基础医学与临床 ›› 2015, Vol. 35 ›› Issue (10): 1375-1381.

• 研究论文 • 上一篇    下一篇

异氟烷减轻人心肌细胞缺氧/复氧损伤的研究

梁冰,方洁   

  1. 河南中医学院第一附属医院
  • 收稿日期:2015-04-16 修回日期:2015-07-01 出版日期:2015-10-05 发布日期:2015-09-30
  • 通讯作者: 方洁 E-mail:fangjiezhengzhou@163.com

Isoflurane attenuates human cardiacmyocytes anoxia/reoxygenation injury

1,   

  • Received:2015-04-16 Revised:2015-07-01 Online:2015-10-05 Published:2015-09-30

摘要: 目的 探讨异氟烷对缺氧/复氧(AR)损伤人心肌细胞的作用及其机制。方法 人心肌细胞株HCM分为对照组(con)、AR组和异氟烷(0.5%、1%、1.5%和2%)组(n=5)。酶标仪检测细胞活力,化学比色法检测LDH活性,Annexin V-FITC/PI双染法检测细胞凋亡,RT-PCR和Western blot检测低氧诱导因子(HIF)-1α表达水平。结果 与对照组比较,AR组细胞活力降低,LDH活性和凋亡细胞升高,HIF-1α表达水平显著上调(P<0.05);异氟烷可缓解AR导致的心肌细胞活力降低、LDH活性和凋亡细胞数增加以及HIF-1α表达水平回降(P<0.05)。siRNA转染组HIF-1α表达水平显著低于AR组(P<0.05);2%异氟烷显著缓解siRNA转染组心肌细胞活力的升高,LDH活性和凋亡细胞数的降低(P<0.05)。结论 异氟烷可通过上调HIF-1α的表达部分减轻AR损伤人心肌细胞。

关键词: 异氟烷, 低氧诱导因子-1α, 心肌细胞, 缺氧/复氧

Abstract: Objective To explore the effect and the mechanism of isoflurane on human cardiac myocytes (HCM) injury induced by anoxia/reoxygenation (AR). Methods HCM cells were divided into control group (con), anoxia/reoxygenation group (AR) and isoflurane (0.5%, 1%, 1.5% and 2%) treatment group (n=6). Cell viability , LDH activity, apoptosis and the expression level of Anoxia inducible factor-1α (HIF-1α) were detected using CCK-8 assay, LDH activity assay kit, Annexin V-FITC/PI staining, PCR and western blot, respectively. Results Compared with the con group, cell viability decreased, LDH activity and apoptosis cells increased in AR group. Isoflurane can significantly relieve the decrease of cell viability, the increase of LDH activity and apoptosis cells, and the down-regulation of the mRNA and protein expression level of HIF-1α induced by AR (P<0.05). Compared with AR group, the mRNA and protein expression level of HIF-1α in siRNA transfected group is significantly decreased (P<0.05). 2% isoflurane significantly relieve the increase of cell viability, and the decrease of LDH activity and apoptotic cells induced by HIF-siRNA in AR injuried HCM cells(P<0.05).Conclusion Isoflurane can protect HCM cells from AR injury partly through up-regulate the expression of HIF-1α.