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Approaching the mechanistic insights towards the genesis of intracellular calcium transient alternans - a simulation study

机译:接近细胞内钙瞬态障碍的成因的机械洞察 - 一种模拟研究

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Mechanical contraction alternans of the heart is associated with fatal cardiac death. It is manifested by T-wave alternans in the ECG, and is thought to be possibly related to intracellular Ca2+ transient alternans released from the sarcoplasmic reticulum (SR). However, it is unclear yet how beat-to-beat alternans of intracellular Ca2+ transient is produced. In this study investigated the mechanism(s) underlying the genesis of intracellular Ca2+ alternans produced at slow pacing rates by using a mathematical model of a spatially extended cardiac cell with a cluster of coupled ryanodine receptor (RyR) elements. It was shown that the intracellular Ca2+ alternans was generated by propagating waves of Ca2+ release and sustained through alternation of SR Ca2+ content that has a stiff relationship with the Ca2+ transient. This study provides novel and fundamental insights to understand mechanisms that may underlie intracellular Ca2+ alternans without the need for refractoriness of L-type Ca or RyR channels under rapid pacing.
机译:心脏的机械收缩交流与致命的心脏死亡有关。它表现为ECG中的T波段,并且被认为可能与从肌动脉内网(SR)释放的细胞内Ca 2 + 瞬态交替。然而,尚不清楚产生细胞内Ca 2 + 瞬态的击败击败的交替。在这项研究中调查的起源的基础的机制(S)细胞内Ca 2 + 交替通过使用具有耦合兰诺定受体的集群中的空间延伸的心脏细胞的数学模型在缓慢起搏率生产(RyR的)元素。结果表明,通过将Ca 2 + 释放的波传播并通过SR Ca 2 + 的交替进行持续来产生细胞内Ca 2 + 替代障碍。与CA 2 + 瞬态具有僵硬关系的内容。该研究提供了新颖的和基本的见解理解可依据细胞内Ca 2 +机制交替,而不需要在快速起搏L-型Ca或RyR的信道的耐火度。

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