JN Fuel your research with LabChart
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


J Neurophysiol 55: 203-226, 1986;
0022-3077/86 $5.00
This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Chapman, C. E.
Right arrow Articles by Lamarre, Y.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Chapman, C. E.
Right arrow Articles by Lamarre, Y.

Journal of Neurophysiology, Vol 55, Issue 2 203-226, Copyright © 1986 by APS


ARTICLES

Activity of dentate neurons during arm movements triggered by visual, auditory, and somesthetic stimuli in the monkey

C. E. Chapman, G. Spidalieri and Y. Lamarre

Single-unit recordings were obtained from 404 neurons in the dentate and interposed nuclei in two monkeys trained to perform simple movements of the elbow in response to three different sensory cues: a light, a tone, and a small, brief perturbation of the trained forearm. Both flexion and extension movements were investigated. Those dentate neurons that showed a clear modulation before the onset of movement (149 of 318 cells recorded) were classified as stimulus related or movement related on the basis of an analysis of the timing of the initial change in discharge. Seventy-one percent of these dentate neurons (106/149) were classified as stimulus related, and 21% (31/149) were classified as movement related. Within the stimulus-related group 87% responded selectively to only one or two of the sensory cues (selective stimulus-related neurons), most often the teleceptive cues, whereas the remaining 13% responded nonselectively to all three cues (nonselective stimulus-related neurons). Interposed neurons, in contrast, showed principally movement-related discharge, and this represented the initial change in discharge in 89% of the neurons. Eleven percent of the interposed cells showed a selective response to the somesthetic cue. The discharge of 28 out of 91 dentate neurons tested with both flexion and extension movements varied with the direction of movement. Few dentate neurons (9%) were found to display any direction sensitivity when considering the discharge preceding the onset of movement, and none of these showed a reciprocal pattern. The discharge of a greater proportion of neurons (24%) was direction sensitive during movement and was occasionally reciprocal. In the same monkeys, however, 78% of the neurons in the neighboring interposed nucleus were direction sensitive, and one-quarter of these displayed reciprocal patterns of discharge. Thus, the discharge of dentate neurons, occurring well in advance of a conditioned movement, cannot specify direction in this simple reaction-time (RT) task. The sensory responses of selective stimulus-related dentate cells ended near the onset of movement but were time locked to the stimulus and not to the movement. When a neuron was responsive to two of the cues the response did not vary with the modality of the stimulus apart from changes in the latency. The initial sensory response was usually followed by later "secondary" changes in discharge that were temporally related to the movement.(ABSTRACT TRUNCATED AT 250 WORDS)


This article has been cited by other articles:


Home page
J. Neurophysiol.Home page
B. Schepens and T. Drew
Descending Signals From the Pontomedullary Reticular Formation Are Bilateral, Asymmetric, and Gated During Reaching Movements in the Cat
J Neurophysiol, November 1, 2006; 96(5): 2229 - 2252.
[Abstract] [Full Text] [PDF]


Home page
J. Physiol.Home page
O. B. Miles, N. L. Cerminara, and D. E. Marple-Horvat
Purkinje cells in the lateral cerebellum of the cat encode visual events and target motion during visually guided reaching
J. Physiol., March 15, 2006; 571(3): 619 - 637.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
C. R. Mason, C. M. Hendrix, and T. J. Ebner
Purkinje Cells Signal Hand Shape and Grasp Force During Reach-to-Grasp in the Monkey
J Neurophysiol, January 1, 2006; 95(1): 144 - 158.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
A. V. Roitman, S. Pasalar, M. T. V. Johnson, and T. J. Ebner
Position, Direction of Movement, and Speed Tuning of Cerebellar Purkinje Cells during Circular Manual Tracking in Monkey
J. Neurosci., October 5, 2005; 25(40): 9244 - 9257.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
N. C. Rowland and D. Jaeger
Coding of Tactile Response Properties in the Rat Deep Cerebellar Nuclei
J Neurophysiol, August 1, 2005; 94(2): 1236 - 1251.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
K. Kurata
Activity Properties and Location of Neurons in the Motor Thalamus That Project to the Cortical Motor Areas in Monkeys
J Neurophysiol, July 1, 2005; 94(1): 550 - 566.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
B. Schepens and T. Drew
Independent and Convergent Signals From the Pontomedullary Reticular Formation Contribute to the Control of Posture and Movement During Reaching in the Cat
J Neurophysiol, October 1, 2004; 92(4): 2217 - 2238.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
B. Schepens and T. Drew
Strategies for the Integration of Posture and Movement During Reaching in the Cat
J Neurophysiol, November 1, 2003; 90(5): 3066 - 3086.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
X. Liu, E. Robertson, and R. C. Miall
Neuronal Activity Related to the Visual Representation of Arm Movements in the Lateral Cerebellar Cortex
J Neurophysiol, March 1, 2003; 89(3): 1223 - 1237.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
R. Courtemanche, J.-P. Pellerin, and Y. Lamarre
Local Field Potential Oscillations in Primate Cerebellar Cortex: Modulation During Active and Passive Expectancy
J Neurophysiol, August 1, 2002; 88(2): 771 - 782.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
S. R. Williams, J. Shenasa, and C. E. Chapman
Time Course and Magnitude of Movement-Related Gating of Tactile Detection in Humans. I. Importance of Stimulus Location
J Neurophysiol, February 1, 1998; 79(2): 947 - 963.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
Q.-G. Fu, D. Flament, J. D. Coltz, and T. J. Ebner
Relationship of Cerebellar Purkinje Cell Simple Spike Discharge to Movement Kinematics in the Monkey
J Neurophysiol, July 1, 1997; 78(1): 478 - 491.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Visit Other APS Journals Online