Loading…

In-vitro recording of adult zebrafish heart electrocardiogram — A platform for pharmacological testing

Recently zebrafish has become a powerful vertebrate model system for cardiac arrhythmia and another advantage is that the heart could be rapidly excised for in-vitro electrophysiological recording. We made direct in-vitro recordings of adult zebrafish heart ECG using the microelectrode and tested th...

Full description

Saved in:
Bibliographic Details
Published in:Clinica chimica acta 2011-10, Vol.412 (21), p.1963-1967
Main Authors: Tsai, Chia-Ti, Wu, Cho-Kai, Chiang, Fu-Tien, Tseng, Chuen-Den, Lee, Jen-Kuang, Yu, Chih-Chieh, Wang, Yi-Chih, Lai, Ling-Ping, Lin, Jiunn-Lee, Hwang, Juey-Jen
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:Recently zebrafish has become a powerful vertebrate model system for cardiac arrhythmia and another advantage is that the heart could be rapidly excised for in-vitro electrophysiological recording. We made direct in-vitro recordings of adult zebrafish heart ECG using the microelectrode and tested the effects of various drugs on zebrafish heart ECG. The QT interval change in the ECG was verified by optically mapped action potential duration (APD). The mean in-vitro heart rate (HR) of the adult zebrafish was 118 ± 22 beats/min. The mean QT interval was 312 ± 36 ms and mean HR corrected QT interval (QTc) 439 ± 39 ms. The mean optically mapped APD was 308 ± 30 ms, which was close to the QT interval in ECG (p = 0.815). We found that sympathomimetic drug isoproterenol increased HR, whereas L-type calcium channel blocker verapamil decreased HR. Sodium channel blocker quinidine and L-type calcium channel activator BayK8644 prolonged QTc interval in a dose-dependent manner (515 ± 24 ms and 519 ± 27 ms, respectively, both p < 0.01). The APD was also prolonged accordingly. Both rapidly and slowly activating delayed rectifier potassium channel (IKr and IKs) blockers E4031 and chromanol 293B, respectively, also prolonged QTc interval in a dose-dependent manner (523 ± 25 ms and 529 ± 27 ms, respectively, both p < 0.01). Quinidine, E4031 and chromanol 293B also decreased HR. Direct in-vitro recording of adult zebrafish heart is an efficient platform for test of drugs which exert electrophysiological effects on cardiomyocytes, and perturbation of ionic channels that are responsible for human long QT syndrome also modulates QT interval in adult zebrafish heart. ► Direct in-vitro recording of adult zebrafish heart is easy to perform. ► It is an efficient platform for test of drugs with anti-arrhythmic properties. ► Drugs that prolong mammalian QT intervals also prolong zebrafish QT intervals.
ISSN:0009-8981
1873-3492
DOI:10.1016/j.cca.2011.07.002