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Updated: Jun 12, 2026

Imaging Cleared Embryonic and Postnatal Hearts at Single-cell Resolution
07:30

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Published on: October 7, 2016

Atrioventricular conduction and arrhythmias at the initiation of beating in embryonic mouse hearts

Fuhua Chen1, Carlos De Diego, Marvin G Chang

  • 1UCLA Cardiovascular Research Laboratory, David Geffen School of Medicine, University of California-Los Angeles, 675 Charles Young Drive South, Los Angeles, CA 90095, USA.

Developmental Dynamics : an Official Publication of the American Association of Anatomists
|June 16, 2010
PubMed

To investigate cardiac physiology at the onset of heart beating in embryonic mouse hearts, we performed optical imaging of membrane potential (Vm) and/or intracellular calcium (Ca(i)). Action potentials and Ca(i) transients were detected in approximately 50% of mouse embryo hearts at E8.5, but in all hearts at E9.0, indicating that beating typically starts between E8-E9. Beating was eliminated by Ca channel blocker nifedipine and the I(f) blocker ZD7288, unaffected by tetrodotoxin and only mildly depressed by disabling sarcoplasmic (SR) and endoplasmic (ER) reticulum Ca cycling. From E8.5 to E10, conduction velocity increased from 0.2-1 mm/s to >5 mm/s in first ventricular and then atrial tissue, while remaining slow in other areas. Arrhythmias included atrioventricular reentry induced by adenosine. In summary, at the onset of beating, I(f)-dependent pacemaking drives both AP propagation and Ca(i) transient generation through activation of voltage-dependent Ca channels. Na channels and intracellular Ca cycling have minor roles.

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