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首页> 外文期刊>Progress in Biophysics and Molecular Biology: An International Review Journal >Electrophysiological modelling of pulmonary artery smooth muscle cells in the rabbits--special consideration to the generation of hypoxic pulmonary vasoconstriction
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Electrophysiological modelling of pulmonary artery smooth muscle cells in the rabbits--special consideration to the generation of hypoxic pulmonary vasoconstriction

机译:兔肺动脉平滑肌细胞的电生理模型-特别考虑缺氧性肺血管收缩的产生

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摘要

In vascular smooth muscle cells, it has been suggested that membrane potential is an important component that initiates contraction. We developed a mathematical model to elucidate the quantitative contributions of major ion currents [a voltage-gated L-type Ca2+ current (ICaL), a voltage-sensitive K+ current (IKV), a Ca2+-activated K+ current (IKCa) and a nonselective cation current (INSC)] to membrane potential. In order to typify the diverse nature of pulmonary artery smooth muscle cells (PASMCs), we introduced parameters that are not fixed (variable parameters). The population of cells with different parameters was constructed and the cells that have the electrophysiological properties of PASMCs were selected. The contributions of each membrane current were investigated by sensitivity analysis and modification of the current parameters. Consequently, IKV and INSC were found to be the most important currents that affect the membrane potential. The occurrence of depolarisation in hypoxic pulmonary vasoconstriction (HPV) was also examined. In hypoxia, IKV and IKCa were reduced, but the consequent depolarisation in simulation was not enough to initiate contractions. If we add an increase of INSC (2.5-fold), the calculated membrane potential was enough to induce contraction. From the results, we conclude that the balance of various ion channel activities determines the resting membrane potential of PASMCs and our model was successful in explaining the depolarisation in HPV. Therefore, this model can be a powerful tool to investigate the various electrical properties of PASMCs in both normal and pathological conditions.
机译:在血管平滑肌细胞中,已经提出膜电位是引发收缩的重要成分。我们开发了一个数学模型来阐明主要离子电流的定量贡献[电压门控L型Ca2 +电流(ICaL),电压敏感K +电流(IKV),Ca2 +激活的K +电流(IKCa)和非选择性阳离子电流(INSC)]到膜电位。为了代表肺动脉平滑肌细胞(PASMC)的多样性,我们引入了不固定的参数(可变参数)。构建具有不同参数的细胞群,并选择具有PASMCs电生理特性的细胞。通过灵敏度分析和修改电流参数来研究每个膜电流的贡献。因此,发现IKV和INSC是影响膜电位的最重要电流。还检查了缺氧性肺血管收缩(HPV)中去极化的发生。在缺氧状态下,IKV和IKCa降低,但是随后的模拟去极化作用不足以引发收缩。如果我们增加INSC(2.5倍),则计算出的膜电位足以引起收缩。从结果可以得出结论,各种离子通道活性的平衡决定了PASMCs的静息膜电位,我们的模型成功地解释了HPV中的去极化现象。因此,该模型可以成为研究正常状态和病理状态下PASMCs各种电特性的强大工具。

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