Optical Mapping Approaches on Muscleblind‐Like Compound Knockout Mice for Understanding Mechanistic Insights Into Ventricular Arrhythmias in Myotonic Dystrophy

BackgroundCardiac arrhythmias are common causes of death in patients with myotonic dystrophy (dystrophia myotonica [DM]). Evidence shows that atrial tachyarrhythmia is an independent risk factor for sudden death; however, the relationship is unclear. Methods and ResultsControl wild‐type (Mbnl1+/+; M...

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Main Authors: Chung‐Chuan Chou, Po‐Cheng Chang, Yi‐Chia Wei, Kuang‐Yung Lee
Format: Article
Language:English
Published: Wiley 2017-04-01
Series:Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease
Subjects:
Online Access:https://www.ahajournals.org/doi/10.1161/JAHA.116.005191
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author Chung‐Chuan Chou
Po‐Cheng Chang
Yi‐Chia Wei
Kuang‐Yung Lee
author_facet Chung‐Chuan Chou
Po‐Cheng Chang
Yi‐Chia Wei
Kuang‐Yung Lee
author_sort Chung‐Chuan Chou
collection DOAJ
description BackgroundCardiac arrhythmias are common causes of death in patients with myotonic dystrophy (dystrophia myotonica [DM]). Evidence shows that atrial tachyarrhythmia is an independent risk factor for sudden death; however, the relationship is unclear. Methods and ResultsControl wild‐type (Mbnl1+/+; Mbnl2+/+) and DM mutant (Mbnl1−/−; Mbnl2+/−) mice were generated by crossing double heterozygous knockout (Mbnl1+/−; Mbnl2+/−) mice. In vivo electrophysiological study and optical mapping technique were performed to investigate mechanisms of ventricular tachyarrhythmias. Transmission electron microscopy scanning was performed for myocardium ultrastructural analysis. DM mutant mice were more vulnerable to anesthesia medications and program electrical pacing: 2 of 12 mice had sudden apnea and cardiac arrest during premedication of general anesthesia; 9 of the remaining 10 had atrial tachycardia and/or atrioventricular block, but none of the wild‐type mice had spontaneous arrhythmias; and 9 of 10 mice had pacing‐induced ventricular tachyarrhythmias, but only 1 of 14 of the wild‐type mice. Optical mapping studies revealed prolonged action potential duration, slower conduction velocity, and steeper conduction velocity restitution curves in the DM mutant mice than in the wild‐type group. Spatially discordant alternans was more easily inducible in DM mutant than wild‐type mice. Transmission electron microscopy showed disarranged myofibrils with enlarged vacuole‐occupying mitochondria in the DM mutant group. ConclusionsThis DM mutant mouse model presented with clinical myofibril ultrastructural abnormality and cardiac arrhythmias, including atrial tachyarrhythmias, atrioventricular block, and ventricular tachyarrhythmias. Optical mapping studies revealed prolonged action potential duration and slow conduction velocity in the DM mice, leading to vulnerability of spatially discordant alternans and ventricular arrhythmia induction to pacing.
