Literature DB >> 6693934

Cerebellar cortical activity during antagonist cocontraction and reciprocal inhibition of forearm muscles.

R C Frysinger, D Bourbonnais, J F Kalaska, A M Smith.   

Abstract

Monkeys were trained to perform a maintained isometric grip of the thumb and forefinger that elicited a simultaneous cocontraction of the antagonist muscles of the forearm. The same monkeys were also trained to flex and extend the wrist against a stop with the fingers extended and to maintain an isometric wrist position for 1.0-1.5 s. During wrist movement, some of the synergist forearm muscles contracted during both flexion and extension. However, during the maintained isometric wrist position, the prime mover and synergist muscles were reciprocally active or silent. In the culmen-simplex region of the cerebellar cortex bordering on the primary fissure, 62% of the Purkinje cells that were identified by the climbing fiber discharge and that changed firing frequency decreased activity during maintained prehension. Almost all of these same Purkinje cells were reciprocally active during isometric wrist flexion and extension, although three neurons had similar discharge patterns during movements in both directions. In contrast, 79% of the unidentified neurons recorded from the same region of the cerebellar cortex increased discharge frequency during prehension. In general, most of these same neurons had reciprocal patterns of discharge during wrist movement even though a few cells were active during the dynamic phase in both directions. Together, the Purkinje cells and the unidentified neurons with bidirectional response patterns were thought to be related to muscles active during both flexion and extension wrist movements. No cells were found that increased discharge with the static isometric wrist torque exerted in both directions. The discharge frequency of some Purkinje and some unidentified neurons could be shown to be related to prehensile force as well as wrist movement velocity and isometric wrist torque. These data suggest that the discharge of about two-thirds of the Purkinje cells related to forearm muscles located along the borders of the primary fissure may depend on whether antagonist muscles are activated reciprocally or coactively. As a consequence, these cells may play a role in the selection or alternation between either of these two modes of muscular contraction. The increased discharge of the remaining one-third of the Purkinje cells excited during antagonist coactivation may provide inhibition of nuclear cells to stabilize the posture at joints other than the wrist and fingers or, alternatively, they may act to reduce nuclear cell discharge in proportion to the intensity of cutaneous stimulation.

Mesh:

Year:  1984        PMID: 6693934     DOI: 10.1152/jn.1984.51.1.32

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


  21 in total

1.  Cerebellar Purkinje cell simple spike discharge encodes movement velocity in primates during visuomotor arm tracking.

Authors:  J D Coltz; M T Johnson; T J Ebner
Journal:  J Neurosci       Date:  1999-03-01       Impact factor: 6.167

2.  Efficient generation of reciprocal signals by inhibition.

Authors:  Sung-min Park; Esra Tara; Kamran Khodakhah
Journal:  J Neurophysiol       Date:  2012-02-01       Impact factor: 2.714

3.  Simple spike firing in the posterior lateral cerebellar cortex of Macaque Mulatta was correlated with success-failure during a visually guided reaching task.

Authors:  Bradley Greger; Scott Norris
Journal:  Exp Brain Res       Date:  2005-11-12       Impact factor: 1.972

4.  Velocity-based planning of rapid elbow movements expands the control scheme of the equilibrium point hypothesis.

Authors:  Masataka Suzuki; Yoshihiko Yamazaki
Journal:  J Comput Neurosci       Date:  2005 Mar-Apr       Impact factor: 1.621

5.  Representation of limb kinematics in Purkinje cell simple spike discharge is conserved across multiple tasks.

Authors:  Angela L Hewitt; Laurentiu S Popa; Siavash Pasalar; Claudia M Hendrix; Timothy J Ebner
Journal:  J Neurophysiol       Date:  2011-07-27       Impact factor: 2.714

Review 6.  What features of limb movements are encoded in the discharge of cerebellar neurons?

Authors:  Timothy J Ebner; Angela L Hewitt; Laurentiu S Popa
Journal:  Cerebellum       Date:  2011-12       Impact factor: 3.847

Review 7.  Muscle coactivation: definitions, mechanisms, and functions.

Authors:  Mark L Latash
Journal:  J Neurophysiol       Date:  2018-03-28       Impact factor: 2.714

8.  Locomotor deficits in the mutant mouse, Lurcher.

Authors:  P A Fortier; A M Smith; S Rossignol
Journal:  Exp Brain Res       Date:  1987       Impact factor: 1.972

9.  Dynamic correspondence between Purkinje cell discharge and forelimb muscle activity during reaching.

Authors:  Robert N Holdefer; Lee E Miller
Journal:  Brain Res       Date:  2009-07-30       Impact factor: 3.252

Review 10.  Physiologic changes associated with cerebellar dystonia.

Authors:  Vikram G Shakkottai
Journal:  Cerebellum       Date:  2014-10       Impact factor: 3.847

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