AJP - Heart Fuel your research with LabChart
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Am J Physiol Heart Circ Physiol 272: H236-H243, 1997;
0363-6135/97 $5.00
This Article
Right arrow Full Text (PDF)
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 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 Minamikawa, T.
Right arrow Articles by Williams, D. A.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Minamikawa, T.
Right arrow Articles by Williams, D. A.

AJP - Heart and Circulatory Physiology, Vol 272, Issue 1 236-H243, Copyright © 1997 by American Physiological Society


ARTICLES

In situ visualization of spontaneous calcium waves within perfused whole rat heart by confocal imaging

T. Minamikawa, S. H. Cody and D. A. Williams
Department of Physiology, University of Melbourne, Parkville, Victoria, Australia. tets@physiol.unimelb.edu.au

We describe the first direct visualization of Ca2+ oscillations in the perfused whole rat heart. Dye loading at a low temperature and enhanced optical-section techniques of confocal microscopy by elimination of the refractive index mismatch with use of saline-immersible objective lens enabled us to image multiple Ca2+ waves in the subepicardial myocardium of the fluo 3-loaded heart. These Ca2+ waves were sporadically seen even with a physiological extracellular Ca2+ perfusion in either a paced or an arrested heart and propagated beyond cellular boundaries within the three-dimensional structures of cardiac muscle. Under these conditions, the velocity of wave propagation was 60-100 microns/s and the frequency of initiation was relatively low (< 2 Hz). With an increase in extracellular Ca2+ concentration, however, the waves became more prevalent and tended to be multifocal, and an increasing fraction of the waves exhibited faster propagation velocities and higher frequencies. These results suggest that perfused rat hearts exhibit spontaneous Ca2+ waves in an apparently resting state and that under Ca(2+)-overload conditions the multifocal and high-frequency waves become more widespread in the heart syncytium, which may provide an understanding of the ionic basis for the summation of afterdepolarizations and triggering of arrhythmias seen under pathological conditions.


This article has been cited by other articles:


Home page
Circ. Res.Home page
K. Fujiwara, H. Tanaka, H. Mani, T. Nakagami, and T. Takamatsu
Burst Emergence of Intracellular Ca2+ Waves Evokes Arrhythmogenic Oscillatory Depolarization via the Na+-Ca2+ Exchanger: Simultaneous Confocal Recording of Membrane Potential and Intracellular Ca2+ in the Heart
Circ. Res., August 29, 2008; 103(5): 509 - 518.
[Abstract] [Full Text] [PDF]


Home page
Physiol. Rev.Home page
H. E. D. J. ter Keurs and P. A. Boyden
Calcium and Arrhythmogenesis
Physiol Rev, April 1, 2007; 87(2): 457 - 506.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Gastrointest. Liver Physiol.Home page
R. R. Roberts, J. F. Murphy, H. M. Young, and J. C. Bornstein
Development of colonic motility in the neonatal mouse-studies using spatiotemporal maps
Am J Physiol Gastrointest Liver Physiol, March 1, 2007; 292(3): G930 - G938.
[Abstract] [Full Text] [PDF]


Home page
J. Appl. Physiol.Home page
O. Eerbeek, E. G. Mik, C. J. Zuurbier, M. v. t Loo, C. Donkersloot, and C. Ince
Ratiometric intracellular calcium imaging in the isolated beating rat heart using indo-1 fluorescence
J Appl Physiol, December 1, 2004; 97(6): 2042 - 2050.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Cell Physiol.Home page
N. Kurebayashi, H. Yamashita, Y. Nakazato, H. Daida, and Y. Ogawa
Behavior of Ca2+ waves in multicellular preparations from guinea pig ventricle
Am J Physiol Cell Physiol, December 1, 2004; 287(6): C1646 - C1656.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Cell Physiol.Home page
M. Rubart, E. Wang, K. W. Dunn, and L. J. Field
Two-photon molecular excitation imaging of Ca2+ transients in Langendorff-perfused mouse hearts
Am J Physiol Cell Physiol, June 1, 2003; 284(6): C1654 - C1668.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Heart Circ. Physiol.Home page
S. O. Suadicani, M. J. Vink, and D. C. Spray
Slow intercellular Ca2+ signaling in wild-type and Cx43-null neonatal mouse cardiac myocytes
Am J Physiol Heart Circ Physiol, December 1, 2000; 279(6): H3076 - H3088.
[Abstract] [Full Text] [PDF]


Home page
Circ. Res.Home page
B. D. Stuyvers, P. A. Boyden, and H. E. D. J. t. Keurs
Calcium Waves : Physiological Relevance in Cardiac Function
Circ. Res., May 26, 2000; 86(10): 1016 - 1018.
[Full Text] [PDF]


Home page
Circ. Res.Home page
T. Kaneko, H. Tanaka, M. Oyamada, S. Kawata, and T. Takamatsu
Three Distinct Types of Ca2+ Waves in Langendorff-Perfused Rat Heart Revealed by Real-Time Confocal Microscopy
Circ. Res., May 26, 2000; 86(10): 1093 - 1099.
[Abstract] [Full Text] [PDF]


Home page
Physiol. Rev.Home page
A. Takahashi, P. Camacho, J. D. Lechleiter, and B. Herman
Measurement of Intracellular Calcium
Physiol Rev, October 1, 1999; 79(4): 1089 - 1125.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Cell Physiol.Home page
R. J. Stevens, J. S. Weinert, and N. G. Publicover
Visualization of origins and propagation of excitation in canine gastric smooth muscle
Am J Physiol Cell Physiol, September 1, 1999; 277(3): C448 - C460.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Visit Other APS Journals Online