哈蚧前背侧室嵴嘴外侧区的纤维联系

用ＨＲＰ顺、逆行追踪技术,对蛤蚧（Gekko gecko)前背侧室嵴嘴外侧区内部,以及该区与其周围结构之间的纤维联系进行了系统研究。结果表明：①蛤蚧前背侧室嵴嘴外侧区内部存在核心部－浅层细胞区环路;②蛤蚧前背侧室嵴嘴外侧区与尾外侧区之间有广泛的纤维联系;③蛤蚧前背侧室嵴嘴外侧区与皮质加厚区之间的环路是２条联系视觉通路的高级中枢。     

蛤蚧前背侧室嵴(ADVR)的分区及细胞形态学研究

采用解剖学方法和绀织学方法仔细观察,分析蛤蚧（Gekko gecko）前背侧室嵴（ADVR）的形态学分区,发现以ADVR表面的浅沟为标记,参照细胞着色深浅,细胞密度分布特征以及细胞形态大小,可将ADVR分为内侧区（ma）、嘴外侧区（rla）和尾外侧区（cla）等3个部分,为ADVR的结构功能的深入研究提供了形态学依据。     

蛤蚧视觉神经核团的细胞形态结构及功能的研究

本研究发现,蛤蚧视觉神经核团有视顶盖（OT）、峡核（NI）、基底视束核（nBOR）、豆状核（LM）、中脑深部核（NPM）、圆核（NR）、前背侧室嵴（ADVR）和皮质加厚区（Pth）等,其中NI和ADVR两核团的体积最大。视觉核团中有各种形状的细胞形态,其中梨形和梭形细胞占的比例较大。神经核团的细胞直径为6～30μm,其中以15～28μm最多。在ADVR和Pth核团中有细胞丛簇存在,其它核团尚未发现有这样的结构。各神经核团问和核团内有广泛而复杂的纤维联系。蛤蚧有关视觉神经核团除具有视觉功能外,可能还与听觉、触觉、嗅觉和平衡感觉等功能有关。     

大鼠海马—小脑皮层—小脑深部核团投射的电生理学和HRP研究

本文用电生理学和HRP示踪法,研究了大鼠海马-小脑皮层投射的空间分布,小脑皮层的海马投射区与其深部核团间的纤维联系。 电生理学的实验结果表明,刺激背侧海马CA_1/CA_3区,均可使小脑皮层第Ⅵ小叶的浦肯野细胞产生顺行多突触的诱发简单锋电位和复杂锋电位反应。提示背侧海马CA_1/CA_3区与小脑皮层之间有经苔状纤维和攀缘纤维的多突触投射。实验证明,大鼠的这一投射的终止区域,集中在小脑皮层第Ⅵ小叶中线外侧0.8—1.4mm的范围内;并且来自CA_1区的投射以对侧性为主,CA_3区的投射以同侧性为主。HRP示踪的实验表明,背侧海马CA_1/CA_3区在小脑皮层第Ⅵ小叶的投射区是小脑纵区组构的间位区,该区皮层与间位核之间存在着交互投射关系。     

蛤蚧豆状核的结构及其与顶盖前端的纤维联系

运用Nissl法和辣根过氧化物酶(horseradish peroxidase,HRP)追踪标记技术,研究蛤蚧(Gekko gecko)豆状核的结构及其与顶盖前端的纤维联系。Nissl染色显示,蛤蚧豆状核细胞大小没有明显差别,由背内侧细胞密集部和腹外侧细胞稀疏部组成。将HRP注射于顶盖前端,结果豆状核背内侧部和腹外侧部分别接受同侧顶盖前端脑室内、外侧纤维的传入,核内标记有浓密的神经丛和大量纤维末梢,并在该核腹外侧部及其邻近区域发现少量大胞体标记细胞。推测豆状核腹外侧部的大胞体细胞及其邻近区域的大胞体细胞可能具有相同的功能,且该核可能形成离顶盖通路和副视系统相联系的交通要道。     

