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Dynamic studies of ototoxicity in mature avian auditory epithelium
K Hirose1, L E Westrum, J S Stone
1Virginia Merrill Bloedel Hearing Research Center, Department of Otolaryngology-Head and Neck Surgery, University of Washington, Seattle 98195, USA.
Abstract:
Hearing loss induced by ototoxicity is a worldwide problem despite the development of newer antibiotics and chemotherapy agents. The cellular mechanisms responsible for aminoglycoside-induced hearing loss are still poorly understood. We have developed two different methods of studying the dynamic cellular and subcellular changes in the chick auditory sensory epithelium that occur during hair cell death. The first study was performed in mature chicks after a single, high dose injection of gentamicin, which results in the rapid loss of all hair cells in the basal third of the cochlea. Chicks were sacrificed at discrete time points after drug treatment, and transmission electron microscopy was performed to study the ultrastructural changes in basal hair cells during the course of cell death. We noted various changes in the cell morphology including accumulation of cytoplasmic inclusion bodies, dispersion of the cytoplasmic polyribosomes, mitochondrial swelling, and cellular extrusion by 24 h after injection. The next two studies were performed using tissue cultures from mature avian auditory sensory epithelium. Cultured cells were labeled using vital fluorescent markers, and levels of intracellular calcium and reactive oxygen species within hair cells were studied following aminoglycoside exposure. We identified a dose-dependent increase in the levels of intracellular calcium, which was blocked by an inhibitor of voltage-gated calcium channels. We also found that levels of reactive oxygen species in hair cells greatly increased after exposure to gentamicin, and this response was blocked by two different antioxidants. These studies serve to identify key cellular and molecular changes in hair cells in response to ototoxic drugs. Further study of these processes may lead to a better understanding of how ototoxicity is induced and to potential preventative interventions.
Insights
Aminoglycoside ototoxicity causes hearing loss. This study reveals gentamicin damages auditory hair cells by increasing intracellular calcium and reactive oxygen species, offering insights for prevention.
Area of Science:
- Ototoxicity research
- Auditory cell biology
- Drug-induced hearing loss mechanisms
Background:
- Ototoxicity from medications like antibiotics and chemotherapy is a global health concern.
- The precise cellular mechanisms behind aminoglycoside-induced hearing loss remain unclear.
- Understanding hair cell death pathways is crucial for developing preventative strategies.
Purpose of the Study:
- To investigate the cellular and subcellular changes in the chick auditory sensory epithelium during hair cell death induced by ototoxic drugs.
- To identify key molecular events, including changes in intracellular calcium and reactive oxygen species, following aminoglycoside exposure.
Main Methods:
- Transmission electron microscopy was used to examine ultrastructural changes in hair cells after gentamicin injection in mature chicks.
- Vital fluorescent markers and tissue culture techniques were employed to study intracellular calcium and reactive oxygen species in cultured avian auditory sensory epithelium exposed to aminoglycosides.
Main Results:
- Gentamicin exposure led to significant morphological changes in hair cells, including inclusion body accumulation and mitochondrial swelling.
- A dose-dependent increase in intracellular calcium, sensitive to calcium channel blockers, was observed in hair cells.
- Elevated reactive oxygen species levels were detected in hair cells post-gentamicin exposure, and these increases were mitigated by antioxidants.
Conclusions:
- This research elucidates critical cellular and molecular alterations in hair cells in response to ototoxic agents like gentamicin.
- The findings highlight the roles of calcium influx and oxidative stress in aminoglycoside-induced ototoxicity.
- Further investigation into these pathways may pave the way for interventions to prevent drug-induced hearing loss.

