Present address: Laboratory of Neurodevelopmental Genetics, Korea University Ansan Hospital, Gojan-dong, Ansan-si, Gyunggi-do 425-707, Korea.
Protective role of edaravone against neomycin-induced ototoxicity in zebrafish
Version of Record online: 3 DEC 2013
Copyright © 2013 John Wiley & Sons, Ltd.
Journal of Applied Toxicology
Volume 34, Issue 5, pages 554–561, May 2014
How to Cite
Choi, J., Chang, J., Jun, H. J., Im, G. J., Chae, S. W., Lee, S. H., Kwon, S.-Y., Jung, H. H., Chung, A.-Y. and Park, H.-C. (2014), Protective role of edaravone against neomycin-induced ototoxicity in zebrafish. J. Appl. Toxicol., 34: 554–561. doi: 10.1002/jat.2964
- Issue online: 26 MAR 2014
- Version of Record online: 3 DEC 2013
- Manuscript Revised: 21 OCT 2013
- Manuscript Accepted: 21 OCT 2013
- Manuscript Received: 28 AUG 2013
Aminoglycosides such as neomycin are one of the most commonly prescribed types of antibiotics worldwide. However, these drugs appear to generate free radicals within the inner ear, which can result in permanent hearing loss. We evaluated the effects of edaravone, a neuroprotective agent, on neomycin-induced ototoxicity in transgenic zebrafish. The 5-day post fertilization (dpf) zebrafish larvae were exposed to 125 μM neomycin and various concentrations of edaravone for 1 h. Hair cell survival was calculated as average numbers of the hair cells in the control group, which was not exposed to neomycin. Ultrastructural changes were evaluated using a scanning electron microscope (SEM) and transmission electron microscope (TEM). Edaravone protected against neomycin-induced hair cell loss in the neuromasts (1000 μM: 11.6 ± 1.1 cells, neomycin only: 5.5 ± 0.5 cells; n = 10, P < 0.05) and decreased the TUNEL reaction for detecting apoptosis. In ultrastructural analysis, structures of mitochondria and hair cells within neuromasts were preserved in zebrafish exposed to 125 μM neomycin and 1000 μM edaravone for 1 h. Edaravone protected against neomycin-induced hair cell loss by preventing apoptosis. Copyright © 2013 John Wiley & Sons, Ltd.