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The contribution of the 'pacemaker' current (if) to generation of spontaneous activity in rabbit sino-atrial node myocytes.

机译:“起搏器”电流(if)对家兔窦房结肌细胞自发活动产生的贡献。

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摘要

1. The contribution to the diastolic depolarization of the hyperpolarization-activated current, if, relative to other components was investigated in isolated rabbit sino-atrial (SA) node myocytes. 2. During the diastolic phase the membrane potential depolarized by 0.1096 +/- 0.014 V/s, which requires only about 3 pA of inward current in a cell with an average capacity of 30 pF. The problem of which ionic component is responsible for initiating the diastolic depolarization was investigated by analysing the composition and the properties of the net inward current in the diastolic range of voltages. 3. The measured instantaneous 'background' current activated during voltage clamp steps from a holding potential of -35 mV was outward positive to approximately -61 mV, and had a region of negative slope conductance from -45 to -35 mV. 4. The instantaneous component lost its rectifying behaviour in the presence of Ni2+ (100 microM) and nitrendipine (10 microM). These blockers of Ca(2+)-dependent currents modified the instantaneous I-V relation at voltages positive to -45 to -50 mV, thus implying that Ca2+ currents become important at less negative potentials than -50 mV, towards the very end of diastolic depolarization. 5. Possible errors introduced by voltage clamp analysis with the whole-cell method on the instantaneous current and on if measurement were evaluated. Leakage through the seal resistance caused the instantaneous I-V relation to be displaced in the inward direction at negative voltages. Correction for the seal leakage moved the reversal potential for the instantaneous current toward the negative direction from -61 to approximately -66 mV. Thus, no depolarization can be driven by the background current beyond -66 mV. 6. During voltage clamp analysis, lack of series-resistance compensation led to lack of intracellular voltage control, as was apparent using a second pipette on the same cell. This slowed activation of if and led to a 1.5- to 2-fold reduction of if size in the range -55 to -115 mV. Thus, uncorrected measurements of the instantaneous component and of if may concur to underestimate the role of if in pacemaking. 7. These results lead to the conclusion that in the SA node cells analysed, pacemaker activity is generated with the essential contribution of the hyperpolarization-activated current, if. Numerical computation of SA node cell activity using an extension of the DiFrancesco-Noble model shows that the if-activation hypothesis can account for the presence of spontaneous action potentials and their sensitivity to if changes.
机译:1.如果在分离的兔窦房(SA)结节心肌细胞中研究了相对于其他成分的超极化激活电流对舒张期去极化的贡献。 2.在舒张期,膜电势以0.1096 +/- 0.014 V / s的速度去极化,这在平均容量为30 pF的电池中仅需要约3 pA的内向电流。通过分析电压的舒张期范围内的净内向电流的组成和性质,研究了哪个离子成分引起舒张期去极化的问题。 3.在电压钳制步骤中从保持电势为-35 mV激活的瞬时瞬时“背景”电流向外正向约为-61 mV,并具有从-45至-35 mV的负斜率电导区域。 4.在Ni2 +(100 microM)和尼群地平(10 microM)的存在下,瞬时成分失去了其整流性能。这些Ca(2+)依赖性电流的阻滞剂在-45至-50 mV的正电压下改变了瞬时IV关系,因此暗示着Ca2 +电流在负电位小于-50 mV时变得非常重要,接近舒张期去极化的终点。 。 5.电压钳夹分析通过全电池方法引入的瞬时电流和评估评估可能引入的误差。密封电阻的泄漏导致瞬时I-V关系在负电压下向内移动。密封泄漏的校正将瞬时电流的反向电位从-61移至负方向,约为-66 mV。因此,超过-66 mV的背景电流不会驱动去极化。 6.在电压钳分析过程中,缺少串联电阻补偿会导致缺乏细胞内电压控制,这在同一细胞上使用第二个移液器很明显。这减慢了if的激活,并导致if大小在-55至-115 mV范围内减少了1.5到2倍。因此,瞬时分量和if的未经校正的测量可能会低估if在起搏中的作用。 7.这些结果得出的结论是,在分析的SA节点细胞中,起搏器活动是由超极化激活电流的主要贡献所产生的。使用DiFrancesco-Noble模型的扩展对SA节点细胞活动进行数值计算表明,如果激活假设可以解释自发动作电位的存在及其对if变化的敏感性。

著录项

  • 作者

    DiFrancesco, D;

  • 作者单位
  • 年度 1991
  • 总页数
  • 原文格式 PDF
  • 正文语种 en
  • 中图分类

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