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The inhibition of nitric oxide synthase enhances PSA-NCAM expression and CREB phosphorylation in the rat hippocampus.一氧化氮合酶的抑制增强了大鼠海马体中PSA-NCAM的表达和CREB的磷酸化。
Neuroreport. 2004 Feb 9;15(2):231-4. doi: 10.1097/00001756-200402090-00003.
2
Vesicular glutamate transporters in the spinal cord, with special reference to sensory primary afferent synapses.脊髓中的囊泡谷氨酸转运体,特别涉及感觉初级传入突触。
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Nitric oxide modulation of the hypothalamo-neurohypophyseal system.一氧化氮对下丘脑 - 神经垂体系统的调节作用。
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NO inhibition of the magnocellular neuroendocrine system in rats is independent of cGMP signaling pathway.大鼠中视上核神经内分泌系统的一氧化氮抑制作用独立于环鸟苷酸信号通路。
Exp Neurol. 2003 Dec;184(2):846-56. doi: 10.1016/S0014-4886(03)00305-4.
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Signalling pathway of nitric oxide in synaptic GABA release in the rat paraventricular nucleus.大鼠室旁核中一氧化氮在突触γ-氨基丁酸释放中的信号通路。
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Visualization of nitric oxide production and intracellular calcium in juxtamedullary afferent arteriolar endothelial cells.近髓质传入小动脉内皮细胞中一氧化氮生成及细胞内钙的可视化
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A calcium-induced calcium influx factor, nitric oxide, modulates the refilling of calcium stores in astrocytes.一种钙诱导的钙内流因子——一氧化氮,可调节星形胶质细胞中钙库的再填充。
J Neurosci. 2003 Nov 12;23(32):10302-10. doi: 10.1523/JNEUROSCI.23-32-10302.2003.
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Application of 4,5-diaminofluorescein to reliably measure nitric oxide released from endothelial cells in vitro.应用4,5-二氨基荧光素可靠地测量体外内皮细胞释放的一氧化氮。
Biol Proced Online. 2003;5:136-142. doi: 10.1251/bpo55. Epub 2003 Jun 15.
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Activation of the cGMP/nitric oxide signal transduction system by nicotine in the retina.尼古丁对视网膜中cGMP/一氧化氮信号转导系统的激活作用。
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10
Nitric oxide inhibits the firing activity of hypothalamic paraventricular neurons that innervate the medulla oblongata: role of GABA.一氧化氮抑制支配延髓的下丘脑室旁核神经元的放电活动:γ-氨基丁酸的作用
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大鼠大细胞神经分泌系统中内源性一氧化氮的细胞来源、靶点及作用

Cellular sources, targets and actions of constitutive nitric oxide in the magnocellular neurosecretory system of the rat.

作者信息

Stern Javier E, Zhang Wenfeng

机构信息

Department of Psychiatry, Genome Research Insitute, University of Cincinnati, 2170 E. Galbraith Road, Cincinnati, OH 45237, USA.

出版信息

J Physiol. 2005 Feb 1;562(Pt 3):725-44. doi: 10.1113/jphysiol.2004.077735. Epub 2004 Nov 18.

DOI:10.1113/jphysiol.2004.077735
PMID:15550458
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1665550/
Abstract

Nitric oxide (NO) is a key activity-dependent modulator of the magnocellular neurosecretory system (MNS) during conditions of high hormonal demand. In addition, recent studies support the presence of a functional constitutive NO tone. The aim of this study was to identify the cellular sources, targets, signalling mechanisms and functional relevance of constitutive NO production within the supraoptic nucleus (SON). Direct visualization of intracellular NO, along with neuronal nitric oxide synthase (nNOS) and cGMP immunohistochemistry, was used to study the cellular sources and targets of NO within the SON, respectively. Our results support the presence of a strong NO basal tone within the SON, and indicate that vasopressin (VP) neurones constitute the major neuronal source and target of basal NO. NO induced-fluorescence and cGMP immunoreactivity (cGMPir) were also found in the glia and microvasculature of the SON, suggesting that they contribute as sources/targets of NO within the SON. cGMPir was also found in association with glutamic acid decarboxylase 67 (GAD67)- and vesicular glutamate transporter 2 (VGLUT2)-positive terminals. Glutamate, acting on NMDA and possibly AMPA receptors, was found to be an important neurotransmitter driving basal NO production within the SON. Finally, electrophysiological recordings obtained from SON neurones in a slice preparation indicated that constitutive NO efficiently restrains ongoing firing activity of these neurones. Furthermore, phasically active (putative VP) and continuously firing neurones appeared to be influenced by NO originating from different sources. The potential roles for basal NO as an autocrine signalling molecule, and one that bridges neuronal-glial-vascular interactions within the MNS are discussed.

摘要

在激素需求旺盛的情况下,一氧化氮(NO)是大细胞神经分泌系统(MNS)中一种关键的活动依赖性调节剂。此外,最近的研究支持功能性组成型NO张力的存在。本研究的目的是确定视上核(SON)内组成型NO产生的细胞来源、靶点、信号传导机制及其功能相关性。分别利用细胞内NO的直接可视化以及神经元型一氧化氮合酶(nNOS)和环磷酸鸟苷(cGMP)免疫组织化学来研究SON内NO的细胞来源和靶点。我们的结果支持SON内存在强大的NO基础张力,并表明血管加压素(VP)神经元是基础NO的主要神经元来源和靶点。在SON的神经胶质细胞和微脉管系统中也发现了NO诱导荧光和cGMP免疫反应性(cGMPir),这表明它们也是SON内NO的来源/靶点。在谷氨酸脱羧酶67(GAD67)和囊泡谷氨酸转运体2(VGLUT2)阳性终末也发现了cGMPir。发现谷氨酸作用于NMDA受体以及可能的AMPA受体,是驱动SON内基础NO产生的重要神经递质。最后,在脑片制备中从SON神经元获得的电生理记录表明,组成型NO有效地抑制了这些神经元的持续放电活动。此外,相位活跃(假定为VP)和持续放电的神经元似乎受到来自不同来源的NO的影响。本文讨论了基础NO作为自分泌信号分子以及在MNS内建立神经元 - 神经胶质 - 血管相互作用的潜在作用。