Ke Jun, Chen Feng, Zhang Cuntai, Xiao Xing, Tu Jing, Dai Musen, Wang Xiaoping, Chen Bing, Chen Min
Department of Emergency, Fujian Provincial Hospital, Provincial College of Clinical Medicine, Fujian Medical University, Fuzhou, 350001, China.
General Department, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430030, China.
J Huazhong Univ Sci Technolog Med Sci. 2012 Aug;32(4):485-489. doi: 10.1007/s11596-012-0084-9. Epub 2012 Aug 11.
Cardiac hypertrophy is an independent risk factor for sudden cardiac death in clinical settings and the incidence of sudden cardiac death and ventricular arrhythmias are closely related. The aim of this study was to determine the effects of the calmodulin-dependent protein kinase (CaMK) II inhibitor, KN-93, on L-type calcium current (I(Ca, L)) and early after-depolarizations (EADs) in hypertrophic cardiomyocytes. A rabbit model of myocardial hypertrophy was constructed through abdominal aortic coarctation (LVH group). The control group (sham group) received a sham operation, in which the abdominal aortic was dissected but not coarcted. Eight weeks later, the degree of left ventricular hypertrophy (LVH) was evaluated using echocardiography. Individual cardiomyocyte was isolated through collagenase digestion. Action potentials (APs) and I(Ca, L) were recorded using the perforated patch clamp technique. APs were recorded under current clamp conditions and I(Ca, L) was recorded under voltage clamp conditions. The incidence of EADs and I(ca, L) in the hypertrophic cardiomyocytes were observed under the conditions of low potassium (2 mmol/L), low magnesium (0.25 mmol/L) Tyrode's solution perfusion, and slow frequency (0.25-0.5 Hz) electrical stimulation. The incidence of EADs and I(ca, L) in the hypertrophic cardiomyocytes were also evaluated after treatment with different concentrations of KN-92 (KN-92 group) and KN-93 (KN-93 group). Eight weeks later, the model was successfully established. Under the conditions of low potassium, low magnesium Tyrode's solution perfusion, and slow frequency electrical stimulation, the incidence of EADs was 0/12, 11/12, 10/12, and 5/12 in sham group, LVH group, KN-92 group (0.5 μmol/L), and KN-93 group (0.5 μmol/L), respectively. When the drug concentration was increased to 1 μmol/L in KN-92 group and KN-93 group, the incidence of EADs was 10/12 and 2/12, respectively. At 0 mV, the current density was 6.7±1.0 and 6.3±0.7 PA·PF(-1) in LVH group and sham group, respectively (P>0.05, n=12). When the drug concentration was 0.5 μmol/L in KN-92 and KN-93 groups, the peak I(Ca, L) at 0 mV was decreased by (9.4±2.8)% and (10.5±3.0)% in the hypertrophic cardiomyocytes of the two groups, respectively (P>0.05, n=12). When the drug concentration was increased to 1 μmol/L, the peak I(Ca, L) values were lowered by (13.4±3.7)% and (40±4.9)%, respectively (P<0.01, n=12). KN-93, a specific inhibitor of CaMKII, can effectively inhibit the occurrence of EADs in hypertrophic cardiomyocytes partially by suppressing I(Ca, L), which may be the main action mechanism of KN-93 antagonizing the occurrence of ventricular arrhythmias in hypertrophic myocardium.
在临床环境中,心脏肥大是心源性猝死的独立危险因素,且心源性猝死的发生率与室性心律失常密切相关。本研究旨在确定钙调蛋白依赖性蛋白激酶(CaMK)II抑制剂KN-93对肥厚型心肌细胞L型钙电流(I(Ca,L))和早期后去极化(EADs)的影响。通过腹主动脉缩窄构建兔心肌肥大模型(左心室肥厚组)。对照组(假手术组)接受假手术,即解剖腹主动脉但不进行缩窄。八周后,使用超声心动图评估左心室肥厚程度。通过胶原酶消化分离单个心肌细胞。使用穿孔膜片钳技术记录动作电位(APs)和I(Ca,L)。在电流钳条件下记录APs,在电压钳条件下记录I(Ca,L)。在低钾(2 mmol/L)、低镁(0.25 mmol/L)的台氏液灌注以及慢频率(0.25 - 0.5 Hz)电刺激条件下,观察肥厚型心肌细胞中EADs的发生率和I(ca,L)。在用不同浓度的KN-92(KN-92组)和KN-93(KN-93组)处理后,也评估肥厚型心肌细胞中EADs的发生率和I(ca,L)。八周后,模型成功建立。在低钾、低镁台氏液灌注以及慢频率电刺激条件下,假手术组、左心室肥厚组、KN-92组(0.5 μmol/L)和KN-93组(0.5 μmol/L)中EADs的发生率分别为0/12、11/12、10/12和5/12。当KN-92组和KN-93组药物浓度增加到1 μmol/L时,EADs的发生率分别为10/12和2/12。在0 mV时,左心室肥厚组和假手术组的电流密度分别为6.7±1.0和6.3±0.7 PA·PF(-1)(P>0.05,n = 12)。当KN-92组和KN-93组药物浓度为0.5 μmol/L时,两组肥厚型心肌细胞在0 mV时的I(Ca,L)峰值分别降低了(9.4±2.8)%和(10.5±3.0)%(P>0.05,n = 12)。当药物浓度增加到1 μmol/L时,I(Ca,L)峰值分别降低了(13.4±3.7)%和(40±4.9)%(P<0.01,n = 12)。CaMKII的特异性抑制剂KN-93可通过部分抑制I(Ca,L)有效抑制肥厚型心肌细胞中EADs的发生,这可能是KN-93拮抗肥厚型心肌中室性心律失常发生的主要作用机制。