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本文引用的文献

1
Early increase in extrasynaptic NMDA receptor signaling and expression contributes to phenotype onset in Huntington's disease mice.早期 extrasynaptic NMDA 受体信号和表达的增加导致亨廷顿病小鼠表型的出现。
Neuron. 2010 Jan 28;65(2):178-90. doi: 10.1016/j.neuron.2010.01.008.
2
State-dependent plasticity in vasopressin neurones: dehydration-induced changes in activity patterning.血管加压素神经元的状态依赖性可塑性:脱水诱导的活动模式变化。
J Neuroendocrinol. 2010 May;22(5):343-54. doi: 10.1111/j.1365-2826.2010.01961.x. Epub 2010 Jan 19.
3
Balance between synaptic versus extrasynaptic NMDA receptor activity influences inclusions and neurotoxicity of mutant huntingtin.突触与突触外NMDA受体活性之间的平衡影响突变型亨廷顿蛋白的包涵体形成和神经毒性。
Nat Med. 2009 Dec;15(12):1407-13. doi: 10.1038/nm.2056. Epub 2009 Nov 15.
4
Dehydration-induced modulation of kappa-opioid inhibition of vasopressin neurone activity.脱水诱导的κ-阿片受体抑制血管加压素神经元活性的调制。
J Physiol. 2009 Dec 1;587(Pt 23):5679-89. doi: 10.1113/jphysiol.2009.180232. Epub 2009 Oct 12.
5
Glutamate uptake triggers transporter-mediated GABA release from astrocytes.谷氨酸摄取引发星形胶质细胞中介的 GABA 释放。
PLoS One. 2009 Sep 24;4(9):e7153. doi: 10.1371/journal.pone.0007153.
6
Regulation of tonic GABA inhibitory function, presympathetic neuronal activity and sympathetic outflow from the paraventricular nucleus by astroglial GABA transporters.星形胶质细胞γ-氨基丁酸转运体对紧张性γ-氨基丁酸抑制功能、交感神经节前神经元活动及室旁核交感神经输出的调节
J Physiol. 2009 Oct 1;587(Pt 19):4645-60. doi: 10.1113/jphysiol.2009.173435. Epub 2009 Aug 24.
7
Neuronal viability is controlled by a functional relation between synaptic and extrasynaptic NMDA receptors.神经元的存活受突触和突触外NMDA受体之间功能关系的控制。
FASEB J. 2008 Dec;22(12):4258-71. doi: 10.1096/fj.08-107268. Epub 2008 Aug 18.
8
Synaptic NMDA receptor activity boosts intrinsic antioxidant defenses.突触N-甲基-D-天冬氨酸受体活性增强内在抗氧化防御能力。
Nat Neurosci. 2008 Apr;11(4):476-87. doi: 10.1038/nn2071. Epub 2008 Mar 23.
9
Dual GABAA receptor-mediated inhibition in rat presympathetic paraventricular nucleus neurons.双GABAA受体介导的大鼠交感神经节前室旁核神经元抑制作用
J Physiol. 2007 Jul 15;582(Pt 2):539-51. doi: 10.1113/jphysiol.2007.133223. Epub 2007 May 10.
10
Tonic activation of NMDA receptors by ambient glutamate of non-synaptic origin in the rat hippocampus.大鼠海马体中非突触起源的环境谷氨酸对NMDA受体的强直性激活。
J Physiol. 2007 Apr 15;580(Pt. 2):373-83. doi: 10.1113/jphysiol.2006.123570. Epub 2006 Dec 21.

神经分泌神经元中星形胶质细胞调节细胞外 NMDA 受体信号的状态依赖性变化。

State-dependent changes in astrocyte regulation of extrasynaptic NMDA receptor signalling in neurosecretory neurons.

机构信息

Department of Physiology, Medical College of Georgia, 1120 15th Street Augusta, GA 30912, USA.

出版信息

J Physiol. 2011 Aug 15;589(Pt 16):3929-41. doi: 10.1113/jphysiol.2011.207340. Epub 2011 Jun 20.

DOI:10.1113/jphysiol.2011.207340
PMID:21690192
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3179993/
Abstract

Despite the long-established presence of glutamate NMDA receptors at extrasynaptic sites (eNMDARs), their functional roles remain poorly understood. Factors influencing the concentration and time course of glutamate in the extrasynaptic space, such as the topography of the neuronal–glial microenvironment, as well as glial glutamate transporters, are expected to affect eNMDAR-mediated signalling strength. In this study, we used in vitro and in vivo electrophysiological recordings to assess the properties, functional relevance and modulation of a persistent excitatory current mediated by activation of eNMDARs in hypothalamic supraoptic nucleus (SON) neurons. We found that ambient glutamate of a non-synaptic origin activates eNMDARs to mediate a persistent excitatory current (termed tonic I(NMDA)), which tonically stimulates neuronal activity. Pharmacological blockade of GLT1 astrocyte glutamate transporters, as well as the gliotoxin α-aminodadipic acid, enhanced tonic I(NMDA) and neuronal activity, supporting an astrocyte regulation of tonic I(NMDA) strength. Dehydration, a physiological challenge known to increase SON firing activity and to induce neuroglial remodelling, including reduced neuronal ensheathment by astrocyte processes, resulted in blunted GLT1 efficacy, enhanced tonic I(NMDA) strength, and increased neuronal activity. Taken together, our studies support the view that glial modulation of tonic I(NMDA) activation contributes to regulation of SON neuronal activity, contributing in turn to neuronal homeostatic responses during a physiological challenge.

摘要

尽管谷氨酸 NMDA 受体在突触外部位(eNMDARs)的存在由来已久,但它们的功能作用仍知之甚少。影响突触外空间中谷氨酸浓度和时程的因素,如神经元-神经胶质微环境的拓扑结构以及神经胶质谷氨酸转运体,预计会影响 eNMDAR 介导的信号转导强度。在这项研究中,我们使用体外和体内电生理记录来评估下丘脑视上核(SON)神经元中 eNMDAR 激活介导的持续兴奋性电流的特性、功能相关性和调节。我们发现,非突触来源的环境谷氨酸激活 eNMDAR 以介导持续的兴奋性电流(称为 tonic I(NMDA)),该电流持续刺激神经元活动。GLT1 星形胶质细胞谷氨酸转运体的药理学阻断以及神经胶质毒素 α-氨基己二酸,增强了 tonic I(NMDA)和神经元活性,支持 tonic I(NMDA)强度的星形胶质细胞调节。脱水是一种已知会增加 SON 放电活动并诱导神经胶质重塑的生理挑战,包括星形胶质细胞过程对神经元包绕的减少,导致 GLT1 功效降低、tonic I(NMDA)强度增强和神经元活性增加。总之,我们的研究支持这样一种观点,即胶质细胞对 tonic I(NMDA)激活的调节有助于调节 SON 神经元活动,进而有助于在生理挑战期间神经元的稳态反应。