Henning B, Zehender M, Meinertz T, Just H
Department of Cardiology, University of Freiburg, F.R.G.
Basic Res Cardiol. 1988 Mar-Apr;83(2):176-89. doi: 10.1007/BF01907272.
The effect of tetrodotoxin (TTX), lidocaine, and quinidine on the transient inward current (TI) was studied in voltage-clamped sheep cardiac Purkinje fibres. The TI was induced by elevation of extracellular Ca or addition of strophanthidin. Reduction of external Na had a biphasic effect on the steady state TI magnitude; a moderate (less than 50%) reduction of external Na had an enhancing effect on the TI; a further decrease of extracellular Na was accompanied by a decline of TI amplitude. The TI could not be induced in Na-free medium (external Ca less than or equal to 9.0 mM). TTX, lidocaine, and quinidine reduced the magnitude of the TI in a dose-dependent way. The blocking effect of these agents could be compensated for by a moderate (less than 50%) reduction of external Na or an elevation of extracellular Ca. It is suggested that the blocking effect of TTX, lidocaine, and quinidine on the TI is due to a reduction of intracellular Na, which causes a decay of intracellular Ca via the Na-Ca exchange mechanism.
在电压钳制的绵羊心脏浦肯野纤维中研究了河豚毒素(TTX)、利多卡因和奎尼丁对瞬时内向电流(TI)的影响。TI由细胞外钙升高或毒毛花苷的添加诱导产生。细胞外钠的减少对稳态TI幅度有双相作用;细胞外钠适度(小于50%)减少对TI有增强作用;细胞外钠进一步减少伴随着TI幅度下降。在无钠培养基(细胞外钙小于或等于9.0 mM)中不能诱导出TI。TTX、利多卡因和奎尼丁以剂量依赖方式降低TI幅度。这些药物的阻断作用可通过细胞外钠适度(小于50%)减少或细胞外钙升高来代偿。提示TTX、利多卡因和奎尼丁对TI的阻断作用是由于细胞内钠减少,通过钠-钙交换机制导致细胞内钙衰减。