Evidence map›Paper›PMID 41559063›Full record

ArticleNature communications2026

Dynamical modulation of hippocampal replay through firing rate adaptation.

Zilong Ji, Tianhao Chu, Xingsi Dong, Changmin Yu, Daniel Bush, Neil Burgess, Si Wu

Abstract read
In one paragraph

Article in Nature communications, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Drift-diffusion dynamics of hippocampal replay.PLoS computational biology · 2026
    Article
  2. The hippocampus as a small-world cognitive map.bioRxiv : the preprint server for biology · 2026
    Article
  3. Article
  4. Review
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

7 authors.

Zilong Ji *School of Psychological and Cognitive Sciences, Peking University, Beijing, China.ORCID http://orcid.org/0000-0001-7868-6178
Tianhao Chu *School of Psychological and Cognitive Sciences, Peking University, Beijing, China.ORCID http://orcid.org/0000-0001-9910-9361
Xingsi Dong *Peking-Tsinghua Center for Life Sciences, Academy for Advanced Interdisciplinary Studies, Peking University, Beijing, China.
Changmin YuComputational and Biological Learning Lab, Department of Engineering, University of Cambridge, Cambridge, UK.
Daniel BushDepartment of Neuroscience, Physiology and Pharmacology, University of College London, London, UK.ORCID http://orcid.org/0000-0002-5097-8117
Neil BurgessInstitute of Cognitive Neuroscience, University College London, London, UK. n.burgess@ucl.ac.uk.ORCID http://orcid.org/0000-0003-0646-6584
Si WuSchool of Psychological and Cognitive Sciences, Peking University, Beijing, China. siwu@pku.edu.cn.ORCID http://orcid.org/0000-0001-9650-6935

Funding

Wellcome TrustWellcome Trust (Wellcome) 222457/Z/21/Z
6 · The paper itself

Abstract

During periods of immobility and sleep, the hippocampus generates diverse self-sustaining sequences of "replay" activity, which exhibit stationary, diffusive, and super-diffusive dynamical patterns. However, the neural mechanisms underlying this diversity in hippocampal sequential dynamics remain largely unknown. Here, we propose a unifying mechanism by showing that modulation of firing-rate adaptation strength within a continuous attractor model of place cells gives rise to these distinct forms of replay. Our model accounts for empirical data and yields several testable predictions. First, more diffusive replay sequences should positively correlate with longer theta sequences, both reflecting stronger adaptation. Second, increased neural activity combined with firing-rate adaptation should reduce the step size of decoded trajectories during replay. Third, the framework is consistent with previous work showing that replay diffusivity can vary within an animal across behavioural states that may influence adaptation (such as wake and sleep). Together, these results suggest that the diverse replay dynamics observed in the hippocampus can be understood through a simple yet powerful neural mechanism, providing insight into the computational role of replay in hippocampal-dependent cognition and its relationship to other electrophysiological phenomena.

Indexed as

Action PotentialsAdaptation, PhysiologicalHippocampusAnimalsModels, NeurologicalNeuronsPlace CellsSleepTheta Rhythm

Identifiers

PMID41559063
PMCPMC12868804

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.