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Automated monitoring of early neurobehavioral changes in mice following traumatic brain injury

Traumatic brain injury often causes a variety of behavioral and emotional impairments that can develop into chronic disorders. Therefore, there is a need to shift towards identifying early symptoms that can aid in the prediction of traumatic brain injury outcomes and behavioral endpoints in patients...

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Autores principales: Qu, Wenrui, Liu, Nai-kui, Xie, Xin-min (Simon), Li, Rui, Xu, Xiao-ming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4810988/
https://www.ncbi.nlm.nih.gov/pubmed/27073377
http://dx.doi.org/10.4103/1673-5374.177732
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author Qu, Wenrui
Liu, Nai-kui
Xie, Xin-min (Simon)
Li, Rui
Xu, Xiao-ming
author_facet Qu, Wenrui
Liu, Nai-kui
Xie, Xin-min (Simon)
Li, Rui
Xu, Xiao-ming
author_sort Qu, Wenrui
collection PubMed
description Traumatic brain injury often causes a variety of behavioral and emotional impairments that can develop into chronic disorders. Therefore, there is a need to shift towards identifying early symptoms that can aid in the prediction of traumatic brain injury outcomes and behavioral endpoints in patients with traumatic brain injury after early interventions. In this study, we used the SmartCage system, an automated quantitative approach to assess behavior alterations in mice during an early phase of traumatic brain injury in their home cages. Female C57BL/6 adult mice were subjected to moderate controlled cortical impact (CCI) injury. The mice then received a battery of behavioral assessments including neurological score, locomotor activity, sleep/wake states, and anxiety-like behaviors on days 1, 2, and 7 after CCI. Histological analysis was performed on day 7 after the last assessment. Spontaneous activities on days 1 and 2 after injury were significantly decreased in the CCI group. The average percentage of sleep time spent in both dark and light cycles were significantly higher in the CCI group than in the sham group. For anxiety-like behaviors, the time spent in a light compartment and the number of transitions between the dark/light compartments were all significantly reduced in the CCI group than in the sham group. In addition, the mice suffering from CCI exhibited a preference of staying in the dark compartment of a dark/light cage. The CCI mice showed reduced neurological score and histological abnormalities, which are well correlated to the automated behavioral assessments. Our findings demonstrate that the automated SmartCage system provides sensitive and objective measures for early behavior changes in mice following traumatic brain injury.
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spelling pubmed-48109882016-04-12 Automated monitoring of early neurobehavioral changes in mice following traumatic brain injury Qu, Wenrui Liu, Nai-kui Xie, Xin-min (Simon) Li, Rui Xu, Xiao-ming Neural Regen Res Research Article Traumatic brain injury often causes a variety of behavioral and emotional impairments that can develop into chronic disorders. Therefore, there is a need to shift towards identifying early symptoms that can aid in the prediction of traumatic brain injury outcomes and behavioral endpoints in patients with traumatic brain injury after early interventions. In this study, we used the SmartCage system, an automated quantitative approach to assess behavior alterations in mice during an early phase of traumatic brain injury in their home cages. Female C57BL/6 adult mice were subjected to moderate controlled cortical impact (CCI) injury. The mice then received a battery of behavioral assessments including neurological score, locomotor activity, sleep/wake states, and anxiety-like behaviors on days 1, 2, and 7 after CCI. Histological analysis was performed on day 7 after the last assessment. Spontaneous activities on days 1 and 2 after injury were significantly decreased in the CCI group. The average percentage of sleep time spent in both dark and light cycles were significantly higher in the CCI group than in the sham group. For anxiety-like behaviors, the time spent in a light compartment and the number of transitions between the dark/light compartments were all significantly reduced in the CCI group than in the sham group. In addition, the mice suffering from CCI exhibited a preference of staying in the dark compartment of a dark/light cage. The CCI mice showed reduced neurological score and histological abnormalities, which are well correlated to the automated behavioral assessments. Our findings demonstrate that the automated SmartCage system provides sensitive and objective measures for early behavior changes in mice following traumatic brain injury. Medknow Publications & Media Pvt Ltd 2016-02 /pmc/articles/PMC4810988/ /pubmed/27073377 http://dx.doi.org/10.4103/1673-5374.177732 Text en Copyright: © Neural Regeneration Research http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Research Article
Qu, Wenrui
Liu, Nai-kui
Xie, Xin-min (Simon)
Li, Rui
Xu, Xiao-ming
Automated monitoring of early neurobehavioral changes in mice following traumatic brain injury
title Automated monitoring of early neurobehavioral changes in mice following traumatic brain injury
title_full Automated monitoring of early neurobehavioral changes in mice following traumatic brain injury
title_fullStr Automated monitoring of early neurobehavioral changes in mice following traumatic brain injury
title_full_unstemmed Automated monitoring of early neurobehavioral changes in mice following traumatic brain injury
title_short Automated monitoring of early neurobehavioral changes in mice following traumatic brain injury
title_sort automated monitoring of early neurobehavioral changes in mice following traumatic brain injury
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4810988/
https://www.ncbi.nlm.nih.gov/pubmed/27073377
http://dx.doi.org/10.4103/1673-5374.177732
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