Purkinje-related Arrhythmias
نویسندگان
چکیده
منابع مشابه
Purkinje-related arrhythmias part ii: polymorphic ventricular tachycardia and ventricular fibrillation.
There has been growing evidence that the Purkinje network plays a pivotal role in both the initiation and perpetuation of ventricular fibrillation (VF). A triggering ventricular premature beat (VPB) with a short-coupling interval could arise from either the right or left Purkinje system in patients with polymorphic ventricular tachycardia (VT) or VF, and that can be suppressed by the catheter a...
متن کاملPurkinje involvement in arrhythmias after coronary artery reperfusion.
Previous studies have indicated that the endocardium may be responsible for a large portion of ventricular tachycardia (VT) seen with reperfusion of ischemic myocardium. To evaluate the role of the Purkinje system in nonreentrant VT arising from the endocardium after reperfusion, the anterior descending coronary artery was occluded for 20 min and then reperfused in 23 dogs after instrumentation...
متن کاملMouse Models of SCN5A-Related Cardiac Arrhythmias
Mutations of SCN5A gene, which encodes the α-subunit of the voltage-gated Na(+) channel Na(V)1.5, underlie hereditary cardiac arrhythmic syndromes such as the type 3 long QT syndrome, cardiac conduction diseases, the Brugada syndrome, the sick sinus syndrome, a trial standstill, and numerous overlap syndromes. Patch-clamp studies in heterologous expression systems have provided important inform...
متن کاملPurkinje Cells as Sources of Arrhythmias in Long QT Syndrome Type 3
Long QT syndrome (LQTS) is characterized by ventricular arrhythmias and sudden cardiac death. Purkinje cells (PC) within the specialized cardiac conduction system have unique electrophysiological properties that we hypothesize may produce the primary sources of arrhythmia in heritable LQTS. LQTS type 3 (LQT3) transgenic mice harboring the ΔKPQ(+/-) mutation were crossed with Contactin2-EGFP BAC...
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ژورنال
عنوان ژورنال: Journal of Arrhythmia
سال: 2011
ISSN: 1880-4276
DOI: 10.1016/s1880-4276(11)80004-9