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Permeation and block of rat GluR6 glutamate receptor channels by internal and external polyamines.内源性和外源性多胺对大鼠GluR6谷氨酸受体通道的通透与阻断作用
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Distribution of neurones expressing inwardly rectifying and Ca(2+)-permeable AMPA receptors in rat hippocampal slices.表达内向整流和Ca(2+)通透性AMPA受体的神经元在大鼠海马切片中的分布。
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Synaptic strengthening through activation of Ca2+-permeable AMPA receptors.通过激活钙离子通透型AMPA受体实现突触增强。
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Pre- and postsynaptic glutamate receptors at a giant excitatory synapse in rat auditory brainstem slices.大鼠听觉脑干切片中一个巨大兴奋性突触处的突触前和突触后谷氨酸受体。
J Physiol. 1995 Oct 15;488 ( Pt 2)(Pt 2):387-406. doi: 10.1113/jphysiol.1995.sp020974.
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A synaptic model of memory: long-term potentiation in the hippocampus.记忆的突触模型:海马体中的长时程增强效应
Nature. 1993 Jan 7;361(6407):31-9. doi: 10.1038/361031a0.
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Patch-clamp recordings from the soma and dendrites of neurons in brain slices using infrared video microscopy.利用红外视频显微镜对脑片神经元的胞体和树突进行膜片钳记录。
Pflugers Arch. 1993 Jun;423(5-6):511-8. doi: 10.1007/BF00374949.
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Heterogeneity of synaptic glutamate receptors on CA3 stratum radiatum interneurones of rat hippocampus.大鼠海马CA3辐射层中间神经元突触谷氨酸受体的异质性
J Physiol. 1993 Mar;462:373-92. doi: 10.1113/jphysiol.1993.sp019560.
10
AMPA receptors with high Ca2+ permeability mediate synaptic transmission in the avian auditory pathway.具有高钙离子通透性的AMPA受体介导鸟类听觉通路中的突触传递。
J Physiol. 1995 Jan 15;482 ( Pt 2)(Pt 2):309-15. doi: 10.1113/jphysiol.1995.sp020519.

通过多胺阻断的活性依赖性解除来促进电流通过大鼠Ca2+通透型AMPA受体通道。

Facilitation of currents through rat Ca2+-permeable AMPA receptor channels by activity-dependent relief from polyamine block.

作者信息

Rozov A, Zilberter Y, Wollmuth L P, Burnashev N

机构信息

Max-Planck-Institut fur medizinische Forschung, Abteilung Zellphysiologie, Jahnstrasse 29, D-69120 Heidelberg, Germany.

出版信息

J Physiol. 1998 Sep 1;511 ( Pt 2)(Pt 2):361-77. doi: 10.1111/j.1469-7793.1998.361bh.x.

DOI:10.1111/j.1469-7793.1998.361bh.x
PMID:9706016
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2231126/
Abstract
  1. In outside-out patches excised from human embryonic kidney (HEK) 293 cells expressing Ca2+-permeable alpha-amino-3-hydroxy-5-methyl-4-isoxazole-propionate receptor (AMPAR) channels, currents activated by 1 ms glutamate pulses at negative membrane potentials facilitated during and following a repetitive (2 to 100 Hz) agonist application. The degree of facilitation depended on subunit type, membrane potential and stimulation frequency being antagonized by a slow recovery from desensitization. 2. Activity-dependent current facilitation occurred in Ca2+-permeable but not in Ca2+-impermeable AMPAR channels. Current facilitation, however, does not depend on Ca2+ flux. Rather it reflects a relief from the block of Ca2+-permeable AMPARs by intracellular polyamines since facilitation occurred only in the presence of polyamines and since facilitated currents had a nearly linear current-voltage relation (I-V). 3. Relief from polyamine block was use dependent and occurred mainly in open channels. The relief mechanism was determined primarily by membrane potential rather than by current flow. 4. In closed channels the degree of polyamine block was independent of membrane potential. The voltage dependence of the rate of relief from the block in open channels rather than the voltage dependence of the block underlies the inwardly rectifying shape of the I-V at negative potentials. 5. Currents through native Ca2+-permeable AMPAR channels in outside-out or nucleated patches from either hippocampal basket cells or a subtype of neocortical layer II nonpyramidal cells also showed facilitation. 6. It is concluded that a use-dependent relief from polyamine block during consecutive AMPAR channel openings underlies current facilitation. This polyamine-AMPAR interaction may represent a new activity-dependent postsynaptic mechanism for control of synaptic signalling.
摘要
  1. 在从表达钙离子通透型α-氨基-3-羟基-5-甲基-4-异恶唑丙酸受体(AMPAR)通道的人胚肾(HEK)293细胞上切下的外向型膜片中,在负膜电位下由1毫秒谷氨酸脉冲激活的电流,在重复(2至100赫兹)激动剂施加期间及之后会增强。增强程度取决于亚基类型、膜电位和刺激频率,脱敏后的缓慢恢复会拮抗这种增强。2. 活性依赖的电流增强发生在钙离子通透型而非钙离子不通透型AMPAR通道中。然而,电流增强并不依赖于钙离子通量。相反,它反映了细胞内多胺对钙离子通透型AMPAR通道阻滞的缓解,因为增强仅在多胺存在时发生,且增强后的电流具有近乎线性的电流-电压关系(I-V)。3. 多胺阻滞的缓解是使用依赖的,主要发生在开放通道中。缓解机制主要由膜电位而非电流流动决定。4. 在关闭通道中,多胺阻滞程度与膜电位无关。开放通道中阻滞缓解速率的电压依赖性而非阻滞的电压依赖性,是负电位下I-V内向整流形状的基础。5. 通过海马篮状细胞或新皮层II层非锥体细胞亚型的外向型或有核膜片中天然钙离子通透型AMPAR通道的电流也显示出增强。6. 得出的结论是,连续AMPAR通道开放期间多胺阻滞的使用依赖缓解是电流增强的基础。这种多胺-AMPAR相互作用可能代表了一种新的活性依赖的突触后机制,用于控制突触信号传递。