昆明小鼠与C57BL6/J小鼠心脏电生理差异。

Teng Wang, Mu Qin, He Huang, Hong-liang Li, Cong-xin Huang
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引用次数: 0

摘要

目的:探讨昆明(KM)和C57BL6/J (C57)小鼠心脏电生理特性的改变及其实质机制,建立稳定的心律失常小鼠模型。方法:采用活体心电图记录QT间期,记录左、右心外膜单相动作电位,诱发常规电刺激和程控电刺激下动作电位持续时间(APD)的变化。利用全细胞膜片钳技术记录左、右单个心外膜肌细胞瞬时外向钾电流。结果:QT间期较C57延长(62.51±4.47 ms vs 52.59±4.85 ms)。结论:QT间期延长和APD的KM小鼠更易发生室性心律失常,这与KM小鼠心室肌细胞Ito密度较C57小鼠低有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cardiac electrophysiological differences between Kunming and C57BL6/J mice.

Objective: To investigate the alterations of cardiac electrophysiological properties and substantial mechanism and find the stable arrhythmia mouse model in Kunming (KM) and C57BL6/J (C57) mice.

Methods: Electrocardiogram recordings were used to analyze the QT interval in vivo, and mono- phasic action potential of right and left ventricular epicardium was recorded to elicit changes of action potential duration (APD) in conventional and programmed electrical stimulation (PES). Transient outward potassium current (Ito) was recorded via whole-cell patch-clamp technique in single right and left epicardial myocytes.

Results: QT interval was prolonged in KM mice relative to C57 mice (62.51±4.47 ms vs. 52.59±4.85 ms, P<0.05) The APD at 50% repolarization of the left ventricular epicardium (18.60±0.91 ms vs. 12.90±0.35 ms), and APDs at 50% (17.31±6.05 ms vs. 12.00±3.24 ms) and 70% repolarization (36.13±5.32 ms vs. 21.95±8.06 ms) of the right ventricular epicardium in KM mice were more sensitive to PES-induced ventricular tachycardia (25%, 3 of 12 hearts), and especially to Burst-induced ventricular tachycardia (50%, 6 of 12 hearts)compared with C57 mice, which were 20% (2 of 10 hearts) and 30% (3 of 10 hearts) respectively. Ito densities both in the left and right ventricular epicardial myocytes from KM mice were significantly decreased compared with C57 mice, respectively (all P<0.01).

Conclusion: Our data showed that KM mice with the prolonged QT interval and APD are vulnerabilities to ventricular arrhythmia, which are attributed to lower Ito densities in ventricular myocytes obtained from KM mice than that from C57 mice.

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