检索规则说明:AND代表“并且”;OR代表“或者”;NOT代表“不包含”;(注意必须大写,运算符两边需空一格)
检 索 范 例 :范例一: (K=图书馆学 OR K=情报学) AND A=范并思 范例二:J=计算机应用与软件 AND (U=C++ OR U=Basic) NOT M=Visual
作 者:朱丹[1] 胡莹[1] 赵欣[2] 马吉芳[1] 郝建兵[1] 任连生[1] 崔蕾[1]
机构地区:[1]哈尔滨医科大学附属第一医院肾内二病房,150070 [2]黑龙江省医院血液透析中心,哈尔滨150001
出 处:《检验医学与临床》2015年第9期1196-1197,共2页Laboratory Medicine and Clinic
基 金:黑龙江省教育厅科学技术研究项目(12521293)
摘 要:目的探讨不同浓度阿托伐他汀对大鼠系膜细胞凋亡的影响。方法体外培养大鼠永生系膜细胞,分为5组:对照(C)组;高糖(30mmol/L)(H)组;高糖(30mmol/L)+阿托伐他汀(10-7 mmol/L)(H+A1)组;高糖(30mmol/L)+阿托伐他汀(10-6 mmol/L)(H+A2)组;高糖(30mmol/L)+阿托伐他汀(10-5 mmol/L)(H+A3)组。采用Annexin V-FITC和PI双染法检测细胞凋亡。采用caspase-3活性检测试剂盒检测系膜细胞caspase-3活性。结果与C组相比,H组系膜细胞凋亡率明显增加,caspase-3活性明显增加,差异有统计学意义(P<0.05)。与H组相比,高糖加不同浓度阿托伐他汀组细胞凋亡率明显降低,caspase-3活性明显降低,差异有统计学意义(P<0.05),且呈浓度依赖。结论阿托伐他汀可以通过caspase途径抑制醛固酮诱导的大鼠系膜细胞凋亡。Objective To investigate the influence of different concentrations of atorvastatin on apoptosis of rat mesangial cells .Methods Rat immortal mesangial cells were cultured in vitro and divided into 5 groups:control (C) group ,hyperglycemia (30 mmol/L ,H)group ,hyperglycemia (30 mmol/L)+ atorvastatin(10^-7 mmol/L)(H+A1) group ,hyperglycemia (30 mmol/L)+ atorvastatin(10^-6 mmol/L)(H + A2)group and hyperglycemia (30 mmol/L)+atorvastatin(10^-5 mmol/L)(H+ A3)group .Apoptosis was detected by Annexin V‐FITC and PI double staining ,and the caspase‐3 activity was assayed by the caspase‐3 activity kit .Results Compared with the group C , the mesangial cells apoptosis rate and caspase‐3 activity in the group H were significantly increased ,the differences were statistically significant(P〈0 .05) .Compared with the group H ,the mesangial cells apoptosis rate and caspase‐3 activity in the H+ A1 ,2 ,3 groups were significantly decreased ,the differences were statistically significant ( P〈0 .05) ,moreover which showing the concentration dependence .Conclusion Atorvastatin may inhibit aldosterone in‐duced mesangial cells apoptosis via caspase pathway .
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在链接到云南高校图书馆文献保障联盟下载...
云南高校图书馆联盟文献共享服务平台 版权所有©
您的IP:216.73.216.229