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. 1988 Apr 1;91(4):573–591. doi: 10.1085/jgp.91.4.573

Functional pacemaking area in the early embryonic chick heart assessed by simultaneous multiple-site optical recording of spontaneous action potentials

PMCID: PMC2216141  PMID: 3392520

Abstract

Pacemaking areas in the early embryonic chick hearts were quantitatively assessed using simultaneous multiple-site optical recordings of spontaneous action potentials. The measuring system with a 10- X 10- or a 12 X 12-element photodiode array had a spatial resolution of 15-30 microns. Spontaneous action potential-related optical signals were recorded simultaneously from multiple contiguous regions in the area in which the pacemaker site was located in seven- to nine-somite embryonic hearts stained with a voltage-sensitive merocyanine-rhodanine dye (NK 2761). In the seven- to early eight- somite embryonic hearts, the location of the pacemaking area is not uniquely determined, and as development proceeds to the nine-somite stage, the pacemaking area becomes confined to the left pre-atrial tissue. Analysis of the simultaneous multiple-site optical recordings showed that the pacemaking area was basically circular in shape in the later eight- to nine-somite embryonic hearts. An elliptical shape also was observed at the seven- to early eight-somite stages of development. The size of the pacemaking area was estimated to be approximately 1,200- 3,000 micron2. We suggest that the pacemaking area is composed of approximately 60-150 cells, and that the pacemaking area remains at a relatively constant size throughout the seven- to nine-somite stages. It is thus proposed that a population of pacemaking cells, rather than a single cell, serves as a rhythm generator in the embryonic chick heart.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Cohen L. B., Salzberg B. M. Optical measurement of membrane potential. Rev Physiol Biochem Pharmacol. 1978;83:35–88. doi: 10.1007/3-540-08907-1_2. [DOI] [PubMed] [Google Scholar]
  2. Fujii S., Hirota A., Kamino K. Optical indications of pace-maker potential and rhythm generation in early embryonic chick heart. J Physiol. 1981 Mar;312:253–263. doi: 10.1113/jphysiol.1981.sp013627. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Fujii S., Hirota A., Kamino K. Optical signals from early embryonic chick heart stained with potential sensitive dyes: evidence for electrical activity. J Physiol. 1980 Jul;304:503–518. doi: 10.1113/jphysiol.1980.sp013339. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Hirota A., Fujii S., Sakai T., Kamino K. Temperature dependence of spontaneous electrical activity in early embryonic heart monitored optically with a potential-sensitive dye. Jpn J Physiol. 1983;33(1):85–100. doi: 10.2170/jjphysiol.33.85. [DOI] [PubMed] [Google Scholar]
  5. Hirota A., Kamino K., Komuro H., Sakai T. Mapping of early development of electrical activity in the embryonic chick heart using multiple-site optical recording. J Physiol. 1987 Feb;383:711–728. doi: 10.1113/jphysiol.1987.sp016437. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Hirota A., Kamino K., Komuro H., Sakai T., Yada T. Early events in development of electrical activity and contraction in embryonic rat heart assessed by optical recording. J Physiol. 1985 Dec;369:209–227. doi: 10.1113/jphysiol.1985.sp015897. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Hirota A., Kamino K., Komuro H., Sakai T., Yada T. Optical studies of excitation-contraction coupling in the early embryonic chick heart. J Physiol. 1985 Sep;366:89–106. doi: 10.1113/jphysiol.1985.sp015786. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Hirota A., Sakai T., Fujii S., Kamino K. Initial development of conduction pattern of spontaneous action potential in early embryonic precontractile chick heart. Dev Biol. 1983 Oct;99(2):517–523. doi: 10.1016/0012-1606(83)90301-9. [DOI] [PubMed] [Google Scholar]
  9. Hiruma T., Hirakow R. An ultrastructural topographical study on myofibrillogenesis in the heart of the chick embryo during pulsation onset period. Anat Embryol (Berl) 1985;172(3):325–329. doi: 10.1007/BF00318980. [DOI] [PubMed] [Google Scholar]
  10. Kamino K., Hirota A., Fujii S. Localization of pacemaking activity in early embryonic heart monitored using voltage-sensitive dye. Nature. 1981 Apr 16;290(5807):595–597. doi: 10.1038/290595a0. [DOI] [PubMed] [Google Scholar]
  11. Komuro H., Hirota A., Yada T., Sakai T., Fujii S., Kamino K. Effects of calcium on electrical propagation in early embryonic precontractile heart as revealed by multiple-site optical recording of action potentials. J Gen Physiol. 1985 Mar;85(3):365–382. doi: 10.1085/jgp.85.3.365. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Manasek F. J. Embryonic development of the heart. I. A light and electron microscopic study of myocardial development in the early chick embryo. J Morphol. 1968 Jul;125(3):329–365. doi: 10.1002/jmor.1051250306. [DOI] [PubMed] [Google Scholar]
  13. Obaid A. L., Orkand R. K., Gainer H., Salzberg B. M. Active calcium responses recorded optically from nerve terminals of the frog neurohypophysis. J Gen Physiol. 1985 Apr;85(4):481–489. doi: 10.1085/jgp.85.4.481. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Orbach H. S., Cohen L. B. Optical monitoring of activity from many areas of the in vitro and in vivo salamander olfactory bulb: a new method for studying functional organization in the vertebrate central nervous system. J Neurosci. 1983 Nov;3(11):2251–2262. doi: 10.1523/JNEUROSCI.03-11-02251.1983. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Sakai T., Hirota A., Fujii S., Kamino K. Flexibility of regional pacemaking priority in early embryonic heart monitored by simultaneous optical recording of action potentials from multiple sites. Jpn J Physiol. 1983;33(3):337–350. doi: 10.2170/jjphysiol.33.337. [DOI] [PubMed] [Google Scholar]
  16. Salzberg B. M., Grinvald A., Cohen L. B., Davila H. V., Ross W. N. Optical recording of neuronal activity in an invertebrate central nervous system: simultaneous monitoring of several neurons. J Neurophysiol. 1977 Nov;40(6):1281–1291. doi: 10.1152/jn.1977.40.6.1281. [DOI] [PubMed] [Google Scholar]
  17. Virágh S., Challice C. E. The development of the early atrioventricular conduction system in the embryonic heart. Can J Physiol Pharmacol. 1983 Aug;61(8):775–792. doi: 10.1139/y83-121. [DOI] [PubMed] [Google Scholar]
  18. Yada T., Sakai T., Komuro H., Hirota A., Kamino K. Development of electrical rhythmic activity in early embryonic cultured chick double-heart monitored optically with a voltage-sensitive dye. Dev Biol. 1985 Aug;110(2):455–466. doi: 10.1016/0012-1606(85)90103-4. [DOI] [PubMed] [Google Scholar]

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