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The Mouse Round-window Approach for Ototoxic Agent Delivery: A Rapid and Reliable Technique for Inducing Cochlear Cell Degeneration
Published on: November 26, 2015
Comparative analysis of combination kanamycin-furosemide versus kanamycin alone in the mouse cochlea
1Department of Otolaryngology, Washington University, 660 South Euclid Avenue, Campus Box 8115, St. Louis, MO 63110, United States. keiko_hirose@post.harvard.edu
Abstract:
Combinations of aminoglycosides and loop diuretics have been known to have a synergistic effect in ototoxic injury. Because murine hair cells are relatively resistant to ototoxicity compared to those of other mammals, investigators have turned to combination therapies to create ototoxic lesions in the mouse inner ear. In this paper, we perform a systematic comparison of hearing thresholds, hair cell damage and monocyte migration into the mouse cochlea after kanamycin versus combined kanamycin/furosemide and explore the pathophysiology of enhanced hair cell loss in aminoglycoside ototoxicity in the presence of loop diuretic. Combined kanamycin-furosemide resulted in elevation of threshold not only in the high frequencies, but across all frequencies with more extensive loss of outer hair cells when compared to kanamycin alone. The stria vascularis was severely atrophied and stellate cells in the spiral limbus were missing in kanamycin-furosemide exposed mice while these changes were not observed in mice receiving kanamycin alone. Monocytes and macrophages were recruited in large numbers to the spiral ligament and spiral ganglion in these mice. Combination therapy resulted in a greater number of macrophages in total, and many more macrophages were present further apically when compared to mice given kanamycin alone. Combined kanamycin-furosemide provides an effective method of addressing the relative resistance to ototoxicity that is observed in most mouse strains. As the mouse becomes increasingly more common in studies of hearing loss, and combination therapies gain popularity, recognition of the overall effects of combined aminoglycoside-loop diuretic therapy will be critical to interpretation of the interventions that follow.
Insights
Combining kanamycin and furosemide effectively induces ototoxicity in mice, causing significant hearing loss and hair cell damage. This combination therapy is crucial for studying hearing loss in mice due to their resistance to ototoxic drugs.
Area of Science:
- Ototoxicology
- Auditory Neuroscience
- Pharmacology
Background:
- Aminoglycosides and loop diuretics synergistically cause ototoxic injury.
- Murine hair cells exhibit relative resistance to ototoxicity, necessitating enhanced methods for creating lesions.
- Combination therapies are increasingly used in mouse models for hearing loss research.
Purpose of the Study:
- To systematically compare hearing thresholds, hair cell damage, and monocyte migration in mice using kanamycin alone versus combined kanamycin/furosemide.
- To explore the pathophysiology of enhanced hair cell loss in aminoglycoside ototoxicity when combined with a loop diuretic.
- To establish an effective method for inducing ototoxicity in mouse models, overcoming their inherent resistance.
Main Methods:
- Systematic comparison of hearing thresholds and hair cell damage.
- Assessment of monocyte and macrophage migration into the mouse cochlea.
- Histological examination of the stria vascularis and spiral limbus.
Main Results:
- Combined kanamycin-furosemide caused threshold elevation across all frequencies and more extensive outer hair cell loss than kanamycin alone.
- Severe stria vascularis atrophy and loss of spiral limbus stellate cells were observed with combination therapy.
- Combination therapy led to increased recruitment of monocytes and macrophages, particularly in apical cochlear regions.
Conclusions:
- Combined kanamycin-furosemide is an effective method to overcome mouse resistance to ototoxicity.
- This combination therapy enhances hair cell loss and inflammatory cell infiltration in the cochlea.
- Understanding these effects is critical for interpreting research on hearing loss using mouse models and combination therapies.

