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Dexamethasone uptake in the murine organ of Corti with transtympanic versus systemic administration

OBJECTIVE: To investigate glucocorticoid uptake in auditory hair cells following transtympanic versus systemic administration of dexamethasone. STUDY DESIGN: Controlled experimental study. SETTING: Translational science experimental laboratory. METHODS: Swiss-Webster mice were injected with dexameth...

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Autores principales: Grewal, Amandeep S, Nedzelski, Julian M, Chen, Joseph M, Lin, Vincent YW
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3651220/
https://www.ncbi.nlm.nih.gov/pubmed/23663237
http://dx.doi.org/10.1186/1916-0216-42-19
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author Grewal, Amandeep S
Nedzelski, Julian M
Chen, Joseph M
Lin, Vincent YW
author_facet Grewal, Amandeep S
Nedzelski, Julian M
Chen, Joseph M
Lin, Vincent YW
author_sort Grewal, Amandeep S
collection PubMed
description OBJECTIVE: To investigate glucocorticoid uptake in auditory hair cells following transtympanic versus systemic administration of dexamethasone. STUDY DESIGN: Controlled experimental study. SETTING: Translational science experimental laboratory. METHODS: Swiss-Webster mice were injected with dexamethasone via transtympanic or systemic administration. At 1, 6, or 12 hours post-injection the temporal bones were harvested. After cryosectioning, immunohistochemical staining was performed using an antibody for dexamethasone. RESULTS: Dexamethasone labelling was greatest at 1 hour. Inner hair cells demonstrated much higher steroid uptake than outer hair cells. Both transtympanic injection and high-dose systemic administration resulted in strong dexamethasone labelling of hair cells, and a decreasing basal-to-apical gradient of hair cell fluorescence intensity was observed. Systemically delivered dexamethasone was rapidly eliminated from the inner ear, demonstrating mild labelling after 6 hours and none after 12 hours. In contrast, the mice receiving transtympanic injection had persistent moderate intensity fluorescence at 6 and 12 hours post-injection. CONCLUSION: There is similar uptake of dexamethasone by auditory hair cells after transtympanic and high-dose systemic delivery. Novel findings include the presence of a decreasing basal-apical gradient of steroid uptake, and demonstration of greater affinity of inner hair cells for dexamethasone compared to outer hair cells. In this animal model transtympanic injection resulted in prolonged steroid uptake. These findings help further our understanding of the pharmacokinetics of steroids in the cochlea, with a focus on auditory hair cells.
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spelling pubmed-36512202013-05-14 Dexamethasone uptake in the murine organ of Corti with transtympanic versus systemic administration Grewal, Amandeep S Nedzelski, Julian M Chen, Joseph M Lin, Vincent YW J Otolaryngol Head Neck Surg Original Research Article OBJECTIVE: To investigate glucocorticoid uptake in auditory hair cells following transtympanic versus systemic administration of dexamethasone. STUDY DESIGN: Controlled experimental study. SETTING: Translational science experimental laboratory. METHODS: Swiss-Webster mice were injected with dexamethasone via transtympanic or systemic administration. At 1, 6, or 12 hours post-injection the temporal bones were harvested. After cryosectioning, immunohistochemical staining was performed using an antibody for dexamethasone. RESULTS: Dexamethasone labelling was greatest at 1 hour. Inner hair cells demonstrated much higher steroid uptake than outer hair cells. Both transtympanic injection and high-dose systemic administration resulted in strong dexamethasone labelling of hair cells, and a decreasing basal-to-apical gradient of hair cell fluorescence intensity was observed. Systemically delivered dexamethasone was rapidly eliminated from the inner ear, demonstrating mild labelling after 6 hours and none after 12 hours. In contrast, the mice receiving transtympanic injection had persistent moderate intensity fluorescence at 6 and 12 hours post-injection. CONCLUSION: There is similar uptake of dexamethasone by auditory hair cells after transtympanic and high-dose systemic delivery. Novel findings include the presence of a decreasing basal-apical gradient of steroid uptake, and demonstration of greater affinity of inner hair cells for dexamethasone compared to outer hair cells. In this animal model transtympanic injection resulted in prolonged steroid uptake. These findings help further our understanding of the pharmacokinetics of steroids in the cochlea, with a focus on auditory hair cells. BioMed Central 2013-02-27 /pmc/articles/PMC3651220/ /pubmed/23663237 http://dx.doi.org/10.1186/1916-0216-42-19 Text en Copyright © 2013 Grewal et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research Article
Grewal, Amandeep S
Nedzelski, Julian M
Chen, Joseph M
Lin, Vincent YW
Dexamethasone uptake in the murine organ of Corti with transtympanic versus systemic administration
title Dexamethasone uptake in the murine organ of Corti with transtympanic versus systemic administration
title_full Dexamethasone uptake in the murine organ of Corti with transtympanic versus systemic administration
title_fullStr Dexamethasone uptake in the murine organ of Corti with transtympanic versus systemic administration
title_full_unstemmed Dexamethasone uptake in the murine organ of Corti with transtympanic versus systemic administration
title_short Dexamethasone uptake in the murine organ of Corti with transtympanic versus systemic administration
title_sort dexamethasone uptake in the murine organ of corti with transtympanic versus systemic administration
topic Original Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3651220/
https://www.ncbi.nlm.nih.gov/pubmed/23663237
http://dx.doi.org/10.1186/1916-0216-42-19
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