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Changes in Membrane Properties of Chick Embryonic Hearts during Development
Open accessAbstract
The electrophysiological properties of embryonic chick hearts (ventricles) change during development; the largest changes occur between days 2 and 8. Resting potential (Em) and peak overshoot potential (+Emax) increase, respectively, from -35 mv and +11 mv at day 2 to -70 mv and +28 mv at days 12–21. Action potential duration does not change significantly. Maximum rate of rise of the action potential (+Vmax) increases from about 20 v/sec at days 2–3 to 150 v/sec at days 18–21; + Vmax of young cells is not greatly increased by applied hyperpolarizing current pulses. In resting Em vs. log [K+]o curves, the slope at high K+ is lower in young hearts (e.g. 30 mv/decade) than the 50–60 mv/decade obtained in old hearts, but the extrapolated [K+]i values (125–140 mM) are almost as high. Input resistance is much higher in young hearts (13 MΩ at day 2 vs. 4.5 MΩ at days 8–21), suggesting that the membrane resistivity (Rm) is higher. The ratio of permeabilities, PNa/PK, is high (about 0.2) in young hearts, due to a low PK, and decreases during ontogeny (to about 0.05). The low K+ conductance (gK) in young hearts accounts for the greater incidence of hyperpolarizing afterpotentials and pacemaker potentials, the lower sensitivity (with respect to loss of excitability) to elevation of [K+]o, and the higher chronaxie. Acetylcholine does not increase gK of young or old ventricular cells. The increase in (Na+, K+)-adenosine triphosphatase (ATPase) activity during development tends to compensate for the increase in gK. +Emax and + Vmax are dependent on [Na+]o in both young and old hearts. However, the Na+ channels in young hearts (2–4 days) are slow, tetrodotoxin (TTX)-insensitive, and activated-inactivated at lower Em. In contrast, the Na+ channels of cells in older hearts (> 8 days) are fast and TTX-sensitive, but they revert back to slow channels when placed in culture.
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Cited by
He, J.-Q., Ma, Y., Lee, Y., Thomson, J. A., & Kamp, T. J. (2003) · Circulation Research · doi:10.1161/01.res.0000080317.92718.99 · Cited by 800
Mechanism of spontaneous excitability in human embryonic stem cell derived cardiomyocytes
Satin, J., Kehat, I., Caspi, O., Huber, I., Arbel, G., Itzhaki, I., Magyar, J., Schroder, E. A., Perlman, I., & Gepstein, L. (2004) · The Journal of Physiology · doi:10.1113/jphysiol.2004.068213 · Cited by 283
Contact inhibition of division: Involvement of the electrical transmembrane potential
Cone, C. D., & Tongier, M. (1973) · Journal of Cellular Physiology · doi:10.1002/jcp.1040820307 · Cited by 123
Metadata
- Authors
- Sperelakis, N., & Shigenobu, K.
- Venue
- The Journal of General Physiology
- Publisher
- Rockefeller University Press
- Published
- 1972-10-01
- Volume
- 60
- Issue
- 4
- Pages
- 430-453
- ISSN
- 0022-1295 (ISSN-L)
- 1540-7748
- OpenAlex
- W2039530429
- Cited by
- 168
- References
- 0
- FWCI
- 12.98
- Type
- journal article
- Language
- en
- Open access
- bronze
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