Zhang Xu, Roppolo James R, de Groat William C, Tai Changfeng
Department of Pharmacology, University of Pittsburgh, Pittsburgh, PA 15261, USA.
IEEE Trans Biomed Eng. 2006 Dec;53(12 Pt 1):2445-54. doi: 10.1109/TBME.2006.884640.
The mechanisms of nerve conduction block induced by high-frequency biphasic electrical currents were investigated using a lumped circuit model of the myelinated axon based on Frankenhaeuser-Huxley (FH) model or Chiu-Ritchie-Rogart-Stagg-Sweeney (CRRSS) model. The FH model revealed that the constant activation of potassium channels at the node under the block electrode, rather than inactivation of sodium channels, is the likely mechanism underlying conduction block of myelinated axons induced by high-frequency biphasic stimulation. However, the CRRSS model revealed a different blocking mechanism where the complete inactivation of sodium channels at the nodes next to the block electrode caused the nerve conduction block. The stimulation frequencies to observe conduction block in FH model agree with the observations from animal experiments (greater than 6 kHz), but much higher frequencies are required in CRRSS model (greater than 15 kHz). This frequency difference indicated that the constant activation of potassium channels might be the underlying mechanism of conduction block observed in animal experiments. Using the FH model, this study also showed that the axons could recover from conduction block within 1 ms after termination of the blocking stimulation, which also agrees very well with the animal experiments where nerve block could be reversed immediately once the blocking stimulation was removed. This simulation study, which revealed two possible mechanisms of nerve conduction block in myelinated axons induced by high-frequency biphasic stimulation, can guide future animal experiments as well as optimize stimulation waveforms for electrical nerve block in clinical applications.
基于弗兰肯豪泽 - 赫胥黎(FH)模型或邱 - 里奇 - 罗加特 - 斯塔格 - 斯威尼(CRRSS)模型,利用有髓轴突的集总电路模型研究了高频双相电流诱导神经传导阻滞的机制。FH模型表明,在阻断电极下方的节点处钾通道的持续激活,而非钠通道的失活,可能是高频双相刺激诱导有髓轴突传导阻滞的潜在机制。然而,CRRSS模型揭示了一种不同的阻断机制,即阻断电极旁边节点处钠通道的完全失活导致神经传导阻滞。在FH模型中观察到传导阻滞的刺激频率与动物实验的观察结果一致(大于6 kHz),但在CRRSS模型中需要更高的频率(大于15 kHz)。这种频率差异表明钾通道的持续激活可能是动物实验中观察到的传导阻滞的潜在机制。利用FH模型,本研究还表明轴突在阻断刺激终止后1毫秒内可从传导阻滞中恢复,这也与动物实验非常吻合,即在去除阻断刺激后神经阻滞可立即逆转。这项模拟研究揭示了高频双相刺激诱导有髓轴突神经传导阻滞的两种可能机制,可为未来的动物实验提供指导,并优化临床应用中电神经阻滞的刺激波形。