Evidence map›Paper›PMID 41223212›Full record

ArticlePLoS biology2025

Cardiac, respiratory, and gastric rhythms independently modulate motor corticospinal excitability in humans.

Tahnée Engelen, Teresa Schuhmann, Alexander T Sack, Catherine Tallon-Baudry

Abstract read
In one paragraph

Article in PLoS biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Dynamic Respiration-Neural Coupling in Substantia Nigra across Sleep and Anesthesia.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2026
    Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Evidence That Respiratory Phase May Modulate Task-Related Neural Representations of Visual Stimuli.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2025
    Article
  12. Article
  13. Article
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

4 authors.

Tahnée EngelenCognitive and Computational Neuroscience Laboratory (LNC2), INSERM U960, Department of Cognitive Studies, Ecole Normale Supérieure, PSL University, Paris, France.ORCID 0000-0001-9285-8968
Teresa SchuhmannSection Brain Stimulation and Cognition, Department of Cognitive Neuroscience, Faculty of Psychology and Neuroscience, Maastricht University, Maastricht, the Netherlands.
Alexander T SackSection Brain Stimulation and Cognition, Department of Cognitive Neuroscience, Faculty of Psychology and Neuroscience, Maastricht University, Maastricht, the Netherlands.
Catherine Tallon-BaudryCognitive and Computational Neuroscience Laboratory (LNC2), INSERM U960, Department of Cognitive Studies, Ecole Normale Supérieure, PSL University, Paris, France.

Funding

Agence Nationale pour la RechercheCanadian Institute For Advanced Research (CIFAR)
6 · The paper itself

Abstract

Interoception refers to the brain's sensing of internal body state and encompasses various bodily systems, notably the cardiac, respiratory, and gastric rhythms. Beyond their roles in physiological regulation and emotional states, each of these visceral rhythms has been shown to influence brain activity and cognition, prompting for the development of various interpretative functional frameworks. However, both experimental data and functional hypothesis leave it unclear whether and how each visceral rhythm acts simultaneously and independently on brain activity. Here, we address this question by measuring in human participants how the corticospinal excitability of the motor system varies with the phase of each of the three visceral rhythms. We applied single pulse transcranial magnetic stimulation (TMS) over the hand region in primary motor cortex to elicit Motor Evoked Potentials (MEPs), whose amplitude reflects corticospinal excitability, and tested whether MEP amplitude depends on the phase of the simultaneously measured cardiac, respiratory, and gastric rhythms. All three visceral rhythms were coupled to motor excitability with similar effect sizes at the group level. However, we found no relation between coupling strengths: participants displaying high coupling with one organ did not necessarily display high coupling to the other organs. These results indicate that independent mechanisms could underly the coupling between the cardiac, respiratory, and gastric rhythms and motor excitability. We further introduce the concept of individual interoceptive profiles and show that such interoceptive profiles obtained from objective coupling strength measures were not explained by self-reported awareness of the organ. Altogether, our results call for refined specifications of the frameworks offering a functional or clinical interpretation of viscera-brain coupling taking into account both independent mechanisms and individual interoceptive profiles.

Indexed as

HeartMotor CortexPyramidal TractsStomachAdultEvoked Potentials, MotorFemaleHeart RateHumansInteroceptionMaleRespirationTranscranial Magnetic StimulationYoung Adult

Identifiers

PMID41223212
PMCPMC12629470

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.