TY - JOUR
T1 - Optogenetic defibrillation terminates ventricular arrhythmia in mouse hearts and human simulations
AU - Bruegmann, Tobias
AU - Boyle, Patrick M.
AU - Vogt, Christoph C.
AU - Karathanos, Thomas V.
AU - Arevalo, Hermenegild J.
AU - Fleischmann, Bernd K.
AU - Trayanova, Natalia A.
AU - Sasse, Philipp
N1 - Funding Information:
We thank F. Holst for technical assistance and Penn Vector Core, Gene Therapy Program (University of Pennsylvania), for providing the AAV9-CAG-hChR2(H134R)-mCherry.WPRE.SV40 virus vector. This work was supported by the German Research Foundation (SA 1785/5-1, SA 1785/7-1 and Research Training Group 1873 to P. Sasse); the BONFOR Program, Medical Faculty, University of Bonn (O-162.0011 to P. Sasse); and the NIH (DP1 HL123271, R01 HL105216, R01 HL103428, and R01 HL126802 to N.A. Trayanova).
PY - 2016/10/3
Y1 - 2016/10/3
N2 - Ventricular arrhythmias are among the most severe complications of heart disease and can result in sudden cardiac death. Patients at risk currently receive implantable defibrillators that deliver electrical shocks to terminate arrhythmias on demand. However, strong electrical shocks can damage the heart and cause severe pain. Therefore, we have tested optogenetic defibrillation using expression of the light-sensitive channel channelrhodopsin-2 (ChR2) in cardiac tissue. Epicardial illumination effectively terminated ventricular arrhythmias in hearts from transgenic mice and from WT mice after adeno-associated virus-based gene transfer of ChR2. We also explored optogenetic defibrillation for human hearts, taking advantage of a recently developed, clinically validated in silico approach for simulating infarct-related ventricular tachycardia (VT). Our analysis revealed that illumination with red light effectively terminates VT in diseased, ChR2-expressing human hearts. Mechanistically, we determined that the observed VT termination is due to ChR2-mediated transmural depolarization of the myocardium, which causes a block of voltage-dependent Na+ channels throughout the myocardial wall and interrupts wavefront propagation into illuminated tissue. Thus, our results demonstrate that optogenetic defibrillation is highly effective in the mouse heart and could potentially be translated into humans to achieve nondamaging and pain-free termination of ventricular arrhythmia.
AB - Ventricular arrhythmias are among the most severe complications of heart disease and can result in sudden cardiac death. Patients at risk currently receive implantable defibrillators that deliver electrical shocks to terminate arrhythmias on demand. However, strong electrical shocks can damage the heart and cause severe pain. Therefore, we have tested optogenetic defibrillation using expression of the light-sensitive channel channelrhodopsin-2 (ChR2) in cardiac tissue. Epicardial illumination effectively terminated ventricular arrhythmias in hearts from transgenic mice and from WT mice after adeno-associated virus-based gene transfer of ChR2. We also explored optogenetic defibrillation for human hearts, taking advantage of a recently developed, clinically validated in silico approach for simulating infarct-related ventricular tachycardia (VT). Our analysis revealed that illumination with red light effectively terminates VT in diseased, ChR2-expressing human hearts. Mechanistically, we determined that the observed VT termination is due to ChR2-mediated transmural depolarization of the myocardium, which causes a block of voltage-dependent Na+ channels throughout the myocardial wall and interrupts wavefront propagation into illuminated tissue. Thus, our results demonstrate that optogenetic defibrillation is highly effective in the mouse heart and could potentially be translated into humans to achieve nondamaging and pain-free termination of ventricular arrhythmia.
UR - https://www.scopus.com/pages/publications/84991737601
UR - https://www.scopus.com/pages/publications/84991737601#tab=citedBy
U2 - 10.1172/JCI88950
DO - 10.1172/JCI88950
M3 - Article
C2 - 27617859
AN - SCOPUS:84991737601
SN - 0021-9738
VL - 126
SP - 3894
EP - 3904
JO - Journal of Clinical Investigation
JF - Journal of Clinical Investigation
IS - 10
ER -