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Results for “GANGLIA, SPINAL”

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At least 343 records · Page 19Linked to original sources

PubMed1997

Age-related decrease of the perineuronal satellite cell number in the rabbit spinal ganglia.

This study was undertaken to establish whether a change in the perineuronal satellite cell number contributes to the age-related reduction of the volume ratio between the perineuronal glial sheaths and their associated nerve cell bodies, observed to occur in rabbit spinal ganglia. The volumes of the nerve cell bodies and the numbers of the related satellite cell nuclei were estimated on serial semithin sections from young adult and old rabbits. As satellite cells are mononucleate, the number of the nuclei corresponds to that of these cells. The satellite cell sheaths in both age groups were also examined under the electron microscope. The mean number of satellite cells was significantly smaller in the aged animals than in the young adults although the mean volume of the nerve cell bodies was significantly larger in the former. Cytoplasmic vacuoles, invaginations of the connective tissue and autophagic vacuoles were more frequent in the old rabbits. Satellite cells with pyknotic nuclei and remnants of degenerated satellite cells were only found in aged animals, although rather rarely. The decrease in the satellite cell number is one of the mechanisms by which the age-related reduction of the volume ratio between the perineuronal glial sheaths and their associated nerve cell bodies takes place. The decrease in the satellite cell number seems to occur, at least in part, through cell degeneration. However, other mechanisms (e.g., detachment of satellite cells from the perineuronal sheaths) cannot be excluded. Since satellite cells play a role in neuronal support, the significant decrease in their number probably has negative consequences for neuronal activity.

Aging↗

PubMed1985

Immunohistochemical demonstration of some putative neurotransmitters in the lamprey spinal cord and spinal ganglia: 5-hydroxytryptamine-, tachykinin-, and neuropeptide-Y-immunoreactive neurons and fibers.

The distribution of some putative neurotransmitters was investigated in the spinal cord and spinal ganglia of the lamprey, a primitive vertebrate, by using immunohistochemical methods. In the spinal cord a midline row of 5-hydroxytryptamine (5-HT)-immunoreactive neurons was present immediately ventral to the central canal over the entire length of the spinal cord. The ventral processes of these neurons formed a dense ventromedial plexus of varicosities. In the dorsal, lateral, and ventral spinal axon columns, several longitudinal 5-HT fibers were present. After chronic spinal transections the distribution of 5-HT fibers was unchanged; it is therefore concluded that there was no substantial descending 5-HT contribution and that the spinal 5-HT neurons supplied the regional 5-HT innervation. The spinal 5-HT cells sent fibers into the dorsal and ventral roots; 5-HT cell bodies and fibers were also present in the spinal dorsal root ganglia, in their dorsal, ventral, and lateral nerve branches, and in the dorsal and ventral branches of the ventral roots. Neurons and fibers containing peptides of the tachykinin (TK) family (to which, amongst others, substance P belongs) were found in the spinal cord. TK neurons in the spinal cord supplied the local TK innervation, as well as TK fibers in the dorsal and ventral roots. Fibers have been found containing either TK, or 5-HT, or both compounds. Neurons containing neuropeptide-Y (NPY)-immunoreactive material were present in a medial column just dorsal to the central canal. The NPY neurons have longitudinal, mainly descending, fibers that provide the local NPY innervation of the lamprey spinal cord. The present results provide evidence for local spinal systems containing 5-HT, TK, 5-HT and TK, or NPY, but in contrast to mammals, these compounds do not seem to arise from supraspinal neurons.

Animals↗

PubMed1998

Veins of the lumbar spinal ganglia in human adults and fetuses.

