Short B G, Steinhagen W H, Swenberg J A
Chemical Industry Institute of Toxicology, Research Triangle Park, North Carolina 27709.
Cancer Res. 1989 Nov 15;49(22):6369-78.
Unleaded gasoline (UG), a nongenotoxic kidney carcinogen in male, but not female, F344 rats or either sex of mice, and 2,2,4-trimethylpentane (TMP), a representative nephrotoxic isoparaffinic component of UG, were tested for potential promoting and cocarcinogenic effects in a kidney initiation-promotion model. The promotion study was conducted with 305 male and 305 female F344 rats fed 170 ppm N-ethyl-N-hydroxyethylnitrosamine in the drinking water for 2 weeks and then inhalation exposed to 0, 10, 70, or 300 ppm UG or 50 ppm TMP for 24 or 59 to 61 weeks. In a sequence reversal study, 390 male F344 rats were inhalation exposed to 0, 10, 70, or 300 ppm UG or 50 ppm TMP for 24 weeks, followed by 170 ppm N-ethyl-N-hydroxyethylnitrosamine in the drinking water during weeks 28 to 30, and killed at weeks 65 to 67. Renal neoplastic lesions were classified as atypical cell foci (ACF) and renal cell tumors (RCT). In the hydrocarbon promotion study, dose related increases were observed in the incidence of ACF in male rats promoted with UG or 50 ppm TMP for 24 or 60 weeks. A significant linear trend in the incidence of RCT was observed in male rats promoted with UG for 24 weeks. The incidence of ACF or RCT was not elevated in female rats promoted with UG or TMP. In the sequence reversal study, a slight increase in ACF was demonstrated in male rats exposed to 300 ppm UG, whereas no increase in RCT was observed in any exposure group. It is concluded that UG and TMP are promoters of ACF and RCT in male, but not female, rats under the conditions of this study. Data from related investigations suggest that the tumor promoting potential of UG and TMP results from reversible binding of metabolites to alpha 2u-globulin, which leads to decreased renal catabolism of this protein, chronic lysosomal overload, cell death, and compensatory cell proliferation.
无铅汽油(UG)在雄性F344大鼠而非雌性F344大鼠或任何性别的小鼠中是一种非遗传毒性肾致癌物,2,2,4-三甲基戊烷(TMP)是UG中一种具有代表性的肾毒性异链烷烃成分,在肾脏启动-促进模型中对其潜在的促进和共致癌作用进行了测试。促进研究使用了305只雄性和305只雌性F344大鼠,给它们饮用含170 ppm N-乙基-N-羟乙基亚硝胺的水2周,然后吸入暴露于0、10、70或300 ppm UG或50 ppm TMP中24周或59至61周。在一项顺序颠倒研究中,390只雄性F344大鼠吸入暴露于0、10、70或300 ppm UG或50 ppm TMP中24周,然后在第28至30周饮用含170 ppm N-乙基-N-羟乙基亚硝胺的水,并在第65至67周处死。肾肿瘤性病变分为非典型细胞灶(ACF)和肾细胞肿瘤(RCT)。在烃类促进研究中,在用UG或50 ppm TMP促进24周或60周的雄性大鼠中,观察到ACF发生率呈剂量相关增加。在用UG促进24周的雄性大鼠中,观察到RCT发生率有显著的线性趋势。在用UG或TMP促进的雌性大鼠中,ACF或RCT的发生率没有升高。在顺序颠倒研究中,暴露于300 ppm UG的雄性大鼠中ACF略有增加,而在任何暴露组中均未观察到RCT增加。得出的结论是,在本研究条件下,UG和TMP是雄性而非雌性大鼠中ACF和RCT的促进剂。相关研究数据表明,UG和TMP的肿瘤促进潜力源于其代谢产物与α2u-球蛋白的可逆结合,这导致该蛋白的肾脏分解代谢减少、慢性溶酶体过载、细胞死亡和代偿性细胞增殖。