Center for Hearing and Deafness, University at Buffalo, State University of New York, NY 14214, USA.
J Zhejiang Univ Sci B. 2011 Oct;12(10):853-61. doi: 10.1631/jzus.B1100040.
It is well known that ethacrynic acid (EA) can potentiate the ototoxicity of aminoglycoside antibiotics (AmAn) such as kanamycin (KM), if they were applied at the same time. Currently, to create the model of EA-KM-induced cochlear lesion in rats, adult rats received a single injection of EA (75 mg/kg, intravenous injection), or followed immediately by KM (500 mg/kg, intramuscular injection). The hearing function was assessed by auditory brainstem response (ABR) measurement in response to click and/or tone bursts at 4, 8, 12, 16, 20, 24, and 32 kHz. The static microcirculation status in the stria vascularis after a single EA injection was evaluated with eosin staining. The pathological changes in cochlear and vestibular hair cells were also quantified after co-administration of EA and KM. After a single EA injection, blood flow in vessels supplying the stria vascularis rapidly diminished. However, the blood supply to the cochlear lateral wall partially recovered 5 h after EA treatment. Threshold changes in ABR were basically parallel to the microcirculation changes in stria vascularis after single EA treatment. Importantly, disposable co-administration of EA and KM resulted in a permanent hearing loss and severe damage to the cochlear hair cells, but spared the vestibular hair cells. Since the cochlear lateral wall is the important part of the blood-cochlea barrier, EA-induced anoxic damage to the epithelium of stria vascularis may enhance the entry of KM to the cochlea. Thus, experimental animal model of selective cochlear damage with normal vestibular systems can be reliably created through co-administration of EA and KM.
众所周知,如果同时应用,依他尼酸(EA)可增强氨基糖苷类抗生素(AmAn)如卡那霉素(KM)的耳毒性。目前,为了在大鼠中创建 EA-KM 诱导的耳蜗病变模型,成年大鼠接受单次 EA(75mg/kg,静脉注射)注射,或随后立即接受 KM(500mg/kg,肌肉注射)。通过听觉脑干反应(ABR)测量对 4、8、12、16、20、24 和 32kHz 的点击和/或纯音爆发来评估听力功能。单次 EA 注射后,用曙红染色评估血管纹的静态微循环状态。在 EA 和 KM 共同给药后,还对耳蜗和前庭毛细胞的病理变化进行了量化。单次 EA 注射后,供应血管纹的血管中的血流迅速减少。然而,EA 处理后 5 小时,耳蜗外侧壁的血液供应部分恢复。ABR 的阈值变化基本上与单次 EA 处理后血管纹微循环变化平行。重要的是,EA 和 KM 的一次性共同给药导致永久性听力损失和耳蜗毛细胞严重损伤,但前庭毛细胞不受影响。由于耳蜗外侧壁是血-耳蜗屏障的重要组成部分,EA 对血管纹上皮的缺氧损伤可能增强 KM 进入耳蜗。因此,通过 EA 和 KM 的共同给药可以可靠地创建具有正常前庭系统的选择性耳蜗损伤的实验动物模型。