Donate Help Contact The AHA Sign In Home
American Heart Association
Circulation Research
Search: search_blue_button Advanced Search
Circulation Research. 1979;44:250-262

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
Right arrowRequest Permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Legato, M. J.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Legato, M. J.

Circulation Research, Vol 44, 250-262, Copyright © 1979 by American Heart Association


ARTICLES

Cellular mechanisms of normal growth in the mammalian heart. I. Qualitative and quantitative features of ventricular architecture in the dog from birth to five months of age

MJ Legato

This paper describes the qualitative and quantitative composition of dog myocardium over the first 5 months of life. The quantitative composition of dog right and left ventricle over this period does not vary. A stereological analysis of electron micrographs representing 32,000 micron2 of tissue surface revealed that 79% of the heart is made up of myofibers, whereas 21% is extracellular space. Twenty-eight percent of the extracellular compartment by volume is vasculature (tissue was preserved by immersion rather than vascular perfusion); 72% is occupied by nonvascular elements and "empty" space. In contrast to the remarkable constancy of quantitative composition of the whole myocardium, myocyte shape and dimensions and the arrangement of intercellular connections vary dramatically over the age period studied. In early postnatal life, the morphology of blood vessels, many of which have completely partitioned lumina, also changes significantly.


This article has been cited by other articles:


Home page
Cardiovasc ResHome page
M.N. M. N. Obreztchikova, E.A. E. A. Sosunov, A. Plotnikov, E.P. E. P. Anyukhovsky, R. Z. Gainullin, P. Danilo Jr., Z.-H. Yeom, R. B. Robinson, and M. R. Rosen
Developmental changes in IKr and IKs contribute to age-related expression of dofetilide effects on repolarization and proarrhythmia
Cardiovasc Res, August 1, 2003; 59(2): 339 - 350.
[Abstract] [Full Text] [PDF]


Home page
Physiol. Rev.Home page
B. Ostadal, I. Ostadalova, and N. S. Dhalla
Development of Cardiac Sensitivity to Oxygen Deficiency: Comparative and Ontogenetic Aspects
Physiol Rev, July 1, 1999; 79(3): 635 - 659.
[Abstract] [Full Text] [PDF]


Home page
Eur Heart JHome page
P.B.J. Burton, M.H. Yacoub, and P.J.R. Barton
Cyclin-dependent kinase inhibitor expression in human heart failure. A comparison with fetal development
Eur. Heart J., April 2, 1999; 20(8): 604 - 611.
[Abstract] [PDF]


Home page
Cardiovasc ResHome page
D. A.M. Norman, M. H. Yacoub, and P. J.R. Barton
Nuclear factor NF-{kappa}B in myocardium: developmental expression of subunits and activation by interleukin-1{beta} in cardiac myocytes in vitro
Cardiovasc Res, August 1, 1998; 39(2): 434 - 441.
[Abstract] [Full Text] [PDF]


Home page
Circ. Res.Home page
B. D. Angst, L. U.R. Khan, N. J. Severs, K. Whitely, S. Rothery, R. P. Thompson, A. I. Magee, and R. G. Gourdie
Dissociated Spatial Patterning of Gap Junctions and Cell Adhesion Junctions During Postnatal Differentiation of Ventricular Myocardium
Circ. Res., January 1, 1997; 80(1): 88 - 94.
[Abstract] [Full Text]