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Neurotoxicity associated with colistin methanesulfonate treatment is enhanced by concomitant sevoflurane inhalation
Colistin methanesulfonate (CMS) is a cyclic polypeptide antibiotic with neurotoxic side effects. Sevoflurane (Sevo), an inhaled anesthetic, is known to enhance the non-depolarizing effect of neuromuscular relaxants; however, its mechanism of action is unclear. In this study, we investigated the augm...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9742878/ https://www.ncbi.nlm.nih.gov/pubmed/36518416 http://dx.doi.org/10.1016/j.toxrep.2022.05.020 |
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author | Gotoda, Mai Enoki, Yuki Shishido, Shino Taguchi, Kazuaki Matsumoto, Kazuaki |
author_facet | Gotoda, Mai Enoki, Yuki Shishido, Shino Taguchi, Kazuaki Matsumoto, Kazuaki |
author_sort | Gotoda, Mai |
collection | PubMed |
description | Colistin methanesulfonate (CMS) is a cyclic polypeptide antibiotic with neurotoxic side effects. Sevoflurane (Sevo), an inhaled anesthetic, is known to enhance the non-depolarizing effect of neuromuscular relaxants; however, its mechanism of action is unclear. In this study, we investigated the augmentation effect of Sevo on CMS-induced neurotoxicity. We prepared a sciatic nerve-skeletal muscle stimulation model using Sprague-Dawley male rats administered CMS with or without Sevo. The muscle contraction inhibition rate was determined from electromyogram measurements. Furthermore, we simulated the pharmacokinetics of CMS and colistin using previous reports, and the relationship between the effect of muscle contraction inhibition and pharmacokinetic parameters was evaluated. We observed a dose-dependent neuromuscular inhibitory effect of Sevo under CMS administration. The 50 % inhibitory dose (ID(50)) values for CMS and CMS+Sevo were 167 ± 12 and 85 ± 5 mg/kg, respectively. The combination of CMS with Sevo showed a 49 % decrease in the ID(50) compared with CMS alone. The simulated area under the time–concentration curve (AUC) values for CMS and colistin administration in rats at 200 mg/kg were 219 and 16.0 mg·h/L, respectively. The predicted AUC values of colistin corresponding to the ID(50) at 0–45 min for CMS alone and CMS+Sevo were 12.0 and 7.0 mg·h/L, respectively. We revealed that the neurotoxic effect of CMS was enhanced by the concomitant use of Sevo. Based on the simulated AUC values, we concluded that this neurotoxic effect may also occur in clinical settings, and concomitant use of CMS and Sevo should be avoided. |
format | Online Article Text |
id | pubmed-9742878 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-97428782022-12-13 Neurotoxicity associated with colistin methanesulfonate treatment is enhanced by concomitant sevoflurane inhalation Gotoda, Mai Enoki, Yuki Shishido, Shino Taguchi, Kazuaki Matsumoto, Kazuaki Toxicol Rep Regular Article Colistin methanesulfonate (CMS) is a cyclic polypeptide antibiotic with neurotoxic side effects. Sevoflurane (Sevo), an inhaled anesthetic, is known to enhance the non-depolarizing effect of neuromuscular relaxants; however, its mechanism of action is unclear. In this study, we investigated the augmentation effect of Sevo on CMS-induced neurotoxicity. We prepared a sciatic nerve-skeletal muscle stimulation model using Sprague-Dawley male rats administered CMS with or without Sevo. The muscle contraction inhibition rate was determined from electromyogram measurements. Furthermore, we simulated the pharmacokinetics of CMS and colistin using previous reports, and the relationship between the effect of muscle contraction inhibition and pharmacokinetic parameters was evaluated. We observed a dose-dependent neuromuscular inhibitory effect of Sevo under CMS administration. The 50 % inhibitory dose (ID(50)) values for CMS and CMS+Sevo were 167 ± 12 and 85 ± 5 mg/kg, respectively. The combination of CMS with Sevo showed a 49 % decrease in the ID(50) compared with CMS alone. The simulated area under the time–concentration curve (AUC) values for CMS and colistin administration in rats at 200 mg/kg were 219 and 16.0 mg·h/L, respectively. The predicted AUC values of colistin corresponding to the ID(50) at 0–45 min for CMS alone and CMS+Sevo were 12.0 and 7.0 mg·h/L, respectively. We revealed that the neurotoxic effect of CMS was enhanced by the concomitant use of Sevo. Based on the simulated AUC values, we concluded that this neurotoxic effect may also occur in clinical settings, and concomitant use of CMS and Sevo should be avoided. Elsevier 2022-06-02 /pmc/articles/PMC9742878/ /pubmed/36518416 http://dx.doi.org/10.1016/j.toxrep.2022.05.020 Text en © 2022 The Authors https://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 | Regular Article Gotoda, Mai Enoki, Yuki Shishido, Shino Taguchi, Kazuaki Matsumoto, Kazuaki Neurotoxicity associated with colistin methanesulfonate treatment is enhanced by concomitant sevoflurane inhalation |
title | Neurotoxicity associated with colistin methanesulfonate treatment is enhanced by concomitant sevoflurane inhalation |
title_full | Neurotoxicity associated with colistin methanesulfonate treatment is enhanced by concomitant sevoflurane inhalation |
title_fullStr | Neurotoxicity associated with colistin methanesulfonate treatment is enhanced by concomitant sevoflurane inhalation |
title_full_unstemmed | Neurotoxicity associated with colistin methanesulfonate treatment is enhanced by concomitant sevoflurane inhalation |
title_short | Neurotoxicity associated with colistin methanesulfonate treatment is enhanced by concomitant sevoflurane inhalation |
title_sort | neurotoxicity associated with colistin methanesulfonate treatment is enhanced by concomitant sevoflurane inhalation |
topic | Regular Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9742878/ https://www.ncbi.nlm.nih.gov/pubmed/36518416 http://dx.doi.org/10.1016/j.toxrep.2022.05.020 |
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