首页> 外文期刊>Acta physiologica Scandinavica >Swelling-induced decrease in spontaneous pacemaker activity of rabbit isolated sino-atrial node cells.
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Swelling-induced decrease in spontaneous pacemaker activity of rabbit isolated sino-atrial node cells.

机译:肿胀诱导的兔离体窦房结细胞自发起搏器活性降低。

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The heart responds to an increase in sino-atrial node wall stress with an augmentation in rate of contraction. It has been suggested that swelling-activated ion channels may play a key role in that response. This paper investigates directly the effects of cell swelling on spontaneous activity of rabbit isolated sino-atrial node pacemaker cells. The main finding is that sino-atrial node cells, studied in current clamp mode using amphotericin-permeabilized patches, decrease their spontaneous pacemaker rate by 24.2 +/- 7.8% (P < 0.01, n = 9) during 75% hyposmotic swelling. This response is opposite to the predicted impact of volume-activation of sarcolemmal ion conductances. Computer modelling (OXSOFT Heart v4.8) suggests that swelling-induced dilution of the cytosol, reduction in intracellular potassium concentration, and decrease in the delayed rectifier potassium current, IK, are leading mechanisms in the response. This is supported by voltage-clamp data that show a swelling-induced positive shift in the reversal potential of IK by between 5 and 10 mV (n = 7) and a reduction in amplitude of its rapidly activating component, IKr, (n = 6). Thus, spontaneously active sino-atrial node cells reduce pacemaking rate during swelling. This response cannot be explained by the known volume-activated sarcolemmal ion conductances, but appears to be dictated by other mechanisms including dilution of the cytosol and reduction in IK. The results re-enforce the view that cardiac responses to cell volume changes may be quite different from those to longitudinal stretch.
机译:心脏对窦房结壁压力的增加作出反应,收缩率增加。已经提出溶胀激活的离子通道可能在该反应中起关键作用。本文直接研究了细胞肿胀对兔离体窦房结起搏器细胞自发活动的影响。主要发现是,在当前钳夹模式下,使用两性霉素可渗透贴片研究的窦房结细胞,在75%的低渗性肿胀过程中,其自发起搏率降低了24.2 +/- 7.8%(P <0.01,n = 9)。这种反应与肌膜离子电导的体积激活的预期影响相反。计算机模型(OXSOFT Heart v4.8)表明,溶胀引起的细胞溶质稀释,细胞内钾浓度降低和延迟整流钾电流IK降低是应答的主要机制。电压钳位数据支持了这一点,电压钳位数据显示了IK的反向电位在5到10 mV(n = 7)之间发生膨胀诱发的正向偏移,并且其快速激活分量IKr的幅度减小了(n = 6 )。因此,自发活跃的窦房结细胞会降低肿胀过程中的起搏率。该反应不能通过已知的体积激活的肌膜离子电导来解释,但是似乎由其他机制决定,包括细胞溶质的稀释和IK的降低。结果进一步证实了这样一种观点,即心脏对细胞体积变化的反应可能与对纵向拉伸的反应完全不同。

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