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Unrepaired decompressive craniectomy worsens motor performance in a rat traumatic brain injury model
Decompressive craniectomy (DC) is often required to manage rising intracranial pressure after traumatic brain injury (TBI). Syndrome of the trephine (SoT) is a reversible neurologic condition that often occurs following DC as a result of the unrepaired skull. The purpose of the present study is to c...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7747615/ https://www.ncbi.nlm.nih.gov/pubmed/33335178 http://dx.doi.org/10.1038/s41598-020-79155-8 |
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author | Andrews, Brian T. Barbay, Scott Townsend, Jakob Detamore, Michael Harris, Janna Tuchek, Chad Nudo, Randolph J. |
author_facet | Andrews, Brian T. Barbay, Scott Townsend, Jakob Detamore, Michael Harris, Janna Tuchek, Chad Nudo, Randolph J. |
author_sort | Andrews, Brian T. |
collection | PubMed |
description | Decompressive craniectomy (DC) is often required to manage rising intracranial pressure after traumatic brain injury (TBI). Syndrome of the trephine (SoT) is a reversible neurologic condition that often occurs following DC as a result of the unrepaired skull. The purpose of the present study is to characterize neurological impairment following TBI in rats with an unrepaired craniectomy versus rats with a closed cranium. Long Evans male rats received a controlled cortical impact (CCI) over the caudal forelimb area (CFA) of the motor cortex. Immediately after CCI, rats received either a hemi-craniectomy (TBI Open Skull Group) or an immediate acrylic cranioplasty restoring cranial anatomy (TBI Closed Skull Group). Motor performance was assessed on a skilled reaching task on post-CCI weeks 1—4, 8, 12, and 16. Three weeks after the CCI injury, the TBI Closed Skull Group demonstrated improved motor performance compared to TBI Open Skull Group. The TBI Closed Skull Group continued to perform better than the TBI Open Skull Group throughout weeks 4, 8, 12 and 16. The protracted recovery of CFA motor performance demonstrated in rats with unrepaired skulls following TBI suggests this model may be beneficial for testing new therapeutic approaches to prevent SoT. |
format | Online Article Text |
id | pubmed-7747615 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-77476152020-12-18 Unrepaired decompressive craniectomy worsens motor performance in a rat traumatic brain injury model Andrews, Brian T. Barbay, Scott Townsend, Jakob Detamore, Michael Harris, Janna Tuchek, Chad Nudo, Randolph J. Sci Rep Article Decompressive craniectomy (DC) is often required to manage rising intracranial pressure after traumatic brain injury (TBI). Syndrome of the trephine (SoT) is a reversible neurologic condition that often occurs following DC as a result of the unrepaired skull. The purpose of the present study is to characterize neurological impairment following TBI in rats with an unrepaired craniectomy versus rats with a closed cranium. Long Evans male rats received a controlled cortical impact (CCI) over the caudal forelimb area (CFA) of the motor cortex. Immediately after CCI, rats received either a hemi-craniectomy (TBI Open Skull Group) or an immediate acrylic cranioplasty restoring cranial anatomy (TBI Closed Skull Group). Motor performance was assessed on a skilled reaching task on post-CCI weeks 1—4, 8, 12, and 16. Three weeks after the CCI injury, the TBI Closed Skull Group demonstrated improved motor performance compared to TBI Open Skull Group. The TBI Closed Skull Group continued to perform better than the TBI Open Skull Group throughout weeks 4, 8, 12 and 16. The protracted recovery of CFA motor performance demonstrated in rats with unrepaired skulls following TBI suggests this model may be beneficial for testing new therapeutic approaches to prevent SoT. Nature Publishing Group UK 2020-12-17 /pmc/articles/PMC7747615/ /pubmed/33335178 http://dx.doi.org/10.1038/s41598-020-79155-8 Text en © The Author(s) 2020 Open Access This 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/. |
spellingShingle | Article Andrews, Brian T. Barbay, Scott Townsend, Jakob Detamore, Michael Harris, Janna Tuchek, Chad Nudo, Randolph J. Unrepaired decompressive craniectomy worsens motor performance in a rat traumatic brain injury model |
title | Unrepaired decompressive craniectomy worsens motor performance in a rat traumatic brain injury model |
title_full | Unrepaired decompressive craniectomy worsens motor performance in a rat traumatic brain injury model |
title_fullStr | Unrepaired decompressive craniectomy worsens motor performance in a rat traumatic brain injury model |
title_full_unstemmed | Unrepaired decompressive craniectomy worsens motor performance in a rat traumatic brain injury model |
title_short | Unrepaired decompressive craniectomy worsens motor performance in a rat traumatic brain injury model |
title_sort | unrepaired decompressive craniectomy worsens motor performance in a rat traumatic brain injury model |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7747615/ https://www.ncbi.nlm.nih.gov/pubmed/33335178 http://dx.doi.org/10.1038/s41598-020-79155-8 |
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