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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
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.
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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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