Acute atrial arrhythmogenicity and altered Ca2+ homeostasis in murine RyR2-P2328S hearts

被引:35
|
作者
Zhang, Yanmin [1 ,2 ]
Fraser, James A. [1 ]
Jeevaratnam, Kamalan [1 ,3 ]
Hao, Xiaojin [4 ]
Hothi, Sandeep S. [1 ]
Grace, Andrew A. [5 ]
Lei, Ming [4 ]
Huang, Christopher L. -H. [1 ]
机构
[1] Univ Cambridge, Physiol Lab, Cambridge CB2 3EG, England
[2] Xi An Jiao Tong Univ, Affiliated Hosp 1, Dept Paediat, Xian 710061, Peoples R China
[3] Int Med Univ, Fac Med, Dept Human Biol, Kuala Lumpur 57000, Malaysia
[4] Univ Manchester, Cardiovasc Grp, Sch Clin & Lab Sci, Manchester M13 9NT, Lancs, England
[5] Univ Cambridge, Dept Biochem, Cardiovasc Biol Grp, Cambridge CB2 1QW, England
基金
英国生物技术与生命科学研究理事会; 英国惠康基金; 英国医学研究理事会;
关键词
RyR2; Atrial arrhythmia; Calcium; Electrocardiography; Monophasic action potentials; POLYMORPHIC VENTRICULAR-TACHYCARDIA; CARDIAC RYANODINE RECEPTOR; RYR2; GENE; FOLLOW-UP; FIBRILLATION; MECHANISMS; MUTATIONS; DEATH; ARRHYTHMIAS; MOUSE;
D O I
10.1093/cvr/cvq229
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aims The experiments explored for atrial arrhythmogenesis and its possible physiological background in recently developed hetero-(RyR2(+/S)) and homozygotic (RyR2(S/S)) RyR2-P2328S murine models for catecholaminergic polymorphic ventricular tachycardia (VT) for the first time. They complement previous clinical and experimental reports describing increased ventricular arrhythmic tendencies associated with physical activity, stress, or catecholamine infusion, potentially leading to VT and ventricular fibrillation. Methods and results Atrial arrhythmogenic properties were compared at the whole animal, Langendorff-perfused heart, and single, isolated atrial myocyte levels using electrophysiological and confocal fluorescence microscopy methods. This demonstrated that: (i) electrocardiographic parameters in intact anaesthetized wild-type (WT), RyR2(+/S) and RyR2(S/S) mice were statistically indistinguishable both before and after addition of isoproterenol apart from increases in heart rates. (ii) Bipolar electrogram and monophasic action potential recordings showed significantly higher incidences of arrhythmogenesis in isolated perfused RyR2(S/S), but not RyR2(+/S), relative to WT hearts during either regular pacing or programmed electrical stimulation. The addition of isoproterenol increased such incidences in all three groups. (iii) However, there were no accompanying differences in cardiac anatomy or action potential durations at 90% repolarization and refractory periods. (iv) In contrast, episodes of diastolic Ca2+ release were observed under confocal microscopy in isolated fluo-3-loaded RyR2(S/S), but not RyR2(+/S) or WT, atrial myocytes. The introduction of isoproterenol resulted in significant diastolic Ca2+ release in all three groups. Conclusions These findings establish acute atrial arrhythmogenic properties in RyR2-P2328S hearts and correlate these with altered Ca2+ homeostasis in an absence of repolarization abnormalities for the first time.
引用
收藏
页码:794 / 804
页数:11
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