Single-dose and chronic dietary neurotoxicity screening studies on 2,4-dichlorophenoxyacetic acid in rats.

J. Mattsson, J. Charles, B. Yano, H. Cunny, R. D. Wilson, J. Bus
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引用次数: 43

Abstract

Forms of 2,4-dichlorophenoxyacetic acid (collectively known as 2,4-D) are herbicides used to control a wide variety of broadleaf and woody plants. Single-dose acute and 1-year chronic neurotoxicity screening studies in male and female Fischer 344 rats (10/sex/dose) were conducted on 2,4-D according to the U.S. EPA 1991 guidelines. The studies emphasized a Functional Observational Battery (which included grip performance and hindlimb splay tests), automated motor activity testing, and comprehensive neurohistopathology of perfused tissues. Dosages were up to 250 mg/kg by gavage for the single-dose study, and up to 150 mg/kg/day in the diet for 52 weeks in the repeated-dose study. In the acute study, gavage with 250 mg/kg test material caused slight transient gait and coordination changes and clearly decreased motor activity at the time of maximal effect on the day of treatment (day 1). Mild locomotor effects occurred in one mid-dose rat (75 mg/kg), on Day 1 only. No gait, coordination, or motor activity effects were noted by day 8. In the chronic study, the only finding of neurotoxicologic significance was retinal degeneration in females in the high-dose group (150 mg/kg/day). Body weights of both sexes were slightly less than controls in the mid-dose group, and 10% less than controls in the high-dose group. In summary, the findings of these studies indicated a mild, transient locomotor effect from high-level acute exposure, and retinal degeneration in female rats from high-level chronic exposure. Based on the results from these two studies, the no-observed-adverse-effect level for acute neurotoxicity was 15 mg/kg/day and for chronic neurotoxicity was 75 mg/kg/day.
2,4-二氯苯氧乙酸对大鼠的单剂量和慢性膳食神经毒性筛选研究。
2,4-二氯苯氧乙酸(统称为2,4-d)是用于控制各种阔叶和木本植物的除草剂。根据美国环保署1991年的指南,对雄性和雌性Fischer 344大鼠(10只/性/剂量)进行了单剂量急性和1年慢性神经毒性筛选研究。这些研究强调功能观察电池(包括握力表现和后肢伸展测试)、自动运动活动测试和灌注组织的综合神经组织病理学。在单剂量研究中,通过灌胃给药的剂量高达250 mg/kg,在重复给药研究中,通过饮食给药的剂量高达150 mg/kg/天,持续52周。在急性研究中,在给药当天(第1天)效果最大时,用250 mg/kg的试验材料给药可引起轻微的短暂性步态和协调改变,并明显减少运动活动。一只中剂量大鼠(75 mg/kg)仅在第1天出现轻度运动作用。到第8天,没有注意到步态、协调或运动活动的影响。在慢性研究中,高剂量组(150 mg/kg/天)女性视网膜变性是唯一有神经毒理学意义的发现。中剂量组男女体重均略低于对照组,高剂量组体重比对照组低10%。总之,这些研究结果表明,高水平急性暴露对雌性大鼠有轻微的、短暂的运动影响,而高水平慢性暴露对雌性大鼠有视网膜变性。根据这两项研究的结果,急性神经毒性的未观察到的不良反应水平为15 mg/kg/天,慢性神经毒性为75 mg/kg/天。
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