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Effect of sialodacryoadenitis virus infection on axonal regeneration
The effect of sialodacryoadenitis virus (SDAV) infection on axonal regeneration and functional recovery was investigated in male Lewis rats. Animals underwent unilateral tibial nerve transection, immediate repair, and treatment with either FK506 (treated) or control vehicle (untreated). Serial walki...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wiley Subscription Services, Inc., A Wiley Company
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4088328/ https://www.ncbi.nlm.nih.gov/pubmed/21866574 http://dx.doi.org/10.1002/micr.20914 |
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author | Yu, Vivian M. Mackinnon, Susan E. Hunter, Daniel A Brenner, Michael J. |
author_facet | Yu, Vivian M. Mackinnon, Susan E. Hunter, Daniel A Brenner, Michael J. |
author_sort | Yu, Vivian M. |
collection | PubMed |
description | The effect of sialodacryoadenitis virus (SDAV) infection on axonal regeneration and functional recovery was investigated in male Lewis rats. Animals underwent unilateral tibial nerve transection, immediate repair, and treatment with either FK506 (treated) or control vehicle (untreated). Serial walking track analyses were performed to assess functional recovery. Nerves were harvested for morphometric analysis on postoperative day 18 after an SDAV outbreak occurred that affected the 12 experimental animals. Histomorphometry and walking track data were compared against 36 historical controls. Rats infected with SDAV demonstrated severely impaired axonal regeneration and diminished functional recovery. Total fiber counts, nerve density, and percent neural tissue were all significantly reduced in infected animals (P < 0.05). Active SDAV infection severely impaired nerve regeneration and negated the positive effect of FK506 on nerve regeneration in rats. Immunosuppressive risks must be weighed carefully against the potential neuroregenerative benefits in the treatment of peripheral nerve injuries. © 2011 Wiley‐Liss, Inc. Microsurgery, 2011. |
format | Online Article Text |
id | pubmed-4088328 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Wiley Subscription Services, Inc., A Wiley Company |
record_format | MEDLINE/PubMed |
spelling | pubmed-40883282014-07-09 Effect of sialodacryoadenitis virus infection on axonal regeneration Yu, Vivian M. Mackinnon, Susan E. Hunter, Daniel A Brenner, Michael J. Microsurgery Research Articles The effect of sialodacryoadenitis virus (SDAV) infection on axonal regeneration and functional recovery was investigated in male Lewis rats. Animals underwent unilateral tibial nerve transection, immediate repair, and treatment with either FK506 (treated) or control vehicle (untreated). Serial walking track analyses were performed to assess functional recovery. Nerves were harvested for morphometric analysis on postoperative day 18 after an SDAV outbreak occurred that affected the 12 experimental animals. Histomorphometry and walking track data were compared against 36 historical controls. Rats infected with SDAV demonstrated severely impaired axonal regeneration and diminished functional recovery. Total fiber counts, nerve density, and percent neural tissue were all significantly reduced in infected animals (P < 0.05). Active SDAV infection severely impaired nerve regeneration and negated the positive effect of FK506 on nerve regeneration in rats. Immunosuppressive risks must be weighed carefully against the potential neuroregenerative benefits in the treatment of peripheral nerve injuries. © 2011 Wiley‐Liss, Inc. Microsurgery, 2011. Wiley Subscription Services, Inc., A Wiley Company 2011-08-22 2011-09 /pmc/articles/PMC4088328/ /pubmed/21866574 http://dx.doi.org/10.1002/micr.20914 Text en Copyright © 2011 Wiley‐Liss, Inc. This article is being made freely available through PubMed Central as part of the COVID-19 public health emergency response. It can be used for unrestricted research re-use and analysis in any form or by any means with acknowledgement of the original source, for the duration of the public health emergency. |
spellingShingle | Research Articles Yu, Vivian M. Mackinnon, Susan E. Hunter, Daniel A Brenner, Michael J. Effect of sialodacryoadenitis virus infection on axonal regeneration |
title | Effect of sialodacryoadenitis virus infection on axonal regeneration |
title_full | Effect of sialodacryoadenitis virus infection on axonal regeneration |
title_fullStr | Effect of sialodacryoadenitis virus infection on axonal regeneration |
title_full_unstemmed | Effect of sialodacryoadenitis virus infection on axonal regeneration |
title_short | Effect of sialodacryoadenitis virus infection on axonal regeneration |
title_sort | effect of sialodacryoadenitis virus infection on axonal regeneration |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4088328/ https://www.ncbi.nlm.nih.gov/pubmed/21866574 http://dx.doi.org/10.1002/micr.20914 |
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