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In vitro toxicity of local anaesthetics and corticosteroids on supraspinatus tenocyte viability and metabolism

BACKGROUND/OBJECTIVE: The purpose of this study was to evaluate supraspinatus tenocyte viability and metabolism in explants exposed to various local anaesthetics and corticosteroids. Our hypothesis was that the tendons exposed to these common injectates would have significantly decreased cell viabil...

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Autores principales: Nuelle, Clayton W., Cook, Cristi R., Stoker, Aaron M., Cook, James L., Sherman, Seth L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Chinese Speaking Orthopaedic Society 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5987053/
https://www.ncbi.nlm.nih.gov/pubmed/30035090
http://dx.doi.org/10.1016/j.jot.2016.08.002
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author Nuelle, Clayton W.
Cook, Cristi R.
Stoker, Aaron M.
Cook, James L.
Sherman, Seth L.
author_facet Nuelle, Clayton W.
Cook, Cristi R.
Stoker, Aaron M.
Cook, James L.
Sherman, Seth L.
author_sort Nuelle, Clayton W.
collection PubMed
description BACKGROUND/OBJECTIVE: The purpose of this study was to evaluate supraspinatus tenocyte viability and metabolism in explants exposed to various local anaesthetics and corticosteroids. Our hypothesis was that the tendons exposed to these common injectates would have significantly decreased cell viability and metabolism compared with controls. METHODS: Supraspinatus tendon explants were obtained from dogs, placed in a culture media, and randomly assigned to one of the following groups: culture media only (control), 1% lidocaine, 0.5% lidocaine, 0.25% bupivacaine, 0.125% bupivacaine, 0.0625% bupivacaine, betamethasone acetate (5 mg), methylprednisolone acetate (40 mg), or triamcinolone acetonide (40 mg). Cell viability was determined on Days 1 and 7 after culture treatment using calcein AM (live cell) and Sytox Blue (dead cell) stains. Tissue metabolism was assessed on Days 1 and 7 using the resazurin blue metabolic assay. Significant differences were evaluated using a one-way analysis of variance with Tukey post hoc analysis. RESULTS: Compared with the controls, there were significant decreases in cell viability noted at Days 1 and 7 in tenocytes exposed to 1% lidocaine, betamethasone, and methylprednisolone. Significant decreases in cell metabolism were also noted at Days 1 and 7 in those groups. Treatment with 0.125% bupivacaine, 0.0625% bupivacaine, and triamcinolone demonstrated no decrease in cell viability or metabolism when compared with controls at any time point. CONCLUSION: This data confirms that peritendinous injection of commonly used local anaesthetics and corticosteroids results in significant supraspinatus tenotoxicity in vitro. Further in vivo studies are required before making definitive clinical recommendations.
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spelling pubmed-59870532018-07-20 In vitro toxicity of local anaesthetics and corticosteroids on supraspinatus tenocyte viability and metabolism Nuelle, Clayton W. Cook, Cristi R. Stoker, Aaron M. Cook, James L. Sherman, Seth L. J Orthop Translat Original Article BACKGROUND/OBJECTIVE: The purpose of this study was to evaluate supraspinatus tenocyte viability and metabolism in explants exposed to various local anaesthetics and corticosteroids. Our hypothesis was that the tendons exposed to these common injectates would have significantly decreased cell viability and metabolism compared with controls. METHODS: Supraspinatus tendon explants were obtained from dogs, placed in a culture media, and randomly assigned to one of the following groups: culture media only (control), 1% lidocaine, 0.5% lidocaine, 0.25% bupivacaine, 0.125% bupivacaine, 0.0625% bupivacaine, betamethasone acetate (5 mg), methylprednisolone acetate (40 mg), or triamcinolone acetonide (40 mg). Cell viability was determined on Days 1 and 7 after culture treatment using calcein AM (live cell) and Sytox Blue (dead cell) stains. Tissue metabolism was assessed on Days 1 and 7 using the resazurin blue metabolic assay. Significant differences were evaluated using a one-way analysis of variance with Tukey post hoc analysis. RESULTS: Compared with the controls, there were significant decreases in cell viability noted at Days 1 and 7 in tenocytes exposed to 1% lidocaine, betamethasone, and methylprednisolone. Significant decreases in cell metabolism were also noted at Days 1 and 7 in those groups. Treatment with 0.125% bupivacaine, 0.0625% bupivacaine, and triamcinolone demonstrated no decrease in cell viability or metabolism when compared with controls at any time point. CONCLUSION: This data confirms that peritendinous injection of commonly used local anaesthetics and corticosteroids results in significant supraspinatus tenotoxicity in vitro. Further in vivo studies are required before making definitive clinical recommendations. Chinese Speaking Orthopaedic Society 2016-09-28 /pmc/articles/PMC5987053/ /pubmed/30035090 http://dx.doi.org/10.1016/j.jot.2016.08.002 Text en © 2016 The Authors 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
Nuelle, Clayton W.
Cook, Cristi R.
Stoker, Aaron M.
Cook, James L.
Sherman, Seth L.
In vitro toxicity of local anaesthetics and corticosteroids on supraspinatus tenocyte viability and metabolism
title In vitro toxicity of local anaesthetics and corticosteroids on supraspinatus tenocyte viability and metabolism
title_full In vitro toxicity of local anaesthetics and corticosteroids on supraspinatus tenocyte viability and metabolism
title_fullStr In vitro toxicity of local anaesthetics and corticosteroids on supraspinatus tenocyte viability and metabolism
title_full_unstemmed In vitro toxicity of local anaesthetics and corticosteroids on supraspinatus tenocyte viability and metabolism
title_short In vitro toxicity of local anaesthetics and corticosteroids on supraspinatus tenocyte viability and metabolism
title_sort in vitro toxicity of local anaesthetics and corticosteroids on supraspinatus tenocyte viability and metabolism
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5987053/
https://www.ncbi.nlm.nih.gov/pubmed/30035090
http://dx.doi.org/10.1016/j.jot.2016.08.002
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