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Intra-articular viscosupplementation of hyaluronic acids in an experimental osteoarthritis model()

OBJECTIVE: To analyze, from the immunohistochemical perspective, the effects of hyaluronic acid of different molecular weights in an experimental model of osteoarthritis in rabbits. METHODS: Forty-four male California rabbits were randomly assigned to three different groups (PR, S, and P) and submit...

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Autores principales: Oliveira, Marcello Zaia, Albano, Mauro Batista, Stirma, Guilherme Augusto, Namba, Mario Massatomo, Vidigal, Leandro, Cunha, Luiz Antonio Munhoz da
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5993877/
https://www.ncbi.nlm.nih.gov/pubmed/29892579
http://dx.doi.org/10.1016/j.rboe.2018.03.009
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author Oliveira, Marcello Zaia
Albano, Mauro Batista
Stirma, Guilherme Augusto
Namba, Mario Massatomo
Vidigal, Leandro
Cunha, Luiz Antonio Munhoz da
author_facet Oliveira, Marcello Zaia
Albano, Mauro Batista
Stirma, Guilherme Augusto
Namba, Mario Massatomo
Vidigal, Leandro
Cunha, Luiz Antonio Munhoz da
author_sort Oliveira, Marcello Zaia
collection PubMed
description OBJECTIVE: To analyze, from the immunohistochemical perspective, the effects of hyaluronic acid of different molecular weights in an experimental model of osteoarthritis in rabbits. METHODS: Forty-four male California rabbits were randomly assigned to three different groups (PR, S, and P) and submitted to the resection of the anterior cruciate ligament of the right knee. Three weeks after the surgical procedure, three intra-articular weekly injections were carried out with low-molecular-weight native hyaluronic acid (Hyalgan(®)) to PR group, high molecular weight branched chain hyaluronic acid (Synvisc(®)) to group S, and saline solution 0.9% to group P. All animals were sacrificed 12 weeks after the surgical procedure, and the tibial plateaus of the infiltrated knees were then dissected. Histological sections of cartilage from the tibial plateau support areas were stained with immunohistochemical markers in order to investigate the amount of metalloproteases (MMPs 3 and 13) and their inhibitors (TIMPs 1 and 3). The staining intensity was quantified on a Zeiss Imager.Z2 Metasystems microscope and analyzed by Metafer4 Msearch software. RESULTS: The chondroprotective effect of the hyaluronic acids used in the study was demonstrated when compared to the control group. However, the comparison between them presented no significant statistical difference regarding chondroprotection. CONCLUSION: The injection of saline solution demonstrated signs of OA development, while adding native hyaluronic acid of low molecular weight (Hyalgan(®)) and hyaluronic acid of high molecular weight (Synvisc(®)) protected the articular cartilage in this model of OA.
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spelling pubmed-59938772018-06-11 Intra-articular viscosupplementation of hyaluronic acids in an experimental osteoarthritis model() Oliveira, Marcello Zaia Albano, Mauro Batista Stirma, Guilherme Augusto Namba, Mario Massatomo Vidigal, Leandro Cunha, Luiz Antonio Munhoz da Rev Bras Ortop Original Article OBJECTIVE: To analyze, from the immunohistochemical perspective, the effects of hyaluronic acid of different molecular weights in an experimental model of osteoarthritis in rabbits. METHODS: Forty-four male California rabbits were randomly assigned to three different groups (PR, S, and P) and submitted to the resection of the anterior cruciate ligament of the right knee. Three weeks after the surgical procedure, three intra-articular weekly injections were carried out with low-molecular-weight native hyaluronic acid (Hyalgan(®)) to PR group, high molecular weight branched chain hyaluronic acid (Synvisc(®)) to group S, and saline solution 0.9% to group P. All animals were sacrificed 12 weeks after the surgical procedure, and the tibial plateaus of the infiltrated knees were then dissected. Histological sections of cartilage from the tibial plateau support areas were stained with immunohistochemical markers in order to investigate the amount of metalloproteases (MMPs 3 and 13) and their inhibitors (TIMPs 1 and 3). The staining intensity was quantified on a Zeiss Imager.Z2 Metasystems microscope and analyzed by Metafer4 Msearch software. RESULTS: The chondroprotective effect of the hyaluronic acids used in the study was demonstrated when compared to the control group. However, the comparison between them presented no significant statistical difference regarding chondroprotection. CONCLUSION: The injection of saline solution demonstrated signs of OA development, while adding native hyaluronic acid of low molecular weight (Hyalgan(®)) and hyaluronic acid of high molecular weight (Synvisc(®)) protected the articular cartilage in this model of OA. Elsevier 2018-04-04 /pmc/articles/PMC5993877/ /pubmed/29892579 http://dx.doi.org/10.1016/j.rboe.2018.03.009 Text en © 2018 Published by Elsevier Editora Ltda. on behalf of Sociedade Brasileira de Ortopedia e Traumatologia. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
Oliveira, Marcello Zaia
Albano, Mauro Batista
Stirma, Guilherme Augusto
Namba, Mario Massatomo
Vidigal, Leandro
Cunha, Luiz Antonio Munhoz da
Intra-articular viscosupplementation of hyaluronic acids in an experimental osteoarthritis model()
title Intra-articular viscosupplementation of hyaluronic acids in an experimental osteoarthritis model()
title_full Intra-articular viscosupplementation of hyaluronic acids in an experimental osteoarthritis model()
title_fullStr Intra-articular viscosupplementation of hyaluronic acids in an experimental osteoarthritis model()
title_full_unstemmed Intra-articular viscosupplementation of hyaluronic acids in an experimental osteoarthritis model()
title_short Intra-articular viscosupplementation of hyaluronic acids in an experimental osteoarthritis model()
title_sort intra-articular viscosupplementation of hyaluronic acids in an experimental osteoarthritis model()
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5993877/
https://www.ncbi.nlm.nih.gov/pubmed/29892579
http://dx.doi.org/10.1016/j.rboe.2018.03.009
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