Evidence map›Paper›PMID 42856344›Full record

ArticlemedRxiv : the preprint server for health sciences2026

A Distal-Proximal Gradient of Hebbian Plasticity in the Human Arm.

Minkyu Lee, Matthew T Farley, Bing Chen, Sina Sangari, Monica A Perez

Abstract readPreprint
In one paragraph

Article in medRxiv : the preprint server for health sciences, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Minkyu LeeShirley Ryan AbilityLab, Chicago, IL, USA.ORCID 0000-0002-8770-585X
Matthew T FarleyShirley Ryan AbilityLab, Chicago, IL, USA.
Bing ChenShirley Ryan AbilityLab, Chicago, IL, USA.
Sina SangariShirley Ryan AbilityLab, Chicago, IL, USA.
Monica A PerezShirley Ryan AbilityLab, Chicago, IL, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Corticospinal-motoneuronal connections are more prominent in distal than proximal upper-limb muscles, but whether this anatomical specialization influences the capacity for activity-dependent plasticity remains unknown. Here, we tested whether Hebbian stimulation targeting corticospinal-motoneuronal connections, induces muscle-specific plasticity in proximal and distal arm muscles in healthy humans. We applied a spike-timing-dependent stimulation protocol comprising 180 paired stimuli, with transcranial magnetic stimulation timed to evoke corticospinal volleys 1-2 ms before motoneurons were antidromically activated by electrical stimulation of the brachial plexus for the biceps brachii or the ulnar nerve for the first dorsal interosseous (FDI). Corticospinal excitability was assessed by measuring motor-evoked potentials (MEPs) before and 30 min after stimulation. Hebbian stimulation increased MEP amplitudes in both muscles, but facilitation was greater in the FDI than in the biceps. Because resting motor threshold was higher for the biceps than for the FDI, in a control experiment we matched stimulation intensities between muscles. Under these conditions, Hebbian stimulation continued producing greater facilitation in the FDI than in the biceps, indicating that the difference was not attributable to stimulation intensity. Moreover, changes in MEP amplitude were associated with maximal MEP size in the FDI but not in the biceps, whereas no muscle-specific association was observed with peripheral responses (M-max), supporting a stronger relationship between corticospinal drive and Hebbian plasticity in the distal than in the proximal arm muscle. Together, these findings identify a distal-to-proximal gradient in Hebbian plasticity across arm muscles, which may contribute to optimizing targeted neuromodulation approaches for upper-limb rehabilitation.

Indexed as

armcorticospinal tracthandHebbian stimulationneuroplasticityupper-limb

Identifiers

PMID42856344
PMCPMC13648674

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