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How to obtain physiologically relevant cardiovascular data with students using chick embryo ventricular cardiomyocytes
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Laura F. Corns ,
James L. Rouse ,
Aidan Seeley
Advances in Physiology Education, Volume: 49, Issue: 4, Pages: 1026 - 1033
Swansea University Author:
Aidan Seeley
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DOI (Published version): 10.1152/advan.00215.2024
Abstract
The chick embryo ventricular cardiomyocyte model provides students easy access to experiments involving fundamental features of cardiac cell physiology and pharmacology. With standard physiology teaching laboratories and basic cell culture equipment, spontaneously beating colonies of electrically co...
| Published in: | Advances in Physiology Education |
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| ISSN: | 1043-4046 1522-1229 |
| Published: |
American Physiological Society
2025
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| Online Access: |
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| URI: | https://cronfa.swan.ac.uk/Record/cronfa70333 |
| Abstract: |
The chick embryo ventricular cardiomyocyte model provides students easy access to experiments involving fundamental features of cardiac cell physiology and pharmacology. With standard physiology teaching laboratories and basic cell culture equipment, spontaneously beating colonies of electrically connected cardiomyocytes can be obtained by the students themselves. Students learn aseptic techniques and cell culture alongside experiments illustrating, at the simplest level of experimentation, how beating rate can be altered physiologically or pharmacologically. In the typical course of the type of experiments presented here, students first observe the effect of temperature (beating rates decline to a third going from 37°C to room temperature; e.g., to 40 from 130 beats/min) and media change (beating rates increase up to 50%) before moving on to the pharmacological characterization of various receptors in these cells. Most obviously, in the cardiac cell context, this involves drugs acting on β-adrenoceptor subtypes. Students can obtain predictable dose-dependent increases in beating rates (up to maximal 100% increases in beating rate; from ∼100 to 200 beats/min typically) with the addition of stimulatory β-adrenoceptor agonists (e.g., isoproterenol) but also observe dose-dependent decreases in beating rate with β3-adrenoceptor agonists (reducing beating rate by up to a third). Consequently, “classical” log dose-response curves can be obtained in the “real world,” enhancing student understanding of fundamental mechanisms of drug action. Although these experiments focus on physiological and pharmacological techniques, the model can be extended to encompass biochemical or molecular biological studies in terms of intracellular signaling systems activated and protein expression patterns. |
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| Keywords: |
chick embryo cardiomyocytes; humane experimental technique; partial replacement; 3Rs |
| College: |
Faculty of Medicine, Health and Life Sciences |
| Issue: |
4 |
| Start Page: |
1026 |
| End Page: |
1033 |