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Published on: December 11, 2017
Low-dose carvedilol reduces transmural heterogeneity of ventricular repolarization in congestive heart failure
Jiang-hua Zhong1, Xiao-pan Chen, Mei-ling Yun
1Department of Cardiology, Affiliated Hospital of Hainan Medical College, Haikou, China.
Insights
Carvedilol treatment reduced transmural heterogeneity of ventricular repolarization in rabbits with congestive heart failure (CHF). This effect in CHF rabbits may stem from carvedilol's direct electrophysiological properties.
Area of Science:
- Cardiology
- Pharmacology
- Electrophysiology
Background:
- Congestive heart failure (CHF) is associated with altered ventricular repolarization.
- Transmural heterogeneity of ventricular repolarization is a key factor in arrhythmogenesis.
Purpose of the Study:
- To investigate the impact of carvedilol on ventricular repolarization heterogeneity in a rabbit model of CHF.
- To determine if carvedilol's effects are linked to its electrophysiological properties or ventricular remodeling.
Main Methods:
- Rabbits were induced with CHF and divided into control, CHF, and carvedilol-treated CHF groups.
- Monophasic action potential duration (MAPD) was measured across three myocardial layers.
- Ventricular fibrillation threshold (VFT) and ventricular remodeling were assessed.
Main Results:
- CHF rabbits exhibited decreased blood pressure, cardiac output, and increased peripheral resistance.
- CHF significantly increased transmural dispersion of repolarization (TDR) and prolonged MAPD, particularly in the midmyocardium.
- Low-dose carvedilol treatment increased VFT and significantly reduced TDR in CHF rabbits, without affecting ventricular remodeling.
Conclusions:
- CHF increases transmural heterogeneity of ventricular repolarization in rabbits.
- Low-dose carvedilol effectively mitigates this heterogeneity in CHF.
- Carvedilol's beneficial electrophysiological effects in CHF appear independent of ventricular remodeling.
Aim:
To study the effects of carvedilol on the transmural heterogeneity of ventricular repolarization in rabbits with congestive heart failure (CHF).
Methods:
Rabbits were randomly divided into 3 groups: control, CHF and carvedilol treated CHF group. Monophasic action potential duration (MAPD) in the 3 myocardial layers was simultaneously recorded.
Results:
All the rabbits in the CHF group had signs of severe CHF. Compared with the control group, the mean blood pressure and cardiac output were significantly decreased, while peripheral resistance was significantly increased in the CHF group. This proved that the CHF model was successful created with adriamycin in this study. Compared to the control group, the ventricular fibrillation threshold (VFT) was remarkably decreased and all MAPD of the 3 myocardial layers were extended in rabbits with CHF. However, the extension of MAPD in the midmyocardium was more obvious. The transmural dispersion of repolarization (TDR) was significantly increased in CHF. Low-dose carvedilol (0.25 mg/kg, twice daily) had no effects on ventricular remodeling. Treatment with low-dose carvedilol significantly increased VFT. Although the MAPD of the 3 myocardial layers were further prolonged in the carvedilol treated CHF group, the prolongation of MAPD in the midmyocardium was shorter than those in the epicardium and endocardium. Treatment with low-dose carvedilol significantly decreased TDR in CHF.
Conclusion:
In the present study, the transmural heterogeneity of ventricular repolarization increased in the rabbits with CHF. Low-dose carvedilol decreased the transmural heterogeneity of ventricular repolarization in CHF, which may be related to its direct electrophysiological property rather than its effect on ventricular remodeling.
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