Home LiteratureArticle Details
PMID: 18708441 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Polarity reversal lowers activation time during diastolic field stimulation of the rabbit ventricles: insights into mechanisms.

American journal of physiology. Heart and circulatory physiology ·Vol. 295 ·No. 4 ·2008-10-00 ·Pages H1626-33

Maleckar MM, Woods MC, Sidorov VY, Holcomb MR, Mashburn DN, Wikswo JP, Trayanova NA

Abstract

To fully characterize the mechanisms of defibrillation, it is necessary to understand the response, within the three-dimensional (3D) volume of the ventricles, to shocks given in diastole. Studies that have examined diastolic responses conducted measurements on the epicardium or on a transmural surface of the left ventricular (LV) wall only. The goal of this study was to use optical imaging experiments and 3D bidomain simulations, including a model of optical mapping, to ascertain the shock-induced virtual electrode and activation patterns throughout the rabbit ventricles following diastolic shocks. We tested the hypothesis that the locations of shock-induced regions of hyperpolarization govern the different diastolic activation patterns for shocks of reversed polarity. In model and experiment, uniform-field monophasic shocks of reversed polarities (cathode over the right ventricle is RV-, reverse polarity is LV-) were applied to the ventricles in diastole. Experiments and simulations revealed that RV- shocks resulted in longer activation times compared with LV- shocks of the same strength. 3D simulations demonstrated that RV- shocks induced a greater volume of hyperpolarization at shock end compared with LV- shocks; most of these hyperpolarized regions were located in the LV. The results of this study indicate that ventricular geometry plays an important role in both the location and size of the shock-induced virtual anodes that determine activation delay during the shock and subsequently affect shock-induced propagation. If regions of hyperpolarization that develop during the shock are sufficiently large, activation delay may persist until shock end.

