The fractal-like complexity of heart rate variability beyond neurotransmitters and autonomic receptors: signaling intrinsic to sinoatrial node pacemaker cells.

Y. Yaniv, A. Lyashkov, E. Lakatta
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引用次数: 28

Abstract

The heart rate and rhythm are controlled by complex chaotic neural, chemical and hormonal networks which are not strictly regular, but exhibit fluctuations across multiple time scales. A careful assessment of the heart rate variability (HRV) offers clues to this complexity. A reduction in HRV, specifically in advanced age, is associated with increase in morbidity and mortality. Mechanisms that induce this decrease, however, have not been fully elucidated. The classical literature characterizes changes in HRV as a result of changes in the balance of competing influences of the sympathetic and parasympathetic autonomic impulses delivered to the heart. It has now become clear, however, that the heart rate and HRV are also determined by intrinsic properties of the pacemaker cells that comprise sinoatrial node, and that these properties respond to autonomic receptor stimulation in a non-linear mode. That HRV is determined by both the intrinsic properties of pacemaker cells in the sinoatrial node and the competing influences of the two branches of the autonomic neural input to the cells requires an expansion of our perspective about mechanisms that govern HRV in the normal heart, and how HRV changes with aging in health and in heart diseases.
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超越神经递质和自主神经受体的心率变异性的分形样复杂性:窦房结起搏器细胞固有的信号。
心率和节律是由复杂混沌的神经、化学和激素网络控制的,这些网络不是严格规则的,而是在多个时间尺度上表现出波动。对心率变异性(HRV)的仔细评估为这种复杂性提供了线索。HRV的减少,特别是在老年时,与发病率和死亡率的增加有关。然而,导致这种减少的机制尚未完全阐明。经典文献将HRV的变化描述为交感神经和副交感神经自主冲动传递到心脏的竞争影响平衡变化的结果。然而,现在已经清楚的是,心率和HRV也由构成窦房结的起搏器细胞的内在特性决定,并且这些特性以非线性模式响应自主受体的刺激。HRV是由窦房结起搏器细胞的内在特性和自主神经输入细胞的两个分支的竞争影响决定的,这需要我们扩大对正常心脏中控制HRV的机制的看法,以及HRV如何随着健康和心脏病的衰老而变化。
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