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作 者:刘占术[1] 罗章琴[1] 张红宾[2] 陈建斌[2] 杨泽松[2] 黄曦[3] 黄宗干[2]
机构地区:[1]重庆医科大学附属永川医院血液内科,重庆402160 [2]重庆医科大学附属第一医院血液内科,重庆400016 [3]重庆市合川区人民医院肿瘤血液中心,重庆401520
出 处:《中成药》2011年第3期400-403,共4页Chinese Traditional Patent Medicine
基 金:重庆市卫生局科研资助项目(08-2-035)
摘 要:目的:探讨p38MAPK活化在中药苦参碱(Matrine,Mat)诱导人Burkitt,s淋巴瘤Raji细胞凋亡中的作用。方法:体外培养Raji细胞,分别用苦参碱(终浓度为0.4、0.8、1.6mg/mL)和在此基础上加入SB203580(p38 MAPK抑制剂)作用48h后,采用AnnexinⅤ–FITC/PI双染法检测细胞凋亡率,应用Western blot检测P-p38MAPK及Caspase-3蛋白表达量。结果:终浓度为0.4、0.8、1.6 mg/mL苦参碱对Raji细胞总凋亡率分别为(15.77±0.53)%、(27.88±1.52)%、(48.08±2.87)%、与加入SB203580比较(11.48±0.64)%、(19.34±0.91)%、(33.98±1.26)%具有统计学意义(P<0.05或P<0.01),与对照组(8.78±0.66)%比较也具有显著性差异(P<0.05或P<0.01);Western blot显示了P-p38MAPK和Caspase-3蛋白表达水平均随苦参碱浓度的提高而增加,加入SB203580后二者表达降低。结论:苦参碱可诱导Raji细胞凋亡,其凋亡可能与p38 MAPK的活化,进而直接或间接激活Caspase-3有关。AIM:To explore the effect and signaling pathway involved in apoptosis of human Burkitt's lympho-ma Raji cells induced by matrine through p38 MAPK activation.METHODS:Raji cells were cultured in vitro,the cells were treated by different final concentrations(0.4,0.8,1.6mg/mL) of matrine or combined with SB203580(p38 MAPK inhibitor) before matrine was added,then cocultured for 48 h,cell apoptosis rate was detected by An-nexinⅤ-FITC/PI double staining method,the P-p38 MAPK and caspase-3 protein expresssion of Raji cells were evaluated by Western blot.RESULTS:After cells were treated by matrine(0.4,0.8,1.6mg/mL),the corresponding total apoptosis rate of treatment-groups was(15.77±0.53)%,(27.88±1.52)%,(48.08±2.87)% re-spectively,had statistical significance compared with adding SB203580 groups(11.48±0.64)%,(19.34±0.91)%,(33.98±1.26)%(P0.05 or P0.01),respectively,also had statistical significance compared with control group(8.78±0.66)%(P0.05 or P0.01).As the concentration of matrine gradually increased.theprotein expresssion levels of p-p38MAPK and caspase-3 also increased,and decreased after SB203580 was added.CONCLUSION:In view of the inducement of matrine to the apoptosis of Raji cells in vitro,we evaluate matrine from bean family that exhibits the activation of caspase-3 through directly and indirectly activating P-p38 MAPK.matrine can induce the apoptosis of Raji cells in vitro,its possible mechanism is that matrine activates caspase-3 directly or indirectly through p38 MAPK activation.
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