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Anterior cingulate cortex regulates pain catastrophizing-like behaviors in rats
Negative pain expectation including pain catastrophizing is a well-known clinical phenomenon whereby patients amplify the aversive value of a painful or oftentimes even a similar, non-painful stimulus. Mechanisms of pain catastrophizing, however, remain elusive. Here, we modeled pain catastrophizing...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10576271/ https://www.ncbi.nlm.nih.gov/pubmed/37833814 http://dx.doi.org/10.1186/s13041-023-01060-8 |
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author | Jee, Hyun Jung Zhu, Elaine Sun, Mengqi Liu, Weizhuo Zhang, Qiaosheng Wang, Jing |
author_facet | Jee, Hyun Jung Zhu, Elaine Sun, Mengqi Liu, Weizhuo Zhang, Qiaosheng Wang, Jing |
author_sort | Jee, Hyun Jung |
collection | PubMed |
description | Negative pain expectation including pain catastrophizing is a well-known clinical phenomenon whereby patients amplify the aversive value of a painful or oftentimes even a similar, non-painful stimulus. Mechanisms of pain catastrophizing, however, remain elusive. Here, we modeled pain catastrophizing behavior in rats, and found that rats subjected to repeated noxious pin pricks on one paw demonstrated an aversive response to similar but non-noxious mechanical stimuli delivered to the contralateral paw. Optogenetic inhibition of pyramidal neuron activity in the anterior cingulate cortex (ACC) during the application of repetitive noxious pin pricks eliminated this catastrophizing behavior. Time-lapse calcium (Ca(2+)) imaging in the ACC further revealed an increase in spontaneous neural activity after the delivery of noxious stimuli. Together these results suggest that the experience of repeated noxious stimuli may drive hyperactivity in the ACC, causing increased avoidance of subthreshold stimuli, and that reducing this hyperactivity may play a role in treating pain catastrophizing. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13041-023-01060-8. |
format | Online Article Text |
id | pubmed-10576271 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-105762712023-10-15 Anterior cingulate cortex regulates pain catastrophizing-like behaviors in rats Jee, Hyun Jung Zhu, Elaine Sun, Mengqi Liu, Weizhuo Zhang, Qiaosheng Wang, Jing Mol Brain Research Negative pain expectation including pain catastrophizing is a well-known clinical phenomenon whereby patients amplify the aversive value of a painful or oftentimes even a similar, non-painful stimulus. Mechanisms of pain catastrophizing, however, remain elusive. Here, we modeled pain catastrophizing behavior in rats, and found that rats subjected to repeated noxious pin pricks on one paw demonstrated an aversive response to similar but non-noxious mechanical stimuli delivered to the contralateral paw. Optogenetic inhibition of pyramidal neuron activity in the anterior cingulate cortex (ACC) during the application of repetitive noxious pin pricks eliminated this catastrophizing behavior. Time-lapse calcium (Ca(2+)) imaging in the ACC further revealed an increase in spontaneous neural activity after the delivery of noxious stimuli. Together these results suggest that the experience of repeated noxious stimuli may drive hyperactivity in the ACC, causing increased avoidance of subthreshold stimuli, and that reducing this hyperactivity may play a role in treating pain catastrophizing. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13041-023-01060-8. BioMed Central 2023-10-13 /pmc/articles/PMC10576271/ /pubmed/37833814 http://dx.doi.org/10.1186/s13041-023-01060-8 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Jee, Hyun Jung Zhu, Elaine Sun, Mengqi Liu, Weizhuo Zhang, Qiaosheng Wang, Jing Anterior cingulate cortex regulates pain catastrophizing-like behaviors in rats |
title | Anterior cingulate cortex regulates pain catastrophizing-like behaviors in rats |
title_full | Anterior cingulate cortex regulates pain catastrophizing-like behaviors in rats |
title_fullStr | Anterior cingulate cortex regulates pain catastrophizing-like behaviors in rats |
title_full_unstemmed | Anterior cingulate cortex regulates pain catastrophizing-like behaviors in rats |
title_short | Anterior cingulate cortex regulates pain catastrophizing-like behaviors in rats |
title_sort | anterior cingulate cortex regulates pain catastrophizing-like behaviors in rats |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10576271/ https://www.ncbi.nlm.nih.gov/pubmed/37833814 http://dx.doi.org/10.1186/s13041-023-01060-8 |
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