Literature DB >> 8983981

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

C F Ekerot1, H Jörntell, M Garwicz.   

Abstract

The functional relation between receptive fields of climbing fibres projecting to the C1, C3 and Y zones and forelimb movements controlled by nucleus interpositus anterior via the rubrospinal tract were studied in cats decerebrated at the pre-collicular level. Microelectrode tracks were made through the caudal half of nucleus interpositus anterior. This part of the nucleus receives its cerebellar cortical projection from the forelimb areas of these three sagittal zones. The C3 zone has been demonstrated to consist of smaller functional units called microzones. Natural stimulation of the forelimb skin evoked positive field potentials in the nucleus. These potentials have previously been shown to be generated by climbing fibre-activated Purkinje cells and were mapped at each nuclear site, to establish the climbing fibre receptive fields of the afferent microzones. The forelimb movement evoked by microstimulation at the same site was then studied. The movement usually involved more than one limb segment. Shoulder retraction and elbow flexion were frequently evoked, whereas elbow extension was rare and shoulder protraction never observed. In total, movements at the shoulder and/or elbow occurred for 96% of the interpositus sites. At the wrist, flexion and extension movements caused by muscles with radial, central or ulnar insertions on the paw were all relatively common. Pure supination and pronation movements were also observed. Movements of the digits consisted mainly of dorsal flexion of central or ulnar digits. A comparison of climbing fibre receptive fields and associated movements for a total of 110 nuclear sites indicated a general specificity of the input-output relationship of this cerebellar control system. Several findings suggested that the movement evoked from a particular site would act to withdraw the area of the skin corresponding to the climbing fibre receptive field of the afferent microzones. For example, sites with receptive fields on the dorsum of the paw were frequently associated with palmar flexion at the wrist, whereas sites with receptive fields on the ventral side of the paw and forearm were associated with dorsiflexion at the wrist. Correspondingly, receptive fields on the lateral side of the forearm and paw were often associated with flexion at the elbow, whereas sites with receptive fields on the radial side of the forearm were associated with elbow extension. The proximal movements that were frequently observed also for distal receptive fields may serve to produce a general shortening of the limb to enhance efficiency of the withdrawal. It has previously been suggested that the cerebellar control of forelimb movements via the rubrospinal tract has a modular organisation. Each module would consist of a cell group in the nucleus interpositus anterior and its afferent microzones in the C1, C3 and Y zones, characterised by a homogenous set of climbing fibre receptive fields. The results of the present study support this organisational principle, and suggest that the efferent action of a module is to withdraw the receptive field from an external stimulus. Possible functional interpretations of the action of this system during explorative and reaching movements are discussed.

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Year:  1995        PMID: 8983981     DOI: 10.1007/bf00231060

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


  39 in total

1.  Purkinje cell activity during motor learning.

Authors:  P F Gilbert; W T Thach
Journal:  Brain Res       Date:  1977-06-10       Impact factor: 3.252

2.  Spinal branching of corticospinal axons in the cat.

Authors:  Y Shinoda; A P Arnold; H Asanuma
Journal:  Exp Brain Res       Date:  1976-10-28       Impact factor: 1.972

3.  Spinal branching of rubrospinal axons in the cat.

Authors:  Y Shinoda; C Ghez; A Arnold
Journal:  Exp Brain Res       Date:  1977-11-24       Impact factor: 1.972

4.  Cerebellar neuronal activity related to whole-arm reaching movements in the monkey.

Authors:  P A Fortier; J F Kalaska; A M Smith
Journal:  J Neurophysiol       Date:  1989-07       Impact factor: 2.714

5.  Unit activity in the cerebellar nuclei related to arm reaching movements.

Authors:  W A MacKay
Journal:  Brain Res       Date:  1988-03-01       Impact factor: 3.252

6.  Climbing fibre induced depression of both mossy fibre responsiveness and glutamate sensitivity of cerebellar Purkinje cells.

Authors:  M Ito; M Sakurai; P Tongroach
Journal:  J Physiol       Date:  1982-03       Impact factor: 5.182

7.  Inferior olivary neurons in the awake cat: detection of contact and passive body displacement.

Authors:  R Gellman; A R Gibson; J C Houk
Journal:  J Neurophysiol       Date:  1985-07       Impact factor: 2.714

8.  Peripheral afferent inputs to the forelimb area of the monkey motor cortex: input-output relations.

Authors:  I Rosén; H Asanuma
Journal:  Exp Brain Res       Date:  1972       Impact factor: 1.972

9.  Movement and electromyographic disorders associated with cerebellar dysmetria.

Authors:  D Flament; J Hore
Journal:  J Neurophysiol       Date:  1986-06       Impact factor: 2.714

10.  Cerebellar nuclear topography of simple and synergistic movements in the alert baboon (Papio papio).

Authors:  L Rispal-Padel; F Cicirata; C Pons
Journal:  Exp Brain Res       Date:  1982       Impact factor: 1.972

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  31 in total

1.  Common principles of sensory encoding in spinal reflex modules and cerebellar climbing fibres.

Authors:  Martin Garwicz; Anders Levinsson; Jens Schouenborg
Journal:  J Physiol       Date:  2002-05-01       Impact factor: 5.182

2.  Central regulation of cerebellar climbing fibre input during motor learning.

Authors:  Richard Apps; Stephen Lee
Journal:  J Physiol       Date:  2002-05-15       Impact factor: 5.182

3.  Receptive field plasticity profoundly alters the cutaneous parallel fiber synaptic input to cerebellar interneurons in vivo.

Authors:  Henrik Jörntell; Carl-Fredrik Ekerot
Journal:  J Neurosci       Date:  2003-10-22       Impact factor: 6.167

Review 4.  Parallel fiber receptive fields: a key to understanding cerebellar operation and learning.

Authors:  Carl-Fredrik Ekerot; Henrik Jörntell
Journal:  Cerebellum       Date:  2003       Impact factor: 3.847

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.  Neural circuits in movement control.

Authors:  Henrik Jörntell
Journal:  J Physiol       Date:  2013-11-15       Impact factor: 5.182

7.  Cutaneous receptive fields and topography of mossy fibres and climbing fibres projecting to cat cerebellar C3 zone.

Authors:  M Garwicz; H Jorntell; C F Ekerot
Journal:  J Physiol       Date:  1998-10-01       Impact factor: 5.182

8.  Topographical organization of projections to cat motor cortex from nucleus interpositus anterior and forelimb skin.

Authors:  H Jörntell; C F Ekerot
Journal:  J Physiol       Date:  1999-01-15       Impact factor: 5.182

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.  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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