Literature DB >> 6716117

Integration of retinal and motor signals of eye movements in striate cortex cells of the alert cat.

K Toyama, Y Komatsu, K Shibuki.   

Abstract

Responses of saccade-depressed (SD) and saccade-excited (SE) cells in the striate cortex to eye movements of alert cats under presentation of a visual pattern were studied under reinforcement of the eye movements with rewards of water. These responses were compared to those on passive displacement of the visual pattern reproducing the movements of the retinal image occurring during eye movements while eye movements were suppressed by withdrawal of reinforcement. Passive displacement of the visual pattern produced in the SD cells depression closely resembled the depression occurring during eye movements under presentation of the visual pattern, in time course as well as in amplitude. Both the saccade depression and the depression due to passive movement of the visual pattern were nonselective to the direction of eye movements. Saccade excitation of the SE cells frequently contained two components occurring at 20 and 80 ms after the onsets of eye movements. Passive displacement of the visual pattern produced in the SE cells excitation comparable with the early component of the saccade excitation. These findings suggest that saccade depression in the SD cells and the early component of the saccade excitation in the SE cells are related to retinal reafference of eye movement. During presentation of visual patterns, saccade excitation in the SE cells was closely related to parameters of eye movements, such as direction, amplitude, duration, and velocity. The correlations were completely lost or strongly reduced in darkness. Lines of evidence were provided that the saccade excitation of the SE cells in darkness or the later component of the saccade excitation under presentation of a visual pattern represents efference copy signals of eye movement transferred to the striate cortex through the Clare-Bishop (CB) cortex. Excitation comparable with saccade excitation in darkness occurred in synchrony with activities of the oculomotor nuclei even after retrobulbar paralysis of eye movement, indicating that the excitation is related to efference copy signals rather than proprioceptive reafference of eye movement.(ABSTRACT TRUNCATED AT 400 WORDS)

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Year:  1984        PMID: 6716117     DOI: 10.1152/jn.1984.51.4.649

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


  11 in total

1.  Modeling LGN responses during free-viewing: a possible role of microscopic eye movements in the refinement of cortical orientation selectivity.

Authors:  M Rucci; G M Edelman; J Wray
Journal:  J Neurosci       Date:  2000-06-15       Impact factor: 6.167

2.  Eye position-dependent activity in the primary visual area as revealed by fMRI.

Authors:  Frédéric Andersson; Marc Joliot; Guy Perchey; Laurent Petit
Journal:  Hum Brain Mapp       Date:  2007-07       Impact factor: 5.038

3.  The temporal impulse response function in infantile nystagmus.

Authors:  Harold E Bedell; Mahalakshmi Ramamurthy; Saumil S Patel; Shobana Subramaniam; Lan-Phuong Vu-Yu; Jianliang Tong
Journal:  Vision Res       Date:  2008-06-11       Impact factor: 1.886

4.  Response properties of relay cells in the A-laminae of the cat's dorsal lateral geniculate nucleus after saccades.

Authors:  W H Fischer; M Schmidt; V Stuphorn; K P Hoffmann
Journal:  Exp Brain Res       Date:  1996-08       Impact factor: 1.972

5.  Distinct fMRI Responses to Self-Induced versus Stimulus Motion during Free Viewing in the Macaque.

Authors:  Brian E Russ; Takaaki Kaneko; Kadharbatcha S Saleem; Rebecca A Berman; David A Leopold
Journal:  J Neurosci       Date:  2016-09-14       Impact factor: 6.167

6.  Motion sensitive cells in the macaque superior temporal polysensory area. I. Lack of response to the sight of the animal's own limb movement.

Authors:  J K Hietanen; D I Perrett
Journal:  Exp Brain Res       Date:  1993       Impact factor: 1.972

7.  Neuronal responsiveness in areas 19 and 21a, and the posteromedial lateral suprasylvian cortex of the cat.

Authors:  K Toyama; K Mizobe; E Akase; T Kaihara
Journal:  Exp Brain Res       Date:  1994       Impact factor: 1.972

8.  Single cell activity in area 18 of the cat's visual cortex during optokinetic nystagmus.

Authors:  K P Hoffmann; R Bauer; H P Huber; M Mayr
Journal:  Exp Brain Res       Date:  1984       Impact factor: 1.972

Review 9.  A physiological perspective on fixational eye movements.

Authors:  D Max Snodderly
Journal:  Vision Res       Date:  2014-12-20       Impact factor: 1.886

10.  Early visual evoked potentials are modulated by eye position in humans induced by whole body rotations.

Authors:  Frédéric Andersson; Olivier Etard; Pierre Denise; Laurent Petit
Journal:  BMC Neurosci       Date:  2004-09-19       Impact factor: 3.288

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