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Development and characterization of an intra-articular fracture mediated model of post-traumatic osteoarthritis
PURPOSE: This study aimed to develop and characterize a closed intra-articular fracture (IAF) mediated post-traumatic osteoarthritis (PTOA) model in rats to serve as a testbed for putative disease modifying interventions. METHODS: Male rats were subject to a 0 Joule (J), 1 J, 3 J, or 5 J blunt-force...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10317931/ https://www.ncbi.nlm.nih.gov/pubmed/37400744 http://dx.doi.org/10.1186/s40634-023-00625-9 |
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author | Valerio, Michael S. Pace, William A. Dolan, Connor P. Edwards, Jorge B. Janakiram, Naveena B. Potter, Benjamin K. Dearth, Christopher L. Goldman, Stephen M. |
author_facet | Valerio, Michael S. Pace, William A. Dolan, Connor P. Edwards, Jorge B. Janakiram, Naveena B. Potter, Benjamin K. Dearth, Christopher L. Goldman, Stephen M. |
author_sort | Valerio, Michael S. |
collection | PubMed |
description | PURPOSE: This study aimed to develop and characterize a closed intra-articular fracture (IAF) mediated post-traumatic osteoarthritis (PTOA) model in rats to serve as a testbed for putative disease modifying interventions. METHODS: Male rats were subject to a 0 Joule (J), 1 J, 3 J, or 5 J blunt-force impact to the lateral aspect of the knee and allowed to heal for 14 and 56 days. Micro-CT was performed at time of injury and at the specified endpoints to assess bone morphometry and bone mineral density measurements. Cytokines and osteochondral degradation markers were assayed from serum and synovial fluid via immunoassays. Histopathological analyses were performed on decalcified tissues and assessed for evidence of osteochondral degradation. RESULTS: High-energy (5 J) blunt impacts consistently induced IAF to the proximal tibia, distal femur, or both while lower energy (1 J and 3 J) impacts did not. CCL2 was found to be elevated in the synovial fluid of rats with IAF at both 14- and 56-days post-injury while COMP and NTX-1 were upregulated chronically relative to sham controls. Histological analysis showed increased immune cell infiltration, increased osteoclasts and osteochondral degradation with IAF relative to sham. CONCLUSION: Based on results from the current study, our data indicates that a 5 J blunt-forced impact adequately and consistently induces hallmark osteoarthritic changes to the articular surface and subchondral bone at 56 days after IAF. Marked development of PTOA pathobiology suggest this model will provide a robust testbed for screening putative disease modifying interventions that might be translated to the clinic for militarily relevant, high-energy joint injuries. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40634-023-00625-9. |
format | Online Article Text |
id | pubmed-10317931 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-103179312023-07-05 Development and characterization of an intra-articular fracture mediated model of post-traumatic osteoarthritis Valerio, Michael S. Pace, William A. Dolan, Connor P. Edwards, Jorge B. Janakiram, Naveena B. Potter, Benjamin K. Dearth, Christopher L. Goldman, Stephen M. J Exp Orthop Original Paper PURPOSE: This study aimed to develop and characterize a closed intra-articular fracture (IAF) mediated post-traumatic osteoarthritis (PTOA) model in rats to serve as a testbed for putative disease modifying interventions. METHODS: Male rats were subject to a 0 Joule (J), 1 J, 3 J, or 5 J blunt-force impact to the lateral aspect of the knee and allowed to heal for 14 and 56 days. Micro-CT was performed at time of injury and at the specified endpoints to assess bone morphometry and bone mineral density measurements. Cytokines and osteochondral degradation markers were assayed from serum and synovial fluid via immunoassays. Histopathological analyses were performed on decalcified tissues and assessed for evidence of osteochondral degradation. RESULTS: High-energy (5 J) blunt impacts consistently induced IAF to the proximal tibia, distal femur, or both while lower energy (1 J and 3 J) impacts did not. CCL2 was found to be elevated in the synovial fluid of rats with IAF at both 14- and 56-days post-injury while COMP and NTX-1 were upregulated chronically relative to sham controls. Histological analysis showed increased immune cell infiltration, increased osteoclasts and osteochondral degradation with IAF relative to sham. CONCLUSION: Based on results from the current study, our data indicates that a 5 J blunt-forced impact adequately and consistently induces hallmark osteoarthritic changes to the articular surface and subchondral bone at 56 days after IAF. Marked development of PTOA pathobiology suggest this model will provide a robust testbed for screening putative disease modifying interventions that might be translated to the clinic for militarily relevant, high-energy joint injuries. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40634-023-00625-9. Springer Berlin Heidelberg 2023-07-04 /pmc/articles/PMC10317931/ /pubmed/37400744 http://dx.doi.org/10.1186/s40634-023-00625-9 Text en © This is a U.S. Government work and not under copyright protection in the US; foreign copyright protection may apply 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 | Original Paper Valerio, Michael S. Pace, William A. Dolan, Connor P. Edwards, Jorge B. Janakiram, Naveena B. Potter, Benjamin K. Dearth, Christopher L. Goldman, Stephen M. Development and characterization of an intra-articular fracture mediated model of post-traumatic osteoarthritis |
title | Development and characterization of an intra-articular fracture mediated model of post-traumatic osteoarthritis |
title_full | Development and characterization of an intra-articular fracture mediated model of post-traumatic osteoarthritis |
title_fullStr | Development and characterization of an intra-articular fracture mediated model of post-traumatic osteoarthritis |
title_full_unstemmed | Development and characterization of an intra-articular fracture mediated model of post-traumatic osteoarthritis |
title_short | Development and characterization of an intra-articular fracture mediated model of post-traumatic osteoarthritis |
title_sort | development and characterization of an intra-articular fracture mediated model of post-traumatic osteoarthritis |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10317931/ https://www.ncbi.nlm.nih.gov/pubmed/37400744 http://dx.doi.org/10.1186/s40634-023-00625-9 |
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