Publication | Open Access
Neural Correlates of Reach Errors
643
Citations
72
References
2005
Year
NeuropsychologyMotor ControlAttentionSocial SciencesNeural MechanismKinesiologyCognitive ElectrophysiologyKinematicsMotor NeuroscienceCognitive NeuroscienceHealth SciencesCognitive ScienceRehabilitationReach ErrorsSensorimotor TransformationAction MonitoringMotor SystemTarget ErrorsNeuroscienceExecution ErrorsHuman MovementFine Motor Control
Reach errors are categorized as target errors, caused by unpredictable target changes, and execution errors, caused by miscalibration of internal models such as altered visual feedback or limb dynamics. The study used fMRI with a compatible robot to identify brain regions processing each error type. Execution errors, unlike target errors, elicit strong trial‑by‑trial adaptation and activate central/postcentral sulci, cerebellar lobules V, VI, VIII, and parietal area 5, whereas target errors mainly engage the striatum and posterior superior parietal lobule, demonstrating a neural and behavioral dissociation between goal‑switching and internal‑model adaptation.
Reach errors may be broadly classified into errors arising from unpredictable changes in target location, called target errors, and errors arising from miscalibration of internal models (e.g., when prisms alter visual feedback or a force field alters limb dynamics), called execution errors. Execution errors may be caused by miscalibration of dynamics (e.g., when a force field alters limb dynamics) or by miscalibration of kinematics (e.g., when prisms alter visual feedback). Although all types of errors lead to similar on-line corrections, we found that the motor system showed strong trial-by-trial adaptation in response to random execution errors but not in response to random target errors. We used functional magnetic resonance imaging and a compatible robot to study brain regions involved in processing each kind of error. Both kinematic and dynamic execution errors activated regions along the central and the postcentral sulci and in lobules V, VI, and VIII of the cerebellum, making these areas possible sites of plastic changes in internal models for reaching. Only activity related to kinematic errors extended into parietal area 5. These results are inconsistent with the idea that kinematics and dynamics of reaching are computed in separate neural entities. In contrast, only target errors caused increased activity in the striatum and the posterior superior parietal lobule. The cerebellum and motor cortex were as strongly activated as with execution errors. These findings indicate a neural and behavioral dissociation between errors that lead to switching of behavioral goals and errors that lead to adaptation of internal models of limb dynamics and kinematics.
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