Literature DB >> 6705862

Single cell studies of the primate putamen. II. Relations to direction of movement and pattern of muscular activity.

M D Crutcher, M R DeLong.   

Abstract

The major goal of this study was to determine whether the activity of single cells in the primate putamen was better related to the direction of limb movement or to the underlying pattern of muscular activity. In addition, the neural responses to load application were studied in order to determine whether the same neurons were also responsive to somatosensory stimuli. Two rhesus monkeys were trained to perform a visuomotor arm tracking task which required elbow flexion/extension movements with assisting and opposing loads in order to dissociate the direction of elbow movement from the pattern of muscular activity required for the movement. Neurons in the putamen were selected for study only if they were related both to the task and to arm movements outside the task. Most (96%) of the cells studied responded to load application: 36% of these showed short-latency (less than 50 ms), "sensory" responses. Forty-four percent of neurons had significant relations to the level of static load as the animal held the arm stationary against the steady loads: in general, static load effects were relatively weak. During the elbow flexion/extension movements in the task, 76% of cells had significant relations to the direction of movement, and 52% of neurons had significant dynamic relations to the level of load. Half of all neurons studied were primarily related to the direction of movement independent of the load. Only thirteen percent of cells in the putamen had a pattern of activity similar to that of muscles. These results indicate that neuronal activity in the putamen is predominantly related to the direction of limb movement rather than to the activity of particular muscles and that the basal ganglia may play a role in the specification of parameters of movement independent of the activity of specific muscles. These results also indicate that the basal ganglia receive proprioceptive input which may be used in the control of ongoing movement.

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Mesh:

Year:  1984        PMID: 6705862     DOI: 10.1007/bf00238154

Source DB:  PubMed          Journal:  Exp Brain Res        ISSN: 0014-4819            Impact factor:   1.972


  36 in total

1.  Reexamination of the force relationship of cortical cell discharge patterns with conditioned wrist movements.

Authors:  E M Schmidt; R G Jost; K K Davis
Journal:  Brain Res       Date:  1975-01-10       Impact factor: 3.252

2.  An autoradiographic analysis of the efferent connections from premotor and adjacent prefrontal regions (areas 6 and 9) in macaca fascicularis.

Authors:  H Künzle
Journal:  Brain Behav Evol       Date:  1978       Impact factor: 1.808

3.  Discharge patterns of basal ganglia neurons during active maintenance of postural stability and adjustment to chair tilt.

Authors:  M E Anderson
Journal:  Brain Res       Date:  1978-03-24       Impact factor: 3.252

4.  Relation of pyramidal tract activity to force exerted during voluntary movement.

Authors:  E V Evarts
Journal:  J Neurophysiol       Date:  1968-01       Impact factor: 2.714

5.  Relation of activity in precentral cortical neurons to force and rate of force change during isometric contractions of finger muscles.

Authors:  A M Smith; M C Hepp-Reymond; U R Wyss
Journal:  Exp Brain Res       Date:  1975-09-29       Impact factor: 1.972

6.  Sensory and motor responses of precentral cortex cells during comparable passive and active joint movements.

Authors:  E E Fetz; D V Finocchio; M A Baker; M J Soso
Journal:  J Neurophysiol       Date:  1980-04       Impact factor: 2.714

7.  Cerebellar participation in generation of prompt arm movements.

Authors:  J Meyer-Lohmann; J Hore; V B Brooks
Journal:  J Neurophysiol       Date:  1977-09       Impact factor: 2.714

8.  Activity of primate precentral neurons during voluntary movements triggered by visual signals.

Authors:  J T Murphy; H C Kwan; W A MacKay; Y C Wong
Journal:  Brain Res       Date:  1982-03-25       Impact factor: 3.252

9.  Bilateral projections from precentral motor cortex to the putamen and other parts of the basal ganglia. An autoradiographic study in Macaca fascicularis.

Authors:  H Künzle
Journal:  Brain Res       Date:  1975-05-02       Impact factor: 3.252

10.  Arm movement performance during reversible basal ganglia lesions in the monkey.

Authors:  J Hore; T Vilis
Journal:  Exp Brain Res       Date:  1980       Impact factor: 1.972

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  63 in total

1.  Spontaneous activity of neostriatal cholinergic interneurons in vitro.

Authors:  B D Bennett; C J Wilson
Journal:  J Neurosci       Date:  1999-07-01       Impact factor: 6.167

2.  Convergent inputs from thalamic motor nuclei and frontal cortical areas to the dorsal striatum in the primate.

Authors:  N R McFarland; S N Haber
Journal:  J Neurosci       Date:  2000-05-15       Impact factor: 6.167

3.  Corticostriatal activity in primary motor cortex of the macaque.

Authors:  R S Turner; M R DeLong
Journal:  J Neurosci       Date:  2000-09-15       Impact factor: 6.167

Review 4.  Role of uncertainty in sensorimotor control.

Authors:  Robert J van Beers; Pierre Baraduc; Daniel M Wolpert
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2002-08-29       Impact factor: 6.237

5.  Neural responses in multiple basal ganglia regions during spontaneous and treadmill locomotion tasks in rats.

Authors:  L H Shi; F Luo; D J Woodward; J Y Chang
Journal:  Exp Brain Res       Date:  2004-04-06       Impact factor: 1.972

6.  Role of primate basal ganglia and frontal cortex in the internal generation of movements. II. Movement-related activity in the anterior striatum.

Authors:  R Romo; E Scarnati; W Schultz
Journal:  Exp Brain Res       Date:  1992       Impact factor: 1.972

7.  Striatal neuronal activity during the initiation and execution of hand movements made in response to visual and vibratory cues.

Authors:  T W Gardiner; R J Nelson
Journal:  Exp Brain Res       Date:  1992       Impact factor: 1.972

8.  Temporal convergence of dynamic cell assemblies in the striato-pallidal network.

Authors:  Avital Adler; Shiran Katabi; Inna Finkes; Zvi Israel; Yifat Prut; Hagai Bergman
Journal:  J Neurosci       Date:  2012-02-15       Impact factor: 6.167

Review 9.  Striatal mechanisms underlying movement, reinforcement, and punishment.

Authors:  Alexxai V Kravitz; Anatol C Kreitzer
Journal:  Physiology (Bethesda)       Date:  2012-06

10.  Acute effects of cocaine on movement-related firing of dorsolateral striatal neurons depend on predrug firing rate and dose.

Authors:  Anthony P Pawlak; Chris C Tang; Cathy Pederson; Martin B Wolske; Mark O West
Journal:  J Pharmacol Exp Ther       Date:  2009-11-11       Impact factor: 4.030

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