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Updated: May 6, 2026

Trans-Tympanic Drug Delivery for the Treatment of Ototoxicity
Published on: March 16, 2018
Dexamethasone otoprotection in a multidose cisplatin ototoxicity mouse model
Amy Lawrason Hughes1, Nighat Hussain, Ryan Pafford
1University of Connecticut Health Center, Department of Surgery, Division of Otolaryngology-Head & Neck Surgery, Farmington, Connecticut, USA.
This study developed a multidose cisplatin mouse model for ototoxicity. Intratympanic dexamethasone did not protect against cisplatin-induced hearing loss in this model.
Area of Science:
- Ototoxicity research
- Translational medicine
- Pharmacology
Background:
- Cisplatin chemotherapy can cause ototoxicity, leading to hearing loss.
- Developing reliable animal models is crucial for studying and preventing cisplatin-induced hearing damage.
Purpose of the Study:
- To establish a multidose cisplatin murine model for ototoxicity research.
- To evaluate the efficacy of intratympanic dexamethasone in preventing cisplatin ototoxicity.
Main Methods:
- CBA/J mice received intraperitoneal cisplatin (2 or 3 mg/kg/day) for 5 or 10 days.
- Auditory brainstem response (ABR) thresholds were measured to assess hearing loss.
- Mice received intratympanic dexamethasone or saline in a controlled study.
Main Results:
- A 5-day regimen of 3 mg/kg/day cisplatin effectively induced hearing threshold elevations with acceptable mortality.
- Significant hearing threshold elevations were observed across all tested frequencies.
- No statistically significant difference in hearing protection was found between intratympanic dexamethasone and saline treatments.
Conclusions:
- Intratympanic dexamethasone demonstrated no otoprotective effect in the developed multidose cisplatin ototoxicity mouse model.
- This finding contrasts with potential benefits observed in single-dose cisplatin ototoxicity models.
- The study highlights the need for further research into effective otoprotective strategies for multidose cisplatin therapy.
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