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豚鼠心脏细胞中通过L型钙通道的生理离子通量的宏观和整体特性。

Macroscopic and unitary properties of physiological ion flux through L-type Ca2+ channels in guinea-pig heart cells.

作者信息

Rose W C, Balke C W, Wier W G, Marban E

机构信息

Department of Medicine, University of Maryland, Baltimore.

出版信息

J Physiol. 1992 Oct;456:267-84. doi: 10.1113/jphysiol.1992.sp019336.

Abstract
  1. We investigated the currents through L-type Ca2+ channels when Ca2+ (1-10 mM) was the charge carrier, as is the case physiologically. 2. Na+ was removed from both the external and internal solutions to eliminate currents through Na+ channels and Na(+)-Ca2+ exchange. 3. From a holding potential of -50 mV only L-type channels were available to open with depolarization. Macroscopic L-type currents were maximal during depolarizing pulses to +10 mV (peak current density of 4.7 +/- 0.3 nA nF-1). 4. During depolarizing steps as long as 180 ms, the decay of current through L-type channels was incomplete, in contrast to that of T-type current. 5. Unitary currents recorded with comparable ionic conditions and voltage protocols exhibited a single-channel conductance of 6.9 pS in 10 mM Ca2+. Ensemble average currents reproduced accurately the features of whole-cell L-type current, including the maintained component. 6. Convolution analysis was employed to clarify the single-channel basis of the complex current waveform of L-type channels. First openings underlie the peak, while the maintained pedestal is generated by multiple re-openings. As with T-type channels, single openings are brief and contribute little to the time course of the average current. 7. The prominent maintained component of macroscopic and ensemble average L-type current cannot be explained by simple Markov models in which current decay reflects the progressive entry of channels into an absorbing inactivated state. 8. We considered the possibility that the maintained component of current arises from the existence of multiple distinct gating patterns, one of which lacks inactivation. Individual sweeps were sorted among three patterns of gating (no openings, active-early and active-late). Patterns of activity are not randomly distributed; instead, they tend to cluster over time. 9. Most of the maintained current is attributable to the 'active-late' pattern of gating. Considered separately, this pattern can be well described by a simple Markov chain lacking an inactivated state. The 'active-early' gating pattern accounts entirely for the initial current transient, and for about one-third of the maintained component; thus, inactivation, even when present, must be reversible rather than absorbing. 10. The unitary current amplitudes and peak open probabilities measured for single L-type channels, when compared to the average macroscopic L-type current density, predict 170 functional channels per picofarad, or 28,000 L-type channels per typical ventricular myocyte.(ABSTRACT TRUNCATED AT 400 WORDS)
摘要
  1. 我们研究了以钙离子(1 - 10 mM)作为电荷载体时通过L型钙通道的电流,生理情况下即是如此。2. 细胞外液和细胞内液中的钠离子均被去除,以消除通过钠通道和钠钙交换产生的电流。3. 从 - 50 mV的钳制电位开始,仅L型通道可在去极化时开放。向 + 10 mV去极化脉冲期间,宏观L型电流最大(峰值电流密度为4.7 ± 0.3 nA nF⁻¹)。4. 在长达180 ms的去极化步骤中,与T型电流不同,通过L型通道的电流衰减不完全。5. 在可比的离子条件和电压方案下记录的单通道电流,在10 mM钙离子中显示单通道电导为6.9 pS。整体平均电流准确再现了全细胞L型电流的特征,包括持续成分。6. 采用卷积分析来阐明L型通道复杂电流波形的单通道基础。峰值由首次开放产生,而持续平台由多次重新开放产生。与T型通道一样,单次开放短暂,对平均电流的时间进程贡献不大。7. 宏观和整体平均L型电流突出的持续成分,无法用简单的马尔可夫模型解释,在该模型中电流衰减反映通道逐渐进入吸收性失活状态。8. 我们考虑了电流持续成分源于多种不同门控模式存在的可能性,其中一种模式缺乏失活。单个扫描被分类为三种门控模式(无开放、早期激活和晚期激活)。活动模式并非随机分布;相反,它们倾向于随时间聚类。9. 大部分持续电流归因于“晚期激活”门控模式。单独考虑时,这种模式可用缺乏失活状态的简单马尔可夫链很好地描述。“早期激活”门控模式完全解释了初始电流瞬变以及约三分之一的持续成分;因此,即使存在失活,也必须是可逆的而非吸收性的。10. 将单个L型通道测量的单通道电流幅度和峰值开放概率与平均宏观L型电流密度相比,预测每皮法有170个功能通道,或每个典型心室肌细胞有28,000个L型通道。(摘要截于400字)

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