Melnick R L, Huff J E, Roycroft J H, Chou B J, Miller R A
National Institute of Environmental Health Sciences, Research Triangle Park, NC 27709.
Environ Health Perspect. 1990 Jun;86:27-36. doi: 10.1289/ehp.908627.
1,3-Butadiene, a large-production volume chemical used mainly in the manufacture of synthetic rubber, was found to induce multiple-organ carcinogenicity in male and female B6C3F1 mice at exposure concentrations (625 and 1250 ppm) equivalent to and below the OSHA standard of 1000 ppm. Since this study was terminated after 60 weeks of exposure because of reduced survival due to fatal tumors, and because dose-response relationships for 1,3-butadiene-induced neoplastic and nonneoplastic lesions were not clearly established, a second long-term inhalation study of 1,3-butadiene in B6C3F1 mice was conducted at lower exposure concentrations, ranging from 6.25 to 625 ppm. Both the histopathological findings from animals dying through week 65 and the results of evaluations of animals exposed for 40 and 65 weeks are presented in this report. Exposure to 1,3-butadiene caused a regenerative anemia at concentrations of 62.5 ppm and higher. Testicular atrophy was induced at 625 ppm, and ovarian atrophy was observed at 20 ppm and higher. During the first 50 weeks of the study, lymphocytic lymphoma was the major cause of death of mice exposed to 625 ppm 1,3-butadiene. Neoplasms of the heart, forestomach, lung, Harderian gland, mammary gland, ovary, and liver were frequently observed in 1,3-butadiene-exposed mice that died between week 40 and week 65 of the study. Studies in which exposure to 1,3-butadiene was stopped after limited periods were also included to assess the relationship between exposure levels and duration of exposures on the outcome of 1,3-butadiene-induced carcinogenicity. In these studies, lymphocytic lymphomas were induced in male mice exposed to 625 ppm 1,3-butadiene for only 13 weeks. The incidence of lymphocytic lymphoma in male mice exposed to 625 ppm 1,3-butadiene for 26 weeks was two times that in mice exposed to 625 ppm for 13 weeks. However, when the exposure concentration was reduced by half to 312 ppm and the exposure duration extended to 52 weeks, the incidence of lymphocytic lymphoma was reduced by 90%. Thus, the multiple of the exposure concentration times the exposure duration did not predict the incidence of lymphocytic lymphoma in mice. The early mortalities resulting from lymphocytic lymphomas in male mice exposed to 625 ppm 1,3-butadiene limited the expression of tumors at other sites. A clearer dose-response for 1,3-butadiene-induced neoplasia should be apparent from experiments in mice exposed to lower concentrations of this chemical for 2 years.
1,3 - 丁二烯是一种大量生产的化学品,主要用于制造合成橡胶。研究发现,在暴露浓度(625和1250 ppm)等于或低于职业安全与健康管理局(OSHA)1000 ppm标准的情况下,1,3 - 丁二烯可诱导雄性和雌性B6C3F1小鼠发生多器官致癌性。由于该研究在暴露60周后因致命肿瘤导致存活率降低而终止,且1,3 - 丁二烯诱导的肿瘤性和非肿瘤性病变的剂量反应关系未明确确立,因此在较低暴露浓度(6.25至625 ppm)下对B6C3F1小鼠进行了第二项1,3 - 丁二烯长期吸入研究。本报告呈现了直至第65周死亡动物的组织病理学发现以及暴露40周和65周动物的评估结果。暴露于1,3 - 丁二烯在浓度为62.5 ppm及更高时会导致再生性贫血。在625 ppm时可诱导睾丸萎缩,在20 ppm及更高时可观察到卵巢萎缩。在研究的前50周,淋巴细胞性淋巴瘤是暴露于625 ppm 1,3 - 丁二烯的小鼠的主要死亡原因。在研究第40周至第65周期间死亡的暴露于1,3 - 丁二烯的小鼠中,经常观察到心脏、前胃、肺、哈德氏腺、乳腺、卵巢和肝脏的肿瘤。还纳入了在有限时间段后停止暴露于1,3 - 丁二烯的研究,以评估暴露水平和暴露持续时间与1,3 - 丁二烯致癌性结果之间的关系。在这些研究中,仅暴露于625 ppm 1,3 - 丁二烯13周的雄性小鼠诱发了淋巴细胞性淋巴瘤。暴露于625 ppm 1,3 - 丁二烯26周的雄性小鼠中淋巴细胞性淋巴瘤的发生率是暴露于625 ppm 13周小鼠的两倍。然而,当暴露浓度减半至312 ppm且暴露持续时间延长至52周时,淋巴细胞性淋巴瘤的发生率降低了90%。因此,暴露浓度乘以暴露持续时间的倍数并不能预测小鼠中淋巴细胞性淋巴瘤的发生率。暴露于625 ppm 1,3 - 丁二烯的雄性小鼠因淋巴细胞性淋巴瘤导致的早期死亡限制了其他部位肿瘤的表现。在暴露于较低浓度该化学品2年的小鼠实验中,1,3 - 丁二烯诱导肿瘤的剂量反应应该会更清晰。