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A quantitative description of membrane current and its application to conduction and excitation in nerve.膜电流的定量描述及其在神经传导和兴奋中的应用。
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Differential subcellular localization of the two alternatively spliced isoforms of the Kv3.1 potassium channel subunit in brain.Kv3.1钾通道亚基两种可变剪接异构体在大脑中的亚细胞定位差异。
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Intrinsic neuronal properties of the chick nucleus angularis.鸡听觉角核的内在神经元特性
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Developmental expression of potassium-channel subunit Kv3.2 within subpopulations of mouse hippocampal inhibitory interneurons.小鼠海马抑制性中间神经元亚群中钾通道亚基Kv3.2的发育表达
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5
Resilient RTN fast spiking in Kv3.1 null mice suggests redundancy in the action potential repolarization mechanism.Kv3.1基因敲除小鼠中具有适应性的快速发放网状丘脑神经元表明动作电位复极化机制存在冗余。
J Neurophysiol. 2002 Mar;87(3):1303-10. doi: 10.1152/jn.00556.2001.
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Presynaptic short-term depression is maintained during regulation of transmitter release at a GABAergic synapse in rat hippocampus.在大鼠海马体的γ-氨基丁酸能突触处调节神经递质释放的过程中,突触前短期抑制持续存在。
J Physiol. 2002 Feb 15;539(Pt 1):201-8. doi: 10.1113/jphysiol.2001.013455.
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Gating, modulation and subunit composition of voltage-gated K(+) channels in dendritic inhibitory interneurones of rat hippocampus.大鼠海马树突状抑制性中间神经元中电压门控钾离子通道的门控、调节及亚基组成
J Physiol. 2002 Jan 15;538(Pt 2):405-19. doi: 10.1113/jphysiol.2001.013066.
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Compartmental models of rat cerebellar Purkinje cells based on simultaneous somatic and dendritic patch-clamp recordings.基于体细胞和树突膜片钳同步记录的大鼠小脑浦肯野细胞房室模型
J Physiol. 2001 Sep 1;535(Pt 2):445-72. doi: 10.1111/j.1469-7793.2001.00445.x.
9
Alcohol hypersensitivity, increased locomotion, and spontaneous myoclonus in mice lacking the potassium channels Kv3.1 and Kv3.3.缺乏钾通道Kv3.1和Kv3.3的小鼠出现酒精过敏、运动增加和自发性肌阵挛。
J Neurosci. 2001 Sep 1;21(17):6657-65. doi: 10.1523/JNEUROSCI.21-17-06657.2001.
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Modulation of excitability by alpha-dendrotoxin-sensitive potassium channels in neocortical pyramidal neurons.新皮质锥体神经元中α-树突毒素敏感钾通道对兴奋性的调节
J Neurosci. 2001 Sep 1;21(17):6553-60. doi: 10.1523/JNEUROSCI.21-17-06553.2001.

Kv3钾离子电导对于海马体中间神经元高频动作电位的产生是必要的,并且在动力学上经过了优化。

Kv3 potassium conductance is necessary and kinetically optimized for high-frequency action potential generation in hippocampal interneurons.

作者信息

Lien Cheng-Chang, Jonas Peter

机构信息

Institute of Physiology, University of Freiburg, D-79104 Freiburg, Germany.

出版信息

J Neurosci. 2003 Mar 15;23(6):2058-68. doi: 10.1523/JNEUROSCI.23-06-02058.2003.

DOI:10.1523/JNEUROSCI.23-06-02058.2003
PMID:12657664
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6742035/
Abstract

Kv3 channels are thought to be essential for the fast-spiking (FS) phenotype in GABAergic interneurons, but how these channels confer the ability to generate action potentials (APs) at high frequency is unknown. To address this question, we developed a fast dynamic-clamp system (approximately 50 kHz) that allowed us to add a Kv3 model conductance to CA1 oriens alveus (OA) interneurons in hippocampal slices. Selective pharmacological block of Kv3 channels by 0.3 mm 4-aminopyridine or 1 mm tetraethylammonium ions led to a marked broadening of APs during trains of short stimuli and a reduction in AP frequency during 1 sec stimuli. The addition of artificial Kv3 conductance restored the original AP pattern. Subtraction of Kv3 conductance by dynamic clamp mimicked the effects of the blockers. Application of artificial Kv3 conductance also led to FS in OA interneurons after complete K+ channel block and even induced FS in hippocampal pyramidal neurons in the absence of blockers. Adding artificial Kv3 conductance with altered deactivation kinetics revealed a nonmonotonic relationship between mean AP frequency and deactivation rate, with a maximum slightly above the original value. Insertion of artificial Kv3 conductance with either lowered activation threshold or inactivation also led to a reduction in the mean AP frequency. However, the mechanisms were distinct. Shifting the activation threshold induced adaptation, whereas adding inactivation caused frequency-dependent AP broadening. In conclusion, Kv3 channels are necessary for the FS phenotype of OA interneurons, and several of their gating properties appear to be optimized for high-frequency repetitive activity.

摘要

Kv3通道被认为对GABA能中间神经元的快速放电(FS)表型至关重要,但这些通道如何赋予高频产生动作电位(AP)的能力尚不清楚。为了解决这个问题,我们开发了一种快速动态钳制系统(约50 kHz),使我们能够向海马切片中的CA1海马伞(OA)中间神经元添加Kv3模型电导。用0.3 mM 4-氨基吡啶或1 mM四乙铵离子对Kv3通道进行选择性药理学阻断,导致短刺激序列期间AP明显展宽,以及1秒刺激期间AP频率降低。添加人工Kv3电导可恢复原始AP模式。通过动态钳制减去Kv3电导模拟了阻断剂的作用。在完全阻断K+通道后,施加人工Kv3电导也导致OA中间神经元出现FS,甚至在没有阻断剂的情况下在海马锥体神经元中诱导出FS。添加具有改变失活动力学的人工Kv3电导揭示了平均AP频率与失活速率之间的非单调关系,最大值略高于原始值。插入具有降低激活阈值或失活的人工Kv3电导也导致平均AP频率降低。然而,其机制不同。改变激活阈值会诱导适应性变化,而添加失活会导致频率依赖性AP展宽。总之,Kv3通道对于OA中间神经元的FS表型是必需的,并且它们的几种门控特性似乎针对高频重复活动进行了优化。