Alghamdi Aaazh M, Boyett Mark R, Hancox Jules C, Zhang Henggui
Biological Physics Group, Department of Physics and Astronomy, The University of Manchester, Manchester, United Kingdom.
Department of Physics, Faculty of Science, University of Jeddah, Jeddah, Saudi Arabia.
Front Physiol. 2020 Dec 3;11:546508. doi: 10.3389/fphys.2020.546508. eCollection 2020.
The function of the sinoatrial node (SAN), the pacemaker of the heart, declines with age, resulting in increased incidence of sinoatrial node dysfunction (SND) in older adults. The present study assesses potential ionic mechanisms underlying age associated SND. Two group studies have identified complex and various changes in some of membrane ion channels in aged rat SAN, the first group (Aging Study-1) indicates a considerable changes of gene expression with up-regulation of mRNA in ion channels of Cav1.2, Cav1.3 and KvLQT1, Kv4.2, and the Ca handling proteins of SERCA2a, and down-regulation of Cav3.1, NCX, and HCN1 and the Ca-clock proteins of RYR2. The second group (Aging Study-2) suggests a different pattern of changes, including down regulation of Cav1.2, Cav1.3 and HCN4, and RYR2, and an increase of NCX and SERCA densities and proteins. Although both data sets shared a similar finding for some specific ion channels, such as down regulation of HCN4, NCX, and RYR2, there are contradictory changes for some other membrane ion channels, such as either up-regulation or down-regulation of Cav1.2, NCX and SERCA2a in aged rat SAN. The present study aims to test a hypothesis that age-related SND may arise from different ionic and molecular remodeling patterns. To test this hypothesis, a mathematical model of the electrical action potential of rat SAN myocytes was modified to simulate the functional impact of age-induced changes on membrane ion channels and intracellular Ca handling as observed in Aging Study-1 and Aging Study-2. The role and relative importance of each individually remodeled ion channels and Ca-handling in the two datasets were evaluated. It was shown that the age-induced changes in ion channels and Ca-handling, based on either Aging Study-1 or Aging Study-2, produced similar bradycardic effects as manifested by a marked reduction in the heart rate (HR) that matched experimental observations. Further analysis showed that although the SND arose from an integrated action of all remodeling of ion channels and Ca-handling in both studies, it was the change to that played the most important influence.
窦房结(SAN)作为心脏的起搏器,其功能会随着年龄的增长而衰退,导致老年人心房结功能障碍(SND)的发病率增加。本研究评估了与年龄相关的SND潜在的离子机制。两项分组研究已经确定了老年大鼠窦房结中一些膜离子通道的复杂多样的变化,第一组(衰老研究-1)表明基因表达有相当大的变化,Cav1.2、Cav1.3以及KvLQT1、Kv4.2离子通道的mRNA上调,肌浆网钙ATP酶2a(SERCA2a)等钙处理蛋白上调,而Cav3.1、钠钙交换体(NCX)、超极化激活的环核苷酸门控阳离子通道1(HCN1)以及兰尼碱受体2(RYR2)等钙钟蛋白下调。第二组(衰老研究-2)显示出不同的变化模式,包括Cav1.2、Cav1.3、HCN4以及RYR2的下调,以及NCX和SERCA密度及蛋白的增加。尽管两组数据集对于某些特定离子通道有相似的发现,比如HCN4、NCX和RYR2的下调,但对于其他一些膜离子通道存在相互矛盾的变化,例如老年大鼠窦房结中Cav1.2、NCX和SERCA2a的上调或下调。本研究旨在验证一个假设,即与年龄相关的SND可能源于不同的离子和分子重塑模式。为了验证这一假设,对大鼠窦房结心肌细胞动作电位的数学模型进行了修改,以模拟衰老研究-1和衰老研究-2中观察到的年龄诱导变化对膜离子通道和细胞内钙处理的功能影响。评估了两个数据集中每个单独重塑的离子通道和钙处理的作用及相对重要性。结果表明,基于衰老研究-1或衰老研究-2,年龄诱导的离子通道和钙处理变化产生了类似的心动过缓效应,表现为心率(HR)显著降低,这与实验观察结果相符。进一步分析表明,尽管在两项研究中SND都源于离子通道和钙处理所有重塑的综合作用,但 的变化起到了最重要的影响。 (原文此处“it was the change to that played the most important influence”表述不完整,翻译时保留原文状态)