Correlation of Nogo A release with glia scar formation in spinal cord injury
Autor(a) principal: | |
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Data de Publicação: | 2021 |
Outros Autores: | , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Research, Society and Development |
Texto Completo: | https://rsdjournal.org/index.php/rsd/article/view/15688 |
Resumo: | Several axonal growth inhibitors have already been identified following spinal cord injury, the most known being myelin-derived proteins, such as Nogo-A. The present study aimed to correlate the formation of glial scar with the beginning of growth inhibitor, Nogo-A, release in rats previously submitted to compressive spinal cord injury. For this, 12 male and female Wistar rats (250 ± 50g) were divided into 3 groups of 4 animals each, according to the animals' euthanasia time after spinal cord injury (G3 - three days; G5 - five days; G7 - seven days). Spinal cord injuries were induced by means of dorsal laminectomy of the T10 vertebra and epidural compression. Histopathological evaluation and immunoreactivity of the Nogo-A axonal growth inhibitor were performed. It was observed that there was the release of the axonal inhibitor Nogo-A after 24h after the occurrence of spinal cord injury, and that the glial scar must be maintained, in this time interval, in order to guarantee the rebalancing of the post-trauma environment. Thus, it is suggested that the glial scar should be maintained in the acute phase of the lesion, guaranteeing its numerous benefits for the rebalancing of the post-injured environment and, after 24 hours, when the release of the studied axonal growth inhibitor begins, it should be removed. |
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Correlation of Nogo A release with glia scar formation in spinal cord injuryCorrelación de la liberación de Nogo A con la formación de cicatrices gliales en la lesión de la médula espinalCorrelação da liberação do Nogo A com a formação da cicatriz da glia na lesão medularCuraciónNeuroglia,Modelos animales.Modelos animalesHealingNeurogliaAnimal models.Animal modelsCicatrizaçãoNeurogliaModelos animaisModelos animais.Several axonal growth inhibitors have already been identified following spinal cord injury, the most known being myelin-derived proteins, such as Nogo-A. The present study aimed to correlate the formation of glial scar with the beginning of growth inhibitor, Nogo-A, release in rats previously submitted to compressive spinal cord injury. For this, 12 male and female Wistar rats (250 ± 50g) were divided into 3 groups of 4 animals each, according to the animals' euthanasia time after spinal cord injury (G3 - three days; G5 - five days; G7 - seven days). Spinal cord injuries were induced by means of dorsal laminectomy of the T10 vertebra and epidural compression. Histopathological evaluation and immunoreactivity of the Nogo-A axonal growth inhibitor were performed. It was observed that there was the release of the axonal inhibitor Nogo-A after 24h after the occurrence of spinal cord injury, and that the glial scar must be maintained, in this time interval, in order to guarantee the rebalancing of the post-trauma environment. Thus, it is suggested that the glial scar should be maintained in the acute phase of the lesion, guaranteeing its numerous benefits for the rebalancing of the post-injured environment and, after 24 hours, when the release of the studied axonal growth inhibitor begins, it should be removed.Ya se han identificado varios inhibidores del crecimiento axonal después de una lesión de la médula espinal, siendo los más conocidos proteínas derivadas de la mielina, como Nogo-A. El presente estudio tuvo como objetivo correlacionar la formación de cicatrices gliales con el comienzo de la liberación del inhibidor del crecimiento. Axonal Nogo-A en ratas previamente sometidas a lesión medular por compresión. Para ello, se dividieron 12 ratas Wistar macho y hembra (250 ± 50g) en 3 grupos de 4 animales cada uno, según el tiempo de eutanasia de los animales tras la lesión medular (G3 - tres días; G5 - cinco días; G7 - siete días). Las lesiones medulares