Literature DB >> 96223

Correlation of neural discharge with pattern and force of muscular activity, joint position, and direction of intended next movement in motor cortex and cerebellum.

W T Thach.   

Abstract

1. Monkeys were trained to grasp a rod movable in a horizontal arc (Fig. 1), and to hold the rod by angulation of the wrist in each of three positions (A,B, C). A maintained load was placed on the rod alternately to oppose flexion and extension. At a light signal, the monkey had to move to the next position in a prescribed sequence (ABCBABCBA, ETC.). The task was designed to dissociate, while holding in position, the following variables: 1) pattern of muscular activity in the forearm required to hold the wrist in position, determined by the direction of the load (flexor or extensor muscles); 2) position of the rod, and thus angulation of the wrist joint (A, B, and C); and 3) set for the direction of the intended next movement (flexor or extensor). These variables are subsequently referred to as MPAT, JPOS, and DSET, respectively. 2. After training, recordings were made of the EMG activity of muscles used in the task and of the discharge of single neurons in the motor cortex of the cerebrum and the interposed and dentate nuclei of the cerebellum. 3. While holding the wrist in position, EMG and interpositus behaved uniformly, with higher discharge frequency under load in one direction and lower discharge frequency under load in the opposite direction. This relation was relatively independent of the position held and of the direction of the intended next movement. Thus, interpositus and EMG both seemed best related to the MPAT variable, as opposed to JPOS and DSET variables. By contrast, neurons in motor cortex and in dentate fell into three categories: one category discharged in relation to the pattern of muscular activity (MPAT), a second to the position of the wrist (JPOS), and a third to the direction of the intended next movement (DSET). While MPAT neurons formed a distinct dissociated group, neurons that were best related to JPOS were often related to DSET, and vice versa. 4. A few of the MPAT neurons in interpositus and motor cortex were further studied by varying the magnitude (as well as the direction) of the loads. Both interpositus and motor cortex MPAT neurons changed firing frequency in relation to the magnitude of load, and though few neurons were thus studied, the relation seemed clearer for interpositus than for motor cortex. 5. Anatomically, the three types of neurons thus classified by firing pattern during the hold periods were intermixed in the arm area of motor cortex. In dentate and interpositus, those neurons thus related to the performance were localized to a narrow strip across the posterior part of both nuclei. Neurons apparently related to eye and drinking movements were located more posteriorly still, suggesting somatotopic representation.

Mesh:

Year:  1978        PMID: 96223     DOI: 10.1152/jn.1978.41.3.654

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


  115 in total

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Authors:  D L Tolbert; H Bantli
Journal:  Exp Brain Res       Date:  1979-08-01       Impact factor: 1.972

2.  Discharges of intracerebellar nuclear cells in monkeys.

Authors:  R J Harvey; R Porter; J A Rawson
Journal:  J Physiol       Date:  1979-12       Impact factor: 5.182

3.  Prediction of muscle activity by populations of sequentially recorded primary motor cortex neurons.

Authors:  M M Morrow; L E Miller
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4.  On-line compensation for perturbations of a reaching movement is cerebellar dependent: support for the task dependency hypothesis.

Authors:  Yury Shimansky; Jian-Jun Wang; Richard A Bauer; Vlastislav Bracha; James R Bloedel
Journal:  Exp Brain Res       Date:  2003-12-03       Impact factor: 1.972

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

7.  Differential force scaling of fine-graded power grip force in the sensorimotor network.

Authors:  Birgit Keisker; Marie-Claude Hepp-Reymond; Armin Blickenstorfer; Martin Meyer; Spyros S Kollias
Journal:  Hum Brain Mapp       Date:  2009-08       Impact factor: 5.038

8.  Excitability of corticospinal neurons during tonic muscle contractions in man.

Authors:  B Brouwer; P Ashby; G Midroni
Journal:  Exp Brain Res       Date:  1989       Impact factor: 1.972

9.  Convergence of vestibular and neck proprioceptive sensory signals in the cerebellar interpositus.

Authors:  Hongge Luan; Martha Johnson Gdowski; Shawn D Newlands; Greg T Gdowski
Journal:  J Neurosci       Date:  2013-01-16       Impact factor: 6.167

10.  Specific modulation of the Hoffmann reflex cutaneous facilitation during a reaction-time task.

Authors:  C Demairé; J Honoré; J Le Bizec; J M Coquery
Journal:  Exp Brain Res       Date:  1989       Impact factor: 1.972

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