Neuroregeneration and immune response after neurorrhaphy are improved with the use of heterologous fibrin biopolymer in addition to suture repair alone
Autor(a) principal: | |
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Data de Publicação: | 2023 |
Outros Autores: | , , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNESP |
Texto Completo: | http://dx.doi.org/10.1002/mus.27815 http://hdl.handle.net/11449/248561 |
Resumo: | Introduction/Aims: Peripheral nerve injuries result in impaired neuromuscular interactions, leading to morphological and functional alterations. Adjuvant suture repair methods have been used to improve nerve regeneration and modulate the immune response. Heterologous fibrin biopolymer (HFB), a scaffold with adhesive properties, plays a critical role in tissue repair. The aim of this study is to evaluate neuroregeneration and immune response focusing on neuromuscular recovery, using suture-associated HFB for sciatic nerve repair. Methods: Forty adult male Wistar rats were distributed into four groups (n = 10): C (control), only sciatic nerve location; D (denervated), neurotmesis and 6-mm gap removal and fixation stumps in subcutaneous tissue; S (suture), neurotmesis followed by suture; and SB (suture + HFB), neurotmesis followed by suture and HFB. Analysis of M2 macrophages (CD206+), as well as the morphology and morphometry of nerves, soleus muscle, and neuromuscular junctions (NMJs), were performed at 7 and 30 days after surgery. Results: The SB group had the highest M2 macrophage area in both periods. After 7 days, SB was the only group similar to the C group regarding the number of axons; furthermore, after 30 days, the SB group was closer to the C group concerning blood vessel and central myonuclear numbers, NMJ angle, and connective tissue volume. After 7 days, increases in nerve area, as well as the number and area of blood vessels, were also observed in SB. Discussion: HFB potentiates the immune response, increases axonal regeneration, induces angiogenesis, prevents severe muscle degeneration, and assists in NMJ recovery. In conclusion, suture-associated HFB has major implications for improved peripheral nerve repair. |
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Neuroregeneration and immune response after neurorrhaphy are improved with the use of heterologous fibrin biopolymer in addition to suture repair aloneheterologous fibrin sealantimmune responsenerve regenerationneuromuscular junctionperipheral nerve injuryIntroduction/Aims: Peripheral nerve injuries result in impaired neuromuscular interactions, leading to morphological and functional alterations. Adjuvant suture repair methods have been used to improve nerve regeneration and modulate the immune response. Heterologous fibrin biopolymer (HFB), a scaffold with adhesive properties, plays a critical role in tissue repair. The aim of this study is to evaluate neuroregeneration and immune response focusing on neuromuscular recovery, using suture-associated HFB for sciatic nerve repair. Methods: Forty adult male Wistar rats were distributed into four groups (n = 10): C (control), only sciatic nerve location; D (denervated), neurotmesis and 6-mm gap removal and fixation stumps in subcutaneous tissue; S (suture), neurotmesis followed by suture; and SB (suture + HFB), neurotmesis followed by suture and HFB. Analysis of M2 macrophages (CD206+), as well as the morphology and morphometry of nerves, soleus muscle, and neuromuscular junctions (NMJs), were performed at 7 and 30 days after surgery. Results: The SB group had the highest M2 macrophage area in both periods. After 7 days, SB was the only group similar to the C group regarding the number of axons; furthermore, after 30 days, the SB group was closer to the C group concerning blood vessel and central myonuclear numbers, NMJ angle, and connective tissue volume. After 7 days, increases in nerve area, as well as the number and area of blood vessels, were also observed in SB. Discussion: HFB potentiates the immune response, increases axonal regeneration, induces angiogenesis, prevents severe muscle degeneration, and assists in NMJ recovery. In conclusion, suture-associated HFB has major implications for improved peripheral nerve repair.Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)São Paulo State University (Unesp) Medical School, São PauloDivision of Anatomy Department of Structural and Functional Biology São Paulo State University (Unesp), Institute of Biosciences, São PauloCenter for the Study of Venoms and Venomous Animals (Cevap) São Paulo State University (Unesp), São PauloDivision of Biostatistics Department of Biodiversity and Biostatistics São Paulo State University (Unesp) Institute of Biosciences, São PauloSão Paulo State University (Unesp) Medical School, São PauloDivision of Anatomy Department of Structural and Functional Biology São Paulo State University (Unesp), Institute of Biosciences, São PauloCenter for the Study of Venoms and Venomous Animals (Cevap) São Paulo State University (Unesp), São PauloDivision of Biostatistics Department of Biodiversity and Biostatistics São Paulo State University (Unesp) Institute of Biosciences, São PauloFAPESP: 17/06472-2CAPES: Finance Code 001Universidade Estadual Paulista (UNESP)Tibúrcio, Felipe Cantore [UNESP]Muller, Kevin Silva [UNESP]Leite, Ana Paula Silveira [UNESP]de Oliveira, Igor Rodrigues Araújo [UNESP]Barraviera, Benedito [UNESP]Ferreira, Rui Seabra [UNESP]Padovani, Carlos Roberto [UNESP]Pinto, Carina Guidi [UNESP]Matheus, Selma Maria Michelin [UNESP]2023-07-29T13:47:21Z2023-07-29T13:47:21Z2023-06-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article522-536http://dx.doi.org/10.1002/mus.27815Muscle and Nerve, v. 67, n. 6, p. 522-536, 2023.1097-45980148-639Xhttp://hdl.handle.net/11449/24856110.1002/mus.278152-s2.0-85150817003Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengMuscle and Nerveinfo:eu-repo/semantics/openAccess2024-04-11T15:28:35Zoai:repositorio.unesp.br:11449/248561Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-06T00:13:48.329027Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
Neuroregeneration and immune response after neurorrhaphy are improved with the use of heterologous fibrin biopolymer in addition to suture repair alone |
title |
Neuroregeneration and immune response after neurorrhaphy are improved with the use of heterologous fibrin biopolymer in addition to suture repair alone |
spellingShingle |
Neuroregeneration and immune response after neurorrhaphy are improved with the use of heterologous fibrin biopolymer in addition to suture repair alone Tibúrcio, Felipe Cantore [UNESP] heterologous fibrin sealant immune response nerve regeneration neuromuscular junction peripheral nerve injury |
title_short |
Neuroregeneration and immune response after neurorrhaphy are improved with the use of heterologous fibrin biopolymer in addition to suture repair alone |
title_full |
Neuroregeneration and immune response after neurorrhaphy are improved with the use of heterologous fibrin biopolymer in addition to suture repair alone |
title_fullStr |
Neuroregeneration and immune response after neurorrhaphy are improved with the use of heterologous fibrin biopolymer in addition to suture repair alone |
title_full_unstemmed |
Neuroregeneration and immune response after neurorrhaphy are improved with the use of heterologous fibrin biopolymer in addition to suture repair alone |
title_sort |
Neuroregeneration and immune response after neurorrhaphy are improved with the use of heterologous fibrin biopolymer in addition to suture repair alone |
author |
Tibúrcio, Felipe Cantore [UNESP] |
author_facet |
Tibúrcio, Felipe Cantore [UNESP] Muller, Kevin Silva [UNESP] Leite, Ana Paula Silveira [UNESP] de Oliveira, Igor Rodrigues Araújo [UNESP] Barraviera, Benedito [UNESP] Ferreira, Rui Seabra [UNESP] Padovani, Carlos Roberto [UNESP] Pinto, Carina Guidi [UNESP] Matheus, Selma Maria Michelin [UNESP] |