To obtain a fundamental knowledge of the morphological relationship between nerve root symptoms and circulatory disorders, the distribution pattern of the veins in the lumbar spinal ganglia from the first to fifth vertebrae was investigated in 5 adult human cadavers (mean age 69.6 years) and 5 human fetuses (mean age 6.6 months). The following results were obtained: 1) In the adults the veins perforating from the outer surface of the fifth lumbar spinal ganglion were smaller in number than those perforating from the first to fourth ganglia. In contrast, in the fetuses the number of such veins was increased in the lower lumbar spinal ganglia. In each of the ganglia, the number of veins emerging through the dorsal side was much higher than the number perforating from the outer surface of the ventral sides. The veins perforating through the outer surface of the ganglion formed weak venous networks (periganglionic venous plexus) surrounding the dorsal ramus of the spinal nerve. 2) The veins communicating with the tributaries from the periganglionic venous plexus were classified into three types. Type 1 veins flowed into the intervertebral veins (the frequency ranged from 9.2 to 18.2 in the adults and from 22.4 to 37.0 in the fetuses). Type 2 veins coursed in the spinal cord along the dorsal root fibers and penetrated the dura mater on the way (the frequency ranged from 0.4 to 4.8 in the adults and from 1.2 to 2.2 in the fetuses). Type 3 veins opened directly into the internal vertebral plexus (the frequency ranged from 0.4 to 1.8 in the adults and from 0 to 0.4 in the fetuses). Type 1 veins were the most frequent among the three types of veins in both adults and fetuses. Few type 3 veins were observed in either group. 3) In the first and second lumbar vertebrae in the adults, three-quarters of each spinal ganglion was situated in the vertebral canal. In the lower lumbar region (L3-L5), three quarters of each spinal ganglion lay on the outside of the vertebral canal. In the fetuses, approximately one half to three-quarters of each lumbar spinal ganglion was located in the vertebral canal.

Aged↗

PubMed1989

Fine structural study of the spinal cord and spinal ganglia in mice afflicted with a hereditary sensory neuropathy, dystonia musculorum.

Dystonia musculorum in mice is a hereditary autosomal recessive disorder, characterized by a progressive neuromuscular incoordination. This paper describes the ultrastructural changes in the spinal cord and compares and correlates the results with changes in the spinal ganglia in dystonic mice. Ganglion cells exhibited various stages of degeneration and pyknosis. The dorsal roots of the spinal nerves showed severe degeneration and loss of myelinated fibres accompanied by fibrosis, whilst the ventral roots appeared normal. Nerve cells within the dorsal and intermediate grey matter (laminae I to VII) of the spinal cord showed chromatolysis, atrophy, and necrosis. Boutons exhibited glycogen accumulation or an increase in their electron density. Axonal changes consisted of focal swellings, marked accumulation of neurofilaments, membranous and dense bodies, and disintegration of axoplasm. Myelin sheath degeneration of Wallerian type and degenerating axons were prominent in the dorsal, lateral and ventral white columns of the spinal cord. Glial reactions in the spinal cord were limited to mild hypertrophy and hyperplasia of astrocytic processes. The process of phagocytic activity was not intense in spite of the presence of an abundance of degenerating myelin and cell debris. This study showed that the ultrastructural changes in the spinal cord are more severe than those seen with routine light microscopy. The detection of definite neuronal degeneration of the dorsal root ganglia and spinal cord suggests that the defect apparently operates at the level of cell bodies, as well as axons, of the primary and second order sensory neurons.

Animals↗

PubMed1981

[Effects of gangliosides on the in vitro growth of cultured spinal ganglia of guinea pigs. Preliminary results on a preparation of gangliosides from the cerebral cortex of cattle].

Brain bovine gangliosides added for 48 hrs. to the culture medium at concentrations ranging from 5.10(-5) mg/ml to 5.10(-7) mg/ml induced a statistically significant (p less than .005 to p less than 000,5) increase of the number of neurites of the outgrowth zone of guinea-pig spinal ganglia. On the contrary, the neurite length was only slightly increased.

Animals↗

PubMed2003

The neurite-stimulating influence of components of medicinal leech salivary gland secretions in organotypic culture of spinal ganglia.