鸣禽栗 新纹状体L复合区与发声控制系统的神经联系

利用辣根过氧化物酶顺、逆行追踪的方法对鸣禽栗端脑新纹状体Ｌ复合区的神经联系进行了研究。结果表明,新纹状体Ｌ复合区中的Ｌ２区主要接受来自丘脑卵圆核的传入,并与Ｌ１和Ｌ３区有纤维联系;而Ｌ１和Ｌ３区传出纤维投射至高级发声中枢腹侧的架区、古纹状体粗核喙背侧的杯区以及上纹状体腹部尾外侧等处;Ｌ复合区亦接受来自新纹状体前部巨细胞核内侧部的传入投射。     

鸣禽栗Wu新纹状体L复合区与发声控制系统的神经联系

利用辣根过氧化物酶顺、逆行追踪的方法对鸣禽栗Ｗｕ端脑新纹状体Ｌ复合区的神经联系进行了研究。结果表明,新纹状体Ｌ复合区中的Ｌ２区主要接受来自丘脑卵圆核的传入,并与Ｌ１和Ｌ３区有纤维联系;而Ｌ１和Ｌ３区传出纤维投射至高级发声中枢腹侧的架区、１古纹状体粗核 背侧的杯区以及上纹状体腹部尾外侧等处;Ｌ复合区亦接受一自新纹状体前部巨细胞核内侧部的传入投射。     

扬子鳄胚胎发育后期端脑背侧区的超微结构观察

背侧区位于大脑半球的外侧沟和终沟之间,向脑腔突入,几乎占满整个脑腔,有视觉,听觉和躯体感觉等重要功能,一些作者称它为脑室背嵴(Dorsal ventricular ridge).爬行类成体端脑背侧区的形态学和超微结构研究在国外有所报道1-3,而其胚胎发育详细资料只见于1987年Yanes对蜥蜴背侧区的研究4.扬子鳄(Alligator sinensis Fauvel)为国家重点保护动物之一,研究其组织胚胎结构在系统进化和饲养方面有着重要意义,同时也可填补国内在爬行类脑研究上的空白.       

大鼠下丘脑内一氧化氮合酶阳性神经元的分布

用ＮＡＤＰＨ－ｄ组织化学方法观察了大白鼠下丘脑内一氧化氮合酶（ＮＤＳ）阳性神经元的分布及形态特征。结果显示：在视上核、室旁核的大细胞部、环状核、穹窿周核、下丘脑外侧区、下丘脑腹内侧核、下丘脑背内侧核、乳头体区大部分核团均可见一氧化氮合酶阳性神经元聚集成团。在视前内侧区、视前外侧区、下丘脑前区、下丘脑背侧区、下丘脑后区、室周核、室旁核小细胞部及穹窿内可见散在的一氧化氮合酶阳性神经元。室周核内可见呈阳性反应的接触脑脊液神经元的胞体及突起。一氧化氮合酶阳性神经元大多可见突起,有的突起上可见１～２级分支,并可见膨体。下丘脑大部分区域内可见阳性神经纤维。弓状核内可见许多弧形纤维连于第三脑室室管膜和正中隆起。     

视前区、下丘脑外侧区对外侧缰核“痛”单位放电的影响

以往工作表明,刺激或损毁缰核可改变动物的痛阈(王绍、李淑捷等,1980),并从外侧缰核发现了与痛有关的神经元(王绍、江岩等,1980)。在痛觉调制的机能联系中,缰核可以调节中缝核(王绍、江岩等1980;Wang等,1977)、蓝斑核(王绍等,1981)的放电活动。而缰核是边缘——中脑环路中一个重要的中转站,它可以会聚许多边缘前脑结构的传入纤维(Miles等,1977)。其中,视前区、下丘脑外侧区的传出纤维直接分布于外侧缰核(Hamilton,1976)。而且电针信号可到达这两个区域(天津医学院针麻研究室,1977;孙文颖等,1979),刺激或损毁它们也可加强或削弱针刺镇痛(唐仲良等,1978;张家驹等,     

Projections of Olfactory Bulbs and Non-Olfactory Telencephalic Structures in Amygdaloid Complex of the Turtle <Emphasis Type="Italic">Testudo horsfieldi</Emphasis>: A Study Using Anterograde Tracer Technique

