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Nonconscious formation and reactivation of semantic associations by way of the medial temporal lobe
Abstract
A successful strategy to memorize unrelated items is to associate them semantically. This learning method is typical for declarative memory and depends on the medial temporal lobe (MTL). Yet, only a small fraction of perceived items emerge into conscious awareness and receive the status of representations in declarative memory. This functional magnetic resonance imaging (fMRI) study tackled the mnemonic fate of unrelated item pairs processed without conscious awareness. Stimuli consisted of a face and a written profession (experimental condition) or of a face (control condition) exposed very briefly between pattern masks. Although the participants were unaware of the stimuli, activity in the hippocampus and perirhinal cortex was changed in the experimental versus the control condition; perirhinal activity changes correlated with the reaction time measure of the later nonconscious retrieval. For retrieval, the previously presented faces were shown again, this time for conscious inspection. The task was to guess the professional category of each face. This task was to induce a nonconscious retrieval of previously formed face-profession associations. Remarkably, activity in the hippocampus and perirhinal cortex was enhanced when subjects were confronted with faces from the experimental versus the control condition. The degree of hippocampal and perirhinal activation changes correlated with the reaction time measure of nonconscious retrieval. Together, our findings suggest that new semantic associations can be formed and retrieved by way of the medial temporal lobe without awareness of the associations or its components at encoding or any awareness that one is remembering at retrieval.
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“Apart from right STG, there was evidence (at less conservative significance levels) of functional overlaps between dialogic inner speech and ToM in an area of right MTG that has been previously linked to retrieval of face-word associations (Henke et al., 2003) and reflection on third-person traits (Kjaer et al., 2002).”
From The brain's conversation with itself: neural substrates of dialogic inner speech (2016) · cites this paper as Henke et al., 2003
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“However, training such skills does not proceed entirely detached from declarative memory mechanisms, especially at an initial stage of training (e.g., Refs. 198, 533, 1013Refs. 198, 533, , 1014Refs. 198, 533, , 1042)).”
From About Sleep's Role in Memory (2013) · cites this paper as [533]
Citations
Cites
Spatial registration and normalization of images
Friston, K. J., Ashburner, J., Frith, C., Poline, J.-B., Heather, J. D., & Frackowiak, R. S. J. (1995) · Human Brain Mapping · doi:10.1002/hbm.460030303 · Cited by 3,744
Analysis of fMRI Time-Series Revisited
Friston, K. J., Holmes, A. P., Poline, J., Grasby, P. M., Williams, S., Frackowiak, R. S. J., & Turner, R. (1995) · NeuroImage · doi:10.1006/nimg.1995.1007 · Cited by 2,504
Cohen, L., Dehaene, S., Naccache, L., Lehéricy, S., Dehaene-Lambertz, G., Hénaff, M.-A., & Michel, F. (2000) · Brain · doi:10.1093/brain/123.2.291 · Cited by 1,954
SEMANTIC DEMENTIA: PROGRESSIVE FLUENT APHASIA WITH TEMPORAL LOBE ATROPHY
HODGES, J. R., PATTERSON, K., OXBURY, S., & FUNNELL, E. (1992) · Brain · doi:10.1093/brain/115.6.1783 · Cited by 1,710
Conscious and unconscious emotional learning in the human amygdala
Morris, J. S., Öhman, A., & Dolan, R. J. (1998) · Nature · doi:10.1038/30976 · Cited by 1,665 · cited 1×
“The latter interpretation receives support by a study [57] in which a significant”
ResultRecognition memory: What are the roles of the perirhinal cortex and hippocampus?
Brown, M. W., & Aggleton, J. P. (2001) · Nature reviews. Neuroscience · doi:10.1038/35049064 · Cited by 1,624
Functional neuroanatomy of face and object processing. A positron emission tomography study.
Sergent, J., Ohta, S., & Macdonald, B. (1992) · Brain : a journal of neurology · doi:10.1093/brain/115.1.15 · Cited by 1,576
The Selective Impairment of Semantic Memory
Warrington, E. (1975) · Quarterly Journal of Experimental Psychology · doi:10.1080/14640747508400525 · Cited by 1,509
Cerebral mechanisms of word masking and unconscious repetition priming
Dehaene, S., Naccache, L., Cohen, L., Bihan, D. L., Mangin, J.-F., Poline, J.-B., & Rivière, D. (2001) · Nature Neuroscience · doi:10.1038/89551 · Cited by 1,305
Functional anatomy of a common semantic system for words and pictures
Vandenberghe, R. R., Price, C. J., Wise, R., Josephs, O., & Frackowiak, R. S. J. (1996) · Nature · doi:10.1038/383254a0 · Cited by 1,172
Research works printed but not linked: 5
- Birkhäuser R. Near-vision test cards. Basel: Birkhäuser Press; 1995.
- Henke, 1999, H215O PET imaging of conscious and unconscious encoding/retrieval of semantic associations, Society for Neuroscience Abstracts, 25, 647
- Kayser A. Heads. New York: Abbeville Press; 1984.
- Paller, 1999, Neural correlates of memory for faces: hemodynamic and electrophysiological differences between retrieval success and retrieval effort, Society for Neuroscience Abstracts, 25, 648
- Tulving, 1999, Positron emission tomography correlations in and beyond medial temporal lobes, Hippocampus, 9, 71, 10.1002/(SICI)1098-1063(1999)9:1<71::AID-HIPO8>3.0.CO;2-F · DOI
Cited by
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Brain mechanisms for emotional influences on perception and attention: What is magic and what is not
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Metadata
- Authors
- Henke, K., Mondadori, C. R. A., Treyer, V., Nitsch, R. M., Buck, A., & Hock, C.
- Affiliations
- University of Zurich (CH)
- University Hospital Zurich (CH)
- Corresponding author
- Henke, Katharina
- ORCID
- Henke, Katharina
- Venue
- Neuropsychologia
- Publisher
- Elsevier BV
- Published
- 2003-01
- Volume
- 41
- Issue
- 8
- Pages
- 863-876
- ISSN
- 0028-3932 (ISSN-L)
- OpenAlex
- W1989493051
- Cited by
- 128
- References
- 86
- Citations by year
- 2026: 4 · 2025: 1 · 2024: 7 · 2023: 9 · 2022: 3 · 2021: 2 · 2020: 2 · 2019: 5 · 2018: 11 · 2017: 4 · 2016: 4 · 2015: 7 · 2014: 6 · 2013: 8 · 2012: 10
- FWCI
- 2.76
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Neuropsychologia (publishedVersion)
- PubMed (publishedVersion)
- Zurich Open Repository and Archive (University of Zurich) (submittedVersion)
- Funders
- Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung
- 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
- semantic association, medial temporal lobe, hippocampus, perirhinal cortex, declarative memory, reaction time
- MeSH terms
- Adult, Association Learning, Brain Mapping, Concept Formation, Face, Humans, Magnetic Resonance Imaging, Male, Memory, Photic Stimulation, Reaction Time, Semantics, Temporal Lobe
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