期刊文献+

房颤患者右心耳组织SIRT1表达以及与氧化应激的相关性 被引量:3

Expression of SIRT1 in right auricle tissues and the relationship with oxidative stress in patients with atrial fibrillation
下载PDF
导出
摘要 目的:观察房颤患者右心耳组织SIRT1的表达及其与心房氧化应激的关系。方法:选择行心脏手术的风湿性心脏病患者共38例,按照是否合并房颤分为两组:持续性房颤组25例(AF组),其房颤持续时间超过6个月;窦性心律组13例(SR组)。在术中取其部分右心耳组织,采用免疫组化法检测右心耳组织SIRT1蛋白表达,同时测定右心耳组织匀浆中丙二醛(MDA)、总超氧化物歧化酶(SOD)活力和金属硫蛋白(MT)的含量。结果:免疫组化结果发现AF组患者SIRT1表达(45.8±4.03)%高于SR组(19.7±2.54)%,差异有统计学意义(P<0.05)。房颤组MDA为(7.24±1.05)nmol/mg,SOD为(1034.25±84.32)U/mg,MT为(7.21±1.46)μg/g,窦性心律组MDA为(3.01±0.47)nmol/mg,SOD为(723.63±65.23)U/mg,MT为(4.31±1.23)μg/g,两者相比有显著性差异(P<0.05)。房颤组SIRT1表达与MDA、SOD、MT呈负相关,相关系数分别为-0.447、-0.521、-0.394(P<0.05)。结论:房颤患者右心耳组织SIRT1表达增加,与氧化应激指标呈负相关,提示SIRT1可能通过抑制氧化应激在房颤中起作用。 AIM:To observe the expression of mammalian sirtuin 1(SIRT1) in right auricle tissues in patients presenting with atrial fibrillation(AF) and make clear the relationship between SIRT1 expression and oxidative stress.METHODS: A total of 38 patients with rheumatic heart disease were divided into 2 groups: AF group(AF lasted more than 6 months,n=25) and SR(sinus rhythm) group(n=13).The expression of SIRT1 in right auricle tissues harvested during heart operations was detected by immunohistochemistry.Oxidative stress was estimated by the amounts of malondialdehyde(MDA) and metallothionein(MT) and the activity of superoxide dismutase(SOD) which were detected using thiobarbituric acid reaction(TBA),enzyme-linked immunosorbent assay(ELISA) and xanthine oxidase assay,respectively.RESULTS: Compared with the SR group,the expression of SIRT1 protein in the atrium significantly increased in AF group [P〈0.05,(45.8±4.03)% vs(19.7±2.54)%].In AF group,MDA was(7.24±1.05) nmol/mg,SOD(1034.25±84.32) U/mg and MT(7.21±1.46) μg/g,all being significantly higher than those in SR group[P〈0.05,MDA:(3.01±0.47) nmol/mg;SOD:(723.63±65.23) U/mg;MT:(4.31±1.23) μg/g].Spearman correlation indicated that the expression of SIRT1 had a significantly negative correlation with the amounts of MDA and MT and the activity of SOD(P〈0.05,r=-0.447,-0.521,-0.394,respectively).CONCLUSION: The expression of SIRT1 increased in patients with AF.SIRT1 maybe effects the AF by means of inhibiting the process of oxidative stress.
出处 《细胞与分子免疫学杂志》 CAS CSCD 北大核心 2012年第9期972-974,共3页 Chinese Journal of Cellular and Molecular Immunology
关键词 SIRT1 房颤 氧化应激 SIRT1 artial fibrillation oxidative stress
  • 相关文献

