Basic concepts in nervous system: Are the nerves wired as we have thought them to be?

Fundamentals of neurology as passed down through the instruction of medical schooling say that nerves are broadly classified into three types; namely the motor, sensory and mixed nerves. But, is this truly so with regard to cranial nerves? This short communication aims at cautioning the pioneers, experts and medical instructors in the field of neurology about the use of misconstrued terminology in the basic concepts of nervous system. May be it is time for us to re-visit the basics of neurology?     

Proprioceptive afferent fibers in the cranial nerves III, IV and VI.

The purpose of the present works was to clarify whether the cranial nerves III, IV and VI carry proprioceptive afferent fibres from the extrinsic ocular muscles. In sheep the picture is now clear. The cranial nerves III, IV and VI carry many large proprioceptive fibres (12-16 micrometer) to the central nervous system. These nerves also contain many small fibres of the y-range (2-6 micrometer) which innervate the intrafusal muscle fibres in the spindles. In man the picture is still vague: most of the spindles are not typical, the large proprioceptive fibres (12-16 micrometer) and the small y-fibres (2-6 micrometer) are very few in the cranial nerves III, IV and VI. It is to be concluded that in sheep the cranial nerves III, IV and VI are not purely motor nerves to the extrinsic ocular muscles, but they also carry many of the large fibres of the proprioceptive function. In man, such large fibres are not found and the pathway of proprioceptive afferents from the orbital muscles is still not certain.     

Dil对鱼类视觉传导通路的形态学研究

目的：应用Dil染色晶体研究罗非鱼脑、脑神经及其视觉传导路的形态分布。方法：罗非鱼6只,体长12．16ctn,进行灌注固定后,在外科显微镜下开颅并确认脑和脑神经根,分别于双侧视神经植入Dil染色晶体。37℃恒温箱放置3个月,待Dil染色晶体扩散后,取出植入Dil染色晶体的视神经和脑,再根据神经走向切片,通过荧光显微镜观察Dil染色晶体在视觉传导路的形态分布。结果：①外科显微镜下可以观察到罗非鱼的脑分为端脑、中脑、间脑、小脑和延脑5部分,并同时观察到10对脑神经。②右侧视神经植入Dil染色晶体后,均可见到标记的右侧视神经纤维,行向后内,穿经视神经管入颅,逐步靠近左侧视神经,进一步行向后内,经过左侧视神经上方,进行完全交叉,形成视交叉,再经左侧视柬连于左侧间脑视盖。结论：罗非鱼的脑分为5部分,脑神经只有10对。罗非鱼视交叉属于完全性交叉,视觉中枢可能位于间脑视盖内。     

SPARCL1-containing neurons in the human brainstem and sensory ganglion

Secreted protein, acidic and rich in cysteine-like 1 (SPARCL1) is a member of the osteonectin family of proteins. In this study, immunohistochemistry for SPARCL1 was performed to obtain its distribution in the human brainstem, cervical spinal cord, and sensory ganglion. SPARCL1-immunoreactivity was detected in neuronal cell bodies including perikarya and proximal dendrites, and the neuropil. The motor nuclei of the IIIrd, Vth, VIth, VIIth, IXth, Xth, XIth, and XIIth cranial nerves and spinal nerves contained many SPARCL1-immunoreactive (-IR) neurons with medium-sized to large cell bodies. Small and medium-sized SPARCL1-IR neurons were distributed in sensory nuclei of the Vth, VIIth, VIIIth, IXth, and Xth cranial nerves. In the medulla oblongata, the dorsal column nuclei also had small to medium-sized SPARCL1-IR neurons. In addition, SPARCL1-IR neurons were detected in the nucleus of the trapezoid body and pontine nucleus within the pons and the arcuate nucleus in the medulla oblongata. In the cervical spinal cord, the ventral horn contained some SPARCL1-IR neurons with large cell bodies. These findings suggest that SPARCL1-containing neurons function to relay and regulate motor and sensory signals in the human brainstem. In the dorsal root (DRG) and trigeminal ganglia (TG), primary sensory neurons contained SPARCL1-immunoreactivity. The proportion of SPARCL1-IR neurons in the TG (mean?±?SD, 39.9?±?2.4%) was higher than in the DRG (30.6?±?2.1%). SPARCL1-IR neurons were mostly medium-sized to large (mean?±?SD, 1494.5?±?708.3?μm²; range, 320.4–4353.4?μm²) in the DRG, whereas such neurons were of various cell body sizes in the TG (mean?±?SD, 1291.2?±?532.8?μm²; range, 209.3–4326.4?μm²). There appears to be a SPARCL1-containing sensory pathway in the ganglion and brainstem of the spinal and trigeminal nervous systems.     

