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Changes in Membrane Properties of Chick Embryonic Hearts during Development

The electrophysiological properties of embryonic chick hearts (ventricles) change during development; the largest changes occur between days 2 and 8. Resting potential (E(m)) and peak overshoot potential (+E (max)) increase, respectively, from -35 mv and +11 mv at day 2 to -70 mv and +28 mv at days...

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Detalles Bibliográficos
Autores principales: Sperelakis, Nick, Shigenobu, K.
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1972
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2226086/
https://www.ncbi.nlm.nih.gov/pubmed/4263008
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author Sperelakis, Nick
Shigenobu, K.
author_facet Sperelakis, Nick
Shigenobu, K.
author_sort Sperelakis, Nick
collection PubMed
description The electrophysiological properties of embryonic chick hearts (ventricles) change during development; the largest changes occur between days 2 and 8. Resting potential (E(m)) and peak overshoot potential (+E (max)) 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 (+V (max)) increases from about 20 v/sec at days 2–3 to 150 v/sec at days 18–21; + V (max) of young cells is not greatly increased by applied hyperpolarizing current pulses. In resting E(m) 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 (R(m)) is higher. The ratio of permeabilities, P (Na)/P (K), is high (about 0.2) in young hearts, due to a low P (K), and decreases during ontogeny (to about 0.05). The low K(+) conductance (g (K)) 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 g (K) of young or old ventricular cells. The increase in (Na(+), K(+))-adenosine triphosphatase (ATPase) activity during development tends to compensate for the increase in g (K). +E (max) and + V (max) 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 E(m). 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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spelling pubmed-22260862008-04-23 Changes in Membrane Properties of Chick Embryonic Hearts during Development Sperelakis, Nick Shigenobu, K. J Gen Physiol Article The electrophysiological properties of embryonic chick hearts (ventricles) change during development; the largest changes occur between days 2 and 8. Resting potential (E(m)) and peak overshoot potential (+E (max)) 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 (+V (max)) increases from about 20 v/sec at days 2–3 to 150 v/sec at days 18–21; + V (max) of young cells is not greatly increased by applied hyperpolarizing current pulses. In resting E(m) 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 (R(m)) is higher. The ratio of permeabilities, P (Na)/P (K), is high (about 0.2) in young hearts, due to a low P (K), and decreases during ontogeny (to about 0.05). The low K(+) conductance (g (K)) 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 g (K) of young or old ventricular cells. The increase in (Na(+), K(+))-adenosine triphosphatase (ATPase) activity during development tends to compensate for the increase in g (K). +E (max) and + V (max) 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 E(m). 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. The Rockefeller University Press 1972-10-01 /pmc/articles/PMC2226086/ /pubmed/4263008 Text en Copyright © 1972 by The Rockefeller University Press This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Article
Sperelakis, Nick
Shigenobu, K.
Changes in Membrane Properties of Chick Embryonic Hearts during Development
title Changes in Membrane Properties of Chick Embryonic Hearts during Development
title_full Changes in Membrane Properties of Chick Embryonic Hearts during Development
title_fullStr Changes in Membrane Properties of Chick Embryonic Hearts during Development
title_full_unstemmed Changes in Membrane Properties of Chick Embryonic Hearts during Development
title_short Changes in Membrane Properties of Chick Embryonic Hearts during Development
title_sort changes in membrane properties of chick embryonic hearts during development
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2226086/
https://www.ncbi.nlm.nih.gov/pubmed/4263008
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