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The waiting game: investigating the neurobiological transition from acute to persistent pain in adolescent rats

Persistent postsurgical pain affects 20% of youth undergoing a surgical procedure, with females exhibiting increased prevalence of chronic pain compared with males. This study sought to examine the sexually-dimorphic neurobiological changes underlying the transition from acute to persistent pain fol...

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Autores principales: Salberg, Sabrina, Doshen, Angela, Yamakawa, Glenn R, Miller, Jillian Vinall, Noel, Melanie, Henderson, Luke, Mychasiuk, Richelle
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10183733/
https://www.ncbi.nlm.nih.gov/pubmed/36610738
http://dx.doi.org/10.1093/cercor/bhac511
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author Salberg, Sabrina
Doshen, Angela
Yamakawa, Glenn R
Miller, Jillian Vinall
Noel, Melanie
Henderson, Luke
Mychasiuk, Richelle
author_facet Salberg, Sabrina
Doshen, Angela
Yamakawa, Glenn R
Miller, Jillian Vinall
Noel, Melanie
Henderson, Luke
Mychasiuk, Richelle
author_sort Salberg, Sabrina
collection PubMed
description Persistent postsurgical pain affects 20% of youth undergoing a surgical procedure, with females exhibiting increased prevalence of chronic pain compared with males. This study sought to examine the sexually-dimorphic neurobiological changes underlying the transition from acute to persistent pain following surgery in adolescence. Male and female Sprague Dawley rats were randomly allocated to a sham or injury (plantar-incision surgery) condition and assessed for pain sensitivity while also undergoing magnetic resonance imaging at both an acute and chronic timepoint within adolescence. We found that injury resulted in persistent pain in both sexes, with females displaying most significant sensitivity. Injury resulted in significant gray matter density increases in brain areas including the cerebellum, caudate putamen/insula, and amygdala and decreases in the hippocampus, hypothalamus, nucleus accumbens, and lateral septal nucleus. Gray matter density changes in the hippocampus and lateral septal nucleus were driven by male rats whereas changes in the amygdala and caudate putamen/insula were driven by female rats. Overall, our results indicate persistent behavioral and neurobiological changes following surgery in adolescence, with sexually-dimorphic and age-specific outcomes, highlighting the importance of studying both sexes and adolescents, rather than extrapolating from male adult literature.
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spelling pubmed-101837332023-05-16 The waiting game: investigating the neurobiological transition from acute to persistent pain in adolescent rats Salberg, Sabrina Doshen, Angela Yamakawa, Glenn R Miller, Jillian Vinall Noel, Melanie Henderson, Luke Mychasiuk, Richelle Cereb Cortex Original Article Persistent postsurgical pain affects 20% of youth undergoing a surgical procedure, with females exhibiting increased prevalence of chronic pain compared with males. This study sought to examine the sexually-dimorphic neurobiological changes underlying the transition from acute to persistent pain following surgery in adolescence. Male and female Sprague Dawley rats were randomly allocated to a sham or injury (plantar-incision surgery) condition and assessed for pain sensitivity while also undergoing magnetic resonance imaging at both an acute and chronic timepoint within adolescence. We found that injury resulted in persistent pain in both sexes, with females displaying most significant sensitivity. Injury resulted in significant gray matter density increases in brain areas including the cerebellum, caudate putamen/insula, and amygdala and decreases in the hippocampus, hypothalamus, nucleus accumbens, and lateral septal nucleus. Gray matter density changes in the hippocampus and lateral septal nucleus were driven by male rats whereas changes in the amygdala and caudate putamen/insula were driven by female rats. Overall, our results indicate persistent behavioral and neurobiological changes following surgery in adolescence, with sexually-dimorphic and age-specific outcomes, highlighting the importance of studying both sexes and adolescents, rather than extrapolating from male adult literature. Oxford University Press 2023-01-04 /pmc/articles/PMC10183733/ /pubmed/36610738 http://dx.doi.org/10.1093/cercor/bhac511 Text en © The Author(s) 2023. Published by Oxford University Press. All rights reserved. For permissions, please e-mail: journals.permission@oup.com https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Original Article
Salberg, Sabrina
Doshen, Angela
Yamakawa, Glenn R
Miller, Jillian Vinall
Noel, Melanie
Henderson, Luke
Mychasiuk, Richelle
The waiting game: investigating the neurobiological transition from acute to persistent pain in adolescent rats
title The waiting game: investigating the neurobiological transition from acute to persistent pain in adolescent rats
title_full The waiting game: investigating the neurobiological transition from acute to persistent pain in adolescent rats
title_fullStr The waiting game: investigating the neurobiological transition from acute to persistent pain in adolescent rats
title_full_unstemmed The waiting game: investigating the neurobiological transition from acute to persistent pain in adolescent rats
title_short The waiting game: investigating the neurobiological transition from acute to persistent pain in adolescent rats
title_sort waiting game: investigating the neurobiological transition from acute to persistent pain in adolescent rats
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10183733/
https://www.ncbi.nlm.nih.gov/pubmed/36610738
http://dx.doi.org/10.1093/cercor/bhac511
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