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Sexual dimorphism in cognitive disorders in a murine model of neuropathic pain

BACKGROUND: A sex-difference in susceptibility to chronic pain is well-known. Although recent studies have begun to reveal the sex-dependent mechanisms of nerve injury-induced pain sensitization, sex differences in the affective and cognitive brain dysfunctions associated with chronic pain have not...

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Autores principales: Won, Soonmi, Park, Keebum, Lim, Hyoungsub, Lee, Sung Joong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6942364/
https://www.ncbi.nlm.nih.gov/pubmed/31901234
http://dx.doi.org/10.1186/s12993-019-0164-0
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author Won, Soonmi
Park, Keebum
Lim, Hyoungsub
Lee, Sung Joong
author_facet Won, Soonmi
Park, Keebum
Lim, Hyoungsub
Lee, Sung Joong
author_sort Won, Soonmi
collection PubMed
description BACKGROUND: A sex-difference in susceptibility to chronic pain is well-known. Although recent studies have begun to reveal the sex-dependent mechanisms of nerve injury-induced pain sensitization, sex differences in the affective and cognitive brain dysfunctions associated with chronic pain have not been investigated. Therefore, we tested whether chronic pain leads to affective and cognitive disorders in a mouse neuropathic pain model and whether those disorders are sexually dimorphic. METHODS: Chronic neuropathic pain was induced in male and female mice by L5 spinal nerve transection (SNT) injury. Pain sensitivity was measured with the von Frey test. Affective behaviors such as depression and anxiety were assessed by the forced swim, tail suspension, and open field tests. Cognitive brain function was assessed with the Morris water maze and the novel object location and novel object recognition tests. RESULTS: Mechanical allodynia was induced and maintained for up to 8 weeks after SNT in both male and female mice. Depressive- and anxiety-like behaviors were observed 8 weeks post-SNT injury regardless of sex. Chronic pain-induced cognitive deficits measured with the Morris water maze and novel object location test were seen only in male mice, not in female mice. CONCLUSIONS: Chronic neuropathic pain is accompanied by anxiety- and depressive-like behaviors in a mouse model regardless of sex, and male mice are more vulnerable than female mice to chronic pain-associated cognitive deficits.
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spelling pubmed-69423642020-01-07 Sexual dimorphism in cognitive disorders in a murine model of neuropathic pain Won, Soonmi Park, Keebum Lim, Hyoungsub Lee, Sung Joong Behav Brain Funct Research BACKGROUND: A sex-difference in susceptibility to chronic pain is well-known. Although recent studies have begun to reveal the sex-dependent mechanisms of nerve injury-induced pain sensitization, sex differences in the affective and cognitive brain dysfunctions associated with chronic pain have not been investigated. Therefore, we tested whether chronic pain leads to affective and cognitive disorders in a mouse neuropathic pain model and whether those disorders are sexually dimorphic. METHODS: Chronic neuropathic pain was induced in male and female mice by L5 spinal nerve transection (SNT) injury. Pain sensitivity was measured with the von Frey test. Affective behaviors such as depression and anxiety were assessed by the forced swim, tail suspension, and open field tests. Cognitive brain function was assessed with the Morris water maze and the novel object location and novel object recognition tests. RESULTS: Mechanical allodynia was induced and maintained for up to 8 weeks after SNT in both male and female mice. Depressive- and anxiety-like behaviors were observed 8 weeks post-SNT injury regardless of sex. Chronic pain-induced cognitive deficits measured with the Morris water maze and novel object location test were seen only in male mice, not in female mice. CONCLUSIONS: Chronic neuropathic pain is accompanied by anxiety- and depressive-like behaviors in a mouse model regardless of sex, and male mice are more vulnerable than female mice to chronic pain-associated cognitive deficits. BioMed Central 2020-01-04 /pmc/articles/PMC6942364/ /pubmed/31901234 http://dx.doi.org/10.1186/s12993-019-0164-0 Text en © The Author(s) 2020 Open AccessThis 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/. The Creative Commons Public Domain Dedication waiver (http://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
Won, Soonmi
Park, Keebum
Lim, Hyoungsub
Lee, Sung Joong
Sexual dimorphism in cognitive disorders in a murine model of neuropathic pain
title Sexual dimorphism in cognitive disorders in a murine model of neuropathic pain
title_full Sexual dimorphism in cognitive disorders in a murine model of neuropathic pain
title_fullStr Sexual dimorphism in cognitive disorders in a murine model of neuropathic pain
title_full_unstemmed Sexual dimorphism in cognitive disorders in a murine model of neuropathic pain
title_short Sexual dimorphism in cognitive disorders in a murine model of neuropathic pain
title_sort sexual dimorphism in cognitive disorders in a murine model of neuropathic pain
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6942364/
https://www.ncbi.nlm.nih.gov/pubmed/31901234
http://dx.doi.org/10.1186/s12993-019-0164-0
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