参考文献2

二级参考文献43

  • 1Blander G,Guarente L.The Sir2 family of protein deacetylases[J].Annu Rev Biochem,2004,73:417-435
  • 2Frye R A.Characterization of five human cDNAs with homology to the yeast SIR2 gene:Sir2-like proteins (sirtuins) metabolize NAD and may have protein ADP-ribosyltransferase activity[J].Biochem Biophys Res Commun,1999,260:273-279
  • 3Frye R A.Phylogenetic classification of prokaryotic and eukaryotic Sir2-like proteins[J].Biochem Biophys Res Commun,2000,273(2):793 -798
  • 4Picard F,Kurtev M,Chung N,et al.Sirt1 promotes fat mobilization in white adipocytes by repressing PPAR-gamma[J].Nature,2004,429 (6993):771-776
  • 5Rodgers J T,Lerin C,Haas W,et al.Nutrient control of glucose homeostasis through a complex of PGC-1alpha SIRT1[J].Nature,2005,434(7029):113-118
  • 6Giannakou M E,Partridge L.The interaction between FOXO and SIRT1:tipping the balance towards survival[J].Trends Cell Biol,2004,14(8):408-412
  • 7Brunet A,Sweeney L B,Sturgill J F,et al.Stress-dependent regulation of FOXO transcription factors by the SIRT1 deacetylase[J].Science,2004,303(5666):2011-2015
  • 8Kobayashi Y,Furukawa-Hibi Y,Chen C,et al.SIRT1 is critical regulator of FOXO-mediated transcription in response to oxidative stress[J].Int J Mol Med,2005,16(2):237-243
  • 9Motta M C,Diveeha N,Lemieux M,et al.Mammalian SIRT1 represses forkhead transcription factors[J].Cell,2004,116(4):551-563
  • 10Horst A,Tertoolen L G,de Vries-Smits L M,et al.FOXO4 is acetylated upon peroxide stress and deacetylated by the longevity protein hSir2 (SIRT1)[J].J Biol Chem,2004,279 (28):28873-28879

共引文献26

同被引文献42

  • 1Mohebbi M,Ghassemian H.Predicting termination of paroxysmal atrial fibrillation using empirical mode decomposition of the atrial activity and statistical features of the heart rate variability[J].Med Biol Eng Comput,2014,52(5):415-427.
  • 2Li J,Song J,Jiang MH,et al.Interleukin-6 promoter polymorphisms and susceptibility to atrial fibrillation in elderly han chinese patients with essential hypertension[J].J Interferon Cytokine Res,2012,3201):542-547.
  • 3Takizawa Y,Kosuge Y,Awaji H,et al.Up-regulation of endothelial nitric oxide synthase(e NOS),silent mating type information regulation 2 homologue 1(SIRT1)and autophagy-related genes by repeated treatments with resveratrol in human umbilical vein endothelial cells[J].Br J Nutr,2013,110(12):2150-2155.
  • 4Mayyas F,Alzoubi KH,Van Wagoner DR.Impact of aldosterone antagonists on the substrate for atrial fibrillation:aldosterone promotes oxidative stress and atrial structural/electrical remodeling[J].Int J Cardiol,2013,168(6):5135-5142.
  • 5Goette A,D'Alessandro A,Bukowska A,et al.Rationale for and design of the CREATIVE-AF trial:randomized,double-blind,placebo-controlled,crossover study of the effect of irbesartan on oxidative stress and adhesion molecules in patients with persistent atrial fibrillation[J].Clin Drug Investig,2008,28(9):565-572.
  • 6Toyama K,Yamabe H,Uemura T,et al.Analysis of oxidative stress expressed by urinary level of 8-hydroxy-2'-deoxyguanosine and biopyrrin in atrial fibrillation:effect of sinus rhythm restoration[J].Int J Cardiol,2013,168(1):80-85.
  • 7Ulas T,Haclbekiroglu T,Sezen H,et al.Comment on:Analysis of oxidative stress expressed by urinary level of 8-hydroxy-2'-deoxyguanosine and biopyrrin in atrial fibrillation:effect of sinus rhythm restoration[J].Int J Cardiol,2013,167(4):1643.
  • 8Ederhy S,Di Angelantonio E,Dufaitre G,et al.C-reactive protein and transesophageal echocardiographic markers of thromboembolism in patients with atrial fibrillation[J].Int J Cardiol,2012,159(1):40-46.
  • 9Lübkemeier I,AndriéR,Lickfett L,et al.The Connexin40A96S mutation from a patient with atrial fibrillation causes decreased atrial conduction velocities and sustained episodes of induced atrial fibrillation in mice[J].J Mol Cell Cardiol,2013(65):19-32.
  • 10Kawashima T,Inuzuka Y,Okuda J,et al.Constitutive SIRT1overexpression impairs mitochondria and reduces cardiac function in mice[J].J Mol Cell Cardiol,2011,51(6):1026-1036.

引证文献3

二级引证文献14

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