期刊文献+

白藜芦醇在大鼠心肌缺血再灌注损伤中的作用及机制 被引量:4

Effects of resveratrol on rat hearts impaired by ischemia/reperfusion
暂未订购
导出
摘要 目的研究白藜芦醇对大鼠心肌缺血再灌注损伤的保护作用,并进一步阐明其作用机制。方法 45只大鼠随机分为3组,假手术组、单纯缺血再灌注组、白藜芦醇预处理组,每组15只。结扎大鼠左冠状动脉前降支建立大鼠心肌缺血再灌注损伤模型。TUNEL法检测心肌细胞的凋亡,Western-blot检测Sirt1、P53及乙酰化P53的表达。结果白藜芦醇能减少大鼠心肌缺血再灌注后心肌细胞的凋亡(P<0.05),使Sirt1表达增高(P<0.05),乙酰化P53表达降低(P<0.05)。结论白藜芦醇对大鼠心肌缺血再灌注损伤具有保护作用,其机制可能与Sirt1-P53通路有关。 AIM To investigate the protective effects of resveratrol against myocardiac ischemia/reperfusion injury and its mechanism.METHODS Forty-five rats were randomly divided into three groups(15 rats each group): sham operation group,ischemia/reperfusion group,resveratrol pretreatment group.The myocardial ischemia-reperfusion injury model in rats was established by ligating left anterior descending coronary artery.TUNEL method was used to detect myocardial cell apoptosis.Protein expression of Sirt1,P53 and acetylation P53 was measured by Western blot.RESULTS The experiment revealed that resveratrol inhibited myocardial cell apoptosis(P〈0.05),increased Sirt1 level(P〈0.05),and decreased the acetylation P53 content(P〈0.05) on rat hearts impaired by ischemia/reperfusion.CONCLUSION Resveratrol shows protective effects against myocytes ischemia/reperfusion injury induced by coronary ligation in rats,and its mechanism is probably related to Sirt1-P53 pathway.
出处 《中成药》 CAS CSCD 北大核心 2012年第5期811-814,共4页 Chinese Traditional Patent Medicine
关键词 心肌缺血 心肌再灌注损伤 细胞凋亡 Sirtl P53 白藜芦醇 myocyte ischemia ischemia/reperfusion injury apotosis Sirt1 P53 resveratrol
  • 相关文献

参考文献12

  • 1陈丽函,王伟,傅玉才,李吉林,许铭炎.白藜芦醇对缺血再灌注心肌细胞凋亡及沉寂信息调节因子2表达的影响[J].中国临床康复,2006,10(19):69-71. 被引量:15
  • 2Yoshida Y,Shioi T,Izumi T,et al.Resveratrol ameliorates ex-perimental auto-immune myocarditis[J].Circ J,2007,71(3):397-404.
  • 3Huang J,Gan Q,Han L,et al.SIRT1overexpression antagoni-zes cellular senescence with activated ERK/S6k1signaling in hu-man diploid fibroblasts[J].Plos One,2008,3(3):e1710.
  • 4Kajstura J,Cheng W,Reiss K,et al.Apoptotic and necrotic myocyte cell deaths are independent contributing variables of in-farct size in rats[J].Lab Invest,1996,74(1):86-107.
  • 5Samuel S M,Thirunavukkarasu M,Penumathsa S V,et al.Akt/FOXO3a/SIRT1-mediated cardioprotection by n-tyrosol against ischemic stress in rat in vivo model of myocardial infarction:switc-hing gears toward survival and longevity[J].J Agric Food Chem,2008,56(20):9692-9698.
  • 6Shinmura K,Tamaki K,Bolli R.Impact of6-mo caloric restric-tion on myo-cardial ischemic tolerance:possible involvement of nitric oxide-dependent increase in nuclear Sirt1[J].Am J Physi-ol Heart Circ Physiol,2008,295(6):H2348-H2355.
  • 7郭宏兴,张吉翔,章诺贝.Sir2基因与端粒沉默的研究进展[J].生理科学进展,2007,38(2):184-186. 被引量:1
  • 8Kikuno N,Shiina H,Urakami S,et al.Genistein mediated his-tone aeetylation and demethylation activates tumou-suppressor genes in prostate cancer eelb[J].Int J Cancer,2008,123(3):552-560.
  • 9朱兆峰,肖宝荣,张国,卢鑫,苏培英,黄德波,李梁.p53和PCNA表达与非小细胞肺癌放射敏感性及预后的关系[J].肿瘤学杂志,2010,16(1):53-55. 被引量:2
  • 10Pierzchalski P,Reiss K,Cheng W,et al.P53induces myocyte apoptosis via the activation of the renin-angiotensin system[J].Exp Cell Res,1997,234(4):57-65.

二级参考文献25

  • 1莫浩元,张昌卿,冯凯涛,张锋,洪明晃,孙折玉.鼻咽癌组织中P53和PCNA表达与临床分期、VCA/IgA、EA/IgA、放射敏感性和预后的关系[J].癌症,2004,23(z1):1551-1554. 被引量:21
  • 2李健强,邵国光,刘琳琳,郑永晨.p53基因BstUⅠ位点多态性与非小细胞肺癌易感性及放射敏感性的相关性研究[J].中国肺癌杂志,2006,9(2):173-176. 被引量:7
  • 3Nadal-Ginard B,Kajstura J,Anversa P,et al.A matter of life and death:cardiac myocyte apoptosis and regeneration.J Clin Invest 2003;111 (10):1457-9.
  • 4Olson EN,Schneider MD.Sizing up the heart:development redux in disease.Genes Dev 2003;17(16):1937-56.
  • 5Sakamoto J,Miura T,Shimamoto K,et al.Predominant expression of Sir2α,an NAD-dependent histone deacetylase,in the embryonic mouse heart and brain.FEBS Letters 2004;556(1-3):281-6.
  • 6Howitz KT,Bitterman K J,Cohen HY,et al.Small molecule activators of sirtuins extend Saccharomyces cerevisiae lifespan.Nature 2003;425 (6954):191-6.
  • 7Alcendor R,Kirshenbaum LA,Imai S,et al.Silent information regulator 2α,a longevity factor and class Ⅲ histone deacetylase,is an essential endogenous apoptosis inhibitor in cardiac myocytes.Circ Res 2004;95 (10):971-80.
  • 8Higuchi M,Aggarwal BB,Yeh ET.Activation of CPP 32-like protease in tumor necrosis factor induced apoptosis is dependent on mitochondrial function.J Clin Invest 1997;99(7):1751-8.
  • 9Cubizolles F,Martino F,Perrod S,et al.A homotrimer-heterotrimer switch in Sir2 structure differentiates rDNA and telomeric silencing.Mol Cell,2006,21:825~836.
  • 10Moazed D.Enzymatic activities of Sir2 and chromatin silencing.Curr Opin Cell Biol,2001,13:232~238.

共引文献15

同被引文献37

引证文献4

二级引证文献11

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