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

机译:探讨细胞内钙瞬变交替发生的机理见解-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:心脏的机械性收缩交替与致命性心脏死亡相关。它由心电图中的T波交替蛋白表现出来,并被认为可能与从肌浆网(SR)释放的细胞内Ca 2 + 瞬时交替蛋白有关。然而,目前尚不清楚如何产生细胞内Ca 2 + 瞬变的逐跳交替信号。在这项研究中,通过使用空间扩展的心脏细胞与耦合的ryanodine受体(RyR)簇的数学模型,研究了以缓慢起搏速率产生的细胞内Ca 2 + 交替RNA发生的潜在机理。 )元素。结果表明,细胞内Ca 2 + 交替表达是通过传播Ca 2 + 释放波而产生的,并通过SR Ca 2 + 的交替而得以维持。含量与Ca 2 + 瞬态有严格的关系。这项研究提供了新的和基本的见解,以了解可能在快速起搏下不需要L型Ca或RyR通道的耐火性的细胞内Ca 2 + 交替分子的机制。

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