Cheng M, Kligerman A D
Mutat Res. 1984 Jul;137(1):51-5. doi: 10.1016/0165-1218(84)90112-5.
o-, m- and p-Cresols were evaluated in both an in vitro and in vivo SCE assay. Dose-dependent SCE increases were not observed in cultured human fibroblasts with any of the isomers at concentrations up to 8 mM. There was a small but significant increase in SCE frequency compared to control at 8 mM o-cresol. A significant decrease in cell-cycle progression as measured by average generation time (AGT), was seen for all isomers at a concentration of 8 mM. Furthermore, no increase in SCE frequencies was observed in bone marrow, alveolar macrophages, and regenerating liver cells of male DBA/2 mice treated with a single i.p. injection of either o-cresol (200 mg/kg), m-cresol (200 mg/kg), or p-cresol (75 mg/kg) 21.5 h prior to sacrifice.
对邻甲酚、间甲酚和对甲酚进行了体外和体内姐妹染色单体交换(SCE)试验评估。在浓度高达8 mM的情况下,培养的人成纤维细胞中,未观察到任何一种异构体导致剂量依赖性的SCE增加。在8 mM邻甲酚时,与对照组相比,SCE频率有小幅但显著的增加。在浓度为8 mM时,所有异构体均出现平均世代时间(AGT)所测量的细胞周期进程显著下降。此外,在处死前21.5小时经腹腔注射邻甲酚(200 mg/kg)、间甲酚(200 mg/kg)或对甲酚(75 mg/kg)处理的雄性DBA/2小鼠的骨髓、肺泡巨噬细胞和再生肝细胞中,未观察到SCE频率增加。