Attenuation of hearing loss in DBA/2J mice by anti-apoptotic treatment

作者：Yang, Linlin; Zhang, Heng; Han, Xu; Zhao, Xin; Hu, Fangyuan; Li, Ping; Xie, Gang; Gao, Lixiang; Cheng, Lin; Song, Xicheng; Han, Fengchan^*

来源：Hearing Research, 2015, 327: 109-116.

DOI：10.1016/j.heares.2015.05.006

• MITOCHONDRIAL-DNA MUTATIONS
• EARLY-ONSET
• C57BL/6J MICE
• AGE
• COCHLEA
• STEREOCILIA
• FASCIN-2
• STRAINS
• FAMILY
• ACTIN

DBA/2J mice are characterized by early onset hearing loss at about 3-4 weeks of age. Mutations in cadherin 23 (Cdh23) and fascin-2 (Fscn2) are responsible for the phenotypes, but the underlying mechanism is unknown. In the present study, DBA/2J mice displayed progressive hair cell loss and degeneration of spiral ganglion neurons (SGNs) after 2 weeks of age; however, the mRNA level of Caspase-3 in the inner ears was much higher at 2 weeks of age than that at 4 or 8 weeks of age. Moreover, transcriptional levels of Caspase-3 and Caspase-9 in the inner ears of DBA/2J mice were significantly higher than those of C57BL/6J mice at 2 or 8 weeks of age. Immunohistochemistry localized Caspase-3 and Caspase-9 mainly to the hair cells, SGNs and stria vascularis of the cochleae. To determine the significance of caspase-dependent apoptosis in the hearing loss, the pan-caspase inhibitor Z-VAD-FMK was given intraperitoneally to DBA/J2 mice over an 8-week period starting at one week of age. Blockage of caspases preserved hearing in the mice by more than 10 dB (dB) sound pressure level (SPL) of the ABR thresholds and significantly reduced outer hair cell loss at the basal turns of the cochleae. These results demonstrate that apoptosis in the cochleae of DBA/J2 mice contributes to the early onset of hearing loss, which can be attenuated by anti-apoptotic treatment.

• 出版日期2015-9
• 单位烟台毓璜顶医院; 滨州医学院