Literature DB >> 6325507

Cerebellar targets of visual pontine cells in the cat.

F R Robinson, J L Cohen, J May, A K Sestokas, M Glickstein.   

Abstract

The cerebellum receives visual mossy fiber input from the cerebral cortex via visual cells in the pons. We identified the regions of cat cerebellum that receive cerebral visual input by injecting orthograde tracers among physiologically identified visual pontine cells. Cerebellar labeling following these injections indicates that the contralateral paraflocculus and the rostral folium of the uvula (vermal lobule IX) receive the heaviest projection from cortically activated pontine visual cells. Lighter visual input reaches much of the rest of the contralateral posterior lobe. A second experiment combined, in the same animal, orthograde tracing of the visual corticopontine pathway with retrograde tracing of the pontocerebellar projection. The results of this experiment confirm that the paraflocculus and uvula receive more cortical visual input than do other regions of the cerebellum. This experiment also shows that uvula-projecting and paraflocculus-projecting cells occupy different parts of the ventromedial pons. Uvula-projecting cells cluster immediately adjacent to the ventral and medial borders of the pyramidal tract and near the midline. Paraflocculus-projecting cells lie ventral and medial to the pyramidal tract but displaced from its border. There are few paraflocculus-projecting cells near the midline.

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Year:  1984        PMID: 6325507     DOI: 10.1002/cne.902230402

Source DB:  PubMed          Journal:  J Comp Neurol        ISSN: 0021-9967            Impact factor:   3.215


  13 in total

1.  Eye movements coordinated with steering benefit performance even when vision is denied.

Authors:  M Wilson; S Stephenson; M Chattington; D E Marple-Horvat
Journal:  Exp Brain Res       Date:  2006-08-05       Impact factor: 1.972

2.  Purkinje cells in the lateral cerebellum of the cat encode visual events and target motion during visually guided reaching.

Authors:  Omür Budanur Miles; Nadia L Cerminara; Dilwyn E Marple-Horvat
Journal:  J Physiol       Date:  2006-01-19       Impact factor: 5.182

Review 3.  Paradoxical inter-hemispheric transfer after section of the cerebral commissures.

Authors:  Mitchell Glickstein
Journal:  Exp Brain Res       Date:  2008-08-23       Impact factor: 1.972

4.  Neuronal activity in the lateral cerebellum of the cat related to visual stimuli at rest, visually guided step modification, and saccadic eye movements.

Authors:  D E Marple-Horvat; J M Criado; D M Armstrong
Journal:  J Physiol       Date:  1998-01-15       Impact factor: 5.182

5.  Cerebro-cerebellar projections from the lateral suprasylvian visual area in the cat.

Authors:  N Kato; S Kawaguchi; H Miyata
Journal:  J Physiol       Date:  1988-01       Impact factor: 5.182

6.  Classical conditioning of the nictitating membrane response of the rabbit. III. Connections of cerebellar lobule HVI.

Authors:  C H Yeo; M J Hardiman; M Glickstein
Journal:  Exp Brain Res       Date:  1985       Impact factor: 1.972

7.  Principal component analysis of cerebellar shape on MRI separates SCA types 2 and 6 into two archetypal modes of degeneration.

Authors:  Brian C Jung; Soo I Choi; Annie X Du; Jennifer L Cuzzocreo; Zhuo Z Geng; Howard S Ying; Susan L Perlman; Arthur W Toga; Jerry L Prince; Sarah H Ying
Journal:  Cerebellum       Date:  2012-12       Impact factor: 3.847

8.  Classical conditioning of the nictitating membrane response of the rabbit. II. Lesions of the cerebellar cortex.

Authors:  C H Yeo; M J Hardiman; M Glickstein
Journal:  Exp Brain Res       Date:  1985       Impact factor: 1.972

9.  Different patterns of corticopontine projections from separate cortical fields within the inferior parietal lobule and dorsal prelunate gyrus of the macaque.

Authors:  J G May; R A Andersen
Journal:  Exp Brain Res       Date:  1986       Impact factor: 1.972

10.  Classical conditioning of the nictitating membrane response of the rabbit. IV. Lesions of the inferior olive.

Authors:  C H Yeo; M J Hardiman; M Glickstein
Journal:  Exp Brain Res       Date:  1986       Impact factor: 1.972

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