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首页> 外文期刊>SIAM Journal on Scientific Computing >LONG-TIME SIMULATIONS ON HIGH RESOLUTION MESHES TO MODEL CALCIUM WAVES IN A HEART CELL
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LONG-TIME SIMULATIONS ON HIGH RESOLUTION MESHES TO MODEL CALCIUM WAVES IN A HEART CELL

机译:高分辨率网格对心室钙波模型的长时间模拟

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A model for the flow of calcium on the scale of one heart cell is given by a system of time-dependent reaction-diffusion equations coupled by nonlinear reaction terms. Calcium ions enter into the cell at release units distributed throughout the cell and then diffuse. At each release unit, the probability for calcium to be released increases along with the concentration of calcium, thus creating a feedback loop of waves regenerating themselves repeatedly. The validation of this model requires simulations on the time scale of several repeated waves and on the spatial scale of the entire cell. This requires long-time studies on spatial meshes that need to have a high resolution to resolve the positions of the calcium release units throughout the entire cell. We detail the development of a special-purpose numerical method and parallel implementation for this problem. Parallel performance studies demonstrate the scalability of the implementation on a distributed-memory cluster with low-latency interconnect. Convergence studies verify convergence to analytical expectations and confirm the appropriateness of all numerical parameters. Application studies on the desired time and length scales confirm that the model exhibits the desired feedback mechanism for calcium currents through the release units at suitable high levels, but the long-time studies demonstrate also that the current model with its present parameters leads to excessive calcium concentrations over time. This phenomenon could only be observed using a computational method able to reach laboratory scale final times for a domain on the scale of a complete cell.
机译:钙在一个心脏细胞尺度上的流动的模型是由一个与时间有关的反应扩散方程组和非线性反应项耦合而成的。钙离子以分布在整个细胞中的释放单元进入细胞,然后扩散。在每个释放单元,钙被释放的可能性随钙浓度的增加而增加,从而形成了一个波的反馈回路,使它们不断地再生。要验证此模型,需要在几个重复波的时间尺度和整个单元的空间尺度上进行仿真。这需要对需要高分辨率的空间网格进行长期研究,以解决整个细胞中钙释放单元的位置。我们详细介绍了专用数值方法的开发以及针对此问题的并行实现。并行性能研究证明了在具有低延迟互连的分布式内存群集上实现的可伸缩性。收敛性研究验证了收敛到分析期望并确认所有数值参数的适当性。关于所需时间和长度范围的应用研究证实,该模型在适当的高水平下显示了通过释放单元的钙电流的所需反馈机制,但长期研究也表明,具有当前参数的当前模型会导致钙过多随着时间的推移浓度。这种现象只能使用能够在整个细胞规模的域中达到实验室规模最终时间的计算方法来观察。

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