XING Sha-sha, JIN Si, XU Gao, et al. Effect of Phenolic Alkaloids of on Cardiac Electrophysiology[J]. Chinese journal of experimental traditional medical formulae, 2015, 21(17): 88-91.
DOI:
XING Sha-sha, JIN Si, XU Gao, et al. Effect of Phenolic Alkaloids of on Cardiac Electrophysiology[J]. Chinese journal of experimental traditional medical formulae, 2015, 21(17): 88-91. DOI: 10.13422/j.cnki.syfjx.2015170088.
Effect of Phenolic Alkaloids of on Cardiac Electrophysiology
RPF)和舒张期去极化速度[velocity of diastolic (phase 4) depolarization
VDD]的影响。 结果: 在豚鼠右心室心肌乳头肌细胞中研究发现
PAMD可以剂量依赖性的显著延长APD和ERP
延缓Vmax。当浓度为10 μmol·L-1时
PAMD对窦房结自律性具有轻度影响
这种作用与对照组比有显著差异。 结论: PAMD对心室肌的作用强于其对窦房结的作用
这表明其具有成为理想的抗室性心律失常的药物的潜力。
Abstract
Objective: To study the effect of phenolic alkaloids of Menispermum dauricum (PAMD) on the action potential in papillary muscles of guinea pig and dominant pacemaker cells of rabbit sinoatrial nodes. Method: Capillary grass microelectrode was used to record the paction potential in papillary muscles of guinea pigs
study the effect of different concentrations (1
3
10 μmol·L-1) of PAMD on action potential duration (APD)
effective refractory period (ERP)
maximum upstroke velocity (Vmax)
amplitude (APA) and overshoot (OS). Capillary grass microelectrode was also used to record the paction potential in dominant pacemaker cells of rabbit sinoatrial nodes and study the effect of different concentrations (1
3
10 μmol·L-1) of PAMD on APD
maximal diastolic potential (MDP)
APA
Vmax
rate of pacemaker firing (RPF)
and velocity of diastolic (phase 4) depolarization (VDD). Result: According to the study for papillary muscle cells of right ventricular myocardia
PAMD can significantly prolong APD and ERP and delay Vmax in a concentration-dependent manner. PAMD also had a mild effect on the automatic rhythmicity of sinus nodes at concentration of 10 μmol·L-1
with a significant difference with the control group. Conclusion: PAMD have a stronger effect on ventricular muscles than sinoatrial nodes
suggesting that it has the potential to be prepared into an ideal drug for ventricular arrhythmia.