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From two competing oscillators to one coupled-clock pacemaker cell system

机译:从两个竞争的振荡器到一个耦合时钟的起搏器单元系统

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摘要

At the beginning of this century, debates regarding “what are the main control mechanisms that ignite the action potential (AP) in heart pacemaker cells” dominated the electrophysiology field. The original theory which prevailed for over 50 years had advocated that the ensemble of surface membrane ion channels (i.e., “M-clock”) is sufficient to ignite rhythmic APs. However, more recent experimental evidence in a variety of mammals has shown that the sarcoplasmic reticulum (SR) acts as a “Ca2+-clock” rhythmically discharges diastolic local Ca2+ releases (LCRs) beneath the cell surface membrane. LCRs activate an inward current (likely that of the Na+/Ca2+ exchanger) that prompts the surface membrane “M-clock” to ignite an AP. Theoretical and experimental evidence has mounted to indicate that this clock “crosstalk” operates on a beat-to-beat basis and determines both the AP firing rate and rhythm. Our review is focused on the evolution of experimental definition and numerical modeling of the coupled-clock concept, on how mechanisms intrinsic to pacemaker cell determine both the heart rate and rhythm, and on future directions to develop further the coupled-clock pacemaker cell concept.
机译:在本世纪初,有关“什么是点燃心脏起搏器细胞中动作电位(AP)的主要控制机制”的争论主导了电生理领域。 50多年来流行的原始理论主张,表面膜离子通道(即“ M-clock”)的整体足以点燃有节奏的AP。然而,最近在各种哺乳动物中的实验证据表明,肌浆网(SR)充当“ Ca 2 + -时钟”,有节奏地释放舒张性局部Ca 2 + 在细胞表面膜下释放(LCR)。 LCR激活一个内向电流(可能是Na + / Ca 2 + 交换器的电流),该电流促使表面膜“ M-clock”点燃AP。理论上和实验上的证据表明,这种时钟“串扰”是逐拍进行的,并确定了AP的发射速率和节奏。我们的研究重点是耦合钟概念的实验定义和数值模型的发展,起搏器细胞的内在机制如何决定心率和心律以及进一步发展耦合钟起搏器细胞概念的未来方向。

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