癌变·畸变·突变
癌變·畸變·突變
암변·기변·돌변
CARCINOGENSES,TERATOGENSIS AND MUTAGENESIS
2010年
2期
126-129
,共4页
周炯林%连勇%彭双清%徐培渝
週炯林%連勇%彭雙清%徐培渝
주형림%련용%팽쌍청%서배투
敌敌畏%乐果%马拉硫磷%遗传毒性%彗星试验
敵敵畏%樂果%馬拉硫燐%遺傳毒性%彗星試驗
활활외%악과%마랍류린%유전독성%혜성시험
dichlorvos%dimethoate%malathion%genotoxicity%comet assay
目的:评价敌敌畏(dichlorvos,DDVP)、乐果(dimethoate, DM)和马拉硫磷(malathion, Mal)3种常用有机磷农药单独及两两组合下诱导HepG2细胞DNA损伤效应,并阐明联合作用模式. 方法:3种有机磷农药分别单独染毒HepG2细胞4 h,联合效应研究采用析因设计分别在高剂量水平和低剂量水平下将3种农药两两混合染毒,同时设溶剂对照(DMSO作用4 h)和阳性对照(0.5 μmol/ml重铬酸钾染毒2 h),染毒结束后进行彗星试验,采集图像并用CASP软件分析,选择尾部DNA百分比、彗星尾长(tail length,TL)和Olive尾矩(Olive tail moment, OTM)表示DNA损伤强度. 结果:3种有机磷农药单独作用时,较高剂量组的尾部DNA百分比、TL和OTM均显著高于对照组(P<0.01);析因分析联合效应结果表明,较低剂量水平下,DDVP与DM之间无交互作用(P>0.05),DDVP与Mal之间以及DM与Mal之间存在交互作用(P<0.01),交互方式均为协同;在较高剂量水平,3种农药两两间均存在交互作用(P<0.05),交互方式均为拮抗. 结论:敌敌畏、乐果和马拉硫磷单独及两两联合作用均可致DNA损伤,在低剂量和高剂量水平下,存在不同的联合作用模式.
目的:評價敵敵畏(dichlorvos,DDVP)、樂果(dimethoate, DM)和馬拉硫燐(malathion, Mal)3種常用有機燐農藥單獨及兩兩組閤下誘導HepG2細胞DNA損傷效應,併闡明聯閤作用模式. 方法:3種有機燐農藥分彆單獨染毒HepG2細胞4 h,聯閤效應研究採用析因設計分彆在高劑量水平和低劑量水平下將3種農藥兩兩混閤染毒,同時設溶劑對照(DMSO作用4 h)和暘性對照(0.5 μmol/ml重鉻痠鉀染毒2 h),染毒結束後進行彗星試驗,採集圖像併用CASP軟件分析,選擇尾部DNA百分比、彗星尾長(tail length,TL)和Olive尾矩(Olive tail moment, OTM)錶示DNA損傷彊度. 結果:3種有機燐農藥單獨作用時,較高劑量組的尾部DNA百分比、TL和OTM均顯著高于對照組(P<0.01);析因分析聯閤效應結果錶明,較低劑量水平下,DDVP與DM之間無交互作用(P>0.05),DDVP與Mal之間以及DM與Mal之間存在交互作用(P<0.01),交互方式均為協同;在較高劑量水平,3種農藥兩兩間均存在交互作用(P<0.05),交互方式均為拮抗. 結論:敵敵畏、樂果和馬拉硫燐單獨及兩兩聯閤作用均可緻DNA損傷,在低劑量和高劑量水平下,存在不同的聯閤作用模式.
목적:평개활활외(dichlorvos,DDVP)、악과(dimethoate, DM)화마랍류린(malathion, Mal)3충상용유궤린농약단독급량량조합하유도HepG2세포DNA손상효응,병천명연합작용모식. 방법:3충유궤린농약분별단독염독HepG2세포4 h,연합효응연구채용석인설계분별재고제량수평화저제량수평하장3충농약량량혼합염독,동시설용제대조(DMSO작용4 h)화양성대조(0.5 μmol/ml중락산갑염독2 h),염독결속후진행혜성시험,채집도상병용CASP연건분석,선택미부DNA백분비、혜성미장(tail length,TL)화Olive미구(Olive tail moment, OTM)표시DNA손상강도. 결과:3충유궤린농약단독작용시,교고제량조적미부DNA백분비、TL화OTM균현저고우대조조(P<0.01);석인분석연합효응결과표명,교저제량수평하,DDVP여DM지간무교호작용(P>0.05),DDVP여Mal지간이급DM여Mal지간존재교호작용(P<0.01),교호방식균위협동;재교고제량수평,3충농약량량간균존재교호작용(P<0.05),교호방식균위길항. 결론:활활외、악과화마랍류린단독급량량연합작용균가치DNA손상,재저제량화고제량수평하,존재불동적연합작용모식.
OBJECTIVE: To invesgate the genotoxicity of dichlorvos(DDVP), dimethoate(DM) and malathion(Mal) in HepC2 cells alone and in combination, and to elucidate the combined genotoxic effects. METHODS: Comet assay (single cell gel electrophoresis assay) was adopted to evaluate the genotoxicity of dichlorvos(DDVP), dimethoate(DM) and malathion(Mal), the images were collected and then analyzed by CASP software. The 2× 2factorial analysis experiment was used to investigate their combined genotoxic effects. RESULTS: DDVP, DM and Mai all induced obvious DNA damage in HepG2 cells after treatmemt for 4 h. At the two higher concentrations of each pesticide, these parameters (percent of Tail DNA, Tail Length and Olive Tail Moment) measuring DNA damage were significantly more serious compared with solvent control. Factorial ANOVA revealed that at lower mixed dose, no interaction was noted between DDVP and DM. But DDVP and Mal, also DM and Mal both exerted synergistic effect; while at higher mixed dose, antagonistic effect were found between DDVP and DM, DDVP and Mal, as well as DM and Mal. CONCLUSION: DDVP,DM and Mal could induce DNA damage both alone and in combination, but the combined effects varied with the mixture concentration.