» Articles » PMID: 15147320

The Basal Ganglia Network Mediates the Planning of Movement Amplitude

Overview
Journal Eur J Neurosci
Specialty Neurology
Date 2004 May 19
PMID 15147320
Citations 39
Authors
Affiliations
Soon will be listed here.
Abstract

This study addresses the hypothesis that the basal ganglia (BG) are involved specifically in the planning of movement amplitude (or covariates). Although often advanced, based on observations that Parkinson's disease (PD) patients exhibit hypokinesia in the absence of significant directional errors, this hypothesis has been challenged by a recent alternative, that parkinsonian hypometria could be caused by dysfunction of on-line feedback loops. To re-evaluate this issue, we conducted two successive experiments. In the first experiment we assumed that if BG are involved in extent planning then PD patients (who exhibit a major dysfunction within the BG network) should exhibit a preserved ability to use a direction precue with respect to normals, but an impaired ability to use an amplitude precue. Results were compatible with this prediction. Because this evidence did not prove conclusively that the BG is involved in amplitude planning (functional deficits are not restricted to the BG network in PD), a second experiment was conducted using positron emission tomography (PET). We hypothesized that if the BG is important for planning movement amplitude, a task requiring increased amplitude planning should produce increased activation in the BG network. In agreement with this prediction, we observed enhanced activation of BG structures under a precue condition that emphasized extent planning in comparison with conditions that emphasized direction planning or no planning. Considered together, our results are consistent with the idea that BG is directly involved in the planning of movement amplitude or of factors that covary with that parameter.

Citing Articles

Medication improves velocity, reaction time, and movement time but not amplitude or error during memory-guided reaching in Parkinson's disease.

Trevarrow M, Munoz M, Rivera Y, Arora R, Drane Q, Pal G Physiol Rep. 2024; 12(17):e16150.

PMID: 39209762 PMC: 11361790. DOI: 10.14814/phy2.16150.


A neurocomputational view of the effects of Parkinson's disease on speech production.

Manes J, Bullock L, Meier A, Turner R, Richardson R, Guenther F Front Hum Neurosci. 2024; 18:1383714.

PMID: 38812472 PMC: 11133703. DOI: 10.3389/fnhum.2024.1383714.


Moving, fast and slow: behavioural insights into bradykinesia in Parkinson's disease.

Herz D, Brown P Brain. 2023; 146(9):3576-3586.

PMID: 36864683 PMC: 10473574. DOI: 10.1093/brain/awad069.


Reaching and Grasping Movements in Parkinson's Disease: A Review.

Fasano A, Mazzoni A, Falotico E J Parkinsons Dis. 2022; 12(4):1083-1113.

PMID: 35253780 PMC: 9198782. DOI: 10.3233/JPD-213082.


Sensorimotor Learning in Response to Errors in Task Performance.

Sadaphal D, Kumar A, Mutha P eNeuro. 2022; 9(2).

PMID: 35110383 PMC: 8938978. DOI: 10.1523/ENEURO.0371-21.2022.