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体内记录的房室结电位变异性:房室结双重生理功能的直接证明。

Variability of AV nodal potentials recorded, in vivo: direct demonstration of dual AV nodal physiology.

作者信息

Scherlag Benjamin J, Yamanashi William S, Yagi Tetsuo, Patterson Eugene, Lazzara Ralph, Jackman Warren M

机构信息

Department of Veterans Affairs Medical Center and Cardiac Arrhythmia Research Institute at the University of Oklahoma Health Sciences Center, Oklahoma City, Oklahoma, USA.

出版信息

J Interv Card Electrophysiol. 2004 Feb;10(1):9-18. doi: 10.1023/B:JICE.0000011479.07333.57.

Abstract

OBJECTIVES OF STUDY

We developed a method to record extracellular A-V nodal potentials in the beating dog heart, in vivo.

METHODS

In eleven Na-pentobarbital anesthetized, open-chest dogs, an octapolar electrode catheter (2 mm rings, 2 mm spacing) was inserted through a purse-string suture in the coronary sinus (CS) distal to the ostium and positioned electrographically so that the tip electrode recorded a His bundle (Hb) potential.

RESULTS

Stable recordings of A-V nodal potentials (amplitude, 178 +/- 94 microV; duration 78 +/- 26 msec) were consistently made during sinus rhythm from the second and/or third bipolar pairs of electrodes. Programmed atrial stimulation and vagal stimulation resulted in loss of amplitude and increased duration of the A-V nodal potentials associated with A-H prolongation. In another series of experiments, crushing the sinus node in 6 dogs resulted in AV nodal rhythms with AV nodal potentials of varying amplitudes (132 to 840 microV) and durations (range 25 to 71 msec) as the earliest activation which preceded the Hb, atrial and ventricular deflections. One dog, showing dual AV nodal physiology as documented from the AV nodal function curve, had two distinctly different AV nodal potentials. The low-level, longer duration potentials were associated with longer (slow pathway) A-H intervals; whereas the shorter higher amplitude potentials (fast pathway) showed shorter A-H intervals, each occurring at a critical paced cycle length.

CONCLUSION

We conclude that consistent extracellular AV nodal electrograms can be recorded in vivo although the configuration of these potentials varies depending on heart rate, autonomic stimulation and different arrhythmic conditions such as AV nodal escape rhythms and dual AV nodal physiology.

摘要

研究目的

我们开发了一种在活体搏动的犬心脏中记录细胞外房室结电位的方法。

方法

在11只戊巴比妥钠麻醉、开胸的犬中,通过冠状窦(CS)开口远端的荷包缝线插入一个八极电极导管(环间距2mm,环直径2mm),并通过心电图定位,使尖端电极记录希氏束(Hb)电位。

结果

在窦性心律期间,从第二和/或第三对双极电极持续稳定记录到房室结电位(振幅,178±94μV;持续时间78±26毫秒)。程控心房刺激和迷走神经刺激导致房室结电位振幅降低和持续时间延长,同时伴有A-H间期延长。在另一系列实验中,6只犬的窦房结被挤压后出现房室结节律,房室结电位振幅(132至840μV)和持续时间(范围25至71毫秒)各不相同,且是先于Hb、心房和心室波的最早激动。一只犬根据房室结功能曲线显示出双房室结生理特性,有两种明显不同的房室结电位。低水平、持续时间较长的电位与较长(慢径路)的A-H间期相关;而较短、较高振幅的电位(快径路)显示较短的A-H间期,每种情况都发生在一个临界起搏周期长度。

结论

我们得出结论,尽管这些电位的形态会因心率、自主神经刺激以及不同的心律失常情况(如房室结逸搏节律和双房室结生理特性)而有所不同,但仍可在活体中持续记录到一致的细胞外房室结电图。

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