Loewe Axel, Lutz Yannick, Nagy Norbert, Fabbri Alan, Schweda Christoph, Varro Andras, Severi Stefano
Annu Int Conf IEEE Eng Med Biol Soc. 2019 Jul;2019:1875-1878. doi: 10.1109/EMBC.2019.8857573.
Changes of serum and extracellular ion concentrations occur regularly in patients with chronic kidney disease (CKD). Recently, hypocalcaemia, i.e. a decrease of the extracellular calcium concentration [Ca], has been suggested as potential pathomechanism contributing to the unexplained high rate of sudden cardiac death (SCD) in CKD patients. In particular, there is a hypothesis that hypocalcaemia could slow down natural pacemaking in the human sinus node to fatal degrees. Here, we address the question whether there are inter-species differences in the response of cellular sinus node pacemaking to changes of [Ca]. Towards this end, we employ computational models of mouse, rabbit and human sinus node cells. The Fabbri et al. human model was updated to consider changes of intracellular ion concentrations. We identified crucial inter-species differences in the response of cellular pacemaking in the sinus node to changes of [Ca] with little changes of cycle length in mouse and rabbit models (<; 83 ms) in contrast to a pronounced bradycardic effect in the human model (up to >1000 ms). Our results suggest that experiments with human sinus node cells are required to investigate the potential mechanism of hypocalcaemia-induced bradycardic SCD in CKD patients and small animal models are not well suited.
慢性肾脏病(CKD)患者血清和细胞外离子浓度会定期发生变化。最近,低钙血症,即细胞外钙浓度[Ca]降低,被认为是导致CKD患者不明原因心脏性猝死(SCD)高发生率的潜在病理机制。特别是,有一种假说认为低钙血症可能会使人类窦房结的自然起搏减慢到致命程度。在此,我们探讨细胞窦房结起搏对[Ca]变化的反应是否存在种间差异。为此,我们采用了小鼠、兔子和人类窦房结细胞的计算模型。对法布里等人的人类模型进行了更新,以考虑细胞内离子浓度的变化。我们发现,窦房结细胞起搏对[Ca]变化的反应存在关键的种间差异,小鼠和兔子模型中周期长度变化很小(<83毫秒),而人类模型中则有明显的心动过缓效应(高达>1000毫秒)。我们的结果表明,需要用人窦房结细胞进行实验,以研究CKD患者低钙血症诱发心动过缓性SCD的潜在机制,小动物模型不太适合。