Literature DB >> 85698

Tectopontine pathway in the cat: laminar distribution of cells of origin and visual properties of target cells in dorsolateral pontine nucleus.

G Mower, A Gibson, M Glickstein.   

Abstract

1. The superior colliculus projects to the dorsolateral nucleus of the pons. Retrograde transport of horseradish peroxidase (HRP) revealed that cells in the superior colliculus, which send their axons to the pons, lie in both superficial (III) and deep (IV--VII) layers. Superficial cells outnumbered deep cells. The inferior colliculus also projects heavily to the dorsolateral pontine nucleus. 2. Dorsolateral pontine visual cells were activated only by visual stimulation. Cells responsive to somatic or auditory stimulation were also found in the dorsolateral nucleus, and they too responded to only one sense modality. 3. Of the dorsolateral pontine visual cells, 69% were directionally selective. 4. Dorsolateral pontine visual cells were responsive to moving targets over a wide range of stimulus velocities. Velocities between 25 and 100 degrees/s were the most effective. No cells responded to a stationary stimulus. 5. Single-spot targets were the most effective stimuli. Stimulus size was a more important parameter than stimulus configuration. Many cells had inhibitory regions outside of their excitatory fields. 6. The excitatory receptive fields of dorsolateral pontine cells were very large (median, 1,100 deg2). 7. Nearly all receptive fields were centered in the contralateral visual hemifield, and 91% of the dorsolateral visual cells were activated from either eye. 8. We conclude that the visual cells in the dorsolateral nucleus have receptive-field properties that are similar to those of cells in the superior colliculus. The preference of dorsolateral cells for single-spot targets contrasts strongly with the multiple-spot preference of medial pontine cells, which receive their input from visual cortex.

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Year:  1979        PMID: 85698     DOI: 10.1152/jn.1979.42.1.1

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


  18 in total

1.  Cerebro-cerebellar projections from the ventral bank of the anterior ectosylvian sulcus in the cat.

Authors:  S Kyuhou
Journal:  J Physiol       Date:  1992       Impact factor: 5.182

2.  Information processing in the hemisphere of the cerebellar cortex for control of wrist movement.

Authors:  Saeka Tomatsu; Takahiro Ishikawa; Yoshiaki Tsunoda; Jongho Lee; Donna S Hoffman; Shinji Kakei
Journal:  J Neurophysiol       Date:  2015-10-14       Impact factor: 2.714

3.  Superficial tectal neurons projecting to the dorsolateral pontine nucleus in the rabbit.

Authors:  L S Simó; F Doñate-Oliver
Journal:  Exp Brain Res       Date:  1991       Impact factor: 1.972

4.  Organization of the auditory area in the posterior cerebellar vermis of the cat.

Authors:  C Huang; G Liu
Journal:  Exp Brain Res       Date:  1990       Impact factor: 1.972

5.  The cerebellotectal pathway in the grey squirrel.

Authors:  P J May; W C Hall
Journal:  Exp Brain Res       Date:  1986       Impact factor: 1.972

6.  Projection from the inferior colliculus to the superior olivary complex in the albino rat.

Authors:  H Faye-Lund
Journal:  Anat Embryol (Berl)       Date:  1986

7.  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

8.  The ability to move to a beat is linked to the consistency of neural responses to sound.

Authors:  Adam Tierney; Nina Kraus
Journal:  J Neurosci       Date:  2013-09-18       Impact factor: 6.167

9.  The initial torsional Ocular Following Response (tOFR) in humans: a response to the total motion energy in the stimulus?

Authors:  B M Sheliga; E J Fitzgibbon; F A Miles
Journal:  J Vis       Date:  2009-11-09       Impact factor: 2.240

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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