神经调制与神经激素通讯

神经调制与神经激素通讯刘桂萍,孙春龄（吉林省白城师专生物学系１３７０００）大约５０多年前人们就认识到,神经元之间以突触相互联系,发生在突触处的信息传递是由一组称为神经递质的化学物质完成的化学传递过程。后来,人们不仅认识到化学传递过程伴有生物电效应,而...     

神经营养因子与神经干细胞

生长因子在神经干细胞的增殖,分化和存活过程中有重要作用。神经营养因子是其中的一类,它包括神经生长因子（NGF）家族,胶质源性神经营养因子（GDNF）家族和其它神经营养因子。NGF家族包括NGF,BDNF,NT－3,NT－4／5和NT－6。这一家族可促进epidermic growth facter(EGF)反应 海马及前脑室管膜下区神经干细胞的存活和分化。GDNF家族包括GDNF,NTN,PSP和ART。GDNF家族促神经发育的作用主要在外周,它促进肠神经嵴前体细胞的存活和增殖,且对外周感觉神经的发育至关重要。其它生长因子如bFGF和EGF,它们能促进神经干细胞增殖和存活;CNTF和LIF等在神经干细胞的分化中也有重要作用。     

神经减压术治疗糖尿病神经病变对神经疼痛及神经电生理学的影响

为了研究神经减压手术治疗痛性糖尿病对患者下肢周围神经病变神经疼痛和神经电生理学的影响,本研究进行回顾性研究,测量疼痛水平数字评级量表。治疗效果通过实质性分类缓解(数值评分量表评分降低至少50%)与术前数字评估量表评分相比或非实质性缓解(在数字评分量表评分中减少了50%或更少)在12个月基于既定的标准。性别、年龄、体重指数、糖尿病的持续时间,糖尿病周围神经病变疼痛的持续时间,使用单变量和逻辑回归分析评估术前数字评分量表和两点辨别感觉,并研究神经减压手术治疗对患者神经电生理学的影响。术前平均数值评分量表(8.65±1.29)术后的6 d明显减少(3.56±2.22)(p0.01),6个月(3.03±2.11)(p0.01),术后12个月(3.44±2.36)(p0.01) 64.7%的患者在12个月后有明显的疼痛缓解。据单变量和逻辑回归分析,两点辨别觉和疼痛的缓解息息相关(OR,3.700;p=0.046,逻辑回归分析)。神经减压手术明显减少了痛性糖尿病周围神经病变患者的疼痛数值评分;在患者神经电生理学方面,神经减压术显著加快了手术患者感觉神经和运动神经传导速度。在神经减压手术后,两点辨别觉可以用来诊断痛性糖尿病周围神经病变的前兆因素。     

神经威武

Rodolfo Llinas采用大胆的方法研究神经生理学，彻底改变了人们对神经元个体的理解，以及对神经元产生运动和意识的过程的认识。     

神经免疫学

近十多年来由于分子生物学和细胞生物学的迅猛发展,对哺乳动物体内最复杂的两大系统——神经系统和免疫系统的研究导致一门新的学科——神经免疫学——即免疫学和神经生物学的交叉学科的出现。这也是一门现代生物医学中的新学科。本文试作一概括地介绍,分三个问题。     

神经分泌

神经元具有分泌功能是沙勒(Scharrer)于1928年首次提出的,当时他在研究鱼下丘脑的形态学时,观察到有些神经元内存在典型的分泌颗粒;50年代他与同事们在哺乳动物的下丘脑也发现有相同的结构,并且观察到颗粒的数量随机体水负荷的状况而改变,同时下丘脑提取液经生物鉴定具有抗利尿活性,于是提出了垂体后叶激素来源于下丘脑的设想。后来,轴浆流(axoplasmic flow)现象的发现,为该设想提供了可靠的证据,即如将垂体柄切断,则可见分泌颗粒堆积在截面的近端。加压素(亦称抗利尿激     

神经导航辅助神经内镜清除脑室血肿

目的:应用神经导航辅助神经内镜清除脑室血肿,探讨一种微创清除自发性脑室血肿的方法。方法:37例脑室血肿患者在神经导航定位下应用神经内镜清除脑室血肿。结果:术后3个月据GOS量表和Barther评分表评定,优18例;良11例;中4例;差3例;死亡1例。良好率达78.37%。结论:神经导航辅助神经内镜清除脑室血肿具有定位精确,视野广阔,术后并发症少等优点,是一种安全有效的微创治疗方法。     

