gouveia, J., & Gilbert, P. (2013) · Clinical Psychology & Psychotherapy · doi:10.1002/cpp.1766 · Cited by 178 · see citing works
Lang, S., Kroll, A., Lipinski, S. J., Wessa, M., Ridder, S., Christmann, C., Schad, L. R., & Flor, H. (2009) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2009.06624.x · Cited by 171 · see citing works
Pinto-Gouveia, J., & Matos, M. (2011) · Applied Cognitive Psychology · doi:10.1002/acp.1689 · Cited by 167 · see citing works
Adrenal stress hormones, amygdala activation, and memory for emotionally arousing experiences
Roozendaal, B., Barsegyan, A., & Lee, S. (2007) · Progress in Brain Research · doi:10.1016/s0079-6123(07)67006-x · Cited by 154 · see citing works
The functional neuroanatomy of odor evoked autobiographical memories cued by odors and words
Arshamian, A., Iannilli, E., Gerber, J. C., Willander, J., Persson, J., Seo, H.-S., Hummel, T., & Larsson, M. (2013) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2012.10.023 · Cited by 148 · see citing works
Young, K. D., Siegle, G. J., Misaki, M., Zotev, V., Phillips, R., Drevets, W. C., & Bodurka, J. (2018) · NeuroImage: Clinical · doi:10.1016/j.nicl.2017.12.004 · Cited by 118 · see citing works
Holland, A. C., Addis, D. R., & Kensinger, E. A. (2011) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2011.07.015 · Cited by 118 · see citing works
St. Jacques, P. L., Botzung, A., Miles, A., & Rubin, D. C. (2011) · Journal of Psychiatric Research · doi:10.1016/j.jpsychires.2010.10.011 · Cited by 112 · see citing works
Self-citationGüroğlu, B., Haselager, G. J. T., van Lieshout, C. F. M., Takashima, A., Rijpkema, M., & Fernández, G. (2008) · NeuroImage · doi:10.1016/j.neuroimage.2007.09.007 · Cited by 107 · see citing works
Inserra, A. (2018) · Frontiers in Pharmacology · doi:10.3389/fphar.2018.00330 · Cited by 91 · see citing works
First-person view of one’s body in immersive virtual reality: Influence on episodic memory
Bréchet, L., Mange, R., Herbelin, B., Theillaud, Q., Gauthier, B., Serino, A., & Blanke, O. (2019) · PLOS ONE · doi:10.1371/journal.pone.0197763 · Cited by 85 · see citing works
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The neurobiology of self-knowledge in depressed and self-injurious youth
Quevedo, K., Martin, J., Scott, H., Smyda, G., & Pfeifer, J. H. (2016) · Psychiatry Research Neuroimaging · doi:10.1016/j.pscychresns.2016.06.015 · Cited by 50 · see citing works
- Authors
- Greenberg, D. L., Rice, H. J., Cooper, J. J., Cabeza, R., Rubin, D. C., & LaBar, K. S.
- Affiliations
- Duke University (US)
- Corresponding author
- LaBar, Kevin S.
- Venue
- Neuropsychologia
- Publisher
- Elsevier BV
- Published
- 2005-01
- Volume
- 43
- Issue
- 5
- Pages
- 659-674
- ISSN
- 0028-3932 (ISSN-L)
- OpenAlex
- W2142343279
- Cited by
- 273
- References
- 117
- Citations by year
- 2026: 2 · 2025: 10 · 2024: 9 · 2023: 6 · 2022: 2 · 2021: 19 · 2020: 11 · 2019: 7 · 2018: 9 · 2017: 26 · 2016: 11 · 2015: 12 · 2014: 12 · 2013: 17 · 2012: 23
- FWCI
- 5.88
- Type
- journal article
- Language
- en
- Open access
- green
- hdl.handle.net
- Licence
- cc-by-nc-nd
- www.elsevier.com/tdm/userlicense/1.0/ (tdm)
- Locations
- Neuropsychologia (publishedVersion)
- PubMed (publishedVersion)
- DukeSpace (Duke University) (submittedVersion, cc-by-nc-nd)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory Processes and Influences
- Social Sciences › Psychology › Developmental and Educational Psychology › Identity, Memory, and Therapy
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Keywords
- autobiographical memory, memory retrieval, amygdala, hippocampus, inferior frontal gyrus, medial temporal lobe, semantic memory retrieval, functional connectivity, recollection
- MeSH terms
- Adolescent, Adult, Amygdala, Brain Mapping, Female, Gyrus Cinguli, Hippocampus, Humans, Image Processing, Computer-Assisted, Functional Laterality, Magnetic Resonance Imaging, Male, Oxygen, Surveys and Questionnaires, Reaction Time, Mental Recall
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.
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