Fechter L D, Liu Y
Toxicology Program, College of Pharmacy, University of Oklahoma Health Sciences Center, Oklahoma City 73190.
Hear Res. 1994 Aug;78(2):189-96. doi: 10.1016/0378-5955(94)90025-6.
Trimethyltin (TMT), a model neurotoxicant, has previously been demonstrated to disrupt auditory thresholds in laboratory subjects. In this experiment we characterized the potency of this ototoxicant by means of a dose response study and then evaluated the functional effects of TMT administration when tone-bursts were presented at supra-threshold levels. Guinea pigs were anaesthetized and prepared for electrophysiological measurement of the compound action potential (CAP) and cochlear microphonic (CM). Subsequently averaged wave forms generated by tone-bursts of 0-80 dB SPL were evaluated in order to calculate both a N1 and a summating potential (SP) input-output function. We show that TMT at doses as low as 0.2 mg/kg produce elevations in N1, but not in the CM isopotential curve. Using exposures to 0.5 mg/kg TMT we show a profound reduction in the slope of the N1 input-output curve, but no shift in the SP. The results are consistent with the hypothesis that TMT disrupts function at the synapse between the inner hair cell and the Type 1 spiral ganglion cell.
三甲基锡(TMT)是一种典型的神经毒素,此前已证实它会破坏实验对象的听觉阈值。在本实验中,我们通过剂量反应研究来确定这种耳毒性物质的效力,然后评估当以阈上水平呈现短纯音时给予TMT后的功能效应。将豚鼠麻醉并准备好用于复合动作电位(CAP)和耳蜗微音电位(CM)的电生理测量。随后,对由0 - 80 dB SPL的短纯音产生的平均波形进行评估,以计算N1和总和电位(SP)的输入 - 输出函数。我们发现,低至0.2 mg/kg的TMT剂量会使N1升高,但不会使CM等电位曲线升高。使用0.5 mg/kg TMT进行暴露实验,我们发现N1输入 - 输出曲线的斜率显著降低,但SP没有偏移。这些结果与TMT破坏内毛细胞与I型螺旋神经节细胞之间突触功能的假设一致。