se indujeron mediante laminectomía dorsal de la vértebra T10 y compresión epidural. Se realizó la evaluación histopatológica y la inmunorreactividad del inhibidor del crecimiento axonal Nogo-A. Se observó que hubo liberación del inhibidor axonal Nogo-A a las 24 h de ocurrida la lesión medular, y que la cicatriz glial debe mantenerse, en este intervalo de tiempo, para garantizar el reequilibrio del postraumatismo. ambiente. Así, se sugiere que la cicatriz glial se mantenga en la fase aguda de la lesión, garantizando sus numerosos beneficios para el reequilibrio del ambiente post-lesionado y, a las 24 horas, cuando comience la liberación del inhibidor del crecimiento axonal estudiado, debería ser eliminado.Diversos inibidores de crescimento axonal já foram identificados acompanhando a lesão medular, sendo as mais conhecidas as proteínas derivadas de mielina, como o Nogo-A. O presente trabalho teve como objetivo correlacionar a formação da cicatriz glial com o início da liberação do inibidor de crescimento axonal Nogo-A em ratos previamente submetidos à lesão medular compressiva. Para isso, 12 ratos Wistar, machos e fêmeas (250 ± 50g), foram divididos em 3 grupos de 4 animais cada, de acordo com o tempo de eutanásia dos animais após a lesão medular (G3 - três dias; G5 - cinco dias; G7 - sete dias). Foi realizada a indução das lesões medulares por meio de laminectomia dorsal da vértebra T10 e compressão epidural. A avaliação histopatológica e da imunorreatividade do inibidor de crescimento axonal Nogo-A foram realizadas. Foi observado que houve a liberação do inibidor axonal Nogo-A a partir de 24h após a ocorrência de lesão medular, e que cicatriz da glia deve ser mantida, nesse intervalo de tempo, para que garanta o reequilíbrio do meio pós-trauma. Dessa forma, sugere-se que a cicatriz glial deve ser mantida na fase aguda da lesão, garantindo seus inúmeros benefícios ao reequilíbrio do ambiente pós-lesionado e, após 24h, quando se inicia a liberação do inibidor de crescimento axonal estudado, esta deve ser removida.Research, Society and Development2021-05-29info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://rsdjournal.org/index.php/rsd/article/view/1568810.33448/rsd-v10i6.15688Research, Society and Development; Vol. 10 No. 6; e25410615688Research, Society and Development; Vol. 10 Núm. 6; e25410615688Research, Society and Development; v. 10 n. 6; e254106156882525-3409reponame:Research, Society and Developmentinstname:Universidade Federal de Itajubá (UNIFEI)instacron:UNIFEIenghttps://rsdjournal.org/index.php/rsd/article/view/15688/14068Copyright (c) 2021 Juliana Casanovas de Carvalho; César Augusto Abreu-Pereira; Lucas Cauê da Silva Assunção; Rosana Costa Casanovas; Ana Lucia Abreu-Silva; Matheus Levi Tajra Feitosahttps://creativecommons.org/licenses/by/4.0info:eu-repo/semantics/openAccessCarvalho, Juliana Casanovas de Abreu-Pereira, César AugustoAssunção, Lucas Cauê da Silva Casanovas, Rosana Costa Abreu-Silva, Ana LuciaFeitosa, Matheus Levi Tajra 2021-06-10T22:51:46Zoai:ojs.pkp.sfu.ca:article/15688Revistahttps://rsdjournal.org/index.php/rsd/indexPUBhttps://rsdjournal.org/index.php/rsd/oairsd.articles@gmail.com2525-34092525-3409opendoar:2024-01-17T09:36:27.282104Research, Society and Development - Universidade Federal de Itajubá (UNIFEI)false |
dc.title.none.fl_str_mv |
Correlation of Nogo A release with glia scar formation in spinal cord injury Correlación de la liberación de Nogo A con la formación de cicatrices gliales en la lesión de la médula espinal Correlação da liberação do Nogo A com a formação da cicatriz da glia na lesão medular |
title |
Correlation of Nogo A release with glia scar formation in spinal cord injury |
spellingShingle |
Correlation of Nogo A release with glia scar formation in spinal cord injury Carvalho, Juliana Casanovas de Curación Neuroglia, Modelos animales. Modelos animales Healing Neuroglia Animal models. Animal models Cicatrização Neuroglia Modelos animais Modelos animais. |
title_short |
Correlation of Nogo A release with glia scar formation in spinal cord injury |
title_full |
Correlation of Nogo A release with glia scar formation in spinal cord injury |
