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窦房结起搏器同步机制:一种新假说。

Mechanisms of sinoatrial pacemaker synchronization: a new hypothesis.

作者信息

Michaels D C, Matyas E P, Jalife J

机构信息

Department of Pharmacology, SUNY/Health Science Center, Syracuse 13210.

出版信息

Circ Res. 1987 Nov;61(5):704-14. doi: 10.1161/01.res.61.5.704.

Abstract

A model of electrically coupled sinus node cells was used to investigate pacemaker coordination and conduction. Individual cells were simulated using differential equations describing transmembrane ionic currents. Intrinsic cycle lengths (periods) were adjusted by applying constant depolarizing or hyperpolarizing bias current, and cells were coupled through ohmic resistances to form two-dimensional arrays. Activation maps of 81-225 coupled cells showed an apparent wavefront conducting from a leading pacemaker region to the rest of the matrix even though the pattern actually resulted from mutual entrainment of all spontaneously beating cells. Apparent conduction time increased with increasing intercellular resistance. Appropriate selection of pacemaker cycle lengths and intercellular resistances permitted the accurate simulation of the activation sequence seen experimentally for the rabbit sinus node. Furthermore, a simulated acetylcholine pulse applied to a randomly selected 20% of the cells in this model produced a pacemaker shift that lasted several beats. These results support the hypothesis that sinus node synchronization occurs through a "democratic" process resulting from the phase-dependent interactions of thousands of pacemakers.

摘要

使用电耦合窦房结细胞模型来研究起搏器的协调性和传导。通过描述跨膜离子电流的微分方程对单个细胞进行模拟。通过施加恒定的去极化或超极化偏置电流来调整固有周期长度(周期),并且细胞通过欧姆电阻耦合以形成二维阵列。81 - 225个耦合细胞的激活图显示,尽管该模式实际上是由所有自发搏动细胞的相互夹带导致的,但仍有一个明显的波前从领先的起搏器区域传导至基质的其余部分。表观传导时间随着细胞间电阻的增加而增加。适当选择起搏器周期长度和细胞间电阻,可以准确模拟实验中观察到的兔窦房结的激活序列。此外,在此模型中,对随机选择的20%的细胞施加模拟乙酰胆碱脉冲会产生持续几个搏动的起搏器移位。这些结果支持了这样一种假设,即窦房结同步是通过数千个起搏器的相位依赖性相互作用所产生的“民主”过程实现的。

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