肠道内神经丛富含神经介素-U

神经介素-U(neuromedin-U,NMU)是近年由日本学者在猪脊髓发现的一个新肽,有NMU-8和NMU-25两种形式,后者的C端8个氨基酸与NMU-8完全相同。大鼠NMU为23肽,C端7个氨基酸组成与猪NMU一致,二者具有完全的免疫交叉反应。NMU存在于神经系统的神经元和神经纤维中,具     

室管膜下区神经干细胞与神经发生的研究进展

室管膜下区(subventricular zone,SVZ)存在着神经干细胞(nueral stem cells,NSCs),是成年哺乳动物脑内重要的神经发生区域。神经发生过程极为复杂,包括一系列的生物学事件。在病理状态下,SVZ区的细胞增殖,新生的神经细胞迁移到病灶处,取代或修复受损的细胞,起到保护脑组织的作用。该文就SVZ区的神经干细胞、神经发生过程及病理状态下神经发生的相关研究做一综述。     

神经营养因子

神经营养因子(Neurotrophin)是一类含量极少,对神经系统生命活动非常重要的、可溶性多肽因子。它们来源于靶细胞,逆向营养神经元,对脊椎动物神经系统的发生、发育、成     

多种神经活性物质在幼年猫和鸡视网膜神经细胞中的共存(简报)

视网膜起源于前脑泡,结构简单层次分明,因此常被视为脑的简化模型。但近期工作证明,视网膜包含的神经活性物质(神经递质、调质和神经肽)种类之多、分布之复杂并不亚于脑。尤其是无长突细胞不仅包含多种递质和肽类,而且还有递质与肽类或肽类与肽类在一个细胞中的共存。对视网膜神经递质、调质和神经肽的研究将是探索脑奥秘的有效途径。     

The anatomy and innervation of the mammalian pineal gland

The parenchymal cells of the mammalian pineal gland are the hormone-producing pinealocytes and the interstitial cells. In addition, perivascular phagocytes are present. The phagocytes share antigenic properties with microglial and antigen-presenting cells. In certain species, the pineal gland also contains neurons and/or neuron-like peptidergic cells. The peptidergic cells might influence the pinealocyte by a paracrine secretion of the peptide. Nerve fibers innervating the mammalian pineal gland originate from perikarya located in the sympathetic superior cervical ganglion and the parasympathetic sphenopalatine and otic ganglia. The sympathetic nerve fibers contain norepinephrine and neuropeptide Y as neurotransmitters. The parasympathetic nerve fibers contain vasoactive intestinal peptide and peptide histidine isoleucine. Recently, neurons in the trigeminal ganglion, containing substance P, calcitonin gene-related peptide, and pituitary adenylate cyclase-activating peptide, have been shown to project to the mammalian pineal gland. Finally, nerve fibers originating from perikarya located in the brain containing, for example, GABA, orexin, serotonin, histamine, oxytocin, and vasopressin innervate the pineal gland directly via the pineal stalk. Biochemical studies have demonstrated numerous receptors on the pinealocyte cell membrane, which are able to bind the neurotransmitters located in the pinealopetal nerve fibers. These findings indicate that the mammalian pinealocyte can be influenced by a plethora of neurotransmitters.     

Comparative marker analysis of the ependymocytes of the subcommissural organ in four different mammalian species

Summary The subcommissural organ (SCO), classified as one of the circumventricular organs, is composed mainly of modified ependymal cells, attributable to a glial lineage. Nevertheless, in the rat, these cells do not possess glial markers such as glial fibrillary acidic protein (GFAP), protein S100, or the enzyme glutamine synthetase (GS). They receive a synaptic 5-HT input and show pharmacological properties for uptake of GABA resembling the uptake mechanism of neurons. In this study, we examine the phenotype of several mammalian SCO (cat, mouse, rabbit) and compare them with the corresponding features of the rat SCO. In all these species, the SCO ependymocytes possess vimentin as an intermediate filament, but never express GFAP or neurofilament proteins. They do not contain GS as do glial cells involved in GABA metabolism, and when they contain protein S100 (rabbit, mouse), its rate is low in comparison to classical glial or ependymal cells. Thus, these ependymocytes display characteristics that differentiate them from other types of glial cells (astrocytes, epithelial ependymocytes and tanycytes). Striking interspecies differences in the capacity of SCO-ependymocytes for uptake of GABA might be related to their innervation and suggest a species-dependent plasticity in their function.     

