Evaluating the efficacy of L-N-acetylcysteine and dexamethasone in combination to provide otoprotection for electrode insertion trauma
Journal of Clinical Medicine, vol.9, no.3, 2020 (SCI-Expanded, Scopus)
- Publication Type: Article / Article
- Volume: 9 Issue: 3
- Publication Date: 2020
- Doi Number: 10.3390/jcm9030716
- Journal Name: Journal of Clinical Medicine
- Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus, Academic Search Premier, EMBASE, Directory of Open Access Journals
- Keywords: Dexamethasone, Electrode insertion trauma, L-N-acetylcysteine, Nitric oxide, Organ of Corti, Oxidative stress, Proinflammatory cytokines, Residual hearing
- Trakya University Affiliated: Yes
Abstract
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.