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Pelvic Pain Alters Functional Connectivity Between Anterior Cingulate Cortex and Hippocampus in Both Humans and a Rat Model
The anterior cingulate cortex (ACC) and hippocampus (HIPP) are two key brain regions associated with pain and pain-related affective processing. However, whether and how pelvic pain alters the neural activity and connectivity of the ACC and HIPP under baseline and during social pain, and the underly...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8210850/ https://www.ncbi.nlm.nih.gov/pubmed/34149369 http://dx.doi.org/10.3389/fnsys.2021.642349 |
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author | Yu, Wenjun Wu, Xiaoyan Chen, Yunan Liang, Zhiying Jiang, Jinxiang Misrani, Afzal Su, Yun Peng, Yigang Chen, Jian Tang, Binliang Sun, Mengyao Long, Cheng Shen, Jun Yang, Li |
author_facet | Yu, Wenjun Wu, Xiaoyan Chen, Yunan Liang, Zhiying Jiang, Jinxiang Misrani, Afzal Su, Yun Peng, Yigang Chen, Jian Tang, Binliang Sun, Mengyao Long, Cheng Shen, Jun Yang, Li |
author_sort | Yu, Wenjun |
collection | PubMed |
description | The anterior cingulate cortex (ACC) and hippocampus (HIPP) are two key brain regions associated with pain and pain-related affective processing. However, whether and how pelvic pain alters the neural activity and connectivity of the ACC and HIPP under baseline and during social pain, and the underlying cellular and molecular mechanisms, remain unclear. Using functional magnetic resonance imaging (fMRI) combined with electrophysiology and biochemistry, we show that pelvic pain, particularly, primary dysmenorrhea (PDM), causes an increase in the functional connectivity between ACC and HIPP in resting-state fMRI, and a smaller reduction in connectivity during social exclusion in PDM females with periovulatory phase. Similarly, model rats demonstrate significantly increased ACC-HIPP synchronization in the gamma band, associating with reduced modulation by ACC-theta on HIPP-gamma and increased levels of receptor proteins and excitation. This study brings together human fMRI and animal research and enables improved therapeutic strategies for ameliorating pain and pain-related affective processing. |
format | Online Article Text |
id | pubmed-8210850 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-82108502021-06-18 Pelvic Pain Alters Functional Connectivity Between Anterior Cingulate Cortex and Hippocampus in Both Humans and a Rat Model Yu, Wenjun Wu, Xiaoyan Chen, Yunan Liang, Zhiying Jiang, Jinxiang Misrani, Afzal Su, Yun Peng, Yigang Chen, Jian Tang, Binliang Sun, Mengyao Long, Cheng Shen, Jun Yang, Li Front Syst Neurosci Neuroscience The anterior cingulate cortex (ACC) and hippocampus (HIPP) are two key brain regions associated with pain and pain-related affective processing. However, whether and how pelvic pain alters the neural activity and connectivity of the ACC and HIPP under baseline and during social pain, and the underlying cellular and molecular mechanisms, remain unclear. Using functional magnetic resonance imaging (fMRI) combined with electrophysiology and biochemistry, we show that pelvic pain, particularly, primary dysmenorrhea (PDM), causes an increase in the functional connectivity between ACC and HIPP in resting-state fMRI, and a smaller reduction in connectivity during social exclusion in PDM females with periovulatory phase. Similarly, model rats demonstrate significantly increased ACC-HIPP synchronization in the gamma band, associating with reduced modulation by ACC-theta on HIPP-gamma and increased levels of receptor proteins and excitation. This study brings together human fMRI and animal research and enables improved therapeutic strategies for ameliorating pain and pain-related affective processing. Frontiers Media S.A. 2021-06-03 /pmc/articles/PMC8210850/ /pubmed/34149369 http://dx.doi.org/10.3389/fnsys.2021.642349 Text en Copyright © 2021 Yu, Wu, Chen, Liang, Jiang, Misrani, Su, Peng, Chen, Tang, Sun, Long, Shen and Yang. https://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) and the copyright owner(s) 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 Yu, Wenjun Wu, Xiaoyan Chen, Yunan Liang, Zhiying Jiang, Jinxiang Misrani, Afzal Su, Yun Peng, Yigang Chen, Jian Tang, Binliang Sun, Mengyao Long, Cheng Shen, Jun Yang, Li Pelvic Pain Alters Functional Connectivity Between Anterior Cingulate Cortex and Hippocampus in Both Humans and a Rat Model |
title | Pelvic Pain Alters Functional Connectivity Between Anterior Cingulate Cortex and Hippocampus in Both Humans and a Rat Model |
title_full | Pelvic Pain Alters Functional Connectivity Between Anterior Cingulate Cortex and Hippocampus in Both Humans and a Rat Model |
title_fullStr | Pelvic Pain Alters Functional Connectivity Between Anterior Cingulate Cortex and Hippocampus in Both Humans and a Rat Model |
title_full_unstemmed | Pelvic Pain Alters Functional Connectivity Between Anterior Cingulate Cortex and Hippocampus in Both Humans and a Rat Model |
title_short | Pelvic Pain Alters Functional Connectivity Between Anterior Cingulate Cortex and Hippocampus in Both Humans and a Rat Model |
title_sort | pelvic pain alters functional connectivity between anterior cingulate cortex and hippocampus in both humans and a rat model |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8210850/ https://www.ncbi.nlm.nih.gov/pubmed/34149369 http://dx.doi.org/10.3389/fnsys.2021.642349 |
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