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作 者:郑红燕[1,2] 饶凯敏[1,2] 姜英[1,2] 杨光涛[1,2] 陈曦[1,2] 王建书[1,2] 汪倩[1,2] 王晶[1,2] 袁晶[1,2]
机构地区:[1]华中科技大学同济医学院公共卫生学院劳动卫生与环境卫生学系,湖北武汉430030 [2]环境与健康教育部重点实验室,湖北武汉430030
出 处:《癌变.畸变.突变》2012年第1期25-29,共5页Carcinogenesis,Teratogenesis & Mutagenesis
基 金:国家自然科学基金项目(30972437)
摘 要:目的:研究邻苯二甲酸单(2-乙基)己酯(mono-2-ethylexyl phthalate,MEHP)对人乳腺癌MCF-7细胞DNA氧化损伤的作用。方法:分别用不同浓度的MEHP(6.25、12.5、25、50和100μmol/L)和二甲基亚砜(溶剂对照,<0.1%)处理MCF-7细胞12和24 h后用MTT比色法检测细胞的存活率。再分别于染毒后1.5、3、6、12和24 h,测定丙二醛(malondialdehyde,MDA)、超氧化物歧化酶(superoxide dismutase,SOD)、谷胱甘肽过氧化物酶(glutathione peroxidase,GSH-Px)和细胞8-羟基脱氧鸟苷(8-hydroxy-2′-deoxyguanosine,8-OHdG)水平。结果:与对照组比较,MEHP染毒12 h,6.25和12.5μmol/L组细胞的存活率显著增加(P<0.05)。MEHP染毒24 h,在较高浓度处理组(≥25μmol/L)的细胞存活率显著降低(P<0.05);各处理组细胞的SOD活性有所增加,细胞MDA水平、GSH-Px活性以及8-OHdG生成量无显著变化(P>0.05)。当MEHP染毒MCF-7细胞较短时间(1.5、3和6 h)时,各处理组MDA水平和8-OHdG生成量均显著升高(P<0.05),而SOD和GSH-Px活性则显著性降低(P<0.05)。结论:一定浓度MEHP作用在短时间内(1.5、3和6 h)可引起MCF-7细胞的氧化应激反应,并触发细胞DNA的氧化性损伤,具体调控机制有待深入研究。OBJECTIVE:Oxidative DNA-damaging effects of mono-2-ethylexyl phthalate(MEHP) on MCF-7 cells were investigated.METHODS:MCF-7 cells were treated with MEHP at various concentrations (6.25,12.5,25,50 and 100μmol/L) or dimethyl sulphoxide alone(DMSO,solvent control,final concentration 1‰). Cell proliferation was measured by the MTT assay at 12 and 24 h after the treatment.At the time points(1.5,3,6,12 and 24 h),the content of malondialdehyde(MDA) and activities of superoxide dismutase(SOD) and glutathione peroxidase (GSH-Px) were measured using the corresponding kits.The level of(8-hydroxy-2'-deoxyguanosine,8-OHdG) in MEHP-treated cells was estimated using high-pressure liquid chromatography with electrochemical detection HPLC-ECD method. RESULTS:At 12 h after treatment,cell proliferation rates significantly increased in MEHP-treated groups(6.25 and 12.5μmol/L,P0.05 for both).However,cell proliferation rates significantly decreased at 24 h after treatment,in the higher MEHP-treated groups(25-100μmol/L,P0.05 for all).There were no significant changes in the levels of MDA,GSH-Px and 8-OHdG(P0.05 for all).After MCF-7 cells were treated with MEHP for short periods(1.5,3 and 6 h),the levels of MDA and 8-OHdG in all treatment groups were increased(P0.05),but SOD and GSH-Px activities were reduced(P0.05 for all).CONCLUSION:Short periods(≤6 h) of treatment with MEHP at a certain concentration induced oxidative stress in MCF-7 cells,and accelerated DNA oxidative damage.The underlying mechanisms of MEHP mediated oxidative DNA damage MCF-7 cells need to be investigated.
关 键 词:邻苯二甲酸单(2-乙基)己酯 氧化应激 DNA氧化损伤 8-羟基脱氧鸟苷
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