A validation study of auditory function in an aminoglycoside-furosemide ototoxicity mouse model: Auditory brainstem response and distortion product otoacoustic emissions

Y. Ahn, Jin Sil Choi, Dae hyun Kim, Temuulen Batsaikhan, Y. Seo
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Abstract

Sensorineural hearing loss due to ototoxic drugs remains as a conflict as the treatment option with aminoglycosides. Ototoxic mouse model was produced with the administration of ototoxic drugs aminoglycoside kanamycin and loop-diuretic furosemide, thus validation of auditory function of the mouse model is needed to determine the efficacy of the drugs. Kanamycin sulfate 550 mg/kg (VWR life sciences, PA, USA) and furosemide 130 mg/kg (Lasix, Handok, Korea) were administered through subcutaneous and intraperitoneal injection respectively. Auditory brainstem response and distortion otoacoustic emission tests were performed on days 3,5,7,10,14 post administration of the ototoxic drug. Thresholds in response to the stimulus given in the auditory brainstem recordings and distortion otoacoustic emission tests were obtained. The hearing threshold shift to high stimulus intensity was observed post administration of the ototoxic drug. Latency of the ABR peak waves were recorded and analyzed, latency delay was observed as hearing threshold increases. These findings will further support in the application of this animal model in various studies regarding ototoxic hearing loss.
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氨基糖苷-呋塞米耳毒性小鼠模型听觉功能的验证研究:听觉脑干反应和畸变产物耳声发射
耳毒性药物引起的感音神经性听力损失与氨基糖苷类药物的治疗选择仍然存在冲突。耳毒性小鼠模型是通过给药氨基糖苷卡那霉素和环利尿剂速尿建立的,因此需要验证小鼠模型的听觉功能,以确定药物的疗效。硫酸卡那霉素550 mg/kg (VWR life sciences, PA, USA)和呋塞米130 mg/kg (Lasix, Handok, Korea)分别皮下注射和腹腔注射。分别于给药后第3、5、7、10、14天进行听性脑干反应和畸变耳声发射试验。在听觉脑干记录和畸变耳声发射测试中获得了对刺激的反应阈值。耳毒性药物给药后,听阈向高刺激强度转移。记录并分析ABR峰波的潜伏期,观察潜伏期随听力阈值的增加而延迟。这些发现将进一步支持该动物模型在耳毒性听力损失的各种研究中的应用。
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