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用于评估窦房传导时间的窦房结活动细胞内和细胞外直流电记录之间的比较。

Comparison between intracellular and extracellular direct current recordings of sinus node activity for evaluation of sinoatrial conduction time.

作者信息

Haberl R, Steinbeck G, Lüderitz B

出版信息

Circulation. 1984 Oct;70(4):760-7. doi: 10.1161/01.cir.70.4.760.

Abstract

For evaluation of sinoatrial conduction time in humans, study of extracellular direct current (DC) electrograms from the sinus node has been proposed. To validate this method, we compared transmembrane potentials from multiple sites (40 to 60, "mapping" of sinoatrial activation by microelectrode technique) and extracellular DC electrograms of the sinus node in 12 isolated rabbit atria. Sinoatrial conduction time, measured by microelectrodes and by extracellular electrograms, was essentially the same if the DC electrode was positioned over the pacemaker center (35 +/- 15 and 33 +/- 15 msec, respectively; deviation less or equal to 2 msec). While in all experiments phase 4 and phase 0 depolarization of dominant pacemaker fibers was reflected in the DC electrogram, it shape was influenced by pacemaker location and duration of sinoatrial impulse propagation. If sinoatrial conduction time was long (greater than 25 msec) the transition from the diastolic to the upstroke slope was smooth and the sinus node potential was clearly separated from atrial activity. If sinoatrial conduction time was short (less or equal to 25 msec) the onset of the upstroke slope was well defined and the upstroke slope directly merged into atrial activity. Extracellular recordings 0.2 mm away from the pacemaker center were fairly unchanged in shape; however, sinoatrial conduction time was significantly underestimated. Underestimation also occurred when the tip size of the extracellular electrode was increased from 0.2 to 0.5 and 1.0 mm. Thus sinus node activity is reflected in extracellular DC recordings; however, measurement of sinoatrial conduction time by this technique requires exact localization of the electrode over the pacemaker center, which cannot be controlled in humans.

摘要

为了评估人类的窦房传导时间,有人提出研究来自窦房结的细胞外直流电(DC)电图。为了验证该方法,我们比较了12只离体兔心房中多个部位(40至60个,通过微电极技术对窦房结激活进行“标测”)的跨膜电位和窦房结的细胞外DC电图。如果将DC电极置于起搏中心上方,通过微电极和细胞外电图测量的窦房传导时间基本相同(分别为35±15毫秒和33±15毫秒;偏差小于或等于2毫秒)。在所有实验中,主导起搏纤维的4期和0期去极化在DC电图中均有反映,但其形态受起搏位置和窦房冲动传播持续时间的影响。如果窦房传导时间较长(大于25毫秒),从舒张期到上升支斜率的转变是平滑的,窦房结电位与心房活动明显分开。如果窦房传导时间较短(小于或等于25毫秒),上升支斜率的起始清晰可辨,上升支斜率直接融入心房活动。在距离起搏中心0.2毫米处的细胞外记录形状相当不变;然而,窦房传导时间被显著低估。当细胞外电极尖端尺寸从0.2毫米增加到0.5毫米和1.0毫米时,也会出现低估。因此,窦房结活动反映在细胞外DC记录中;然而,用该技术测量窦房传导时间需要将电极精确地定位在起搏中心上方,而这在人体中无法控制。

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