Filament proteins in central,cranial, and peripheral mammalian nerves

Several classes of 10-nm filaments have been reported in mammalian cells and they can be distinguished by the size of their protein subunit. We have studied the distribution of these filaments in nerves from calves and other mammals. From the display on polyacrylamide electrophoretic gels of proteins in extracts from fibroblast and central, cranial and peripheral nerves, we cut the appropriate stained bands and prepared iodinated peptide maps. The similarities between the respective maps provide strong evidence for the presence of vimentin in cranial and peripheral nerves. The glial fibrillary acidic protein was found in axon preparations from the central nervous system, but was not identified in distal segments of some cranial nerves, nor in peripheral nerve.     

Fibulin-1 is required for morphogenesis of neural crest-derived structures

Here we report that mouse embryos homozygous for a gene trap insertion in the fibulin-1 (Fbln1) gene are deficient in Fbln1 and exhibit cardiac ventricular wall thinning and ventricular septal defects with double outlet right ventricle or overriding aorta. Fbln1 nulls also display anomalies of aortic arch arteries, hypoplasia of the thymus and thyroid, underdeveloped skull bones, malformations of cranial nerves and hemorrhagic blood vessels in the head and neck. The spectrum of malformations is consistent with Fbln1 influencing neural crest cell (NCC)-dependent development of these tissues. This is supported by evidence that Fbln1 expression is associated with streams of cranial NCCs migrating adjacent to rhombomeres 2-7 and that Fbln1-deficient embryos display patterning anomalies of NCCs forming cranial nerves IX and X, which derive from rhombomeres 6 and 7. Additionally, Fbln1-deficient embryos show increased apoptosis in areas populated by NCCs derived from rhombomeres 4, 6 and 7. Based on these findings, it is concluded that Fbln1 is required for the directed migration and survival of cranial NCCs contributing to the development of pharyngeal glands, craniofacial skeleton, cranial nerves, aortic arch arteries, cardiac outflow tract and cephalic blood vessels.     

The emerging role of cranial nerves in shaping craniofacial development

Organs and structures of the vertebrate head perform a plethora of tasks including visualization, digestion, vocalization/communication, auditory functions, and respiration in response to neuronal input. This input is primarily derived from afferent and efferent fibers of the cranial nerves (sensory and motor respectively) and efferent fibers of the cervical sympathetic trunk. Despite their essential contribution to the function and integration of processes necessary for survival, how organ innervation is established remains poorly understood. Furthermore, while it has been appreciated for some time that innervation of organs by cranial nerves is regulated in part by secreted factors and cell surface ligands expressed by those organs, whether nerves also regulate the development of facial organs is only beginning to be elucidated. This review will provide an overview of cranial nerve development in relation to the organs they innervate, and outline their known contributions to craniofacial development, thereby providing insight into how nerves may shape the organs they innervate during development. Throughout, the interaction between different cell and tissue types will be highlighted.     

Sex steroids and 5-en-3 beta-hydroxysteroids in specific regions of the human brain and cranial nerves

Sex steroids and 5-en-3 beta-hydroxysteroids were determined by radioimmunoassay in specific regions of the human brain, in the anterior and posterior pituitary, in one sensory organ, the retina and in the cranial nerves. Progesterone, androstenedione, testosterone and estrone were found in all areas of the brain and in all the cranial nerves but not in all cases. There was no sex difference except in the case of androstenedione where values were higher in women in some brain areas. Estrone values were always higher than those of estradiol in both men and women. No 5 alpha-dihydrotestosterone was detected in any of the samples studied. The values for pregnenolone, dehydroepiandrosterone and their sulfates were much higher than those of the sex steroids in all areas of the brain and in all the cranial nerves. Values for pregnenolone were greater than those of its sulfate while those of dehydroepiandrosterone were in general equal to or higher than those of its sulfate. The values for pregnenolone were greater than those of dehydroepiandrosterone. There were no obvious regional differences in the concentrations of the 5-en-3 beta-hydroxysteroids either in specific areas of the brain or in the cranial nerves. But there was a definite trend for the free dehydroepiandrosterone values to be higher in women. The possible significance of these observations is discussed.     

