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Visual deprivation selectively reshapes the intrinsic functional architecture of the anterior insula subregions
The anterior insula (AI) is the core hub of salience network that serves to identify the most relevant stimuli among vast sensory inputs and forward them to higher cognitive regions to guide behaviour. As blind subjects were usually reported with changed perceptive abilities for salient non-visual s...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5372462/ https://www.ncbi.nlm.nih.gov/pubmed/28358391 http://dx.doi.org/10.1038/srep45675 |
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author | Liu, Lihua Yuan, Congcong Ding, Hao Xu, Yongjie Long, Miaomiao Li, YanJun Liu, Yong Jiang, Tianzi Qin, Wen Shen, Wen Yu, Chunshui |
author_facet | Liu, Lihua Yuan, Congcong Ding, Hao Xu, Yongjie Long, Miaomiao Li, YanJun Liu, Yong Jiang, Tianzi Qin, Wen Shen, Wen Yu, Chunshui |
author_sort | Liu, Lihua |
collection | PubMed |
description | The anterior insula (AI) is the core hub of salience network that serves to identify the most relevant stimuli among vast sensory inputs and forward them to higher cognitive regions to guide behaviour. As blind subjects were usually reported with changed perceptive abilities for salient non-visual stimuli, we hypothesized that the resting-state functional network of the AI is selectively reorganized after visual deprivation. The resting-state functional connectivity (FC) of the bilateral dorsal and ventral AI was calculated for twenty congenitally blind (CB), 27 early blind (EB), 44 late blind (LB) individuals and 50 sighted controls (SCs). The FCs of the dorsal AI were strengthened with the dorsal visual stream, while weakened with the ventral visual stream in the blind than the SCs; in contrast, the FCs of the ventral AI of the blind was strengthened with the ventral visual stream. Furthermore, these strengthened FCs of both the dorsal and ventral AI were partially negatively associated with the onset age of blindness. Our result indicates two parallel pathways that selectively transfer non-visual salient information between the deprived “visual” cortex and salience network in blind subjects. |
format | Online Article Text |
id | pubmed-5372462 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-53724622017-03-31 Visual deprivation selectively reshapes the intrinsic functional architecture of the anterior insula subregions Liu, Lihua Yuan, Congcong Ding, Hao Xu, Yongjie Long, Miaomiao Li, YanJun Liu, Yong Jiang, Tianzi Qin, Wen Shen, Wen Yu, Chunshui Sci Rep Article The anterior insula (AI) is the core hub of salience network that serves to identify the most relevant stimuli among vast sensory inputs and forward them to higher cognitive regions to guide behaviour. As blind subjects were usually reported with changed perceptive abilities for salient non-visual stimuli, we hypothesized that the resting-state functional network of the AI is selectively reorganized after visual deprivation. The resting-state functional connectivity (FC) of the bilateral dorsal and ventral AI was calculated for twenty congenitally blind (CB), 27 early blind (EB), 44 late blind (LB) individuals and 50 sighted controls (SCs). The FCs of the dorsal AI were strengthened with the dorsal visual stream, while weakened with the ventral visual stream in the blind than the SCs; in contrast, the FCs of the ventral AI of the blind was strengthened with the ventral visual stream. Furthermore, these strengthened FCs of both the dorsal and ventral AI were partially negatively associated with the onset age of blindness. Our result indicates two parallel pathways that selectively transfer non-visual salient information between the deprived “visual” cortex and salience network in blind subjects. Nature Publishing Group 2017-03-30 /pmc/articles/PMC5372462/ /pubmed/28358391 http://dx.doi.org/10.1038/srep45675 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Liu, Lihua Yuan, Congcong Ding, Hao Xu, Yongjie Long, Miaomiao Li, YanJun Liu, Yong Jiang, Tianzi Qin, Wen Shen, Wen Yu, Chunshui Visual deprivation selectively reshapes the intrinsic functional architecture of the anterior insula subregions |
title | Visual deprivation selectively reshapes the intrinsic functional architecture of the anterior insula subregions |
title_full | Visual deprivation selectively reshapes the intrinsic functional architecture of the anterior insula subregions |
title_fullStr | Visual deprivation selectively reshapes the intrinsic functional architecture of the anterior insula subregions |
title_full_unstemmed | Visual deprivation selectively reshapes the intrinsic functional architecture of the anterior insula subregions |
title_short | Visual deprivation selectively reshapes the intrinsic functional architecture of the anterior insula subregions |
title_sort | visual deprivation selectively reshapes the intrinsic functional architecture of the anterior insula subregions |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5372462/ https://www.ncbi.nlm.nih.gov/pubmed/28358391 http://dx.doi.org/10.1038/srep45675 |
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