利多卡因对急性缺血的影响:一项计算机模拟研究

K. Cardona, J. Saiz, J. Ferrero, Miguel Ángel Martínez, G. Moltó, V. Hernández
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引用次数: 0

摘要

利多卡因是一种以pH值、频率和浓度依赖的方式阻断钠通道的药物。在这项工作中,我们使用了我们小组开发的利多卡因数学模型,并将其纳入了Luo Rudy心室动作电位模型。我们研究了利多卡因对缺血组织钠电流(INa)、最大上冲速度(dV/dt)和传导速度(CV)的影响。结果表明,100 μ mol/L的利多卡因在模拟急性缺血条件下,使正常区(细胞54)的INa、dV/dt和CV分别降低42%、41%和24%,而边界区(细胞94)的降低幅度为37%;相同参数下分别为44%和18%。最后,我们发现利多卡因减少了BW,因此药物倾向于消除UDB。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effect of lidocaine in acute ischemic situations: A computer modelling study
Lidocaine is a drug that blocks the sodium channel in a pH, frequency and concentration dependent manner. In this work, we have used a mathematical model of lidocaine developed by our group and incorporated it into the Luo Rudy model of ventricular action potential. We have studied the action of lidocaine on the sodium current (INa), maximum upstroke velocity (dV/dt) and conduction velocity (CV) in ischemic tissue. Additionally, we measured the block window (BW) in different concentrations of drug .Our results show that 100 mumol/L of lidocaine under simulated acute ischemic conditions reduces the INa, dV/dt and CV a 42%, 41% and 24% in the normal zone (cell 54), respectively while in the border zone (cell 94) the decreased was 37%; 44% and 18% for the same parameters. Finally, we have found that lidocaine diminished the BW, thus the drug tends to eliminate the UDB.
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