Literature DB >> 7714572

Neurons in monkey parietal area LIP are tuned for eye-movement parameters in three-dimensional space.

J W Gnadt1, L E Mays.   

Abstract

1. A functional class of neurons in area LIP on the lateral bank of the intraparietal sulcus were shown previously (Gnadt and Andersen 1988) to be related to the metrics of saccadic eye movements. In this study, we tested LIP neurons at different depths with respect to the plane of fixation. 2. Sixty-one neurons were identified for their increased activity before saccadic eye movements. While holding the location of the target constant at the center of the frontoparallel (saccadic) response field, the neurons were tested systematically during eye movements to target positions proximal (near) to the plane of fixation, at the plane of fixation, and distal (far) to the plane of fixation. By necessity, the movements of these targets required a combination of saccadic and vergence movements. 3. Seventy-two percent of the neurons were found to change their activity as a function of target depth relative to the plane of fixation. The neurons had broad tuning curves for depth. Some cells preferred "near" target positions, some preferred "far" positions, and others responded best in the frontoparallel plane of fixation. 4. The location of a neuron's response field in the frontoparallel plane remained constant regardless of target depth. However, the magnitude of the neuron's response increased when the target was positioned at the preferred depth and it decreased for targets positioned at nonpreferred depths. This indicated that the neurons always were related to the same frontoparallel coordinates, but responded more vigorously when the target was positioned at its preferred depth. 5. The visual display apparatus allowed independent presentation of two stimulus cues for depth: binocular disparity and accommodative demand whereas other cues were held constant. For many neurons, either cue was sufficient to tune the activity in depth, though most neurons responded best for the geometrically appropriate combination of the two cues. 6. Comparison of the binocular tuning for depth with the individual monocular responses showed that the tuning for depth was not produced by simple linear combination of two monocular response fields. 7. We tested a subset of the neurons in a double-movement task that dissociated the retinal coordinates of the visual stimuli from the eye-movement coordinates of the second movement. These tests confirmed earlier findings that this functional class of neurons are active when the eye-movement coordinates matched the neurons' response field. It was not necessary for a visual stimulus to fall within the neurons' response field for them to become active.(ABSTRACT TRUNCATED AT 400 WORDS)

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Year:  1995        PMID: 7714572     DOI: 10.1152/jn.1995.73.1.280

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


  37 in total

1.  EEG activity related to preparation and suppression of eye movements in three-dimensional space.

Authors:  Areti Tzelepi; Antoine Lutz; Zoi Kapoula
Journal:  Exp Brain Res       Date:  2004-01-17       Impact factor: 1.972

2.  Motion parallax is computed in the updating of human spatial memory.

Authors:  W Pieter Medendorp; Douglas B Tweed; J Douglas Crawford
Journal:  J Neurosci       Date:  2003-09-03       Impact factor: 6.167

3.  Parallel updating and weighting of multiple spatial maps for visual stability during whole body motion.

Authors:  J J Tramper; W P Medendorp
Journal:  J Neurophysiol       Date:  2015-10-21       Impact factor: 2.714

4.  Anterior regions of monkey parietal cortex process visual 3D shape.

Authors:  Jean-Baptiste Durand; Koen Nelissen; Olivier Joly; Claire Wardak; James T Todd; J Farley Norman; Peter Janssen; Wim Vanduffel; Guy A Orban
Journal:  Neuron       Date:  2007-08-02       Impact factor: 17.173

5.  Parietal reach region encodes reach depth using retinal disparity and vergence angle signals.

Authors:  Rajan Bhattacharyya; Sam Musallam; Richard A Andersen
Journal:  J Neurophysiol       Date:  2009-05-13       Impact factor: 2.714

6.  Effects of diazepam on the latency of saccades for luminance and binocular disparity defined stimuli.

Authors:  Cunguo Wang; Jianliang Tong; Fuchuan Sun
Journal:  Exp Brain Res       Date:  2005-04-08       Impact factor: 1.972

7.  A distinct representation of three-dimensional shape in macaque anterior intraparietal area: fast, metric, and coarse.

Authors:  Siddharth Srivastava; Guy A Orban; Patrick A De Mazière; Peter Janssen
Journal:  J Neurosci       Date:  2009-08-26       Impact factor: 6.167

8.  Visual form discrimination from texture cues: a PET study.

Authors:  B Gulyás; A Cowey; C A Heywood; D Popplewell; P E Roland
Journal:  Hum Brain Mapp       Date:  1998       Impact factor: 5.038

9.  Task-modulated coactivation of vergence neural substrates.

Authors:  Rajbir Jaswal; Suril Gohel; Bharat B Biswal; Tara L Alvarez
Journal:  Brain Connect       Date:  2014-06-19

10.  Fine discrimination training alters the causal contribution of macaque area MT to depth perception.

Authors:  Syed A Chowdhury; Gregory C DeAngelis
Journal:  Neuron       Date:  2008-10-23       Impact factor: 17.173

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