Literature DB >> 411917

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

R J Harvey, R Porter, J A Rawson.   

Abstract

1. Conscious monkeys were trained with food rewards to perform movement tasks with the left hand and to accept manipulation of the joints and muscles and natural non-noxious stimulation of the skin of both forelimbs.2. Recordings were made from 230 Purkinje cells situated in the paravermal region of lobules V and VI or immediately adjacent folia of the left cerebellum in a region from 2 to 7 mm from the mid line. These neurones were all in a zone which was demonstrated to receive inputs from the ipsilateral hand and which is known to receive projections, via the pontine nuclei from the ;arm area' of motor cortex in the right hemisphere.3. Modulation of the natural activity of 182 of these 230 Purkinje cells (79%) occurred in a reproducible manner in temporal association, each with a particular phase of the self-paced movement tasks performed by the animal using the ipsilateral arm and hand. The patterns of modulation of Purkinje cell firing in this limited zone of cerebellar cortex could be classified into one of four groups, and each cell's discharge was associated with a particular aspect of movement such as general arm flexion, shoulder retraction, elbow extension or elbow flexion whenever it occurred.4. The cells were spontaneously active at rest. Most commonly, marked accelerations of the discharge were related to one direction of the particular aspect of movement and a reduction of activity or even total silence accompanied movement in the opposite direction.5. Variation of the amount of discharge demonstrated during a movement performance with which this discharge was characteristically associated could be related to the range of the movement or its duration, more activity being characteristic of more prolonged movement performance through larger angles of joint displacement.6. Both simple spikes and complex spikes of some cells showed characteristic modulation of their activity during the monkey's self-initiated movements. Cells whose simple spikes did not change in frequency during the movement task, also showed no modification of complex spike discharge.7. Of the 182 neurones whose discharges changed during active movement performance, 105 (roughly 60%) were demonstrated to be in receipt of an input from peripheral receptors in the hand which could be activated by brisk tapping of the skin or brushing of hairs. In contrast, none of the Purkinje cells whose discharges were unchanged during arm movements could be demonstrated to receive such an input.8. Movement of joints through their full range and prodding of muscles were completely ineffective stimuli for causing changes in Purkinje cell firing in this zone of the cerebellar cortex while the animal was passive and relaxed. Imposed perturbations of movement performance injected unexpectedly during the execution of a movement task were also ineffective in modifying the discharge of these Purkinje cells in relation to the task.

Entities:  

Mesh:

Year:  1977        PMID: 411917      PMCID: PMC1353584          DOI: 10.1113/jphysiol.1977.sp012012

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


  14 in total

1.  Relationship between the activity of precentral neurones during active and passive movements in conscious monkeys.

Authors:  R N Lemon; J A Hanby; R Porter
Journal:  Proc R Soc Lond B Biol Sci       Date:  1976-10-29

2.  Excitatory and inhibitory processes acting upon individual Purkinje cells of the cerebellum in cats.

Authors:  R GRANIT; C G PHILLIPS
Journal:  J Physiol       Date:  1956-09-27       Impact factor: 5.182

3.  The cerebellum of the cat and the monkey.

Authors:  O LARSELL
Journal:  J Comp Neurol       Date:  1953-08       Impact factor: 3.215

4.  Cerebrocerebellar relationships in the monkey.

Authors:  R S SNIDER; E ELDRED
Journal:  J Neurophysiol       Date:  1952-01       Impact factor: 2.714

5.  Spike discharges of single units in the cerebellar cortex.

Authors:  J M BROOKHART; G MORUZZI; R S SNIDER
Journal:  J Neurophysiol       Date:  1950-11       Impact factor: 2.714

6.  A headpiece for recording discharges of neurons in unrestrained monkeys.

Authors:  R Porter; M M Lewis; G F Linklater
Journal:  Electroencephalogr Clin Neurophysiol       Date:  1971-01

7.  Discharge of cerebellar neurons related to two maintained postures and two prompt movements. II. Purkinje cell output and input.

Authors:  W T Thach
Journal:  J Neurophysiol       Date:  1970-07       Impact factor: 2.714

8.  Discharge of cerebellar neurons related to two maintained postures and two prompt movements. I. Nuclear cell output.

Authors:  W T Thach
Journal:  J Neurophysiol       Date:  1970-07       Impact factor: 2.714

9.  The excitatory synaptic action of climbing fibres on the Purkinje cells of the cerebellum.

Authors:  J C Eccles; R Llinás; K Sasaki
Journal:  J Physiol       Date:  1966-01       Impact factor: 5.182

10.  Somatosensory receptive fields of single units in cat cerebellar cortex.

Authors:  W T Thach
Journal:  J Neurophysiol       Date:  1967-07       Impact factor: 2.714

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  30 in total

1.  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

2.  Movement-related discharge in the cerebellar nuclei persists after local injections of GABA(A) antagonists.

Authors:  R N Holdefer; J C Houk; L E Miller
Journal:  J Neurophysiol       Date:  2004-08-25       Impact factor: 2.714

3.  Neuronal activity in the lateral cerebellum of trained monkeys, related to visual stimuli or to eye movements.

Authors:  D E Marple-Horvat; J F Stein
Journal:  J Physiol       Date:  1990-09       Impact factor: 5.182

4.  Gcn5 loss-of-function accelerates cerebellar and retinal degeneration in a SCA7 mouse model.

Authors:  Yi Chun Chen; Jennifer R Gatchel; Rebecca W Lewis; Chai-An Mao; Patrick A Grant; Huda Y Zoghbi; Sharon Y R Dent
Journal:  Hum Mol Genet       Date:  2011-10-14       Impact factor: 6.150

Review 5.  Activation of climbing fibers.

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

6.  Frequency-dependent reliability of spike propagation is function of axonal voltage-gated sodium channels in cerebellar Purkinje cells.

Authors:  Zhilai Yang; Jin-Hui Wang
Journal:  Cerebellum       Date:  2013-12       Impact factor: 3.847

Review 7.  The neuronal code(s) of the cerebellum.

Authors:  Detlef H Heck; Chris I De Zeeuw; Dieter Jaeger; Kamran Khodakhah; Abigail L Person
Journal:  J Neurosci       Date:  2013-11-06       Impact factor: 6.167

8.  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

9.  Gating of cutaneous input to cerebellar climbing fibres during a reaching task in the cat.

Authors:  R Apps; M J Atkins; M Garwicz
Journal:  J Physiol       Date:  1997-07-01       Impact factor: 5.182

10.  Functional relation between corticonuclear input and movements evoked on microstimulation in cerebellar nucleus interpositus anterior in the cat.

Authors:  C F Ekerot; H Jörntell; M Garwicz
Journal:  Exp Brain Res       Date:  1995       Impact factor: 1.972

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