国际医学寄生虫病杂志
國際醫學寄生蟲病雜誌
국제의학기생충병잡지
INTERNATIONAL JOURNAL OF MEDICAL PARASITIC DISEASES
2014年
4期
218-222
,共5页
薛丹%程慧芳%毋海兰%赵青%王锐利%张淑秋
薛丹%程慧芳%毌海蘭%趙青%王銳利%張淑鞦
설단%정혜방%무해란%조청%왕예리%장숙추
SYBR green Ⅰ法%流式细胞术%青蒿素%蒿甲醚%双氢青蒿素%恶性疟原虫
SYBR green Ⅰ法%流式細胞術%青蒿素%蒿甲醚%雙氫青蒿素%噁性瘧原蟲
SYBR green Ⅰ법%류식세포술%청호소%호갑미%쌍경청호소%악성학원충
SYBR green Ⅰ%Flow cytometry%Artimisinin%Artemether%Dihydroartemisinine%Plasmodium falciparum
目的 用SYBR green Ⅰ法和流式细胞术评价3种青蒿素类药物对体外培养恶性疟原虫的抗疟活性. 方法 采用SYBR green Ⅰ法观察不同浓度的青蒿素(arteminisinin,ART)、蒿甲醚(artemether,AM)及双氢青蒿素(dihydroartemisinin,DHA)对体外培养的恶性疟原虫增殖的抑制作用.ART、AM、DHA的抑制浓度依次为6、6×10-1、6×10-2、6×10-3、6×10-4 μmol/L,4、4×10-1、4×10-2、4×10-3、4× 10-4 μmol/L及3×10-1、3×10-2、3×10-3、3×10-4、3×10-5 μmol/L,设空白组与对照组.体外药物作用72 h后,SYBR green Ⅰ法测得其抑制率,用50%抑制浓度(50% inhibitory concentraton,IC50)及95%抑制浓度(95% inhibitory concentraton,IC95)反映其抑制作用,并与流式细胞术所测得的疟原虫DNA含量的变化进行比较. 结果 SYBR green Ⅰ法结果显示其抑制率随药物浓度的增加而增大,ART、AM与DHA的IC50值分别为11.29、3.32、0.66 nmol/L,IC95值分别为42.55、17.89、4.02 nmol/L;流式细胞术结果中其DNA含量随药物浓度的降低而增加,与SYBR green Ⅰ法结果一致且更具直观性. 结论 SYBR green Ⅰ法的灵敏性与流式细胞术的直观性可以满足体外测定抗疟药对疟原虫抑制作用的需要,均可适于抗疟药物体外活性评价;ART、AM与DHA的体外抗疟活性由高到低的次序为DHA>AM>ART.
目的 用SYBR green Ⅰ法和流式細胞術評價3種青蒿素類藥物對體外培養噁性瘧原蟲的抗瘧活性. 方法 採用SYBR green Ⅰ法觀察不同濃度的青蒿素(arteminisinin,ART)、蒿甲醚(artemether,AM)及雙氫青蒿素(dihydroartemisinin,DHA)對體外培養的噁性瘧原蟲增殖的抑製作用.ART、AM、DHA的抑製濃度依次為6、6×10-1、6×10-2、6×10-3、6×10-4 μmol/L,4、4×10-1、4×10-2、4×10-3、4× 10-4 μmol/L及3×10-1、3×10-2、3×10-3、3×10-4、3×10-5 μmol/L,設空白組與對照組.體外藥物作用72 h後,SYBR green Ⅰ法測得其抑製率,用50%抑製濃度(50% inhibitory concentraton,IC50)及95%抑製濃度(95% inhibitory concentraton,IC95)反映其抑製作用,併與流式細胞術所測得的瘧原蟲DNA含量的變化進行比較. 結果 SYBR green Ⅰ法結果顯示其抑製率隨藥物濃度的增加而增大,ART、AM與DHA的IC50值分彆為11.29、3.32、0.66 nmol/L,IC95值分彆為42.55、17.89、4.02 nmol/L;流式細胞術結果中其DNA含量隨藥物濃度的降低而增加,與SYBR green Ⅰ法結果一緻且更具直觀性. 結論 SYBR green Ⅰ法的靈敏性與流式細胞術的直觀性可以滿足體外測定抗瘧藥對瘧原蟲抑製作用的需要,均可適于抗瘧藥物體外活性評價;ART、AM與DHA的體外抗瘧活性由高到低的次序為DHA>AM>ART.
