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完整兔心脏的电和机械反应与兴奋间隔的关系。与离体乳头肌标本的比较。

Electrical and mechanical responses of the intact rabbit heart in relation to the excitation interval. A comparison with the isolated papillary muscle preparation.

作者信息

Wohlfart B, Elzinga G

出版信息

Acta Physiol Scand. 1982 Jul;115(3):331-40. doi: 10.1111/j.1748-1716.1982.tb07086.x.

DOI:10.1111/j.1748-1716.1982.tb07086.x
PMID:6184947
Abstract

Experiments were performed on anesthetized open thorax rabbits with complete heart block and on isolated papillary muscles from rabbit hearts. Both preparations were basically paced at 1.0 Hz. Two consecutive test stimuli (denoted 1 and 2, respectively) were applied at various intervals. Action potentials were recorded; using suction electrodes in the intact heart and microelectrodes in the isolated tissue. Peak rate of rise of left ventricular pressure (DP) and of isometric force (DF, in vitro) were taken as measures of the contractile response. Action potential duration (AP), at 50% repolarization, were longer in vivo (175 ms) than in vitro (130 ms). AP and DP (DF) of the test contractions were similarly related to the test pulse intervals in the two preparations. DP2 was significantly correlated with DP1 and AP1 (r: 0.92-0.96). The regression coefficient for the dependence of DP2 on DP1 was significantly greater in vivo (0.61) than in vitro (0.21). This was interpreted to mean that recirculation of activator calcium from one heart beat to another was greater in vivo than in vitro. The isolated tissue would therefore be more dependent on calcium entering during the action potential. This could explain the greater postextrasystolic potentiation in vitro than in vivo (255% and 141% of steady state-responses, respectively).

摘要

实验在麻醉开胸的完全性心脏传导阻滞兔以及兔心脏分离乳头肌上进行。两种标本基本均以1.0赫兹起搏。以不同间隔施加两个连续的测试刺激(分别记为1和2)。记录动作电位;在完整心脏中使用吸引电极,在分离组织中使用微电极。左心室压力上升的峰值速率(DP)和等长力(体外为DF)作为收缩反应的指标。动作电位持续时间(AP)在复极化50%时,体内(175毫秒)比体外(130毫秒)长。测试收缩的AP和DP(DF)在两种标本中与测试脉冲间隔的关系相似。DP2与DP1和AP1显著相关(r:0.92 - 0.96)。DP2对DP1依赖性的回归系数在体内(0.61)显著大于体外(0.21)。这被解释为意味着从一次心跳到另一次心跳的激活钙再循环在体内比体外更大。因此,分离组织将更依赖于动作电位期间进入的钙。这可以解释体外比体内更大的期外收缩后增强(分别为稳态反应的255%和141%)。

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