Wang Dandan, Liu Tao, Shi Shaobo, Li Ran, Shan Yingguang, Huang Yan, Hu Dan, Huang Congxin
Department of Cardiology, Renmin Hospital of Wuhan University, Wuhan, China Cardiovacular Research Institute, Wuhan University, Wuhan, China.
Department of Cardiology, Renmin Hospital of Wuhan University, Wuhan, China Cardiovacular Research Institute, Wuhan University, Wuhan, China Masonic Medical Research Laboratory, Utica, NY, USA.
J Cardiovasc Pharmacol Ther. 2016 Nov;21(6):526-535. doi: 10.1177/1074248416628676. Epub 2016 Jan 27.
Catestatin (CST), which is emerging as a novel cardiac modulator, can protect the heart against excessive sympathetic drive in hypertensive cardiomyopathy. The aim of this study is to investigate whether exogenous CST decreases excessive cardiac sympathetic drive and improves autonomic function and exerts cardioprotective effects in myocardial infarction (MI) rats. Rats were divided into a sham group, MI group, and MI plus CST (MI + CST) group. Four weeks later, the autonomic function of the animals was assessed by analyzing heart rate variability (HRV) and measuring plasma catecholamine. Cardiac function was evaluated via echocardiography. Electrophysiological characteristics were assessed in Langendorff-perfused hearts. Compared to the MI group, the chronic administration of CST significantly increased the standard deviation of normal-normal intervals (P < .01) and low-frequency (LF) and high-frequency (HF) HRV and decreased the ratio of LF-HF HRV (P < .01 for all). Additionally, the level of plasma catecholamine was reduced in the MI + CST group compared to the MI group (P < .01). Treatment with CST significantly increased ejection fraction (EF) and fraction shorting (FS) and significantly decreased the left ventricular end-systolic diameter and left ventricular end-diastolic diameter at 28 days postmyocardial infraction (P < .05 for all). After MI, the ventricular repolarization duration, such as QTc intervals and action potential duration (APD) at 90% repolarization, was prolonged, and this prolongation could be decreased by CST (P < .05 for all). The CST also increased the threshold of ADP alternans (P < .01). Moreover, ventricular arrhythmias were induced in 83% of the MI group but only 33% of the MI + CST group (P < .05). These results suggested that the chronic administration of CST plays a role in cardioprotection in MI rats, which may function by decreasing the cardiac sympathetic drive and improving autonomic function.
癌抑制素(CST)作为一种新型心脏调节剂,可保护心脏免受高血压性心肌病中过度交感神经驱动的影响。本研究旨在探讨外源性CST是否能降低心肌梗死(MI)大鼠过度的心脏交感神经驱动,改善自主神经功能并发挥心脏保护作用。将大鼠分为假手术组、MI组和MI加CST(MI + CST)组。四周后,通过分析心率变异性(HRV)和测量血浆儿茶酚胺来评估动物的自主神经功能。通过超声心动图评估心脏功能。在Langendorff灌注心脏中评估电生理特征。与MI组相比,长期给予CST可显著增加正常到正常间期的标准差(P <.01)以及低频(LF)和高频(HF)HRV,并降低LF-HF HRV比值(所有P <.01)。此外,与MI组相比,MI + CST组的血浆儿茶酚胺水平降低(P <.01)。CST治疗在心肌梗死后28天显著增加射血分数(EF)和缩短分数(FS),并显著降低左心室收缩末期直径和左心室舒张末期直径(所有P <.05)。MI后,心室复极持续时间,如QTc间期和90%复极时的动作电位持续时间(APD)延长,而CST可减少这种延长(所有P <.05)。CST还增加了ADP交替的阈值(P <.01)。此外,MI组83%诱发室性心律失常,而MI + CST组仅33%(P <.05)。这些结果表明,长期给予CST在MI大鼠的心脏保护中起作用,其作用机制可能是通过降低心脏交感神经驱动和改善自主神经功能。