Why the study?
Does Wenxin Keli shorten action potential duration and reduce L-type calcium current in rats with TAC-induced heart failure?
Does Wenxin Keli shorten action potential duration and reduce L-type calcium current in rats with TAC-induced heart failure?
WXKL shortens action potential duration and blocks L-type calcium currents in hypertrophied rat myocytes, providing a potential mechanism for its antiarrhythmic effects in heart failure.
May support antiarrhythmic mechanism of WXKL in HF models; leaves open clinical translation pending human trials.
Objective. We investigated the effects of WXKL on the action potential (AP) and the L-type calcium current (I Ca-L) in normal and hypertrophied myocytes. Methods. Forty male rats were randomly divided into two groups: the control group and the transverse aortic constriction- (TAC-) induced heart failure group. Cardiac hypertrophy was induced by TAC surgery, whereas the control group underwent a sham operation. Eight weeks after surgery, single cardiac ventricular myocytes were isolated from the hearts of the rats. The APs and I Ca-L were recorded using the whole-cell patch clamp technique. Results. The action potential duration (APD) of the TAC group was prolonged compared with the control group and was markedly shortened by WXKL treatment in a dose-dependent manner. The current densities of the I Ca-L in the TAC group treated with 5 g/L WXKL were significantly decreased compared with the TAC group. We also determined the effect of WXKL on the gating mechanism of the I Ca-L in the TAC group. We found that WXKL decreased the I Ca-L by accelerating the inactivation of the channels and delaying the recovery time from inactivation. Conclusions. The results suggest that WXKL affects the AP and blocked the I Ca-L, which ultimately resulted in the treatment of arrhythmias.
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Chen et al. (2013) studied this question.
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