Acetylcholine receptors of the neuromuscular junctions present normal distribution after peripheral nerve injury and repair through nerve guidance associated with fibrin biopolymer
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/10.1016/j.injury.2022.11.047 http://hdl.handle.net/11449/248000 |
Resumo: | Peripheral nerve injuries (PNI) lead to alterations in the Agrin-LRP4-MuSK pathway. This results in disaggregation of AChRs and change from epsilon (mature, innervated) to gamma (immature, denervated) subunit. Tubulization technique has been shown to be effective for PNI repair and it also allows the use of adjuvants, such as fibrin biopolymer (FB). This study evaluated the effect of the association of tubulization with FB after PNI on AChRs and associated proteins. Fifty-two adults male Wistar rats were used, distributed in 4 experimental groups: Sham Control (S), Denervated Control (D); Tubulization (TB) and Tubulization + Fibrin Biopolymer (TB+FB). Catwalk was performed every 15 days. Ninety days after surgery the right soleus muscles and ischiatic nerves were submitted to the following analyses: (a) morphological and morphometric analysis of AChRs by confocal microscopy; (b) morphological and morphometric analysis of the ischiatic nerve; (c) protein quantification of AChRs: alpha, gama, and epsilon, of Schwann cells, agrin, LRP4, MuSK, rapsyn, MMP3, MyoD, myogenin, MURF1 and atrogin-1. The main results were about the NMJs that in the TB+FB group presented morphological and morphometric approximation (compactness index; area of the AChRs and motor plate) to the S group. In addition, there were also an increase of S100 and AChRε protein expression and a decrease of MyoD. These positive association resulted in AChRs stabilization that potentiate the neuromuscular regeneration, which strengthens the use of TB for severe injuries repair and the beneficial effect of FB, along with tubulization technique. |
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Acetylcholine receptors of the neuromuscular junctions present normal distribution after peripheral nerve injury and repair through nerve guidance associated with fibrin biopolymerAcetylcholine receptorsFibrin biopolymerNeuromuscular junctionPeripheral nerve injuryPolycaprolactonePeripheral nerve injuries (PNI) lead to alterations in the Agrin-LRP4-MuSK pathway. This results in disaggregation of AChRs and change from epsilon (mature, innervated) to gamma (immature, denervated) subunit. Tubulization technique has been shown to be effective for PNI repair and it also allows the use of adjuvants, such as fibrin biopolymer (FB). This study evaluated the effect of the association of tubulization with FB after PNI on AChRs and associated proteins. Fifty-two adults male Wistar rats were used, distributed in 4 experimental groups: Sham Control (S), Denervated Control (D); Tubulization (TB) and Tubulization + Fibrin Biopolymer (TB+FB). Catwalk was performed every 15 days. Ninety days after surgery the right soleus muscles and ischiatic nerves were submitted to the following analyses: (a) morphological and morphometric analysis of AChRs by confocal microscopy; (b) morphological and morphometric analysis of the ischiatic nerve; (c) protein quantification of AChRs: alpha, gama, and epsilon, of Schwann cells, agrin, LRP4, MuSK, rapsyn, MMP3, MyoD, myogenin, MURF1 and atrogin-1. The main results were about the NMJs that in the TB+FB group presented morphological and morphometric approximation (compactness index; area of the AChRs and motor plate) to the S group. In addition, there were also an increase of S100 and AChRε protein expression and a decrease of MyoD. These positive association resulted in AChRs stabilization that potentiate the neuromuscular regeneration, which strengthens the use of TB for severe injuries