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Inward current activated during hyperpolarization in the rabbit sinoatrial node cell.兔窦房结细胞超极化时激活的内向电流。
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A voltage-clamp analysis of inward (anomalous) rectification in mouse spinal sensory ganglion neurones.小鼠脊髓感觉神经节神经元内向(反常)整流的电压钳分析。
J Physiol. 1983 Jul;340:19-45. doi: 10.1113/jphysiol.1983.sp014747.
3
Ionic basis for the electro-responsiveness and oscillatory properties of guinea-pig thalamic neurones in vitro.豚鼠丘脑神经元在体外电反应性和振荡特性的离子基础
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Lateral geniculate nucleus unitary discharge in sleep and waking: state- and rate-specific aspects.睡眠和清醒状态下外侧膝状体的单位放电:状态和频率特异性方面。
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Sleep-related variations of membrane potential in the lateral geniculate body relay neurons of the cat.猫外侧膝状体中继神经元膜电位的睡眠相关变化。
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Neuronal discharges of the ventrolateral nucleus of the thalamus during sleep and wakefulness in the cat. I. Spontaneous activity.猫睡眠和觉醒期间丘脑腹外侧核的神经元放电。I. 自发活动。
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Abolition of spindle oscillations in thalamic neurons disconnected from nucleus reticularis thalami.与丘脑网状核分离的丘脑神经元中纺锤体振荡的消除。
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超极化激活阳离子电流的特性及其在丘脑中继神经元节律性振荡中的作用。

Properties of a hyperpolarization-activated cation current and its role in rhythmic oscillation in thalamic relay neurones.

作者信息

McCormick D A, Pape H C

机构信息

Section of Neuroanatomy, Yale University School of Medicine, New Haven, CT 06510.

出版信息

J Physiol. 1990 Dec;431:291-318. doi: 10.1113/jphysiol.1990.sp018331.

DOI:10.1113/jphysiol.1990.sp018331
PMID:1712843
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1181775/
Abstract
  1. The physiological and functional features of time-dependent anomalous rectification activated by hyperpolarization and the current which underlies it, Ih, were examined in guinea-pig and cat thalamocortical relay neurones using in vitro intracellular recording techniques in thalamic slices. 2. Hyperpolarization of the membrane from rest with a constant-current pulse resulted in time-dependent rectification, expressed as a depolarizing sag of the membrane potential back towards rest. Under voltage clamp conditions, hyperpolarizing steps to membrane potentials negative to approximately -60 mV were associated with the activation of a slow inward current, Ih, which showed no inactivation with time. 3. The activation curve of the conductance underlying Ih was obtained through analysis of tail currents and ranged from -60 to -90 mV, with half-activation occurring at -75 mV. The time course of activation of Ih was well fitted by a single-exponential function and was strongly voltage dependent, with time constants ranging from greater than 1-2 s at threshold to an average of 229 ms at -95 mV. The time course of de-activation was also described by a single-exponential function, was voltage dependent, and the time constant ranged from an average of 1000 ms at -80 mV to 347 ms at -55 mV. 4. Raising [K+]o from 2.5 to 7.5 mM enhanced, while decreasing [Na+]o from 153 to 26 mM reduced, the amplitude of Ih. In addition, reduction of [Na+]o slowed the rate of Ih activation. These results indicate that Ih is carried by both Na+ and K+ ions, which is consistent with the extrapolated reversal potential of -43 mV. Replacement of Cl- in the bathing medium with isethionate shifted the chloride equilibrium potential positive by approximately 30-70 mV, evoked an inward shift of the holding current at -50 mV, and resulted in a marked reduction of instantaneous currents as well as Ih, suggesting a non-specific blocking action of impermeable anions. 5. Local (2-10 mM in micropipette) or bath (1-2 mM) applications of Cs+ abolished Ih over the whole voltage range tested (-60 to -110 mV), with no consistent effects on instantaneous currents. Barium (1 mM, local; 0.3-0.5 mM, bath) evoked a steady inward current, reduced the amplitude of instantaneous currents, and had only weak suppressive effects on Ih. 6. Block of Ih with local application of Cs+ resulted in a hyperpolarization of the membrane from the resting level, a decrease in apparent membrane conductance, and a block of the slow after-hyperpolarization that appears upon termination of depolarizing membrane responses, indicating that Ih contributes substantially to the resting and active membrane properties of thalamocortical relay neurones.(ABSTRACT TRUNCATED AT 400 WORDS)
摘要
  1. 利用丘脑切片的体外细胞内记录技术,在豚鼠和猫的丘脑皮质中继神经元中研究了超极化激活的时间依赖性异常整流及其基础电流Ih的生理和功能特性。2. 用恒流脉冲使膜从静息状态超极化会导致时间依赖性整流,表现为膜电位朝着静息方向的去极化下陷。在电压钳制条件下,向负于约 -60 mV的膜电位进行超极化阶跃与一种缓慢内向电流Ih的激活相关,该电流不随时间失活。3. 通过对尾电流的分析获得了Ih基础电导的激活曲线,范围为 -60至 -90 mV,半激活发生在 -75 mV。Ih的激活时间进程很好地拟合为单指数函数,并且强烈依赖电压,时间常数范围从阈值处大于1 - 2秒到 -95 mV时平均为229毫秒。失活的时间进程也用单指数函数描述,依赖电压,时间常数范围从 -80 mV时平均1000毫秒到 -55 mV时347毫秒。4. 将细胞外钾离子浓度从2.5 mM提高到7.5 mM会增强Ih的幅度,而将细胞外钠离子浓度从153 mM降低到26 mM会降低Ih的幅度。此外,降低细胞外钠离子浓度会减慢Ih的激活速率。这些结果表明Ih由钠离子和钾离子共同携带,这与推断的 -43 mV反转电位一致。用羟乙基磺酸替代灌流液中的氯离子使氯离子平衡电位正向移动约30 - 70 mV,在 -50 mV时诱发钳制电流向内偏移,并导致瞬时电流以及Ih显著降低,表明不可渗透阴离子的非特异性阻断作用。5. 局部(微电极内2 - 10 mM)或浴液(1 - 2 mM)施加铯离子在整个测试电压范围(-60至 -110 mV)内消除了Ih,对瞬时电流没有一致的影响。钡离子(局部1 mM;浴液0.3 - 0.5 mM)诱发稳定的内向电流,降低瞬时电流的幅度,对Ih只有微弱的抑制作用。6. 局部施加铯离子阻断Ih导致膜从静息水平超极化,表观膜电导降低,并阻断去极化膜反应终止时出现的缓慢后超极化,表明Ih对丘脑皮质中继神经元的静息和活动膜特性有重要贡献。(摘要截短至400字)