Cargando…

Sex Differences in the Behavioural Aspects of the Cuprizone-Induced Demyelination Model in Mice

Multiple sclerosis is an autoimmune disease characterised by demyelination in the central nervous system. The cuprizone-induced demyelination model is often used in mice to test novel treatments for multiple sclerosis. However, despite significant demyelination, behavioural deficits may be subtle or...

Descripción completa

Detalles Bibliográficos
Autores principales: Paton, Kelly F., Hong, Sheein, Biggerstaff, Andrew, Kivell, Bronwyn M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9775311/
https://www.ncbi.nlm.nih.gov/pubmed/36552147
http://dx.doi.org/10.3390/brainsci12121687
_version_ 1784855613333831680
author Paton, Kelly F.
Hong, Sheein
Biggerstaff, Andrew
Kivell, Bronwyn M.
author_facet Paton, Kelly F.
Hong, Sheein
Biggerstaff, Andrew
Kivell, Bronwyn M.
author_sort Paton, Kelly F.
collection PubMed
description Multiple sclerosis is an autoimmune disease characterised by demyelination in the central nervous system. The cuprizone-induced demyelination model is often used in mice to test novel treatments for multiple sclerosis. However, despite significant demyelination, behavioural deficits may be subtle or have mixed results depending on the paradigm used. Furthermore, the sex differences within the model are not well understood. In the current study, we have sought to understand the behavioural deficits associated with the cuprizone-induced demyelination model in both male and female C57BL/6J mice. Using Black gold II stain, we found that cuprizone administration over 6 weeks caused significant demyelination in the corpus callosum that was consistent across both sexes. Cuprizone administration caused increased mechanical sensitivity when measured using an electronic von Frey aesthesiometer, with no sex differences observed. However, cuprizone administration decreased motor coordination, with more severe deficits seen in males in the horizontal bar and passive wire hang tests. In contrast, female mice showed more severe deficits in the motor skill sequence test. Cuprizone administration caused more anxiety-like behaviours in males compared to females in the elevated zero maze. Therefore, this study provides a better understanding of the sex differences involved in the behavioural aspects of cuprizone-induced demyelination, which could allow for a better translation of results from the laboratory to the clinic.
format Online
Article
Text
id pubmed-9775311
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-97753112022-12-23 Sex Differences in the Behavioural Aspects of the Cuprizone-Induced Demyelination Model in Mice Paton, Kelly F. Hong, Sheein Biggerstaff, Andrew Kivell, Bronwyn M. Brain Sci Article Multiple sclerosis is an autoimmune disease characterised by demyelination in the central nervous system. The cuprizone-induced demyelination model is often used in mice to test novel treatments for multiple sclerosis. However, despite significant demyelination, behavioural deficits may be subtle or have mixed results depending on the paradigm used. Furthermore, the sex differences within the model are not well understood. In the current study, we have sought to understand the behavioural deficits associated with the cuprizone-induced demyelination model in both male and female C57BL/6J mice. Using Black gold II stain, we found that cuprizone administration over 6 weeks caused significant demyelination in the corpus callosum that was consistent across both sexes. Cuprizone administration caused increased mechanical sensitivity when measured using an electronic von Frey aesthesiometer, with no sex differences observed. However, cuprizone administration decreased motor coordination, with more severe deficits seen in males in the horizontal bar and passive wire hang tests. In contrast, female mice showed more severe deficits in the motor skill sequence test. Cuprizone administration caused more anxiety-like behaviours in males compared to females in the elevated zero maze. Therefore, this study provides a better understanding of the sex differences involved in the behavioural aspects of cuprizone-induced demyelination, which could allow for a better translation of results from the laboratory to the clinic. MDPI 2022-12-08 /pmc/articles/PMC9775311/ /pubmed/36552147 http://dx.doi.org/10.3390/brainsci12121687 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Paton, Kelly F.
Hong, Sheein
Biggerstaff, Andrew
Kivell, Bronwyn M.
Sex Differences in the Behavioural Aspects of the Cuprizone-Induced Demyelination Model in Mice
title Sex Differences in the Behavioural Aspects of the Cuprizone-Induced Demyelination Model in Mice
title_full Sex Differences in the Behavioural Aspects of the Cuprizone-Induced Demyelination Model in Mice
title_fullStr Sex Differences in the Behavioural Aspects of the Cuprizone-Induced Demyelination Model in Mice
title_full_unstemmed Sex Differences in the Behavioural Aspects of the Cuprizone-Induced Demyelination Model in Mice
title_short Sex Differences in the Behavioural Aspects of the Cuprizone-Induced Demyelination Model in Mice
title_sort sex differences in the behavioural aspects of the cuprizone-induced demyelination model in mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9775311/
https://www.ncbi.nlm.nih.gov/pubmed/36552147
http://dx.doi.org/10.3390/brainsci12121687
work_keys_str_mv AT patonkellyf sexdifferencesinthebehaviouralaspectsofthecuprizoneinduceddemyelinationmodelinmice
AT hongsheein sexdifferencesinthebehaviouralaspectsofthecuprizoneinduceddemyelinationmodelinmice
AT biggerstaffandrew sexdifferencesinthebehaviouralaspectsofthecuprizoneinduceddemyelinationmodelinmice
AT kivellbronwynm sexdifferencesinthebehaviouralaspectsofthecuprizoneinduceddemyelinationmodelinmice