To confirm the discrete character of projections of telencephalic olfactory and non-olfactory structures to the amygdaloid complex (AC) in the terrestrial turtle Testudo horsfieldi, a study was performed by the method of anterograde axonal transport of tracers (HRP, BDA). After a massive injection of the tracers into the main and accessory olfactory bulb, a dense accumulation of labeled fibers and terminals was found in ventral part of AC in the neuropil zones of nbam (J) and ncoam and very scanty—in nmam and ncam. After a massive injection of the tracers into non-olfactory telencephalic structures including dorsal cortex, pallidal enlargement, and ADVR, a very dense terminal field was observed in the dorsal AC part and a less dense one, with predominance of labeled fibers, in its ventral part. Local administration of the tracers separately into the dorsolateral (visual area) and the ventromedial (auditory-somatic area) parts of the ADVR allowed revealing discrete projections, respectively, to the laterocentral and mediocentral areas of the dorsal AC part with a relative overlapping in the central AC area. In all experiments, retrogradely labeled neurons in AC were also observed in zones of the corresponding bulbar and rostrotelencephalic projections. Thus, it has been shown that in the turtle AC there exist not only separation of direct olfactory and non-olfactory projections, but also discrete projections of different sensory areas of ADVR. Reciprocity of these connections is also confirmed. Organization of afferent olfactory and non-olfactory telencephalic connections in AC is similar in reptiles and in mammals.     

Anterior dorsal ventricular ridge in the lizard: Embryonic development

In lacertids the telencephalic vesicle starts its development at stage E = 30, at which time it is lined by a homogeneous nucleated zone in which particular ventricular zone territories or sulci cannot be distinguished. At stage E = 32 coinciding with the initial development of the anterior dorsal ventricular ridge (ADVR), one may distinguish the ventricular zone b in the dorsolateral wall of the ventricle adjacent to the sulcus lateralis. The ADVR continues growing by incorporation of cells produced in two proliferative zones (zone b and wall of the sulcus lateralis) and appears fully developed in postnatal lizards. Ultrastructural characteristics of young ADVR neurons between stages E-32 and E-33 are typical of those in immature cells. Beginning at stage E-34, some of these neurons appear to be degenerating (pycnotic). Thereafter, neurons of the ADVR develop abundant cytoplasmic organelles and the neuropile grows quickly. Myelination starts in the ADVR between stages E-38 and E-40, but is not observed in other striatal masses in the same period. Vascularization begins and is well developed at E-40. The first synaptic contacts were observed in embryos of stage E=38; they are chiefly axo-dendritic, although some are axo-somatic. Degenerating neurons were found in the ADVR up to hatching. From stage E-40 onward, the ADVR shows a greater and more rapid differentiation than all other striatal nuclei, including the ventral and amygdaloid complex.     

Golgi study of the anterior dorsal ventricular ridge in a lizard. I. neuronal typology in the adult

Using Golgi techniques we have studied neuronal cell types in the anterior dorsal ventricular ridge (ADVR) of the adult lizard Gallotia galloti. Multipolar, bitufted, and juxtaependymal neuronal forms were found. The multipolar and bitufted neurons are present in both the periventricular and central ADVR zones. Multipolar neurons can be subdivided into multipolar neurons with polygonal somata and four to six main dendritic trunks and multipolar neurons with pyramidal somata and three or more dendritic trunks. The former are the cells most frequently impregnated in the ADVR. In the population of bitufted neurons, we distinguish subtypes I, II, and III according to the number of dendritic trunks that emerge from the somata. Juxtaependymal neurons are restricted to a cell-poor zone, adjacent to ependymal cells. Their dendrites either are orientated parallel to the ventricular surface or extend into the periventricular zone. The dendrites of ADVR neurons have pedunculated spines with knob-like tips. However, such spines do not appear on the somata or on the primary dendritic trunks. The number of spines is scarce or moderate. The periventricular neuronal clusters contain two to five cells. The morphology of these neurons is mainly multipolar, but we also found some bitufted neurons.     

