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铯可消除豚鼠心室肌细胞中钡诱导的起搏电位和电流。

Cesium abolishes the barium-induced pacemaker potential and current in guinea pig ventricular myocytes.

作者信息

Shen J B, Vassalle M

机构信息

Department of Physiology, State University of New York, Health Science Center, Brooklyn 11203.

出版信息

J Cardiovasc Electrophysiol. 1994 Dec;5(12):1031-44. doi: 10.1111/j.1540-8167.1994.tb01145.x.

Abstract

INTRODUCTION

The ability of cesium to block barium-induced diastolic depolarization ("Ba-DD") and pacemaker current was tested in isolated ventricular myocytes. Because Ba-DD is due to decreasing K+ conductance and there is no I(f) at the resting potential, this approach permits verification of whether Cs+ is a specific blocker of i(f) or if it instead also blocks a K+ pacemaker current.

METHODS AND RESULTS

Guinea pig isolated ventricular myocytes were studied by a discontinuous, single electrode, voltage clamp method. During hyperpolarizing voltage clamp steps from -80 up to -140 mV in Tyrode's solution, the inward current increased as a function of voltage but did not change as a function of time (no I(f) or K+ depletion). Cesium (4 mM) reduced the current size during the hyperpolarizing steps but did not induce or unmask time-dependent currents. Barium (0.05 to 0.1 mM) induced diastolic depolarization, and, in its presence, depolarizing voltage clamp steps were followed by an outward tail current that reversed at -92.0 +/- 1.3 mV. Outward tail currents were larger at -50 mV than at the resting potential, and inward tail currents decayed more rapidly and to a larger extent during larger hyperpolarizing steps. In the presence of Ba2+, Cs+ (4 mM) had little effect on the steady-state current but markedly reduced or abolished undershoot, Ba-DD, and time-dependent tail currents at potentials both positive and negative to the resting potential. Cs+ had a smaller effect on the steady-state current-voltage (I-V) relation in the presence than in the absence of Ba2+, as part of the IK1 channels were already blocked by Ba2+ and the time-dependent changes induced by Ba2+ were not present. Both Ba2+ and Cs+ had little blocking effect on the steady-state current positive to the negative slope region of the I-V relation.

CONCLUSION

In ventricular myocytes, Cs+ abolishes the Ba(2+)-induced pacemaker current by blocking the time-dependent change in K+ conductance, not by blocking I(f). Because Cs+ can also block a decaying K+ pacemaker current, the abolition of a pacemaker current by Cs+ in other cardiac tissues cannot be taken as unequivocal proof that the blocked current is I(f).

摘要

引言

在分离的心室肌细胞中测试了铯阻断钡诱导的舒张期去极化(“Ba-DD”)和起搏电流的能力。由于Ba-DD是由于钾离子电导降低所致,且静息电位时不存在I(f),因此该方法可以验证Cs+是否是I(f)的特异性阻滞剂,或者它是否也阻断钾离子起搏电流。

方法与结果

采用间断单电极电压钳法研究豚鼠分离的心室肌细胞。在台氏液中从-80 mV到-140 mV进行超极化电压钳制步骤时,内向电流随电压增加但不随时间变化(无I(f)或钾离子耗竭)。铯(4 mM)在超极化步骤中减小了电流大小,但未诱导或揭示时间依赖性电流。钡(0.05至0.1 mM)诱导舒张期去极化,在其存在时,去极化电压钳制步骤后跟随一个外向尾电流,其反转电位为-92.0±1.3 mV。-50 mV时的外向尾电流大于静息电位时的,且在更大的超极化步骤中内向尾电流衰减更快且程度更大。在Ba2+存在时,Cs+(4 mM)对稳态电流影响不大,但显著降低或消除了静息电位正负两侧电位下的超射、Ba-DD和时间依赖性尾电流。与不存在Ba2+时相比,存在时Cs+对稳态电流-电压(I-V)关系的影响较小,因为部分IK1通道已被Ba2+阻断,且不存在Ba2+诱导的时间依赖性变化。Ba2+和Cs+对I-V关系负斜率区域正向的稳态电流几乎没有阻断作用。

结论

在心室肌细胞中,Cs+通过阻断钾离子电导的时间依赖性变化而非阻断I(f)来消除Ba(2+)诱导的起搏电流。由于Cs+也可阻断衰减的钾离子起搏电流,因此在其他心脏组织中Cs+消除起搏电流不能明确证明被阻断的电流是I(f)。

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