author_role |
author |
author2 |
Muller, Kevin Silva [UNESP] Leite, Ana Paula Silveira [UNESP] de Oliveira, Igor Rodrigues Araújo [UNESP] Barraviera, Benedito [UNESP] Ferreira, Rui Seabra [UNESP] Padovani, Carlos Roberto [UNESP] Pinto, Carina Guidi [UNESP] Matheus, Selma Maria Michelin [UNESP] |
author2_role |
author author author author author author author author |
dc.contributor.none.fl_str_mv |
Universidade Estadual Paulista (UNESP) |
dc.contributor.author.fl_str_mv |
Tibúrcio, Felipe Cantore [UNESP] Muller, Kevin Silva [UNESP] Leite, Ana Paula Silveira [UNESP] de Oliveira, Igor Rodrigues Araújo [UNESP] Barraviera, Benedito [UNESP] Ferreira, Rui Seabra [UNESP] Padovani, Carlos Roberto [UNESP] Pinto, Carina Guidi [UNESP] Matheus, Selma Maria Michelin [UNESP] |
dc.subject.por.fl_str_mv |
heterologous fibrin sealant immune response nerve regeneration neuromuscular junction peripheral nerve injury |
topic |
heterologous fibrin sealant immune response nerve regeneration neuromuscular junction peripheral nerve injury |
description |
Introduction/Aims: Peripheral nerve injuries result in impaired neuromuscular interactions, leading to morphological and functional alterations. Adjuvant suture repair methods have been used to improve nerve regeneration and modulate the immune response. Heterologous fibrin biopolymer (HFB), a scaffold with adhesive properties, plays a critical role in tissue repair. The aim of this study is to evaluate neuroregeneration and immune response focusing on neuromuscular recovery, using suture-associated HFB for sciatic nerve repair. Methods: Forty adult male Wistar rats were distributed into four groups (n = 10): C (control), only sciatic nerve location; D (denervated), neurotmesis and 6-mm gap removal and fixation stumps in subcutaneous tissue; S (suture), neurotmesis followed by suture; and SB (suture + HFB), neurotmesis followed by suture and HFB. Analysis of M2 macrophages (CD206+), as well as the morphology and morphometry of nerves, soleus muscle, and neuromuscular junctions (NMJs), were performed at 7 and 30 days after surgery. Results: The SB group had the highest M2 macrophage area in both periods. After 7 days, SB was the only group similar to the C group regarding the number of axons; furthermore, after 30 days, the SB group was closer to the C group concerning blood vessel and central myonuclear numbers, NMJ angle, and connective tissue volume. After 7 days, increases in nerve area, as well as the number and area of blood vessels, were also observed in SB. Discussion: HFB potentiates the immune response, increases axonal regeneration, induces angiogenesis, prevents severe muscle degeneration, and assists in NMJ recovery. In conclusion, suture-associated HFB has major implications for improved peripheral nerve repair. |
publishDate |
2023 |
dc.date.none.fl_str_mv |
2023-07-29T13:47:21Z 2023-07-29T13:47:21Z 2023-06-01 |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://dx.doi.org/10.1002/mus.27815 Muscle and Nerve, v. 67, n. 6, p. 522-536, 2023. 1097-4598 0148-639X http://hdl.handle.net/11449/248561 10.1002/mus.27815 2-s2.0-85150817003 |
url |
http://dx.doi.org/10.1002/mus.27815 http://hdl.handle.net/11449/248561 |
identifier_str_mv |
Muscle and Nerve, v. 67, n. 6, p. 522-536, 2023. 1097-4598 0148-639X 10.1002/mus.27815 2-s2.0-85150817003 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Muscle and Nerve |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
522-536 |
dc.source.none.fl_str_mv |
Scopus reponame:Repositório Institucional da UNESP instname:Universidade Estadual Paulista (UNESP) instacron:UNESP |
instname_str |
Universidade Estadual Paulista (UNESP) |
instacron_str |
UNESP |
institution |
UNESP |
reponame_str |
Repositório Institucional da UNESP |
collection |
Repositório Institucional da UNESP |
repository.name.fl_str_mv |
Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP) |
repository.mail.fl_str_mv |
|
_version_ |
1808129597922869248 |