Abstract
AbstractPathological hypertrophy underlies sudden cardiac death due to its high incidence of occurrence of ventricular arrhythmias. The alteration of transmural electrophysiological properties in hypertrophic cardiac murine tissue has never been explored previously. In this dataset, we have for the first time conducted high-throughput simultaneous optical imaging of transmembrane potential and calcium transients (CaT) throughout the entire hypertrophic murine hearts at high temporal and spatial resolution. Using ElectroMap, we have conducted multiple parameters analysis including action potential duration/calcium transient duration, conduction velocity, alternans and diastolic interval. Voltage-calcium latency was measured as time difference between action potential and CaT peak. The dataset therefore provides the first high spatial resolution transmural electrophysiological profiling of the murine heart, allowing interrogation of mechanisms driving ventricular arrhythmias associated with pathological hypertrophy. The dataset allows for further reuse and detailed analyses of geometrical, topological and functional analyses and reconstruction of 2-dimensional and 3-dimentional models.
Funder
British Heart Foundation
RCUK | Engineering and Physical Sciences Research Council
the National Natural Science Foundation of China
Publisher
Springer Science and Business Media LLC
Subject
Library and Information Sciences,Statistics, Probability and Uncertainty,Computer Science Applications,Education,Information Systems,Statistics and Probability
Reference16 articles.
1. Refaat, M. M., Hotait, M. & London, B. Genetics of sudden cardiac death. Curr Cardiol. Rep. 17, 606 (2015).
2. He, S. et al. A protocol for transverse cardiac slicing and optical mapping in murine heart. Front. Physiol. 10, 755 (2019).
3. Liu, W. et al. Pak1 as a novel therapeutic target for antihypertrophic treatment in the heart. Circulation 124, 2702–2715 (2011).
4. Tavakoli, R., Nemska, S., Jamshidi, P., Gassmann, M. & Frossard, N. Technique of minimally invasive transverse aortic constriction in mice for induction of left ventricular hypertrophy. J. Vis. Exp. 25, 56231 (2017).
5. Zhang, P. et al. Contribution of DNA methylation in chronic stress-induced cardiac remodeling and arrhythmias in mice. FASEB. J. 33, 12240–12252 (2019).
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