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Improved recovery from spinal cord injury in rats with chronic parvovirus serotype-1a infection
OBJECTIVES: A vendor informed us that rats shipped to us and used by us in a spinal cord contusion injury experiment were infected by rat parvovirus type 1a (RPV-1a). Our aim was therefore to determine whether this infection may have altered locomotor recovery or tissue pathology. SETTING: Stockholm...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5399164/ https://www.ncbi.nlm.nih.gov/pubmed/26690859 http://dx.doi.org/10.1038/sc.2015.208 |
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author | Kjell, J Olson, L Abrams, M B |
author_facet | Kjell, J Olson, L Abrams, M B |
author_sort | Kjell, J |
collection | PubMed |
description | OBJECTIVES: A vendor informed us that rats shipped to us and used by us in a spinal cord contusion injury experiment were infected by rat parvovirus type 1a (RPV-1a). Our aim was therefore to determine whether this infection may have altered locomotor recovery or tissue pathology. SETTING: Stockholm, Sweden. METHODS: We induced a moderate contusion injury of the spinal cord in rats received from an (unknown to us) RPV-1a-contaminated facility. We compared the hind limb locomotor function between RPV-1a-infected rats and non-infected controls with the same spinal cord lesions, obtained before (historical control), as well as after infection (future controls). Histologically, we assessed spinal tissue sparing, astrocyte reactivity and the amount of macrophages/activated microglia. RESULTS: RPV-1a-infected rats had significantly better hind limb locomotor recovery compared with both ‘historical' and ‘future' controls. We also observed significantly better tissue sparing and axonal sparing around the injury site, as well as significant reductions in macrophages/activated microglia and astrocyte reactivity in the spinal cords of RPV-1a-infected rats. CONCLUSION: The results stress the importance of knowing the health status of animals used to study central nervous system trauma and support the notion that acquired infections, even if asymptomatic, may alter response to injury in mammals. Furthermore, the results demonstrate that virus infections may have positive effects on functional recovery after spinal cord injury and indicate that RPV-1a infection may be neuroprotective by dampening secondary damage. |
format | Online Article Text |
id | pubmed-5399164 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-53991642017-05-09 Improved recovery from spinal cord injury in rats with chronic parvovirus serotype-1a infection Kjell, J Olson, L Abrams, M B Spinal Cord Original Article OBJECTIVES: A vendor informed us that rats shipped to us and used by us in a spinal cord contusion injury experiment were infected by rat parvovirus type 1a (RPV-1a). Our aim was therefore to determine whether this infection may have altered locomotor recovery or tissue pathology. SETTING: Stockholm, Sweden. METHODS: We induced a moderate contusion injury of the spinal cord in rats received from an (unknown to us) RPV-1a-contaminated facility. We compared the hind limb locomotor function between RPV-1a-infected rats and non-infected controls with the same spinal cord lesions, obtained before (historical control), as well as after infection (future controls). Histologically, we assessed spinal tissue sparing, astrocyte reactivity and the amount of macrophages/activated microglia. RESULTS: RPV-1a-infected rats had significantly better hind limb locomotor recovery compared with both ‘historical' and ‘future' controls. We also observed significantly better tissue sparing and axonal sparing around the injury site, as well as significant reductions in macrophages/activated microglia and astrocyte reactivity in the spinal cords of RPV-1a-infected rats. CONCLUSION: The results stress the importance of knowing the health status of animals used to study central nervous system trauma and support the notion that acquired infections, even if asymptomatic, may alter response to injury in mammals. Furthermore, the results demonstrate that virus infections may have positive effects on functional recovery after spinal cord injury and indicate that RPV-1a infection may be neuroprotective by dampening secondary damage. Nature Publishing Group 2016-07 2015-12-22 /pmc/articles/PMC5399164/ /pubmed/26690859 http://dx.doi.org/10.1038/sc.2015.208 Text en Copyright © 2016 International Spinal Cord Society http://creativecommons.org/licenses/by-nc-sa/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/4.0/ |
spellingShingle | Original Article Kjell, J Olson, L Abrams, M B Improved recovery from spinal cord injury in rats with chronic parvovirus serotype-1a infection |
title | Improved recovery from spinal cord injury in rats with chronic parvovirus serotype-1a infection |
title_full | Improved recovery from spinal cord injury in rats with chronic parvovirus serotype-1a infection |
title_fullStr | Improved recovery from spinal cord injury in rats with chronic parvovirus serotype-1a infection |
title_full_unstemmed | Improved recovery from spinal cord injury in rats with chronic parvovirus serotype-1a infection |
title_short | Improved recovery from spinal cord injury in rats with chronic parvovirus serotype-1a infection |
title_sort | improved recovery from spinal cord injury in rats with chronic parvovirus serotype-1a infection |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5399164/ https://www.ncbi.nlm.nih.gov/pubmed/26690859 http://dx.doi.org/10.1038/sc.2015.208 |
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