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Hippocampal Theta Coordinates Memory Processing During Visual Exploration

Overview
Journal Elife
Specialty Biology
Date 2020 Mar 14
PMID 32167468
Citations 26
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Abstract

The hippocampus supports memory encoding and retrieval, which may occur at distinct phases of the theta cycle. These processes dynamically interact over rapid timescales, especially when sensory information conflicts with memory. The ability to link hippocampal dynamics to memory-guided behaviors has been limited by experiments that lack the temporal resolution to segregate encoding and retrieval. Here, we simultaneously tracked eye movements and hippocampal field potentials while neurosurgical patients performed a spatial memory task. Phase-locking at the peak of theta preceded fixations to retrieved locations, indicating that the hippocampus coordinates memory-guided eye movements. In contrast, phase-locking at the trough of theta followed fixations to novel object-locations and predicted intact memory of the original location. Theta-gamma phase amplitude coupling increased during fixations to conflicting visual content, but predicted memory updating. Hippocampal theta thus supports learning through two interleaved processes: strengthening encoding of novel information and guiding exploration based on prior experience.

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References
1.
Vaz A, Inati S, Brunel N, Zaghloul K . Coupled ripple oscillations between the medial temporal lobe and neocortex retrieve human memory. Science. 2019; 363(6430):975-978. PMC: 6478623. DOI: 10.1126/science.aau8956. View

2.
Landau A, Schreyer H, van Pelt S, Fries P . Distributed Attention Is Implemented through Theta-Rhythmic Gamma Modulation. Curr Biol. 2015; 25(17):2332-7. DOI: 10.1016/j.cub.2015.07.048. View

3.
Colgin L . Do slow and fast gamma rhythms correspond to distinct functional states in the hippocampal network?. Brain Res. 2015; 1621:309-15. PMC: 4499490. DOI: 10.1016/j.brainres.2015.01.005. View

4.
Brodeur M, Dionne-Dostie E, Montreuil T, Lepage M . The Bank of Standardized Stimuli (BOSS), a new set of 480 normative photos of objects to be used as visual stimuli in cognitive research. PLoS One. 2010; 5(5):e10773. PMC: 2879426. DOI: 10.1371/journal.pone.0010773. View

5.
Bicanski A, Burgess N . A Computational Model of Visual Recognition Memory via Grid Cells. Curr Biol. 2019; 29(6):979-990.e4. PMC: 6428694. DOI: 10.1016/j.cub.2019.01.077. View