ReviewThe Journal of neuroscience : the official journal of the Society for Neuroscience2025
Sensorimotor Transformations for Postural Control in the Vermis of the Cerebellum.
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.
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The trial behind it
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Who cites it
9 citing papers in PubMed.
- Effect of cerebellar vermis intermittent theta-burst stimulation on balance function in frail older adults: a randomized controlled trial.BMC geriatrics · 2026Trial
- Wearable Technologies for Gait Instability Rehabilitation: Mechanisms, Clinical Evidence, and Future Directions.Bioengineering (Basel, Switzerland) · 2026Review
- Loss of YY1 in Purkinje cells triggers cerebellar ataxia via Wnt10b-mediated impairment of dendrite development.iScience · 2026Article
- Specialized outputs and behavioral contributions of Purkinje cell subtypes.bioRxiv : the preprint server for biology · 2026Article
- Postural Balance and Human Movement: An Integrative Framework for Mechanisms, Assessment, and Functional Implications.Journal of clinical medicine · 2026Review
- Optic Flow Simulating Self-Motion Does Not Modulate the Hoffmann Reflex in the Soleus During Upright Standing in Healthy Young Adults.Brain sciences · 2026Article
- Ground-truth encoding of self-motion in the primate cerebellar nodulus and uvula.Nature communications · 2026Article
- Cerebellar dysfunction in glaucoma patients.Brain communications · 2025Article
- Altered spontaneous brain activity and functional connectivity in persistent postural-perceptual dizziness.Frontiers in neurologyArticle
Corrections and comments
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Authors and funding
2 authors.
Funding
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.
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Registered trials
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.