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  • 1
    Digitale Medien
    Digitale Medien
    Oxford, UK : Blackwell Publishing Ltd
    Journal of neurochemistry 18 (1971), S. 0 
    ISSN: 1471-4159
    Quelle: Blackwell Publishing Journal Backfiles 1879-2005
    Thema: Medizin
    Notizen: —The development of ganglioside sialidase and of four different p-nitrophenyl glycosidases in human brain was investigated including both prenatal and postnatal periods. The developmental curve for sialidase was different from that of the other glycosidases. While p-nitrophenyl glycosidases showed high activities at an early stage of development (21 foetal weeks), and remained at about the same level, ganglioside sialidase was not detected before the foetal age of 15-20 weeks. The sialidase activity at term reached about half the adult level and there was a possible decrease in activity during the first year. The sialidase activity then increased, approaching the adult level at about the age of 5 years. The development of the ganglioside sialidase activity in human brain can be related to changes in the concentration of individual brain ganglioside components. The late maturation of the sialidase system in relation to other glycohydrolases is also discussed as a possible protective mechanism for sialic acid-containing compounds during the early period of development.
    Materialart: Digitale Medien
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  • 2
    Digitale Medien
    Digitale Medien
    Oxford, UK : Blackwell Publishing Ltd
    Journal of neurochemistry 18 (1971), S. 0 
    ISSN: 1471-4159
    Quelle: Blackwell Publishing Journal Backfiles 1879-2005
    Thema: Medizin
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 3
    Digitale Medien
    Digitale Medien
    Oxford, UK : Blackwell Publishing Ltd
    Journal of neurochemistry 18 (1971), S. 0 
    ISSN: 1471-4159
    Quelle: Blackwell Publishing Journal Backfiles 1879-2005
    Thema: Medizin
    Notizen: Abstract— The developmental profiles of individual gangliosides of human brain were compared with those of rat brain. Interest was focused mainly on the pre- and early postnatal development. Human frontal lobe cortex covering the period from 10 foetal weeks to adult age and the cerebrum of rat from birth to 21 days were analysed. Lipid-NANA and lipid-P were followed; in the rat, also protein and brain weight. A limited number of samples of human cerebral white matter and cerebellar cortex were also studied. The following major results were obtained:〈list xml:id="l1" style="custom"〉1The ganglioside concentration increased approximately three-fold within a short period: in rat cerebrum, from birth to the 17th day; in human cerebral cortex, from the 15th foetal week to the age of about 6 months. The largest increase in the rat brain occurred by the 11th to the 13th day; in human brain by term. The relative increase of gangliosides during this period was more rapid than that of phospholipids.2A hitherto unknown distinct early period of ganglioside and phospholipid formation in rat occurred by the second to fourth day.3The changes in brain ganglioside pattern, characteristic of the developmental stages of the rat, were found to be equally pronounced in the human brain.4Regional developmental differences in the ganglioside pattern were demonstrated in human brain. A characteristic white matter pattern, rich in monosialogangliosides, had developed by the age of 1 year. The increase in ganglioside concentration and the formation of the definitive ganglioside pattern of cerebellar cortex occurred later than in cerebral cortex. This cerebellar pattern was characterized by a very large trisialoganglioside fraction.5The two periods of rapid ganglioside metabolism in rat brain preceded the two periods of rapid protein biosynthesis.
    Materialart: Digitale Medien
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  • 4
    Digitale Medien
    Digitale Medien
    Oxford, UK : Blackwell Publishing Ltd
    Journal of neurochemistry 18 (1971), S. 0 
    ISSN: 1471-4159
    Quelle: Blackwell Publishing Journal Backfiles 1879-2005
    Thema: Medizin
    Notizen: —A subcellular fractionation was performed on forebrain cortex from three human brains and the fractions obtained were assayed for ganglioside sialidase and four p-nitrophenyl glycohydrolases. Differences in the sedimentation patterns of the enzymes were observed. From 53 to 77 per cent of the recovered sialidase activity was found in the synaptosomal fraction, while the p-nitrophenyl glycosidases were mainly recovered in the lysosome-enriched fraction. Three possible interpretations of the sialidase sedimentation pattern are suggested: (1) The ganglioside sialidase is bound to the limiting membrane structure of the nerve ending. (2) The ganglioside sialidase is lysosomal, although bound to lysosomes of low density. (3) The enzyme occurs mainly in lysosomes primarily located in the nerve endings, being trapped under the formation of the synaptosomes.