MeSH Terms
Animals Computer Simulation Diastole Electric Countershock/methods Fluorescent Dyes/administration & dosage Heart Conduction System/physiology Heart Ventricles/anatomy & histology In Vitro Techniques Injections Models, Cardiovascular Pericardium/physiology Pyridinium Compounds/administration & dosage Rabbits Time Factors Ventricular Function
Chemicals
Fluorescent Dyes Pyridinium Compounds 1-(3-sulfonatopropyl)-4-(beta)(2-(di-n-butylamino)-6-naphthylvinyl)pyridinium betaine
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Maleckar M M
Department of Biomedical Engineering and Institute for Computational Medicine, Johns Hopkins University, Baltimore, Maryland 21218, USA.
Woods M C
Sidorov V Y
Holcomb M R
Mashburn D N
Wikswo J P
Trayanova N A
References (31)
31 references, click to expand
  1. Role of intramural virtual electrodes in shock-induced activation of left ventricle: optical measurements from the intact epicardial surface.
    Heart Rhythm. 2006 Sep;3(9):1063-73 PMID: 16945803
  2. Tunnel propagation of postshock activations as a hypothesis for fibrillation induction and isoelectric window.
    Circ Res. 2008 Mar 28;102(6):737-45 PMID: 18218982
  3. Experimental evidence of improved transthoracic defibrillation with electroporation-enhancing pulses.
    IEEE Trans Biomed Eng. 2006 Oct;53(10):1901-10 PMID: 17019853
  4. Optical transmembrane potential measurements during defibrillation-strength shocks in perfused rabbit hearts.
    Circ Res. 1995 Sep;77(3):593-602 PMID: 7641329
  5. Synthesis of voltage-sensitive optical signals: application to panoramic optical mapping.
    Biophys J. 2006 Apr 15;90(8):2938-45 PMID: 16443665
  6. Virtual electrodes in cardiac tissue: a common mechanism for anodal and cathodal stimulation.
    Biophys J. 1995 Dec;69(6):2195-210 PMID: 8599628
  7. A high-voltage cardiac stimulator for field shocks of a whole heart in a bath.
    Rev Sci Instrum. 2007 Oct;78(10):104302 PMID: 17979442
  8. Virtual cathode effects during stimulation of cardiac muscle. Two-dimensional in vivo experiments.
    Circ Res. 1991 Feb;68(2):513-30 PMID: 1991354
  9. Termination of spiral waves with biphasic shocks: role of virtual electrode polarization.
    J Cardiovasc Electrophysiol. 2000 Dec;11(12):1386-96 PMID: 11196563
  10. Virtual electrode-induced phase singularity: a basic mechanism of defibrillation failure.
    Circ Res. 1998 May 4;82(8):918-25 PMID: 9576111
  11. Asymmetry in membrane responses to electric shocks: insights from bidomain simulations.
    Biophys J. 2004 Oct;87(4):2271-82 PMID: 15454429
  12. Shock-induced epicardial and endocardial virtual electrodes leading to ventricular fibrillation via reentry, graded responses, and transmural activation.
    J Cardiovasc Electrophysiol. 2004 Jan;15(1):79-87 PMID: 15028078
  13. The role of photon scattering in optical signal distortion during arrhythmia and defibrillation.
    Biophys J. 2007 Nov 15;93(10):3714-26 PMID: 17978166
  14. Success and failure of the defibrillation shock: insights from a simulation study.
    J Cardiovasc Electrophysiol. 2000 Jul;11(7):785-96 PMID: 10921796
  15. Electrical stimulation of cardiac tissue: a bidomain model with active membrane properties.
    IEEE Trans Biomed Eng. 1994 Mar;41(3):232-40 PMID: 8045575
  16. Direct evidence of the role of virtual electrode-induced phase singularity in success and failure of defibrillation.
    J Cardiovasc Electrophysiol. 2000 Aug;11(8):861-8 PMID: 10969748
  17. Success and failure of biphasic shocks: results of bidomain simulations.
    Math Biosci. 2001 Dec;174(2):91-109 PMID: 11730859
  18. Examination of optical depth effects on fluorescence imaging of cardiac propagation.
    Biophys J. 2003 Dec;85(6):4134-45 PMID: 14645100
  19. Roles of electric field and fiber structure in cardiac electric stimulation.
    Biophys J. 1999 Sep;77(3):1404-17 PMID: 10465752
  20. Responses of the transmembrane potential of myocardial cells during a shock.
    J Cardiovasc Electrophysiol. 1995 Apr;6(4):252-63 PMID: 7647950
  21. Differences between left and right ventricular anatomy determine the types of reentrant circuits induced by an external electric shock. A rabbit heart simulation study.
    Prog Biophys Mol Biol. 2006 Jan-Apr;90(1-3):399-413 PMID: 16055175
  22. Intramural virtual electrodes in ventricular wall: effects on epicardial polarizations.
    Circulation. 2004 May 18;109(19):2349-56 PMID: 15117837
  23. Virtual electrode polarization in the far field: implications for external defibrillation.
    Am J Physiol Heart Circ Physiol. 2000 Sep;279(3):H1055-70 PMID: 10993768
  24. Differences between left and right ventricular chamber geometry affect cardiac vulnerability to electric shocks.
    Circ Res. 2005 Jul 22;97(2):168-75 PMID: 15976315
  25. Diastolic shocking experience: do virtual electrodes exist only during systole?
    J Cardiovasc Electrophysiol. 2003 Nov;14(11):1223-4 PMID: 14678139
  26. Photon density measured over a cut surface: implications for optical mapping of the heart.
    IEEE Trans Biomed Eng. 2008 Aug;55(8):2102-4 PMID: 18632373
  27. Evaluating intramural virtual electrodes in the myocardial wedge preparation: simulations of experimental conditions.
    Biophys J. 2008 Mar 1;94(5):1904-15 PMID: 17993491
  28. Intramural virtual electrodes during defibrillation shocks in left ventricular wall assessed by optical mapping of membrane potential.
    Circulation. 2002 Aug 20;106(8):1007-14 PMID: 12186808
  29. Optical mapping of transmural activation induced by electrical shocks in isolated left ventricular wall wedge preparations.
    J Cardiovasc Electrophysiol. 2003 Nov;14(11):1215-22 PMID: 14678138
  30. High-resolution optical mapping of intramural virtual electrodes in porcine left ventricular wall.
    Cardiovasc Res. 2004 Dec 1;64(3):448-56 PMID: 15537498
  31. Photon scattering effects in optical mapping of propagation and arrhythmogenesis in the heart.
    J Electrocardiol. 2007 Nov-Dec;40(6 Suppl):S75-80 PMID: 17993334
Article Info
Journal
American journal of physiology. Heart and circulatory physiology
Abbr.
Am J Physiol Heart Circ Physiol
ISSN
0363-6135
Published
2008-10-00
Epub
2008-00-15
Pages
H1626-33
Language
English
Region
United States
NLM ID
100901228
PMCID
PMC2593523
Subset
IM
Grants
NHLBI NIH HHS · HL058241 · United States
NHLBI NIH HHS · HL063195 · United States
NHLBI NIH HHS · HL082729 · United States
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: [email protected]