首页> 美国卫生研究院文献>Frontiers in Neuroscience >Correlation of Ventricular Arrhythmogenesis with Neuronal Remodeling of Cardiac Postganglionic Parasympathetic Neurons in the Late Stage of Heart Failure after Myocardial Infarction
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Correlation of Ventricular Arrhythmogenesis with Neuronal Remodeling of Cardiac Postganglionic Parasympathetic Neurons in the Late Stage of Heart Failure after Myocardial Infarction

机译:心肌梗死后心力衰竭晚期心律后副交感神经元心室心律失常与神经元重塑的相关性

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摘要

>Introduction: Ventricular arrhythmia is a major cause of sudden cardiac death in patients with chronic heart failure (CHF). Our recent study demonstrates that N-type Ca2+ currents in intracardiac ganglionic neurons are reduced in the late stage of CHF rats. Rat intracardiac ganglia are divided into the atrioventricular ganglion (AVG) and sinoatrial ganglion. Only AVG nerve terminals innervate the ventricular myocardium. In this study, we tested the correlation of electrical remodeling in AVG neurons with ventricular arrhythmogenesis in CHF rats.>Methods and Results: CHF was induced in male Sprague-Dawley rats by surgical ligation of the left coronary artery. The data from 24-h continuous radiotelemetry ECG recording in conscious rats showed that ventricular tachycardia/fibrillation (VT/VF) occurred in 3 and 14-week CHF rats but not 8-week CHF rats. Additionally, as an index for vagal control of ventricular function, changes of left ventricular systolic pressure (LVSP) and the maximum rate of left ventricular pressure rise (LV dP/dtmax) in response to vagal efferent nerve stimulation were blunted in 14-week CHF rats but not 3 or 8-week CHF rats. Results from whole-cell patch clamp recording demonstrated that N-type Ca2+ currents in AVG neurons began to decrease in 8-week CHF rats, and that there was also a significant decrease in 14-week CHF rats. Correlation analysis revealed that N-type Ca2+ currents in AVG neurons negatively correlated with the cumulative duration of VT/VF in 14-week CHF rats, whereas there was no correlation between N-type Ca2+ currents in AVG neurons and the cumulative duration of VT/VF in 3-week CHF.>Conclusion: Malignant ventricular arrhythmias mainly occur in the early and late stages of CHF. Electrical remodeling of AVG neurons highly correlates with the occurrence of ventricular arrhythmias in the late stage of CHF.
机译:>简介:室性心律失常是慢性心力衰竭(CHF)患者突发心源性死亡的主要原因。我们最近的研究表明,在CHF大鼠的晚期,心内神经节神经元中的N型Ca 2 + 电流降低。大鼠心内神经节分为房室神经节(AVG)和窦房神经节。只有AVG神经末梢可影响心室心肌。在本研究中,我们测试了CHF大鼠AVG神经元电重构与室性心律失常的相关性。>方法和结果:通过外科结扎左冠状动脉在雄性Sprague-Dawley大鼠中诱发CHF。在清醒的大鼠中进行24小时连续无线电遥测ECG记录的数据显示,在3周和14周的CHF大鼠中发生了室性心动过速/心律颤动(VT / VF),而在8周的CHF大鼠中没有发生。此外,作为迷走神经控制心室功能的指标,在​​迷走神经传入神经刺激下,左心室收缩压(LVSP)的变化和左心室最大压力上升率(LV dP / dtmax)在14周的CHF中减弱大鼠,但不包括3或8周的CHF大鼠。全细胞膜片钳记录的结果表明,在8周的CHF大鼠中,AVG神经元中的N型Ca 2 + 电流开始降低,而在14周的CHF中也显着降低大鼠。相关分析表明,AVG神经元中N型Ca 2 + 电流与14周CHF大鼠的VT / VF累积持续时间呈负相关,而N型Ca 2 + 电流和3周CHF中VT / VF的累积持续时间。>结论:恶性室性心律失常主要发生在CHF的早期和晚期。 AVG神经元的电重构与CHF晚期室性心律失常的发生高度相关。

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