    Materialart: Digitale Medien
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  • 5
    ISSN: 1435-1463
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Medizin
    Notizen: Summary The antipsychotic effect ofα-methyltyrosine (α-MT) in combination with thioridazine was investigated by means of rating scales for “social behaviour” and “mental symptoms” The clinical effect was also evaluated in relation to the serum concentrations ofα-MT and thioridazine and to the increase in prolactin secretion in response to the interaction with hypothalamic dopaminergic mechanisms. The interactions between the serum levels ofα-MT and those of the transmitter precursors phenylalanine and tyrosine were analysed. The results confirmed the ability ofα-MT (2g/day) to potentiate the antipsychotic effect of thioridazine, whereby the dose of neuroleptic drug required to control psychotic symptoms may be markedly reduced. None of the four patients who completed the trial showed side effects that could be ascribed toα-MT. The antipsychotic effect of thioridazine, alone or in combination withα-MT, correlated well with the prolactin response in the individual patient. No important interference with serum phenylalanine or tyrosine levels was noted during treatment withα-MT.
    Materialart: Digitale Medien
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  • 6
    Digitale Medien
    Digitale Medien
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 299 (1977), S. 105-114 
    ISSN: 1432-1912
    Schlagwort(e): Haloperidol ; Dopa ; Prolactin ; Pharmacokinetics ; Behaviour
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Medizin
    Notizen: Summary A method has been developed for the quantitative determination of haloperidol in brain and other tissues. Such determinations have been made after acute and chronic administration of haloperidol to Sprague-Dawley rats. Different regions of the brain including the striatum, the limbic forebrain and the cerebellum have been analyzed separately. The haloperidol effects on Dopa formation have been studied in the same tissue samples. The stimulation of prolactin secretion via blockade of hypothalamic dopaminergic mechanisms and behavioural effects of the drug have been evaluated in parallel experiments. The elimination of haloperidol from brain tissue is a multiphasic process. The fourth phase of elimination is the slowest with a half life of 4 days. No strict correlation was found between serum and brain concentrations of haloperidol. Both after acute and chronic administration there exists apparently a saturating dose above which the brain concentration of the drug increases very little. The dose seems to coincide with that beyond which little increase in Dopa formation is observed. A pharmacokinetic analysis suggests an element of saturable binding or transfer of haloperidol to brain tissue. This mechanism is not preferentially localized to areas of brain rich in dopaminergic synapses. A good correlation was found between the haloperidol concentration in the brain on the one hand and its effects on behaviour, on serum prolactin values and on Dopa formation on the other.
    Materialart: Digitale Medien
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  • 7
    Digitale Medien
    Digitale Medien
    Springer
    European journal of clinical pharmacology 14 (1978), S. 111-116 
    ISSN: 1432-1041
    Schlagwort(e): Serum prolactin ; Thioridazine ; antipsychotic effect ; dopamine ; psychiatric rating ; psychosis ; schizophrenia
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie , Medizin
    Notizen: Summary Neuroleptic drugs may exert their antipsychotic effect by interference with central dopaminergic mechanisms. Tuberoinfundibular dopaminergic neurons may also be affected, which will increase prolactin secretion from the pituitary. Accordingly, a study has been made in 23 patients with acute paranoid psychosis, treated with thioridazine, of repeated ratings of psychiatric symptoms (CPRS) and of serum prolactin concentration. There was a close correlation between the serum concentration of prolactin and low doses of thioridazine, but at higher doses the increase in prolactin level gradually levelled off. At a given dose the prolactin response to thioridazine showed large interindividual variation and female patients had higher serum prolactin concentrations than males. The prolactin response to thioridazine was unaffected by time of treatment, age or body weight. In individual patients a correlation was found between serum prolactin level and amelioration of psychiatric symptoms, as reflected by the psychiatric rating score (p〈0.001). After normalization of the data, the same relationship was also found for the entire group of patients. The dose-response relationship of prolactin to thioridazine showed saturation kinetics and linear transformation by a Woolfe-plot was done. Therefore, it appears possible to predict the thioridazine dose that would give the maximal prolactin response (and maximal clinical effect) and thereby optimize the regimen of antipsychotic medication in the individual patient.
    Materialart: Digitale Medien
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  • 8
    Digitale Medien
    Digitale Medien
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 286 (1974), S. 113-124 
    ISSN: 1432-1912
    Schlagwort(e): Butyrophenones ; Gas Chromatography ; Haloperidol ; Serum ; Concentrations ; Pharmacokinetics
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Medizin
    Notizen: Summary A quick, specific and precise method for determining haloperidol in serum is described. The method is based on gas chromatography and the use of a structurally similar internal standard. Serum concentrations of haloperidol determined in patients treated with haloperidol, were in the range of 0.5 to 10 ng/ml. The precision of the method was ±8.3%. Of the many drugs tested so far, only thioridazine and dibenzepim interfere with the determinations. Preliminary pharmacokinetic studies based on the intravenous injection of haloperidol demontrated typical apparent volumes of distribution as large as 2,000 l and serum half-lives of 12.6–22.0 hrs. Inter-individual differences in these parameters were demonstrated.
    Materialart: Digitale Medien
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