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  • 1
    ISSN: 1471-4159
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Developmental changes in pyruvate kinase (PK), lactate dehydrogenase (LDH), α-glycerophosphate dehydrogenase (α-GPD), glucose-6-phosphate dehydrogenase (G6P), succinate dehydrogenase (SDH), glutamate dehydrogenase (GDH), choline acetyltransferase (CAT), glutamate decarboxylase (GAD), activities were measured in early autopsy material in the following areas of human neocortex: area 4 (motor cortex), area 17 (visual cortex), area 40 (gyrus supramarginalis, associative cortex). Changes with age were analysed from 8 fetal weeks to adult age. The important points emerging from this study are: 1. Enzymes associated with glycolytic pathways show a high activity in early fetal period, decline through to the end of the active phase of neurogenesis and then, rise continuously to the end of the first year of life. 2. G6P, an enzyme associated with the oxidative segment of the pentose phosphate pathway, shows a high activity at 8 fetal weeks and, gradually declines through to the end of the active phase of neurogenesis; it then either does not change significantly (motor cortex) or increases slightly. 3. Enzymes related to the tricarboxylic pathway have a low level of activity throughout the first half of gestation, and then rise markedly during the last fetal months and the first year after birth. SDH increase is of much higher magnitude (× 10) than that observed for glycolytic enzymes (×4). For the enzymes of oxidative metabolism, motor cortex is the most advanced area, while associative cortex matures more slowly. 4. CAT activity at 8 fetal weeks is high in visual cortex and declines to the fifth month. After that time, there is a continuous rise until the age of 11 years. Although the time pattern in reaching the adult value is different in motor and associative cortex, there exists a continuous increase from fetal onset to adult level in both areas. Developmental changes in GAD activity are very unusual. The development of activity lags behind that of CAT and commences after birth. After a steady rise in the first year of life, the activity decreases after this age.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Acta neuropathologica 15 (1970), S. 251-271 
    ISSN: 1432-0533
    Keywords: Capillary Walls N. S. ; Maturation ; Histoenzymology
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Résumé La maturation de l'équipement enzymatique des parois vasculaires du système nerveux a été étudiée par des techniques histochimiques chez le rat et l'enfant. Dans les capillaires du rat, l'activité des phosphatases acides et des estérases carboxyliques non spécifiques apparaît dans les péricytes vers le 10e jour, mais des estérases carboxyliques endothéliales existent dès la naissance et disparaissent ensuite au cours de la maturation. L'activité de l'ATPase et de la NADH tétrazolium reductase apparaît vers le 20e jour. L'inosine diphosphatase, les phosphatases alcalines et la butyrylcholinestérase sont déjà présents chez le rat nouveau-né, mais des modifications dans la localisation des deux dernières activités on été notées en fonction de lâge. Chez l'enfant, les estérases carboxyliques dans les péricytes ne font leur apparition qu'après la naissance alors que les phosphatases alcalines, la NADH tétrazolium reductase et l'ATPase sont déjà présents chez un foetus de 3 mois. Les phosphatases alcalines diminuent dans les vaisseaux de la substance blanche après la fin de la myélinisation alors que l'activité de la NADH tétrazolium reductase et celle de l'ATPase augmente. Les rapports entre la maturation de l'équipement enzymatique des parois vasculaires et celle du fonctionnement de la barrière hémo-encéphalique sont discutés de même que les rapports avec la maturation ultrastructurale des capillaires.
    Notes: Summary A histochemical study was done on the enzymatic equipment of the vessel walls of the brain during maturation in the rat and in children. Acid phosphatases and nonspecific carboxylic esterases appear in the pericytes of newborn rats at the 10th day, however endothelial carboxylic esterases are present at birth and later disappear during maturation. The activities of NADH tetrazolium reductase and ATPase appears in the capillaries only around the 20th day. Inosine diphosphatase, alkaline phosphatase and butyrylcholinesterase are present in the vessels of newborn rats but the localization of these two last activities undergoe modifications during maturation. In children there is a progressive increase of carboxylic esterases in the pericytes after birth but alkaline phosphatases, NADH tetrazolium reductase and ATPases are already present in the vessel walls of a 3 months old foetus. The activity of alkaline phosphatases decreases in the capillaries of the white substance after myelination when those of NADH tetrazolium reductase and ATPase increases. The relation between the maturation of enzymatic equipment of vessel walls and that of blood brain barier (BBB) function is discussed as well as relations with the ultrastructural development of capillary walls.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1432-0533
    Keywords: Leukoencophalopathy ; Genetic disorders ; Metabolic diseases ; Cogenital lactic acidosis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Résumé Des anomalies graves de la substance blanche sont décrites chez deux sœurs décédées l'une à 8 jours, l'autre à 10 mois 1/2. L'étude biochimique a mis en évidence chez l'une d'entre elles une acidose lactique congénitale. Les altérations de la substance blanche chez nos deux sœurs sont superposables compte-tenu de leur âge. Elles sont caractérisées par: a) des kystes périventriculaires bilatéraux et symétriques, frontaux, temporaux et cérébelleux; b) une spongiose lache au voisinage des kystes s'étendant parfois à distance; c) un retard massif de la myélinisation correspondant à celle d'un foetus de 7 mois pour l'enfant de 8 jours et à celle d'un enfant de 2 à 3 mois pour la sœur aïnée; d) et par une démyélinisation dans les zones déjà myélinisées. Des éclaircissements myéliniques existent dans le pallidum et la calotte bulbo protubérantielle de l'aïnée; les deux sœurs présentent des foyers de myélinolyse pontique. Les auteurs pensent que les lésions décrites sont le substratum neuropathologique de l'acidose lactique congénitale.
