Kohlhardt M, Kübler M
Naunyn Schmiedebergs Arch Pharmacol. 1975;290(2-3):265-74. doi: 10.1007/BF00510555.
The effect of metabolic alterations of isolated trabeculae and papillary muscles of cats upon the transmembrane slow inward current was studied in voltage clamp experiments using the double sucrose gap technique. The slow inward current which is mainly carried by Ca ions was separated from the fast Na current by applying the conditioning clamp technique. 1. After inhibition of the oxidative phosphorylation of the myocardial cell caused by cyanide (100 mg/l), the transmembrane slow inward current decreased by 25% on average within 25 min. The same diminution appeared after poisoning with 2.4 dinitrophenol (40 mg/l) which amounted to 46% on an average. In both cases the extrapolated reversal potential of the slow inward current was shifted to less positive values. The reduction of the slow inward current seems to reflect a diminished Ca driving force due to a metabolically evoked increase in intracellular free Ca. But these metabolic inhibitors might exert some direct effects upon the membrane since after the treatment with cyanide and 2.4 dinitrophenol, respectively, a slight delay of current inactivation could be observed. Nevertheless, the kinetics of the recovery from inactivation remained unaffected. 2. Metabolic poisoning abolished the normal response of the slow inward current to an increase of the extracellular Ca concentration or to the addition of Sr ions. Excess Ca failed to augment the current, and in some cases even a slight diminution occurred. If at all 5.5 mM Sr caused an increase by not more than 20%. These unusual reactions may also result from a reduced driving force for Ca or Sr, respectively. 3. Catecholamines still exerted their promoting effects upon the slow inward current after poisoning with cyanide or 2,4 dinitrophenol. The addition of 5 mg/l isoproterenol not only neutralized the effect of these metabolic inhibitors but caused an increase of the slow inward current even surpassing the initial control values.
采用双蔗糖间隙技术,在电压钳实验中研究了猫离体小梁和乳头肌代谢改变对跨膜缓慢内向电流的影响。通过应用条件钳技术,将主要由钙离子携带的缓慢内向电流与快速钠电流分离。1. 在用氰化物(100mg/l)抑制心肌细胞的氧化磷酸化后,跨膜缓慢内向电流在25分钟内平均下降了25%。在用2,4-二硝基苯酚(40mg/l)中毒后也出现了同样的减少,平均减少量为46%。在这两种情况下,缓慢内向电流的外推反转电位都向较不正值的方向移动。缓慢内向电流的减少似乎反映了由于代谢引起的细胞内游离钙增加导致的钙驱动力减弱。但这些代谢抑制剂可能对膜有一些直接作用,因为在用氰化物和2,4-二硝基苯酚处理后,分别观察到电流失活有轻微延迟。然而,失活恢复的动力学不受影响。2. 代谢中毒消除了缓慢内向电流对细胞外钙浓度增加或添加锶离子的正常反应。过量的钙未能增强电流,在某些情况下甚至出现轻微减少。如果有作用,5.5mM的锶引起的增加不超过20%。这些异常反应也可能分别是由于钙或锶的驱动力降低所致。3. 在用氰化物或2,4-二硝基苯酚中毒后,儿茶酚胺仍对缓慢内向电流发挥其促进作用。添加5mg/l异丙肾上腺素不仅抵消了这些代谢抑制剂的作用,甚至使缓慢内向电流增加超过初始对照值。