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A spontaneous neural replay account for involuntary autobiographical memories and déjà vu experiences

Published online by Cambridge University Press:  14 November 2023

Mohith M. Varma
Affiliation:
Department of Management, School of Business, Hong Kong Baptist University, Hong Kong, S.A.R. China rongjunyu@hkbu.edu.hk
Rongjun Yu
Affiliation:
Department of Management, School of Business, Hong Kong Baptist University, Hong Kong, S.A.R. China rongjunyu@hkbu.edu.hk

Abstract

Barzykowski and Moulin argue both involuntary autobiographical memories and déjà vu experiences rely on the same involuntary memory retrieval processes but their underlying neurological basis remains unclear. We propose spontaneous neural replay in the default mode network (DMN) and hippocampus as the basis for involuntary autobiographical memories, whereas for déjà vu experiences such transient activation is limited to the DMN.

Type
Open Peer Commentary
Copyright
Copyright © The Author(s), 2023. Published by Cambridge University Press

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References

Cabeza, R., & St Jacques, P. (2007). Functional neuroimaging of autobiographical memory. Trends in Cognitive Sciences, 11(5), 219227.CrossRefGoogle ScholarPubMed
Deuker, L., Olligs, J., Fell, J., Kranz, T. A., Mormann, F., Montag, C., … Axmacher, N. (2013). Memory consolidation by replay of stimulus-specific neural activity. Journal of Neuroscience, 33(49), 1937319383.CrossRefGoogle ScholarPubMed
Dickey, C. W., Verzhbinsky, I. A., Jiang, X., Rosen, B. Q., Kajfez, S., Stedelin, B., … Halgren, E. (2022). Widespread ripples synchronize human cortical activity during sleep, waking, and memory recall. Proceedings of the National Academy of Sciences, 119(28), e2107797119.CrossRefGoogle ScholarPubMed
Gillespie, A. K., Maya, D. A. A., Denovellis, E. L., Liu, D. F., Kastner, D. B., Coulter, M. E., … Frank, L. M. (2021). Hippocampal replay reflects specific past experiences rather than a plan for subsequent choice. Neuron, 109(19), 31493163.CrossRefGoogle ScholarPubMed
Goode, T. D., Tanaka, K. Z., Sahay, A., & McHugh, T. J. (2020). An integrated index: Engrams, place cells, and hippocampal memory. Neuron, 107(5), 805820.CrossRefGoogle ScholarPubMed
Higgins, C., Liu, Y., Vidaurre, D., Kurth-Nelson, Z., Dolan, R., Behrens, T., & Woolrich, M. (2021). Replay bursts in humans coincide with activation of the default mode and parietal alpha networks. Neuron, 109(5), 882893.CrossRefGoogle ScholarPubMed
Kaefer, K., Stella, F., McNaughton, B. L., & Battaglia, F. P. (2022). Replay, the default mode network and the cascaded memory systems model. Nature Reviews Neuroscience, 23(10), 628640.CrossRefGoogle ScholarPubMed
Kvavilashvili, L., Niedźwieńska, A., Gilbert, S. J., & Markostamou, I. (2020). Deficits in spontaneous cognition as an early marker of Alzheimer's disease. Trends in Cognitive Sciences, 24(4), 285301.CrossRefGoogle ScholarPubMed
Liu, Y., Nour, M. M., Schuck, N. W., Behrens, T. E., & Dolan, R. J. (2022). Decoding cognition from spontaneous neural activity. Nature Reviews Neuroscience, 23(4), 204214.CrossRefGoogle ScholarPubMed
McCormick, C., Rosenthal, C. R., Miller, T. D., & Maguire, E. A. (2018). Mind-wandering in people with hippocampal damage. Journal of Neuroscience, 38(11), 27452754.CrossRefGoogle ScholarPubMed
O'Callaghan, C., Shine, J. M., Lewis, S. J., Andrews-Hanna, J. R., & Irish, M. (2015). Shaped by our thoughts – a new task to assess spontaneous cognition and its associated neural correlates in the default network. Brain and Cognition, 93, 110.CrossRefGoogle ScholarPubMed
Palmqvist, S., Schöll, M., Strandberg, O., Mattsson, N., Stomrud, E., Zetterberg, H., … Hansson, O. (2017). Earliest accumulation of β-amyloid occurs within the default-mode network and concurrently affects brain connectivity. Nature Communications, 8(1), 113.CrossRefGoogle ScholarPubMed
Philippi, C. L., Tranel, D., Duff, M., & Rudrauf, D. (2015). Damage to the default mode network disrupts autobiographical memory retrieval. Social Cognitive and Affective Neuroscience, 10(3), 318326.CrossRefGoogle Scholar
Schuck, N. W., & Niv, Y. (2019). Sequential replay of nonspatial task states in the human hippocampus. Science, 364(6447).CrossRefGoogle ScholarPubMed
Scoville, W. B., & Milner, B. (1957). Loss of recent memory after bilateral hippocampal lesions. Journal of Neurology, Neurosurgery, and Psychiatry, 20(1), 11.CrossRefGoogle ScholarPubMed
Simons, J. S., Ritchey, M., & Fernyhough, C. (2022). Brain mechanisms underlying the subjective experience of remembering. Annual Review of Psychology, 73, 159186.CrossRefGoogle ScholarPubMed
Vaz, A. P., Wittig, J. H. Jr., Inati, S. K., & Zaghloul, K. A. (2020). Replay of cortical spiking sequences during human memory retrieval. Science, 367(6482), 11311134.CrossRefGoogle ScholarPubMed