Author
Listed:
- Leila Reddy
(Université de Toulouse, Centre de Recherche Cerveau et Cognition, Université Paul Sabatier
CNRS, UMR 5549, Faculté de Médecine de Purpan
Artificial and Natural Intelligence Toulouse Institute (ANITI))
- Matthew W. Self
(Netherlands Institute for Neuroscience (KNAW))
- Benedikt Zoefel
(Université de Toulouse, Centre de Recherche Cerveau et Cognition, Université Paul Sabatier
CNRS, UMR 5549, Faculté de Médecine de Purpan)
- Marlène Poncet
(Université de Toulouse, Centre de Recherche Cerveau et Cognition, Université Paul Sabatier
CNRS, UMR 5549, Faculté de Médecine de Purpan)
- Jessy K. Possel
(Netherlands Institute for Neuroscience (KNAW))
- Judith C. Peters
(Netherlands Institute for Neuroscience (KNAW)
Faculty of Psychology and Neuroscience, Maastricht University)
- Johannes C. Baayen
(Amsterdam University Medical Centers, location VUmc, Departments of Neurophysiology and Neurosurgery)
- Sander Idema
(Amsterdam University Medical Centers, location VUmc, Departments of Neurophysiology and Neurosurgery)
- Rufin VanRullen
(Université de Toulouse, Centre de Recherche Cerveau et Cognition, Université Paul Sabatier
CNRS, UMR 5549, Faculté de Médecine de Purpan
Artificial and Natural Intelligence Toulouse Institute (ANITI))
- Pieter R. Roelfsema
(Netherlands Institute for Neuroscience (KNAW)
Centre for Neurogenomics and Cognitive Research, Vrije Universiteit
Psychiatry Department, Academic Medical Center)
Abstract
The ability to maintain a sequence of items in memory is a fundamental cognitive function. In the rodent hippocampus, the representation of sequentially organized spatial locations is reflected by the phase of action potentials relative to the theta oscillation (phase precession). We investigated whether the timing of neuronal activity relative to the theta brain oscillation also reflects sequence order in the medial temporal lobe of humans. We used a task in which human participants learned a fixed sequence of pictures and recorded single neuron and local field potential activity with implanted electrodes. We report that spikes for three consecutive items in the sequence (the preferred stimulus for each cell, as well as the stimuli immediately preceding and following it) were phase-locked at distinct phases of the theta oscillation. Consistent with phase precession, spikes were fired at progressively earlier phases as the sequence advanced. These findings generalize previous findings in the rodent hippocampus to the human temporal lobe and suggest that encoding stimulus information at distinct oscillatory phases may play a role in maintaining sequential order in memory.
Suggested Citation
Leila Reddy & Matthew W. Self & Benedikt Zoefel & Marlène Poncet & Jessy K. Possel & Judith C. Peters & Johannes C. Baayen & Sander Idema & Rufin VanRullen & Pieter R. Roelfsema, 2021.
"Theta-phase dependent neuronal coding during sequence learning in human single neurons,"
Nature Communications, Nature, vol. 12(1), pages 1-9, December.
Handle:
RePEc:nat:natcom:v:12:y:2021:i:1:d:10.1038_s41467-021-25150-0
DOI: 10.1038/s41467-021-25150-0
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Citations
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Cited by:
- Louis Kang & Taro Toyoizumi, 2024.
"Distinguishing examples while building concepts in hippocampal and artificial networks,"
Nature Communications, Nature, vol. 15(1), pages 1-19, December.
- Miles Wischnewski & Harry Tran & Zhihe Zhao & Sina Shirinpour & Zachary J. Haigh & Jonna Rotteveel & Nipun D. Perera & Ivan Alekseichuk & Jan Zimmermann & Alexander Opitz, 2024.
"Induced neural phase precession through exogenous electric fields,"
Nature Communications, Nature, vol. 15(1), pages 1-15, December.
- Michele N. Insanally & Badr F. Albanna & Jade Toth & Brian DePasquale & Saba Shokat Fadaei & Trisha Gupta & Olivia Lombardi & Kishore Kuchibhotla & Kanaka Rajan & Robert C. Froemke, 2024.
"Contributions of cortical neuron firing patterns, synaptic connectivity, and plasticity to task performance,"
Nature Communications, Nature, vol. 15(1), pages 1-21, December.
- Daniel Müller-Komorowska & Baris Kuru & Heinz Beck & Oliver Braganza, 2023.
"Phase information is conserved in sparse, synchronous population-rate-codes via phase-to-rate recoding,"
Nature Communications, Nature, vol. 14(1), pages 1-18, December.
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