Expression pattern of the Rsk2, Rsk4 and Pdk1 genes during murine embryogenesis

The ribosomal S6 kinase family members RSK2 (RPS6KA3) and RSK4 (RPS6KA6) belong to the group of X chromosomal genes, in which defects cause unspecific mental retardation (MRX) in humans. In this study, we investigated the spatiotemporal expression pattern of these genes during mouse development with emphasis to midgestation stages. Additionally, we analyzed the expression of the phosphoinositide-dependent protein kinase-1 gene, Pdk1 (Pspk1), which is essential for the activation of Rsk family members and thus regulates their function. During midgestation we observed specifically enhanced expression of Rsk2 first in somites, later restricted to the dermatomyotome of the somites, then in the sensory ganglia of cranial nerves and in the dorsal root ganglia of the spinal nerves. High Rsk2 expression in the cranial nerve ganglia persists throughout development and is correlated with Pdk1 expression. In the brain of 2-day-old mice, Pdk1 is expressed in the cortical plate of the cerebral cortex and in the stratum pyramidale of the hippocampus, whereas Rsk2 expression is lower in these structures. For Rsk4 ubiquitous expression at lower levels was observed throughout development.     

Cranial Nerve Development Requires Co-Ordinated Shh and Canonical Wnt Signaling

Cranial nerves govern sensory and motor information exchange between the brain and tissues of the head and neck. The cranial nerves are derived from two specialized populations of cells, cranial neural crest cells and ectodermal placode cells. Defects in either cell type can result in cranial nerve developmental defects. Although several signaling pathways are known to regulate cranial nerve formation our understanding of how intercellular signaling between neural crest cells and placode cells is coordinated during cranial ganglia morphogenesis is poorly understood. Sonic Hedgehog (Shh) signaling is one key pathway that regulates multiple aspects of craniofacial development, but whether it co-ordinates cranial neural crest cell and placodal cell interactions during cranial ganglia formation remains unclear. In this study we examined a new Patched1 (Ptch1) loss-of-function mouse mutant and characterized the role of Ptch1 in regulating Shh signaling during cranial ganglia development. Ptch1^{Wig/ Wig} mutants exhibit elevated Shh signaling in concert with disorganization of the trigeminal and facial nerves. Importantly, we discovered that enhanced Shh signaling suppressed canonical Wnt signaling in the cranial nerve region. This critically affected the survival and migration of cranial neural crest cells and the development of placodal cells as well as the integration between neural crest and placodes. Collectively, our findings highlight a novel and critical role for Shh signaling in cranial nerve development via the cross regulation of canonical Wnt signaling.     

Diverse mechanisms for assembly of branchiomeric nerves

The formation of branchiomeric nerves (cranial nerves V, VII, IX and X) from their sensory, motor and glial components is poorly understood. The current model for cranial nerve formation is based on the Vth nerve, in which sensory afferents are formed first and must enter the hindbrain in order for the motor efferents to exit. Using transgenic zebrafish lines to discriminate between motor neurons, sensory neurons and peripheral glia, we show that this model does not apply to the remaining three branchiomeric nerves. For these nerves, the motor efferents form prior to the sensory afferents, and their pathfinding show no dependence on sensory axons, as ablation of cranial sensory neurons by ngn1 knockdown had no effect. In contrast, the sensory limbs of the IXth and Xth nerves (but not the Vth or VIIth) were misrouted in gli1 mutants, which lack hindbrain bmn, suggesting that the motor efferents are crucial for appropriate sensory axon projection in some branchiomeric nerves. For all four nerves, peripheral glia were the intermediate component added and had a critical role in nerve integrity but not in axon guidance, as foxd3 null mutants lacking peripheral glia exhibited defasciculation of gVII, gIX, and gX axons. The bmn efferents were unaffected in these mutants. These data demonstrate that multiple mechanisms underlie formation of the four branchiomeric nerves. For the Vth, sensory axons initiate nerve formation, for the VIIth the sensory and motor limbs are independent, and for the IXth/Xth the motor axons initiate formation. In all cases the glia are patterned by the initiating set of axons and are needed to maintain axon fasciculation. These results reveal that coordinated interactions between the three neural cell types in branchiomeric nerves differ according to their axial position.     

