期刊文献+

白藜芦醇对低氧内皮细胞活性的影响及机制研究 被引量:1

The research on the effect and mechanism of resveratrol on the inflammatory response of endothelial cells induced by hypoxia
下载PDF
导出
摘要 目的探讨白藜芦醇(RSV)对低氧内皮细胞炎症反应的影响及机制。方法 HUVECs分为常氧、低氧、低氧+DMSO、低氧+RSV(低、中、高剂量)组。分别采用CCK8法检测细胞活力,qRT-PCR及Western blot法检测SIRT1、IL-6和ICAM-1 mRNA及SIRT1、PGC-1α和NF-κB p65蛋白的表达,流式细胞术检测活性氧(ROS)含量。结果低氧能抑制HUVECs细胞活力,下调SIRT1、PGC-1α蛋白表达(P<0.05);上调IL-6、ICAM-1 mRNA及磷酸化NF-κB p65蛋白表达(P<0.05);促进ROS生成(P<0.05)。RSV能促进低氧HUVECs细胞活力,上调SIRT1、PGC-1α表达(P<0.05);下调IL-6、ICAM-1及磷酸化NF-κB p65蛋白的表达(P<0.05);抑制ROS生成(P<0.05)。结论 RSV可促进低氧HUVECs细胞活力,其机制可能与RSV抑制低氧HUVECs炎症反应有关。 Objective To study the effect and mechanism of resveratrol on the inflammatory response of endothelial cells induced by hypoxia. Methods Human umbilical vein endothelial cells were divided into normal group,hypoxia group,DMSO group and low,medium and high doses of RSV groups. The cell viability was detected by CCK8 assay,The mRNA contents of SIRT1,IL-6 and ICAM- 1 were detected by real- time PCR method,the protein contents of SIRT1,PGC- 1α and NF- κB p65 were detected by western blot method,the contents of ROS were detected by flow cytometry method. Results Compared with normal group,the cell viability and contents of SIRT1 and PGC- 1α protein were decreased markedly in hypoxia group,the contents of IL- 6 mRNA,ICAM- 1 mRNA,p- NF- κB p65 protein and ROS were increased markedly. Compared with DMOS group,the cell viability and contents of SIRT1 and PGC- 1α protein were increased markedly in RSV groups,the contents of IL- 6 mRNA,ICAM- 1 mRNA,p- NF- κB p65 protein and ROS were decreased markedly in RSV groups. Conclusion RSV could promote the cell viability of HUVECs induced by hypoxia. This maybe be concerned with that RSV could inhibit the inflammatory response of HUVECs induced by hypoxia..
出处 《时珍国医国药》 CAS CSCD 北大核心 2016年第6期1296-1299,共4页 Lishizhen Medicine and Materia Medica Research
基金 国家自然科学基金面上项目(No.81470247)
关键词 白藜芦醇 内皮细胞 炎症反应 SIRT1 Resveratrol Endothelial cell Inflammation SIRT1
  • 相关文献

参考文献1

二级参考文献1

共引文献6

同被引文献12

引证文献1

二级引证文献1

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部