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兔窦房结细胞中超级化激活阳离子电流的阳离子依赖性门控。

Cation-dependent gating of the hyperpolarization-activated cation current in the rabbit sino-atrial node cells.

作者信息

Maruoka F, Nakashima Y, Takano M, Ono K, Noma A

机构信息

Department of Physiology, Faculty of Medicine, Kyushu University, Fukuoka, Japan.

出版信息

J Physiol. 1994 Jun 15;477 ( Pt 3)(Pt 3):423-35. doi: 10.1113/jphysiol.1994.sp020204.

Abstract
  1. The gating properties of the hyperpolarization-activated cation current (I(f) or Ih) were investigated in single pacemaker cells dissociated from the rabbit sino-atrial node. 2. The whole-cell I(f) was recorded in the presence of different external cations. The inward I(f) was increased when external Na+ was replaced with K+, and was decreased in Li+ or Rb+ solution. In Tris+ and Cs+ solutions, the inward I(f) was negligible. The outward tail current recorded upon depolarization was largest in Li+ solution and smaller in a sequence of Na+, Tris+ and K+ solutions. In Rb+ and Cs+ solutions, only a small tail current was recorded. 3. The outward tail current had a 'shoulder' in Na+ solution, which was much delayed by replacing Na+ with Li+. In K+ solution, the decay of the tail current was much faster, and no obvious shoulder was recorded. The tail current was slowest in Li(+)-rich and 0 mM K+ solution, and was progressively accelerated by adding K+ over the range from 0 to 3 mM. The tail current at 30 mM [K+]o showed only a small shoulder. A common binding site to modulate the I(f) deactivation was suggested for monovalent cations. 4. The shoulder of the I(f) tail became more evident as I(f) was activated to a larger extent either by prolonging the duration or by increasing the amplitude of the preceding hyperpolarization in both Na+ and Li+ solutions. 5. The I(f) was first activated by hyperpolarizing the membrane to -110 mV, and then deactivated by depolarization. The inward tail current at -50 mV showed a single exponential decay. At more positive potentials, the shoulder of the outward tail currents became more evident and the rate of the final decay was increased. 6. The time course of I(f) activation was well fitted with the sum of two exponential functions. Time constants of both components were not affected by the external cation (Na+, K+ or Li+) replacement. Likewise, the quasi-steady state activation was conserved when external Na+ was replaced with Li+. 7. Two closed and three open states were assumed in a sequential state model of the I(f) channel. The cation effects were well simulated by assuming that the deactivation rate was selectively modulated. The flow of I(f) during the spontaneous action potential was calculated. The activation of I(f) started on repolarization to the maximum diastolic potential and reached a maximum in the middle of the diastolic period. Its peak amplitude was 14% of the net inward current during the diastolic period.
摘要
  1. 在从兔窦房结分离出的单个起搏细胞中研究了超极化激活阳离子电流(I(f) 或 Ih)的门控特性。2. 在不同的细胞外阳离子存在的情况下记录全细胞 I(f)。当细胞外 Na+ 被 K+ 取代时,内向 I(f) 增加,而在 Li+ 或 Rb+ 溶液中则降低。在 Tris+ 和 Cs+ 溶液中,内向 I(f) 可忽略不计。去极化时记录到的外向尾电流在 Li+ 溶液中最大,在 Na+、Tris+ 和 K+ 溶液中依次减小。在 Rb+ 和 Cs+ 溶液中,仅记录到小的尾电流。3. 外向尾电流在 Na+ 溶液中有一个“肩部”,用 Li+ 取代 Na+ 后该肩部明显延迟。在 K+ 溶液中,尾电流的衰减快得多,未记录到明显的肩部。在富含 Li+ 且 0 mM K+ 的溶液中尾电流最慢,在 0 至 3 mM 的范围内添加 K+ 可使其逐渐加速。在 30 mM [K+]o 时尾电流仅显示出小的肩部。推测单价阳离子存在一个共同的结合位点来调节 I(f) 的失活。4. 在 Na+ 和 Li+ 溶液中,通过延长前超极化的持续时间或增加其幅度,使 I(f) 激活程度更大时,I(f) 尾电流的肩部变得更明显。5. 通过将膜超极化至 -110 mV 首先激活 I(f),然后通过去极化使其失活。-50 mV 时的内向尾电流呈单指数衰减。在更正的电位下,外向尾电流的肩部变得更明显且最终衰减速率增加。6. I(f) 的激活时间进程与两个指数函数之和拟合良好。两个成分的时间常数不受细胞外阳离子(Na+、K+ 或 Li+)取代的影响。同样,当用 Li+ 取代细胞外 Na+ 时,准稳态激活得以保留。7. 在 I(f) 通道的顺序状态模型中假设存在两个关闭状态和三个开放状态。通过假设失活速率被选择性调节,很好地模拟了阳离子效应。计算了自发动作电位期间 I(f) 的流动情况。I(f) 的激活在复极化至最大舒张电位时开始,并在舒张期中期达到最大值。其峰值幅度为舒张期内向净电流的 14%。

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引用本文的文献

本文引用的文献

1
Cardiac pacemaking in the sinoatrial node.窦房结的心脏起搏
Physiol Rev. 1993 Jan;73(1):197-227. doi: 10.1152/physrev.1993.73.1.197.

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