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心肌细胞中自发钙释放的时间统计。

The timing statistics of spontaneous calcium release in cardiac myocytes.

机构信息

Department of Physics and Astronomy, California State University Northridge, Northridge, California, United States of America.

出版信息

PLoS One. 2013 May 17;8(5):e62967. doi: 10.1371/journal.pone.0062967. Print 2013.

Abstract

A variety of cardiac arrhythmias are initiated by a focal excitation that disrupts the regular beating of the heart. In some cases it is known that these excitations are due to calcium (Ca) release from the sarcoplasmic reticulum (SR) via propagating subcellular Ca waves. However, it is not understood what are the physiological factors that determine the timing of these excitations at both the subcellular and tissue level. In this paper we apply analytic and numerical approaches to determine the timing statistics of spontaneous Ca release (SCR) in a simplified model of a cardiac myocyte. In particular, we compute the mean first passage time (MFPT) to SCR, in the case where SCR is initiated by spontaneous Ca sparks, and demonstrate that this quantity exhibits either an algebraic or exponential dependence on system parameters. Based on this analysis we identify the necessary requirements so that SCR occurs on a time scale comparable to the cardiac cycle. Finally, we study how SCR is synchronized across many cells in cardiac tissue, and identify a quantitative measure that determines the relative timing of SCR in an ensemble of cells. Using this approach we identify the physiological conditions so that cell-to-cell variations in the timing of SCR is small compared to the typical duration of an SCR event. We argue further that under these conditions inward currents due to SCR can summate and generate arrhythmogenic triggered excitations in cardiac tissue.

摘要

各种心律失常都是由破坏心脏正常跳动的局灶兴奋引起的。在某些情况下,已知这些兴奋是由于通过传播的亚细胞 Ca 波从肌浆网(SR)中释放钙(Ca)引起的。然而,尚不清楚是什么生理因素决定了亚细胞和组织水平上这些兴奋的时间。在本文中,我们应用分析和数值方法来确定简化的心肌细胞模型中自发 Ca 释放(SCR)的定时统计。特别是,我们计算了 SCR 由自发 Ca 火花引发时的 SCR 平均首次通过时间(MFPT),并证明该数量与系统参数呈代数或指数依赖性。基于此分析,我们确定了必要的要求,以使 SCR 发生在与心脏周期相当的时间尺度上。最后,我们研究了 SCR 如何在心脏组织中的许多细胞之间同步,并确定了一个定量度量标准,该标准确定了细胞集合中 SCR 的相对定时。使用这种方法,我们确定了生理条件,使得 SCR 的定时变化与 SCR 事件的典型持续时间相比很小。我们进一步认为,在这些条件下,由于 SCR 引起的内向电流可以累积并在心脏组织中产生心律失常性触发兴奋。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/98a1/3656860/6a8f860b7799/pone.0062967.g001.jpg

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