Literature DB >> 6875930

Origin and sagittal termination areas of cerebro-cerebellar climbing fibre paths in the cat.

G Andersson, J Nyquist.   

Abstract

Climbing fibre responses were recorded in the cerebellar anterior lobe on stimulation of the cerebral cortex. A zonal pattern was demonstrated in the cortical projection, which was related to the cerebellar sagittal zones, as identified from peripheral climbing fibre input. In all zones, except c2, a co-variation of the responses evoked on peripheral nerve stimulation and on stimulation of the corresponding part of the sensorimotor cortex was found. There was a bilateral projection to the a, b, c2 and d1 zones which also, to a varying extent, receive a bilateral peripheral input. The x, c1 and c3 zones, receiving an ipsilateral peripheral input, were activated exclusively from the contralateral cortex. Stimulation of the posterior sigmoid gyrus (p.s.g.) evoked responses in all the zones. These responses had, in all zones except d1, lower thresholds and shorter latencies than the responses from other cortical areas. Two separate p.s.g. areas were shown to project to the pars intermedia zones (c1, c2, c3 and d1), the lateral area to the caudal parts and the medial area to the rostral parts of the zones. In contrast, the b zone received a projection from only one p.s.g. area, centred between, but overlapping, the two areas projecting to the pars intermedia zones. Stimulation of the anterior sigmoid gyrus evoked short-latency responses in the d1 zone and long-latency responses in all other zones. Stimulation of the first and second somatosensory areas (SI and SII) was generally less effective in evoking climbing fibre responses than was stimulation of the p.s.g. The only exception was the c2 zone, in which responses were evoked from the SII with nearly as low thresholds and short latencies as on p.s.g. stimulation. From the parietal cortex, long-latency responses were regularly evoked in the d1 zone and less frequently in the a, b and c2 zones.

Entities:  

Mesh:

Year:  1983        PMID: 6875930      PMCID: PMC1199106          DOI: 10.1113/jphysiol.1983.sp014623

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


  78 in total

1.  Responses to a spino-olivo-cerebellar pathway in the cat.

Authors:  D M Armstrong; R J Harvey
Journal:  J Physiol       Date:  1968-01       Impact factor: 5.182

2.  Analysis of electrical potentials evoked in the cerebellar anterior lobe by stimulation of hindlimb and forelimb nerves.

Authors:  J C Eccles; L Provini; P Strata; H Táboríková
Journal:  Exp Brain Res       Date:  1968       Impact factor: 1.972

3.  Mossy and climbing fibre organization on the anterior lobe of the cerebellum activated by forelimb and hindlimb areas of the sensorimotor cortex.

Authors:  L Provini; S Redman; P Strata
Journal:  Exp Brain Res       Date:  1968       Impact factor: 1.972

4.  Projection and convergence patterns in climbing fibre paths to cerebellar anterior lobe activated from cerebral cortex and spinal cord.

Authors:  S Miller; N Nezlina; O Oscarsson
Journal:  Brain Res       Date:  1969-06       Impact factor: 3.252

5.  Projection to cerebral cortex of group I muscle afferents from the cat's hind limb.

Authors:  S Landgren; H Silfvenius
Journal:  J Physiol       Date:  1969-02       Impact factor: 5.182

6.  Inferior olive of the cat: intracellular recording.

Authors:  W E Crill; T T Kennedy
Journal:  Science       Date:  1967-08-11       Impact factor: 47.728

7.  Short-latency projections to the cat's cerebral cortex from skin and muscle afferents in the contralateral forelimb.

Authors:  O Oscarsson; I Rosén
Journal:  J Physiol       Date:  1966-01       Impact factor: 5.182

8.  Corticofugal influences on transmission to the dorsal spinocerebellar tract from hindlimb primary afferents.

Authors:  T Hongo; Y Okada; M Sato
Journal:  Exp Brain Res       Date:  1967       Impact factor: 1.972

9.  Effects from the sensorimotor cortex on the spinal cord in cats with transected pyramids.

Authors:  T Hongo; E Jankowska
Journal:  Exp Brain Res       Date:  1967       Impact factor: 1.972

10.  Cortically evoked pre- and postsynaptic inhibition of impulse transmission to the dorsal spinocerebellar tract.

Authors:  T Hongo; Y Okada
Journal:  Exp Brain Res       Date:  1967       Impact factor: 1.972

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  7 in total

1.  Changes in excitability of ascending and descending inputs to cerebellar climbing fibers during locomotion.

Authors:  Joanne Pardoe; Stephen A Edgley; Trevor Drew; Richard Apps
Journal:  J Neurosci       Date:  2004-03-17       Impact factor: 6.167

2.  A novel site of synaptic relay for climbing fibre pathways relaying signals from the motor cortex to the cerebellar cortical C1 zone.

Authors:  Rochelle Ackerley; Joanne Pardoe; Richard Apps
Journal:  J Physiol       Date:  2006-08-03       Impact factor: 5.182

3.  Stimulation of cat cutaneous nociceptive C fibres causing tonic and synchronous activity in climbing fibres.

Authors:  C F Ekerot; O Oscarsson; J Schouenborg
Journal:  J Physiol       Date:  1987-05       Impact factor: 5.182

4.  Activation of cerebellar climbing fibres to rat cerebellar posterior lobe from motor cortical output pathways.

Authors:  M R Baker; M Javid; S A Edgley
Journal:  J Physiol       Date:  2001-11-01       Impact factor: 5.182

5.  Distinct and overlapping functional zones in the cerebellum defined by resting state functional connectivity.

Authors:  Jill X O'Reilly; Christian F Beckmann; Valentina Tomassini; Narender Ramnani; Heidi Johansen-Berg
Journal:  Cereb Cortex       Date:  2009-08-14       Impact factor: 5.357

Review 6.  What we do not know about cerebellar systems neuroscience.

Authors:  Jan Voogd
Journal:  Front Syst Neurosci       Date:  2014-12-18

7.  Electrophysiological mapping of novel prefrontal - cerebellar pathways.

Authors:  Thomas C Watson; Matthew W Jones; Richard Apps
Journal:  Front Integr Neurosci       Date:  2009-08-11
  7 in total

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