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心室心肌细胞中局部Ca2+释放单元的高效且详细的模型。

Efficient and detailed model of the local Ca2+ release unit in the ventricular cardiac myocyte.

作者信息

Schendel Thomas, Falcke Martin

机构信息

Max Delbrück Centre of Moleculare Medicine, Robert-Rössle-Str. 10, Berlin, Germany, 13092, Germany.

出版信息

Genome Inform. 2010 Jan;22:142-55.

Abstract

We present here an efficient but detailed approach to modelling Ca(2+)-induced Ca(2+) release in the diadic cleft of cardiac ventricular myocytes. In this Framework we developed a spatial resolved Ca(2+) release unit (CaRU), consisting of the junctional sarcoplasmic reticulum and the diadic cleft, with a well defined channel placement. By taking advantage of time scale separation, the model could be finally reduced to only one ordinary differential equation for describing Ca(2+) fluxes and diffusion. Additionally the channel gating is described in a stochastic way. The resulting model is able to reproduce experimental findings like the gradedness of SR release, the voltage dependence of ECC gain and typical spark life time. Due to the numerical efficiency of the model, it is suitable to use for whole cell simulations. The approach we want to use extend the developed (CaRU) to such a whole cell model is already outlined in this work.

摘要

我们在此展示一种高效且详细的方法,用于模拟心室肌细胞二联体裂隙中Ca(2+)诱导的Ca(2+)释放。在此框架下,我们开发了一种空间解析的Ca(2+)释放单元(CaRU),它由连接肌浆网和二联体裂隙组成,具有明确的通道布局。通过利用时间尺度分离,该模型最终可简化为仅一个常微分方程,用于描述Ca(2+)通量和扩散。此外,通道门控以随机方式描述。所得模型能够重现诸如肌浆网释放的分级性、兴奋-收缩偶联增益的电压依赖性以及典型的钙火花寿命等实验结果。由于该模型的数值效率,它适用于全细胞模拟。我们想要用于将已开发的(CaRU)扩展到此类全细胞模型的方法已在本工作中概述。

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