No CrossRef data available.
Article contents
Does inhibitory (dys)function account for involuntary autobiographical memory and déjà vu experience?
Published online by Cambridge University Press: 14 November 2023
Abstract
External cues and internal configuration states are the likely instigators of involuntary autobiographical memories (IAMs) and déjà vu experience. Indeed, Barzykowski and Moulin discuss relevant neuroscientific evidence in this direction. A complementary line of enquiry and evidence is the study of inhibition and its role in memory retrieval, and particularly how its (dys)function may contribute to IAMs and déjà vu.
- Type
- Open Peer Commentary
- Information
- Copyright
- Copyright © The Author(s), 2023. Published by Cambridge University Press
References
Atallah, B. V., & Scanziani, M. (2009). Instantaneous modulation of gamma oscillation frequency by balancing excitation with inhibition. Neuron, 62, 566–577.CrossRefGoogle ScholarPubMed
Barzykowski, K., Radel, R., Niedźwieńska, A., & Kvavilashvili, L. (2019). Why are we not flooded by involuntary thoughts about the past and future? Testing the cognitive inhibition dependency hypothesis. Psychological Research, 83(4), 666–683.CrossRefGoogle Scholar
Barzykowski, K., Staugaard, S. R., & Mazzoni, G. (2021). Retrieval effort or intention: Which is more important for participants’ classification of involuntary and voluntary memories? British Journal of Psychology, 112(4), 1080–1102.CrossRefGoogle ScholarPubMed
Burns, T. F., Haga, T., & Fukai, T. (2022). Multiscale and extended retrieval of associative memory structures in a cortical model of local-global inhibition balance. eNeuro, 9(3), ENEURO.0023-22.2022. https://doi.org/10.1523/ENEURO.0023-22.2022CrossRefGoogle Scholar
Colgin, L. L. (2016). Rhythms of the hippocampal network. Nature Reviews Neuroscience, 17, 239–249.CrossRefGoogle ScholarPubMed
Conway, M. A., & Pleydell-Pearce, C. W. (2000). The construction of autobiographical memories in the self-memory system. Psychological Review, 107(2), 261.CrossRefGoogle ScholarPubMed
Gan, J., Ming Weng, S., Pernía-Andrade, A. J., Csicsvari, J., & Jonas, P. (2017). Phase-locked inhibition, but not excitation, underlies hippocampal ripple oscillations in awake mice in vivo. Neuron, 93, 308–314.CrossRefGoogle Scholar
Haga, T., & Fukai, T. (2019). Extended temporal association memory by modulations of inhibitory circuits. Physical Review Letters, 123, 078101.CrossRefGoogle ScholarPubMed
Holtmaat, A., & Caroni, P. (2016). Functional and structural underpinnings of neuronal assembly formation in learning. Nature Neuroscience, 19, 1553–1562.CrossRefGoogle ScholarPubMed
Isaacson, J. S., & Scanziani, M. (2011). How inhibition shapes cortical activity. Neuron, 72, 231–243.CrossRefGoogle ScholarPubMed
Koolschijn, R. S., Emir, U. E., Pantelides, A. C., Nili, H., Behrens, T. E., & Barron, H. C. (2019). The hippocampus and neocortical inhibitory engrams protect against memory interference. Neuron, 101, 528–541.e6.CrossRefGoogle ScholarPubMed
Kuchibhotla, K. V., Gill, J. V., Lindsay, G. W., Papadoyannis, E. S., Field, R. E., Sten, T. A., … Froemke, R. C. (2017). Parallel processing by cortical inhibition enables context-dependent behavior. Nature Neuroscience, 20, 62–71.CrossRefGoogle ScholarPubMed
Letzkus, J. J., Wolff, S. B., & Lüthi, A. (2015). Disinhibition, a circuit mechanism for associative learning and memory. Neuron, 88, 264–276.CrossRefGoogle ScholarPubMed
Mongillo, G., Rumpel, S., & Loewenstein, Y. (2018). Inhibitory connectivity defines the realm of excitatory plasticity. Nature Neuroscience, 21, 1463–1470.CrossRefGoogle ScholarPubMed
Sayette, M. A., Reichle, E. D., & Schooler, J. W. (2009). Lost in the sauce: The effects of alcohol on mind wandering. Psychological Science, 20(6), 747–752. https://doi.org/10.1111/j.1467-9280.2009.02351.xCrossRefGoogle ScholarPubMed
Vogels, T., & Abbott, L. (2007). Gating deficits in model networks: A path to schizophrenia? Pharmacopsychiatry, 40, S73.CrossRefGoogle ScholarPubMed
Wimber, M., Alink, A., Charest, I., Kriegeskorte, N., & Anderson, M. C. (2015). Retrieval induces adaptive forgetting of competing memories via cortical pattern suppression. Nature Neuroscience, 18, 582–589.CrossRefGoogle ScholarPubMed
Yizhar, O., & Fenno, L. (2011). Neocortical excitation/inhibition balance in information processing and social dysfunction. Nature, 477, 171–178.CrossRefGoogle ScholarPubMed
Target article
Are involuntary autobiographical memory and déjà vu natural products of memory retrieval?
Related commentaries (27)
A possible shared underlying mechanism among involuntary autobiographical memory and déjà vu
A rational analysis and computational modeling perspective on IAM and déjà vu
A spontaneous neural replay account for involuntary autobiographical memories and déjà vu experiences
Accommodating the continuum hypothesis with the déjà vu/déjà vécu distinction
Accounting for the strangeness, infrequency, and suddenness of déjà vu
Are involuntary autobiographical memory and déjà vu cognitive failures?
Cueing involuntary memory
Deconstructing spontaneous expressions of memory in dementia
Distinguishing involuntary autobiographical memories and déjà vu experiences: Different types of cues and memory representations?
Does inhibitory (dys)function account for involuntary autobiographical memory and déjà vu experience?
Déjà vu and involuntary autobiographical memories as two distinct cases of familiarity in patients with Alzheimer's disease
Déjà vu may be illusory gist identification
Déjà vu: A botched memory operation, illegitimate to start with
Evolutionary mismatch and anomalies in the memory system
From jamais to déjà vu: The respective roles of semantic and episodic memory in novelty monitoring and involuntary memory retrieval
Intracranial electrical brain stimulation as an approach to studying the (dis)continuum of memory experiential phenomena
Involuntary autobiographical memories and déjà vu: When and why attention makes a difference
Involuntary memories are not déjà vu
Involuntary memory signals in the medial temporal lobe
Neuropsychological predictions on involuntary autobiographical memory and déjà vu
Oh it's me again: Déjà vu, the brain, and self-awareness
On pattern completion, cues and future-oriented cognition
On the frequency and nature of the cues that elicit déjà vu and involuntary autobiographical memories
The misidentification syndromes and source memory deficits with their neuroanatomical correlates from neuropsychological perspective
The need for a unified framework: How Tulving's framework of memory systems, memory processes, and the SPI-model can guide and sharpen the understanding of déjà vu and involuntary autobiographical memories and add to conceptual clarity
The relation of subjective experience to cognitive processing
What do we gain (or lose) by considering déjà vu a part of autobiographical memory?
Author response
Further advancing theories of retrieval of the personal past