耳毒性
氨基糖苷
新霉素
毛细胞
卡那霉素
通道阻滞剂
药理学
化学
耳蜗
医学
斑马鱼
庆大霉素
内耳
解剖
抗生素
内科学
生物化学
钙
顺铂
化疗
基因
作者
Emma J. Kenyon,Nerissa K. Kirkwood,Siân R. Kitcher,Richard J. Goodyear,Marco Derudas,Daire Cantillon,Sarah Baxendale,Antonio de la Vega de León,Virginia N. Mahieu,Richard T. Osgood,Charlotte Donald Wilson,James C. Bull,Simon J. Waddell,Tanya T. Whitfield,Simon E. Ward,Corné J. Kros,Guy P. Richardson
出处
期刊:JCI insight
[American Society for Clinical Investigation]
日期:2021-03-18
卷期号:6 (7)
被引量:33
标识
DOI:10.1172/jci.insight.145704
摘要
To identify small molecules that shield mammalian sensory hair cells from the ototoxic side effects of aminoglycoside antibiotics, 10,240 compounds were initially screened in zebrafish larvae, selecting for those that protected lateral-line hair cells against neomycin and gentamicin. When the 64 hits from this screen were retested in mouse cochlear cultures, 8 protected outer hair cells (OHCs) from gentamicin in vitro without causing hair-bundle damage. These 8 hits shared structural features and blocked, to varying degrees, the OHC's mechano-electrical transducer (MET) channel, a route of aminoglycoside entry into hair cells. Further characterization of one of the strongest MET channel blockers, UoS-7692, revealed it additionally protected against kanamycin and tobramycin and did not abrogate the bactericidal activity of gentamicin. UoS-7692 behaved, like the aminoglycosides, as a permeant blocker of the MET channel; significantly reduced gentamicin–Texas red loading into OHCs; and preserved lateral-line function in neomycin-treated zebrafish. Transtympanic injection of UoS-7692 protected mouse OHCs from furosemide/kanamycin exposure in vivo and partially preserved hearing. The results confirmed the hair-cell MET channel as a viable target for the identification of compounds that protect the cochlea from aminoglycosides and provide a series of hit compounds that will inform the design of future otoprotectants.
科研通智能强力驱动
Strongly Powered by AbleSci AI