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本文引用的文献

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L-type calcium channel-mediated plateau potentials in barrelette cells during structural plasticity.结构可塑性过程中桶状小体细胞中L型钙通道介导的平台电位
J Neurophysiol. 2002 Aug;88(2):794-801. doi: 10.1152/jn.2002.88.2.794.
2
Synaptic mechanisms regulating the activation of a Ca(2+)-mediated plateau potential in developing relay cells of the LGN.调节外膝体发育中继细胞中钙介导的平台电位激活的突触机制。
J Neurophysiol. 2002 Mar;87(3):1175-85. doi: 10.1152/jn.00715.1999.
3
Neural activity: sculptor of 'barrels' in the neocortex.神经活动:新皮层中“桶状结构”的塑造者。
Trends Neurosci. 2001 Oct;24(10):589-95. doi: 10.1016/s0166-2236(00)01958-5.
4
Roles of serine/threonine phosphatases in hippocampal synaptic plasticity.丝氨酸/苏氨酸磷酸酶在海马突触可塑性中的作用。
Nat Rev Neurosci. 2001 Jul;2(7):461-74. doi: 10.1038/35081514.
5
Neonatal deafferentation does not alter membrane properties of trigeminal nucleus principalis neurons.新生儿去传入并不改变三叉神经脑桥核主神经元的膜特性。
J Neurophysiol. 2001 Mar;85(3):1088-96. doi: 10.1152/jn.2001.85.3.1088.
6
Afferent ingrowth and onset of activity in the rat trigeminal nucleus.大鼠三叉神经核中的传入神经长入及活动起始
Eur J Neurosci. 2000 Aug;12(8):2781-92. doi: 10.1046/j.1460-9568.2000.00161.x.
7
Synaptic regulation of L-type Ca(2+) channel activity and long-term depression during refinement of the retinocollicular pathway in developing rodent superior colliculus.发育中小鼠上丘视网膜-视顶盖通路精细化过程中L型钙通道活性的突触调节与长时程抑制
J Neurosci. 2000 Feb 1;20(3):RC58. doi: 10.1523/JNEUROSCI.20-03-j0003.2000.
8
Electrophysiological properties and synaptic responses of cells in the trigeminal principal sensory nucleus of postnatal rats.新生大鼠三叉神经感觉主核中细胞的电生理特性和突触反应
J Neurophysiol. 1999 Nov;82(5):2765-75. doi: 10.1152/jn.1999.82.5.2765.
9
Spontaneous activity in the perinatal trigeminal nucleus of the rat.
Neuroreport. 1999 Feb 25;10(3):659-64. doi: 10.1097/00001756-199902250-00039.
10
Developmental changes in the electrophysiological properties of brain stem trigeminal neurons during pattern (barrelette) formation.
J Neurophysiol. 1998 Mar;79(3):1295-306. doi: 10.1152/jn.1998.79.3.1295.

在小棒形成和巩固期间三叉神经主核中的突触可塑性。

Synaptic plasticity in the trigeminal principal nucleus during the period of barrelette formation and consolidation.

作者信息

Guido W, Lo F S, Erzurumlu R S

机构信息

Department of Cell Biology and Anatomy, Neuroscience Center for Excellence, Louisiana State Health Science Center, New Orleans, LA 70112, USA.

出版信息

Brain Res Dev Brain Res. 2001 Dec 14;132(1):97-102. doi: 10.1016/s0165-3806(01)00283-8.

DOI:10.1016/s0165-3806(01)00283-8
PMID:11744112
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3676670/
Abstract

We examined whether the postsynaptic responses of cells in the principal sensory nucleus of the trigeminal nerve (PrV) are subject to long-term changes in synaptic strength, and if such changes were correlated the whisker-specific patterning during and just after the critical period for pattern formation. We used an in vitro brainstem preparation in which the trigeminal ganglion (TG) and PrV remained attached. By electrically activating TG afferents, we evoked large-amplitude extracellular field potentials. These responses were postsynaptic in origin and blocked by the glutamate antagonist, DNQX. At P1, a time when barrelettes are consolidating, high frequency stimulation of their afferents led to an immediate (<1 min) and long-lasting (> or =90 min) reduction (35%) in the amplitude of the evoked response. At P3-7, when the pattern of barrelettes have stabilized, the same form of tetanus led to an immediate and long-lasting increase (40%) in the amplitude of the response. Both forms of synaptic plasticity were mediated by the activation of L-type Ca(2+) channels. Application of the L-type channel blocker, nitrendipine, led to a complete blockade of any the tetanus induced changes. These associative processes may regulate the patterning and maintenance of whisker-specific patterns in the brainstem trigeminal nuclei.

摘要

我们研究了三叉神经主感觉核(PrV)中细胞的突触后反应是否会发生突触强度的长期变化,以及这种变化是否与模式形成关键期及之后的胡须特异性模式相关。我们使用了一种体外脑干制备方法,其中三叉神经节(TG)和PrV保持相连。通过电刺激TG传入神经,我们诱发了大幅度的细胞外场电位。这些反应起源于突触后,且被谷氨酸拮抗剂DNQX阻断。在P1期,此时小桶状结构正在巩固,对其传入神经进行高频刺激会导致诱发反应的幅度立即(<1分钟)且持久(≥90分钟)降低(35%)。在P3 - 7期,当小桶状结构的模式已经稳定时,相同形式的强直刺激会导致反应幅度立即且持久增加(40%)。两种形式的突触可塑性均由L型钙通道的激活介导。应用L型通道阻滞剂尼群地平会导致完全阻断任何强直刺激诱导的变化。这些关联过程可能调节脑干三叉神经核中胡须特异性模式的形成和维持。