氯沙坦通过下调单核细胞趋化蛋白1受体表达抑制单核细胞活化
DOI:
作者:
作者单位:

作者简介:

通讯作者:

基金项目:


Inhibitory Effect of Losartan on Monocytic Activation via Downregulation of Monocyte Chemoattractant Protein-1 Receptor Expression
Author:
Affiliation:

Fund Project:

  • 摘要
  • |
  • 图/表
  • |
  • 访问统计
  • |
  • 参考文献
  • |
  • 相似文献
  • |
  • 引证文献
  • |
  • 资源附件
    摘要:

    目的探讨血管紧张素Ⅱ对单核细胞趋化蛋白1受体CCR2表达的影响及氯沙坦的干预作用。方法人单核细胞株与血管紧张素Ⅱ(10-7mol/L)孵育,加或不加氯沙坦(10-7、10-6和10-5mol/L),检测上清液中单核细胞趋化蛋白1水平、单核和内皮细胞粘附情况以及CCR2mRNA的表达。结果与对照组比较,血管紧张素Ⅱ明显增加单核细胞培养上清液中单核细胞趋化蛋白1水平(26.46±3.58ng/L比10.56±2.34ng/L,p<0.01),增加单核内皮细胞间粘附(596±27比268±16,p<0.01)。血管紧张素Ⅱ刺激细胞后明显上调CCR2mRNA表达,氯沙坦能显著抑制血管紧张素Ⅱ的作用,降低单核细胞趋化蛋白1的水平,减少单核内皮细胞间粘附,下调CCR2 mRNA表达。结论氯沙坦通过下调单核细胞趋化蛋白1受体CCR2基因表达抑制单核细胞活化。

    Abstract:

    Aim To investigate the effect of angiotensin Ⅱ(AngⅡ)on the expression of monocyte chemoattractant protein-1(MCP-1)receptor CCR2 and therapeutic effect of losartan on atherosclerosis.Methods Human monocytoid cell(THP-1)were treated with AngⅡ(10-7 mol/L)for 24 h in the absence or presence of losartan(10-7,10-6,10-5 mol/L).The level of MCP-1 in the medium,the adhesion of monocytes to endothelial cell and the expression of CCR2 mRNA were determined.Results Compared with control,incubation of THP-1 with AngⅡ(10-7 mol/L)for 24 h significantly elevated the concentrations of MCP-1(26.46 ±3.58 ng/L vs.10.56 ±2.34 ng/L,p<0.01),increased the number of monocytes binding to endothelial cell(596±27 vs.268±16,p<0.01)and upregulated the expression of CCR2 mRNA.Treatment with losartan decreased the levels of MCP-1,inhibited monocytic binding to endothelial cell,and downregulated the expression of CCR2 mRNA by AngⅡ.Conclusions These data suggest that treatment with losartan in vitro inhibits monocytic activation via downregulation of MCP-1 receptor CCR2 genetic expression.

    参考文献
    相似文献
    引证文献
引用本文

陈美芳,谢秀梅,杨天伦,陈志雄,李元建.氯沙坦通过下调单核细胞趋化蛋白1受体表达抑制单核细胞活化[J].中国动脉硬化杂志,2007,15(1):51~53.

复制
分享
文章指标
  • 点击次数:
  • 下载次数:
历史
  • 收稿日期:2006-08-11
  • 最后修改日期:2006-12-20
  • 录用日期:
  • 在线发布日期: