三氯乙烯的耳毒性:高浓度、短时间动物暴露数据的推断和相关性

K.M. Crofton , X. Zhao
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引用次数: 0

摘要

吸入暴露于高浓度的1,1,2-三氯乙烯(TCE)已被证明会损害大鼠中频范围内的听力。本研究直接评估了高浓度、短期暴露于TCE以预测长期暴露所产生的神经毒性的充分性。将成年雄性Long-Evans大鼠(每组10-12只)在1 m3不锈钢通流室中(全身)吸入TCE,每天6小时,每周5天。使用以下暴露:1天(4000 - 8000ppm)、1周(1000 - 4000ppm)、4周(800 - 3200ppm)和13周(800 - 3200ppm)。只接触空气的动物作为对照。在接触16 khz音调3-5周后使用反射修正听力学测定听觉阈值。结果重复了先前的研究结果,即在所有暴露时间内,在16千赫频率下都有听力损失。暴露1天、1周、4周和13周时,16 khz阈值的dB15浓度(阈值增加15 dB的浓度)分别为6218、2992、2592和2160 ppm。这些数据表明,TCE的耳毒性小于严格的浓度×时间关系预测的耳毒性。这些数据还表明,简单的外推模型(即C × t = k,哈伯定律)在从短时间外推到长时间暴露时高估了TCE的效力。此外,这些数据表明,相对于环境或职业暴露,TCE对大鼠的耳毒性是一种高浓度效应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Ototoxicity of Trichloroethylene: Extrapolation and Relevance of High-Concentration, Short-Duration Animal Exposure Data

Inhalation exposure to high concentrations of 1,1,2-trichloroethylene (TCE) has been shown to damage hearing in the mid-frequency range in the rat. The present study directly evaluated the adequacy of high-concentration, short-term exposures to TCE for predicting the neurotoxicity produced by longer duration exposures. Adult male Long–Evans rats (n= 10–12 per group) were exposed to TCE via inhalation (whole body) in 1-m3stainless steel flow-through chambers for 6 hr/day, 5 days/week. The following exposures were used: 1 day (4000–8000 ppm), 1 week (1000–4000 ppm), 4 weeks (800–3200 ppm), and 13 weeks (800–3200 ppm). Air-only exposed animals served as controls. Auditory thresholds were determined for a 16-kHz tone 3–5 weeks after exposure using reflex modification audiometry. Results replicated previous findings of a hearing loss at 16 kHz for all exposure durations. The dB15 concentrations (concentration that increases thresholds by 15 dB) for 16-kHz thresholds were 6218, 2992, 2592, and 2160 ppm for the 1-day, 1-week, 4-week and 13-week exposures, respectively. These data demonstrate that the ototoxicity of TCE was less than that predicted by a strict concentration × time relationship. These data also demonstrate that simple models of extrapolation (i.e.,C × t = k, Haber's Law) overestimate the potency of TCE when extrapolating from short-duration to longer-duration exposures. Furthermore, these data suggest that, relative to ambient or occupational exposures, the ototoxicity of TCE in the rat is a high-concentration effect.

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