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罗匹尼罗对犬心室肌细胞动作电位特征及相关离子电流的影响。

Effects of ropinirole on action potential characteristics and the underlying ion currents in canine ventricular myocytes.

机构信息

Department of Cardiology, Institute of Medicine, Semmelweis Health Care Center, Miskolc, Hungary.

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 2010 Sep;382(3):213-20. doi: 10.1007/s00210-010-0538-1. Epub 2010 Jul 29.

Abstract

In spite of its widespread clinical application, there is little information on the cellular cardiac effects of the dopamine receptor agonist ropinirole. In the present study, therefore, the concentration-dependent effects of ropinirole on action potential morphology and the underlying ion currents were studied in enzymatically dispersed canine ventricular cardiomyocytes using standard microelectrode, conventional whole-cell patch clamp, and action potential voltage clamp techniques. At concentrations > or = 1 microM, ropinirole increased action potential duration (APD(90)) and suppressed the rapid delayed rectifier K(+) current (I (Kr)) with an IC(50) value of 2.7 +/- 0.25 microM and Hill coefficient of 0.92 +/- 0.09. The block increased with increasing depolarizations to more positive voltages, but paradoxically, the activation of I (Kr) was accelerated by 3 muM ropinirole (time constant decreased from 34 +/- 4 to 14 +/- 1 ms). No significant changes in the fast and slow deactivation time constants were observed with ropinirole. At higher concentrations, ropinirole decreased the amplitude of early repolarization (at concentrations > or = 10 microM), reduced the maximum rate of depolarization and caused depression of the plateau (at concentrations > or = 30 microM), and shortened APD measured at 50% repolarization (at 300 microM) indicating a concentration-dependent inhibition of I (to), I (Na), and I (Ca). Suppression of I (Kr), I (to), and I (Ca) has been confirmed under conventional patch clamp and action potential voltage clamp conditions. I (Ks) and I (K1) were not influenced significantly by ropinirole at concentrations less than 300 microM. All these effects of ropinirole were fully reversible upon washout. The results indicate that ropinirole treatment may carry proarrhythmic risk for patients with inherited or acquired long QT syndrome due to inhibition of I (Kr)-especially in cases of accidental overdose or intoxication.

摘要

尽管多巴胺受体激动剂罗匹尼罗已广泛应用于临床,但有关其对心肌细胞电活动影响的资料却很少。本研究采用酶解法分离犬心室肌细胞,应用标准微电极技术、常规全细胞膜片钳技术和动作电位电压钳技术,观察了不同浓度罗匹尼罗对心肌细胞动作电位时程(APD)及其离子电流的影响。结果表明:浓度大于或等于 1μmol/L 的罗匹尼罗可使 APD(90)延长,并抑制快激活延迟整流钾电流(I(Kr)),其半数有效浓度(IC(50))为 2.7±0.25μmol/L,Hill 系数为 0.92±0.09。随着去极化程度的增加,I(Kr)阻滞逐渐增强,但令人奇怪的是,3μmol/L 的罗匹尼罗可加速 I(Kr)激活(激活时间常数由 34±4ms 缩短至 14±1ms)。罗匹尼罗对快、慢失活时间常数无明显影响。较高浓度(大于或等于 10μmol/L)的罗匹尼罗可引起早期复极时程缩短,最大去极化速率和平台期幅度降低,复极 50%时程(APD50)缩短(在 300μmol/L 时),提示罗匹尼罗可浓度依赖性抑制内向整流钾电流(I(to))、钠电流(I(Na))和钙电流(I(Ca))。在常规全细胞膜片钳和动作电位电压钳技术条件下,进一步证实了罗匹尼罗对 I(Kr)、I(to)和 I(Ca)的抑制作用。在浓度小于 300μmol/L 时,罗匹尼罗对内向整流钾电流(I(Ks))和延迟整流钾电流(I(K1))无明显影响。上述作用均随洗脱而完全逆转。提示罗匹尼罗可通过抑制 I(Kr)而导致心律失常,特别是在长 QT 综合征患者中,其致心律失常作用可能与 I(Kr)抑制相关,故对于此类患者,应避免意外过量或药物中毒。

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