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Visual instrumental learning in blindsight monkeys
Blindsight is the residual visuo-motor ability without subjective awareness observed after lesions of the primary visual cortex (V1). Various visual functions are retained, however, instrumental visual associative learning remains to be investigated. Here we examined the secondary reinforcing proper...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8292513/ https://www.ncbi.nlm.nih.gov/pubmed/34285293 http://dx.doi.org/10.1038/s41598-021-94192-7 |
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author | Kato, Rikako Zeghbib, Abdelhafid Redgrave, Peter Isa, Tadashi |
author_facet | Kato, Rikako Zeghbib, Abdelhafid Redgrave, Peter Isa, Tadashi |
author_sort | Kato, Rikako |
collection | PubMed |
description | Blindsight is the residual visuo-motor ability without subjective awareness observed after lesions of the primary visual cortex (V1). Various visual functions are retained, however, instrumental visual associative learning remains to be investigated. Here we examined the secondary reinforcing properties of visual cues presented to the hemianopic field of macaque monkeys with unilateral V1 lesions. Our aim was to test the potential role of visual pathways bypassing V1 in reinforcing visual instrumental learning. When learning the location of a hidden area in an oculomotor search task, conditioned visual cues presented to the lesion-affected hemifield operated as an effective secondary reinforcer. We noted that not only the hidden area location, but also the vector of the saccade entering the target area was reinforced. Importantly, when the visual reinforcement signal was presented in the lesion-affected field, the monkeys continued searching, as opposed to stopping when the cue was presented in the intact field. This suggests the monkeys were less confident that the target location had been discovered when the reinforcement cue was presented in the affected field. These results indicate that the visual signals mediated by the residual visual pathways after V1 lesions can access fundamental reinforcement mechanisms but with impaired visual awareness. |
format | Online Article Text |
id | pubmed-8292513 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-82925132021-07-22 Visual instrumental learning in blindsight monkeys Kato, Rikako Zeghbib, Abdelhafid Redgrave, Peter Isa, Tadashi Sci Rep Article Blindsight is the residual visuo-motor ability without subjective awareness observed after lesions of the primary visual cortex (V1). Various visual functions are retained, however, instrumental visual associative learning remains to be investigated. Here we examined the secondary reinforcing properties of visual cues presented to the hemianopic field of macaque monkeys with unilateral V1 lesions. Our aim was to test the potential role of visual pathways bypassing V1 in reinforcing visual instrumental learning. When learning the location of a hidden area in an oculomotor search task, conditioned visual cues presented to the lesion-affected hemifield operated as an effective secondary reinforcer. We noted that not only the hidden area location, but also the vector of the saccade entering the target area was reinforced. Importantly, when the visual reinforcement signal was presented in the lesion-affected field, the monkeys continued searching, as opposed to stopping when the cue was presented in the intact field. This suggests the monkeys were less confident that the target location had been discovered when the reinforcement cue was presented in the affected field. These results indicate that the visual signals mediated by the residual visual pathways after V1 lesions can access fundamental reinforcement mechanisms but with impaired visual awareness. Nature Publishing Group UK 2021-07-20 /pmc/articles/PMC8292513/ /pubmed/34285293 http://dx.doi.org/10.1038/s41598-021-94192-7 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Kato, Rikako Zeghbib, Abdelhafid Redgrave, Peter Isa, Tadashi Visual instrumental learning in blindsight monkeys |
title | Visual instrumental learning in blindsight monkeys |
title_full | Visual instrumental learning in blindsight monkeys |
title_fullStr | Visual instrumental learning in blindsight monkeys |
title_full_unstemmed | Visual instrumental learning in blindsight monkeys |
title_short | Visual instrumental learning in blindsight monkeys |
title_sort | visual instrumental learning in blindsight monkeys |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8292513/ https://www.ncbi.nlm.nih.gov/pubmed/34285293 http://dx.doi.org/10.1038/s41598-021-94192-7 |
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