Literature DB >> 843923

The pontine projection to the cerebellar vermal visual area studied by means of the retrograde axonal transport of horseradish peroxidase.

G H Hoddevik, A Brodal, K Kawamura, T Hashikawa.   

Abstract

Following injections of horseradish peroxidase (HRP) in cerbellar vermal lobules VI, VIIA and B, VIIA and B in the cat, the distribution of labeled cells in the pontine nuclei was mapped in drawings of serial transverse and horizontal sections. The labeled pontine cells are distributed in 4 largely longitudinal columns, situated in the dorsolateral, peduncular, lateral and paramedian pontine nucleus (referred to as columns A, B, C and D, respectively). The majority of afferents to the vermal, visual areas come from colums A and B. To some extent cells projecting to the various sublobules have their preferential location within each column (Fig. 5). The majority of the fibers end in lobule VII. Available data from the literature show that only columns A, D and rostral part of B may be involved in the transmission of visual impulses to the vermal area, since these columns receive afferents from the superior colliculus, the lateral geniculate body and the visual cortex, respectively. The route via the superior colliculus-dorsolateral nucleus appears to be quantitatively the most important. As judged from data on fiber connections, impulses from various sources (inferior colliculus, cerebellar nuclei and "non-visual" parts of the cerebral cortex) are transmitted to certain parts of the 4 columns. The functional importance of this convergence and some general features in the organization of the pons are discussed.

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Year:  1977        PMID: 843923     DOI: 10.1016/0006-8993(77)90475-9

Source DB:  PubMed          Journal:  Brain Res        ISSN: 0006-8993            Impact factor:   3.252


  13 in total

1.  Connections of the anterior ectosylvian visual area (AEV).

Authors:  M Norita; L Mucke; G Benedek; B Albowitz; Y Katoh; O D Creutzfeldt
Journal:  Exp Brain Res       Date:  1986       Impact factor: 1.972

2.  Retrograde labeling of ascending and descending neurons in the inferior colliculus. A fluorescent double labelling study in the cat.

Authors:  T Hashikawa; K Kawamura
Journal:  Exp Brain Res       Date:  1983       Impact factor: 1.972

3.  Coding of visual information by units in the cat cerebellar vermis.

Authors:  I M Donaldson; M E Hawthorne
Journal:  Exp Brain Res       Date:  1979-01-02       Impact factor: 1.972

4.  Discharges of Purkinje cells and mossy fibres in the cerebellar vermis of the monkey during saccadic eye movements and fixation.

Authors:  M Kase; D C Miller; H Noda
Journal:  J Physiol       Date:  1980-03       Impact factor: 5.182

5.  Visual cortical projections to the paraflocculus in the rat. An electrophysiologic study.

Authors:  R A Burne; D J Woodward
Journal:  Exp Brain Res       Date:  1983       Impact factor: 1.972

6.  The projection from nucleus reticularis tegmenti pontis onto the cerebellum in the cat. A study using the methods of anterograde degeneration and retrograde axonal transport of horseradish peroxidase.

Authors:  G H Hoddevik
Journal:  Anat Embryol (Berl)       Date:  1978-06-12

7.  The pontocerebellar projection of the uvula in the cat.

Authors:  A Brodal; G H Hoddevik
Journal:  Exp Brain Res       Date:  1978-05-12       Impact factor: 1.972

8.  The pontine projection to the crebellar anterior lobe. An experimental study in the cat with retrograde transport of horseradish peroxidase.

Authors:  P Brodal; F Walberg
Journal:  Exp Brain Res       Date:  1977-08-31       Impact factor: 1.972

9.  Smooth pursuit eye movement deficits after pontine nuclei lesions in humans.

Authors:  B Gaymard; C Pierrot-Deseilligny; S Rivaud; S Velut
Journal:  J Neurol Neurosurg Psychiatry       Date:  1993-07       Impact factor: 10.154

10.  Ocular Fixation Abnormality in Patients with Autism Spectrum Disorder.

Authors:  Aya Shirama; Chieko Kanai; Nobumasa Kato; Makio Kashino
Journal:  J Autism Dev Disord       Date:  2016-05
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