Literature DB >> 119847

Discharges of intracerebellar nuclear cells in monkeys.

R J Harvey, R Porter, J A Rawson.   

Abstract

1. Conscious monkeys were trained with food rewards to perform movement tasks with the left forelimb and to accept manipulation of the joints and muscles and natural non-noxious stimulation of the skin of all four limbs. 2. Recordings were made from 217 cells situated in the left interpositus and dentate nuclei of the cerebellum. The identity of seventy-seven cells as cerebellar projection neurones was definitively established by activating them antidromically from the brachium conjunctivum near the contralateral red nucleus. 3. Modulation in the natural activity of 129 of these crebellar nuclear cells (sixty in interpositus; sixty-nine in dentate) occurred in a reproducible manner in temporal association with a phase of the self-paced movement tasks performed by the animal using the ipsilateral arm and hand. The discharges during motor performance of forty-two dentate and forty-five interpositus cells were shown to be associated with movement about a particular joint or region of the forelimb whenever that movement occurred. 4. Cells whose discharges were related to proximal joint movements (shoulder, elbow) and cells related to distal joint movements (wrist, fingers) were encountered in both the dentate and interposed nuclei. 5. The cells were tonically active at rest. Most commonly, accelerations in the discharge were related to movement of a joint or the limb in one direction and a reduction or cessation of activity accompanied movement in the opposite direction. 6. For some cells, variation of the amount of discharge demonstrated during movement performance 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. 7. The dentate and interpositus cells whose discharges were most strongly and consistently related to movements of the forelimb were concentrated in the mid region and caudal half of either nucleus. 8. None of seventy-three dentate neurones examined showed appreciable responses to stimulation of the skin or manipulation of joints and muscles of the fore- or hind limbs and only two cells responded to unexpected perturbation of movement performance. 9. No influence resulting from peripheral afferent input from the ipsilateral forelimb was detected in any interpositus cell whose firing was unchanged during ipsilateral arm movements. 10. Of the sixty interpositus cells whose discharge rates changed during motor performance, twenty-eight were demonstrated to be in receipt of input from receptors in the ipsilateral hand or arm, which could be activated by brisk tapping of the skin and sometimes by gentle squeezing of the forearm. 11. In the passive relaxed animal, manipulation of joints was ineffective in modifying the discharges of most interpositus neurones and, in all cases, prolonged pressure upon the skin elicited only transient responses...

Mesh:

Year:  1979        PMID: 119847      PMCID: PMC1458737          DOI: 10.1113/jphysiol.1979.sp013057

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


  22 in total

1.  Functional localization in the cerebellum. II. Somatotopic organization in cortex and nuclei.

Authors:  W W CHAMBERS; J M SPRAGUE
Journal:  AMA Arch Neurol Psychiatry       Date:  1955-12

2.  Functional localization in the cerebellum. I. Organization in longitudinal cortico-nuclear zones and their contribution to the control of posture, both extrapyramidal and pyramidal.

Authors:  W W CHAMBERS; J M SPRAGUE
Journal:  J Comp Neurol       Date:  1955-08       Impact factor: 3.215

3.  Convergence of cerebral inputs onto dentate neurons in monkey.

Authors:  G I Allen; P F Gilbert; T C Yin
Journal:  Exp Brain Res       Date:  1978-06-19       Impact factor: 1.972

4.  Electrophysiological studies on the cerebellocerebral projections in monkeys.

Authors:  K Sasaki; S Kawaguchi; H Oka; M Sakai; N Mizuno
Journal:  Exp Brain Res       Date:  1976-03-15       Impact factor: 1.972

Review 5.  Functional significance of connections of the inferior olive.

Authors:  D M Armstrong
Journal:  Physiol Rev       Date:  1974-04       Impact factor: 37.312

6.  Synaptic excitation of red nucleus neurones by fibres from interpositus nucleus.

Authors:  K Toyama; N Tsukahara; K Kosaka; K Matsunami
Journal:  Exp Brain Res       Date:  1970       Impact factor: 1.972

7.  The lateral reticular nucleus in the cat. III. Organization of component activated from ipsilateral forelimb tract.

Authors:  M Clendenin; C F Ekerot; O Oscarsson
Journal:  Exp Brain Res       Date:  1974       Impact factor: 1.972

8.  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

9.  Integration of cerebral and peripheral inputs by interpositus neurons in monkey.

Authors:  G I Allen; P F Gilbert; R Marini; W Schultz; T C Yin
Journal:  Exp Brain Res       Date:  1977-01-18       Impact factor: 1.972

10.  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

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  32 in total

1.  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

2.  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

3.  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

4.  Unravelling cerebellar pathways with high temporal precision targeting motor and extensive sensory and parietal networks.

Authors:  Fahad Sultan; Mark Augath; Salah Hamodeh; Yusuke Murayama; Axel Oeltermann; Alexander Rauch; Peter Thier
Journal:  Nat Commun       Date:  2012-06-26       Impact factor: 14.919

5.  Bilateral representation in the deep cerebellar nuclei.

Authors:  Demetris S Soteropoulos; Stuart N Baker
Journal:  J Physiol       Date:  2008-01-10       Impact factor: 5.182

6.  Complex spike synchrony dependent modulation of rat deep cerebellar nuclear activity.

Authors:  Tianyu Tang; Timothy A Blenkinsop; Eric J Lang
Journal:  Elife       Date:  2019-01-09       Impact factor: 8.140

7.  Control of voluntary and optogenetically perturbed locomotion by spike rate and timing of neurons of the mouse cerebellar nuclei.

Authors:  Rashmi Sarnaik; Indira M Raman
Journal:  Elife       Date:  2018-04-16       Impact factor: 8.140

Review 8.  Processing of limb kinematics in the interpositus nucleus.

Authors:  Antonino Casabona; Gianfranco Bosco; Vincenzo Perciavalle; Maria Stella Valle
Journal:  Cerebellum       Date:  2010-03       Impact factor: 3.847

9.  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

10.  Cerebellar Control of Reach Kinematics for Endpoint Precision.

Authors:  Matthew I Becker; Abigail L Person
Journal:  Neuron       Date:  2019-06-04       Impact factor: 17.173

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