CELLULAR DISTRIBUTION OF 16S ACETYLCHOLINESTERASE

Multiple molecular forms of acetylcholinesterase (AChE; EC 3.1.1.7), in crude extracts of various tissues from the rat, were distinguished by velocity sedimentation analysis on linear sucrose gradients. Skeletal muscle samples containing end-plate regions showed three different forms of AChE with apparent sedimentation coefficients of 16, 10 and 4s. The 16s form was not detected in non-innervated regions of skeletal muscle, large intestine smooth muscle, whole brain tissue, red blood cells or plasma. Spinal cord, a predominantly motor cranial nerve and mixed (sensory and motor) peripheral nerves contained 16, 10, 6.5 and 4S AChE. Ventral motor roots, supplying the sciatic nerve, contained these four forms of the enzyme, while corresponding dorsal sensory roots were devoid of the 16S form. The 16s-AChE confined to ventral roots can be attributed totally to motor neurons and not to Schwann cells composing these roots. Whether the 16s-AChE presently found in motor nerves has chemical identity with that found at motor end-plates is the basis of future experiments.     

Brain Structure in Calamoichthys calabaricus Smith 1865 (Polypteridae,Brachiopterygii)

The brain of Calamoichthys calabaricus is reconstructed including the arrangement of the parts of the brain and the cranial nerves and their nuclei. Histologically, the analysis includes structure of the rhombencephalon with its cranial and tegmental nuclei, and the cerebellum.     

Cranial nerve growth in birds is preceded by cholinesterase expression during neural crest cell migration and the formation of an HNK-1 scaffold

Summary The expression of the neural crest cell (NCC) markers acetylcholinesterase (AChE) and the HNK-1-epitope is compared from the emigration of cephalic NCC until the formation of the cranial nerves V-X in chicken and quail hindbrain. We show that NCC transiently express acetylcholinesterase (AChE) activity during their emigration; NCC migrate into butyrylcholinesterase (BChE)-positive areas of the cranial mesenchyme. Along these migratory tracks that foreshadow the course of later projecting cranial nerves, BChE increases strongly in cells that may represent immature Schwann cells. Both AChE and BChE, but not HNK-1, are expressed in the ectodermal placodes. In NCC, HNK-1 is expressed strongly only when they approach their destination sites. Their intense expression of HNK-1 then leads to the establishment of tunnel-shaped HNK-1 matrices, within which G4-positive cranial neurites begin to extend. We conclude that AChE and HNK-1 expression in cephalic NCC serve different functions, since AChE is related to their migration, and HNK-1 to their aggregation and the formation of an extracellular neurite scaffold.     

三峡地区最晚更新世的梅氏犀兼述中国南方更新世的犀牛化石

重庆市巫山县迷宫洞是一处重要的晚更新世晚期的古人类遗址, 其绝对年代为距今13150±190年。本文研究了这一遗址出土的犀牛化石, 材料包括头骨碎块、下颌、牙齿及数件头后骨骼。这些材料被鉴定为梅氏犀或称基什贝尔格犀(Stephanorhinus kirchbergensis), 是这个种已知时代最晚和分布最为靠南的记录。适合温带气候的S.kirchbergensis在中-晚更新世南下至长江流域, 可能是受到冰期寒冷气候的压迫所致。以迷宫洞和其他长江流域的S.kirchbergensis为基础, 通过对比, 认为我国南方、北方以及欧洲的S.kirchbergensis在颊齿形态上存在明显的区别, 从而将这个种分为三个类型。另外, 本文还对我国南方更新世的犀牛种类, 特别是中国犀(Rhinoceros sinensis), 进行了全面地厘定。     

Reductions of neural activities to upper airway muscles after elevations in static lung volume.

We evaluated the hypothesis that the tonic discharge of pulmonary stretch receptors significantly influences the respiratory-modulated activities of cranial nerves. Decerebrate and paralyzed cats were ventilated with a servo-respirator, which produced changes in lung volume in parallel with integrated phrenic activity. Activities of the facial, hypoglossal, and recurrent laryngeal nerves and nerves to the thyroarytenoid muscle and triangularis sterni were recorded. After a stereotyped pattern of lung inflation, tracheal pressure was held at 1, 2, 4, or 6 cmH2O during the subsequent ventilatory cycle. Increases in tracheal pressure caused progressive reductions in both inspiratory and expiratory cranial nerve activities and progressive elevations in triangularis sterni discharge; peak levels of phrenic activity declined modestly. Similar changes were observed in normocapnia and hypercapnia. We conclude that the tonic discharge of pulmonary stretch receptors is an important determinant of the presence and magnitude of respiratory-modulated cranial nerve activity. This reflex mechanism may maintain upper airway patency and also regulate expiratory airflow.     

