Changes in activation sequence of embryonic chick atria correlate with developing myocardial architecture
Language English Country United States Media print-electronic
Document type Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't
Grant support
HD-39446
NICHD NIH HHS - United States
HL-50582
NHLBI NIH HHS - United States
HL-52813
NHLBI NIH HHS - United States
RR-16434
NCRR NIH HHS - United States
PubMed
16679393
DOI
10.1152/ajpheart.01007.2005
PII: 01007.2005
Knihovny.cz E-resources
- MeSH
- Electrophysiology MeSH
- Myocardial Contraction physiology MeSH
- Chick Embryo MeSH
- Myocardium cytology MeSH
- Atrioventricular Node physiology MeSH
- Sinoatrial Node physiology MeSH
- Heart Conduction System cytology physiology MeSH
- Atrial Function physiology MeSH
- Heart Atria cytology embryology MeSH
- Animals MeSH
- Check Tag
- Chick Embryo MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Research Support, N.I.H., Extramural MeSH
To characterize developmental changes in impulse propagation within atrial musculature, we performed high-speed optical mapping of activation sequence of the developing chick atria using voltage-sensitive dye. The activation maps were correlated with detailed morphological studies using scanning electron microscopy, histology, and whole mount confocal imaging with three-dimensional reconstruction. A preferential pathway appeared during development within the roof of the atria, transmitting the impulse rapidly from the right-sided sinoatrial node to the left atrium. The morphological substrate of this pathway, the bundle of Bachman, apparent from stage 29 onward, was a prominent ridge of pectinate muscles continuous with the terminal crest. Further acceleration of impulse propagation was noted along the ridges formed by the developing pectinate muscles, ramifying from the terminal crest toward the atrioventricular groove. In contrast, when the impulse reached the interatrial septum, slowing was often observed, suggesting that the septum acts as a barrier or sink for electrical current. We conclude that these inhomogeneities in atrial impulse propagation are consistent with existence of a specialized network of fast-conducting tissues. The purpose of these preferential pathways appears to be to assure synchronous atrial activation and contraction rather than rapid impulse conduction between the sinoatrial and atrioventricular nodes.
References provided by Crossref.org
Low incidence of atrial septal defects in nonmammalian vertebrates
Erbb2 is required for cardiac atrial electrical activity during development
Embryogenesis of the heart muscle