期刊文献+

青壮年猝死综合征心肌细胞内Cx43的表达 被引量:5

Expression of connexin 43 in cardiomyocytes of sudden manhood death syndrome
在线阅读 下载PDF
导出
摘要 目的观察连接蛋白43(Cx43)在青壮年猝死综合征(SMDS)者心肌细胞的表达,并探讨其法医学意义。方法筛选法医尸检案例45例,其中SMDS组、冠心病猝死组及对照组各15例。采用免疫组织化学和图像分析技术对不同组别Cx43蛋白在心肌细胞内的表达进行阳性单位(PU)定量检测,分析Cx43蛋白在各组表达的差异。所得数据进行统计学分析。结果 SMDS组心肌Cx43染色明显减弱,阳性着色条带分布不均、深浅不一,有的呈散在颗粒状;冠心病猝死组亦见类似变化;对照组未见明显变化。经统计分析发现,3组心肌细胞内Cx43表达的PU值存在显著性差异(P<0.05)。结论 SMDS死前存在心肌缺血及心电紊乱,应属心性猝死范畴。 Objective To study the expression of connexin43 (Cx43) in cardiomyocytes in cases of sudden manhood death syndrome(SMDS) and explore its medicolegal significance. Methods Obtained 45 autopsy cases from 3 different groups (SMDS group,coronary atherosclerotic heart disease group and control group). Cx43 protein in myocardium was detected by immunohistochemical techniques. Computerized image analysis was employed to measure the Cx43 positive units(PU) of cardiomyocytes,the data were analyzed statistically. Results Expression of Cx43 in myocardium decreased obviously in SMDS group. Similar changes were also observed in coronary atherosclerotic heart disease group but no obvious changes in the control group. There were significant differences of Cx43 positive units in the myocardium among the three groups (P0.05). Conclusions Immunohistochemical detection of Cx43 in myocardium may effectively help postmortem diagnosis of SMDS.
出处 《中国法医学杂志》 CSCD 北大核心 2010年第3期159-161,共3页 Chinese Journal of Forensic Medicine
基金 国家自然科学基金资助项目(39700167)
关键词 法医病理学 连接蛋白43 青壮年猝死综合征 免疫组织化学 forensic pathology connexin43(Cx43) sudden manhood death syndrome(SMDS) immunohistochemical method
  • 相关文献

参考文献9

二级参考文献46

  • 1申洪,陆药丹.免疫组织化学染色的定量方法研究[J].生物医学工程学杂志,1993,10(4):281-284. 被引量:127
  • 2陈新山,金秀文,张益鹄.心肌病猝死者心肌连接蛋白43的免疫组化染色观察[J].中国法医学杂志,2006,21(2):76-78. 被引量:9
  • 3苏德淳,常志文,范书英.缝隙连接在大鼠缺血预适应心肌保护中的作用[J].中华心血管病杂志,2006,34(8):690-694. 被引量:14
  • 4杨军,伍卫,梁蔚文,王景峰,潘秋辉,方昶,黄至斌.血管紧张素Ⅱ诱导心肌细胞肥大后缝隙连接蛋白Cx43表达的变化[J].中山大学学报(医学科学版),2007,28(3):292-296. 被引量:6
  • 5Herve J C,Sarrouilhe D.Protein phosphatase modulation of the intercellular junctional communication:Importance in cardiac myocytes[J].Prog Biophys Mol Biol,2006,90 (1-3):225-248.
  • 6Saffitz J E.Regulation ofintercellular coupling in acute and chronic heart disease[J].Braz J Med Res,2000,33(4):407-413.
  • 7Kirchhof S,Kin J S,Hngendorf A,et al.Abnormal cardiac conduction and morphogenesis in connexin40 and connexin43 double-deficient mice[J].Circ Res,2000,87(5):346-348.
  • 8Peters N S.New insights into myocardial arrhythmogenesis:distribution of gap junctional coupling in normal,isehaemic and hypertrophied human hearts[J].Clin Sci (Lond),1996,90(6):447-452.
  • 9Peters N S,Coromilas J,Severs N J,et al.Disturbed connexin43 gap junction distribution correlates with the location of reentrant circuits in the epicardial border zone of healing canine infarcts that cause ventricular taehycardia[J].Circulation,1997,95(4):988-996.
  • 10Peters N S,Wit A L.Myocardial architecture and ventricular arrhythmogenesis[J].Circulation,1998,97(17):1746-1754.

共引文献420

同被引文献54

引证文献5

二级引证文献8

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