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本文引用的文献

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Local axon collaterals of lamina I projection neurons in the spinal cord of young rats.幼年大鼠脊髓 I 层投射神经元的局部轴突侧支。
J Comp Neurol. 2010 Jul 15;518(14):2645-65. doi: 10.1002/cne.22391.
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Multisegmental A{delta}- and C-fiber input to neurons in lamina I and the lateral spinal nucleus.多节段 A{delta}-和 C-纤维向 I 层和脊髓外侧核神经元的传入。
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Transmission efficacy and plasticity in glutamatergic synapses formed by excitatory interneurons of the substantia gelatinosa in the rat spinal cord.在大鼠脊髓胶状质中兴奋性中间神经元形成的谷氨酸能突触的传递效率和可塑性。
PLoS One. 2009 Nov 30;4(11):e8047. doi: 10.1371/journal.pone.0008047.
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Reporting ethical matters in the Journal of Physiology: standards and advice.《生理学杂志》中的伦理问题报告:标准与建议
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Role of ionotropic glutamate receptors in long-term potentiation in rat hippocampal CA1 oriens-lacunosum moleculare interneurons.离子型谷氨酸受体在大鼠海马CA1区原层-分子层间隙神经元长时程增强中的作用
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Advanced technique of infrared LED imaging of unstained cells and intracellular structures in isolated spinal cord, brainstem, ganglia and cerebellum.用于对分离的脊髓、脑干、神经节和小脑中未染色细胞及细胞内结构进行红外发光二极管成像的先进技术。
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Numbers, densities, and colocalization of AMPA- and NMDA-type glutamate receptors at individual synapses in the superficial spinal dorsal horn of rats.大鼠脊髓背角浅层单个突触处AMPA型和NMDA型谷氨酸受体的数量、密度及共定位情况。
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Monosynaptic convergence of C- and Adelta-afferent fibres from different segmental dorsal roots on to single substantia gelatinosa neurones in the rat spinal cord.来自大鼠脊髓不同节段背根的C类和Aδ类传入纤维对单个脊髓胶状质神经元的单突触汇聚。
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Translocation of GluR1-containing AMPA receptors to a spinal nociceptive synapse during acute noxious stimulation.急性伤害性刺激期间含GluR1的AMPA受体向脊髓伤害性突触的转运。
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来自相邻 I 层神经元的单突触兴奋性输入到脊髓 I 层前外侧束投射神经元。

Monosynaptic excitatory inputs to spinal lamina I anterolateral-tract-projecting neurons from neighbouring lamina I neurons.

机构信息

Instituto de Biologia Molecular e Celular, Universidade do Porto, Rua do Campo Alegre 823, 4150-180 Porto, Portugal.

出版信息

J Physiol. 2010 Nov 15;588(Pt 22):4489-505. doi: 10.1113/jphysiol.2010.197012. Epub 2010 Sep 27.

DOI:10.1113/jphysiol.2010.197012
PMID:20876196
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3008853/
Abstract

Spinal lamina I receives nociceptive primary afferent input to project through diverse ascending pathways, including the anterolateral tract (ALT). Large projection neurons (PNs) form only a few per cent of the cell population in this layer, and little is known about their local input from other lamina I neurons. We combined single-cell imaging in the isolated spinal cord, paired recordings, 3-D reconstructions of biocytin-labelled neurons and computer simulations to study the monosynaptic input to large ALT-PNs from neighbouring (somata separated by less than 80 μm) large lamina I neurons. All 11 connections identified were excitatory. We have found that an axon of a presynaptic neuron forms multiple synapses on an ALT-PN, and both Ca(2+)-permeable and Ca(2+)-impermeable AMPA receptors are involved in transmission. The monosynaptic EPSC latencies (1-12 ms) are determined by both post- and presynaptic factors. The postsynaptic delay, resulting from the electrotonic EPSC propagation in the dendrites of an ALT-PN, could be 4 ms at most. The presynaptic delay, caused by the spike propagation in a narrow highly branched axon of a local-circuit neuron, can be about 10 ms for neighbouring ALT-PNs and longer for more distant neurons. In many cases, the EPSPs evoked by release from a lamina I neuron were sufficient to elicit a spike in an ALT-PN. Our data show that ALT-PNs can receive input from both lamina I local-circuit neurons and other ALT-PNs. We suggest that lamina I is a functionally interconnected layer. The intralaminar network described here can amplify the overall output from the principal spinal nociceptive projection area.

摘要

脊髓板层 I 接收伤害性初级传入输入,通过多种上升途径投射,包括前外侧束 (ALT)。 大投射神经元 (PN) 在该层的细胞群体中只占少数,它们来自其他板层 I 神经元的局部输入知之甚少。 我们结合了离体脊髓中的单细胞成像、成对记录、生物素标记神经元的 3D 重建和计算机模拟,研究了来自邻近(相隔小于 80 μm 的胞体)大板层 I 神经元的大 ALT-PN 的单突触输入。 鉴定的 11 个连接都是兴奋性的。 我们发现,一个前突神经元的轴突可以在一个 ALT-PN 上形成多个突触,并且 Ca(2+)-可渗透和 Ca(2+)-不可渗透的 AMPA 受体都参与了传递。 单突触 EPSC 潜伏期(1-12 ms)取决于突触后和突触前因素。 来自局部回路神经元的狭窄高度分支轴突中的尖峰传播引起的突触前延迟最多可以是 4 ms。 来自板层 I 神经元释放引起的 EPSP 在 ALT-PN 的树突中进行电紧张传播,其突触后延迟可以是 4 ms,对于邻近的 ALT-PN 可以是 10 ms 左右,对于更远的神经元则更长。 在许多情况下,来自板层 I 神经元释放引起的 EPSP 足以在 ALT-PN 中引发尖峰。 我们的数据表明,ALT-PN 可以接收来自板层 I 局部回路神经元和其他 ALT-PN 的输入。 我们认为板层 I 是一个功能上相互连接的层。 这里描述的板层内网络可以放大来自主要脊髓伤害性投射区域的整体输出。