Stern Javier E, Zhang Wenfeng
Department of Psychiatry, Genome Research Insitute, University of Cincinnati, 2170 E. Galbraith Road, Cincinnati, OH 45237, USA.
J Physiol. 2005 Feb 1;562(Pt 3):725-44. doi: 10.1113/jphysiol.2004.077735. Epub 2004 Nov 18.
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.
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。