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Pain modulatory network is influenced by sex and age in a healthy state and during osteoarthritis progression in rats
Old age and female sex are risk factors for the development of osteoarthritis (OA) and chronic pain. We investigated the effects of sex and age on pain modulatory networks in a healthy state and during OA progression. We used functional MRI to determine the effects of sex and age on periaqueductal g...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7884031/ https://www.ncbi.nlm.nih.gov/pubmed/33400367 http://dx.doi.org/10.1111/acel.13292 |
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author | Da Silva, Joyce T. Tricou, Christina Zhang, Youping Tofighbakhsh, Amir Seminowicz, David A. Ro, Jin Y. |
author_facet | Da Silva, Joyce T. Tricou, Christina Zhang, Youping Tofighbakhsh, Amir Seminowicz, David A. Ro, Jin Y. |
author_sort | Da Silva, Joyce T. |
collection | PubMed |
description | Old age and female sex are risk factors for the development of osteoarthritis (OA) and chronic pain. We investigated the effects of sex and age on pain modulatory networks in a healthy state and during OA progression. We used functional MRI to determine the effects of sex and age on periaqueductal gray functional connectivity (PAG FC) in a healthy state (pre‐OA) and during the early and late phases of monosodium iodoacetate‐induced OA in rats. We then examined how sex and age affect longitudinal changes in PAG FC in OA. In a healthy state, females exhibited more widespread PAG FC than males, and this effect was exaggerated with aging. Young males had moderate PAG FC changes during the early phase but recruited additional brain regions, including the rostral anterior cingulate cortex (ACC), during the late phase. Young females exhibited widespread PAG FC in the early phase, which includes connections to insula, caudal ACC, and nucleus accumbens (NAc). Older groups had strong PAG FC with fewer regions in the early phase, but they recruited additional brain regions, including NAc, in the late phase. Overall, our findings show that PAG FC is modulated by sex and age in a healthy state. A widespread PAG network in the early phase of OA pain may contribute to the transition from acute to chronic OA pain and the increased risk of developing chronic pain for females. Enhanced PAG FC with the reward system may represent a potential mechanism underlying chronic OA pain in elderly patients. |
format | Online Article Text |
id | pubmed-7884031 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-78840312021-02-19 Pain modulatory network is influenced by sex and age in a healthy state and during osteoarthritis progression in rats Da Silva, Joyce T. Tricou, Christina Zhang, Youping Tofighbakhsh, Amir Seminowicz, David A. Ro, Jin Y. Aging Cell Original Papers Old age and female sex are risk factors for the development of osteoarthritis (OA) and chronic pain. We investigated the effects of sex and age on pain modulatory networks in a healthy state and during OA progression. We used functional MRI to determine the effects of sex and age on periaqueductal gray functional connectivity (PAG FC) in a healthy state (pre‐OA) and during the early and late phases of monosodium iodoacetate‐induced OA in rats. We then examined how sex and age affect longitudinal changes in PAG FC in OA. In a healthy state, females exhibited more widespread PAG FC than males, and this effect was exaggerated with aging. Young males had moderate PAG FC changes during the early phase but recruited additional brain regions, including the rostral anterior cingulate cortex (ACC), during the late phase. Young females exhibited widespread PAG FC in the early phase, which includes connections to insula, caudal ACC, and nucleus accumbens (NAc). Older groups had strong PAG FC with fewer regions in the early phase, but they recruited additional brain regions, including NAc, in the late phase. Overall, our findings show that PAG FC is modulated by sex and age in a healthy state. A widespread PAG network in the early phase of OA pain may contribute to the transition from acute to chronic OA pain and the increased risk of developing chronic pain for females. Enhanced PAG FC with the reward system may represent a potential mechanism underlying chronic OA pain in elderly patients. John Wiley and Sons Inc. 2021-01-05 2021-02 /pmc/articles/PMC7884031/ /pubmed/33400367 http://dx.doi.org/10.1111/acel.13292 Text en © 2021 The Authors. Aging Cell published by the Anatomical Society and John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Papers Da Silva, Joyce T. Tricou, Christina Zhang, Youping Tofighbakhsh, Amir Seminowicz, David A. Ro, Jin Y. Pain modulatory network is influenced by sex and age in a healthy state and during osteoarthritis progression in rats |
title | Pain modulatory network is influenced by sex and age in a healthy state and during osteoarthritis progression in rats |
title_full | Pain modulatory network is influenced by sex and age in a healthy state and during osteoarthritis progression in rats |
title_fullStr | Pain modulatory network is influenced by sex and age in a healthy state and during osteoarthritis progression in rats |
title_full_unstemmed | Pain modulatory network is influenced by sex and age in a healthy state and during osteoarthritis progression in rats |
title_short | Pain modulatory network is influenced by sex and age in a healthy state and during osteoarthritis progression in rats |
title_sort | pain modulatory network is influenced by sex and age in a healthy state and during osteoarthritis progression in rats |
topic | Original Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7884031/ https://www.ncbi.nlm.nih.gov/pubmed/33400367 http://dx.doi.org/10.1111/acel.13292 |
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