Cortical field potential associated with hand movement on warning-imperative visual stimulus and cerebellum in the monkey
Abstract
Latent time of the hand movement in response to a visual stimulus was found to be very short when a monkey was enough trained with a visual imperative stimulus preceded by a visual warning stimulus at a fixed time interval. Cerebellar hemispherectomy scarcely prolonged the reaction time of the warning-imperative, visually initiated (W-VI) movement in contrast to its marked delaying action upon the simple visually initiated reaction-time (S-VI) movement. Between the warning and imperative stimuli, sustained surface-negative, depth-positive field potentials were recorded in various areas of the prefrontal and premotor cortices and the supplementary motor area of both cerebral hemispheres, besides gradually increasing surface-negative, depth-positive deflections in the motor and somatosensory cortices contralateral to the moving hand. These observations suggest that the sustained activities in the prefrontal and premotor cortices elicited by the warning stimulus overcome deficiency of the cerebellar function for performing fast and stable timing movements.
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Abnormal cerebellum and basal ganglia related to tremor and akinetic-rigid symptoms lead to longer RT or MT in PD patients.
“The abnormal cerebellum and basal ganglia that related to tremor [14, 22, 43, 44] and akinetic-rigid symptoms [6–9, 42] also lead to the longer RT or MT in PD patients.”
From Evaluation of tremor interference with control of voluntary reaching movements in patients with Parkinson's disease (2019) · cites this paper as [44]
PD patients with tremor often have less bradykinesia or rigidity but may have additional cerebellar malfunction that affects movement initiation.
“PD patients with the symptom of tremor often accompany less bradykinesia or rigidity, but may have additional malfunction in the cerebellum that affects movement initiation [43, 44].”
From Evaluation of tremor interference with control of voluntary reaching movements in patients with Parkinson's disease (2019) · cites this paper as [44]
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Deecke, L., Scheid, P., & Kornhuber, H. (1969) · Experimental Brain Research · doi:10.1007/bf00235441 · Cited by 748 · see citing works
Brain wave components of the contingent negative variation in humans
Rohrbaugh, J. W., Syndulko, K., & Lindsley, D. B. (1976) · Science · doi:10.1126/science.1251217 · Cited by 373 · see citing works
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Hu, Z., Hao, M., Xu, S., Xiao, Q., & Lan, N. (2019) · Journal of NeuroEngineering and Rehabilitation · doi:10.1186/s12984-019-0505-0 · Cited by 38 · see citing works
- Authors
- Sasaki, K., Gemba, H., & Tsujimoto, T.
- Affiliations
- Kyoto University (JP)
- Corresponding author
- Sasaki, Kazuo
- ORCID
- Sasaki, Kazuo
- Venue
- Brain Research
- Publisher
- Elsevier BV
- Published
- 1990-06
- Volume
- 519
- Issue
- 1-2
- Pages
- 343-346
- ISSN
- 0006-8993 (ISSN-L)
- OpenAlex
- W2003951628
- Cited by
- 18
- References
- 2
- Citations by year
- 2019: 2 · 2012: 1
- FWCI
- 0.24
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Brain Research (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Motor Control and Adaptation
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural and Behavioral Psychology Studies
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
- Keywords
- hand movement, reaction time, prefrontal cortex, premotor cortex, supplementary motor area, cortical field potentials, motor timing
- MeSH terms
- Animals, Cerebellum, Cerebral Cortex, Electrophysiology, Evoked Potentials, Visual, Hand, Functional Laterality, Macaca, Motor Cortex, Movement, Photic Stimulation, Somatosensory Cortex, Time Factors
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