GABA release induced by aspartate-mediated activation of NMDA receptors is modulated by dopamine in a selective subpopulation of amacrine cells

Glutamate and GABA are the major excitatory and inhibitory neurotransmitters in the CNS, including the retina. In the chick retina, GABA is located in horizontal and amacrine cells and in some cells in the ganglion cell layer. It has been shown that glutamate and its agonists, NMDA, kainate, and aspartate, promote the release of GABA from isolated retina and from cultured retinal cells. Dopamine, the major catecholamine in the retina, inhibits the induction of GABA release by NMDA. Two to seven-day-old intact chicken retinas were stimulated with different glutamatergic agonists and the GABA remaining in the tissue was detected by immunohistochemical procedures. The exposure of retinas to 100 μ M NMDA for 30 minutes resulted in 50% reduction in the number of GABA-immunoreactive amacrine cells. Aspartate (100 μ M) treatment also resulted in 60% decrease in the number of GABA-immunoreactive amacrine cells. The number of GABA-immunoreactive horizontal cells was not affected by either NMDA or aspartate. In addition, dopamine reversed by 50% the reduction of the number of GABA-immunoreactive amacrine cells exposed to NMDA or aspartate. Kainate stimulation promoted a 50% reduction in the number of both GABA-immunoreactive amacrine and horizontal cells. Dopamine did not interfere with the kainate effect. While in control and in non-stimulated retinas a continuous and homogeneous immunolabeling was observed throughout the inner plexiform layer, retinas exposed to NMDA, kainate and aspartate displayed only a faint punctate labeling in the inner plexiform layer. It is concluded that, under our experimental conditions, both NMDA and aspartate induce the release of GABA exclusively from amacrine cells, and that the release is modulated by dopamine. On the other hand, kainate stimulates GABA release from both amacrine and horizontal cells with no interference of dopamine.     

The neurons of the ground squirrel retina as revealed by immunostains for calcium binding proteins and neurotransmitters

Ground squirrel retinas were immunostained with antibodies against calcium binding proteins (CBPs) and classical neurotransmitters in order to describe neuronal phenotypes in a diurnal mammalian retina and to then compare these neurons with those of more commonly studied nocturnal retinas like cats' and rabbits'. Double immunostained tissue was examined by confocal microscopy using antibodies against the following: rhodopsin and the CBPs, calbindin, calretinin, parvalbumin, calmodulin and recoverin (CB, CR, PV, CM, RV), glycine, GABA, choline acetyltransferase (CHAT) and tyrosine hydroxylase (TOH). In ground squirrel retina, the traditional cholinergic mirror symmetric amacrine cells colocalize CHAT with PV and GABA and faintly with glycine. A second cholinergic amacrine cell type colocalizes glycine alone. CR is found in at least 3 different amacrine cell types. The CR-immunoreactive (IR) cell population is a mixture of glycinergic and GABAergic types. The dopamine cell type IR to tyrosine hydroxylase has the typical morphology of a wide field cell with dendrites in S1 but the “rings” seen in cat or rabbit retina are not as numerous. TOH-IR amacrine cells send large club-shaped processes to the outer plexiform layer. CB and CR are in bipolar cells, A- and B-type horizontal cells and several amacrine cell types. Anti-rhodopsin labels the low density rod photoreceptor population in this species. Anti-recoverin labels cones and some bipolar cells while PKC is found in several different bipolar cell types. One ganglion cell with dendritic branching in S3 is strongly CR-IR. We find no evidence for an AII amacrine cell in the ground squirrel, with either anti-CR or anti-PV. An amacrine cell with similarity to the DAP1-3 cell of rabbit is CR-IR and glycine-IR. We discuss this labeling pattern in relationship to other mammalian species. The differences in staining patterns and phenotypes revealed suggest a functional diversity in the populations of amacrine cells according to whether the retinas are rod or cone dominated.     

Visualization of neuropeptide expression, transport, and exocytosis in Drosophila melanogaster.

Neuropeptides affect an extremely diverse set of physiological processes. Neuropeptides are often coreleased with neurotransmitters but, unlike neurotransmitters, the neuropeptide target cells may be distant from the site(s) of secretion. Thus, it is often difficult to measure the amount of neuropeptide release in vivo by electrophysiological methods. Here we establish an in vivo system for studying the developmental expression, processing, transport, and release of neuropeptides. A GFP-tagged atrial natriuretic factor fusion (preproANF-EMD) was expressed in the Drosophila nervous system with the panneural promoter, elav. During embryonic development, proANF-EMD was first seen to accumulate in synaptic regions of the CNS in stage 17 embryos. By the third instar larval stage, highly fluorescent neurons were evident throughout the CNS. In the adult, fluorescence was pronounced in the mushroom bodies, antennal lobe, and the central complex. At the larval neuromuscular junction, proANF-EMD was concentrated in nerve terminals. We compared the release of proANF-EMD from synaptic boutons of NMJ 6/7, which contain almost exclusively glutamate-containing clear vesicles, to those of NMJ 12, which include the peptidergic type III boutons. Upon depolarization, approximately 60% of the tagged neuropeptide was released from NMJs of both muscles in 15 min, as assayed by decreased fluorescence. Although the elav promoter was equally active in the motor neurons that innervate both NMJs 6/7 and 12, NMJ 12 contained 46-fold more neuropeptide and released much more proANF-EMD during stimulation than did NMJ 6/7. Our results suggest that peptidergic neurons have an enhanced ability to accumulate and/or release neuropeptides as compared to neurons that primarily release classical neurotransmitters.     

