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豚鼠窦房结起搏细胞中延迟整流钾电流的快速和慢速激活成分

Rapidly and slowly activating components of delayed rectifier K(+) current in guinea-pig sino-atrial node pacemaker cells.

作者信息

Matsuura Hiroshi, Ehara Tsuguhisa, Ding Wei-Guang, Omatsu-Kanbe Mariko, Isono Takahiro

机构信息

Department of Physiology, Shiga University of Medical Science, Shiga 520-2192, Japan.

出版信息

J Physiol. 2002 May 1;540(Pt 3):815-30. doi: 10.1113/jphysiol.2001.016741.

Abstract

The components and properties of the delayed rectifier K(+) current (I(K)) in isolated guinea-pig sino-atrial (SA) node pacemaker cells were investigated using the whole-cell configuration of the patch-clamp technique. An envelope of tails test was conducted by applying depolarizing pulses from a holding potential of -50 mV to +30 mV for various durations ranging from 40 to 2000 ms. The ratio of the tail current amplitude elicited upon return to the holding potential to the magnitude of the time-dependent outward current activated during depolarizing steps was dependent on the pulse duration, while after exposure to the selective I(Kr) inhibitor E-4031 (5 microM) this current ratio became practically constant irrespective of the pulse duration. These observations are consistent with the presence of the E-4031-sensitive, rapidly activating and E-4031-resistant, slowly activating components of I(K) (I(Kr) and I(Ks), respectively) in guinea-pig SA node cells. The activation range for I(Kr), defined as the E-4031-sensitive current (half-maximal activation voltage (V(1/2)) of -26.2 mV) was much more negative than that for I(Ks), defined as the E-4031-resistant current (V(1/2) of +17.2 mV). I(Kr) exhibited a marked inward rectification at potentials positive to -50 mV, whereas I(Ks) showed only a slight rectification. In the current-clamp experiments, bath application of E-4031 (0.5 and 5 microM) initially slowed the repolarization at potentials negative to approximately -30 mV and produced a significant depolarization of the maximum diastolic potential, followed by the arrest of electrical activity, thus indicating that the late phase of the repolarization leading to the maximum diastolic potential at around -60 mV in spontaneous action potentials is primarily produced by I(Kr) in guinea-pig SA node cells. External application of the selective I(Ks) inhibitor 293B (30 microM) also delayed the repolarization process at potentials negative to about -20 mV and induced moderate depolarization of the maximum diastolic potential leading to the arrest of the spontaneous activity. These results provide evidence to suggest that both I(Kr) and I(Ks) are present and play crucial roles in the spontaneous electrical activity of guinea-pig SA node pacemaker cells.

摘要

采用膜片钳技术的全细胞模式,研究了豚鼠离体窦房(SA)结起搏细胞中延迟整流钾电流(I(K))的组成成分和特性。通过从 -50 mV 的钳制电位施加去极化脉冲至 +30 mV,持续时间从 40 到 2000 ms 不等,进行了尾电流包络测试。回到钳制电位时诱发的尾电流幅度与去极化步骤期间激活的时间依赖性外向电流幅度之比取决于脉冲持续时间,而在暴露于选择性 I(Kr) 抑制剂 E - 4031(5 μM)后,该电流比值几乎保持恒定,与脉冲持续时间无关。这些观察结果与豚鼠 SA 结细胞中存在 E - 4031 敏感的、快速激活的 I(K) 成分和 E - 4031 抗性的、缓慢激活的 I(K) 成分(分别为 I(Kr) 和 I(Ks))一致。I(Kr) 的激活范围(定义为 E - 4031 敏感电流,半最大激活电压(V(1/2))为 -26.2 mV)比 I(Ks) 的激活范围(定义为 E - 4031 抗性电流,V(1/2) 为 +17.2 mV)更负。I(Kr) 在电位高于 -50 mV 时表现出明显的内向整流,而 I(Ks) 仅表现出轻微的整流。在电流钳实验中,浴槽施加 E - 4031(0.5 和 5 μM)最初使电位低于约 -30 mV 时的复极化减慢,并使最大舒张电位显著去极化,随后电活动停止,这表明在豚鼠 SA 结细胞中,自发动作电位中导致约 -60 mV 最大舒张电位的复极化后期主要由 I(Kr) 产生。外部施加选择性 I(Ks) 抑制剂 293B(30 μM)也使电位低于约 -20 mV 时的复极化过程延迟,并诱导最大舒张电位适度去极化,导致自发活动停止。这些结果提供了证据表明 I(Kr) 和 I(Ks) 均存在,并在豚鼠 SA 结起搏细胞的自发电活动中起关键作用。

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