title_fullStr |
Correlation of Nogo A release with glia scar formation in spinal cord injury |
title_full_unstemmed |
Correlation of Nogo A release with glia scar formation in spinal cord injury |
title_sort |
Correlation of Nogo A release with glia scar formation in spinal cord injury |
author |
Carvalho, Juliana Casanovas de |
author_facet |
Carvalho, Juliana Casanovas de Abreu-Pereira, César Augusto Assunção, Lucas Cauê da Silva Casanovas, Rosana Costa Abreu-Silva, Ana Lucia Feitosa, Matheus Levi Tajra |
author_role |
author |
author2 |
Abreu-Pereira, César Augusto Assunção, Lucas Cauê da Silva Casanovas, Rosana Costa Abreu-Silva, Ana Lucia Feitosa, Matheus Levi Tajra |
author2_role |
author author author author author |
dc.contributor.author.fl_str_mv |
Carvalho, Juliana Casanovas de Abreu-Pereira, César Augusto Assunção, Lucas Cauê da Silva Casanovas, Rosana Costa Abreu-Silva, Ana Lucia Feitosa, Matheus Levi Tajra |
dc.subject.por.fl_str_mv |
Curación Neuroglia, Modelos animales. Modelos animales Healing Neuroglia Animal models. Animal models Cicatrização Neuroglia Modelos animais Modelos animais. |
topic |
Curación Neuroglia, Modelos animales. Modelos animales Healing Neuroglia Animal models. Animal models Cicatrização Neuroglia Modelos animais Modelos animais. |
description |
Several axonal growth inhibitors have already been identified following spinal cord injury, the most known being myelin-derived proteins, such as Nogo-A. The present study aimed to correlate the formation of glial scar with the beginning of growth inhibitor, Nogo-A, release in rats previously submitted to compressive spinal cord injury. For this, 12 male and female Wistar rats (250 ± 50g) were divided into 3 groups of 4 animals each, according to the animals' euthanasia time after spinal cord injury (G3 - three days; G5 - five days; G7 - seven days). Spinal cord injuries were induced by means of dorsal laminectomy of the T10 vertebra and epidural compression. Histopathological evaluation and immunoreactivity of the Nogo-A axonal growth inhibitor were performed. It was observed that there was the release of the axonal inhibitor Nogo-A after 24h after the occurrence of spinal cord injury, and that the glial scar must be maintained, in this time interval, in order to guarantee the rebalancing of the post-trauma environment. Thus, it is suggested that the glial scar should be maintained in the acute phase of the lesion, guaranteeing its numerous benefits for the rebalancing of the post-injured environment and, after 24 hours, when the release of the studied axonal growth inhibitor begins, it should be removed. |
publishDate |
2021 |
dc.date.none.fl_str_mv |
2021-05-29 |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
https://rsdjournal.org/index.php/rsd/article/view/15688 10.33448/rsd-v10i6.15688 |
url |
https://rsdjournal.org/index.php/rsd/article/view/15688 |
identifier_str_mv |
10.33448/rsd-v10i6.15688 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
https://rsdjournal.org/index.php/rsd/article/view/15688/14068 |
dc.rights.driver.fl_str_mv |
https://creativecommons.org/licenses/by/4.0 info:eu-repo/semantics/openAccess |
rights_invalid_str_mv |
https://creativecommons.org/licenses/by/4.0 |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.publisher.none.fl_str_mv |
Research, Society and Development |
publisher.none.fl_str_mv |
Research, Society and Development |
dc.source.none.fl_str_mv |
Research, Society and Development; Vol. 10 No. 6; e25410615688 Research, Society and Development; Vol. 10 Núm. 6; e25410615688 Research, Society and Development; v. 10 n. 6; e25410615688 2525-3409 reponame:Research, Society and Development instname:Universidade Federal de Itajubá (UNIFEI) instacron:UNIFEI |
instname_str |
Universidade Federal de Itajubá (UNIFEI) |
instacron_str |
UNIFEI |
institution |
UNIFEI |
reponame_str |
Research, Society and Development |
collection |
Research, Society and Development |
repository.name.fl_str_mv |
Research, Society and Development - Universidade Federal de Itajubá (UNIFEI) |
repository.mail.fl_str_mv |
rsd.articles@gmail.com |
_version_ |
1797052785658691584 |