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Simultaneous changes in the equilibrium potential and potassium conductance in voltage clamped Ranvier node in the frog.青蛙有髓神经纤维郎飞结电压钳制下平衡电位与钾电导的同步变化。
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本文引用的文献

1
Potassium ion current in the squid giant axon: dynamic characteristic.鱿鱼巨轴突中的钾离子电流:动态特性
Biophys J. 1960 Sep;1(1):1-14. doi: 10.1016/s0006-3495(60)86871-3.
2
Fully activated potassium current-voltage relationship in the Ranvier node: discrepancy between the results of two methods of analysis.郎飞结中完全激活的钾电流-电压关系:两种分析方法结果之间的差异
Pflugers Arch. 1980 Mar;384(1):49-56. doi: 10.1007/BF00589513.
3
Simultaneous changes in the equilibrium potential and potassium conductance in voltage clamped Ranvier node in the frog.青蛙有髓神经纤维郎飞结电压钳制下平衡电位与钾电导的同步变化。
J Physiol. 1981 Sep;318:279-95. doi: 10.1113/jphysiol.1981.sp013864.
4
Outward membrane currents activated in the plateau range of potentials in cardiac Purkinje fibres.在心脏浦肯野纤维动作电位平台期激活的外向膜电流。
J Physiol. 1969 Jan;200(1):205-31. doi: 10.1113/jphysiol.1969.sp008689.
5
Two fast transient current components during voltage clamp on snail neurons.蜗牛神经元电压钳制期间的两种快速瞬态电流成分。
J Gen Physiol. 1971 Jul;58(1):36-53. doi: 10.1085/jgp.58.1.36.
6
Slow changes in potassium permeability in skeletal muscle.骨骼肌中钾通透性的缓慢变化。
J Physiol. 1970 Jul;208(3):645-68. doi: 10.1113/jphysiol.1970.sp009140.
7
Potassium inactivation in single myelinated nerve fibres of Xenopus laevis.非洲爪蟾单根有髓神经纤维中的钾离子失活
Pflugers Arch. 1971;330(1):61-73. doi: 10.1007/BF00588735.
8
Block of potassium channels of the nodal membrane by 4-aminopyridine and its partial removal on depolarization.4-氨基吡啶对结区膜钾通道的阻断及其在去极化时的部分解除。
Pflugers Arch. 1976 Nov 30;367(1):77-87. doi: 10.1007/BF00583659.
9
Effect of conditioning potential on potassium current kinetics in the frog node.条件电位对蛙神经节钾电流动力学的影响。
Biophys J. 1976 Mar;16(3):261-73. doi: 10.1016/S0006-3495(76)85686-X.
10
Late sodium current in the node of Ranvier.郎飞结处的晚钠电流。
Pflugers Arch. 1975;357(1-2):145-8. doi: 10.1007/BF00584552.

青蛙郎飞结膜中存在三种类型钾通道的证据。

Evidence for the existence of three types of potassium channels in the frog Ranvier node membrane.

作者信息

Dubois J M

出版信息

J Physiol. 1981 Sep;318:297-316. doi: 10.1113/jphysiol.1981.sp013865.