NEUROLOGIC COMPLICATIONS OF DIABETES

Peripheral neuropathy is a common complication of diabetes and may appear as the first manifestation of the disease. It is likely to occur in even the mildest cases of diabetes.Careful regulation of diabetes is necessary for effective treatment of the neuropathy. In early cases the prognosis is excellent.The peripheral nerves, autonomic nerves, cranial nerves, spinal cord and brain are all frequently involved in diabetes.The possibility of diabetes should be considered in the differential diagnosis of many neurologic conditions.     

Morphological alterations induced by sodium valproate on somites and spinal nerves in rat embryos

The antiepileptic drug valproic acid is a well-known teratogenic agent; its main target organ is the neural tube, though skeletal malformations have also been described. In our recent work, respecifications of vertebrae were described in rat fetuses after treatment with 400 mg/kg of sodium valproate at specific somitogenic stages. The observed malformations were stage-dependent. Morphological segmental respecification was observed at the level of segments in formation at the moment of exposure and at the level of more posterior segments. Recently, specific alterations in the development of cranial nerves and ganglia were described in mouse embryos after in vitro exposure to VPA. The aim of the present work was to analyze dysmorphogenetic effects of VPA on embryonic metameric structures: somites, spinal and cranial nerves, and ganglia. Sodium valproate (400 mg/kg) was subcutaneously injected at specific gestational times corresponding to embryonic stages: presomitic or at about 2, 6, 10, 14, 18, or 22 somites. Females were sacrificed on the day 12 post coitum, and embryos were examined. Morphological examination of somites was performed by staining with acridine orange. Morphological examination of nerves and ganglia was performed by immunostaining, using monoclonal antibodies to the 160-kD neurofilament protein. No abnormalities were observed in the cranial nerves and ganglia. Specific and stage-dependent alterations were observed both at the level of the somites and at the level of the spinal nerves. The following characteristic malformations were observed: fusions, duplications, and reductions of somites and corresponding spinal nerves and ganglia. Our morphological data suggest a morphogenetic action of VPA at the level of the axial segments, with a possible respecification of the identity of the interested segments and their derivatives.     

The Lateral Line System of Hagfishes (Craniata: Myxinoidea)

The morphology of the peripheral lateral line system in Eptatretus stoutii is described using a combination of electron microscopical, histological and immunocytochemical techniques. The epidermis and cranial nerves of Myxine glutinosa were also examined for evidence of a lateral line system. Together with results previously published by other researchers, we conclude that most or all eptatretid hagfish possess a lateral line system composed of shallow trenches, or grooves, lined with a single class of flask-shaped receptive cells. No species of myxinid hagfish has been shown to possess any component of this system. Three groups of lateral line grooves are present in eptatretids: preoptic, dorsal postoptic, and ventral postoptic groups. The preoptic grooves are innervated by a single pair of ganglionated cranial nerves and the two postoptic series of grooves are innervated by a pair of cranial nerves which each possess two ganglia, possibly as a result of fusion of two pairs of ganglionated nerves. Morphometric analysis indicates that these grooves continue to grow throughout life and that the variability in the distribution of grooves between animals may result from developmental instability in lateral line ontogeny. The morphology of the receptive organs is compared to neuromasts of the vertebrate lateral line system and ciliated receptor cells of other chordates. The morphology of hagfish lateral line receptors may represent the primitive condition for craniate lateral line organs, or more likely, they are highly derived as a result of regressive evolution. © 1997 The Royal Swedish Academy of Sciences. Published by Elsevier Science Ltd.     

Ghrelin 对脑功能的影响

Ghrelin是生长激素促分泌素受体(growth hormone secretagogue receptor,GHSR)的内源性配体,在大鼠胃组织中首次被发现,通过与其特异性受体结合发挥生物学作用。近年来随着对其研究的深入,发现Ghrelin在多种组织中合成分泌,不仅在消化、内分泌等系统产生重要作用,对脑功能也有很大影响,可提高学习记忆能力、影响睡眠、与应激焦虑关系密切并且对脑神经起保护作用。本文总结近几年的文章,旨在通过对Ghrelin对脑功能影响的介绍,为以后的相关研究奠定基础。