Fei Chenzhong, Zhang Jie, Lin Yang, Wang Xiaoyang, Zhang Keyu, Zhang Lifang, Zheng Wenli, Wang Mi, Li Tao, Xiao Sui, Xue Feiqun, Wang Chunmei
Key Laboratory of Veterinary Drug Safety Evaluation and Residues Research, Shanghai Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Shanghai 200241, PR China.
Chinese Medicine Hospital of Pudong New Area, Shanghai 201200, PR China.
Regul Toxicol Pharmacol. 2015 Apr;71(3):585-9. doi: 10.1016/j.yrtph.2015.01.011. Epub 2015 Jan 30.
Nitromezuril (NZL) is a novel triazine compound that exhibits remarkable anticoccidial activity. However, mutagenicity and genotoxicity of NZL have not been evaluated to date. This study evaluated the potential risks of NZL by testing for bacterial reverse mutation (Ames), mouse sperm abnormality (SA), bone marrow micronucleus (MN) and chromosomal aberration (CA). Mice were orally administered with NZL at 385, 192 and 96 mg/kg, corresponding to 0.5 ×, 0.25 × and 0.125 × the LD50 of NZL, respectively. No significant increases in SA and CA were found in mice treated with NZL for 5d and 3d, respectively (P>0.05). NZL at 96-385 mg/kg did not have significant influence on micronucleated polychromatic erythrocyte counts (P>0.05). These results suggest that NZL is not genotoxic. However, Ames test results were positive both with and without the S9 system for Salmonella typhimurium TA98 and TA100, suggesting that NZL may be mutagenic. The mutagenic effects of NZL were different in in vitro and in vivo assays. Further studies should be conducted to confirm the safety of using and developing NZL as a novel anticoccidial drug.
硝美珠利(NZL)是一种新型三嗪化合物,具有显著的抗球虫活性。然而,NZL的致突变性和遗传毒性迄今尚未评估。本研究通过细菌回复突变试验(Ames试验)、小鼠精子畸形试验(SA)、骨髓微核试验(MN)和染色体畸变试验(CA)来评估NZL的潜在风险。分别以385、192和96mg/kg的剂量给小鼠口服NZL,相应剂量分别为NZL半数致死量(LD50)的0.5倍、0.25倍和0.125倍。用NZL处理5天和3天的小鼠,其精子畸形率和染色体畸变率均未显著增加(P>0.05)。96 - 385mg/kg的NZL对多染性红细胞微核计数无显著影响(P>0.05)。这些结果表明NZL无遗传毒性。然而,在鼠伤寒沙门氏菌TA98和TA100菌株中,无论有无S9系统,Ames试验结果均为阳性,提示NZL可能具有致突变性。NZL的致突变作用在体外和体内试验中有所不同。应进一步开展研究以确认将NZL作为新型抗球虫药物使用和开发的安全性。