Vladimir Matchkov

A characterization of the electrophysiological properties of the cardiomyocytes from ventricle, atrium and sinus venosus of the snake heart.

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A characterization of the electrophysiological properties of the cardiomyocytes from ventricle, atrium and sinus venosus of the snake heart. / Abramochkin, Denis; Matchkov, Vladimir; Wang, Tobias.

In: Journal of Comparative Physiology B: Biochemical, Systems, and Environmental Physiology, Vol. 190, No. 1, 01.2020, p. 63-73.

Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaperJournal articleResearchpeer-review

Harvard

Abramochkin, D, Matchkov, V & Wang, T 2020, 'A characterization of the electrophysiological properties of the cardiomyocytes from ventricle, atrium and sinus venosus of the snake heart.', Journal of Comparative Physiology B: Biochemical, Systems, and Environmental Physiology, vol. 190, no. 1, pp. 63-73. https://doi.org/10.1007/s00360-019-01253-5

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Abramochkin D, Matchkov V, Wang T. A characterization of the electrophysiological properties of the cardiomyocytes from ventricle, atrium and sinus venosus of the snake heart. Journal of Comparative Physiology B: Biochemical, Systems, and Environmental Physiology. 2020 Jan;190(1):63-73. Epub 2019. doi: 10.1007/s00360-019-01253-5

Author

Abramochkin, Denis ; Matchkov, Vladimir ; Wang, Tobias. / A characterization of the electrophysiological properties of the cardiomyocytes from ventricle, atrium and sinus venosus of the snake heart. In: Journal of Comparative Physiology B: Biochemical, Systems, and Environmental Physiology. 2020 ; Vol. 190, No. 1. pp. 63-73.

Bibtex

@article{a657a7ea2f784262bbef31d4c4a22200,
title = "A characterization of the electrophysiological properties of the cardiomyocytes from ventricle, atrium and sinus venosus of the snake heart.",
abstract = "A detailed description of the electrophysiological features of cardiomyocytes in the various contractile chambers of the vertebrate heart is essential to understand the evolution of cardiac electrical activity, yet very little is known about reptiles. The present study characterizes major ionic currents (I Na, I CaL, I Kr, I K1 and I KACh) and action potential (AP) configuration in cardiomyocytes from the ventricle, the right atrium and the sinus venosus (SV) of Burmese pythons (Python molurus) using sharp microelectrode and patch clamp recordings. Special attention was given to SV, since it consists of myocardial cells and appears to contribute to right atrial filling in snakes. We demonstrate that most of the SV in pythons has a stable resting potential of − 82.3 ± 2.6 mV (n = 9) and lacks pacemaker activity. AP duration at 50% repolarization was similar in cells from SV and atria (350.2 ± 8.7 and 330.4 ± 17.2 ms, respectively; n = 7), but shorter than ventricular APs (557.6 ± 19.2 ms, n = 5) at 30 °C. The densities of ionic currents, however, differed substantially between atrial and SV cells, where the latter had much lower densities of I Na, I CaL and I Kr than atrial and ventricular myocytes. I K1 in ventricle was ninefold greater than in atrial cells and 23-fold greater than in myocytes from SV. However, I KACh was absent in ventricular cells, while it was equally large in atrial and SV myocytes. Consistent with this observation, APs of atrium and SV, but not ventricle, were greatly shortened upon addition of acetylcholine (10 −6 M). Thus, snake SV, right atrium and ventricle have distinct patterns of ionic currents, but the resulting electrical activity is similar in atrium and SV. ",
keywords = "Acetylcholine, Action potential, Heart, Ionic current, Pacemaker, Python molurus, Reptile, Sinus venosus",
author = "Denis Abramochkin and Vladimir Matchkov and Tobias Wang",
year = "2020",
month = jan,
doi = "10.1007/s00360-019-01253-5",
language = "English",
volume = "190",
pages = "63--73",
journal = "Journal of Comparative Physiology B: Biochemical, Systems, and Environmental Physiology",
issn = "0174-1578",
publisher = "Springer",
number = "1",

}

RIS

TY - JOUR

T1 - A characterization of the electrophysiological properties of the cardiomyocytes from ventricle, atrium and sinus venosus of the snake heart.

