期刊文献+

氢气治疗心肌缺血再灌注损伤的作用机制及展望

Hydrogen for treatment of myocardial ischemia-reperfusion injury:mechanism and prospect
原文传递
导出
摘要 心肌缺血再灌注损伤是导致心血管疾病心肌损伤的最重要原因,常见于冠心病和心脏手术围手术期,发生率和死亡率高,其机制涉及氧化应激、炎性反应和细胞凋亡等。目前的治疗措施包括药物治疗和物理治疗,但效果不佳。氢气作为一种小分子无毒还原性气体,在细胞缺血再灌注损伤中有明显保护作用,是未来治疗缺血再灌注损伤的重要方向,本文就氢气治疗心肌缺血再灌注损伤的作用机制及其未来应用临床的初步展望进行综述。 Myocardial ischemia-reperfusion injury(MIRI)is one of the key causes of myocardial injury,secondary to cardiovascular diseases,which is mostly present in coronary heart disease and during the perioperative period of cardiac surgery.MIRI elicits oxidative stress,inflammatory activity,and cell apoptosis,with a high incidence and mortality rate.The current treatments for MIRI include medicines and physical therapy,but with unsatisfactory effects.As a small molecule non-toxic reducing gas,hydrogen has a clear protective effect against cell ischemia-reperfusion,and has therefore become a promising treatment for MIRI.This paper reviews the mechanism of hydrogen for the treatment of MIRI and the preliminary prospect of its clinical application in the future.
作者 张敏洁 张小杉 段莎莎 施依璐 赵捷 白天昊 王雅晳 Zhang Minjie;Zhang Xiaoshan;Duan Shasha;Shi Yilu;Zhao Jie;Bai Tianhao;Wang Yaxi(Inner Mongolia Medical University,Hohhot 010110,China;Department of Ultrasound,Affiliated Hospital of Inner Mongolia Medical University,Hohhot 010050,China)
出处 《中华临床医师杂志(电子版)》 CAS 北大核心 2023年第6期744-748,共5页 Chinese Journal of Clinicians(Electronic Edition)
基金 中央引导地方科技发展资金项目(2021ZY0026) 内蒙古自治区教育厅“高校青年科技英才”项目(NJYT22021) 内蒙古自治区医疗卫生科技计划项目(202201310)
关键词 心肌缺血再灌注损伤 氢气 氧化应激 炎性反应 凋亡 Myocardial ischemia-reperfusion injury Hydrogen Oxidative stress Inflammation Apoptosis
  • 相关文献

参考文献9

二级参考文献52

  • 1王幼林,陈念航,丁建花.丹参酮ⅡA磺酸钠对大鼠心,脑微粒体Na~+,K~+-ATP酶的抑制作用[J].中国药理学与毒理学杂志,1994,8(1):19-23. 被引量:4
  • 2肖本见,谭志鑫,陈国栋,李玉山.富硒板党对小鼠益智和低氧/复氧损伤的保护[J].中国公共卫生,2005,21(11):1368-1369. 被引量:9
  • 3左玉姣,李颖庆,王刚.丹参酮ⅡA磺酸钠对冠心病心绞痛及血液流变学疗效观察[J].现代生物医学进展,2007,7(5):732-734. 被引量:22
  • 4Simkhovich BZ, Marjoram P, Poizat C, et al. Brief episode of ischemia activates protective genetic program in rat heart: A gene chip study. Cardiovasc Res, 2003,59(2) :450-459.
  • 5Nordlie MA, Wold LE, Simkhovich BZ, et al. Molecular aspects of ischemic heart disease: ischemia/reperfusion-induced genetic changes and potential applications of gene and RNA interference therapy. J Cardiovasc Pharmacol Ther, 2006,11 ( 1 ) :17-30.
  • 6Okubo S, Wildner O, Shah MR, et al. Gene transfer of heat-shock protein 70 reduces infarct size in vivo after ischemia/reperfusion in rabbit heart. Circulation, 2001,103 (6) : 877-881.
  • 7Das DK, Maulik N, Moratu Ⅱ. Gene expression in acute myocardial stress. Induction by hypoxia, ischemia, reperfusion, hyperthermia and oxidative stress. J Mol Cell Cardiol, 1995,27( 1 ) :181-193.
  • 8Nobori K, Ito H, Tamamori-Adachi M, et al. ATF3 inhibits doxorubicin-induced apoptopsis in cardiac myocytes: A novel eardioprotective role of ATF3. J Mol Cell Cardiol, 2002,34 (10) : 1387-1397.
  • 9Melo LG, Pachori AS, Gnecchi M, et al. Genetic therapies for cardiovascular diseases. Trends Mol Med, 2005,11 (5) : 240-250.
  • 10Valen G. Signal transduction through nuclear factor kappa B in ischemia-reperfusion and heart failure. Basic Res Cardiol, 2004,99 ( 1 ) : 1-7.

共引文献101

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