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出 处:《沈阳医学院学报》2012年第4期223-225,共3页Journal of Shenyang Medical College
基 金:辽宁省博士启动基金资助项目(No.20091082)
摘 要:目的:探讨氯化锌(ZnCl2)和N-乙酰半胱氨酸(N-acetyl cysteine,NAC)对镉所致人正常肝细胞HL-7702凋亡的拮抗作用。方法:体外培养的人正常肝细胞HL-7702分别以0、10、20、40、80、160μmol/L的氯化镉(CdCl2)处理24h,ZnCl2和NAC预处理组分别在各浓度的CdCl2处理前以25.0、50.0、100.0、200.0μmol/L的氯化锌和2.5、5.0、10.0、20.0 mmol/L NAC预处理24 h,MTT法测定各组HL-7702细胞的相对存活率;流式细胞术Annexin-V-PI双染法检测细胞凋亡百分率。结果:随着镉处理浓度的增加,氯化镉对细胞活力的抑制作用增强,40、80、160μmol/L的镉处理组细胞相对存活率明显降低,50μmol/L锌预处理组在CdCl2剂量为40、80μmol/L时,细胞相对存活率显著高于相应剂量的单纯镉处理组(P<0.01),10 mmol/L NAC预处理组只在40 mmol/L CdCl2组细胞相对存活率显著高于相应剂量的单纯镉处理组(P<0.05);与0μmol/L镉处理组比较,40、80、160μmol/L镉处理组HL-7702细胞的凋亡百分率显著升高(P<0.01);与40μmol/L镉处理组比较,100μmol/L锌预处理组细胞凋亡率显著降低(P<0.01);5.0、10.0、20.0 mmol/L NAC预处理可有效拮抗镉诱导的HL-7702细胞凋亡(P<0.05)。结论:锌和NAC对镉致HL-7702细胞损伤和凋亡有明显的拮抗作用。Objective: To study the antagonism of zinc chloride ( ZnCl2 ) and N-acetyl Cysteine (NAC) on apoptosis of normal human hepatoeyte HL-7702 cells induced by cadmium. Methods: Normal human hepatocyte HL-7702 ceils were incubated with 0, 10, 20, 40, 80, 160 μmol/L Cdcl2 for 24 h. The cells in groups of ZnC12 and NAC pretreatment were treated with 25.0, 50. 0, 100.0, 200.0 μmol/L ZnCl2 and2.5, 5.0, 10.0, 20.0 mmol/L NAC for24 h before incubated with 0, 10, 20, 40, 80, 160 μmol/L CdC12. Cells viability were measured by MTT. The rate of apoptosis was measured by Flowcytometry Staining of cells with phosphatidylserine (PS) -annexin- V. Results: The cells viability decreased obviously in the incubating cell with 40, 80, 160 μmol/L cadmium. The cells viability of 50. 0 μmol/L ZnC12 pretreatment group obviously increased compared with simple 40, 80 μmol/L cadmium incubating cell (P 〈 0. 01 ). The cells viability of 10 mmol/L NAC pretreatment group increased compared with simple 40 μmol/L cadmium incubating cell ( P 〈 0. 05 ). The apoptosis rate increased obviously in cells incubated with 40, 80, 160μmol/L cadmium compared with that in 0 p,mol/L cadmium group. The apoptosis rate in 100 μmol/L ZnC12 pretreatment decreased obriously compared with that in 40μmol/L codmium group and 5.0, 10. 0, 20. 0 mmol/L NAC pretreatment could suppress signifi- cantly cadmium-induced cell apoptosis ( P 〈 0. 05 ). Conclusions : ZnCl2 and NAC may suppress the apoptosis rate induced by cad- mium.
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