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Treatment with Human Amniotic Suspension Allograft Improves Tendon Healing in a Rat Model of Collagenase-Induced Tendinopathy

Treatment of tendon injuries is challenging, with neither conservative nor surgical approaches providing full recovery. Placental-derived tissues represent a promising tool for the treatment of tendon injuries. In this study, human amniotic suspension allograft (ASA) was investigated in a pre-clinic...

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Autores principales: de Girolamo, Laura, Morlin Ambra, Luiz Felipe, Perucca Orfei, Carlotta, McQuilling, John P., Kimmerling, Kelly A., Mowry, Katie C., Johnson, Kimberly A., Phan, Amy T., Whited, Jessica L., Gomoll, Andreas H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6912389/
https://www.ncbi.nlm.nih.gov/pubmed/31717431
http://dx.doi.org/10.3390/cells8111411
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author de Girolamo, Laura
Morlin Ambra, Luiz Felipe
Perucca Orfei, Carlotta
McQuilling, John P.
Kimmerling, Kelly A.
Mowry, Katie C.
Johnson, Kimberly A.
Phan, Amy T.
Whited, Jessica L.
Gomoll, Andreas H.
author_facet de Girolamo, Laura
Morlin Ambra, Luiz Felipe
Perucca Orfei, Carlotta
McQuilling, John P.
Kimmerling, Kelly A.
Mowry, Katie C.
Johnson, Kimberly A.
Phan, Amy T.
Whited, Jessica L.
Gomoll, Andreas H.
author_sort de Girolamo, Laura
collection PubMed
description Treatment of tendon injuries is challenging, with neither conservative nor surgical approaches providing full recovery. Placental-derived tissues represent a promising tool for the treatment of tendon injuries. In this study, human amniotic suspension allograft (ASA) was investigated in a pre-clinical model of Achilles tendinopathy. Collagenase type I was injected in the right hind limb of Sprague Dawley rats to induce disease. Contralateral tendons were either left untreated or injected with saline as controls. Seven days following induction, tendons were injected with saline, ASA, or left untreated. Rats were sacrificed 14 and 28 days post-treatment. Histological and biomechanical analysis of tendons was completed. Fourteen days after ASA injection, improved fiber alignment and reduced cell density demonstrated improvement in degenerated tendons. Twenty-eight days post-treatment, tendons in all treatment groups showed fewer signs of degeneration, which is consistent with normal tendon healing. No statistically significant differences in histological or biomechanical analyses were observed between treatment groups at 28 days independent of the treatment they received. In this study, ASA treatment was safe, well-tolerated, and resulted in a widespread improvement of the tissue. The results of this study provide preliminary insights regarding the potential use of ASA for the treatment of Achilles tendinopathy.
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spelling pubmed-69123892020-01-02 Treatment with Human Amniotic Suspension Allograft Improves Tendon Healing in a Rat Model of Collagenase-Induced Tendinopathy de Girolamo, Laura Morlin Ambra, Luiz Felipe Perucca Orfei, Carlotta McQuilling, John P. Kimmerling, Kelly A. Mowry, Katie C. Johnson, Kimberly A. Phan, Amy T. Whited, Jessica L. Gomoll, Andreas H. Cells Article Treatment of tendon injuries is challenging, with neither conservative nor surgical approaches providing full recovery. Placental-derived tissues represent a promising tool for the treatment of tendon injuries. In this study, human amniotic suspension allograft (ASA) was investigated in a pre-clinical model of Achilles tendinopathy. Collagenase type I was injected in the right hind limb of Sprague Dawley rats to induce disease. Contralateral tendons were either left untreated or injected with saline as controls. Seven days following induction, tendons were injected with saline, ASA, or left untreated. Rats were sacrificed 14 and 28 days post-treatment. Histological and biomechanical analysis of tendons was completed. Fourteen days after ASA injection, improved fiber alignment and reduced cell density demonstrated improvement in degenerated tendons. Twenty-eight days post-treatment, tendons in all treatment groups showed fewer signs of degeneration, which is consistent with normal tendon healing. No statistically significant differences in histological or biomechanical analyses were observed between treatment groups at 28 days independent of the treatment they received. In this study, ASA treatment was safe, well-tolerated, and resulted in a widespread improvement of the tissue. The results of this study provide preliminary insights regarding the potential use of ASA for the treatment of Achilles tendinopathy. MDPI 2019-11-08 /pmc/articles/PMC6912389/ /pubmed/31717431 http://dx.doi.org/10.3390/cells8111411 Text en © 2019 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
de Girolamo, Laura
Morlin Ambra, Luiz Felipe
Perucca Orfei, Carlotta
McQuilling, John P.
Kimmerling, Kelly A.
Mowry, Katie C.
Johnson, Kimberly A.
Phan, Amy T.
Whited, Jessica L.
Gomoll, Andreas H.
Treatment with Human Amniotic Suspension Allograft Improves Tendon Healing in a Rat Model of Collagenase-Induced Tendinopathy
title Treatment with Human Amniotic Suspension Allograft Improves Tendon Healing in a Rat Model of Collagenase-Induced Tendinopathy
title_full Treatment with Human Amniotic Suspension Allograft Improves Tendon Healing in a Rat Model of Collagenase-Induced Tendinopathy
title_fullStr Treatment with Human Amniotic Suspension Allograft Improves Tendon Healing in a Rat Model of Collagenase-Induced Tendinopathy
title_full_unstemmed Treatment with Human Amniotic Suspension Allograft Improves Tendon Healing in a Rat Model of Collagenase-Induced Tendinopathy
title_short Treatment with Human Amniotic Suspension Allograft Improves Tendon Healing in a Rat Model of Collagenase-Induced Tendinopathy
title_sort treatment with human amniotic suspension allograft improves tendon healing in a rat model of collagenase-induced tendinopathy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6912389/
https://www.ncbi.nlm.nih.gov/pubmed/31717431
http://dx.doi.org/10.3390/cells8111411
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