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机构地区:[1]杭州师范大学生命与环境科学学院,浙江杭州310036
出 处:《杭州师范大学学报(自然科学版)》2010年第6期430-433,共4页Journal of Hangzhou Normal University(Natural Science Edition)
基 金:浙江省自然科学基金项目(Y2090698);浙江省钱江人才计划项目(2010R10062);生物科学国家特色专业建设项目
摘 要:为探讨硫辛酸对甲醛诱发人HepG2细胞DNA损伤的保护作用,体外培养的HepG2细胞经甲醛(0.25,2.5,25μmol/L)单独处理或甲醛与硫辛酸((5+20),(5+40)μmol/L)同时处理2 h后,分别运用彗星试验(comet assay)结合彗星图像分析软件(CASP)分析细胞尾部DNA百分率(tail DNA%)变化.结果显示:不同浓度甲醛处理后HepG2细胞尾部DNA百分率以浓度依赖性方式显著升高(P<0.01);但甲醛与硫辛酸同时处理后HepG2细胞尾部DNA百分率明显降低并与硫辛酸浓度呈依赖关系,与甲醛单独处理组(5μmol/L)相比差异显著(P<0.05或P<0.01).此结果说明硫辛酸对甲醛诱发的人HepG2细胞DNA损伤有保护作用.To investigate the protecting role of lipoic acid on DNA damage induced by formaldehyde in human HepG2 cells,cultured HepG2 cells were treated with formaldehyde(0.25,2.5,25 μmol/L) alone or treated with formaldehyde and lipoic acid together((5+20),(5+40) μmol/L) for 2 h.After the treatment,the tail DNA % of HepG2 cells was analyzed using the comet assay combined with the comet image analyzing software(CASP).The results have showed that when treated with different concentrations of formaldehyde alone, the tail DNA ~ of HepG2 cells has significantly increased with the concentration-effect dependent manner (P〈0.01). However, when treated with formaldehyde and lipoic acid together, the tail DNA ~ of HepG2 cells has obviously decreased with the lipoic aci&dependent mode, and has distinct difference comparing to the formaldehyde alone(5μmol/L)-treated cells (P〈0.05 or P〈0.01). The paper has concluded that lipoic acid has the role of protecting the formaldehyde induced DNA damage in HepG2 cells.
关 键 词:硫辛酸 甲醛 HEPG2细胞 彗星试验 DNA损伤
分 类 号:R114[医药卫生—卫生毒理学]
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