甲苯对雄性和雌性大鼠的急性毒性:单次口服剂量暴露2周的研究

C. S. Mehta, P. Sun, A. Kuhn
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引用次数: 6

摘要

有毒物质和疾病登记局(ATSDR)在对甲苯的优先数据需求中已确定口服途径为主要接触途径,神经毒性为关注的终点。研究了甲苯对雄性和雌性Sprague-Dawley大鼠的急性口服神经毒性。剂量选择相对于基准剂量(BD)。BD被定义为最大非致死神经毒性剂量,并通过测距研究进行检查。3种口服(灌胃)剂量分别为3.0 ml/kg (50% BD)、4.5 ml/kg (75% BD)和6.0 ml/kg (100% BD)。为了表征其神经毒性,在给药后的第1天(分别为FOB和SMA暴露后2-3小时和4-7小时)、第7天和第14天测量了功能观察电池(FOB)和自发运动活动(SMA)。数据表明,与生理盐水对照组相比,暴露于甲苯的大鼠(雄性剂量为4.5和6.0 ml/kg,雌性剂量为6.0 ml/kg)在第1天表现出显著(p < 0.05)更大的视界…
本文章由计算机程序翻译,如有差异,请以英文原文为准。
ACUTE TOXICITY OF TOLUENE IN MALE AND FEMALE RATS:A SINGLE ORAL DOSE EXPOSURE 2-WEEK STUDY
The Agency for Toxic Substances and Disease Registry (ATSDR) has identified the oral route as the primary route of exposure, and neurotoxicity as the endpoint of concern, in the priority data needs for toluene. The acute oral neurotoxicity of toluene was investigated in male and female Sprague-Dawley rats. Dose selection was made relative to a benchmark dose (BD). The BD was defined as the maximum nonlethal neurotoxic dose and was examined by range-finding studies. The 3 oral (gavage) doses were 3.0 ml/kg (50% BD), 4.5 ml/kg (75% BD), and 6.0 ml/kg (100% BD). To characterize its neurotoxicity, a functional observational battery (FOB) and spontaneous motor activity (SMA) were measured on d 1 (2-3 h and 4-7 h postexposure times for FOB and SMA, respectively), 7, and 14 following toluene administration. The data indicate that on d 1, when compared with the saline controls, toluene-exposed rats (males at 4.5- and 6.0-ml/kg doses and females at 6.0-ml/kg dose) exhibited significantly ( p <.05) greater horiz...
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