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Collagenase-Induced Patellar Tendinopathy with Neovascularization: First Results towards a Piglet Model of Musculoskeletal Embolization

Background: Therapeutic strategies targeting neovessels responsible for musculoskeletal chronic pain have emerged, including neovessels embolization. Our study aimed to develop a large animal model of patellar tendinopathy with neovascularization. Methods: Nine 3-month-old male piglets (18 patellar...

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Autores principales: Ghelfi, Julien, Bacle, Marylène, Stephanov, Olivier, de Forges, Hélène, Soulairol, Ian, Roger, Pascal, Ferretti, Gilbert R., Beregi, Jean-Paul, Frandon, Julien
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8773136/
https://www.ncbi.nlm.nih.gov/pubmed/35052682
http://dx.doi.org/10.3390/biomedicines10010002
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author Ghelfi, Julien
Bacle, Marylène
Stephanov, Olivier
de Forges, Hélène
Soulairol, Ian
Roger, Pascal
Ferretti, Gilbert R.
Beregi, Jean-Paul
Frandon, Julien
author_facet Ghelfi, Julien
Bacle, Marylène
Stephanov, Olivier
de Forges, Hélène
Soulairol, Ian
Roger, Pascal
Ferretti, Gilbert R.
Beregi, Jean-Paul
Frandon, Julien
author_sort Ghelfi, Julien
collection PubMed
description Background: Therapeutic strategies targeting neovessels responsible for musculoskeletal chronic pain have emerged, including neovessels embolization. Our study aimed to develop a large animal model of patellar tendinopathy with neovascularization. Methods: Nine 3-month-old male piglets (18 patellar tendons) received percutaneous injections of increasing doses of collagenase (0 to 50 mg) at day 0 (D0). Tendinopathy was evaluated by ultrasound (D7 and D14). Neovascularization was evaluated visually and on angiographies. Bonar score was used for histological analysis (D14). Correlations were evaluated using Spearman’s rank (Rs) test. Results: Research protocol was well tolerated. All tendons were enlarged with a median increase of 31.58% [25–40.28] at D7 (p = 0.244) at D7 and 57.52% [48.41–91.45] at D14 (p = 0.065). Tendons with collagenase injection had more hypoechoic changes, with one tendon rupture (p = 0.012). Neovascularization was reported above 5 mg collagenase (p < 0.01) at D7 and D14 with dose-related neovessels induction (Rs = 0.8, p < 0.001). The Bonar score increased above 5 mg collagenase, correlated with the dose (Rs = 0.666, p = 0.003). Conclusions: The study shows the feasibility, safety and reproducibility of this new large animal model of patellar tendinopathy with neovascularization after collagenase injection. It will allow studying new treatments on direct embolization of neovessels by endovascular approach.
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spelling pubmed-87731362022-01-21 Collagenase-Induced Patellar Tendinopathy with Neovascularization: First Results towards a Piglet Model of Musculoskeletal Embolization Ghelfi, Julien Bacle, Marylène Stephanov, Olivier de Forges, Hélène Soulairol, Ian Roger, Pascal Ferretti, Gilbert R. Beregi, Jean-Paul Frandon, Julien Biomedicines Article Background: Therapeutic strategies targeting neovessels responsible for musculoskeletal chronic pain have emerged, including neovessels embolization. Our study aimed to develop a large animal model of patellar tendinopathy with neovascularization. Methods: Nine 3-month-old male piglets (18 patellar tendons) received percutaneous injections of increasing doses of collagenase (0 to 50 mg) at day 0 (D0). Tendinopathy was evaluated by ultrasound (D7 and D14). Neovascularization was evaluated visually and on angiographies. Bonar score was used for histological analysis (D14). Correlations were evaluated using Spearman’s rank (Rs) test. Results: Research protocol was well tolerated. All tendons were enlarged with a median increase of 31.58% [25–40.28] at D7 (p = 0.244) at D7 and 57.52% [48.41–91.45] at D14 (p = 0.065). Tendons with collagenase injection had more hypoechoic changes, with one tendon rupture (p = 0.012). Neovascularization was reported above 5 mg collagenase (p < 0.01) at D7 and D14 with dose-related neovessels induction (Rs = 0.8, p < 0.001). The Bonar score increased above 5 mg collagenase, correlated with the dose (Rs = 0.666, p = 0.003). Conclusions: The study shows the feasibility, safety and reproducibility of this new large animal model of patellar tendinopathy with neovascularization after collagenase injection. It will allow studying new treatments on direct embolization of neovessels by endovascular approach. MDPI 2021-12-21 /pmc/articles/PMC8773136/ /pubmed/35052682 http://dx.doi.org/10.3390/biomedicines10010002 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Ghelfi, Julien
Bacle, Marylène
Stephanov, Olivier
de Forges, Hélène
Soulairol, Ian
Roger, Pascal
Ferretti, Gilbert R.
Beregi, Jean-Paul
Frandon, Julien
Collagenase-Induced Patellar Tendinopathy with Neovascularization: First Results towards a Piglet Model of Musculoskeletal Embolization
title Collagenase-Induced Patellar Tendinopathy with Neovascularization: First Results towards a Piglet Model of Musculoskeletal Embolization
title_full Collagenase-Induced Patellar Tendinopathy with Neovascularization: First Results towards a Piglet Model of Musculoskeletal Embolization
title_fullStr Collagenase-Induced Patellar Tendinopathy with Neovascularization: First Results towards a Piglet Model of Musculoskeletal Embolization
title_full_unstemmed Collagenase-Induced Patellar Tendinopathy with Neovascularization: First Results towards a Piglet Model of Musculoskeletal Embolization
title_short Collagenase-Induced Patellar Tendinopathy with Neovascularization: First Results towards a Piglet Model of Musculoskeletal Embolization
title_sort collagenase-induced patellar tendinopathy with neovascularization: first results towards a piglet model of musculoskeletal embolization
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8773136/
https://www.ncbi.nlm.nih.gov/pubmed/35052682
http://dx.doi.org/10.3390/biomedicines10010002
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