Generoso W M, Cain K T, Cornett C V, Cacheiro N L, Hughes L A
Biology Division, Oak Ridge National Laboratory, TN 37831-8077.
Environ Mol Mutagen. 1990;16(2):126-31. doi: 10.1002/em.2850160209.
Male mice were subjected to repeated inhalation exposures to different concentrations (165, 204, 250, or 300 ppm) of ethylene oxide (EtO) during an 8.5-week period. Transmitted clastogenic effects of these exposures were measured in terms of induction of dominant lethal mutations and heritable translocations. The concentration-response curves for both endpoints are not linear but are markedly concave upward. Significant increases in dominant lethals were detected at all concentrations, except the lowest one. In comparison, the incidences of heritable translocations were significantly increased at all concentrations.
在8.5周的时间内,让雄性小鼠反复吸入不同浓度(165、204、250或300 ppm)的环氧乙烷(EtO)。通过检测显性致死突变和可遗传易位的诱导情况来衡量这些暴露所产生的遗传断裂效应。这两个终点的浓度-反应曲线并非线性,而是明显向上凹陷。除最低浓度外,在所有浓度下均检测到显性致死率显著增加。相比之下,在所有浓度下可遗传易位的发生率均显著增加。