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Evaluating the Efficacy of L-N-acetylcysteine and Dexamethasone in Combination to Provide Otoprotection for Electrode Insertion Trauma
Background: Electrode insertion trauma (EIT) during cochlear implantation (CI) can cause loss of residual hearing. L-N-acetylcysteine (L-NAC) and dexamethasone (Dex) have been individually shown to provide otoprotection albeit at higher concentrations that may be associated with adverse effects. Obj...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7141216/ https://www.ncbi.nlm.nih.gov/pubmed/32155788 http://dx.doi.org/10.3390/jcm9030716 |
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author | Eshraghi, Adrien A. Shahal, David Davies, Camron Mittal, Jeenu Shah, Viraj Bulut, Erdogan Garnham, Carolyn Sinha, Priyanka Mishra, Dibyanshi Marwede, Hannah Mittal, Rahul |
author_facet | Eshraghi, Adrien A. Shahal, David Davies, Camron Mittal, Jeenu Shah, Viraj Bulut, Erdogan Garnham, Carolyn Sinha, Priyanka Mishra, Dibyanshi Marwede, Hannah Mittal, Rahul |
author_sort | Eshraghi, Adrien A. |
collection | PubMed |
description | Background: Electrode insertion trauma (EIT) during cochlear implantation (CI) can cause loss of residual hearing. L-N-acetylcysteine (L-NAC) and dexamethasone (Dex) have been individually shown to provide otoprotection albeit at higher concentrations that may be associated with adverse effects. Objective/Aims: The aim of this study is to determine whether L-NAC and Dex could be combined to decrease their effective dosage. Materials and Methods: The organ of Corti (OC) explants were divided into various groups: 1) control; 2) EIT; 3) EIT treated with different concentrations of Dex; 4) EIT treated with different concentrations of L-NAC; 5) EIT treated with L-NAC and Dex in combination. Hair cell (HC) density, levels of oxidative stress, proinflammatory cytokines and nitric oxide (NO) was determined. Results: There was a significant loss of HCs in explants subjected to EIT compared to the control group. L-NAC and Dex in combination was able to provide significant otoprotection at lower concentrations compared to individual drugs. Conclusions and Significance: A combination containing L-NAC and Dex is effective in protecting sensory cells at lower protective doses than each compound separately. These compounds can be combined allowing a decrease of potential side effects of each compound and providing significant otoprotection for EIT. |
format | Online Article Text |
id | pubmed-7141216 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-71412162020-04-10 Evaluating the Efficacy of L-N-acetylcysteine and Dexamethasone in Combination to Provide Otoprotection for Electrode Insertion Trauma Eshraghi, Adrien A. Shahal, David Davies, Camron Mittal, Jeenu Shah, Viraj Bulut, Erdogan Garnham, Carolyn Sinha, Priyanka Mishra, Dibyanshi Marwede, Hannah Mittal, Rahul J Clin Med Article Background: Electrode insertion trauma (EIT) during cochlear implantation (CI) can cause loss of residual hearing. L-N-acetylcysteine (L-NAC) and dexamethasone (Dex) have been individually shown to provide otoprotection albeit at higher concentrations that may be associated with adverse effects. Objective/Aims: The aim of this study is to determine whether L-NAC and Dex could be combined to decrease their effective dosage. Materials and Methods: The organ of Corti (OC) explants were divided into various groups: 1) control; 2) EIT; 3) EIT treated with different concentrations of Dex; 4) EIT treated with different concentrations of L-NAC; 5) EIT treated with L-NAC and Dex in combination. Hair cell (HC) density, levels of oxidative stress, proinflammatory cytokines and nitric oxide (NO) was determined. Results: There was a significant loss of HCs in explants subjected to EIT compared to the control group. L-NAC and Dex in combination was able to provide significant otoprotection at lower concentrations compared to individual drugs. Conclusions and Significance: A combination containing L-NAC and Dex is effective in protecting sensory cells at lower protective doses than each compound separately. These compounds can be combined allowing a decrease of potential side effects of each compound and providing significant otoprotection for EIT. MDPI 2020-03-06 /pmc/articles/PMC7141216/ /pubmed/32155788 http://dx.doi.org/10.3390/jcm9030716 Text en © 2020 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 Eshraghi, Adrien A. Shahal, David Davies, Camron Mittal, Jeenu Shah, Viraj Bulut, Erdogan Garnham, Carolyn Sinha, Priyanka Mishra, Dibyanshi Marwede, Hannah Mittal, Rahul Evaluating the Efficacy of L-N-acetylcysteine and Dexamethasone in Combination to Provide Otoprotection for Electrode Insertion Trauma |
title | Evaluating the Efficacy of L-N-acetylcysteine and Dexamethasone in Combination to Provide Otoprotection for Electrode Insertion Trauma |
title_full | Evaluating the Efficacy of L-N-acetylcysteine and Dexamethasone in Combination to Provide Otoprotection for Electrode Insertion Trauma |
title_fullStr | Evaluating the Efficacy of L-N-acetylcysteine and Dexamethasone in Combination to Provide Otoprotection for Electrode Insertion Trauma |
title_full_unstemmed | Evaluating the Efficacy of L-N-acetylcysteine and Dexamethasone in Combination to Provide Otoprotection for Electrode Insertion Trauma |
title_short | Evaluating the Efficacy of L-N-acetylcysteine and Dexamethasone in Combination to Provide Otoprotection for Electrode Insertion Trauma |
title_sort | evaluating the efficacy of l-n-acetylcysteine and dexamethasone in combination to provide otoprotection for electrode insertion trauma |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7141216/ https://www.ncbi.nlm.nih.gov/pubmed/32155788 http://dx.doi.org/10.3390/jcm9030716 |
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