Evidence map›Paper›PMID 35040779›Full record

ArticleeLife2022

Hippocampal sharp wave-ripples and the associated sequence replay emerge from structured synaptic interactions in a network model of area CA3.

András Ecker, Bence Bagi, Eszter Vértes, Orsolya Steinbach-Németh, Mária R Karlócai, Orsolya I Papp, István Miklós, Norbert Hájos, Tamás F Freund, Attila I Gulyás and 1 more

Abstract read
In one paragraph

Article in eLife, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

29 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Effects of Novelty and Temporal Distance on Postexperience Spike Patterns of Hippocampal Place Cells Encoding Multiple Environments.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2026
    Article
  6. Conditions for replay of neuronal assemblies.PLoS computational biology · 2026
    Article
  7. Article
  8. Behavioral Timescale Synaptic Plasticity: A Burst in the Field of Learning and Memory.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2025
    Review
  9. Behavioral Timing of Interictal Spikes, But Not Rate, Correlates with Impaired Working Memory Performance.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2025
    Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Review
  15. Review
  16. Article
  17. Article
  18. Article
  19. Distinct mechanisms and functions of episodic memory.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2024
    Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

András EckerInstitute of Experimental Medicine, Eötvös Loránd Research Network, Budapest, Hungary.ORCID 0000-0001-9635-4169
Bence BagiInstitute of Experimental Medicine, Eötvös Loránd Research Network, Budapest, Hungary.
Eszter VértesInstitute of Experimental Medicine, Eötvös Loránd Research Network, Budapest, Hungary.
Orsolya Steinbach-NémethInstitute of Experimental Medicine, Eötvös Loránd Research Network, Budapest, Hungary.
Mária R KarlócaiInstitute of Experimental Medicine, Eötvös Loránd Research Network, Budapest, Hungary.
Orsolya I PappInstitute of Experimental Medicine, Eötvös Loránd Research Network, Budapest, Hungary.
István MiklósAlfréd Rényi Institute of Mathematics, Eötvös Loránd Research Network, Budapest, Hungary.
Norbert HájosInstitute of Experimental Medicine, Eötvös Loránd Research Network, Budapest, Hungary.
Tamás F FreundInstitute of Experimental Medicine, Eötvös Loránd Research Network, Budapest, Hungary.
Attila I GulyásInstitute of Experimental Medicine, Eötvös Loránd Research Network, Budapest, Hungary.
Szabolcs KáliInstitute of Experimental Medicine, Eötvös Loránd Research Network, Budapest, Hungary.ORCID 0000-0002-2740-6057

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hippocampal place cells are activated sequentially as an animal explores its environment. These activity sequences are internally recreated ('replayed'), either in the same or reversed order, during bursts of activity (sharp wave-ripples [SWRs]) that occur in sleep and awake rest. SWR-associated replay is thought to be critical for the creation and maintenance of long-term memory. In order to identify the cellular and network mechanisms of SWRs and replay, we constructed and simulated a data-driven model of area CA3 of the hippocampus. Our results show that the chain-like structure of recurrent excitatory interactions established during learning not only determines the content of replay, but is essential for the generation of the SWRs as well. We find that bidirectional replay requires the interplay of the experimentally confirmed, temporally symmetric plasticity rule, and cellular adaptation. Our model provides a unifying framework for diverse phenomena involving hippocampal plasticity, representations, and dynamics, and suggests that the structured neural codes induced by learning may have greater influence over cortical network states than previously appreciated.

Indexed as

AnimalsBrain WavesCA3 Region, HippocampalHippocampusInterneuronsLearningMemoryMiceModels, TheoreticalPlace CellsSleepWakefulnesscomputational biologycomputational modelinghippocampusmouseneuroscienceplace cellsequence replayspike-timing-dependent plasticitysystems biology

Identifiers

PMID35040779
PMCPMC8865846

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.