Evidence map›Paper›PMID 40785043›Full record

ArticleThe Journal of physiology2025

Transcutaneous spinal cord stimulation at alternating intensities preferentially prevents the development of spasticity after contusion SCI in rat.

Dillon C Malloy, Jadwiga N Bilchak, Marie-Pascale Côté

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 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Trial
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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.

Dillon C MalloyMarion Murray Spinal Cord Research Center, Department of Neurobiology and Anatomy, Drexel University College of Medicine, Philadelphia, PA, USA.
Jadwiga N BilchakMarion Murray Spinal Cord Research Center, Department of Neurobiology and Anatomy, Drexel University College of Medicine, Philadelphia, PA, USA.
Marie-Pascale CôtéMarion Murray Spinal Cord Research Center, Department of Neurobiology and Anatomy, Drexel University College of Medicine, Philadelphia, PA, USA.ORCID 0000-0003-1145-2179

Funding

Mechanisms of Action Contributing to Decrease Spasticity and Improve Motor Recovery with Repeated Transcutaneous Stimulation After Spinal Cord InjuryR01NS119475 · NINDS · DREXEL UNIVERSITY · PI COTE, MARIE-PASCALE · 2021 to 2025
$1.8M
NINDS NIH HHS R01 NS119475
6 · The paper itself

Abstract

Transcutaneous spinal cord stimulation (tSCS) has become an increasingly popular and effective research intervention for functional recovery after spinal cord injury (SCI). Despite its surge in application for clinical investigations, there is a current lack of systematic approaches to investigate the optimal design of electrical stimulation protocols for a desired outcome. Important parameters that can affect the outcome are stimulation frequency and intensity. Previous work in humans and rodents have identified tSCS as a promising strategy to reduce spasticity and hyperreflexia after SCI. However, the stimulation intensities used in these studies vary widely and it remains unknown whether sub- or supra-motor threshold stimulation intensity is preferable for restoring spinal inhibition and mitigating spasticity after SCI. The objective of this study was to deliver 6 weeks of tSCS to rats with a severe contusion injury using a stimulation protocol with the intensity set (1) above motor threshold, (2) below motor threshold or (3) alternating between supra- and subthreshold, and evaluate whether it differentially influenced diverse outcome measures associated with spasticity. Here, we show that these various protocols distinctly affect different aspects of spasticity. Collectively, multiple sessions of tSCS at alternating intensities more profoundly (1) decreased hyperreflexia, (2) increased the frequency-dependent modulation of the H-reflex, (3) reduced antagonist ankle muscle co-contractions and aberrant crossed-extensor reflexes, and (4) prevented the development of SCI-induced KCC2 membrane downregulation in lumbar motoneurons, when compared to the supra- and sub-motor threshold intensity protocols. Together, these results suggest that an alternating stimulation intensity protocol is preferential to supra- or subthreshold stimulation alone for treating spastic symptoms after SCI and begins to elucidate the impact of varying stimulation parameters in promoting neuroplasticity and functional recovery after SCI. KEY POINTS: Transcutaneous spinal cord stimulation (tSCS) has shown potential for targeting and improving spasticity after spinal cord injury (SCI) in both human and rodent research settings. However, the stimulation protocols used are variable and without consensus on the optimal stimulation parameters for targeting spasticity and hyperreflexia following SCI. We do not yet understand how various stimulation parameters, like frequency and intensity, influence neuroplasticity and functional recovery. Recent human and rodent work has identified a low frequency tSCS protocol to be effective for targeting spasticity after SCI. We used this established frequency to investigate the ideal tSCS intensity protocol for mitigating spasticity. We show that tSCS at alternating supra- and sub-motor threshold intensities preferentially improves hyperreflexia, the frequency-dependent modulation of the H-reflex, behavioural reflex activity, and neuroanatomical plasticity, collectively, compared to supra- or subthreshold stimulation alone. This study elucidates the impact of the stimulation intensity parameter on decreasing spasticity after SCI.

Indexed as

Muscle SpasticitySpinal Cord InjuriesSpinal Cord StimulationTranscutaneous Electric Nerve StimulationAnimalsFemaleRatsRats, Sprague-DawleySpinal Cordchloride homeostasisKCC2neuromodulationneuroplasticityspasticityspinal cord injurytranscutaneous spinal cord stimulation

Identifiers

PMID40785043
PMCPMC12400786

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LicenceCC BY-NC-ND
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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.