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Comparative Study
. 2013 Feb 27;42(1):19.
doi: 10.1186/1916-0216-42-19.

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

Affiliations
Comparative Study

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

Amandeep S Grewal et al. J Otolaryngol Head Neck Surg. .

Abstract

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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Figures

Figure 1
Figure 1
(A) Apical region of control mouse; (B) Basal region of control mouse; (C) Apical region of extreme high dose positive control mouse at 1 hour post-injection; (D) Basal region of positive control mouse at 1 hour; (E) Apical region of positive control mouse at 6 hours; (F) Basal region of positive control mouse at 6 hours; (G) Apical region of positive control mouse at 12 hours; (H) Basal region of positive control mouse at 12 hours. Blue arrow in Panel F marks inner hair cell and yellow arrow marks outer hair cells. White bar in Panel B represents 10 μm.
Figure 2
Figure 2
(A) Apical region of transtympanic mouse at 1 hour post-injection; (B) Basal region of transtympanic mouse at 1 hour; (C) Apical region of high dose systemic mouse at 1 hour post-injection; (D) Basal region of systemic mouse at 1 hour. White bar in Panel B represents 10 μm.
Figure 3
Figure 3
(A) Basal region of transtympanic mouse at 1 hour post-injection; (B) Basal region of transtympanic mouse at 6 hours; (C) Basal region of transtympanic mouse at 12 hours; (D) Basal region of high dose systemic mouse at 1 hour post-injection; (E) Basal region of systemic mouse at 6 hours; (F) Basal region of systemic mouse at 12 hours. Blue arrow in Panel A marks Inner hair cell and yellow arrow marks outer hair cells. White bar in Panel B represents 10 μm.

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