목적 용SYBR green Ⅰ법화류식세포술평개3충청호소류약물대체외배양악성학원충적항학활성. 방법 채용SYBR green Ⅰ법관찰불동농도적청호소(arteminisinin,ART)、호갑미(artemether,AM)급쌍경청호소(dihydroartemisinin,DHA)대체외배양적악성학원충증식적억제작용.ART、AM、DHA적억제농도의차위6、6×10-1、6×10-2、6×10-3、6×10-4 μmol/L,4、4×10-1、4×10-2、4×10-3、4× 10-4 μmol/L급3×10-1、3×10-2、3×10-3、3×10-4、3×10-5 μmol/L,설공백조여대조조.체외약물작용72 h후,SYBR green Ⅰ법측득기억제솔,용50%억제농도(50% inhibitory concentraton,IC50)급95%억제농도(95% inhibitory concentraton,IC95)반영기억제작용,병여류식세포술소측득적학원충DNA함량적변화진행비교. 결과 SYBR green Ⅰ법결과현시기억제솔수약물농도적증가이증대,ART、AM여DHA적IC50치분별위11.29、3.32、0.66 nmol/L,IC95치분별위42.55、17.89、4.02 nmol/L;류식세포술결과중기DNA함량수약물농도적강저이증가,여SYBR green Ⅰ법결과일치차경구직관성. 결론 SYBR green Ⅰ법적령민성여류식세포술적직관성가이만족체외측정항학약대학원충억제작용적수요,균가괄우항학약물체외활성평개;ART、AM여DHA적체외항학활성유고도저적차서위DHA>AM>ART.
Objective To evaluate the antimalarial activity against Plasmodiumfalciparum in vitro by SYBR green Ⅰ and flow cytometry.Methods SYBR green Ⅰ was used to evaluate the inhibition to proliferation of Plasmodium falciparum in vitro treated by artimisinin(ART),artemether(AM) and dihydroartemisinine(DHA) at different concentrations.The intervention concentrations of ART,AM and DHA were 6,6×10-1,6×10-2,6×103,6×10-4μmol/L,4,4×10-1,4×10-2,4×10-3,4×10-4 μmol/L,and 3×10-1,3×10-2,3×10-3,3×10-4,3×10-5 μmol/L respectively,a blank control group was set up.After 72 h of drug intervention in vitro,the inhibition rate was measured using SYBR green Ⅰ,the 50% inhibitory concentration (IC50) and 95% inhibition concentration (IC95) were used to reflect the inhibition activity,then compared with the changes of DNA content of malaria parasites measured by flow cytometry.Results SYBR green Ⅰ showed the inhibition rates increased as dose of ART increased,The IC5o values of ART,AM and DHA were 11.29,3.32,0.66 nmol/L; IC95 values were 42.55,17.89,4.02 nmol/L respectively.At the same time,the results of the flow cytometry showed the content of DNA decreased with the increase of drug concentration,agreeing with the results of SYBR green Ⅰ and being objectively perceived.Conclusion The sensitivity of SYBR green Ⅰ and intuitiveness of flow cytometry could meet the requirements of evaluation on antimalarial activity of artemisinin-based antimalarial drugs against Plasmodiumfalciparum in vitro; The order from high to low of antimalarial activity is DHA>AM>ART.