Interbeat interval variability in isolated working rat hearts at various dynamic conditions and temperatures.

S F Langer, M Lambertz, P Langhorst, H D Schmidt
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引用次数: 26

Abstract

This study quantifies the effect of afterload and preload changes and of temperature on interbeat interval variability of the intact isolated heart. Ventricular pressure pulse records were obtained from isolated working rat hearts. The variability of interbeat intervals (BIs) was quantified by C90, the central 90% range of the BIs during 10 min periods; predominant frequencies were searched for by power spectral analysis. At 37 degrees C the BI lengths oscillated pseudo-randomly with BI variability C90< or =4 ms. Alternating signs of consecutive BI differences were predominant, and no peaks. were seen in the power spectra. Changes in end-diastolic and aortic pressure had little effect. From 37 degrees C down to 27 degrees C the variability increased about sevenfold, run phase length became randomly distributed, and individual, time-variant peaks occurred in the power spectra. BI variability vanished during atrial pacing. We conclude that: (1) effective mutual synchronization with minimal fluctuation happens within the sino-atrial node of intact rat hearts at body temperature, and synchronization is not affected even by extreme changes in pre- and afterload, (2) the sino-atrial node is the sole source of BI variability in the intact isolated rat heart, (3) low temperature hampers this functional organization which can be reestablished by sinus node accelerating agents (isoprenaline, theophylline), (4) decreasing frequency by N6-Cyclopentyladenosine at normothermia also increases BI variability but less pronouncedly than hypothermia does.

不同动态条件和温度下离体工作大鼠心脏的搏动间隔变异性。
本研究量化了负荷后和负荷前的变化以及温度对完整离体心脏搏动间隔变异性的影响。从离体工作的大鼠心脏获得心室压脉冲记录。心跳间隔(BIs)的变异性用C90 (10 min内BIs的中心90%范围)来量化;通过功率谱分析寻找主频率。在37℃时,BI长度伪随机振荡,BI变异性为C90<或=4 ms。连续BI差异的交替迹象占主导地位,没有峰值。在功率谱中可见。舒张末期和主动脉压的变化影响不大。从37℃下降到27℃,变异性增加了约7倍,运行相长变得随机分布,功率谱中出现个别的时变峰。心房起搏时BI变异性消失。我们的结论是:(1)在体温下,完整大鼠心脏窦房结内发生波动最小的有效相互同步,即使前负荷和后负荷的极端变化也不影响同步;(2)窦房结是完整离体大鼠心脏BI变异性的唯一来源;(3)低温阻碍了窦房结加速剂(异丙肾上腺素、茶碱)可重建的这种功能组织。(4)在体温正常时,n6 -环戊基腺苷降低的频率也会增加BI变异性,但不像低温那么明显。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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