repair and the beneficial effect of FB, along with tubulization technique.Medical School São Paulo State University (Unesp), SPDivision of Anatomy Department of Structural and Functional Biology Institute of Biosciences São Paulo State University (Unesp), SPDivision of Biostatistics Department of Biostatistics Vegetal Biology Parasitology and Zoology Institute of Biosciences São Paulo State University (Unesp), SPCenter for the Study of Venoms and Venomous Animals (Cevap) São Paulo State University (Unesp), SPSchool of Mechanical Engineering University of Campinas (Unicamp), SPMedical School São Paulo State University (Unesp), SPDivision of Anatomy Department of Structural and Functional Biology Institute of Biosciences São Paulo State University (Unesp), SPDivision of Biostatistics Department of Biostatistics Vegetal Biology Parasitology and Zoology Institute of Biosciences São Paulo State University (Unesp), SPCenter for the Study of Venoms and Venomous Animals (Cevap) São Paulo State University (Unesp), SPUniversidade Estadual Paulista (UNESP)Universidade Estadual de Campinas (UNICAMP)Leite, Ana Paula Silveira [UNESP]Pinto, Carina Guidi [UNESP]Tibúrcio, Felipe Cantore [UNESP]Muller, Kevin Silva [UNESP]Padovani, Carlos Roberto [UNESP]Barraviera, Benedito [UNESP]Junior, Rui Seabra Ferreira [UNESP]Leal, Claudenete VieiraMatsumura, Cintia Yuri [UNESP]Matheus, Selma Maria Michelin [UNESP]2023-07-29T13:31:44Z2023-07-29T13:31:44Z2023-02-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article345-361http://dx.doi.org/10.1016/j.injury.2022.11.047Injury, v. 54, n. 2, p. 345-361, 2023.1879-02670020-1383http://hdl.handle.net/11449/24800010.1016/j.injury.2022.11.0472-s2.0-85143544360Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengInjuryinfo:eu-repo/semantics/openAccess2024-04-11T15:28:35Zoai:repositorio.unesp.br:11449/248000Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestrepositoriounesp@unesp.bropendoar:29462024-04-11T15:28:35Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
Acetylcholine receptors of the neuromuscular junctions present normal distribution after peripheral nerve injury and repair through nerve guidance associated with fibrin biopolymer |
title |
Acetylcholine receptors of the neuromuscular junctions present normal distribution after peripheral nerve injury and repair through nerve guidance associated with fibrin biopolymer |
spellingShingle |
Acetylcholine receptors of the neuromuscular junctions present normal distribution after peripheral nerve injury and repair through nerve guidance associated with fibrin biopolymer Leite, Ana Paula Silveira [UNESP] Acetylcholine receptors Fibrin biopolymer Neuromuscular junction Peripheral nerve injury Polycaprolactone |
title_short |
Acetylcholine receptors of the neuromuscular junctions present normal distribution after peripheral nerve injury and repair through nerve guidance associated with fibrin biopolymer |
title_full |
Acetylcholine receptors of the neuromuscular junctions present normal distribution after peripheral nerve injury and repair through nerve guidance associated with fibrin biopolymer |
title_fullStr |
Acetylcholine receptors of the neuromuscular junctions present normal distribution after peripheral nerve injury and repair through nerve guidance associated with fibrin biopolymer |
title_full_unstemmed |
Acetylcholine receptors of the neuromuscular junctions present normal distribution after peripheral nerve injury and repair through nerve guidance associated with fibrin biopolymer |
title_sort |
Acetylcholine receptors of the neuromuscular junctions present normal distribution after peripheral nerve injury and repair through nerve guidance associated with fibrin biopolymer |
author |
Leite, Ana Paula Silveira [UNESP] |
author_facet |