Structure of anterior dorsal ventricular ridge in snakes.

Anterior dorsal ventricular ridge (ADVR) is a major subcortical, telencephalic nucleus in snakes. Its structure was studied in Nissl, Golgi, and electron microscopic preparations in several species of snakes. Neurons in ADVR form a homogeneous population. They have large nuclei, scattered cisternae of rough endoplasmic reticulum in their cytoplasm, and bear dendrites from all portions of their somata. The dendrites have a moderate covering of pedunculated spines. Clusters of two to five cells with touching somata can be seen in Nissl, Golgi, and electron microscopic preparations. The area of apposition may contain a series of specialized junctions which resemble gap junctions. Three populations of axons can be identified in rapid Golgi preparations of snake ADVR. Type 1 axons course from the lateral forebrain bundle and bear small varicosities about 1 mu long. Type 2 axons arise from ADVR neurons and bear large varicosities about 5 mu long. The origin of the very thin type 3 axons is not known; they bear small varicosities about 1 mu long. The majority of axon terminals in ADVR are small (1 mu to 2 mu long), contain round synaptic vesicles, and form asymmetric active zones. This type of axon terminates on dendritic spines and shafts and on somata. A small percentage of terminals are large, 5 mu in length, contain round synaptic vesicles, and form asymmetric active zones. This type of axon terminates only on dendritic spines. A small percentage of terminals are small, contain pleomorphic synaptic vesicles, and form symmetric active zones. This type of axon terminates on dendritic shafts and on somata.     

Structural analysis of human FANCL, the E3 ligase in the Fanconi anemia pathway

The Fanconi anemia (FA) pathway is essential for the repair of DNA interstrand cross-links. At the heart of this pathway is the monoubiquitination of the FANCI-FANCD2 (ID) complex by the multiprotein "core complex" containing the E3 ubiquitin ligase FANCL. Vertebrate organisms have the eight-protein core complex, whereas invertebrates apparently do not. We report here the structure of the central domain of human FANCL in comparison with the recently solved Drosophila melanogaster FANCL. Our data represent the first structural detail into the catalytic core of the human system and reveal that the central fold of FANCL is conserved between species. However, there are macromolecular differences between the FANCL proteins that may account for the apparent distinctions in core complex requirements between the vertebrate and invertebrate FA pathways. In addition, we characterize the binding of human FANCL with its partners, Ube2t, FANCD2, and FANCI. Mutational analysis reveals which residues are required for substrate binding, and we also show the domain required for E2 binding.     

Drosophila neuropeptide F mediates integration of chemosensory stimulation and conditioning of the nervous system by food

The conserved neuropeptide Y (NPY) signaling pathway has been strongly implicated in the stimulation of food uptake in vertebrates as well as in the regulation of food conditioned foraging behaviors of Caenorhabditis elegans. Using in situ RNA hybridization and immunocytochemistry, we report the neuronal network of Drosophila neuropeptide F (dNPF), a human NPY homologue, in the larval central nervous system and its food-dependent modifications. We provide indications that gustatory stimulation by sugar, but not its ingestion or metabolism, is sufficient to trigger long-term, dose-dependent alterations of the dNPF neuronal circuit through both dnpf activation and increased synaptic transmission. Our results strongly suggest that the dNPF neuronal circuit is an integral part of the sensory system that mediates food signaling, providing the neural basis for understanding how invertebrate NPY regulates food response.     

Golgi study of the anterior dorsal ventricular ridge in a lizard. II. Neuronal cytodifferentiation

The development of the morphologic features of neurons in the anterior dorsal ventricular ridge (ADVR) has been followed in Golgi preparations from the lizard Gallotia galloti between embryonic stage 32 and post-eclosion stages of specimens 3.6–4.5 cm in length. The differentiation sequence of multipolar and bitufted neurons was established. Dendritic growth cones are present after stage 34. Filiform dendritic processes are replaced later on by spines. Clusters of neurons first appear at stage 39 in the periventricular zone, the cells becoming Golgi-impregnated in pairs. After hatching, the number of impregnated cells per cluster increases.