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Saccade-induced image motion cannot account for post-saccadic enhancement of visual processing in primate MST

Primates use saccadic eye movements to make gaze changes. In many visual areas, including the dorsal medial superior temporal area (MSTd) of macaques, neural responses to visual stimuli are reduced during saccades but enhanced afterwards. How does this enhancement arise—from an internal mechanism as...

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Autores principales: Cloherty, Shaun L., Crowder, Nathan A., Mustari, Michael J., Ibbotson, Michael R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4555012/
https://www.ncbi.nlm.nih.gov/pubmed/26388747
http://dx.doi.org/10.3389/fnsys.2015.00122
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author Cloherty, Shaun L.
Crowder, Nathan A.
Mustari, Michael J.
Ibbotson, Michael R.
author_facet Cloherty, Shaun L.
Crowder, Nathan A.
Mustari, Michael J.
Ibbotson, Michael R.
author_sort Cloherty, Shaun L.
collection PubMed
description Primates use saccadic eye movements to make gaze changes. In many visual areas, including the dorsal medial superior temporal area (MSTd) of macaques, neural responses to visual stimuli are reduced during saccades but enhanced afterwards. How does this enhancement arise—from an internal mechanism associated with saccade generation or through visual mechanisms activated by the saccade sweeping the image of the visual scene across the retina? Spontaneous activity in MSTd is elevated even after saccades made in darkness, suggesting a central mechanism for post-saccadic enhancement. However, based on the timing of this effect, it may arise from a different mechanism than occurs in normal vision. Like neural responses in MSTd, initial ocular following eye speed is enhanced after saccades, with evidence suggesting both internal and visually mediated mechanisms. Here we recorded from visual neurons in MSTd and measured responses to motion stimuli presented soon after saccades and soon after simulated saccades—saccade-like displacements of the background image during fixation. We found that neural responses in MSTd were enhanced when preceded by real saccades but not when preceded by simulated saccades. Furthermore, we also observed enhancement following real saccades made across a blank screen that generated no motion signal within the recorded neurons' receptive fields. We conclude that in MSTd the mechanism leading to post-saccadic enhancement has internal origins.
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spelling pubmed-45550122015-09-18 Saccade-induced image motion cannot account for post-saccadic enhancement of visual processing in primate MST Cloherty, Shaun L. Crowder, Nathan A. Mustari, Michael J. Ibbotson, Michael R. Front Syst Neurosci Neuroscience Primates use saccadic eye movements to make gaze changes. In many visual areas, including the dorsal medial superior temporal area (MSTd) of macaques, neural responses to visual stimuli are reduced during saccades but enhanced afterwards. How does this enhancement arise—from an internal mechanism associated with saccade generation or through visual mechanisms activated by the saccade sweeping the image of the visual scene across the retina? Spontaneous activity in MSTd is elevated even after saccades made in darkness, suggesting a central mechanism for post-saccadic enhancement. However, based on the timing of this effect, it may arise from a different mechanism than occurs in normal vision. Like neural responses in MSTd, initial ocular following eye speed is enhanced after saccades, with evidence suggesting both internal and visually mediated mechanisms. Here we recorded from visual neurons in MSTd and measured responses to motion stimuli presented soon after saccades and soon after simulated saccades—saccade-like displacements of the background image during fixation. We found that neural responses in MSTd were enhanced when preceded by real saccades but not when preceded by simulated saccades. Furthermore, we also observed enhancement following real saccades made across a blank screen that generated no motion signal within the recorded neurons' receptive fields. We conclude that in MSTd the mechanism leading to post-saccadic enhancement has internal origins. Frontiers Media S.A. 2015-09-01 /pmc/articles/PMC4555012/ /pubmed/26388747 http://dx.doi.org/10.3389/fnsys.2015.00122 Text en Copyright © 2015 Cloherty, Crowder, Mustari and Ibbotson. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Cloherty, Shaun L.
Crowder, Nathan A.
Mustari, Michael J.
Ibbotson, Michael R.
Saccade-induced image motion cannot account for post-saccadic enhancement of visual processing in primate MST
title Saccade-induced image motion cannot account for post-saccadic enhancement of visual processing in primate MST
title_full Saccade-induced image motion cannot account for post-saccadic enhancement of visual processing in primate MST
title_fullStr Saccade-induced image motion cannot account for post-saccadic enhancement of visual processing in primate MST
title_full_unstemmed Saccade-induced image motion cannot account for post-saccadic enhancement of visual processing in primate MST
title_short Saccade-induced image motion cannot account for post-saccadic enhancement of visual processing in primate MST
title_sort saccade-induced image motion cannot account for post-saccadic enhancement of visual processing in primate mst
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4555012/
https://www.ncbi.nlm.nih.gov/pubmed/26388747
http://dx.doi.org/10.3389/fnsys.2015.00122
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