The effects of components from medicinal leech (Hirudo medicinalis) salivary gland secretions and the therapeutic agent Piyavit on the growth of chick embryo neurites in organotypic culture were studied. Native destabilase and bdellin A at concentrations of 0.01, 0.02, 0.05, and 0.1 ng/ml, bdellin B at a concentration of 0.05 ng/ml, and eglin at a concentration of 0.1 ng/ml had neurite-stimulating activity, evident on the third day of organotypic culture of spinal ganglia. The stimulatory activity of destabilase was lost after revere-phase chromatography. The neurite-stimulating activity of the extract of the therapeutic agent Piyavit (200 ng/ml) in organotypic ganglion culture appeared to result from the neurite-stimulating salivary gland components within this agent, suggesting that Piyavit could be used for the treatment of neurodegenerative disorders.

Animals↗

PubMed1983

Restricted replication of herpes simplex virus in spinal ganglia of resistant mice is accompanied by an early infiltration of immunoglobulin G-bearing cells.

In an attempt to define the nature of the difference in the susceptibility of C57BL/6 (resistant) and A/J (susceptible) mice to herpes simplex virus type 1, we initiated a study of virus progression through the nervous system. After inoculation of virus in a rear footpad, C57BL/6 mice were found to be more than 500-fold more resistant, but resistance did not extend to pseudorabies virus. In additional investigations, it was found that the virus was selectively restricted at the level of spinal ganglia in C57BL/6 mice. No intrinsic difference in the ability of this tissue from either mouse strain to replicate virus was found. However, by 4 days after infection, morphological investigations indicated that a mononuclear cell infiltrate was present surrounding infected neurons and satellite cells both earlier and in greater numbers in the ganglia of C57BL/6 mice. Immunohistochemical methods showed that most of these cells did not express Thy 1.2 antigen, but the vast majority bore immunoglobulin G. The mechanism by which these infiltrating cells could restrict virus spread is discussed.

Animals↗

PubMed1999

Evidence that Hoxa expression domains are evolutionarily transposed in spinal ganglia, and are established by forward spreading in paraxial mesoderm.

Transposition of anatomical structures along the anteroposterior axis has been a commonly used mechanism for changing body proportions during the course of evolutionary time. Earlier work (Gaunt, S.J., 1994. Conservation in the Hox code during morphological evolution. Int. J. Dev. Biol. 38, 549-552; Burke, A.C., Nelson, C.E., Morgan, B.A., Tabin, C., 1995. Hox genes and the evolution of vertebrate axial morphology. Development 121, 333-346) showed how transposition in mesodermal derivatives (vertebrae) could be attributed to transposition in the expression of Hox genes along the axial series of somites. We now show how transposition in the segmental arrangement of the spinal nerves can also be correlated with shifts in the expression domains of Hox genes. Specifically, we show how the expression domains of Hoxa-7, a-9 and a-10 in spinal ganglia correspond similarly in both mouse and chick with the positions of the brachial and lumbosacral plexuses, and that this is true even though the brachial plexus of chick is shifted posteriorly, relative to mouse, by seven segmental units. In spite of these marked species differences in the boundaries of Hoxa-7 expression, cis regulatory elements located up to 5 kb upstream of the chick Hoxa-7 gene showed much functional and structural conservation with those described in the mouse (Puschel, A.W., Balling, R., Gruss, P., 1991. Separate elements cause lineage restriction and specify boundaries of Hox-1.1 expression. Development 112, 279-287; Knittel, T., Kessel, M., Kim, M.H., Gruss, P., 1995. A conserved enhancer of the human and murine Hoxa-7 gene specifies the anterior boundary of expression during embryonal development. Development 121, 1077-1088). We also show that chick Hoxa-7 and a-10 expression domains spread forward into regions of somites that are initially negative for the expression of these genes. We discuss this as evidence that Hox expression in paraxial mesoderm spreads forward, as earlier found for neurectoderm and lateral plate mesoderm, in a process that occurs independently of cell movement.