    Notes: Summary Severe lesions of the white matter are described in two sisters who died of the age of 8 days and $$10{\raise0.7ex\hbox{$1$} \!\mathord{\left/ {\vphantom {1 2}}\right.\kern-\nulldelimiterspace}\!\lower0.7ex\hbox{$2$}}$$ months respectively. Biochemical studies in the older child showed modifications seen in congenital lactic acidosis. The neuropathological findings in the two sisters where similar. Both had: 1. bilateral and symetrical periventricular cysts, 2. spongy state and gliosis of the white matter near the cysts, 3. Severe delay in myelination and 4. demyelination in the myelinated tracts. Some demyelination was also noted in the pallidum and the superior medullar tegmentum of the older child. Both sisters had myelinolytic foci in the ventral part of the pons. Authors think that the lesions described are characteristic of congenital lactic acidosis.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Acta neuropathologica 21 (1972), S. 272-281 
    ISSN: 1432-0533
    Keywords: Jimpy Mice ; Myelination ; Oligodendroglia ; Maturation Defect
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Abnormalities were found in the glial population of white matter in Jimpy mice. These abnormalities consist in: a) low density of glial cells; b) a defect in maturation and proliferation of oligodendrocytes; c) an absence of disposition of these elements in rows; d) a scarcity of mature oligodendrocytes; e) the presence of numerous bipolar elements, probably glioblasts, and f) a proliferation of fibrous astrocytes. Differences in glial population between Jimpy and control mice become striking with age and are specially marked in the regions which myelinate later. The defect in maturation of oligodendroglia and the lack of accumulation of myelin lipids, indicate that the lack of myelin in Jimpy mice must be attributed to the interruption of the myelination process. The defect in maturation and proliferation of oligodendroglia shown, is probably responsible for the arrest of myelin formation as well as for the multienzymatic deficiencies found in the CNS of Jimpy.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1432-0533
    Keywords: Herpes simplex encephalitis ; Histochemistry ; Capillaries
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary An enzyme histochemical study of experimental herpes simplex encephalitis of the mouse has revealed a decrease in the number of capillaries displaying alkaline phosphatase activity. Glial cells showed increased Inosine 5 diphosphatase and ATPase activity. These enzyme histochemical changes were distributed throughout the nervous parenchyma while the lesions, seen by light microscopy, are localized to well defined areas. Mice inoculated with a pure culture of irradiated HSV failed to show the above mentioned modifications.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 1432-0533
    Keywords: Leukodystrophy ; Familial Encephalopathy ; Subacute Necrotizing Encephalopathy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Two cases of a peculiar progressive encephalopathy clinically resembling a leukodystrophy, occurring in siblings, are reported. In both cases there was diffuse involvement of the white matter, with necrosis and vascular proliferation, the histological picture being similar to that observed in subacute necrotizing encephalomyelopathy. All grey structures were normal, except for a slight spongiosis of the locus niger in both cases. An observation of subacute necrotizing encephalopathy with very extensive involvement of the white matter is presented and compared with these cases. The relationship between our first two cases and Leigh's disease are discussed. It is concluded that they cannot be considered cases of subacute necrotizing encephalopathy as presently described.
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 1432-0533
    Keywords: Cerebral Ischaemia ; Recirculation ; Enzyme Histochemistry ; Electron Microscopy ; Dendrite Swelling ; Pinocytosis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Complete cerebral ischaemia of 30 and 90 min was produced in normothermic barbiturized cats by clamping the innominate and subclavian arteries and lowering the systemic blood pressure. When the brains were adequatly recirculated after 30 min of ischaemia, electron microscopical and histochemical changes observed at the end of the circulatory arrest, were almost fully reversible. Endothelial cells of capillaries showed increased number and size of pinocytotic vesicles and numerous intraluminal flaps. ATPase activity was increased in the capillary walls and glial cells. Opposite to this, severe and irreversible ultrastructural changes were observed after 90 min of ischaemia, and all the enzyme activities studied were sharply decreased.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Acta neuropathologica 33 (1975), S. 245-256 
    ISSN: 1432-0533
    Keywords: Herpes simplex encephalitis ; Blood-vessels ; Reactive microglia ; Electron microscopy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Generalized vascular changes and diffused proliferation of reactive microglia were observed in an experimental model of HSV encephalitis of mice. The wide spread of these changes contrasted with the localized character of virus replication and the confined areas of damaged nervous tissue. The vascular and microglial changes were precocious in animals inoculated with concentrated virus suspension (105.5LD50) while they appeared late in mice inoculated with diluted virus suspension (100 LD50). After inoculation with U.V. inactivated virus no changes were seen. The results obtained in this study suggest that the vascular and microglial modifications are not related to a direct cytopathic effect of the virus but dependent on the amount of virus present in the central nervous system and linked to the virus DNA.
    Type of Medium: Electronic Resource
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