AU - Abramochkin, Denis

AU - Matchkov, Vladimir

AU - Wang, Tobias

PY - 2020/1

Y1 - 2020/1

N2 - A detailed description of the electrophysiological features of cardiomyocytes in the various contractile chambers of the vertebrate heart is essential to understand the evolution of cardiac electrical activity, yet very little is known about reptiles. The present study characterizes major ionic currents (I Na, I CaL, I Kr, I K1 and I KACh) and action potential (AP) configuration in cardiomyocytes from the ventricle, the right atrium and the sinus venosus (SV) of Burmese pythons (Python molurus) using sharp microelectrode and patch clamp recordings. Special attention was given to SV, since it consists of myocardial cells and appears to contribute to right atrial filling in snakes. We demonstrate that most of the SV in pythons has a stable resting potential of − 82.3 ± 2.6 mV (n = 9) and lacks pacemaker activity. AP duration at 50% repolarization was similar in cells from SV and atria (350.2 ± 8.7 and 330.4 ± 17.2 ms, respectively; n = 7), but shorter than ventricular APs (557.6 ± 19.2 ms, n = 5) at 30 °C. The densities of ionic currents, however, differed substantially between atrial and SV cells, where the latter had much lower densities of I Na, I CaL and I Kr than atrial and ventricular myocytes. I K1 in ventricle was ninefold greater than in atrial cells and 23-fold greater than in myocytes from SV. However, I KACh was absent in ventricular cells, while it was equally large in atrial and SV myocytes. Consistent with this observation, APs of atrium and SV, but not ventricle, were greatly shortened upon addition of acetylcholine (10 −6 M). Thus, snake SV, right atrium and ventricle have distinct patterns of ionic currents, but the resulting electrical activity is similar in atrium and SV.

AB - A detailed description of the electrophysiological features of cardiomyocytes in the various contractile chambers of the vertebrate heart is essential to understand the evolution of cardiac electrical activity, yet very little is known about reptiles. The present study characterizes major ionic currents (I Na, I CaL, I Kr, I K1 and I KACh) and action potential (AP) configuration in cardiomyocytes from the ventricle, the right atrium and the sinus venosus (SV) of Burmese pythons (Python molurus) using sharp microelectrode and patch clamp recordings. Special attention was given to SV, since it consists of myocardial cells and appears to contribute to right atrial filling in snakes. We demonstrate that most of the SV in pythons has a stable resting potential of − 82.3 ± 2.6 mV (n = 9) and lacks pacemaker activity. AP duration at 50% repolarization was similar in cells from SV and atria (350.2 ± 8.7 and 330.4 ± 17.2 ms, respectively; n = 7), but shorter than ventricular APs (557.6 ± 19.2 ms, n = 5) at 30 °C. The densities of ionic currents, however, differed substantially between atrial and SV cells, where the latter had much lower densities of I Na, I CaL and I Kr than atrial and ventricular myocytes. I K1 in ventricle was ninefold greater than in atrial cells and 23-fold greater than in myocytes from SV. However, I KACh was absent in ventricular cells, while it was equally large in atrial and SV myocytes. Consistent with this observation, APs of atrium and SV, but not ventricle, were greatly shortened upon addition of acetylcholine (10 −6 M). Thus, snake SV, right atrium and ventricle have distinct patterns of ionic currents, but the resulting electrical activity is similar in atrium and SV.

KW - Acetylcholine

KW - Action potential

KW - Heart

KW - Ionic current

KW - Pacemaker

KW - Python molurus

KW - Reptile

KW - Sinus venosus

U2 - 10.1007/s00360-019-01253-5

DO - 10.1007/s00360-019-01253-5

M3 - Journal article

C2 - 31853628

VL - 190

SP - 63

EP - 73

JO - Journal of Comparative Physiology B: Biochemical, Systems, and Environmental Physiology

JF - Journal of Comparative Physiology B: Biochemical, Systems, and Environmental Physiology

SN - 0174-1578

IS - 1

ER -