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Resting-state connectivity in the default mode network and insula during experimental low back pain
Functional magnetic resonance imaging studies have shown that the insular cortex has a significant role in pain identification and information integration, while the default mode network is associated with cognitive and memory-related aspects of pain perception. However, changes in the functional co...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4146160/ https://www.ncbi.nlm.nih.gov/pubmed/25206794 http://dx.doi.org/10.4103/1673-5374.125341 |
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author | Zhang, Shanshan Wu, Wen Huang, Guozhi Liu, Ziping Guo, Shigui Yang, Jianming Wang, Kangling |
author_facet | Zhang, Shanshan Wu, Wen Huang, Guozhi Liu, Ziping Guo, Shigui Yang, Jianming Wang, Kangling |
author_sort | Zhang, Shanshan |
collection | PubMed |
description | Functional magnetic resonance imaging studies have shown that the insular cortex has a significant role in pain identification and information integration, while the default mode network is associated with cognitive and memory-related aspects of pain perception. However, changes in the functional connectivity between the default mode network and insula during pain remain unclear. This study used 3.0 T functional magnetic resonance imaging scans in 12 healthy subjects aged 24.8 ± 3.3 years to compare the differences in the functional activity and connectivity of the insula and default mode network between the baseline and pain condition induced by intramuscular injection of hypertonic saline. Compared with the baseline, the insula was more functionally connected with the medial prefrontal and lateral temporal cortices, whereas there was lower connectivity with the posterior cingulate cortex, precuneus and inferior parietal lobule in the pain condition. In addition, compared with baseline, the anterior cingulate cortex exhibited greater connectivity with the posterior insula, but lower connectivity with the anterior insula, during the pain condition. These data indicate that experimental low back pain led to dysfunction in the connectivity between the insula and default mode network resulting from an impairment of the regions of the brain related to cognition and emotion, suggesting the importance of the interaction between these regions in pain processing. |
format | Online Article Text |
id | pubmed-4146160 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-41461602014-09-09 Resting-state connectivity in the default mode network and insula during experimental low back pain Zhang, Shanshan Wu, Wen Huang, Guozhi Liu, Ziping Guo, Shigui Yang, Jianming Wang, Kangling Neural Regen Res Research and Report Functional magnetic resonance imaging studies have shown that the insular cortex has a significant role in pain identification and information integration, while the default mode network is associated with cognitive and memory-related aspects of pain perception. However, changes in the functional connectivity between the default mode network and insula during pain remain unclear. This study used 3.0 T functional magnetic resonance imaging scans in 12 healthy subjects aged 24.8 ± 3.3 years to compare the differences in the functional activity and connectivity of the insula and default mode network between the baseline and pain condition induced by intramuscular injection of hypertonic saline. Compared with the baseline, the insula was more functionally connected with the medial prefrontal and lateral temporal cortices, whereas there was lower connectivity with the posterior cingulate cortex, precuneus and inferior parietal lobule in the pain condition. In addition, compared with baseline, the anterior cingulate cortex exhibited greater connectivity with the posterior insula, but lower connectivity with the anterior insula, during the pain condition. These data indicate that experimental low back pain led to dysfunction in the connectivity between the insula and default mode network resulting from an impairment of the regions of the brain related to cognition and emotion, suggesting the importance of the interaction between these regions in pain processing. Medknow Publications & Media Pvt Ltd 2014-01-15 /pmc/articles/PMC4146160/ /pubmed/25206794 http://dx.doi.org/10.4103/1673-5374.125341 Text en Copyright: © Neural Regeneration Research http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research and Report Zhang, Shanshan Wu, Wen Huang, Guozhi Liu, Ziping Guo, Shigui Yang, Jianming Wang, Kangling Resting-state connectivity in the default mode network and insula during experimental low back pain |
title | Resting-state connectivity in the default mode network and insula during experimental low back pain |
title_full | Resting-state connectivity in the default mode network and insula during experimental low back pain |
title_fullStr | Resting-state connectivity in the default mode network and insula during experimental low back pain |
title_full_unstemmed | Resting-state connectivity in the default mode network and insula during experimental low back pain |
title_short | Resting-state connectivity in the default mode network and insula during experimental low back pain |
title_sort | resting-state connectivity in the default mode network and insula during experimental low back pain |
topic | Research and Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4146160/ https://www.ncbi.nlm.nih.gov/pubmed/25206794 http://dx.doi.org/10.4103/1673-5374.125341 |
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