Literature DB >> 3193157

Relations of motor cortex neural discharge to kinematics of passive and active elbow movements in the monkey.

D Flament1, J Hore.   

Abstract

1. Bedingham and Tatton recently reported that in cats trained not to resist imposed limb perturbations, some motor cortex (area 4) neurons responded predominantly to acceleration or jerk (the third derivative of position). The questions arose whether motor cortex neurons responding to higher derivatives of limb displacement exist in the primate in a resist-perturbation task and, if so, whether discharge of such neurons responds to the same kinematics in active (voluntary) movements. 2. To answer these questions we studied the discharge patterns of 203 motor cortex neurons that responded to torque pulse perturbations about the elbow and fired during active elbow flexions and extensions in four monkeys. Detailed analysis was performed on 66 neurons that responded reciprocally in both situations. 3. Reciprocal neurons discharged at short latency (20-40 ms) for one direction of arm perturbation. For the opposite direction they were initially silent or inhibited and then discharged at a variety of latencies but in apparent relation to limb kinematics. Based on the timing and overall pattern of their discharge the majority of neurons (68%) were classified as being acceleration-like. 4. Twenty-four (36%) of these reciprocal neurons had only sensory (kinematic)-like properties in active movements, i.e., they discharged after (and not before) movement onset. Discharge of these neurons followed the timing, but not the magnitude, of acceleration (20 neurons) or velocity (4 neurons). The discharge of these neurons also had a static component as the arm was held stationary. 5. Twenty-nine (44%) of reciprocal neurons commenced firing before movement onset for one direction of active movement, while for the opposite direction their discharge occurred after movement onset. Thus their discharge appeared to be muscle-related: both when the muscle was contracting as an agonist and stretched as an antagonist. 6. Although in these tasks discharge of MCNs could be generated either by sensory feedback or by motor responses, the strong response sensitivity of many neurons to acceleration supports the hypothesis that feedback based on higher derivatives of limb displacement could represent a "predictive" control system for accurate regulation of limb motion.

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Mesh:

Year:  1988        PMID: 3193157     DOI: 10.1152/jn.1988.60.4.1268

Source DB:  PubMed          Journal:  J Neurophysiol        ISSN: 0022-3077            Impact factor:   2.714


  27 in total

1.  Time-varying changes in corticospinal excitability accompanying the triphasic EMG pattern in humans.

Authors:  C D MacKinnon; J C Rothwell
Journal:  J Physiol       Date:  2000-11-01       Impact factor: 5.182

2.  Sensing with the motor cortex.

Authors:  Nicholas G Hatsopoulos; Aaron J Suminski
Journal:  Neuron       Date:  2011-11-03       Impact factor: 17.173

3.  Cortical activation during rhythmic hand movements performed under three types of control: an fMRI study.

Authors:  R A Bernard; D A Goran; S T Sakai; T H Carr; D McFarlane; B Nordell; T G Cooper; E J Potchen
Journal:  Cogn Affect Behav Neurosci       Date:  2002-09       Impact factor: 3.282

4.  A frequency analysis of neuronal activity in monkey thalamus, motor cortex and electromyograms in wrist oscillations.

Authors:  E G Butler; M K Horne; P R Churchward
Journal:  J Physiol       Date:  1992-01       Impact factor: 5.182

5.  The activity of monkey thalamic and motor cortical neurones in a skilled, ballistic movement.

Authors:  E G Butler; M K Horne; N J Hawkins
Journal:  J Physiol       Date:  1992-01       Impact factor: 5.182

6.  Sensory characteristics of monkey thalamic and motor cortex neurones.

Authors:  E G Butler; M K Horne; J A Rawson
Journal:  J Physiol       Date:  1992-01       Impact factor: 5.182

Review 7.  Optimal feedback control and the long-latency stretch response.

Authors:  J Andrew Pruszynski; Stephen H Scott
Journal:  Exp Brain Res       Date:  2012-02-28       Impact factor: 1.972

8.  Partition of voluntary command to antagonist muscles during cyclic flexion-extension of the hand.

Authors:  Roberto Esposti; Paolo Cavallari; Fausto Baldissera
Journal:  Exp Brain Res       Date:  2005-02-03       Impact factor: 1.972

9.  Direct comparison of the task-dependent discharge of M1 in hand space and muscle space.

Authors:  M M Morrow; L R Jordan; L E Miller
Journal:  J Neurophysiol       Date:  2006-11-22       Impact factor: 2.714

10.  Influence of ipsilateral transcranial magnetic stimulation on the triphasic EMG pattern accompanying fast ballistic movements in humans.

Authors:  Kerstin Irlbacher; Martin Voss; Bernd-Ulrich Meyer; John C Rothwell
Journal:  J Physiol       Date:  2006-03-31       Impact factor: 5.182

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