首页> 外文期刊>Journal of cardiovascular electrophysiology >Diminished Cardiac Fibrosis in Heart Failure is Associated with Altered Ventricular Arrhythmia Phenotype.
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Diminished Cardiac Fibrosis in Heart Failure is Associated with Altered Ventricular Arrhythmia Phenotype.

机译:心力衰竭中的心脏纤维化减弱与室性心律失常表型改变有关。

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Diminished Ventricular Fibrosis and Tachyarrhythmias. Objectives: We sought to define the role of interstitial fibrosis in the proarrhythmic phenotype of failing ventricular myocardium. Background: Multiple cellular events that occur during pathological remodeling of the failing ventricle are implicated in the genesis of ventricular tachycardia (VT), including interstitial fibrosis. Recent studies suggest that ventricular fibrosis is reversible, and current anti-remodeling therapies attenuate ventricular fibrosis. However, the role of interstitial fibrosis in the proarrhythmic phenotype of failing ventricular myocardium is currently not well defined. Methods: Class II histone deacetylases (HDACs) have been implicated in promoting collagen biosynthesis. As these enzymes are inhibited by protein kinase D1 (PKD1), we studied mice with cardiomyocyte-specific transgenic over-expression of a constitutively active mutant of PKD1 (caPKD). caPKD mice were compared with animals in which cardiomyopathy was induced by severe thoracic aortic banding (sTAB). Hearts were analyzed by echocardiographic and electrocardiographic means. Interstitial fibrosis was assessed by histology and quantified biochemically. Ventricular arrhythmias were induced by closed-chest, intracardiac pacing. Results: Similar degrees of hypertrophic growth, systolic dysfunction and mortality were observed in the two models. In sTAB mice, robust ventricular fibrosis was readily detected, but myocardial collagen content was significantly reduced in caPKD mice. As expected, VT was readily inducible by programmed stimulation in sTAB mice and VT was less inducible in caPKD mice. Surprisingly, episodes of VT manifested longer cycle lengths and longer duration in caPKD mice. Conclusion: Attenuated ventricular fibrosis is associated with reduced VT inducibility, increased VT duration, and significantly longer arrhythmia cycle length. (J Cardiovasc Electrophysiol, Vol. 21, pp. 1031-1037, September 2010).
机译:心室纤维化和快速性心律失常减少。目的:我们试图确定间质纤维化在心室衰竭的心律失常表型中的作用。背景:在衰竭心室的病理重塑过程中发生的多种细胞事件与室性心动过速(VT)的发生有关,包括间质纤维化。最近的研究表明,心室纤维化是可逆的,当前的抗重塑疗法可减轻心室纤维化。然而,间质纤维化在衰竭心室心肌的心律失常表型中的作用目前尚不清楚。方法:II类组蛋白脱乙酰基酶(HDACs)与促进胶原蛋白的生物合成有关。由于这些酶被蛋白激酶D1(PKD1)抑制,因此我们研究了具有PKD1(caPKD)组成型活性突变体的心肌细胞特异性转基因过表达的小鼠。将caPKD小鼠与通过严重胸主动脉束带(sTAB)诱发心肌病的动物进行了比较。通过超声心动图和心电图手段分析心脏。间质纤维化通过组织学评估和生化定量。闭胸,心内起搏诱发室性心律失常。结果:在两个模型中观察到相似程度的肥大性生长,收缩功能障碍和死亡率。在sTAB小鼠中,很容易检测到强健的心室纤维化,但是在caPKD小鼠中,心肌胶原含量明显降低。如预期的那样,在sTAB小鼠中通过编程刺激很容易诱导VT,而在caPKD小鼠中VT诱导较少。出乎意料的是,caPKD小鼠中VT发作表现出更长的周期长度和更长的持续时间。结论:室性纤维化减弱与室速诱发性降低,室速持续时间增加以及心律失常周期时间明显延长有关。 (J Cardiovasc Electrophysiol,Vol.21,pp.1031-1037,2010年9月)。

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