Evidence map›Paper›PMID 32525480›Full record

ArticleeLife2020

mPFC spindle cycles organize sparse thalamic activation and recently active CA1 cells during non-REM sleep.

Carmen Varela, Matthew A Wilson

Open access · goldAbstract read
In one paragraph

Article in eLife, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
3.9field-weighted citation impact, top 6% of its field
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

22 citing papers in PubMed, 51 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. A Distinct Down-to-Up Transition Assembly in the Retrosplenial Cortex during Slow-Wave Sleep.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2025
    Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Mapping sleep's oscillatory events as a biomarker of Alzheimer's disease.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2024
    Article
  12. Article
  13. Article
  14. Accelerating Maturation of Spatial Memory Systems by Experience: Evidence from Sleep Oscillation Signatures of Memory Processing.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2023
    Article
  15. How our understanding of memory replay evolves.Journal of neurophysiology · 2023
    Review
  16. Article
  17. Frontiers in neuroscience · 2022
    Article
  18. Rhythmic Memory Consolidation in the Hippocampus.Frontiers in neural circuits · 2022
    Article
  19. 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

2 authors at 2 institutions in 1 country.

Carmen VarelaMassachusetts Institute of Technology, Cambridge, United States.ORCID 0000-0003-0398-2567
Matthew A WilsonMassachusetts Institute of Technology, Cambridge, United States.
Florida Atlantic University · USMassachusetts Institute of Technology · US

Funding

Brain & Behavior Research Foundation 22852Caja Madrid Foundation Convocatoria 2008NIH HHS TR01-GM10498NSF STC CCF-1231216
6 · The paper itself

Abstract

Sleep oscillations in the neocortex and hippocampus are critical for the integration of new memories into stable generalized representations in neocortex. However, the role of the thalamus in this process is poorly understood. To determine the thalamic contribution to non-REM oscillations (sharp-wave ripples, SWRs; slow/delta; spindles), we recorded units and local field potentials (LFPs) simultaneously in the limbic thalamus, mPFC, and CA1 in rats. We report that the cycles of neocortical spindles provide a key temporal window that coordinates CA1 SWRs with sparse but consistent activation of thalamic units. Thalamic units were phase-locked to delta and spindles in mPFC, and fired at consistent lags with other thalamic units within spindles, while CA1 units that were active during spatial exploration were engaged in SWR-coupled spindles after behavior. The sparse thalamic firing could promote an incremental integration of recently acquired memory traces into neocortical schemas through the interleaved activation of thalamocortical cells.

Indexed as

Action PotentialsAnimalsCA1 Region, HippocampalElectrodes, ImplantedMaleMemoryNeuronsPrefrontal CortexRatsRats, Long-EvansSleepThalamushippocampusmemory consolidationneuroscienceratripplessleepspindlesthalamus

Identifiers

PMID32525480
PMCPMC7319772
OpenAlexW3034050939

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.