Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Liu, Lihua, Yuan, Congcong, Ding, Hao, Xu, Yongjie, Long, Miaomiao, Li, YanJun, Liu, Yong, Jiang, Tianzi, Qin, Wen, Shen, Wen, Yu, Chunshui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
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
_version_ 1782518621527867392
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
work_keys_str_mv AT liulihua visualdeprivationselectivelyreshapestheintrinsicfunctionalarchitectureoftheanteriorinsulasubregions
AT yuancongcong visualdeprivationselectivelyreshapestheintrinsicfunctionalarchitectureoftheanteriorinsulasubregions
AT dinghao visualdeprivationselectivelyreshapestheintrinsicfunctionalarchitectureoftheanteriorinsulasubregions
AT xuyongjie visualdeprivationselectivelyreshapestheintrinsicfunctionalarchitectureoftheanteriorinsulasubregions
AT longmiaomiao visualdeprivationselectivelyreshapestheintrinsicfunctionalarchitectureoftheanteriorinsulasubregions
AT liyanjun visualdeprivationselectivelyreshapestheintrinsicfunctionalarchitectureoftheanteriorinsulasubregions
AT liuyong visualdeprivationselectivelyreshapestheintrinsicfunctionalarchitectureoftheanteriorinsulasubregions
AT jiangtianzi visualdeprivationselectivelyreshapestheintrinsicfunctionalarchitectureoftheanteriorinsulasubregions
AT qinwen visualdeprivationselectivelyreshapestheintrinsicfunctionalarchitectureoftheanteriorinsulasubregions
AT shenwen visualdeprivationselectivelyreshapestheintrinsicfunctionalarchitectureoftheanteriorinsulasubregions
AT yuchunshui visualdeprivationselectivelyreshapestheintrinsicfunctionalarchitectureoftheanteriorinsulasubregions