Evidence map›Paper›PMID 42566537›Full record

ArticleScience advances2026

Distributed burst firing mediates optimized cortical encoding of natural self-motion.

Jerome Carriot, Isabelle Mackrous, Kathleen E Cullen, Maurice J Chacron

Abstract read
In one paragraph

Article in Science advances, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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.

Jerome CarriotDepartment of Physiology, McGill University, Montreal, Canada.ORCID 0000-0003-0352-2245
Isabelle MackrousDepartment of Physiology, McGill University, Montreal, Canada.ORCID 0009-0001-6892-6278
Kathleen E CullenDepartment of Biomedical Engineering, Johns Hopkins University, Baltimore, MD, USA.ORCID 0000-0002-9348-0933
Maurice J ChacronDepartment of Physiology, McGill University, Montreal, Canada.ORCID 0000-0002-3032-452X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Accurate perception of self-motion requires that vestibular input be transformed into neural representations suitable for integrating multisensory cues to guide action. Here, we demonstrate that vestibular cortical neurons represent the self-motion stimuli encountered during everyday activities in a fundamentally different manner than the artificial self-motion stimuli typically used. Using stimuli whose waveforms reproduce the head dynamics encountered in natural behavior, we found that neural activity no longer tracked stimulus velocity through graded firing-rate changes, as observed during artificial sinusoidal stimulation, but instead reliably encoded distinct motion features through burst firing. At the population level, these bursts formed a distributed code that enhanced information transmission by reducing redundancy. This transformation emerged only during natural stimulation and was absent in the vestibular thalamus. Together, our results demonstrate that the vestibular cortex constructs a distributed, feature-based representation of natural self-motion, fundamentally reshaping our understanding of how cortical circuits encode vestibular signals to mediate perception.

Indexed as

Action PotentialsMotion PerceptionNeuronsVestibule, LabyrinthAnimalsMotion

Identifiers

PMID42566537
PMCPMC13450226

What Socratic holds

Textmetadata
LicenceCC BY-NC
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 Socratic graph.