ArticlePloS one2017
Cerebellar anodal tDCS increases implicit learning when strategic re-aiming is suppressed in sensorimotor adaptation.
Article in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.
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Who cites it
12 citing papers in PubMed, 27 citations in OpenAlex.
- A software tool for at-home measurement of sensorimotor adaptation.bioRxiv : the preprint server for biology · 2023Article
- Neurophysiology of cerebellar ataxias and gait disorders.Clinical neurophysiology practice · 2023Review
- Transcranial Direct-Current Stimulation Does Not Affect Implicit Sensorimotor Adaptation: A Randomized Sham-Controlled Trial.Brain sciences · 2022Article
- A Brief History of Cerebellar Neurostimulation.Cerebellum (London, England) · 2022Review
- Residual errors in visuomotor adaptation persist despite extended motor preparation periods.Journal of neurophysiology · 2022Article
- Does anodal cerebellar tDCS boost transfer of after-effects from throwing to pointing during prism adaptation?Frontiers in psychology · 2022Article
- The acute effects of aerobic exercise on sensorimotor adaptation in chronic stroke.Restorative neurology and neuroscience · 2021Article
- Article
- Visual statistical learning and integration of perceptual priors are intact in attention deficit hyperactivity disorder.PloS one · 2020Article
- How different effectors and action effects modulate the formation of separate motor memories.Scientific reports · 2019Article
- Differential plasticity of extensor and flexor motor cortex representations following visuomotor adaptation.Experimental brain research · 2018Article
- Neural changes associated with cerebellar tDCS studied using MR spectroscopy.Experimental brain research · 2018Article
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Authors and funding
4 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Neurophysiological and neuroimaging work suggests that the cerebellum is critically involved in sensorimotor adaptation. Changes in cerebellar function alter behaviour when compensating for sensorimotor perturbations, as shown by non-invasive stimulation of the cerebellum and studies involving patients with cerebellar degeneration. It is known, however, that behavioural responses to sensorimotor perturbations reflect both explicit processes (such as volitional aiming to one side of a target to counteract a rotation of visual feedback) and implicit, error-driven updating of sensorimotor maps. The contribution of the cerebellum to these explicit and implicit processes remains unclear. Here, we examined the role of the cerebellum in sensorimotor adaptation to a 30° rotation of visual feedback of hand position during target-reaching, when the capacity to use explicit processes was manipulated by controlling movement preparation times. Explicit re-aiming was suppressed in one condition by requiring subjects to initiate their movements within 300ms of target presentation, and permitted in another condition by requiring subjects to wait approximately 1050ms after target presentation before movement initiation. Similar to previous work, applying anodal transcranial direct current stimulation (tDCS; 1.5mA) to the right cerebellum during adaptation resulted in faster compensation for errors imposed by the rotation. After exposure to the rotation, we evaluated implicit remapping in no-feedback trials after providing participants with explicit knowledge that the rotation had been removed. Crucially, movements were more adapted in these no-feedback trials following cerebellar anodal tDCS than after sham stimulation in both long and short preparation groups. Thus, cerebellar anodal tDCS increased implicit remapping during sensorimotor adaptation, irrespective of preparation time constraints. The results are consistent with the possibility that the cerebellum contributes to the formation of new visuomotor maps that correct perturbations in sensory feedback, even when explicit processes are suppressed during sensorimotor adaptation.
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