Kalantari Heibatullah, Rezaei Mohsen, Mahdavinia Masoud, Kalantar Mojtaba, Amanpour Zivar, Varnaseri Golnaz
Faculty of Pharmacy, Toxicology Research Center, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran.
Adv Pharm Bull. 2012;2(2):245-8. doi: 10.5681/apb.2012.037. Epub 2012 Aug 15.
The increasing use of herbal drugs and their easy availability have necessitated the use of mutagenicity test to analyze their toxicity and safety. The aim of this study was to evaluate the genotoxicity of Supermint herbal medicine in DNA breakage of rat hepatocytes in comparison with sodium dichromate by single cell gel electrophoresis technique or comet assay.
Hepatocytes were prepared from male wistar rats and were counted and kept in a bioreactor for 30 minutes. Then cells were exposed to the Supermint herbal medicine at doses of 125, 250 and 500 µl/ml. Buffer 4 (incubation buffer) and sodium dichromate were used as negative and positive control for one hour respectively. Then cell suspension with low melting point agarose were put on precoated slides and covered with agarose gel. Then lysing, electrophoresis, neutralization and staining were carried out. Finally the slides were analyzed with fluorescence microscope. The parameter under this analysis was the type of migration which was determined according to Kobayashi pattern.
With increased dose of Supermint herbal medicine the DNA damage was slightly increased (P<0001). Conlusion: In overall compared to the positive control significant differences is observed which convinced that the crude extract of Supermint in vitro did not have mutagenic effect. Conlusion: In overall compared to the positive control significant differences is observed which convinced that the crude extract of Supermint in vitro did not have mutagenic effect.
草药的使用日益增加且易于获取,因此有必要使用致突变性试验来分析其毒性和安全性。本研究的目的是通过单细胞凝胶电泳技术或彗星试验,比较超薄荷草药与重铬酸钠对大鼠肝细胞DNA断裂的遗传毒性。
从雄性Wistar大鼠制备肝细胞,计数后置于生物反应器中30分钟。然后将细胞分别以125、250和500微升/毫升的剂量暴露于超薄荷草药。缓冲液4(孵育缓冲液)和重铬酸钠分别用作阴性和阳性对照1小时。然后将含有低熔点琼脂糖的细胞悬液置于预先包被的载玻片上,并用琼脂糖凝胶覆盖。接着进行裂解、电泳、中和及染色。最后用荧光显微镜分析载玻片。该分析的参数是根据小林模式确定的迁移类型。
随着超薄荷草药剂量的增加,DNA损伤略有增加(P<0.001)。结论:总体而言,与阳性对照相比观察到显著差异,这表明超薄荷粗提物在体外没有致突变作用。结论:总体而言,与阳性对照相比观察到显著差异,这表明超薄荷粗提物在体外没有致突变作用。