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Rate dependency of delayed rectifier currents during the guinea-pig ventricular action potential

机译:豚鼠心室动作电位期间延迟整流电流的速率依赖性

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摘要

class="enumerated" style="list-style-type:decimal">The action potential clamp technique was exploited to evaluate the rate dependency of delayed rectifier currents (IKr and IKs) during physiological electrical activity. IKr and IKs were measured in guinea-pig ventricular myocytes at pacing cycle lengths (CL) of 1000 and 250 ms.A shorter CL, with the attendant changes in action potential shape, was associated with earlier activation and increased magnitude of both IKr and IKs. Nonetheless, the relative contributions of IKr and IKs to total transmembrane current were independent of CL.Shortening of diastolic interval only (constant action potential shape) enhanced IKs, but not IKr.IKr was increased by a change in the action potential shape only (constant diastolic interval).In ramp clamp experiments, IKr amplitude was directly proportional to repolarization rate at values within the low physiological range (< 1.0 V s−1); at higher repolarization rates proportionality became shallower and finally reversed.When action potential duration (APD) was modulated by constant current injection (I-clamp), repolarization rates > 1.0 V s−1 were associated with a reduced effect of IKr block on APD. The effect of changes in repolarization rate was independent of CL and occurred in the presence of IKs blockade.In spite of its complexity, the behaviour of IKr was accurately predicted by a numerical model based entirely on known kinetic properties of the current.Both IKr and IKs may be increased at fast heart rates, but this may occur through completely different mechanisms. The mechanisms identified are such as to contribute to abnormal rate dependency of repolarization in prolonged repolarization syndromes.
机译:class =“ enumerated” style =“ list-style-type:decimal”> <!-list-behavior =枚举前缀-word = mark-type = decimal max-label-size = 0-> 动作电位钳技术被用来评估生理电活动期间延迟整流电流(IKr和IKs)的速率依赖性。在豚鼠心室肌​​细胞中,IKr和IKs在起搏周期长度(CL)为1000和250 ms时进行测量。 较短的CL伴随着动作电位形状的改变,与较早的激活和IKr和IK的幅度都增加了。尽管如此,IKr和IKs对总跨膜电流的相对贡献与CL无关。 仅缩短舒张间隔(恒定动作电位形状)可以增强IKs,但不能改善IKr。 IKr仅通过动作电位形状的改变(恒定的舒张间隔)而增加。 在斜坡钳位实验中,IKr幅度在低生理范围内(<1.0 V s时)与复极化率成正比。 -1 ); 当通过恒流注入(I型钳位)调节动作电位持续时间(APD)时,复极化率> 1.0 V s -1 sup>与IKr阻滞对APD的作用降低有关。复极化率变化的影响与CL无关,并在存在IKs阻滞的情况下发生。 尽管IKr具有复杂性,但它是通过完全基于已知动力学特性的数值模型准确预测的 I Kr和 I Ks 都可能在心跳加快时增加,但这可能会发生通过完全不同的机制。所确定的机制有助于长期复极化综合征中复极化的异常速率依赖性。

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