Hatzopoulos S, Di Stefano M, Albertin A, Martini A
Department of ENT, Service of Audiology, University of Ferrara, Italy.
Ann N Y Acad Sci. 1999 Nov 28;884:211-25. doi: 10.1111/j.1749-6632.1999.tb08643.x.
The ototoxic effects of cisplatin were evaluated by otoacoustic emissions and evoked auditory responses. A transient otoacoustic emissions protocol indicated no significant ototoxic effects in rats treated intravenously with 7.5 mg/kg/week for 2-weeks. A chronic 6-week treatment (2.5 mg/kg/week) monitored by 2F1-F2 distortion product emissions presented significant SNR alterations in a narrow range of frequencies (5.04-5.66 kHz). An acute treatment of 15 mg/kg, using slow 30-min intraperitoneal infusion, presented the highest DP and ABR alterations. The SNR at the 2F1-F2 frequencies 6.34, 7.13, and 7.56 kHz was found significantly decreased, and ABR latency measurements from 8-kHz burst stimuli verified these alterations.
通过耳声发射和诱发听觉反应评估顺铂的耳毒性作用。瞬态耳声发射方案表明,每周静脉注射7.5 mg/kg共2周的大鼠未出现明显耳毒性作用。通过2F1-F2畸变产物发射监测的6周慢性治疗(每周2.5 mg/kg)在窄频率范围(5.04-5.66 kHz)呈现出显著的信噪比改变。采用30分钟缓慢腹腔内输注进行的15 mg/kg急性治疗呈现出最高的畸变产物(DP)和听性脑干反应(ABR)改变。发现在6.34、7.13和7.56 kHz的2F1-F2频率处信噪比显著降低,并且来自8 kHz猝发声刺激的ABR潜伏期测量结果证实了这些改变。