Yi-Cheng FU, Yu ZHANG, Liu-Yang TIAN, Nan LI, Xi CHEN, Zhong-Qi CAI, Chao ZHU, Yang LI. Effects of allocryptopine on outward potassium current and slow delayed rec-tifier potassium current in rabbit myocardium[J]. Journal of Geriatric Cardiology, 2016, 13(4): 316-325. DOI: 10.11909/j.issn.1671-5411.2016.04.008
Citation: Yi-Cheng FU, Yu ZHANG, Liu-Yang TIAN, Nan LI, Xi CHEN, Zhong-Qi CAI, Chao ZHU, Yang LI. Effects of allocryptopine on outward potassium current and slow delayed rec-tifier potassium current in rabbit myocardium[J]. Journal of Geriatric Cardiology, 2016, 13(4): 316-325. DOI: 10.11909/j.issn.1671-5411.2016.04.008

Effects of allocryptopine on outward potassium current and slow delayed rec-tifier potassium current in rabbit myocardium

  • Objective Allocryptopine (ALL) is an effective alkaloid of Corydalis decumbens (Thunb.) Pers. Papaveraceae and has proved to be anti-arrhythmic. The purpose of our study is to investigate the effects of ALL on transmural repolarizing ionic ingredients of outward potassium current (Ito) and slow delayed rectifier potassium current (IKs). Methods The monophasic action potential (MAP) technique was used to record the MAP duration of the epicardium (Epi), myocardium (M) and endocardium (Endo) of the rabbit heart and the whole cell patch clamp was used to record Ito and IKs in cardiomyocytes of Epi, M and Endo layers that were isolated from rabbit ventricles. Results The effects of ALL on MAP of Epi, M and Endo layers were disequilibrium. ALL could effectively reduce the transmural dispersion of repolarization (TDR) in rabbit transmural ventricular wall. ALL decreased the current densities of Ito and IKs in a voltage and concentration dependent way and narrowed the repolarizing differences among three layers. The analysis of gating kinetics showed ALL accelerated the channel activation of Ito in M layers and partly inhibit the channel openings of Ito in Epi, M and Endo cells. On the other hand, ALL mainly slowed channel deactivation of IKs channel in Epi and Endo layers without affecting its activation. Conclusions Our study gives partially explanation about the mechanisms of transmural inhibition of Ito and IKs channels by ALL in rabbit myocardium. These findings provide novel perspective regarding the anti-arrhythmogenesis application of ALL in clinical settings.
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