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Experimental rat model for cervical compressive myelopathy

Previously, a rat model of chronic compressive myelopathy that uses a water-absorbing polymer inserted under a spinal lamina was reported. However, the best size and coefficient of expansion of the polymer sheet have not yet been established. The aim of the present study was to optimize these proper...

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Autores principales: Ijima, Yasushi, Furuya, Takeo, Koda, Masao, Matsuura, Yusuke, Saito, Junya, Kitamura, Mitsuhiro, Miyamoto, Takuya, Orita, Sumihisa, Inage, Kazuhide, Suzuki, Takane, Yamazaki, Masashi, Ohtori, Seiji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5704668/
https://www.ncbi.nlm.nih.gov/pubmed/28957944
http://dx.doi.org/10.1097/WNR.0000000000000907
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author Ijima, Yasushi
Furuya, Takeo
Koda, Masao
Matsuura, Yusuke
Saito, Junya
Kitamura, Mitsuhiro
Miyamoto, Takuya
Orita, Sumihisa
Inage, Kazuhide
Suzuki, Takane
Yamazaki, Masashi
Ohtori, Seiji
author_facet Ijima, Yasushi
Furuya, Takeo
Koda, Masao
Matsuura, Yusuke
Saito, Junya
Kitamura, Mitsuhiro
Miyamoto, Takuya
Orita, Sumihisa
Inage, Kazuhide
Suzuki, Takane
Yamazaki, Masashi
Ohtori, Seiji
author_sort Ijima, Yasushi
collection PubMed
description Previously, a rat model of chronic compressive myelopathy that uses a water-absorbing polymer inserted under a spinal lamina was reported. However, the best size and coefficient of expansion of the polymer sheet have not yet been established. The aim of the present study was to optimize these properties in an ideal rat model of cervical compressive myelopathy. Thirty rats were used in this study. A sheet of water-absorbing polymer was inserted under the cervical laminae. Rats were divided randomly into five experimental groups by the expansion rate (350 or 200%) and thickness (0.5 or 0.7 mm) and the control. After the surgery, the severity of paralysis was evaluated for 12 weeks. At 12 weeks after the surgery, cresyl violet staining was performed to assess the number of motor neurons in the anterior horn at the C4/C5 segment and Luxol Fast Blue staining was performed to assess demyelination in the corticospinal tract at the C7 segment. ‘Slow-progressive’ paralysis appeared at 4–8 weeks postoperatively in rat models using sheets with 200% expansion. By contrast, only temporary paralysis was observed in rat models using sheets with 350% expansion. A loss of motor neurons in the anterior horn was observed in all groups, except for the control. Demyelination in the corticospinal tract was observed in rat models using sheets with 200% expansion, but not rat models using sheets with 350% expansion. A polymer sheet that expands its volume by 200% is an ideal material for rat models of cervical compressive myelopathy.
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spelling pubmed-57046682017-12-11 Experimental rat model for cervical compressive myelopathy Ijima, Yasushi Furuya, Takeo Koda, Masao Matsuura, Yusuke Saito, Junya Kitamura, Mitsuhiro Miyamoto, Takuya Orita, Sumihisa Inage, Kazuhide Suzuki, Takane Yamazaki, Masashi Ohtori, Seiji Neuroreport Degeneration and Repair Previously, a rat model of chronic compressive myelopathy that uses a water-absorbing polymer inserted under a spinal lamina was reported. However, the best size and coefficient of expansion of the polymer sheet have not yet been established. The aim of the present study was to optimize these properties in an ideal rat model of cervical compressive myelopathy. Thirty rats were used in this study. A sheet of water-absorbing polymer was inserted under the cervical laminae. Rats were divided randomly into five experimental groups by the expansion rate (350 or 200%) and thickness (0.5 or 0.7 mm) and the control. After the surgery, the severity of paralysis was evaluated for 12 weeks. At 12 weeks after the surgery, cresyl violet staining was performed to assess the number of motor neurons in the anterior horn at the C4/C5 segment and Luxol Fast Blue staining was performed to assess demyelination in the corticospinal tract at the C7 segment. ‘Slow-progressive’ paralysis appeared at 4–8 weeks postoperatively in rat models using sheets with 200% expansion. By contrast, only temporary paralysis was observed in rat models using sheets with 350% expansion. A loss of motor neurons in the anterior horn was observed in all groups, except for the control. Demyelination in the corticospinal tract was observed in rat models using sheets with 200% expansion, but not rat models using sheets with 350% expansion. A polymer sheet that expands its volume by 200% is an ideal material for rat models of cervical compressive myelopathy. Lippincott Williams & Wilkins 2017-12-13 2017-11-15 /pmc/articles/PMC5704668/ /pubmed/28957944 http://dx.doi.org/10.1097/WNR.0000000000000907 Text en Copyright © 2017 The Author(s). Published by Wolters Kluwer Health, Inc. This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (http://creativecommons.org/licenses/by-nc-nd/4.0/) (CCBY-NC-ND), where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc-nd/4.0/
spellingShingle Degeneration and Repair
Ijima, Yasushi
Furuya, Takeo
Koda, Masao
Matsuura, Yusuke
Saito, Junya
Kitamura, Mitsuhiro
Miyamoto, Takuya
Orita, Sumihisa
Inage, Kazuhide
Suzuki, Takane
Yamazaki, Masashi
Ohtori, Seiji
Experimental rat model for cervical compressive myelopathy
title Experimental rat model for cervical compressive myelopathy
title_full Experimental rat model for cervical compressive myelopathy
title_fullStr Experimental rat model for cervical compressive myelopathy
title_full_unstemmed Experimental rat model for cervical compressive myelopathy
title_short Experimental rat model for cervical compressive myelopathy
title_sort experimental rat model for cervical compressive myelopathy
topic Degeneration and Repair
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5704668/
https://www.ncbi.nlm.nih.gov/pubmed/28957944
http://dx.doi.org/10.1097/WNR.0000000000000907
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