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Systemic effects of oral tolerance in bone healing

Bone fractures cause acute inflammation that, despite being important for initial repair, may delay the healing of the damaged bone. Parenteral injection of dietary protein has been shown to decrease inflammation and accelerate the repair of skin wounds and other inflammatory pathologies. Thus, our...

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Autores principales: Costa, Bruno Henrique, Rezende, Alisson Kennedy, Costa, Lais, Neves, Gabrielle Fernanda Monteiro, Shimano, Antônio Carlos, de Oliveira Penoni, Álvaro, Carvalho, Claudia Rocha, Costa, Raquel Alves, de Alvarenga, Erika Costa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10113372/
https://www.ncbi.nlm.nih.gov/pubmed/37072616
http://dx.doi.org/10.1038/s41598-023-33591-4
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author Costa, Bruno Henrique
Rezende, Alisson Kennedy
Costa, Lais
Neves, Gabrielle Fernanda Monteiro
Shimano, Antônio Carlos
de Oliveira Penoni, Álvaro
Carvalho, Claudia Rocha
Costa, Raquel Alves
de Alvarenga, Erika Costa
author_facet Costa, Bruno Henrique
Rezende, Alisson Kennedy
Costa, Lais
Neves, Gabrielle Fernanda Monteiro
Shimano, Antônio Carlos
de Oliveira Penoni, Álvaro
Carvalho, Claudia Rocha
Costa, Raquel Alves
de Alvarenga, Erika Costa
author_sort Costa, Bruno Henrique
collection PubMed
description Bone fractures cause acute inflammation that, despite being important for initial repair, may delay the healing of the damaged bone. Parenteral injection of dietary protein has been shown to decrease inflammation and accelerate the repair of skin wounds and other inflammatory pathologies. Thus, our aim was to evaluate whether the intraperitoneal (i.p.) immunization with zein, an abundant protein in rodent chow, would favor bone healing. Wistar rats received i.p. immunization: saline (SG), adjuvant (AG) and zein associated with adjuvant (ZG). Then, a 2 mm of defect bone was performed on the right tibia, and on days 7, 14, 28 and 45 thereafter, analyses were performed. The results showed that the injection of zein reduced inflammation without impairing bone mineralization. Moreover, biomechanical tests demonstrated higher levels of maximum force (N) in ZG, indicating better mechanical resistance in relation to the others. The computerized tomography also indicated lower levels of medullary content in the ZG than in the SG, suggesting the absence of trabeculae in the medullary region in the ZG. These findings suggest that the injection of zein in previously tolerated animals may improve bone repair, leading to mechanically functional bone formation.
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spelling pubmed-101133722023-04-20 Systemic effects of oral tolerance in bone healing Costa, Bruno Henrique Rezende, Alisson Kennedy Costa, Lais Neves, Gabrielle Fernanda Monteiro Shimano, Antônio Carlos de Oliveira Penoni, Álvaro Carvalho, Claudia Rocha Costa, Raquel Alves de Alvarenga, Erika Costa Sci Rep Article Bone fractures cause acute inflammation that, despite being important for initial repair, may delay the healing of the damaged bone. Parenteral injection of dietary protein has been shown to decrease inflammation and accelerate the repair of skin wounds and other inflammatory pathologies. Thus, our aim was to evaluate whether the intraperitoneal (i.p.) immunization with zein, an abundant protein in rodent chow, would favor bone healing. Wistar rats received i.p. immunization: saline (SG), adjuvant (AG) and zein associated with adjuvant (ZG). Then, a 2 mm of defect bone was performed on the right tibia, and on days 7, 14, 28 and 45 thereafter, analyses were performed. The results showed that the injection of zein reduced inflammation without impairing bone mineralization. Moreover, biomechanical tests demonstrated higher levels of maximum force (N) in ZG, indicating better mechanical resistance in relation to the others. The computerized tomography also indicated lower levels of medullary content in the ZG than in the SG, suggesting the absence of trabeculae in the medullary region in the ZG. These findings suggest that the injection of zein in previously tolerated animals may improve bone repair, leading to mechanically functional bone formation. Nature Publishing Group UK 2023-04-18 /pmc/articles/PMC10113372/ /pubmed/37072616 http://dx.doi.org/10.1038/s41598-023-33591-4 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Costa, Bruno Henrique
Rezende, Alisson Kennedy
Costa, Lais
Neves, Gabrielle Fernanda Monteiro
Shimano, Antônio Carlos
de Oliveira Penoni, Álvaro
Carvalho, Claudia Rocha
Costa, Raquel Alves
de Alvarenga, Erika Costa
Systemic effects of oral tolerance in bone healing
title Systemic effects of oral tolerance in bone healing
title_full Systemic effects of oral tolerance in bone healing
title_fullStr Systemic effects of oral tolerance in bone healing
title_full_unstemmed Systemic effects of oral tolerance in bone healing
title_short Systemic effects of oral tolerance in bone healing
title_sort systemic effects of oral tolerance in bone healing
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10113372/
https://www.ncbi.nlm.nih.gov/pubmed/37072616
http://dx.doi.org/10.1038/s41598-023-33591-4
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