Evidence map›Paper›PMID 39874961›Full record

ArticleNeuron2025

Topography of putative bi-directional interaction between hippocampal sharp-wave ripples and neocortical slow oscillations.

Rachel A Swanson, Elisa Chinigò, Daniel Levenstein, Mihály Vöröslakos, Navid Mousavi, Xiao-Jing Wang, Jayeeta Basu, György Buzsáki

Abstract read
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In one paragraph

Article in Neuron, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 citing papers in PubMed.

  1. Article
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  9. Subspace communication in the hippocampal-retrosplenial axis.bioRxiv : the preprint server for biology · 2026
    Article
  10. Long-Term Memory Updating Parallels Altered Awake and Sleep Hippocampal Replays.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  11. Time, space, memory and brain-body rhythms.Nature reviews. Neuroscience · 2026
    Review
  12. Review
  13. Article
  14. Article
  15. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors.

Rachel A SwansonNeuroscience Institute, Langone Medical Center, New York University, New York, NY, USA.
Elisa ChinigòCenter for Neural Science, New York University, New York, NY, USA.
Daniel LevensteinDepartment of Neurology and Neurosurgery, McGill University Montreal, QC, Canada; Mila - The Quebec AI Institute, Montreal, QC, Canada.
Mihály VöröslakosNeuroscience Institute, Langone Medical Center, New York University, New York, NY, USA.
Navid MousaviNeuroscience Institute, Langone Medical Center, New York University, New York, NY, USA.
Xiao-Jing WangCenter for Neural Science, New York University, New York, NY, USA.
Jayeeta BasuNeuroscience Institute, Langone Medical Center, New York University, New York, NY, USA; Department of Physiology and Neuroscience, Langone Medical Center, New York University, New York, NY, USA; Department of Psychiatry, Langone Medical Center, New York University, New York, NY, USA. Electronic address: jayeeta.basu@nyulangone.org.
György BuzsákiNeuroscience Institute, Langone Medical Center, New York University, New York, NY, USA; Department of Physiology and Neuroscience, Langone Medical Center, New York University, New York, NY, USA; Department of Neurology, Langone Medical Center, New York University, New York, NY, USA. Electronic address: gyorgy.buzsaki@nyulangone.org.

Funding

Transformation of Neuronal Activity in the Entorhinal-hippocampal-neocortex PathR01MH122391 · NIMH · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI BASU, JAYEETA, BUZSAKI, GYORGY · 2020 to 2024
$3.3M
Linking Plasticity of Hippocampal Representation across the Single Neuron and Circuit LevelsR01NS109994 · NINDS · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI BASU, JAYEETA, CLOPATH, CLAUDIA · 2018 to 2022
$2.4M
Training program in computational approaches to brain and behaviorR90DA060339 · NIDA · NEW YORK UNIVERSITY · PI Wei Ji Ma · 2023 to 2026
$1.3M
NIDA NIH HHS R90 DA060339NIMH NIH HHS R01 MH122391NINDS NIH HHS R01 NS109994
6 · The paper itself

Abstract

Systems consolidation relies on coordination between hippocampal sharp-wave ripples (SWRs) and neocortical UP/DOWN states during sleep. However, whether this coupling exists across the neocortex and the mechanisms enabling it remains unknown. By combining electrophysiology in mouse hippocampus (HPC) and retrosplenial cortex (RSC) with wide-field imaging of the dorsal neocortex, we found spatially and temporally precise bi-directional hippocampo-neocortical interaction. HPC multi-unit activity and SWR probability were correlated with UP/DOWN states in the default mode network (DMN), with the highest modulation by the RSC in deep sleep. Further, some SWRs were preceded by the high rebound excitation accompanying DMN DOWN → UP transitions, whereas large-amplitude SWRs were often followed by DOWN states originating in the RSC. We explain these electrophysiological results with a model in which the HPC and RSC are weakly coupled excitable systems capable of bi-directional perturbation and suggest that the RSC may act as a gateway through which SWRs can perturb downstream cortical regions via cortico-cortical propagation of DOWN states.

Indexed as

Brain WavesHippocampusNeocortexSleepAnimalsElectroencephalographyMaleMiceMice, Inbred C57BLNerve NetNeural Pathwaysdefault mode networkexcitable systemsextracellular electrophysiologyhippocampusinfraslow oscillationmean-field modelretrosplenial cortexsleepsystems consolidationwide-field imaging

Identifiers

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.