Evidence map›Paper›PMID 39365821›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2024

Synaptic weight dynamics underlying memory consolidation: Implications for learning rules, circuit organization, and circuit function.

Brandon J Bhasin, Jennifer L Raymond, Mark S Goldman

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. Cerebellar microcircuits enable robust evidence-based decisions through cortico-cerebellar coupling.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  2. Article
  3. Article
  4. Flexible Coupling of Synaptic and Intrinsic Plasticity in a Cerebellar Circuit.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2026
    Article
  5. Review
  6. Review
  7. Article
  8. Article
  9. How neural systems transform synaptic plasticity into behavioral learning.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  10. Article
  11. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors.

Brandon J BhasinDepartment of Bioengineering, Stanford University, Stanford, CA 94305.ORCID 0000-0002-0995-7656
Jennifer L RaymondDepartment of Neurobiology, Stanford University School of Medicine, Stanford, CA 94305.ORCID 0000-0002-8145-747X
Mark S GoldmanCenter for Neuroscience, University of California, Davis, CA 95616.ORCID 0000-0002-8257-2314

Funding

VESTIBULAR AND VISUAL CONTROL OF EYE MOVEMENTR01DC004154 · NIDCD · STANFORD UNIVERSITY · PI GOLDMAN, MARK S, RAYMOND, JENNIFER L · 1999 to 2025
$9.6M
Instructive Signals for Motor LearningR01NS072406 · NINDS · STANFORD UNIVERSITY · PI Jennifer L Raymond · 2010 to 2026
$7.6M
Activity-Dependent Mechanisms of Memory ConsolidationR01EY031972 · NEI · STANFORD UNIVERSITY · PI GOLDMAN, MARK S, RAYMOND, JENNIFER L · 2021 to 2025
$3.0M
The computational importance of cerebellar processingR01EY021581 · NEI · WEILL MEDICAL COLL OF CORNELL UNIV · PI AKSAY, EMRE R · 2012 to 2016
$2.8M
NEI NIH HHS R01 EY021581NEI NIH HHS R01 EY031972NIDCD NIH HHS R01 DC004154NINDS NIH HHS R01 NS072406Simons Foundation (SF) 543031
6 · The paper itself

Abstract

Systems consolidation is a common feature of learning and memory systems, in which a long-term memory initially stored in one brain region becomes persistently stored in another region. We studied the dynamics of systems consolidation in simple circuit architectures with two sites of plasticity, one in an early-learning and one in a late-learning brain area. We show that the synaptic dynamics of the circuit during consolidation of an analog memory can be understood as a temporal integration process, by which transient changes in activity driven by plasticity in the early-learning area are accumulated into persistent synaptic changes at the late-learning site. This simple principle naturally leads to a speed-accuracy tradeoff in systems consolidation and provides insight into how the circuit mitigates the stability-plasticity dilemma of storing new memories while preserving core features of older ones. Furthermore, it imposes two constraints on the circuit. First, the plasticity rule at the late-learning site must stably support a continuum of possible outputs for a given input. We show that this is readily achieved by heterosynaptic but not standard Hebbian rules. Second, to turn off the consolidation process and prevent erroneous changes at the late-learning site, neural activity in the early-learning area must be reset to its baseline activity. We provide two biologically plausible implementations for this reset that propose functional roles in stabilizing consolidation for core elements of the cerebellar circuit.

Indexed as

LearningMemory ConsolidationModels, NeurologicalNeuronal PlasticitySynapsesAnimalsBrainHumansMemoryMemory, Long-TermNerve Netcerebellumcomputational modelheterosynaptic plasticitymemory consolidation

Identifiers

PMID39365821
PMCPMC11474072

What OpenQuestion holds

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Registered trials

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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.