DOI:10.1113/jphysiol.1981.sp013865
PMID:6275068
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1245492/
Abstract
  1. In voltage clamped myelinated fibres, the K+ current was recorded in high-K+ media to allow analysis without complications due to K+ accumulation. 2. After a depolarization, the tail of K+ current following repolarization decreases in two phases: a fast phase lasting about 20 msec and a slow exponential phase lasting several hundred milliseconds. When the duration of the depolarization is increased, the amplitude at time zero of the fast phase increases (activation of the conductance) and then decreases slowly (inactivation of the conductance). Simultaneously, the amplitude of the slow phase, extrapolated to time zero of repolarization, increases slowly and reaches a steady-state level (about 20% of the maximum instantaneous current) after about 600 msec of depolarization. 3. The fast phase of the tail current is blocked by external application of 4-aminopyridine (4-AP) (KD = 10(-5)M). The slow phase is unaltered by 4-AP (10(-7)-10(-2)M). 4. In the presence of 4-AP (10-3M), the remaining slow K+ current, activated by depolarizations, does not inactivate. 5. During depolarizations and repolarizations, the conductance of the slow current (GKs) varies exponentially. The steady-state value of the slow conductance and its time constant of activation vary with voltage. The variation of the slow conductance with time and voltage can be described by a closed-open mode, assuming that each channel is gated by one particle. The activation kinetics of the slow current is unaltered by long lasting (500 msec) prepolarizations. 6. The fast K+ conductance, calculated from the fast tail current, is fully inactivated at the end of a 3 min depolarization to 0 mV. 7. The fast K+ conductance can be decomposed into two components: one component (GKf1) activating between -80 and -30 mV and inactivating very slowly (tau = 45 sec at E = 0 mV); one component (GKf2) activating between -40 mV and +30 mV and inactivating slowly (tau = 2 sec at E = 0 mV). t = 12 degrees C. 8. The maximum slow and fast conductances increase with [K]0. While the maximum fast conductance tends to saturate at high external K+ concentrations, the maximum slow conductance shows no sign of saturation. 9. A comparison between motor and sensory fibres shows that, while the amplitude of maximum slow and fast conductances are identical for both types of fibres, the amplitude of fast-1 conductance is larger and consequently the amplitude of fast-2 is smaller in motor than in sensory fibres. The different spike frequency adaptations observed on both types of fibres are discussed in relation to these different relative fast conductances amplitudes. 10. It is concluded that the K+ conductance of the nodal membrane is composed of three components (GKS, GKf1 and GKf2) corresponding to three different and distinct types of K+ channels.
摘要
  1. 在电压钳制的有髓纤维中,在高钾培养基中记录钾离子电流,以便在不存在因钾离子积累而产生并发症的情况下进行分析。2. 去极化后,复极化后钾离子电流的尾电流分两个阶段下降:一个快速阶段持续约20毫秒,一个缓慢的指数阶段持续数百毫秒。当去极化持续时间增加时,快速阶段在时间零点的幅度增加(电导激活),然后缓慢下降(电导失活)。同时,缓慢阶段的幅度,外推到复极化的时间零点,缓慢增加,并在约600毫秒的去极化后达到稳态水平(约为最大瞬时电流的20%)。3. 尾电流的快速阶段可被外部施加的4-氨基吡啶(4-AP)(KD = 10^(-5)M)阻断。缓慢阶段不受4-AP(10^(-7)-10^(-2)M)影响。4. 在4-AP(10^(-3)M)存在的情况下,由去极化激活的剩余缓慢钾离子电流不会失活。5. 在去极化和复极化期间,缓慢电流(GKs)的电导呈指数变化。缓慢电导的稳态值及其激活时间常数随电压而变化。缓慢电导随时间和电压的变化可以用一种开闭模式来描述,假设每个通道由一个粒子门控。缓慢电流的激活动力学不受长时间(500毫秒)预极化的影响。6. 根据快速尾电流计算出的快速钾离子电导,在去极化至0 mV 3分钟结束时完全失活。7. 快速钾离子电导可分解为两个成分:一个成分(GKf1)在-80至-30 mV之间激活,失活非常缓慢(在E = 0 mV时,τ = 45秒);一个成分(GKf2)在-40 mV至+30 mV之间激活,失活缓慢(在E = 0 mV时,τ = 2秒)。温度t = 12℃。8. 最大缓慢和快速电导随[K]0增加。虽然最大快速电导在高外部钾离子浓度下趋于饱和,但最大缓慢电导没有饱和迹象。9. 运动纤维和感觉纤维的比较表明,虽然两种类型纤维的最大缓慢和快速电导幅度相同,但运动纤维中快速-1电导的幅度较大,因此快速-2的幅度比感觉纤维小。根据这些不同的相对快速电导幅度,讨论了在两种类型纤维上观察到的不同的动作电位频率适应性。10. 得出结论,结区膜的钾离子电导由三个成分(GKS、GKf1和GKf2)组成,对应于三种不同且独特的钾离子通道类型。