Literature DB >> 7151935

Development and change of cortical field potentials during learning processes of visually initiated hand movements in the monkey.

K Sasaki, H Gemba.   

Abstract

Field potentials on the surface and at 2.5-3.0 mm depth in the cerebral cortex were recorded in various areas with chronically implanted electrodes and the potentials which preceded hand movements in response to a light stimulus were observed during the process of learning the skilled conditioned movement. A naive monkey had to lift a lever by wrist extension within duration of the light stimulus lasting for 900, 700 or 510 ms depending on the stage of the learning process. In addition to some responses in the striate gyrus, significant short-latency responses to the light stimulus appeared bilaterally in certain areas of the prefrontal and prestriate cortices at an early stage of learning in which the monkey still lifted the lever randomly, and they became gradually larger as the monkey was trained further. Short-latency responses were also often noted in the bilateral premotor cortices during an early stage of learning. When the monkey started to respond to the stimulus by the appropriate movement, early surface-positive (s-P), depth-negative (d-N) premovement potentials appeared in the forelimb motor cortex, and the responses in the premotor cortex increased in size. As the movement became faster and more skillful, late s-N, d-P premovement potentials, that are known to be mediated by the neocerebellum and superficial thalamo-cortical projections, emerged after the early s-P, d-N potentials and became more marked, larger and steeper in the forelimb motor cortex contralateral to the moving hand. All the premovement potentials in the different cortical areas thus developed into steady and constant states and remained so for many months thus maintaining their established patterns. Such successive appearances of premovement field potentials in various cortical areas were related to learning processes of the movement and the implication of these findings was discussed.

Mesh:

Year:  1982        PMID: 7151935     DOI: 10.1007/bf00238619

Source DB:  PubMed          Journal:  Exp Brain Res        ISSN: 0014-4819            Impact factor:   1.972


  16 in total

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Journal:  Brain Res       Date:  1981-02-02       Impact factor: 3.252

3.  Further observations on corticofrontal connections in the rhesus monkey.

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5.  A cortical evoked potential that reflects the conditioned, positive incentive value of the stimulus. I. The evoked potential.

Authors:  E S Boyd; E H Boyd; L E Brown
Journal:  Electroencephalogr Clin Neurophysiol       Date:  1977-03

6.  Cortical field potentials preceding visually initiated hand movements and cerebellar actions in the monkey.

Authors:  K Sasaki; H Gemba; N Mizuno
Journal:  Exp Brain Res       Date:  1982       Impact factor: 1.972

7.  Distribution of premovement slow cortical potentials associated with self-paced hand movements in monkeys.

Authors:  H Gemba; K Sasaki; S Hashimoto
Journal:  Neurosci Lett       Date:  1980-11       Impact factor: 3.046

8.  Relationships of precentral premotor and prefrontal cortex to the mediodorsal and intralaminar nuclei of the monkey thalamus.

Authors:  K Akert; K Hartmann-von Monakow
Journal:  Acta Neurobiol Exp (Wars)       Date:  1980       Impact factor: 1.579

9.  Premovement slow cortical potentials on self-paced hand movements and thalamocortical and corticocortical responses in the monkey.

Authors:  K Sasaki; H Gemba; S Hashimoto
Journal:  Exp Neurol       Date:  1981-04       Impact factor: 5.330

10.  Organization of the thalamo-cortical connexions to the frontal lobe in the rhesus monkey.

Authors:  J Kievit; H G Kuypers
Journal:  Exp Brain Res       Date:  1977-09-28       Impact factor: 1.972

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  21 in total

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5.  Reorganization of activity in the supplementary motor area associated with motor learning and functional recovery.

Authors:  H Aizawa; M Inase; H Mushiake; K Shima; J Tanji
Journal:  Exp Brain Res       Date:  1991       Impact factor: 1.972

6.  Changes of slow cortical negative DC-potentials during the acquisition of a complex finger motor task.

Authors:  J Niemann; T Winker; J Gerling; B Landwehrmeyer; R Jung
Journal:  Exp Brain Res       Date:  1991       Impact factor: 1.972

7.  Scaling of the metrics of visually-guided arm movements during motor learning in primates.

Authors:  C L Ojakangas; T J Ebner
Journal:  Exp Brain Res       Date:  1991       Impact factor: 1.972

8.  Supplementary motor area activation while tapping bimanually different rhythms in musicians.

Authors:  W Lang; H Obrig; G Lindinger; D Cheyne; L Deecke
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9.  Population interactions between parietal and primary motor cortices during reach.

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10.  A hierarchical neural-network model for control and learning of voluntary movement.

Authors:  M Kawato; K Furukawa; R Suzuki
Journal:  Biol Cybern       Date:  1987       Impact factor: 2.086

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