High dose sodium salicylate causes moderate, reversible hearing loss and tinnitus. Salicylate-induced hearing loss is believed to arise from a reduction in the electromotile response of outer hair cells (OHCs) and/or reduction of KCNQ4 potassium currents in OHCs, which decreases the driving force for the transduction current. Therefore, enhancing OHC potassium currents could potentially prevent salicylate-induced temporary hearing loss. In this study, we tested whether opening voltage-gated potassium channels using ICA-105665, a novel small molecule that opens KCNQ2/3 and KCNQ3/5 channels, can reduce salicylate-induced hearing loss. We found that systemic application of ICA-105665 at 10âmg/kg prevented the salicylate-induced amplitude reduction and threshold shift in the compound action potentials recorded at the round window of the cochlea. ICA-105665 also prevented the salicylate-induced reduction of distortion-product otoacoustic emission. These results suggest that ICA-105665 partially compensates for salicylate-induced cochlear hearing loss by enhancing KCNQ2/3 and KCNQ3/5 potassium currents and the motility of OHCs.
Potassium channel activator attenuates salicylate-induced cochlear hearing loss potentially ameliorating tinnitus.
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作者:Sun Wei, Liu Jun, Zhang Chao, Zhou Na, Manohar Senthilvelan, Winchester Wendy, Miranda Jason A, Salvi Richard J
| 期刊: | Frontiers in Neurology | 影响因子: | 2.800 |
| 时间: | 2015 | 起止号: | 2015 Apr 7; 6:77 |
| doi: | 10.3389/fneur.2015.00077 | ||
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