首页> 外文期刊>Toxicological sciences: An official journal of the Society of Toxicology >Chronic toxicity/oncogenicity study of styrene in CD rats by inhalation exposure for 104 weeks.
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Chronic toxicity/oncogenicity study of styrene in CD rats by inhalation exposure for 104 weeks.

机译:吸入暴露104周对CD大鼠体内苯乙烯的慢性毒性/致癌性研究。

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摘要

Groups of 70 male and 70 female Charles River CD (Sprague-Dawley-derived) rats were exposed whole body to styrene vapor at 0, 50, 200, 500, or 1000 ppm 6 h/day 5 days/week for 104 weeks. The rats were observed daily, body weights and food and water consumption were measured periodically, and a battery of hematologic and clinical pathology examinations was conducted at weeks 13, 26, 52, 78, and 104. Nine or 10 rats per sex per group were necropsied after 52 weeks of exposure and the remaining survivors were necropsied after 104 weeks. Control and high-exposure rats received a complete histopathologic examination, while target organs, gross lesions, and all masses were examined in the lower exposure groups. Styrene had no effect on survival in males, but females exposed to 500 or 1000 ppm had a dose-related increase in survival. Levels of styrene in the blood at the end of a 6-h exposure during week 95 were proportional to exposure concentration. Levels of styrene oxide in the blood of rats exposed to 200 ppm or greater styrene were proportional to styrene exposure concentration. There were no changes of toxicologic significance in hematology, clinical chemistry, urinalysis, or organ weights. Males exposed to 500 or 1000 ppm gained less weight than the controls during the first year and maintained the difference during the second year. Females exposed to 200, 500, or 1000 ppm gained less weight during the first year; those exposed to 500 or 1000 ppm continued to gain less during months 13-18. Styrene-related non-neoplastic histopathologic changes were confined to the olfactory epithelium of the nasal mucosa. There was no evidence that styrene exposure caused treatment-related increases of any tumor type in males or females or in the number of tumor-bearing rats in the exposed groups compared to controls. In females, there were treatment-related decreases in pituitary adenomas and mammary adenocarcinomas. Based on an overall evaluation of eight oncogenicity studies, there is clear evidence that styrene does not induce cancer in rats.
机译:将70只雄性和70只雌性Charles River CD(Sprague-Dawley衍生)大鼠的组在0、50、200、500或1000 ppm的条件下于6天/天,5天/周,整周暴露于苯乙烯蒸气中104周。每天观察大鼠,定期测量体重,食物和水的消耗,并在第13、26、52、78和104周进行一系列血液学和临床病理学检查。每组每性别分别有9或10只大鼠。暴露52周后进行尸检,其余幸存者在104周后进行尸检。对照和高暴露大鼠接受了完整的组织病理学检查,而较低暴露水平的组则检查了靶器官,肉眼可见的病变和所有肿块。苯乙烯对男性的存活率没有影响,但是暴露于500或1000 ppm的女性的存活率与剂量相关。在第95周的6小时暴露结束后,血液中苯乙烯的水平与暴露浓度成正比。暴露于200 ppm或更高的苯乙烯的大鼠血液中的氧化苯乙烯水平与苯乙烯的暴露浓度成正比。在血液学,临床化学,尿液分析或器官重量方面,毒理学意义没有改变。在第一年,暴露于500或1000 ppm的男性体重减轻得比对照组少,在第二年保持这种差异。在第一年,暴露于200、500或1000 ppm的女性体重减轻了;在13至18个月中,那些暴露于500或1000 ppm的人的增幅继续降低。苯乙烯相关的非肿瘤组织病理学改变仅限于鼻黏膜的嗅上皮。没有证据表明,与对照组相比,暴露于苯乙烯的雄性或雌性引起的与治疗有关的任何肿瘤类型的增加,或暴露组中荷瘤大鼠的数量增加。在女性中,垂体腺瘤和乳腺腺癌的治疗相关减少。根据对八项致癌性研究的总体评估,有明确的证据表明苯乙烯不会在大鼠中诱发癌症。

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