Animals↗

PubMed1993

Unilateral forelimb amputation affects protein synthesis in ipsilateral and contralateral spinal cord and spinal ganglia neurons of the newt in vivo.

The aim of this investigation was to analyze the effect of urodele limb amputation and blastema growth on the protein synthesis in spinal cord and spinal ganglia neurons corresponding to the 3rd and 4th spinal segment of young, postmetamorphic Triturus vulgaris, in vivo. Protein synthesis was studied on both trunk sides as a function of right forelimb amputation at the distal stylopodium, and blastema development, during a critical period of 22 days post amputation (dpa). Protein synthesis was assessed by counting silver grains on autoradiographs obtained after pulse labeling with tritiated phenylalanine. An electronic image analyzer was used to evaluate the results. During the period of observation, several statistically significant, yet moderate changes were observed in the protein synthesis of motor neurons. In contrast, the studied metabolic parameter exhibited considerable augmentation in sensory neurons and spinal nerve. The main results may be summarized as follows: (a) Limb amputation triggers protein synthesis in both ipsilateral and contralateral neural elements; (b) protein synthesis is higher on the ipsilateral than on the contralateral side; (c) as the aftermath of forelimb amputation, the 4th ipsilateral ganglion responds with an approximately 20% higher protein synthesis in comparison to the 3rd one; (d) peaks in protein synthesis are encountered mainly at two time points: 3 hpa and 14 dpa. Protein synthesis returns to control levels after 22 days of limb regeneration.

Amputation, Surgical↗

PubMed1992

Synchronous appearance of antigen-positive and latently infected neurons in spinal ganglia of mice infected with a virulent strain of herpes simplex virus.

Studies with replication-defective mutants of herpes simplex virus (HSV) have defined the minimum requirements for establishment of latency, but their behaviour may not reflect the course of events following infection by wild-type HSV, in which ability to express viral genes has not been precluded by a genetic lesion. To address this issue we devised a strategy for studying establishment of latency by a virulent strain of HSV, based on the distinctive molecular characteristics of latently infected neurons. By combining in situ hybridization for detection of latency-associated transcripts with immunohistochemical analysis of viral proteins we demonstrate here that antigen-positive and latently infected neurons appear synchronously in spinal ganglia during the earliest stages of acute ganglionic infection. This is consistent with early divergence of the molecular pathways leading to productive and latent infection, supporting and extending the results obtained with viral mutants.

Animals↗

PubMed1981

On the mechanism of the inhibition of fast axonal transport caused by exposure of frog spinal ganglia to the sodium-deficient medium.

Substitution of choline or sucrose for Na+ in the medium surrounding frog spinal ganglia causes an inhibition of fast axonal transport in vitro. Since an increase Ca2+ influx into neurons does occur in these media, the present experiments examined the possibility that the effect on transport is mediated by an increase in intracellular free Ca2+. The combination of the choline substitution with a 3-fold increase in extracellular Ca2+ reduced transport of [3H] proteins to 75% of control (as compared to the 63% obtained previously with choline alone), thus providing no evidence of an enhancement of choline's effect by a second factor which promotes an increase in intracellular Ca2+. When Li+ was substituted for Na+, the quantity of [3H] proteins transported fell to 40% of control despite the fact that the Li+ substitution does not modify Ca+ fluxes across the plasma membrane in neurons of the frog spinal nerve. The present findings suggest that removal of Na+ interferes with fast axonal transport by a mechanism other than an increase in intracellular Ca2+

Animals↗

PubMed1991

Clusters of nerve cell bodies enclosed within a common connective tissue envelope in the spinal ganglia of the lizard and rat.

