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:李春梅[1] 王馨[1] 周立群[2] 康立勋[1] 李海清[1] 马晟利[1]
机构地区:[1]黑龙江省医院口腔科,黑龙江哈尔滨150001 [2]黑龙江省医院产科,黑龙江哈尔滨150001
出 处:《系统医学》2016年第6期8-11,共4页Systems Medicine
基 金:哈尔滨市科技局科技创新人才研究专项基金(2014RFQGJ018)
摘 要:目的探讨淫羊藿苷对高糖培养条件下大鼠颌骨骨髓基质细胞成骨能力的影响。方法选取2015年6月—2016年4月黑龙江省医院实验室的8只大鼠,实验分组(每个基因进行5个复孔平行实验):正常组(2%胎牛血清+DMEM培养的细胞),高糖组(2%胎牛血清+高糖-DMEM培养的细胞),淫羊藿苷组1(2%胎牛血清+DMEM+淫羊藿苷培养的细胞),淫羊藿苷组2(2%胎牛血清+高糖-DMEM+淫羊藿苷培养的细胞),每组进行5个复孔平行实验。荧光定量测定成骨相关基因BMP2、OPN、BSP基因的表达。结果淫羊藿苷组1(1.78±0.10)与其它组比较:BMP2(1.37±0.04)、OPN(1.38±0.09)、BSP(1.50±0.05)基因的表达均高于其相应的对照组(P<0.05)。结论淫羊藿苷对高糖培养条件下大鼠颌骨骨髓基质细胞成骨能力有加强作用。Objective To investigate the effect of the content of the bone marrow stromal cells in the bone marrow stromal cells induced by high glucose in rats under high concentration of glucose. Methods Selected June 2015- 2016 in April in Heilongjiang Province Hospital Laboratory of 8 rats, experimental groups(each gene of five hole complex parallel experiment): normal group(2% FBS DMEM culture cells), high glucose group(2% fetal bovine serum + glucose of both cultured cells), icariin group 1(2% fetal bovine serum DMEM + icariin cultured cells) and icariin group 2(2% fetal bovine serum and high glucose increased + icariin cultured cells), every five holes in parallel experiments. The expression of BMP2, OPN and BSP genes in the bone related genes was determined by fluorescence quantitative. Results Compared with other groups, the expression of BMP2(1.37 ±0.04), OPN(1.38 ±0.09)and BSP(1.50 ±0.05)genes in the group of 1(1.78 ±0.10) and other groups was higher than that in the control group(P〈0.05). Conclusion The effect of the content of the bone marrow stromal cells in the bone marrow stromal cells of rats under high glucose condition was enhanced by the high concentration of glucose in the rat bone marrow stromal cells.
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