How to correct Goldman- Hodgkin-Katz ion channel models to include gating nonlinearity based on available Hodgkin_Huxley models

Mohammad Saeid Imani Moqadam, Nasrin Sadat Hashemi, Seyedeh Hoda Asnaashari Namaqi, S. M. Saviz
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Abstract

To simulate the bioelectric response of cells to electric and magnetic fields, we should model the nonlinear behavior of membrane ion channels by mathematical equations. More than 19 types of ion channels have been identified and modeled by the Hodgkin_Huxley (HH) model. Nevertheless, the Hodgkin_Huxley model has a significant simulation problem. In other words, these models cannot produce the expected nonlinear physical response at high frequencies since they explicitly model gating nonlinearity and not adjustable concentration nonlinearity. In this study, we suggested a complete model representing two kinds of nonlinearity, gating and concentration nonlinearity, to produce the expected nonlinear physical response of different voltage-gated channels. We incorporated the gating nonlinearity into the permeability coefficient defined in the Goldman- Hodgkin-Katz model (GHK), expressing concentration nonlinearity, and eventually achieved a modified GHK model for a wide variety of channels. Also, we verified these results using response diagrams of these channels available on the Channelpedia website.
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如何修正高盛-霍奇金-卡茨离子通道模型,以包括基于现有霍奇金-赫胥黎模型的门控非线性
为了模拟细胞对电场和磁场的生物电响应,我们应该用数学方程来模拟膜离子通道的非线性行为。超过19种类型的离子通道已经被确定并通过霍奇金-赫胥黎(HH)模型建模。然而,霍奇金-赫胥黎模型有一个显著的模拟问题。换句话说,这些模型不能在高频下产生预期的非线性物理响应,因为它们明确地模拟了门控非线性而不是可调浓度非线性。在这项研究中,我们提出了一个完整的模型来表示两种非线性,门控和浓度非线性,以产生期望的不同电压门控通道的非线性物理响应。我们将门控非线性纳入到高盛-霍奇金-卡茨模型(GHK)中定义的渗透率系数中,表达浓度非线性,并最终获得了适用于各种通道的修正GHK模型。此外,我们使用Channelpedia网站上提供的这些频道的响应图来验证这些结果。
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