AJP - Heart Calcium Transients and Cell-Sarcomere
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Am J Physiol Heart Circ Physiol 288: H344-H351, 2005. First published August 26, 2004; doi:10.1152/ajpheart.00770.2004
0363-6135/05 $8.00
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Supplemental Video Files
Right arrow All Versions of this Article:
288/1/H344    most recent
00770.2004v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
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 ISI Web of Science (7)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Rothenberg, F.
Right arrow Articles by Efimov, I. R.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Rothenberg, F.
Right arrow Articles by Efimov, I. R.

Electrophysiology and anatomy of embryonic rabbit hearts before and after septation

F. Rothenberg,1 V. P. Nikolski,1 M. Watanabe,2 and I. R. Efimov1

1Department of Biomedical Engineering and 2Rainbow Babies and Children's Hospital, Case Western Reserve University, Cleveland, Ohio

Submitted 30 July 2004 ; accepted in final form 24 August 2004

Mechanisms of cardiac pacemaking and conduction system (CPCS) development are difficult to study, in part because of the absence of models that are physiologically similar to humans in which we can label the entire CPCS. Investigations of the adult rabbit heart have provided insight into normal and abnormal cardiac conduction. The adult and the embryonic rabbit have an endogenous marker of the entire cardiac conduction system, neurofilament 160 (NF-160). Previous work suggested that ventricular septation correlates with critical phases in avian CPCS development, in contrast to the mouse CPCS. Combining high-resolution optical mapping with immunohistochemical analysis of the embryonic rabbit heart, we investigated the significance of ventricular septation in patterning the rabbit embryonic conduction system. We hypothesized that 1) completion of ventricular septation does not correlate with changes in the ventricular activation sequence in rabbit embryos and 2) CPCS anatomy determines the activation sequence of the embryonic heart. We found that preseptated (days 11–13, n = 13) and postseptated (day 15, n = 5) hearts had similar "apex-to-base" ventricular excitation. PR intervals were not significantly different in either group. CPCS anatomy revealed continuity of the NF-160-positive tract connecting the presumptive sinoatrial node, atrioventricular (AV) junction, and ventricular conduction system. The presence of collagen in the AV junction coincided with the appearance of an AV interval. We conclude that the apex-to-base ventricular activation sequence in the rabbit embryo is present before completion of ventricular septation. CPCS anatomy reflects global cardiac activation as demonstrated by high-resolution optical mapping.

rabbit embryo; optical mapping; cardiac conduction system



Address for reprint requests and other correspondence: F. Rothenberg, Pediatrics/Neonatology Div., Neonatal/Perinatal Research Inst., Duke Univ. Medical Center, Bell Research Dr., Box 3179 DUMC, Durham, NC 27710 (E-mail: fgr{at}duke.edu)




This article has been cited by other articles:


Home page
Am. J. Physiol. Heart Circ. Physiol.Home page
D. Sedmera, A. Wessels, T. C. Trusk, R. P. Thompson, K. W. Hewett, and R. G. Gourdie
Changes in activation sequence of embryonic chick atria correlate with developing myocardial architecture
Am J Physiol Heart Circ Physiol, October 1, 2006; 291(4): H1646 - H1652.
[Abstract] [Full Text] [PDF]


Home page
CirculationHome page
M. Valderrabano, F. Chen, A. S. Dave, S. T. Lamp, T. S. Klitzner, and J. N. Weiss
Atrioventricular Ring Reentry in Embryonic Mouse Hearts
Circulation, August 8, 2006; 114(6): 543 - 549.
[Abstract] [Full Text] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
Y. N. Tallini, M. Ohkura, B.-R. Choi, G. Ji, K. Imoto, R. Doran, J. Lee, P. Plan, J. Wilson, H.-B. Xin, et al.
Imaging cellular signals in the heart in vivo: Cardiac expression of the high-signal Ca2+ indicator GCaMP2
PNAS, March 21, 2006; 103(12): 4753 - 4758.
[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 HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Visit Other APS Journals Online
Copyright © 2005 by the American Physiological Society.