Gisbert M P, Mery P F, Fischmeister R
Laboratory of Cardiac Cellular Physiology, INSERM U-241, Paris-Sud University, Orsay, France.
Drugs Exp Clin Res. 1988;14(2-3):109-15.
The effects of extracellular application of cicletanine on the voltage-sensitive calcium current (ICa) was studied in isolated cells from frog ventricle. Myocytes were isolated by enzymatic dissociation and ICa was measured using the whole-cell configuration of the patch-clamp technique modified to permit intracellular perfusion with various substances. Cicletanine (10 to 100 microM) had no effect on control ICa. However, when ICa was enhanced by superfusion of the cell with saturating doses of beta-adrenergic agonist (isoprenaline, 2 microM) or by intracellular perfusion with maximal doses of cAMP (20 microM), cicletanine exerted a dual effect on ICa. At 10 microM, cicletanine generally induced a transient or sustained stimulation of ICa (5 to 40%), while 100 microM of the drug generally reduced ICa. The effects of cicletanine were reversible and not voltage-dependent. These results suggest that cicletanine affects ICa by acting on a mechanism occurring after cAMP synthesis, by enhancing cAMP concentration (e.g. through an inhibition of cAMP phosphodiesterase) or facilitating cAMP-dependent phosphorylation of the Ca channels.
研究了细胞外应用西氯他宁对蛙心室分离细胞电压敏感性钙电流(ICa)的影响。通过酶解分离心肌细胞,并使用膜片钳技术的全细胞模式测量ICa,该模式经过改良以允许用各种物质进行细胞内灌注。西氯他宁(10至100微摩尔)对对照ICa无影响。然而,当通过用饱和剂量的β-肾上腺素能激动剂(异丙肾上腺素,2微摩尔)对细胞进行灌流或通过用最大剂量的cAMP(20微摩尔)进行细胞内灌注来增强ICa时,西氯他宁对ICa产生双重作用。在10微摩尔时,西氯他宁通常会引起ICa的短暂或持续刺激(5%至40%),而100微摩尔的该药物通常会降低ICa。西氯他宁的作用是可逆的,且不依赖电压。这些结果表明,西氯他宁可通过作用于cAMP合成后的机制来影响ICa,即通过提高cAMP浓度(例如通过抑制cAMP磷酸二酯酶)或促进钙通道的cAMP依赖性磷酸化。