Evidence map›Paper›PMID 42321009›Full record

Trial reportThe Journal of physiology2026

Transcutaneous auricular vagus nerve stimulation during short-term motor practice drives cortical plasticity without behavioural improvement.

Kento Nakagawa, Rieko Osu

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in The Journal of physiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Kento NakagawaFaculty of Human Sciences, Waseda University, Tokorozawa, Saitama, Japan.ORCID https://orcid.org/0000-0002-6203-6602
Rieko OsuFaculty of Human Sciences, Waseda University, Tokorozawa, Saitama, Japan.

Funding

JSPS KAKENHI 21H04425JSPS KAKENHI 22H03498JSPS KAKENHI 23H00459
6 · The paper itself

Abstract

Transcutaneous auricular vagus nerve stimulation (taVNS) is emerging as a promising non-invasive neuromodulation technique to augment neurorehabilitation; however, its mechanisms in humans remain poorly understood. Animal studies indicate that VNS during motor skill practice drives task-specific plasticity in the primary motor cortex (M1), but direct evidence in humans is limited. Here, we demonstrate that taVNS paired with dexterous motor skill practice selectively enhances cortical plasticity without boosting motor performance during short-term training. Thirty-one healthy adults practiced a two-ball rotation task for 15 min. Participants were randomised to receive taVNS to the left tragus or sham stimulation during practice. Motor performance, M1 representation (transcranial magnetic stimulation mapping) and spinal excitability (F-wave) were assessed pre- and post-practice, while pupil diameter was monitored during practice. Motor performance improved similarly in both groups, whereas cortical map expansion was significantly greater in the taVNS group than in the sham group. F-wave amplitude increased in the sham group but not in the taVNS group, suggesting a relative shift in the expression of practice-related plasticity toward cortical circuits when training was paired with taVNS. This pattern suggests that taVNS may influence the hierarchical expression of motor plasticity. Moreover, taVNS elicited pupil dilation during practice, consistent with noradrenergic engagement. These findings suggest that taVNS facilitates task-specific cortical reorganization in humans independent of immediate behavioural improvement. By relating taVNS-induced plasticity to noradrenergic engagement and revealing differential cortical and spinal responses, this study offers novel mechanistic insights into how pairing taVNS with motor training may establish a neural basis for motor recovery. KEY POINTS: Previous research has shown that transcutaneous auricular vagus nerve stimulation (taVNS) is a promising neuromodulatory method, yet its effects on human motor learning and underlying plasticity mechanisms remain unclear. This study shows that, in healthy adults, taVNS paired with dexterous motor practice enhanced cortical plasticity (increased M1 map size) without immediate behavioural improvement. By contrast, sham stimulation alone increased F-wave amplitude, suggesting that taVNS may promote a relative shift in the expression of plasticity toward cortical circuits. Pupillometric monitoring revealed enhanced noradrenergic activity during taVNS‑paired training, suggesting a neuromodulatory pathway associated with cortical plasticity. These findings highlight the potential of taVNS to modulate central plasticity mechanisms, offering a novel strategy that could be translated into rehabilitation interventions targeting neural recovery in neurological disorders.

Indexed as

Motor CortexMotor SkillsNeuronal PlasticityTranscutaneous Electric Nerve StimulationVagus Nerve StimulationAdultEvoked Potentials, MotorFemaleHumansMaleYoung AdultF‐wavelocus coeruleusmotor cortexmotor learningneuromodulationnoradrenalinevagus nerve stimulation

Identifiers

PMID42321009
PMCPMC13370720

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.