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腺苷对豚鼠抗室性心律失常作用的电生理研究

An electrophysiological study on the anti-ventricular arrhythmic effect of adenosine in the guinea pig.

作者信息

Zhao Zheng-Hang, Zang Wei-Jin, Yu Xiao-Jiang, Zang Yi-Min

机构信息

Department of Pharmacology, School of Medicine, Xi an Jiaotong University, Xi an 710061.

出版信息

Sheng Li Xue Bao. 2003 Feb 25;55(1):36-41.

Abstract

Using whole-cell patch clamp technique this study investigated the effects of adenosine (Ado) on action potential, L-type calcium current (I(Ca.L)), delayed afterdepolarizations (DADs), and transient inward current (I(ti)) induced by isoproterenol (Iso) in guinea pig isolated single ventricular myocytes. The results showed: (1) Ado alone had no significant direct effects on action potential and I(Ca.L) in guinea pig ventricular myocytes at 20-100 micromol/L. However, Ado significantly attenuated the prolongation of action potential duration (APD) and the increase of the peak amplitude of I(Ca.L) induced by Iso. Iso (10 nmol/L) markedly increased APD(50) and APD(90) from 340+/-21 ms to 486+/-28 ms and from 361+/-17 ms to 501+/-29 ms, respectively (P<0.01), and increased the amplitude of I(Ca.L) from 6.53+/-1.4 pA/pF to 18.28+/-2.4 pA/pF (P<0.01). The peak potential of current-potential relationship shifted to the left. Ado (50 micromol/L) abbreviated APD(50), APD(90) to 403+/-19 ms and 419+/-26 ms (P<0.01), and decreased the peak amplitude of I(Ca.L) to 10.2+/-1.5 pA/pF (P<0.01 vs Iso), but did not change resting membrane potential (RMP), action potential amplitude (APA), and overshoot (OS). (2) Iso (30 nmol/L) reproducibly elicited DADs with 100% incidence of DADs under this condition. Ado (50 micromol/L) completely inhibited Iso from inducing DADs. Iso (30 nmol/L) elicited I(ti) with 2-second depolarizing voltage-clamp pulses rising to +20 mV from a holding potential of -40 mV, the incidence of I(ti) being 100%, and the I(ti) was suppressed in the presence of Ado (50 micromol/L) with the incidence of I(ti) decreased to 14.3% (P<0.05). These data indicate that Ado antagonizes the stimulatory effect of Iso, and that the antiarrhythmic mechanism of Ado preventing Iso-induced DADs is due to the inhibition of intracellular Ca(2+) overload through attenuating the prolongation of APD, the enhance of I(Ca.L) and I(ti).

摘要

本研究采用全细胞膜片钳技术,研究了腺苷(Ado)对豚鼠离体单个心室肌细胞中异丙肾上腺素(Iso)诱导的动作电位、L型钙电流(I(Ca.L))、延迟后去极化(DADs)和短暂内向电流(I(ti))的影响。结果显示:(1)在20 - 100 μmol/L浓度下,单独的Ado对豚鼠心室肌细胞的动作电位和I(Ca.L)无明显直接影响。然而,Ado能显著减弱Iso诱导的动作电位时程(APD)延长和I(Ca.L)峰值幅度增加。Iso(10 nmol/L)使APD(50)和APD(90)分别从340±21 ms显著增加到486±28 ms以及从361±17 ms增加到501±29 ms(P<0.01),并使I(Ca.L)幅度从6.53±1.4 pA/pF增加到18.28±2.4 pA/pF(P<0.01)。电流 - 电压关系的峰值电位向左移动。Ado(50 μmol/L)使APD(50)、APD(90)缩短至403±19 ms和419±26 ms(P<0.01),并使I(Ca.L)峰值幅度降至10.2±1.5 pA/pF(与Iso相比,P<0.01),但不改变静息膜电位(RMP)、动作电位幅度(APA)和超射(OS)。(2)在此条件下,Iso(30 nmol/L)可重复性地引发DADs,DADs发生率为100%。Ado(50 μmol/L)完全抑制Iso诱导DADs。Iso(30 nmol/L)通过从 - 40 mV的 holding 电位升至 +20 mV的2秒去极化电压钳脉冲引发I(ti),I(ti)发生率为100%,在Ado(50 μmol/L)存在时I(ti)受到抑制,I(ti)发生率降至14.3%(P<0.05)。这些数据表明,Ado拮抗Iso的刺激作用,且Ado预防Iso诱导的DADs的抗心律失常机制是通过减弱APD延长、I(Ca.L)和I(ti)增强来抑制细胞内Ca(2+)超载。

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