期刊文献+

DCM猝死与晚期DCM心肌Cx43表达的比较 被引量:1

Expression of myocardial Cx43 in cases of sudden unexpected death with DCM and in patients with serious DCM
原文传递
导出
摘要 目的观察和探讨扩张型心肌病(DCM)猝死与晚期DCM心肌中心肌连接蛋白(connexin,Cx)43表达差异及其意义。方法收集13例DCM猝死者心脏(A组)和5例晚期DCM患者行心脏移植手术切除的心脏(B组),运用免疫组化染色和图像分析技术,检测心肌Cx43阳性表达产物的平均光密度(OD)值和面积(S)值,比较两组间和左右心室间的差异。结果 Cx43阳性表达在A组明显减少,分布不均;在B组表达清晰,主要位于闰盘处。A组与B组心肌Cx43的S值之间的差异有统计学意义(P<0.01),而各组左、右心室肌间相比,差异无统计学意义(P>0.05);心肌Cx43的OD值,在A组与B组之间,以及各组左、右心室肌间差异均无统计学意义(P>0.05)。结论 DCM猝死心肌Cx43表达较晚期DCM心肌明显减少,这种变化可能与DCM患者因心律失常发生猝死有关。 Objective This research was aimed to observe and probe into the expressions and differences of myocardial connexin (Cx)43 between the cases of sudden unexpected death with DCM and patients with a clinical diagnosis of serious DCM. Methods Collect 13 cases of sudden unexpected death with DCM as group A, and 5 patients with serious DCM as group B, then Myocardial Cx43 expression was detected and analyzed by immunohistochemical staining and computerized image analysis. Results Myocardial Cx43 expression was obviously decreased in group A compared to group B. The quantitative data showed that there was significant difference between two groups about Cx43 expressive area ( P 〈 0. 01 ) , but no difference between left and right ventricles in each group itself (P 〉 0. 05 ) and no difference between two groups about average optical density of expression ( P 〉 0. 05 ). Conclusion Myocardial Cx43 expression was obviously reduced in group A. The alterations of quantity and distribution were probably related to sudden death of the patients with DCM.
出处 《中国法医学杂志》 CSCD 2016年第1期18-21,共4页 Chinese Journal of Forensic Medicine
基金 湖北省科技攻关计划项目(2007AA301B31-3) 武汉市科技攻关计划项目(201060626254)
关键词 法医病理学 扩张型心肌病 免疫组化 连接蛋白43 forensic pathology dilated cardiomyopathy immnohistochemistry connexin43
  • 相关文献

参考文献13

  • 1VALIUNAS V,BEYER E C,BRINK P R.Cardiac gap junction channels show quantitative differences in selectivity[J].Circ Res,2002,91(2):104-111.
  • 2李玉林.病理学[M].6版.北京:人民卫生出版社,2003:1.
  • 3ECKARDT D,THEIS M,DEGEN J,et al.Functional role of connexin43 gap junction channels in adult mouse heart assessed by inducible gene deletion[J].J Mol Cell Cardiol,2004,6(1):101-110.
  • 4徐振平,郭志坤,张光谋,文小军.新生儿心肌连接蛋白43、45的表达[J].解剖学研究,2002,24(3):177-179. 被引量:4
  • 5郭继鸿.缝隙连接与心脏的传导[J].临床心电学杂志,2003,12(3):194-199. 被引量:11
  • 6THOMAS S A,SCHUESSHER R B.Disparate dffects of deficient expression of connexin 43 on atrial and ventricular conduction:determinants of conduction[J].Cardiovasc Res,2005,67(2):97-103.
  • 7JEFFREY E,SATTITZ H,LEE K H,et al.Tissue specific and ventricular myocardium[J].Cir Res,1994,74:1065-1070.
  • 8SEVERS N J.The cardiac gap junction and intercalated disc[J].Int J Cardiol,1990,26:137-173.
  • 9CHEN X S,ZHANG Y G.Myocardial Cx43 expression in the cases of sudden death due to dilated cardiomyopathy[J].Forensic Sci Int,2006,162(3):170-173.
  • 10LIAO Y,DAY K H,DAMON D N,et al.Endothelial cellspecific knock-out of connexin 4 3 causes hypotention bradycardiain mice[J].Proc Natl Scad Sci USA,2001,98(17):9989-9994.

二级参考文献33

  • 1Figueroa X F, Duling B R. Gap Junctions in the Control of Vascular Function [J].Antioxid Redox Signal, 2009, 11: 251-266.
  • 2Scemes E, Spray D C, Meda P. Connexins, pannexins, innexins: novel roles of "hemi-channels" [J]. Pflugers Arch Eur J Physiol, 2009, 457(6) : 1207-1226.
  • 3Boengler K, Stahlhofen S, Vandesand A, et al. Presence of connexin 43 in subsarcolemmal, but not in interfibrillar cardiomyocyte mitochondria [J]. Basic Res Cardiol, 2009, 104(2) : 141-147.
  • 4Sato T, Ohkusa T, Honjo H, et al. Altered expression of connexin43 contributes to the arrhythmogenie substrate during the development of heart failure in eardiomyopathie hamster [J]. Am J Physiol Heart Cire Physiol, 2008,294 ( 3 ) : H 1164- H 1173.
  • 5Peter N S, Green C R, Poole-wison P A.Reduced content of connexin43 gapjunction in ventricular myocardium from hypertrophied and ischemie human heart [J]. Circulation, 1993, 88(3): 864-875.
  • 6Peters N S. New insights into myocardial arrhythmogenesis : distribution of gap-junctional coupling in normal, ischaemic and hypertrophied human hearts [J]. Clin Sci, 1996, 90(6):447-452.
  • 7Garcia-Dorado D, Rodriguez-Sinovas A, Ruiz-Meana M, et al. Gap Junction medialed spread of cell injury and death during myocardial ischemia- reperfusion [J]. Cardiovasc Res, 2004, 61(3) :386-401.
  • 8Johansen D, Sanden E, Hagve M, et al. Heptanol triggers cardioprotection via mitochondrial mechanisms and mitochondrial potassium channel opening in rat hearts [J]. Acta Physiologica, 2011, 201 ( 2 ) : 435-444.
  • 9Heinzel F R, Luo Y, Li X, et al. Impairment of diazoxide-induced formation of reactive oxygen species and loss of cardioprotection in connexin 43 deficient mice [J]. Circ Res, 2005, 97(6) : 583-586.
  • 10Kazuyuki N, Toshiyuki Y, Tetsuji M, et al. Roles of Cx43-associated protein kinases in suppression of gap junction- mediated chemical coupling by ischemic preconditioning [J]. Am J Physiol Heart Circ Physiol, 2009, 296 (2) : H396-H403.

共引文献29

同被引文献45

引证文献1

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