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Ketamine decreases cell viability of bone explants and impairs bone healing in rats
BACKGROUND: Ketamine is a widely used anesthetic in experimental medicine. We have also used ketamine for surgical interventions and imaging in rats and found significantly impaired ossification between identically performed experiments, which only differed in the number of anesthetic events. In ord...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7014735/ https://www.ncbi.nlm.nih.gov/pubmed/32046745 http://dx.doi.org/10.1186/s13018-020-1579-x |
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author | Horváthy, Dénes B. Szántó, Péter Marschall, Bence Bagó, Marcell Csery, Márton Hornyák, István Doros, Attila Lacza, Zsombor |
author_facet | Horváthy, Dénes B. Szántó, Péter Marschall, Bence Bagó, Marcell Csery, Márton Hornyák, István Doros, Attila Lacza, Zsombor |
author_sort | Horváthy, Dénes B. |
collection | PubMed |
description | BACKGROUND: Ketamine is a widely used anesthetic in experimental medicine. We have also used ketamine for surgical interventions and imaging in rats and found significantly impaired ossification between identically performed experiments, which only differed in the number of anesthetic events. In order to investigate this phenomenon, we estimated the absorbed ionizing radiation and also studied whether ketamine administration has disadvantageous effect on bone cell viability. METHODS: Spongious bone chips and parietal bone disks were harvested from rats. Explants were incubated in stem cell media containing 0.02, 0.2 and 2 mM ketamine. After 3 days of incubation, tetrazolium-based spectrophotometric assay was performed to measure cell viability. Size-specific dose estimation was used to calculate ionizing radiation of computed tomography imaging. RESULTS: We found that ketamine supplementation with 0.2 mM slightly decreased cell viability, while 2 mM caused significant reduction both in the spongious and cortical explants. The cumulative ionizing radiation was found to be negligible compared to irradiation dosages used to impair ossification. CONCLUSIONS: We conclude that multiple ketamine administration was responsible for the diminished regenerative potential of bone tissue in the present experimental setup. For this reason, we suggest that ketamine anesthesia should be avoided in studies investigating bone regeneration. |
format | Online Article Text |
id | pubmed-7014735 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-70147352020-02-20 Ketamine decreases cell viability of bone explants and impairs bone healing in rats Horváthy, Dénes B. Szántó, Péter Marschall, Bence Bagó, Marcell Csery, Márton Hornyák, István Doros, Attila Lacza, Zsombor J Orthop Surg Res Research Article BACKGROUND: Ketamine is a widely used anesthetic in experimental medicine. We have also used ketamine for surgical interventions and imaging in rats and found significantly impaired ossification between identically performed experiments, which only differed in the number of anesthetic events. In order to investigate this phenomenon, we estimated the absorbed ionizing radiation and also studied whether ketamine administration has disadvantageous effect on bone cell viability. METHODS: Spongious bone chips and parietal bone disks were harvested from rats. Explants were incubated in stem cell media containing 0.02, 0.2 and 2 mM ketamine. After 3 days of incubation, tetrazolium-based spectrophotometric assay was performed to measure cell viability. Size-specific dose estimation was used to calculate ionizing radiation of computed tomography imaging. RESULTS: We found that ketamine supplementation with 0.2 mM slightly decreased cell viability, while 2 mM caused significant reduction both in the spongious and cortical explants. The cumulative ionizing radiation was found to be negligible compared to irradiation dosages used to impair ossification. CONCLUSIONS: We conclude that multiple ketamine administration was responsible for the diminished regenerative potential of bone tissue in the present experimental setup. For this reason, we suggest that ketamine anesthesia should be avoided in studies investigating bone regeneration. BioMed Central 2020-02-11 /pmc/articles/PMC7014735/ /pubmed/32046745 http://dx.doi.org/10.1186/s13018-020-1579-x Text en © The Author(s). 2020 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Horváthy, Dénes B. Szántó, Péter Marschall, Bence Bagó, Marcell Csery, Márton Hornyák, István Doros, Attila Lacza, Zsombor Ketamine decreases cell viability of bone explants and impairs bone healing in rats |
title | Ketamine decreases cell viability of bone explants and impairs bone healing in rats |
title_full | Ketamine decreases cell viability of bone explants and impairs bone healing in rats |
title_fullStr | Ketamine decreases cell viability of bone explants and impairs bone healing in rats |
title_full_unstemmed | Ketamine decreases cell viability of bone explants and impairs bone healing in rats |
title_short | Ketamine decreases cell viability of bone explants and impairs bone healing in rats |
title_sort | ketamine decreases cell viability of bone explants and impairs bone healing in rats |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7014735/ https://www.ncbi.nlm.nih.gov/pubmed/32046745 http://dx.doi.org/10.1186/s13018-020-1579-x |
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