国家毒理学规划关于1,2,4,5-四氯苯对F344/N大鼠和B6C3F1小鼠毒性研究的技术报告(饲料研究)(CAS No. 95-94-3)。

Toxicity report series Pub Date : 1991-01-01
>M. McDonald
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引用次数: 0

摘要

毒理学研究通过将F344/N大鼠和B6C3F1小鼠各组暴露于1,2,4,5-四氯苯(大于99%;在配方饲料中添加不同浓度的纯的,持续14天或13周。在为期14天的研究中,膳食中1,2,4,5-四氯苯的浓度分别为0、30、100、300、1,000或3,000 ppm。所有的大鼠都活到了研究结束,但3000 -ppm组的所有小鼠都死亡了(每组5只)。组织学上,暴露的雄性大鼠在肾皮质上皮中有异常透明液滴的积累。在雌性大鼠或雌雄小鼠中均未见明显的组织学病变。在为期13周的研究中,饮食中1,2,4,5-四氯苯的浓度分别为0、30、100、300、1,000或2,000 ppm(每组10只动物)。所有的大鼠都存活到研究结束;在2000ppm组中,两只雌性老鼠在垂死状态下被杀死。高剂量组的大鼠和小鼠的体重增加比对照组的要少。在暴露的雄性大鼠中,病变包括肾皮质小管上皮透明液滴形成,皮质小管再生,髓质颗粒铸型和矿化。雄性大鼠肾脏病变的频谱与描述为“碳氢化合物或透明液滴肾病”的实体一致。在一些雌性大鼠(30至2000 ppm组)中,肾皮质小管细胞再生,肾皮质上皮中积累了一种不明的黄棕色色素。暴露的雄性和雌性大鼠肝脏小叶中心肝细胞肥大。在小鼠中,1,000和2,000 ppm组的雄性小鼠和2,000 ppm组的雌性小鼠存在轻微至轻度的小叶中心肝细胞肥大。在2000 -ppm组中,每个性别的小鼠都出现了轻微到轻度的个体肝细胞变性。在雄性和雌性小鼠的两个最高剂量组中,观察到血清山梨醇脱氢酶和丙氨酸转氨酶活性升高,表明肝细胞损伤。300- 2000 -ppm组的雄性大鼠和100- 2000 -ppm组的雌性大鼠甲状腺滤泡细胞肥大。300- 2000 ppm组的雄性大鼠和30- 2000 ppm组的雌性大鼠的游离甲状腺素和总甲状腺素浓度下降表明原发性甲状腺功能减退。大鼠的血液学结果显示,摄入1000或2000 ppm的雄性大鼠的红细胞压积值、血红蛋白浓度和红细胞计数显著降低,雌性大鼠的平均细胞体积下降;对于小鼠,在2000 ppm组中,雄性小鼠的血红蛋白浓度、平均红细胞血红蛋白、红细胞压积和平均细胞体积都有所下降,在1000和2000 ppm组中,雌性小鼠的血红蛋白浓度、平均红细胞血红蛋白、红细胞压积和平均细胞体积都有所下降。这些发现表明,这两个物种都有再生障碍性贫血。对雄性和雌性大鼠的组织学病变的无观察效应水平(NOEL)为30ppm。雌雄小鼠组织学病变的NOEL均为300ppm。同义词:s-tetrachlorobenzene;四氯化苯。(注:这些研究的部分资金来自《综合环境反应、赔偿和责任法案》信托基金(超级基金),并与美国公共卫生服务局有毒物质和疾病登记处达成了机构间协议。)
本文章由计算机程序翻译,如有差异,请以英文原文为准。
NTP technical report on the toxicity studies of 1,2,4,5-Tetrachlorobenzene in F344/N Rats and B6C3F1 Mice (Feed Studies) (CAS No. 95-94-3).

Toxicology studies were conducted by exposing groups of F344/N rats and B6C3F1 mice of each sex to 1,2,4,5-tetrachlorobenzene (greater than 99%percnt; pure) at various concentrations in formulated diets for 14 days or 13 weeks. Dietary concentrations were 0, 30, 100, 300, 1,000, or 3,000 ppm 1,2,4,5-tetrachlorobenzene in the 14 day studies. All rats survived to the end of the studies, but all mice in the 3,000-ppm groups died (five animals per group). Histologically, exposed male rats had an accumulation of abnormal hyaline droplets in the renal cortical epithelium. Significant histologic lesions were not seen in female rats or in mice of either sex. Dietary concentrations were 0, 30, 100, 300, 1,000, or 2,000 ppm 1,2,4,5-tetrachlorobenzene in the 13-week studies (10 animals per group). All rats survived to the end of the studies; two female mice in the 2,000-ppm group were killed in a moribund condition. Body weight gains in the higher dose groups of rats and mice were less than those of controls. In exposed male rats, lesions included renal cortical tubular epithelial hyaline droplet formation, cortical tubular regeneration, and medullary granular casts and mineralization. This spectrum of renal lesions in male rats is consistent with the entity described as "hydrocarbon or hyaline droplet nephropathy." In some exposed female rats (30- to 2,000-ppm groups), there was renal cortical tubular cell regeneration plus accumulation of an unidentified yellow-brown pigment in the renal cortical epithelium. Centrilobular hepatocellular hypertrophy was observed in the livers of exposed male and female rats. In mice, minimal-to-mild centrilobular hepatocellular hypertrophy was present in males in the 1,000 and 2,000-ppm groups and in females in the 2,000-ppm group. Minimal-to-mild individual hepatocyte degeneration occurred in mice of each sex in the 2,000-ppm groups. Increased serum sorbitol dehydrogenase and alanine aminotransferase activity was observed in the two highest dose groups of male and female mice and indicated hepatocellular injury. Thyroid follicular cell hypertrophy was present in male rats in the 300- to 2,000-ppm groups and in female rats in the 100- to 2,000-ppm groups. Decreased free thyroxin and total thyroxin concentrations in male rats in the 300- to 2,000 ppm groups and female rats in the 30- to 2,000-ppm groups indicated a primary hypothyroid state. Hematologic findings for rats that received 1,000 or 2,000 ppm included significantly decreased hematocrit values, hemoglobin concentration, and erythrocyte counts for males and decreased mean cell volume for females; for mice, decreased hemoglobin concentrations, mean corpuscular hemoglobin, hematocrit, and mean cell volume were observed in males in the 2,000-ppm group and in females in the 1,000- and 2,000-ppm groups. These findings suggest a poorly regenerative anemia in both species. The no-observed-effect level (NOEL) for histologic lesions was 30 ppm for male and female rats. The NOEL for histologic lesions in male and female mice was 300 ppm. Synonyms: s-tetrachlorobenzene; benzene tetrachloride. (NOTE: These studies were supported in part by funds from the Comprehensive Environmental Response, Compensation, and Liability Act trust fund (Superfund) by an interagency agreement with the Agency for Toxic Substances and Disease Registry, U.S. Public Health Service.)

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