A careful search for groups of nerve cell bodies enclosed within a common connective envelope was made in the spinal ganglia of the lizard and rat using a serial-section technique. Nerve cell bodies sharing a common connective envelope were found to be more common in the lizard (9.4%) than in the rat (5.6%). These nerve cell bodies were arranged in pairs, or, less frequently, in groups of three. At times, they appeared to be in immediate contact, with no intervening satellite cells; at others, they remained separated from one another by a satellite cell sheet. The clusters of nerve cell bodies enclosed within a common connective envelope probably result from the arrest of developmental processes in the spinal ganglion. It is possible that, as a result of the cell arrangement here described, certain neurons electrically influence other sensory neurons at the level of the ganglion.

Animals↗

PubMed1983

Development of a nonneuronal cell line derived from porcine spinal ganglia.

A cell line from porcine spinal ganglion (PSPG) tissue was initiated and characterized. The PSPG cell line contained epithelioid, fibroblast-like, and stellate-like cells. There were numerous intercellular communications between cells in the culture. Neuronal cells were not present in the PSPG cell line. The PSPG cell line was aneuploid at the 5th and 45th subculture levels. Seven porcine viruses replicated in cultures of PSPG cells, and 2 pseudorabies virus strains infected the cells after being diluted 10(-7).

Animals↗

PubMed1988

Acute and chronic effects of the neurolytic agent ricin on dorsal root ganglia, spinal cord, and nerves.

The short- and long-term effects of ricin injections into nerves have been evaluated with light microscopy in the dorsal root ganglia, spinal cord, and peripheral nerves in rats and cats. Dorsal root ganglion cells initially exhibited chromatolysis, followed by gliosis and cell death. These changes were associated with Fink-Heimer degeneration in the somatotopically appropriate region of the dorsal horn. There were no signs of chromatolysis in dorsal horn neurons in ricin-injected animals, but chromatolytic motoneurons were observed. Ricin produced acute necrosis of injected nerves and dissolution of axoplasm. At long survival times (greater than 4 weeks) some apparently regenerating axons were seen in the injection sites of rats. Cell counts indicated that a substantial percentage of dorsal root ganglion neurons associated with the injected nerves were killed, but the presence of regenerating axons suggested that some cells survived the ricin treatment. Although the lesion may not always be complete, even with maximum sublethal doses, this method appears to be useful for specifically destroying afferent fibers associated with a particular nerve without transynaptic destruction of dorsal horn neurons.

Animals↗

PubMed2005

An immunocytochemical study of calbindin-D28K in laminae I and II of the dorsal horn and spinal ganglia in the chicken with special reference to the relation to substance P-containing primary afferent neurons.

The localization of calbindin-D28K (CB) was studied immunocytochemically in laminae I and II of the dorsal horn and in spinal ganglia in the chicken, and compared with the distribution of substance P (SP) using double immunolabeling. At the light microscopic level, CB immunoreactivity was observed most intensely in the lamina II using the avidin-biotinylated peroxidase complex (ABC) and immunofluorescence methods. At the electron microscopic level using the ABC method, CB immunoreactivity was observed in the following three neuronal elements: 1) the scalloped central terminal with many dense-cored vesicles (DCVs) in the synaptic glomerulus; 2) some vesicle-containing dendrites (VCDs) inside or outside the synaptic glomerulus; and 3) some axon terminals outside the synaptic glomerulus. The CB-immunoreactive (IR) VCDs in the synaptic glomerulus often formed reciprocal synapses with the central terminal. Strong immunoreactivity was observed at the postsynaptic membrane of CB-IR elements. Double immunofluorescence and immunolabeling methods at the electron microscopic level showed that CB and SP colocalized in the scalloped central terminal with DCVs of the synaptic glomerulus. Almost all SP-IR neurons in the spinal ganglion revealed the coexistence of CB in serial sections in the chicken. In light of previous biochemical and physiological reports, our findings suggest that CB - coexisting with SP - plays an important role in the control of pain transmission through its strong Ca(2+)-buffering action in the chicken.

Animals↗

PubMed1986

Origin and distribution of cerebral vascular innervation from superior cervical, trigeminal and spinal ganglia investigated with retrograde and anterograde WGA-HRP tracing in the rat.

