J Physiol JP - online manuscript tracking
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


J Physiol Volume 555, Number 1, 267-279, February 15, 2004 DOI: 10.1113/jphysiol.2003.054064
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
555/1/267    most recent
jphysiol.2003.054064v1
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Liu, G.
Right arrow Articles by Kavanagh, K. M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Liu, G.
Right arrow Articles by Kavanagh, K. M.

In vivo temporal and spatial distribution of depolarization and repolarization and the illusive murine T wave

Gang Liu1, Jason B. Iden1, Kay Kovithavongs1, Rashida Gulamhusein1, Henry J. Duff2 and Katherine M. Kavanagh1

1 Department of Medicine, University of Alberta, Edmonton, Canada2 Department of Medicine, University of Calgary, Calgary, Canada

This study assessed in vivo temporal and spatial electrophysiological properties of murine hearts and the effect of manipulation of transmural action potential durations (APDs) on T wave morphology. Monophasic action potentials (MAPs) were acquired from multiple left ventricular sites. All MAPs exhibited a plateau phase, with a spike and dome appearance being present in epicardial recordings. Activation occurred from endocardial apex to epicardial apex and apex to base while repolarization occurred from base (shortest 90 {eta}0 level of repolarization (MAP90), 95.4 ± 8.9 ms) to apex and epicardium to endocardium (longest MAP90, 110.77 ± 10.6 ms). The peak of phase 0 of the epicardial base MAP correlated with the return to baseline of the initial and usually dominant waveform of the QRS and the onset of the second usually smaller wave, which clearly occurred in early repolarization, thus establishing where depolarization ended and repolarization began on the murine ECG. This second waveform was similar to the J wave seen in larger animals. Despite temporal and spatial electrophysiological similarities, a T wave is frequently not seen on a murine ECG. There are several determinants of T wave morphology, including transmural activation time, slope of phase 3 repolarization and differences in epicardial, endocardial and M cell APDs. Experimental manipulation of murine transmural gradients by shortening epicardial MAP90 to 84% of endocardial MAP90 the epicardial/endocardial ratio in larger mammals when a positive T wave is present, resulted in a positive murine T wave. Thus, manipulation of the transmural gradients such that they are similar to larger mammals can result in T waves with similar morphology.

(Received 26 August 2003; accepted after revision 14 November 2003; first published online 21 November 2003)
Corresponding author K. M. Kavanagh: 2C2.32 Walter Mackenzie Centre, University of Alberta, Edmonton, Alberta, Canada T6G 2B7.  Email: katherine.kavanagh{at}ualberta.ca




This article has been cited by other articles:


Home page
Physiol. GenomicsHome page
J. M. Lignon, Z. Bichler, B. Hivert, F. E. Gannier, P. Cosnay, J. A. del Rio, D. Migliore-Samour, and C. O. Malecot
Altered heart rate control in transgenic mice carrying the KCNJ6 gene of the human chromosome 21
Physiol Genomics, April 21, 2008; 33(2): 230 - 239.
[Abstract] [Full Text] [PDF]


Home page
J. Physiol.Home page
I. N. Sabir, M. J. Killeen, C. A. Goddard, G. Thomas, S. Gray, A. A. Grace, and C. L.-H. Huang
Transient alterations in transmural repolarization gradients and arrhythmogenicity in hypokalaemic Langendorff-perfused murine hearts
J. Physiol., May 15, 2007; 581(1): 277 - 289.
[Abstract] [Full Text] [PDF]


Home page
J Am Coll CardiolHome page
P. P. Sengupta, B. K. Khandheria, J. Korinek, A. Jahangir, S. Yoshifuku, I. Milosevic, and M. Belohlavek
Left Ventricular Isovolumic Flow Sequence During Sinus and Paced Rhythms: New Insights From Use of High-Resolution Doppler and Ultrasonic Digital Particle Imaging Velocimetry
J. Am. Coll. Cardiol., February 27, 2007; 49(8): 899 - 908.
[Abstract] [Full Text] [PDF]


Home page
J. Physiol.Home page
G. Thomas, M. J. Killeen, I. S. Gurung, P. Hakim, R. Balasubramaniam, C. A. Goddard, A. A. Grace, and C. L.-H. Huang
Mechanisms of ventricular arrhythmogenesis in mice following targeted disruption of KCNE1 modelling long QT syndrome 5
J. Physiol., January 1, 2007; 578(1): 99 - 114.
[Abstract] [Full Text] [PDF]


Home page
J Am Coll CardiolHome page
P. P. Sengupta, B. K. Khandheria, J. Korinek, J. Wang, A. Jahangir, J. B. Seward, and M. Belohlavek
Apex-to-Base Dispersion in Regional Timing of Left Ventricular Shortening and Lengthening
J. Am. Coll. Cardiol., January 3, 2006; 47(1): 163 - 172.
[Abstract] [Full Text] [PDF]


Home page
EuropaceHome page
J. V. Tranquillo, J. Hlavacek, and C. S. Henriquez
An integrative model of mouse cardiac electrophysiology from cell to torso
Europace, January 1, 2005; 7(s2): S56 - S70.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 2004 The Physiological Society.