摘要
用常规玻璃微电极技术,观察3,6-(二甲氨基)-二苯骈碘杂环依地酸盐(IHC-72)对豚鼠右000室乳头肌细胞膜部分除极引发的慢反应动作电位(SAP)、哇巴因引发的延迟后除极(DAD)及触发活动(TA)的影响。2.54μMIHC-72对SAP各参数均无影响;25.4,101.6μMIHC-72分别使动作电位幅值(APA)减少7.4%和19.3%,0相最大上升速率(V_(max))减少2.5%和39.1%,复极100%的动作电位时程(APD_(100))缩短7.1%和41%。有效不应期(ERP)相对延长4.9%和9l.3%,静息膜电位(RMP)不受影响。浓度为25.4μMIHC-72对复极50%的动作电位时程(APD_(50))无影响,而浓度为101.6μM时能使APD_(50)缩短42.9%,且能抑制由哇巴因诱发的DAD及TA。结果表明:IHC-72对慢钙内流有直接抑制作用;其抑制触发性心律失常的机理与钙拮抗有关。
Standard microelectrode technique was used to study the effects of 3,6-dimethylamino-dibenzopyriodonium edetate(IHC-72)on the slow response action potential(SAP)by partial depolarization,ouabain-induced delayed afterde polarization(DAD)and triggered activity(TA)of isolated guinea pig right ventricular papillary muscles.2.54μMIHC 72 did not affect the parameters of SAP.25.4,101.6μM IHC-72 decreased action potential amplitude(APA)by 7.4% and 19.3%,maximum upstroke velocity(Vmax) by 2.5%and 39.1%,action potential duration at 100%repolarization(APD100) by 7.1%and 41%,The effective refractory period (ERP) was relatively prolonged by 4.9%and 91.3%,and the resting membrane potential(RMP)was not influenced. 25.4 μM IHC-72 did not affect action potential duration at 50%repolarization(APD50),but l01. 6 μMIHC-72 shortened APD50 by 42.9%and inhibited ouabain-induced DAD and TA. It indicates that IHC-72 has a direct inhibitory effect on slow calcium inward current and can inhibit triggered arrhythmia.
关键词
乳头肌
延迟后除极
IHC-72
碘杂环化合物
Dimethylamino-dibenzopyrhdonium edetate Papillary muscle Slow response action potential Delayed afterdepolarization Triggered activity