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四氢姜黄素对H9c2细胞缺血再灌注损伤的影响及机制研究

冯建梅 冯建宇 吴岩 翟蒙恩 冯笑 金振晓 曹磊

中国体外循环杂志2019,Vol.17Issue(1):48-53,6.
中国体外循环杂志2019,Vol.17Issue(1):48-53,6.DOI:10.13498/j.cnki.chin.j.ecc.2019.01.11

四氢姜黄素对H9c2细胞缺血再灌注损伤的影响及机制研究

Protective effects of tetrahydrocurcum on myocardial ischemia reperfusion injury of H9c2 cells

冯建梅 1冯建宇 2吴岩 2翟蒙恩 2冯笑 2金振晓 2曹磊3

作者信息

  • 1. 空军军医大学唐都医院麻醉科 710038 西安
  • 2. 空军军医大学西京医院心血管外科 710032 西安
  • 3. 西安电力中心医院心内科 710032 西安
  • 折叠

摘要

Abstract

Objective To investigate the protective effects and underlying mechanisms of tetrahydrocurcumin (THC) pretreatment on ischemia reperfusion injury (IRI) of H9c2 cells. Methods To mimic the in vivo ischemia reperfusion model, H9c2 cells were exposed to an ischemic buffer for 1 h followed by serum-free DMEM for 4 h. Prior to this procedure, cells were treated with or without THC. They were divided into four groups: Control group, THC group, SIR group and SIR+THC group, respectively. Four hours after the reperfusion, cell viability, reactive oxygen species (ROS) production, malonaldehyde (MDA) content, activities of superoxide dismutase (SOD) and glutathione peroxidase (GSH-Px) as well as the expression levels of Bax, Bcl-2 and Caspase-3 were measured in each group. Results Compared with SIR group, THC pretreatment increased the cell viability, the expression of Bcl-2 and the activities of SOD and GSH-Px in H9c2 cells. In addition, THC also significantly decreased the apoptotic ratio, the expression of Bax and Caspase-3, ROS production and MDA content. Conclusion THC pretreatment could effectively attenuate myocardial IRI by reducing SIR-induced oxidative stress and apoptosis.

关键词

四氢姜黄素/细胞/缺血再灌注损伤/凋亡/氧化应激/预处理

Key words

Tetrahydrocurcumin/Cell/Myocardial ischemia reperfusion injury/Apoptosis/Oxidative stress/Pretreatment

引用本文复制引用

冯建梅,冯建宇,吴岩,翟蒙恩,冯笑,金振晓,曹磊..四氢姜黄素对H9c2细胞缺血再灌注损伤的影响及机制研究[J].中国体外循环杂志,2019,17(1):48-53,6.

基金项目

国家自然科学基金资助项目 (81570231) (81570231)

中国体外循环杂志

OACSTPCD

1672-1403

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