Literature DB >> 6887028

Simple and complex spike activity of cerebellar Purkinje cells during active and passive movements in the awake monkey.

E Bauswein, F P Kolb, B Leimbeck, F J Rubia.   

Abstract

Two Rhesus monkeys (Macaca mulatta) were trained to pursue a target light signal by moving the hand at the wrist joint. Additionally, a d.c. motor could be attached to the lever in order to perform similar passive movements. During performance of the task, single Purkinje cells were recorded from the intermediate part of the cerebellar anterior lobe. Electromyographic activity of the flexor and extensor muscles of the forearm was recorded simultaneously. Passive hand movements evoked changes in the complex spike and simple spike discharge of Purkinje cell. The complex spike responded most sensitively to the beginning of the movement; the activity pattern had phasic character and could be related specifically to the movement direction. The simple spike response was usually weak and hence revealed-less specific relations. During active movements the simple spike frequency change was generally stronger than during passive movements and reached a maximum (or minimum) at the beginning of hand deflexion. The complex spike activity during active movements was characterized by a contrast between the time phases before and after the movement onset. In most of the cases, where a phase of increased activity stopped at the movement onset, the sensory feed-back signal seen during passive movements was cancelled. The possible consequences of the convergence of the complex and simple spike signal for the motor control function of the cerebellum are discussed.

Entities:  

Mesh:

Year:  1983        PMID: 6887028      PMCID: PMC1199167          DOI: 10.1113/jphysiol.1983.sp014722

Source DB:  PubMed          Journal:  J Physiol        ISSN: 0022-3751            Impact factor:   5.182


  31 in total

1.  Climbing fiber responses of cerebellar Purkinje cells to passive movement of the cat forepaw.

Authors:  D S Rushmer; W J Roberts; G K Augter
Journal:  Brain Res       Date:  1976-04-16       Impact factor: 3.252

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

Authors:  W T Thach
Journal:  J Neurophysiol       Date:  1978-05       Impact factor: 2.714

Review 3.  The mammalian cerebellum and its contribution to movement control.

Authors:  D M Armstrong
Journal:  Int Rev Physiol       Date:  1978

4.  Activity patterns of cerebellar cortical neurones and climbing fibre afferents in the awake cat.

Authors:  D M Armstrong; J A Rawson
Journal:  J Physiol       Date:  1979-04       Impact factor: 5.182

5.  The natural discharges of Purkinje cells in paravermal regions of lobules V and VI of the monkey's cerebellum.

Authors:  R J Harvey; R Porter; J A Rawson
Journal:  J Physiol       Date:  1977-10       Impact factor: 5.182

6.  Responses of primate dentate neurons to different trajectories of the limb.

Authors:  L T Robertson; R J Grimm
Journal:  Exp Brain Res       Date:  1975-11-14       Impact factor: 1.972

7.  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

8.  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

9.  The activity of dentate neurons during an arm movement sequence.

Authors:  R J Grimm; D S Rushmer
Journal:  Brain Res       Date:  1974-05-17       Impact factor: 3.252

10.  Responses of cerebellar units to a passive movement in the decerebrate cat.

Authors:  F J Rubia; F P Kolb
Journal:  Exp Brain Res       Date:  1978-03-15       Impact factor: 1.972

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  27 in total

Review 1.  Consensus paper: roles of the cerebellum in motor control--the diversity of ideas on cerebellar involvement in movement.

Authors:  Mario Manto; James M Bower; Adriana Bastos Conforto; José M Delgado-García; Suzete Nascimento Farias da Guarda; Marcus Gerwig; Christophe Habas; Nobuhiro Hagura; Richard B Ivry; Peter Mariën; Marco Molinari; Eiichi Naito; Dennis A Nowak; Nordeyn Oulad Ben Taib; Denis Pelisson; Claudia D Tesche; Caroline Tilikete; Dagmar Timmann
Journal:  Cerebellum       Date:  2012-06       Impact factor: 3.847

2.  Changes in excitability of ascending and descending inputs to cerebellar climbing fibers during locomotion.

Authors:  Joanne Pardoe; Stephen A Edgley; Trevor Drew; Richard Apps
Journal:  J Neurosci       Date:  2004-03-17       Impact factor: 6.167

Review 3.  Activation of climbing fibers.

Authors:  Alan R Gibson; Kris M Horn; Milton Pong
Journal:  Cerebellum       Date:  2004       Impact factor: 3.847

4.  The sensory guidance of movement: a comparison of the cerebellum and basal ganglia.

Authors:  M Jueptner; I H Jenkins; D J Brooks; R S Frackowiak; R E Passingham
Journal:  Exp Brain Res       Date:  1996-12       Impact factor: 1.972

5.  Changes in Purkinje cell simple spike encoding of reach kinematics during adaption to a mechanical perturbation.

Authors:  Angela L Hewitt; Laurentiu S Popa; Timothy J Ebner
Journal:  J Neurosci       Date:  2015-01-21       Impact factor: 6.167

6.  Cerebellar metabolic involvement and its correlations with clinical parameters in vestibular neuritis.

Authors:  Marco Alessandrini; Alessandro Micarelli; Agostino Chiaravalloti; Matteo Candidi; Ernesto Bruno; Barbara Di Pietro; Johanna Öberg; Orazio Schillaci; Marco Pagani
Journal:  J Neurol       Date:  2014-08-01       Impact factor: 4.849

7.  Cerebellar unit responses of the mossy fibre system to passive movements in the decerebrate cat. I. Responses to static parameters.

Authors:  F P Kolb; F J Rubia; E Bauswein
Journal:  Exp Brain Res       Date:  1987       Impact factor: 1.972

8.  Cerebellar learning using perturbations.

Authors:  Guy Bouvier; Johnatan Aljadeff; Claudia Clopath; Célian Bimbard; Jonas Ranft; Antonin Blot; Jean-Pierre Nadal; Nicolas Brunel; Vincent Hakim; Boris Barbour
Journal:  Elife       Date:  2018-11-12       Impact factor: 8.140

9.  A simple method for reliable separation of cerebellar Purkinje cell complex and simple spikes.

Authors:  F P Kolb
Journal:  Pflugers Arch       Date:  1983-09       Impact factor: 3.657

10.  The primate cerebellum selectively encodes unexpected self-motion.

Authors:  Jessica X Brooks; Kathleen E Cullen
Journal:  Curr Biol       Date:  2013-05-16       Impact factor: 10.834

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