Evidence map›Paper›PMID 40399043›Full record

ReviewThe Journal of neuroscience : the official journal of the Society for Neuroscience2025

Sensorimotor Transformations for Postural Control in the Vermis of the Cerebellum.

Robyn L Mildren, Kathleen E Cullen

Abstract readReview
In one paragraph

Review in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 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

2 authors.

Robyn L MildrenDepartment of Biomedical Engineering, Johns Hopkins University, Baltimore, Maryland 21205.
Kathleen E CullenDepartment of Biomedical Engineering, Johns Hopkins University, Baltimore, Maryland 21205 kathleen.cullen@jhu.edu.ORCID https://orcid.org/0000-0002-9348-0933

Funding

The Physiology of Vestibular CompensationR01DC002390 · NIDCD · JOHNS HOPKINS UNIVERSITY · PI Kathleen E Cullen · 1995 to 2026
$10.7M
Neural Computations Underlying Cancellation of the Vestibular Consequences of Voluntary MovementR01DC018061 · NIDCD · JOHNS HOPKINS UNIVERSITY · PI Kathleen E Cullen · 2019 to 2026
$4.0M
NIDCD NIH HHS R01 DC002390NIDCD NIH HHS R01 DC018061
6 · The paper itself

Abstract

The cerebellar vermis plays an essential role in maintaining posture and balance by integrating sensory inputs from multiple modalities to effectively coordinate movement. By transforming convergent sensory information into precise motor commands, it ensures smooth, adaptive motor control, enabling the body to maintain stability in dynamic environments. This review examines recent findings that investigate the distinct neural computations performed by the anterior vermis and posterior vermis (nodulus/uvula). Specifically, we examine how Purkinje cells in these regions integrate vestibular and proprioceptive signals to convert self-motion information from a head-centered to a body-centered reference frame, which is essential for maintaining precise postural control in response to unexpected movements. Additionally, we consider recent findings showing that, during voluntary self-motion, Purkinje cells in the anterior vermis selectively suppress responses in the vestibulospinal pathway by integrating motor inputs with sensory signals. Given the anterior vermis's role in maintaining balance during voluntary behaviors such as locomotion, its suppression prevents counterproductive stabilizing reflexes, enabling goal-directed movement through space. In contrast, the posterior vermis, encompassing the nodulus and uvula, integrates vestibular inputs from both the otoliths and semicircular canals to maintain equilibrium relative to gravitational forces. We thus hypothesize that Purkinje cells in the nodulus/uvula do not generate suppression signals like those observed in the anterior vermis but instead continuously compute our orientation in space, regardless of whether movement is voluntarily generated or unexpected. If our hypothesis is correct, the nodulus/uvula would effectively provide consistent "ground truth" information about self-motion relative to gravity.

Indexed as

Cerebellar VermisCerebellumPostural BalancePosturePsychomotor PerformanceAnimalsHumansProprioceptionPurkinje Cellsbalancecerebellummultisensory integrationproprioceptionPurkinje cellsself-motionvestibular

Identifiers

PMID40399043
PMCPMC12096040

What OpenQuestion holds

Textmetadata
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.