您的位置：山东大学 -> 科技期刊社 -> 《山东大学学报（医学版）》

山东大学学报(医学版) ›› 2013, Vol. 51 ›› Issue (7): 1-5.

• 基础医学 •    下一篇

rhEPO对氧化应激时心肌细胞及心肌梗死后心脏的保护作用

王福1，刘善文1，李彬2，耿海华3，孙帅1，李睿1，肖洁1，季晓平1   

  1. 1.山东大学齐鲁医院心内科， 济南 250012; 2.山东大学附属济南市中心医院保健科， 济南 250013；
    3.南通大学附属医院心内科， 江苏 南通 226001
  • 收稿日期:2012-11-15 出版日期:2013-07-10 发布日期:2013-07-10
  • 通讯作者: 季晓平， E-mail：xpj64@163.com

Protective effects of rhEPO on oxidative stress damage in cardiomyocytes and on heart after myocardial infarction

WANG Fu1, LIU Shan-wen1, LI Bin2, GENG Hai-hua3, SUN Shuai1, LI Rui1, XIAO Jie1， JI Xiao-ping1   

  1. 1.Department of Cardiology, Qilu Hospital of Shandong University, Jinan 250012, China;
    2. Department of Health, Jinan Central Hospital Affiliated to Shandong University, Jinan 250013, China;
    3. Department of Cardiology, Affiliated Hospital of Nantong University, Nantong 226001, Jiangsu, China
  • Received:2012-11-15 Online:2013-07-10 Published:2013-07-10

PDF (PC)

288

摘要：

目的   初步探讨重组人促红细胞生成素(rhEPO)对氧化应激时乳鼠心肌细胞及心肌梗死后小鼠心脏的保护作用。方法   建立乳鼠心肌细胞的氧化应激损伤模型后，加入rhEPO进行干预。以噻唑蓝(MTT)比色法和流式细胞术(FCM)检测rhEPO对心肌细胞凋亡的影响。同时应用Western blotting检测凋亡效应酶胱天蛋白酶-3(caspase3)、Bax、Bcl-2蛋白的表达水平。将小鼠随机分为假手术组(Sham组)、模型组(MI组)和rhEPO组，通过结扎左冠状动脉前降支建立小鼠心梗模型，14d后取心脏组织，HE染色观察rhEPO对心肌梗死面积的影响。结果   在氧化应激损伤过程中，rhEPO可以明显降低心肌细胞的凋亡率，下调caspase-3和Bax蛋白的表达，上调Bcl-2蛋白的表达。HE染色结果显示，rhEPO可以明显缩小小鼠心肌梗死面积。结论   在氧化应激时，rhEPO可对抗过氧化氢引起的心肌细胞损伤；rhEPO还可缩小小鼠心肌梗死面积。

关键词: 重组人促红细胞生成素；心肌细胞；氧化应激损伤；心肌梗死

Abstract:

Objective   To study the protective effects of recombinant human erythropoietin(rhEPO)on cardiomyocytes against oxidative damage and on mice hearts after myocardial infarction. Methods   Isolated neonatal rat cardiomyocytes were treated with rhEPO in vitro after the establishment of oxidative damage experimental models. Thiazolyl blue (MTT) assay and flow cytometry (FCM) were used to detect the apoptosis rate of cardiomyocytes. Protein expression levels of caspase-3, Bax and Bcl-2 were detected by Western blotting. Mice were randomly divided into the sham group, the myocardial infarction group and the rhEPO treatment group. Myocardial infarction models were induced by the ligation of the left anterior descending artery in mice. Mouse heart was harvested after 14 days. HE staining was used to investigate the effects of rhEPO on the myocardial infarct size. Results   In the process of oxidative damage, rhEPO could significantly reduce the apoptosis rate of cardiomyocytes and the expressions of caspase-3 and Bax, but could raise the expression of Bcl-2. HE staining showed that rhEPO could significantly reduce the myocardial infarct size of mouse heart. Conclusion   RhEPO can protect cardiomyocytes from oxidative stress damage induced by H2O2 and reduce the myocardial infarct size in mice after myocardial infarction.

Key words: Recombinant human erythropoietin; Cardiomyocytes; Oxidative stress damage; Myocardial infarction

中图分类号: 

  • R542.2
[1] 申晓倩1，张文东2，何源流3，丛晓4，苏国海4，郝恩魁1. 曲妥珠单抗诱导大鼠心功能降低及其机制的探讨[J]. 山东大学学报(医学版), 2013, 51(12): 11-14.
[2] 阚丽丽1，蒋方国1，安丰双2. 心肌纤维化模型大鼠心肌组织中GRK2的表达以及对胶原合成的影响[J]. 山东大学学报(医学版), 2013, 51(9): 22-25.
[3] 索菲1，胡和生2，薛梅2，王晔1，轩永丽1，闫素华2. 心肌梗死后Neurturin动态表达与心脏迷走神经重构的相关性[J]. 山东大学学报(医学版), 2013, 51(5): 1-5.
[4] 赵立祥，吴新宁，王希，李娜，陈桐帅，刘军妮，卜培莉. NAD对AngII诱导的心肌成纤维细胞I型胶原mRNA表达的影响[J]. 山东大学学报(医学版), 2013, 51(3): 1-5.
[5] 陆冠延1，崔彬2，刘忠良3，李玉瑭4，刘雪飞3，马晓静1，朱贵月1，苑海涛1. 缬沙坦对慢性病毒性心肌炎小鼠Th17/Treg免疫平衡的影响[J]. 山东大学学报(医学版), 2013, 51(2): 1-.
[6] 王其磊1，任满意2，王德金1，徐冬玲1，杜贻萌1，王旭平3，隋树建1. TWEAK通过P38MAPK途径促进大鼠心肌成纤维细胞Ⅰ型胶原和MMP-1的表达[J]. 山东大学学报(医学版), 2012, 50(11): 43-47.
[7] 王德金1,任满意2,陈慧娜1,王旭平3，隋树建1. TWEAK通过NF-κB途径促进大鼠成纤维细胞表达基质金属蛋白酶9[J]. 山东大学学报(医学版), 2011, 49(11): 13-17.
[8] 阚丽丽1,2，安丰双2 . E/E′对肥厚型心肌病患者药物治疗前后左室舒张功能的评价[J]. 山东大学学报(医学版), 2011, 49(7): 105-108.
[9] 马丽娜1，姚民强2，王佩显1. 症状期酒精性心肌病患者心脏结构和功能的超声评价[J]. 山东大学学报(医学版), 2011, 49(1): 82-85.
[10] . 心肌肥厚患者中Fabry病发病状况的临床研究[J]. 山东大学学报(医学版), 2010, 48(3): 116-119.
[11] 巩祖顺1，邢启崇2. 心肌肌钙蛋白T对心肌梗死危险因素的分层定量研究[J]. 山东大学学报(医学版), 2009, 47(11): 114-117.
Viewed
Full text


Abstract

Cited
  Shared   
  Discussed   
No Suggested Reading articles found!
版权所有 © 2018 《山东大学学报(医学版)》编辑部　
地址:山东大学科技期刊社（济南市历城区山大南路27号山东大学中心校区明德楼B座721室） 电话: 0531-88366918 E-mail: xbyxb@sdu.edu.cn
本系统由北京玛格泰克科技发展有限公司设计开发