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房颤患者心房肌I_f电流mRNA表达的变化 被引量:1

Alterations of I_f mRNA expression in atria of patients with persistent atrial fibrillation
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摘要 目的 观察了房颤患者If电流mRNA表达的变化 ,从分子水平探讨房颤发生的机制。方法  2 6例因冠状动脉粥样硬化性心脏病、风湿性心脏瓣膜病或先天性心脏病行开胸心脏手术的患者 ,术中取右心耳 5 0mg。分为两组 :窦性心律组 15例 ;持续房颤组 11例。采用逆转录聚合酶链反应的方法测定两组患者起搏电流离子通道mRNA表达的变化。结果 持续房颤患者左心房内径明显较窦性心律患者大 (5 1.18± 9.12mm∶3 4.2 7± 4.0 6mm ,P <0 .0 1)。其他临床特征匹配。房颤患者If 基因表达明显增加 (0 .3 0± 0 .0 3∶0 .3 4± 0 .0 5P <0 .0 5 )。结论 无论窦性心律患者还是持续房颤患者 ,其心房中都有If 的表达 ,证明If 不仅存在于起搏细胞 ,也在非起搏细胞心房肌组织中有表达。持续房颤患者IfmRNA表达明显高于窦性心律患者 ,提示此电流可能参与房颤发生的某种机制。 Objectives To measure I f channel mRNA expression in atrial tissue of patients with AF and without AF in order to study on the mechanism of AF. Method Right atrial appendages were obtained from 26 patients undergoing open heart surgery including patients with coronary heart disease, rheumatic heart disease and congenital heart disease. Among them 11 had persistent AF and 15 were matched controls in sinus rhythm. Funny channel mRNA were measured by semiquantitative polymerase chain reaction.Results Clinical parameters were matched between 2 groups except that left atrial diameter were larger in patients with AF than in patients with sinus rhythm (51.18±9.12mm vs 34.27±4.06mm, P <0.01). mRNA levels of I f were increased from 0.30±0.03 in patients with AF to 0.34±0.05 in patients with sinus rhythm ( P <0.05).Conclusions I f exists in atria regardless of patient with sinus rhythm or AF, which shows that I f exists both in pacing cells and in nonpacing tissue-atria. Moreover, mRNA of I f is increased among AF patients compared with patients with sinus rhythm, which suggests that this channel may be involved in some mechanism of AF onset.
出处 《中国医刊》 CAS 2004年第8期31-32,共2页 Chinese Journal of Medicine
关键词 MRNA 表达 心房颤动 先天性心脏病 起搏电流 atrial fibrillation I f channel mRNA
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参考文献4

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同被引文献24

  • 1周自强,胡大一,陈捷,张仁汉,李奎宝,赵秀丽.中国心房颤动现状的流行病学研究[J].中华内科杂志,2004,43(7):491-494. 被引量:1398
  • 2Schotten U, Verheule S IKirchhof P, et al.Pathophysiological n anisms of atrial fibrillation: a translational appraisal. Physiol2011,91:265-325.
  • 3Miyasaka Y, Barnes ME, Gersh BJ, et al.Time trends of ischemic stroke incidence and mortality in patients diagnosed with first atrial fibrillation in 1980 to 2000: report of a community-based study. Stroke, 2005,36 : 2362-2366.
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  • 6Herrmann S, Layh B, Ludwig A.Novel insights into the distribution of cardiac HCN channels : an expression study in the mouse heart.J Mol Cell Cardiol,2011,51:997-1006.
  • 7Michels G, Er F, Khan I, et al. Single-channel properties support a potential contribution of hyperpolarization-activated cyclic nueleo- tide-gated channels and /f to cardiac arrhythmias. Circulation, 2005,111:399-404.
  • 8Hoppe UC, Beuckelmann DJ. Characterization of the hyperpolariza- tion-activated inward current in isolated human atrial myocytes. Cardiovase Res, 1998,38 : 788- 801.
  • 9Zorn-Pauly K,Schaffer P,Pelzmann B,et al.if in left human atri- um : a potential contributor to atrial eetopy. Cardiovasc Res, 2004, 64 : 250-259.
  • 10Fernandez-Velasco M, Goren N, Benito G, et al.Regional distribu- tion of hyperpolarization-aetivated current(If) and hyperpolariza- tion-aetivated cyclic nueleotide-gated channel mRNA expression in ventrieular cells from control and hypertrophied rat hearts. J Physiol, 2003,553 : 395 - 405.

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