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膜电位在钡离子诱导豚鼠心肌细胞自动节律性中的作用

Role of membrane potential in Ba2+ induced automaticity in guinea pig cardiac myocytes.

作者信息

Valenzuela F, Vassalle M

机构信息

Departamento de Fisiologia, Instituto Nacional de Cardiologia, Mexico DF, Mexico.

出版信息

Cardiovasc Res. 1991 May;25(5):421-30. doi: 10.1093/cvr/25.5.421.

Abstract

STUDY OBJECTIVE

The aim was to study in isolated myocardial cells the role of membrane potential in barium induced spontaneous activity and the ionic mechanism of the underlying pacemaker current.

DESIGN

The membrane potential and resistance of single myocytes were studied at different voltage levels by means of current and voltage clamp steps in the absence and presence of barium (Ba).

EXPERIMENTAL MATERIAL

The membrane potentials and currents of single guinea pig ventricular myocytes were recorded by means of an intracellular microelectrode through which current could also be passed.

MEASUREMENTS AND MAIN RESULTS

In the presence of Ba (0.1-0.2 mM), stepwise depolarisations induced a transient overshoot and initiated action potentials followed by an undershoot, diastolic depolarisation and spontaneous discharge. During progressive depolarisations, membrane resistance (Rm) increased, decreased transiently at the end of the action potential, and reincreased during diastole. Stepwise repolarisations had opposite effects. Hyperpolarisations reversed diastolic depolarisation and could unmask oscillatory potentials (Vos). Voltage clamp steps to +20 mV were followed by outward tail currents during which Rm increased. Larger or longer depolarisations were followed by larger outward tail currents at resting potential level. The outward tail current reversed at potentials negative to EK.

CONCLUSIONS

In the presence of Ba, applied depolarisation facilitates the induction of spontaneous activity through an interplay between voltage dependent and time dependent Ba block and unblock of gK1, voltage dependent increase in Rm, increased potassium driving force, and negative shift in the slow inward current threshold and sometimes Vos. The pacemaker potential underlying spontaneous activity is due to the slow re-establishment of Ba block of IK1 during diastole.

摘要

研究目的

本研究旨在探讨在分离的心肌细胞中膜电位在钡诱导的自发活动中的作用以及潜在起搏电流的离子机制。

设计

在有无钡(Ba)的情况下,通过电流钳和电压钳步骤在不同电压水平研究单个心肌细胞的膜电位和电阻。

实验材料

通过可通过电流的细胞内微电极记录单个豚鼠心室肌细胞的膜电位和电流。

测量与主要结果

在存在Ba(0.1 - 0.2 mM)的情况下,逐步去极化诱导短暂的超射并引发动作电位,随后是下冲、舒张期去极化和自发放电。在逐步去极化过程中,膜电阻(Rm)增加,在动作电位结束时短暂降低,并在舒张期再次增加。逐步复极化有相反的作用。超极化可逆转舒张期去极化并可揭示振荡电位(Vos)。电压钳步进到 +20 mV 后跟随外向尾电流,在此期间 Rm 增加。更大或更长时间的去极化后,在静息电位水平会有更大的外向尾电流。外向尾电流在比 EK 更负的电位处逆转。

结论

在存在Ba的情况下,施加的去极化通过电压依赖性和时间依赖性的Ba对gK1的阻滞和解除阻滞、电压依赖性的Rm增加、钾驱动力增加以及缓慢内向电流阈值的负向偏移以及有时Vos之间的相互作用,促进自发活动的诱导。自发活动背后的起搏电位是由于舒张期IK1的Ba阻滞缓慢重新建立。

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