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spelling doaj.art-826197e77a1b41b58f0940e95a5854002022-12-21T18:11:39ZengWileyJournal of the American Heart Association: Cardiovascular and Cerebrovascular Disease2047-99802017-04-016410.1161/JAHA.116.005191Optical Mapping Approaches on Muscleblind‐Like Compound Knockout Mice for Understanding Mechanistic Insights Into Ventricular Arrhythmias in Myotonic DystrophyChung‐Chuan Chou0Po‐Cheng Chang1Yi‐Chia Wei2Kuang‐Yung Lee3Department of Cardiology, Chang Gung Memorial Hospital, Linkou, TaiwanDepartment of Cardiology, Chang Gung Memorial Hospital, Linkou, TaiwanDepartment of Neurology, Chang Gung Memorial Hospital, Keelung, TaiwanDepartment of Neurology, Chang Gung Memorial Hospital, Keelung, TaiwanBackgroundCardiac arrhythmias are common causes of death in patients with myotonic dystrophy (dystrophia myotonica [DM]). Evidence shows that atrial tachyarrhythmia is an independent risk factor for sudden death; however, the relationship is unclear. Methods and ResultsControl wild‐type (Mbnl1+/+; Mbnl2+/+) and DM mutant (Mbnl1−/−; Mbnl2+/−) mice were generated by crossing double heterozygous knockout (Mbnl1+/−; Mbnl2+/−) mice. In vivo electrophysiological study and optical mapping technique were performed to investigate mechanisms of ventricular tachyarrhythmias. Transmission electron microscopy scanning was performed for myocardium ultrastructural analysis. DM mutant mice were more vulnerable to anesthesia medications and program electrical pacing: 2 of 12 mice had sudden apnea and cardiac arrest during premedication of general anesthesia; 9 of the remaining 10 had atrial tachycardia and/or atrioventricular block, but none of the wild‐type mice had spontaneous arrhythmias; and 9 of 10 mice had pacing‐induced ventricular tachyarrhythmias, but only 1 of 14 of the wild‐type mice. Optical mapping studies revealed prolonged action potential duration, slower conduction velocity, and steeper conduction velocity restitution curves in the DM mutant mice than in the wild‐type group. Spatially discordant alternans was more easily inducible in DM mutant than wild‐type mice. Transmission electron microscopy showed disarranged myofibrils with enlarged vacuole‐occupying mitochondria in the DM mutant group. ConclusionsThis DM mutant mouse model presented with clinical myofibril ultrastructural abnormality and cardiac arrhythmias, including atrial tachyarrhythmias, atrioventricular block, and ventricular tachyarrhythmias. Optical mapping studies revealed prolonged action potential duration and slow conduction velocity in the DM mice, leading to vulnerability of spatially discordant alternans and ventricular arrhythmia induction to pacing.https://www.ahajournals.org/doi/10.1161/JAHA.116.005191conduction blockMbnl knockout micemyotonic dystrophyoptical mappingventricular tachyarrhythmias
spellingShingle Chung‐Chuan Chou
Po‐Cheng Chang
Yi‐Chia Wei
Kuang‐Yung Lee
Optical Mapping Approaches on Muscleblind‐Like Compound Knockout Mice for Understanding Mechanistic Insights Into Ventricular Arrhythmias in Myotonic Dystrophy
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease
conduction block
Mbnl knockout mice
myotonic dystrophy
optical mapping
ventricular tachyarrhythmias
title Optical Mapping Approaches on Muscleblind‐Like Compound Knockout Mice for Understanding Mechanistic Insights Into Ventricular Arrhythmias in Myotonic Dystrophy
title_full Optical Mapping Approaches on Muscleblind‐Like Compound Knockout Mice for Understanding Mechanistic Insights Into Ventricular Arrhythmias in Myotonic Dystrophy
title_fullStr Optical Mapping Approaches on Muscleblind‐Like Compound Knockout Mice for Understanding Mechanistic Insights Into Ventricular Arrhythmias in Myotonic Dystrophy
title_full_unstemmed Optical Mapping Approaches on Muscleblind‐Like Compound Knockout Mice for Understanding Mechanistic Insights Into Ventricular Arrhythmias in Myotonic Dystrophy
title_short Optical Mapping Approaches on Muscleblind‐Like Compound Knockout Mice for Understanding Mechanistic Insights Into Ventricular Arrhythmias in Myotonic Dystrophy
title_sort optical mapping approaches on muscleblind like compound knockout mice for understanding mechanistic insights into ventricular arrhythmias in myotonic dystrophy
topic conduction block
Mbnl knockout mice
myotonic dystrophy
optical mapping
ventricular tachyarrhythmias
url https://www.ahajournals.org/doi/10.1161/JAHA.116.005191
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AT yichiawei opticalmappingapproachesonmuscleblindlikecompoundknockoutmiceforunderstandingmechanisticinsightsintoventriculararrhythmiasinmyotonicdystrophy
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