Evidence map›Paper›PMID 40019812›Full record

ArticleThe Journal of physiology2025

The interplay between Hebbian and homeostatic plasticity in the adult visual cortex.

Antoine Prosper, Thomas Blanchard, Claudia Lunghi

Abstract read
In one paragraph

Article in The Journal of physiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Orientation-Specific Inhibitory Plasticity in Binocular Rivalry.Investigative ophthalmology & visual science · 2026
    Article
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  3. Review
  4. Article
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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

3 authors.

Antoine ProsperLaboratoire des Systèmes Perceptifs, Département d'études Cognitives, École Normale Supérieure, PSL University, CNRS, Paris, France.ORCID 0000-0002-6005-0419
Thomas BlanchardLaboratoire des Systèmes Perceptifs, Département d'études Cognitives, École Normale Supérieure, PSL University, CNRS, Paris, France.
Claudia LunghiLaboratoire des Systèmes Perceptifs, Département d'études Cognitives, École Normale Supérieure, PSL University, CNRS, Paris, France.

Funding

Agence Nationale de la Recherche (ANR) ANR-17-EURE-0017-FrontCogEC | ERC | HORIZON EUROPE European Research Council (ERC) 94836-HOPLA
6 · The paper itself

Abstract

Homeostatic and Hebbian plasticity co-operate during the critical period, refining neuronal circuits; however, the interaction between these two forms of plasticity is still unclear, especially in adulthood. Here, we directly investigate this issue in adult humans using two consolidated paradigms to elicit each form of plasticity in the visual cortex: the long-term potentiation-like change of the visual evoked potential (VEP) induced by high-frequency stimulation (HFS) and the shift of ocular dominance induced by short-term monocular deprivation (MD). We tested homeostatic and Hebbian plasticity independently, then explored how they interacted by inducing them simultaneously in a group of adult healthy volunteers. We successfully induced both forms of plasticity: 60 min of MD induced a reliable change in ocular dominance and HFS reliably modulated the amplitude of the P1 component of the VEP. Importantly, we found that, across participants, homeostatic and Hebbian plasticity were negatively correlated, indicating related neural mechanisms, potentially linked to intracortical excitation/inhibition balance. On the other hand, we did not find an interaction when the two forms of plasticity were induced simultaneously. Our results indicate a largely preserved plastic potential in the visual cortex of the adult brain, for both short-term homeostatic and Hebbian plasticity. Crucially, we show for the first time a direct relationship between these two forms of plasticity in the adult human visual cortex, which could inform future research and treatment protocols for neurological diseases. KEY POINTS: Homeostatic and Hebbian plasticity co-operate during the critical period to refine neuronal circuits in the visual cortex. The interaction between these two forms of plasticity is still unknown, especially after the closure of the critical periods and in humans. We directly investigate the interplay between Hebbian and homeostatic visual plasticity in adult humans using non-invasive paradigms. We found a negative correlation between these forms of plasticity showing for the first time a direct relationship between Hebbian and homeostatic plasticity. Our results could inform future research and treatment protocols for neurological diseases.

Indexed as

HomeostasisNeuronal PlasticityVisual CortexAdultDominance, OcularEvoked Potentials, VisualFemaleHumansMaleSensory DeprivationYoung Adultadult humansHebbian plasticityhomeostatic plasticityocular dominance plasticitypsychophysicsvisual cortexvisual evoked potentials

Identifiers

PMID40019812
PMCPMC11908499

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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.