Literature DB >> 8433135

Movement-related inputs to intermediate cerebellum of the monkey.

P L van Kan1, A R Gibson, J C Houk.   

Abstract

1. The primary goal of this study was to characterize the information about single-joint forelimb movements supplied to intermediate cerebellar cortex by mossy fibers. Discharge of mossy fibers and Golgi cells was studied while monkeys operated six devices that required movements about specific joints. Additional control experiments in anesthetized cats and monkeys established criteria for identification of mossy fibers and Golgi cells. 2. The control experiments demonstrate that mossy fibers can be distinguished from Purkinje and Golgi cells by the waveshapes of their action potentials. Asynaptic activation from the inferior cerebellar peduncle, in combination with histological localization of recording sites in granular layer or subcortical white matter, verified that mossy fibers produce a variety of waveshapes that are characterized by brief initial phases and relatively small amplitudes. The same waveshapes were observed for the mossy fiber recordings from awake monkeys, and many identified mossy fibers had sensory properties similar to those found in the awake animals. From these combined criteria, we conclude that the recordings in the awake animals were from mossy fibers. Golgi cells, recorded exclusively in the granular layer of cerebellar cortex, were characterized by action potentials of longer duration and larger amplitude as compared with mossy fibers, and none were asynaptically activated from the inferior cerebellar peduncle. 3. Units were isolated while the monkeys made free-form and tracking movements. We studied movement-related discharge of 80 mossy fibers and 12 Golgi cells. Mossy fibers showed high modulations during use of at least one of the six manipulanda and had clear preferences for movement about a specific joint, although they often showed consistent but weaker firing during movement about a neighboring joint. Separation of movements by more than one joint produced a large reduction in discharge: shoulder units never fired well to movements of the finger, and finger units never fired well to movement of the shoulder. 4. The tracking task required maintenance of fixed limb positions (a static phase) as well as movements between these positions (a dynamic phase). Of 80 mossy fibers, 18% had purely tonic discharge patterns, 63% were phasic-tonic, and 20% were purely phasic. Discharge patterns were reciprocal (45%), bidirectional (42%), or unidirectional (13%). 5. Eighty percent of the mossy fibers exhibited tonic discharge that was significantly (P < 0.01) correlated with joint angle (r = 0.65 +/- 0.19, mean +/- SD), and about one third had phasic components that were significantly correlated with movement velocity.(ABSTRACT TRUNCATED AT 400 WORDS)

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Year:  1993        PMID: 8433135     DOI: 10.1152/jn.1993.69.1.74

Source DB:  PubMed          Journal:  J Neurophysiol        ISSN: 0022-3077            Impact factor:   2.714


  90 in total

1.  Cerebellar Purkinje cell simple spike discharge encodes movement velocity in primates during visuomotor arm tracking.

Authors:  J D Coltz; M T Johnson; T J Ebner
Journal:  J Neurosci       Date:  1999-03-01       Impact factor: 6.167

2.  GABA spillover from single inhibitory axons suppresses low-frequency excitatory transmission at the cerebellar glomerulus.

Authors:  S J Mitchell; R A Silver
Journal:  J Neurosci       Date:  2000-12-01       Impact factor: 6.167

3.  Long-term potentiation of intrinsic excitability at the mossy fiber-granule cell synapse of rat cerebellum.

Authors:  S Armano; P Rossi; V Taglietti; E D'Angelo
Journal:  J Neurosci       Date:  2000-07-15       Impact factor: 6.167

Review 4.  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

5.  Ultrastructural contributions to desensitization at cerebellar mossy fiber to granule cell synapses.

Authors:  Matthew A Xu-Friedman; Wade G Regehr
Journal:  J Neurosci       Date:  2003-03-15       Impact factor: 6.167

6.  The contribution of NMDA and AMPA conductances to the control of spiking in neurons of the deep cerebellar nuclei.

Authors:  Volker Gauck; Dieter Jaeger
Journal:  J Neurosci       Date:  2003-09-03       Impact factor: 6.167

7.  Abnormal Purkinje cell activity in vivo in experimental allergic encephalomyelitis.

Authors:  Carl Y Saab; Matthew J Craner; Yuko Kataoka; Stephen G Waxman
Journal:  Exp Brain Res       Date:  2004-04-29       Impact factor: 1.972

8.  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

9.  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

Review 10.  Discovery and rediscoveries of Golgi cells.

Authors:  Elisa Galliano; Paolo Mazzarello; Egidio D'Angelo
Journal:  J Physiol       Date:  2010-10-01       Impact factor: 5.182

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