De Mello Walmor C
School of Medicine, Medical Sciences Campus, UPR, San Juan, PR 00936-5067, USA.
Regul Pept. 2013 Feb 10;181:45-9. doi: 10.1016/j.regpep.2012.12.015. Epub 2013 Jan 11.
The influence of intracellular renin injection on the electrical properties of the intact left ventricle from adult Sprague Dawley rat heart was investigated. Intracellular renin injection was performed using intracellular microelectrodes filled with solution containing renin (120pM). Pressure pulses (40-70psi) for short periods of time (20ms), were applied to the micropipette while recording the action potential simultaneously from the same fiber. The results indicated that intracellular renin caused a depolarization of ventricular fibers of 7.3±2±mV (n=38) (4 animals) (P<0.05) and a decrease of the action potential duration at 50% and at 90% repolarization, respectively. Moreover, the refractoriness was significantly decreased with consequent generation of triggered activity. The effect of intracellular renin was seen within 3min of enzyme injection. The shortening of the action potential was related to an increase of potassium current which was measured in isolated ventricular myocytes before and after intracellular dialysis of renin (10(-9)M) using a voltage whole cell clamp configuration. Valsartan (10(-8)M) dialyzed together with renin (120pM) into the cell decreased drastically the effect of renin on potassium current. An increment of potassium current was also found when intracellular renin was dialyzed into cardiomyocytes exposed to Krebs solution containing valsartan (10(-8)M) for 10min prior to renin administration. Bis-1 which is a specific inhibitor of PKC, abolished the effect of intracellular renin on potassium current.
intracellular renin decreases the action potential duration and cardiac refractoriness in the intact left ventricle of adult Sprague Dawley rats. The shortening of the action potential was related to an increase in total potassium current. The effect of renin on total potassium currents was inhibited by valsartan and by Bis-1. Implication for cardiac arrhythmias was discussed.
研究了向成年斯普拉格-道利大鼠心脏完整左心室内注射细胞内肾素对其电生理特性的影响。使用充满含肾素溶液(120pM)的细胞内微电极进行细胞内肾素注射。在通过同一纤维同时记录动作电位时,对微量移液器施加短时间(20毫秒)的压力脉冲(40 - 70磅力/平方英寸)。结果表明,细胞内肾素使心室纤维去极化7.3±2±毫伏(n = 38)(4只动物)(P < 0.05),并分别使动作电位在50%和90%复极化时的持续时间缩短。此外,不应期显著缩短,随之产生触发活动。细胞内肾素的作用在酶注射后3分钟内即可观察到。动作电位的缩短与钾电流增加有关,该钾电流是在使用电压全细胞钳模式对肾素(10⁻⁹M)进行细胞内透析前后的离体心室肌细胞中测量的。与肾素(120pM)一起透析到细胞内的缬沙坦(10⁻⁸M)显著降低了肾素对钾电流的影响。当在给予肾素之前将细胞内肾素透析到预先在含缬沙坦(10⁻⁸M)的 Krebs 溶液中暴露10分钟的心肌细胞中时,也发现了钾电流的增加。作为蛋白激酶C的特异性抑制剂的Bis - 1消除了细胞内肾素对钾电流的影响。
细胞内肾素可缩短成年斯普拉格-道利大鼠完整左心室的动作电位持续时间并降低心脏不应期。动作电位的缩短与总钾电流增加有关。肾素对总钾电流的作用受到缬沙坦和Bis - 1的抑制。文中讨论了其对心律失常的影响。