Identification of initially appearing glycine‐immunoreactive neurons in the embryonic zebrafish brain

Glycine is a major inhibitory neurotransmitter in the central nervous system of vertebrates. Here, we report the initial development of glycine‐immunoreactive (Gly‐ir) neurons and fibers in zebrafish. The earliest Gly‐ir cells were found in the hindbrain and rostral spinal cord by 20 h post‐fertilization (hpf). Gly‐ir cells in rhombomeres 5 and 6 that also expressed glycine transporter 2 (glyt2) mRNA were highly stereotyped; they were bilaterally located and their axons ran across the midline and gradually turned caudally, joining the medial longitudinal fascicles in the spinal cord by 24 hpf. Gly‐ir neurons in rhombomere 5 were uniquely identified, since there was one per hemisegment, whereas the number of Gly‐ir neurons in rhombomere 6 were variable from one to three per hemisegment. Labeling of these neurons by single‐cell electroporation and tracing them until the larval stage revealed that they became MiD2cm and MiD3cm, respectively. The retrograde labeling of reticulo‐spinal neurons in Tg(glyt2:gfp) larva, which express GFP in Gly‐ir cells, and a genetic mosaic analysis with glyt2:gfp DNA construct also supported this notion. Gly‐ir cells were also distributed widely in the anterior brain by 27 hpf, whereas glyt2 was hardly expressed. Double staining with anti‐glycine and anti‐GABA antibodies demonstrated distinct distributions of Gly‐ir and GABA‐ir cells, as well as the presence of doubly immunoreactive cells in the brain and placodes. These results provide evidence of identifiable glycinergic (Gly‐ir/glyt2‐positive) neurons in vertebrate embryos, and they can be used in further studies of the neurons' development and function at the single‐cell level. © 2013 Wiley Periodicals, Inc. Develop Neurobiol 74: 616–632, 2014     

Peptidergic inputs to sympathetic preganglionic neurons

This paper presents data showing that the sympathetic autonomic areas of the cat thoracolumbar spinal cord contain nerve terminals and fibres with immunoreactivity for at least seven neuropeptides. The distribution in the intermediolateral cell column of the terminals and fibres which contain enkephalin-, neuropeptide Y-, neurotensin-, substance P-, and neurophysin II-like immunoreactivity (ENK, NPY, NT, SP, and NP2, respectively) suggests that these peptides are involved in more generalized functions of the autonomic nervous system. On the other hand, peaks in density of immunoreactivity at certain levels suggest that different levels of influence of sympathetic preganglionic neurons by the various peptides may occur along the length of the thoracolumbar cord. The distribution of terminals and fibres containing somatostatin- and oxytocin-like immunoreactivity (SS and OXY) suggests that these peptides may be part of specific pathways to particular sympathetic preganglionic neurons. The possible sources of the terminals and fibres containing ENK, NPY, NT, SS, and SP include the spinal cord and supraspinal areas, whereas the source of these structures with OXY and NP2 is most likely supraspinal. The data suggest that coexistence of peptides and interactions between structures containing different neuropeptides occur in the spinal autonomic areas. It is speculated that neuropeptides have an important role to play in the regulation of the cardiovascular division of the autonomic nervous system.     

Colocalization of (3H)-adenosine accumulation and GABA immunoreactivity in the chicken and rabbit retinas

Using combined autoradiography and immunohistochemistry, we have compared (3H)-adenosine accumulation and GABA immunoreactivity in the chicken and rabbit retinas. Colocalization of the two markers was observed in a subset of amacrine cells and in certain cell bodies in the ganglion cell layer in both species and in a few horizontal cells in the chicken retina. Cells that contained only (3H)-adenosine or GABA were also seen. The degree of colocalization differed greatly between the two species. The results demonstrate a morphological relationship between the adenosine and GABA systems and provides information on the possible anatomical substrates underlying at least some types of functional interactions.