Verkerk Arie O, Wilders Ronald
Department of Medical Biology, Amsterdam Cardiovascular Sciences, Amsterdam UMC, University of Amsterdam, 1105 AZ Amsterdam, The Netherlands.
Department of Experimental Cardiology, Heart Center, Amsterdam Cardiovascular Sciences, Amsterdam UMC, University of Amsterdam, 1105 AZ Amsterdam, The Netherlands.
Rev Cardiovasc Med. 2024 May 28;25(6):194. doi: 10.31083/j.rcm2506194. eCollection 2024 Jun.
Clinical and experimental data on the cardiac effects of acute hypernatremia are scarce and inconsistent. We aimed to determine and understand the effects of different levels of acute hypernatremia on the human ventricular action potential.
We performed computer simulations using two different, very comprehensive models of the electrical activity of a single human ventricular cardiomyocyte, , the Tomek-Rodriguez model following the O'Hara-Rudy dynamic (ORd) model and the Bartolucci-Passini-Severi model as published in 2020 (known as the ToR-ORd and BPS2020 models, respectively). Mild to extreme levels of hypernatremia were introduced into each model based on experimental data on the effects of hypernatremia on cell volume and individual ion currents.
In both models, we observed an increase in the intracellular sodium and potassium concentrations, an increase in the peak amplitude of the intracellular calcium concentration, a hyperpolarization of the resting membrane potential, a prolongation of the action potential, an increase in the maximum upstroke velocity, and an increase in the threshold stimulus current at all levels of hypernatremia and all stimulus rates tested. The magnitude of all of these effects was relatively small in the case of mild to severe hypernatremia but substantial in the case of extreme hypernatremia. The effects on the action potential were related to an increase in the sodium-potassium pump current, an increase in the sodium-calcium exchange current, a decrease in the rapid and slow delayed rectifier potassium currents, and an increase in the fast and late sodium currents.
The effects of mild to severe hypernatremia on the electrical activity of human ventricular cardiomyocytes are relatively small. In the case of extreme hypernatremia, the effects are more pronounced, especially regarding the increase in threshold stimulus current.
关于急性高钠血症对心脏影响的临床和实验数据稀缺且不一致。我们旨在确定并了解不同程度的急性高钠血症对人心室动作电位的影响。
我们使用两种不同的、非常全面的单个人心室心肌细胞电活动模型进行计算机模拟,即遵循奥哈拉 - 鲁迪动态(ORd)模型的托梅克 - 罗德里格斯模型以及2020年发表的巴托卢奇 - 帕西尼 - 塞韦里模型(分别称为ToR - ORd和BPS2020模型)。根据高钠血症对细胞体积和单个离子电流影响的实验数据,将轻度至极端程度的高钠血症引入每个模型。
在两个模型中,我们观察到在所有测试的高钠血症水平和所有刺激速率下,细胞内钠和钾浓度增加、细胞内钙浓度峰值幅度增加、静息膜电位超极化、动作电位延长、最大上升速度增加以及阈刺激电流增加。在轻度至重度高钠血症情况下,所有这些影响的幅度相对较小,但在极端高钠血症情况下则较为显著。对动作电位的影响与钠钾泵电流增加、钠钙交换电流增加、快速和慢速延迟整流钾电流减少以及快速和晚期钠电流增加有关。
轻度至重度高钠血症对人心室心肌细胞电活动的影响相对较小。在极端高钠血症情况下,影响更为明显,尤其是阈刺激电流的增加。