Department of Biochemistry & Biotechnology, Annamalai University, Annamalai Nagar, Tamil Nadu, India.
Pathol Oncol Res. 2012 Jan;18(1):69-77. doi: 10.1007/s12253-011-9418-3. Epub 2011 Jun 25.
The present study was aimed to evaluate the antigenotoxic effect of Mosinone-A on 7,12-dimethylbenz[a]anthracene induced genotoxicity. The frequency of micronucleated polychromatic erythrocytes [MnPCEs], chromosomal aberrations [CA], DNA damage (comet assay) as cytogenetic markers and the status of lipid peroxidation byproducts, antioxidants and phase II detoxification agents were used as biochemical markers to assess the antigenotoxic effect of Mosinone-A on DMBA induced genotoxicity. A single intraperitoneal injection of DMBA (30 mg/kg b.wt) to golden Syrian hamsters, resulted in marked elevation in the frequency of MnPCEs, aberrations in the chromosomal structure were found in bone marrow and DNA damage (comet assay) was found in blood cells and altered level of lipid peroxidation, antioxidants, and phase II detoxification agents. Oral pretreatment of Mosinone-A (2 mg/kg b.wt) for 5 days to DMBA treated animals significantly reduced the frequency of MnPCEs, chromosomal abnormalities such as chromosomal break, gap, minute, fragment, DNA damage and reversed the status of biochemical variables. Our results thus demonstrated the antigenotoxic effect of Mosinone-A on DMBA induced genotoxicity in male golden Syrian hamsters.
本研究旨在评估 Mosinone-A 对 7,12-二甲基苯并[a]蒽诱导遗传毒性的抗原毒作用。微核多染红细胞(MnPCEs)的频率、染色体畸变(CA)、DNA 损伤(彗星试验)作为细胞遗传学标志物以及脂质过氧化产物、抗氧化剂和 II 相解毒剂的状态被用作生化标志物来评估 Mosinone-A 对 DMBA 诱导遗传毒性的抗原毒作用。单次腹腔注射 DMBA(30mg/kg 体重)给金黄地鼠,导致 MnPCEs 的频率显著升高,骨髓中发现染色体结构的畸变,并且在血细胞中发现 DNA 损伤(彗星试验)和脂质过氧化、抗氧化剂和 II 相解毒剂水平的改变。Mosinone-A(2mg/kg 体重)对 DMBA 处理动物的口服预处理 5 天,显著降低了 MnPCEs 的频率、染色体异常如染色体断裂、缺口、微核、片段、DNA 损伤,并逆转了生化变量的状态。因此,我们的结果表明 Mosinone-A 对雄性金黄地鼠 DMBA 诱导遗传毒性具有抗原毒作用。