Bányász T, Magyar J, Varró A, Kovács A, Gyönös I, Szénási G, Nánási P P
Department of Physiology, University Medical School of Debrecen, Hungary.
Gen Pharmacol. 1999 Mar;32(3):329-33. doi: 10.1016/s0306-3623(98)00197-9.
EGIS-7229 is a novel antiarrhythmic candidate having multiple mechanisms of action with class III predominance. In this study, the effects of EGIS-7229 and sotalol on action potential duration (APD) and incidence of early afterdepolarizations (EADs) were studied and compared in rabbit papillary muscle by using conventional microelectrode techniques. In control bathing solution, both drugs increased APD in a concentration-dependent manner; however, the prolongation of APD was greater with sotalol than with EGIS-7229 when the same drug concentrations were compared. EAD developed in 3 of the 11 preparations (27%) bathed with a solution containing 3.6 mmol/l CsCl + 2 mmol/l KCl within the first 120 min of superfusion. The addition of 100 micromol/l sotalol to this superfusate increased the incidence of EAD to 83% (10 from 12), whereas the addition of the same concentration of EGIS-7229 prevented the development of EAD in all of the 9 preparations studied. These differences in incidence of EAD are likely attributable to differences in drug-induced increases of APD-50 in the presence of CsCl. Prolongation of APD-90 showed less correlation with incidence of EAD than changes in APD-50. On the basis of these in vitro results, high concentrations of EGIS-7229 cannot be expected to be torsadogenic in vivo--in contrast with sotalol--presumably owing to the combined class III + IV activity of the compound.
EGIS-7229是一种新型抗心律失常候选药物,具有多种作用机制,以III类为主。在本研究中,采用传统微电极技术,研究并比较了EGIS-7229和索他洛尔对兔乳头肌动作电位时程(APD)和早期后除极(EAD)发生率的影响。在对照浴液中,两种药物均以浓度依赖性方式增加APD;然而,当比较相同药物浓度时,索他洛尔对APD的延长作用比EGIS-7229更大。在灌注的最初120分钟内,11个标本中有3个(27%)在含有3.6 mmol/l CsCl + 2 mmol/l KCl的溶液中浸泡时出现了EAD。向该灌流液中加入100 μmol/l索他洛尔可使EAD发生率增加至83%(12个中有10个),而加入相同浓度的EGIS-7229可防止所有9个研究标本中EAD的发生。EAD发生率的这些差异可能归因于在CsCl存在下药物诱导的APD-50增加的差异。APD-90的延长与EAD发生率的相关性低于APD-50的变化。基于这些体外结果,与索他洛尔相反,高浓度的EGIS-7229在体内预计不会致尖端扭转型室速,这可能是由于该化合物具有III类和IV类联合活性。