Peripheral sources of cerebral vascular innervation have been investigated with retrograde and anterograde neuronal tracing of wheat germ agglutinin conjugated with horseradish peroxidase (WGA-HRP) in the rat. For retrograde identification of sources of innervation, WGA-HRP was applied to the exposed basilar artery through a fine slit in the overlying meninges, and sections of brain and peripheral ganglia were reacted with tetramethylbenzidine for detection of the tracer. A high density of tetramethylbenzidine reaction product was observed around the basilar artery and in the surrounding pial tissue, but the application sites were not completely selective since some tracer always had spread into the ventral brain stem. Retrogradely labelled cell bodies were identified in the superior cervical, stellate, first and second spinal, and trigeminal ganglia, i.e. these ganglia may represent origins of basilar artery innervation. In a second series of experiments, microinjections of WGA-HRP were placed into the indicated ganglia to obtain anterograde labelling of nerve fibres on whole-mounts of the cerebral vessels. Injections into trigeminal ganglia labelled nerve fibres on the ipsilateral half of the circle of Willis, as well as the contralateral anterior cerebral artery and the rostral part of the basilar artery. The first and second spinal ganglia projected to the vertebrobasilar arteries, while the ipsilateral part of the internal carotid (outside the circle of Willis) received fibres from the second spinal ganglion. Nerve fibres originating in trigeminal and spinal ganglia were organised in bundles, and between these a sparse plexus of thin single fibres appeared. Injection of WGA-HRP into superior cervical ganglion labelled a plexus of nerve fibres on the ipsilateral circle of Willis and the (rostral) basilar artery. These experiments demonstrated the origin and distribution of sympathetic and sensory innervation to major cerebral arteries in the rat.

Animals↗

PubMed1964

THE DISTRIBUTION OF EXOGENOUS FERRITIN IN TOAD SPINAL GANGLIA AND THE MECHANISM OF ITS UPTAKE BY NEURONS.

Toad spinal ganglion cells are individually enclosed in sheaths consisting of one or more attenuated layers of satellite cell cytoplasm surrounded externally by a basement membrane. Narrow ( approximately 150 A) extracellular channels separate these layers from one another and from the underlying neuron. In both in vivo and in vitro experiments it was found that molecules of ferritin, a water-soluble protein, are to some extent able to pass across the basement membrane and through these channels to reach the neuronal plasma membrane. Ferritin particles arriving at the neuronal surface are engulfed by the neuron in 0.1 to 0.2 micro "coated" vesicles. The concentration of ferritin in these vesicles is higher than in the perineuronal space. The ferritin incorporated into the neuron is segregated, apparently intact, in multivesicular bodies. It is inferred that the 150A channels in the satellite cell sheath are patent, aqueous spaces through which molecules with a diameter as large as 95 A are able to pass, and that these neurons are capable of taking up whole protein from their immediate environment by the process of pinocytosis.

Anura↗

PubMed1979

Types of neural cells in the spinal ganglia of human embryos and early fetuses.

Spinal ganglial of human embryos and fetuses ranging in C.-R. length from 15 to 74 mm and in age from 6 1/2 to 11 postovulatory weeks were studied by light and electron microscopy. A sequence of events in differentiation and maturation enabled five types of cells to be distinguished: 1. apolar, undifferentiated neuroblasts are the main cells at 6 1/2 to 7 1/2 weeks; 2. early bipolar neuroblasts (strictly speaking, types 2 to 5 are immature neurons) predominate at the end of the embryonic period proper (8 postovulatory weeks); 3. intermediate bipolar neuroblasts are characteristic of the early fetal period; 4. late bipolar neuroblasts, in which two proceses arise separately from one pole of the cell, appear at about 10 postovulatory weeks; 5. unipolar neuroblasts are found within another week and, by that time, cells of types 1 and 2 are no longer present.

Cell Differentiation↗