Kurata K, Yamamoto M, Tsukuda R, Suzuki T, Sato S
Drug Safety Research Laboratories, Takeda Chemical Industries, Ltd., Osaka, Japan.
J Vet Med Sci. 1997 Jan;59(1):9-15. doi: 10.1292/jvms.59.9.
The acute effects of aspirin on auditory functions were examined electrophysiologically in conscious rats with chronically implanted electrodes for auditory brainstem response (ABR) recording. A single intravenous injection of aspirin at a dose of 225 mg/kg caused a reduction in the amplitude of the ABR P1 wave evoked by a 2 kHz tone pip 1 and 24 hr after dosing at almost all sound intensity levels, while the P1 amplitude at 4 kHz was reduced mainly 1 hr after dosing, and the P1 amplitude at 8 kHz was not significantly affected at middle and high intensities even 1 hr after dosing. The audiogram obtained from the P1 amplitude showed a significant increase in the sound threshold 1 and 24 hr after dosing at 2 kHz, and 1 hr after dosing at 4 kHz, but not at 8 kHz. The peak latency of the P1 wave was also prolonged. Furthermore, reduction of the P2 and P4 wave amplitude and prolongation of the P1-P2 and P2-P4 interpeak latency were also observed at 2 kHz but not a 4 or 8 kHz. These results suggest that the rat auditory function for low frequency is vulnerable to the effects of aspirin. This paradigm, i.e., frequency selectivity, n rats may be useful to further assess the different outer hair cells along the cochlear duct and provide additional evidence for the mechanism(s) or site underlying aspirin ototoxicity.
通过在慢性植入电极的清醒大鼠中进行电生理检查,以记录听觉脑干反应(ABR),研究了阿司匹林对听觉功能的急性影响。单次静脉注射剂量为225mg/kg的阿司匹林后,在给药后1小时和24小时,几乎在所有声音强度水平下,2kHz短纯音诱发的ABR P1波振幅均降低;而4kHz处的P1波振幅主要在给药后1小时降低,8kHz处的P1波振幅在给药后1小时即使在中高强度下也未受到显著影响。从P1波振幅获得的听力图显示,在2kHz给药后1小时和24小时以及4kHz给药后1小时,声音阈值显著升高,但8kHz处未出现这种情况。P1波的峰潜伏期也延长。此外,在2kHz处还观察到P2和P4波振幅降低以及P1 - P2和P2 - P4峰间潜伏期延长,但在4kHz或8kHz处未观察到。这些结果表明,大鼠的低频听觉功能易受阿司匹林的影响。这种在大鼠中的频率选择性模式可能有助于进一步评估沿耳蜗管的不同外毛细胞,并为阿司匹林耳毒性的潜在机制或部位提供额外证据。