Leite, Ana Paula Silveira [UNESP] Pinto, Carina Guidi [UNESP] Tibúrcio, Felipe Cantore [UNESP] Muller, Kevin Silva [UNESP] Padovani, Carlos Roberto [UNESP] Barraviera, Benedito [UNESP] Junior, Rui Seabra Ferreira [UNESP] Leal, Claudenete Vieira Matsumura, Cintia Yuri [UNESP] Matheus, Selma Maria Michelin [UNESP] |
author_role |
author |
author2 |
Pinto, Carina Guidi [UNESP] Tibúrcio, Felipe Cantore [UNESP] Muller, Kevin Silva [UNESP] Padovani, Carlos Roberto [UNESP] Barraviera, Benedito [UNESP] Junior, Rui Seabra Ferreira [UNESP] Leal, Claudenete Vieira Matsumura, Cintia Yuri [UNESP] Matheus, Selma Maria Michelin [UNESP] |
author2_role |
author author author author author author author author author |
dc.contributor.none.fl_str_mv |
Universidade Estadual Paulista (UNESP) Universidade Estadual de Campinas (UNICAMP) |
dc.contributor.author.fl_str_mv |
Leite, Ana Paula Silveira [UNESP] Pinto, Carina Guidi [UNESP] Tibúrcio, Felipe Cantore [UNESP] Muller, Kevin Silva [UNESP] Padovani, Carlos Roberto [UNESP] Barraviera, Benedito [UNESP] Junior, Rui Seabra Ferreira [UNESP] Leal, Claudenete Vieira Matsumura, Cintia Yuri [UNESP] Matheus, Selma Maria Michelin [UNESP] |
dc.subject.por.fl_str_mv |
Acetylcholine receptors Fibrin biopolymer Neuromuscular junction Peripheral nerve injury Polycaprolactone |
topic |
Acetylcholine receptors Fibrin biopolymer Neuromuscular junction Peripheral nerve injury Polycaprolactone |
description |
Peripheral nerve injuries (PNI) lead to alterations in the Agrin-LRP4-MuSK pathway. This results in disaggregation of AChRs and change from epsilon (mature, innervated) to gamma (immature, denervated) subunit. Tubulization technique has been shown to be effective for PNI repair and it also allows the use of adjuvants, such as fibrin biopolymer (FB). This study evaluated the effect of the association of tubulization with FB after PNI on AChRs and associated proteins. Fifty-two adults male Wistar rats were used, distributed in 4 experimental groups: Sham Control (S), Denervated Control (D); Tubulization (TB) and Tubulization + Fibrin Biopolymer (TB+FB). Catwalk was performed every 15 days. Ninety days after surgery the right soleus muscles and ischiatic nerves were submitted to the following analyses: (a) morphological and morphometric analysis of AChRs by confocal microscopy; (b) morphological and morphometric analysis of the ischiatic nerve; (c) protein quantification of AChRs: alpha, gama, and epsilon, of Schwann cells, agrin, LRP4, MuSK, rapsyn, MMP3, MyoD, myogenin, MURF1 and atrogin-1. The main results were about the NMJs that in the TB+FB group presented morphological and morphometric approximation (compactness index; area of the AChRs and motor plate) to the S group. In addition, there were also an increase of S100 and AChRε protein expression and a decrease of MyoD. These positive association resulted in AChRs stabilization that potentiate the neuromuscular regeneration, which strengthens the use of TB for severe injuries repair and the beneficial effect of FB, along with tubulization technique. |
publishDate |
2023 |
dc.date.none.fl_str_mv |
2023-07-29T13:31:44Z 2023-07-29T13:31:44Z 2023-02-01 |
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/10.1016/j.injury.2022.11.047 Injury, v. 54, n. 2, p. 345-361, 2023. 1879-0267 0020-1383 http://hdl.handle.net/11449/248000 10.1016/j.injury.2022.11.047 2-s2.0-85143544360 |
url |
http://dx.doi.org/10.1016/j.injury.2022.11.047 http://hdl.handle.net/11449/248000 |
identifier_str_mv |
Injury, v. 54, n. 2, p. 345-361, 2023. 1879-0267 0020-1383 10.1016/j.injury.2022.11.047 2-s2.0-85143544360 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Injury |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
345-361 |
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 |
repositoriounesp@unesp.br |
_version_ |
1834483919773237248 |