Li Chunmei, Gao Yonglin, Wang Yunzhi, Li Guisheng, Fan Xiaochen, Li Yanshen, Guo Chenghua, Tao Jun
School of Pharmacy, Key Laboratory of Molecular Pharmacology and Drug Evaluation (Yantai University), Ministry of Education, Collaborative Innovation Center of Advanced Drug Delivery System and Biotech Drugs in Universities of Shandong, Yantai University, Yantai 264005, PR China.
School of Life Sciences, Yantai University, Yantai 264005, PR China.
Regul Toxicol Pharmacol. 2017 Jun;86:374-378. doi: 10.1016/j.yrtph.2017.04.005. Epub 2017 Apr 10.
As part of a safety evaluation, we evaluated the potential genotoxicity of sodium formononetin-3'-sulphonate (Sul-F) using bacterial reverse mutation assay, chromosomal aberrations detection, and mouse micronucleus test. In bacterial reverse mutation assay using five strains of Salmonella typhimurium (TA97, TA98, TA100, TA102 and TA1535), Sul-F (250, 500, 1000, 2000, 4000 μg/plate) did not increase the number of revertant colonies in any tester strain with or without S9 mix. In a chromosomal assay using Chinese hamster lung fibroblast (CHL) cells, there were no increases in either kind of aberration at any dose of Sul-F (400, 800, and 1600 μg/mL) treatment groups with or without S9 metabolic activation. In an in vivo bone marrow micronucleus test in ICR mice, Sul-F at up to 2000 mg/kg (intravenous injection) showed no significant increases in the incidence of micronucleated polychromatic erythrocytes, and the proportion of immature erythrocytes to total erythrocytes. The results demonstrated that Sul-F does not show mutagenic or genotoxic potential under these test conditions.
作为安全性评估的一部分,我们使用细菌回复突变试验、染色体畸变检测和小鼠微核试验评估了芒柄花素 - 3'-磺酸钠(Sul-F)的潜在遗传毒性。在使用五株鼠伤寒沙门氏菌(TA97、TA98、TA100、TA102和TA1535)的细菌回复突变试验中,无论有无S9混合液,Sul-F(250、500、1000、2000、4000μg/平板)均未增加任何测试菌株中的回复菌落数。在使用中国仓鼠肺成纤维细胞(CHL)的染色体试验中,无论有无S9代谢活化,任何剂量的Sul-F(400、800和1600μg/mL)处理组中两种类型的畸变均未增加。在ICR小鼠的体内骨髓微核试验中,高达2000mg/kg(静脉注射)的Sul-F在微核多染红细胞的发生率以及未成熟红细胞与总红细胞的比例方面均未显示出显著增加。结果表明,在这些测试条件下,Sul-F不显示诱变或遗传毒性潜力。