ArticleAmerican journal of physiology. Heart and circulatory physiology2014
Cardiac electrophysiology and the susceptibility to sustained ventricular tachycardia in intact, conscious mice.
Article in American journal of physiology. Heart and circulatory physiology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.
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Who cites it
8 citing papers in PubMed, 13 citations in OpenAlex.
- Systolic-dominant coronary flow in rats and mice: Challenging the diastolic paradigm across conscious and anaesthetized states.Experimental physiology · 2026Article
- Magnetic vagus nerve stimulation alleviates myocardial ischemia-reperfusion injury by the inhibition of pyroptosis through the MJournal of nanobiotechnology · 2023Article
- Open thoracic surgical implantation of cardiac pacemakers in rats.Nature protocols · 2023Review
- A single electrical pulse within the protective zone of each cardiac cycle prevented reperfusion-induced ventricular tachycardia in conscious mice.Physiological reports · 2018Article
- Fundamental hemodynamic mechanisms mediating the response to myocardial ischemia in conscious paraplegic mice: cardiac output versus peripheral resistance.Physiological reports · 2017Article
- Complex and interacting influences of the autonomic nervous system on cardiac electrophysiology in conscious mice.Autonomic neuroscience : basic & clinical · 2016Article
- The 24 h pattern of arterial pressure in mice is determined mainly by heart rate-driven variation in cardiac output.Physiological reports · 2014Article
- Reperfusion-induced sustained ventricular tachycardia, leading to ventricular fibrillation, in chronically instrumented, intact, conscious mice.Physiological reports · 2014Article
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Authors and funding
2 authors at 1 institution in 1 country.
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Abstract
Cardiac electrophysiological dysfunction is a major cause of death in humans. Accordingly, electrophysiological testing is routinely performed in intact, conscious, humans to evaluate arrhythmias and disorders of cardiac conduction. However, to date, in vivo electrophysiological studies in mice are limited to anesthetized open-chest or closed-chest preparations. However, cardiac electrophysiology in anesthetized mice or mice with surgical trauma may not adequately represent what occurs in conscious mice. Accordingly, an intact, conscious murine model of cardiac electrophysiology has the potential to be of major importance for advancing the concepts and methods that drive cardiovascular therapies. Therefore, we describe, for the first time, the use of an intact, conscious, murine model of cardiac electrophysiology. The conscious mouse model permits measurements of atrioventricular interval, sinus cycle length, sinus node recovery time (SNRT), SNRT corrected for spontaneous sinus cycle, Wenckebach cycle length, the ventricular effective refractory period (VERP) and the electrical stimulation threshold to induce sustained ventricular tachyarrhythmias in an intact, complex model free of the confounding influences of anesthetics and surgical trauma. This is an important consideration because anesthesia and surgical trauma markedly reduced cardiac output and heart rate as well as altered cardiac electrophysiology parameters. Most importantly, anesthesia and surgical trauma significantly increased the VERP and virtually eliminated the ability to induce sustained ventricular tachyarrhythmias. Accordingly, the methodology allows for the accurate documentation of cardiac electrophysiology in complex, conscious mice and may be adopted for advancing the concepts and ideas that drive cardiovascular research.
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