Literature DB >> 6747896

Discharges of Purkinje cells in the paravermal part of the cerebellar anterior lobe during locomotion in the cat.

D M Armstrong, S A Edgley.   

Abstract

Extracellular recordings were made from 124 Purkinje cells in the paravermal part of lobule V of the cerebellum in cats walking steadily at a speed of 0.5 m/s on a moving belt. All cells tested had a tactile receptive field from which simple spikes could be evoked and 96% of these were on the ipsilateral forelimb. Seventy-six of the cells were also studied whilst the animals sat or lay quietly without movement. Complex spikes were discharged at 1-2/s and these were accompanied by simple spikes in fifty-nine cells (78%); in the remaining cells there were no or few simple spikes. The over-all mean discharge rate (including both types of spike) was 37.8 +/- 27 impulses/s (+/- S.D.). During locomotion all cells discharged both types of spike and the over-all mean rate was 57.6 +/- 29 impulses/s (+/- S.D.). In all cells but one, the frequency of the simple spikes was modulated rhythmically in time with the stepping movements but the phasing relative to the step cycle varied widely between cells. Peak rates also varied widely, the average being 91.5 +/- 44 impulses/s (+/- S.D.). Most cells (63%) generated one period of accelerated discharge per step but others generated two (35%) or three (2%) such periods. Despite the individual variations in discharge timing the population as a whole was considerably more active during the swing than the stance phase of the step cycle in the ipsilateral forelimb (68 impulses/s as compared with 49 impulses/s on average). Thirty-four cells were electrophysiologically identified as lying in the c1 zone of the cortex and twenty-five as being in the c2 zone (nomenclature of Oscarsson, 1980). During locomotion, the population activity in the two zones differed slightly: activity in the c1 population was phase advanced by approximately one-tenth of the step cycle. The results are discussed, with particular emphasis on the finding that population activity in the Purkinje cells of the c1 zone fluctuated during the step cycle in parallel with that in the part of nucleus interpositus to which they project.

Entities:  

Mesh:

Year:  1984        PMID: 6747896      PMCID: PMC1193220          DOI: 10.1113/jphysiol.1984.sp015300

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


  23 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.  Temporal sequence of cerebellar Purkinje and nuclear activity in relation to the acoustic startle response.

Authors:  J A Mortimer
Journal:  Brain Res       Date:  1973-02-28       Impact factor: 3.252

Review 3.  The cerebellum as a computer: patterns in space and time.

Authors:  J C Eccles
Journal:  J Physiol       Date:  1973-02       Impact factor: 5.182

4.  Changes of simple and complex spike activity of cerebellar purkinje cells with sleep and waking.

Authors:  N Mano
Journal:  Science       Date:  1970-12-18       Impact factor: 47.728

5.  Spontaneous discharge rates of cat cerebellar Purkinje cells in sleep and waking.

Authors:  J A Hobson; R W McCarley
Journal:  Electroencephalogr Clin Neurophysiol       Date:  1972-11

6.  Activity of vestibulospinal neurons during locomotion.

Authors:  G N Orlovsky
Journal:  Brain Res       Date:  1972-11-13       Impact factor: 3.252

7.  Termination and functional organization of the dorsolateral spino-olivocerebellar path.

Authors:  B Larson; S Miller; O Oscarsson
Journal:  J Physiol       Date:  1969-08       Impact factor: 5.182

8.  A spinocerebellar climbing fibre path activated by the flexor reflex afferents from all four limbs.

Authors:  B Larson; S Miller; O Oscarsson
Journal:  J Physiol       Date:  1969-08       Impact factor: 5.182

9.  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

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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  46 in total

1.  Rhythmic neuronal activity in the lateral cerebellum of the cat during visually guided stepping.

Authors:  D E Marple-Horvat; J M Criado
Journal:  J Physiol       Date:  1999-07-15       Impact factor: 5.182

Review 2.  The great gate: control of sensory information flow to the cerebellum.

Authors:  Anna Devor
Journal:  Cerebellum       Date:  2002 Jan-Mar       Impact factor: 3.847

3.  The organization of cortical activity in the anterior lobe of the cat cerebellum during hindlimb stepping.

Authors:  M S Valle; J Eian; G Bosco; R E Poppele
Journal:  Exp Brain Res       Date:  2011-11-19       Impact factor: 1.972

4.  Gating in the spino-olivocerebellar pathways to the c1 zone of the cerebellar cortex during locomotion in the cat.

Authors:  M Lidierth; R Apps
Journal:  J Physiol       Date:  1990-11       Impact factor: 5.182

5.  Cerebellar cortical activity in the cat anterior lobe during hindlimb stepping.

Authors:  M S Valle; J Eian; G Bosco; R E Poppele
Journal:  Exp Brain Res       Date:  2008-02-22       Impact factor: 1.972

6.  Locomotion-related variations in excitability of spino-olivocerebellar paths to cat cerebellar cortical c2 zone.

Authors:  R Apps; M Lidierth; D M Armstrong
Journal:  J Physiol       Date:  1990-05       Impact factor: 5.182

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.  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

9.  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

10.  The estrous cycle and the olivo-cerebellar circuit. I. Contrast enhancement of sensorimotor-correlated cerebellar discharge.

Authors:  S S Smith; J K Chapin
Journal:  Exp Brain Res       Date:  1996-10       Impact factor: 1.972

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