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Microsurgical reconstruction affects the outcome in a translational mouse model for Achilles tendon healing

BACKGROUND: Animal models are one of the first steps in translation of basic science findings to clinical practice. For tendon healing research, transgenic mouse models are important to advance therapeutic strategies. However, the small size of the structures complicates surgical approaches, histolo...

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Autores principales: Michel, Philipp A., Kronenberg, Daniel, Neu, Gertje, Stolberg-Stolberg, Josef, Frank, Andre, Pap, Thomas, Langer, Martin, Fehr, Michael, Raschke, Michael J., Stange, Richard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Chinese Speaking Orthopaedic Society 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7260609/
https://www.ncbi.nlm.nih.gov/pubmed/32489862
http://dx.doi.org/10.1016/j.jot.2020.04.003
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author Michel, Philipp A.
Kronenberg, Daniel
Neu, Gertje
Stolberg-Stolberg, Josef
Frank, Andre
Pap, Thomas
Langer, Martin
Fehr, Michael
Raschke, Michael J.
Stange, Richard
author_facet Michel, Philipp A.
Kronenberg, Daniel
Neu, Gertje
Stolberg-Stolberg, Josef
Frank, Andre
Pap, Thomas
Langer, Martin
Fehr, Michael
Raschke, Michael J.
Stange, Richard
author_sort Michel, Philipp A.
collection PubMed
description BACKGROUND: Animal models are one of the first steps in translation of basic science findings to clinical practice. For tendon healing research, transgenic mouse models are important to advance therapeutic strategies. However, the small size of the structures complicates surgical approaches, histological assessment, and biomechanical testing. In addition, available models are not standardized and difficult to compare. How surgery itself affects the healing outcome has not been investigated yet. The focus of the study was to develop a procedure that includes a transection and microsurgical reconstruction of the Achilles tendon but, unlike other models, preserves the sciatic nerve. We wanted to examine how distinct parts of the technique influenced healing. METHODS: For this animal model study, we used 96 wild-type male C57BL/6 mice aged 8–12 weeks. We evaluated different suture techniques and macroscopically confirmed the optimal combination of suture material and technique to minimize tendon gap formation. A key element is the detailed, step-by-step illustration of the surgery. In addition, we assessed histological (Herovici and Alcian blue staining) outcome parameters at 1–16 weeks postoperatively. Microcomputed tomography (micro-CT) was performed to measure the bone volume of heterotopic ossifications (HOs). Biomechanical analyses were carried out using a viscoelastic protocol on the biomechanical testing machine LM1. RESULTS: A modified 4-strand suture combined with a cerclage for immobilization without transection of the sciatic nerve reliably eliminated gap formation. The maximal dorsal extension of the hindlimb at the upper ankle joint from the equinus position (limited by the immobilization cerclage) increased over time postoperatively (operation: 28.8 ± 2.2°; 1 week: 54 ± 36°; 6 weeks: 80 ± 11.7°; 16 weeks: 96 ± 15.8°, p > 0.05). Histological staining revealed a maturation of collagen fibres within 6 weeks, whereas masses of cartilage were visible throughout the healing period. Micro-CT scans detected the development of HOs starting at 4 weeks and further progression at 6 and 16 weeks (bone volume, 4 weeks: 0.07604 ± 0.05286 mm(3); 6 weeks: 0.50682 ± 0.68841 mm(3); 16 weeks: 2.36027 ± 0.85202 mm(3), p > 0.001). In-depth micro-CT analysis of the different surgical elements revealed that an injury of the tendon is a key factor for the development of HOs. Immobilization alone does not trigger HOs. Biomechanical properties of repaired tendons were greatly altered and remained inferior 6 weeks after surgery. CONCLUSION: With this study, we demonstrated that the microsurgical technique greatly influences the short- and longer-term healing outcome. When the sciatic nerve is preserved, the best surgical reconstruction of the tendon defect is achieved by a 4-strand core suture in combination with a tibiofibular cerclage for postoperative immobilization. The cerclage promotes a gradual increase in the range of motion of the upper ankle joint, comparable with an early mobilization rehabilitation protocol. HO, as a key mechanism for poor tendon healing, is progressive and can be monitored early in the model. THE TRANSLATIONAL POTENTIAL OF THIS ARTICLE: The study enhances the understanding of model dependent factors of healing. The described reconstruction technique provides a reproducible and translational rodent model for future Achilles tendon healing research. In combination with transgenic strains, it can be facilitated to advance therapeutic strategies to improve the clinical results of tendon injuries.
