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白藜芦醇调控大鼠心力衰竭模型氧化应激相关基因的作用 被引量:6

The Influence of Resveratrol on the Myocardial Oxidation Related Genes in Rat Models with Heart Failure
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摘要 目的探讨白藜芦醇调控大鼠心力衰竭模型氧化应激相关基因的作用。方法采用腹主动脉缩窄法制备SD大鼠心力衰竭模型,测定心脏重量指数变化,Real-Time PCR定量分析超氧化物歧化酶(SOD)、血红素氧合酶(HO-1)、谷胱甘肽过氧化物酶(GPx)表达;免疫组织化学法检测SOD。结果白藜芦醇干预组和模型组比较,心脏重量指数改善,高剂量组更为显著;心衰大鼠SOD、GPx、HO-1表达水平明显降低(P<0.05或P<0.01),白藜芦醇干预后,SOD、GPx、HO-1表达水平均有所升高,其中以SOD改善明显(P<0.0 5),高剂量组SOD表达甚至高过假手术组。结论白藜芦醇能提高大鼠心力衰竭模型心肌各氧化相关基因的表达,改善心功能。 Objective To observe the effect of resveratrol( RES) on the myocardial oxidation related genes in rat models with heart failure( HF). Methods Sprague-Dawley( SD) rat models with HF were established by partially banding abdominal aortic artery. The cardiac fibrosis was evaluated by heart weight index( HWI). The expression of superoxide dismutase( SOD 1),heme oxygenase( HO-1),glutathione peroxidase( GPX) were measured by real-time polymerase chain reaction( RT-PCR). SOD was detected by immunohistochemistry. Results Compared with model group,HWI was significantly increased in RES group,especially RES high dose group. The expression levels of SOD1,GPx,HO-1 were decreased in model group(P〈0. 01 or P〈0. 05). The expression levels of SOD1,GPx,HO-1 were increased in RES group(P〈0. 05),especially SOD. The activity of SOD in RES high dose group was higher than that in sham operation group. Conclusion RES can improve the expression of the myocardial oxidation related genes in rats with heart failure.
出处 《中西医结合心脑血管病杂志》 2016年第7期704-706,共3页 Chinese Journal of Integrative Medicine on Cardio-Cerebrovascular Disease
基金 江苏省南通市人才工作专项基金(No.s8008)
关键词 心力衰竭 白藜芦醇 氧化应激 大鼠 超氧化物歧化酶 血红素氧合酶 谷胱甘肽过氧化物 heart failure resveratrol oxidative stress rat Superoxide dismutase heme oxygenase glutathione peroxidase
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  • 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
  • 2Samuel SM, Thirunavukkarasu M, Penumathsa SV, et al. Akt/FOXO3a/ SIRTl-mediated cardioprotection by n-tyrosol against ischemic stress in rat in vivo model of myocardial infarction:switching gears toward survival and longevity[ J]. J Agrie Food Chem ,2008 ;56 (20) :9692-8.
  • 3Shinmura K, Tamaki K, Bolli R. Impact of 6-mo caloric restriction on myocardial ischemic tolerance:possible involvement of nitric oxide-dependent increase in nuclear Sirtl [J]. Am J Physiol Heart Circ Physiol,2008 ;295 (6) : H2348-55.
  • 4Yoshida Y, Shioi T, Izumi T. Resveratrol ameliorates experimental autoimmune myocarditis[ J]. Cite J,2007 ;71 ( 3 ) :397-404.
  • 5Huang J, Gala Q, Han L, et al. SIRTI overexpression antagonizes cellular senescence with activated ERK./S6kl signaling in human diploid fibroblasts [ J ]. PLOS ONE,2008 ;3 ( 3 ) : e1710.
  • 6Song JQ, Teng X, Cai Y, et al. Activation of Akt/GSK-3beta signaling pathway is involved in intermedin (1-53) protection against myocardial apoptosis induced by ischemia/reperfusion[ J ]. Apoptosis, 2009;14 (9) : 1061-9.
  • 7Zhang C, Feng Y, Qu S, et al. Resveratrol attenuates doxorubicin-induced cardiomyocyte apoptosis in mice through SIRTl-mediated deaeetylation of p53 [J]. Cardiovase Res ,2011 ;90 ( 3 ) :538-45.
  • 8Nadtochiy SM, Redman E, Rahman I, et al. Lysine deaeetylation in isehemic preconditioning : the role of SIRT1 [J].Cardiovasc Res,2011 ;89 ( 3 ) : 643 -9.
  • 9Sundaresan NR, Pillai VB, Gupta MP. Emerging roles of SIRT1 deacetylase in regulating cardiomyocyte survival and hypertrophy [ J ]. J Mol Cell Cardiol,2011 ;51 (4) :614-8.
  • 10Wong CY, Chaudhry SI, Desai MM, et al. Trends in comorbidity, disability and polypharmacy in heart failure. Am J Med, 2011, 124: 136-143.

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