Department of Internal Medicine II, University Hospital Regensburg, Regensburg, Germany.
Department of Internal Medicine III, University Hospital Regensburg, Regensburg, Germany.
Basic Res Cardiol. 2022 Sep 6;117(1):45. doi: 10.1007/s00395-022-00949-0.
Tachycardiomyopathy is characterised by reversible left ventricular dysfunction, provoked by rapid ventricular rate. While the knowledge of mitochondria advanced in most cardiomyopathies, mitochondrial functions await elucidation in tachycardiomyopathy. Pacemakers were implanted in 61 rabbits. Tachypacing was performed with 330 bpm for 10 days (n = 11, early left ventricular dysfunction) or with up to 380 bpm over 30 days (n = 24, tachycardiomyopathy, TCM). In n = 26, pacemakers remained inactive (SHAM). Left ventricular tissue was subjected to respirometry, metabolomics and acetylomics. Results were assessed for translational relevance using a human-based model: induced pluripotent stem cell derived cardiomyocytes underwent field stimulation for 7 days (TACH-iPSC-CM). TCM animals showed systolic dysfunction compared to SHAM (fractional shortening 37.8 ± 1.0% vs. 21.9 ± 1.2%, SHAM vs. TCM, p < 0.0001). Histology revealed cardiomyocyte hypertrophy (cross-sectional area 393.2 ± 14.5 µm vs. 538.9 ± 23.8 µm, p < 0.001) without fibrosis. Mitochondria were shifted to the intercalated discs and enlarged. Mitochondrial membrane potential remained stable in TCM. The metabolite profiles of ELVD and TCM were characterised by profound depletion of tricarboxylic acid cycle intermediates. Redox balance was shifted towards a more oxidised state (ratio of reduced to oxidised nicotinamide adenine dinucleotide 10.5 ± 2.1 vs. 4.0 ± 0.8, p < 0.01). The mitochondrial acetylome remained largely unchanged. Neither TCM nor TACH-iPSC-CM showed relevantly increased levels of reactive oxygen species. Oxidative phosphorylation capacity of TCM decreased modestly in skinned fibres (168.9 ± 11.2 vs. 124.6 ± 11.45 pmol·O·s·mg tissue, p < 0.05), but it did not in isolated mitochondria. The pattern of mitochondrial dysfunctions detected in two models of tachycardiomyopathy diverges from previously published characteristic signs of other heart failure aetiologies.
心动过速性心肌病的特征为左心室功能障碍可逆,由快速心室率引起。尽管大多数心肌病中线粒体的知识有所进展,但心动过速性心肌病中线粒体的功能仍有待阐明。61 只兔子被植入起搏器。以 330bpm 的频率进行快速起搏 10 天(n=11,早期左心室功能障碍)或 30 天内以高达 380bpm 的频率起搏(n=24,心动过速性心肌病,TCM)。在 n=26 中,起搏器保持不活动(SHAM)。左心室组织接受呼吸测定法、代谢组学和乙酰化组学检测。使用基于人类的模型评估翻译相关性:诱导多能干细胞衍生的心肌细胞接受场刺激 7 天(TACH-iPSC-CM)。TCM 动物与 SHAM 相比表现出收缩功能障碍(短轴缩短率 37.8±1.0%比 21.9±1.2%,SHAM 比 TCM,p<0.0001)。组织学显示心肌细胞肥大(横截面积 393.2±14.5µm 比 538.9±23.8µm,p<0.001)而无纤维化。线粒体转移到闰盘并增大。TCM 中线粒体膜电位保持稳定。ELVD 和 TCM 的代谢物谱特征为三羧酸循环中间产物深度耗竭。氧化还原平衡向更氧化状态转移(还原型与氧化型烟酰胺腺嘌呤二核苷酸的比值为 10.5±2.1 比 4.0±0.8,p<0.01)。线粒体乙酰组学基本保持不变。TCM 或 TACH-iPSC-CM 均未显示明显增加的活性氧水平。TCM 去皮纤维的氧化磷酸化能力略有下降(168.9±11.2 比 124.6±11.45pmol·O·s·mg 组织,p<0.05),但在分离的线粒体中没有。在两种心动过速性心肌病模型中检测到的线粒体功能障碍模式与先前发表的其他心力衰竭病因的特征标志不同。