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spelling pubmed-72606092020-06-01 Microsurgical reconstruction affects the outcome in a translational mouse model for Achilles tendon healing Michel, Philipp A. Kronenberg, Daniel Neu, Gertje Stolberg-Stolberg, Josef Frank, Andre Pap, Thomas Langer, Martin Fehr, Michael Raschke, Michael J. Stange, Richard J Orthop Translat Original Article BACKGROUND: Animal models are one of the first steps in translation of basic science findings to clinical practice. For tendon healing research, transgenic mouse models are important to advance therapeutic strategies. However, the small size of the structures complicates surgical approaches, histological assessment, and biomechanical testing. In addition, available models are not standardized and difficult to compare. How surgery itself affects the healing outcome has not been investigated yet. The focus of the study was to develop a procedure that includes a transection and microsurgical reconstruction of the Achilles tendon but, unlike other models, preserves the sciatic nerve. We wanted to examine how distinct parts of the technique influenced healing. METHODS: For this animal model study, we used 96 wild-type male C57BL/6 mice aged 8–12 weeks. We evaluated different suture techniques and macroscopically confirmed the optimal combination of suture material and technique to minimize tendon gap formation. A key element is the detailed, step-by-step illustration of the surgery. In addition, we assessed histological (Herovici and Alcian blue staining) outcome parameters at 1–16 weeks postoperatively. Microcomputed tomography (micro-CT) was performed to measure the bone volume of heterotopic ossifications (HOs). Biomechanical analyses were carried out using a viscoelastic protocol on the biomechanical testing machine LM1. RESULTS: A modified 4-strand suture combined with a cerclage for immobilization without transection of the sciatic nerve reliably eliminated gap formation. The maximal dorsal extension of the hindlimb at the upper ankle joint from the equinus position (limited by the immobilization cerclage) increased over time postoperatively (operation: 28.8 ± 2.2°; 1 week: 54 ± 36°; 6 weeks: 80 ± 11.7°; 16 weeks: 96 ± 15.8°, p > 0.05). Histological staining revealed a maturation of collagen fibres within 6 weeks, whereas masses of cartilage were visible throughout the healing period. Micro-CT scans detected the development of HOs starting at 4 weeks and further progression at 6 and 16 weeks (bone volume, 4 weeks: 0.07604 ± 0.05286 mm(3); 6 weeks: 0.50682 ± 0.68841 mm(3); 16 weeks: 2.36027 ± 0.85202 mm(3), p > 0.001). In-depth micro-CT analysis of the different surgical elements revealed that an injury of the tendon is a key factor for the development of HOs. Immobilization alone does not trigger HOs. Biomechanical properties of repaired tendons were greatly altered and remained inferior 6 weeks after surgery. CONCLUSION: With this study, we demonstrated that the microsurgical technique greatly influences the short- and longer-term healing outcome. When the sciatic nerve is preserved, the best surgical reconstruction of the tendon defect is achieved by a 4-strand core suture in combination with a tibiofibular cerclage for postoperative immobilization. The cerclage promotes a gradual increase in the range of motion of the upper ankle joint, comparable with an early mobilization rehabilitation protocol. HO, as a key mechanism for poor tendon healing, is progressive and can be monitored early in the model. THE TRANSLATIONAL POTENTIAL OF THIS ARTICLE: The study enhances the understanding of model dependent factors of healing. The described reconstruction technique provides a reproducible and translational rodent model for future Achilles tendon healing research. In combination with transgenic strains, it can be facilitated to advance therapeutic strategies to improve the clinical results of tendon injuries. Chinese Speaking Orthopaedic Society 2020-05-11 /pmc/articles/PMC7260609/ /pubmed/32489862 http://dx.doi.org/10.1016/j.jot.2020.04.003 Text en © 2020 The Author(s) 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
Michel, Philipp A.
Kronenberg, Daniel
Neu, Gertje
Stolberg-Stolberg, Josef
Frank, Andre
Pap, Thomas
Langer, Martin
Fehr, Michael
Raschke, Michael J.
Stange, Richard
Microsurgical reconstruction affects the outcome in a translational mouse model for Achilles tendon healing
title Microsurgical reconstruction affects the outcome in a translational mouse model for Achilles tendon healing
title_full Microsurgical reconstruction affects the outcome in a translational mouse model for Achilles tendon healing
title_fullStr Microsurgical reconstruction affects the outcome in a translational mouse model for Achilles tendon healing
title_full_unstemmed Microsurgical reconstruction affects the outcome in a translational mouse model for Achilles tendon healing
title_short Microsurgical reconstruction affects the outcome in a translational mouse model for Achilles tendon healing
title_sort microsurgical reconstruction affects the outcome in a translational mouse model for achilles tendon healing
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7260609/
https://www.ncbi.nlm.nih.gov/pubmed/32489862
http://dx.doi.org/10.1016/j.jot.2020.04.003
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