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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Journal of agricultural and food chemistry 26 (1978), S. 442-446 
    ISSN: 1520-5118
    Source: ACS Legacy Archives
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition , Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 296 (1976), S. 25-30 
    ISSN: 1432-1912
    Keywords: (+)Amphetamine ; Haloperidol ; Monoamine synthesis ; Dopamine release ; Cerebral hemitransection
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary (+)Amphetamine is known to produce feedback inhibition of catecholamine-containing neurons in the central nervous system due to its indirect receptor stimulating properties. This feedback control may involve postsynaptic receptors and neuronal loops or presynaptic receptors and may be restricted to the catecholaminergic terminal system. In order to study the effect of (+)amphetamine on catecholamine synthesis and metabolism in the terminal system changes in impulse flow were eliminated by cutting the ascending monoaminergic axons. Axotomy of the ascending monoaminergic fibers by means of a complete transverse cerebral hemisection resulted in a 3-fold increase in Dopa formation in the lesioned forebrain during 30 min after inhibition of the aromatic amino acid decarboxylase with 3-hydroxybenzylhydrazine HCl, 100 mg/kg i.p. (+)-Amphetamine sulfate, 10 mg/kg i.p. antagonized the hemisection-induced increase in Dopa formation and reduced the formation of 5-hydroxytryptophan. Pre-treatment with haloperidol, 5 mg/kg i.p. failed to counteract the effect of (+)amphetamine. In the intact forebrain the stimulation of Dopa accumulation was more than additive after combined treatment with haloperidol and (+)amphetamine. Hemitransection retarded the disappearance of dopamine and noradrenaline after administration of α-methyl-p-tyrosine methylester HCl, 300 mg/kg. (+)-Amphetamine, 10 mg/kg accelerated the utilization of dopamine on the lesioned side. Hemitransection reduced the formation of 3-methoxytyramine during 1 h after pargyline, 75 mg/kg i.p. After (+)amphetamine 3-methoxytyramine formation in the intact forebrain was 3 times higher than in the lesioned forebrain. The action of (+)amphetamine on dopamine synthesis and release appears to be dependent on the firing rate in dopamine neurons.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 274 (1972), S. 273-280 
    ISSN: 1432-1912
    Keywords: DOPA ; Tyrosine ; 5-Hydroxytryptophan ; Brain ; Dowex 50W, X-4
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The method is an extension of the chromatographic separation procedure for 5-HIAA and 5-HTP published by Lindqvist (1971). Brain tissue is extracted with perchloric acid. After adjustment of the pH to 2 the extract is passed through a Dowex 50W, X-4 column. 5-HIAA is eluted with 60% aqueous methanol, DOPA and tyrosine with 0.1 M sodium citrate buffer pH 4.5 and 5-HTP and tryptophan with 0.1 M sodium phosphate buffer pH 6.5. If the above procedure is combined with that published by Atack and Magnusson (1970) 9 different compounds can be estimated after a single column procedure. DOPA is assayed fluorimetrically using a modification of the trihydroxy-indole (THI) assay for noradrenaline (Bertler et al., 1958). The level of DOPA found in a normal rat brain was below the sensitivity of the method (10 ng/g). After inhibition of the aromatic amino acid decarboxylase a compound indistinguishable from authentic l-DOPA accumulated in the rat brain.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 290 (1975), S. 347-356 
    ISSN: 1432-1912
    Keywords: l-3-Methoxytyrosine ; Monoamine Synthesis in Rat Brain ; Dopa ; 5-Hydroxytryptophan ; NSD 1015 (3-Hydroxybenzylhydrazine HCl)
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Rats were injected i.p. with l-3-methoxytyrosine, 100 or 300 mg/kg. One h later brain, liver, heart and blood plama were analyzed for catecholamines and their precursors. In brain Dopa as well as dopamine and noradrenaline levels were unchanged, while demethylation of l-3-methoxytyrosine might have occurred in peripheral organs since Dopa levels in liver and dopamine in heart were elevated. 3-Methoxytyramine could not be detected in brain and liver after treatment with l-3-methoxytyrosine. Monoamine synthesis in vivo was measured in whole brain by determining the accumulation of Dopa and 5-hydroxytryptophan 30 min after the i.p. injection of NSD 1015 (3-hydroxybenzylhydrazine HCl, 100 mg/kg), an inhibitor of the aromatic amino acid decarboxylase. l-3-Methoxytyrosine attenuated the formation of Dopa and 5-hydroxytryptophan by about 25% in brain tissue. The effect was paralleled by a decrease in the brain concentration of tryptophan.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 300 (1977), S. 19-23 
    ISSN: 1432-1912
    Keywords: Dopa ; Methoxytyrosine ; Catechol-O-methyltransferase ; Rat liver ; Catechol-O-methyltransferase inhibitors ; 3-Hydroxybenzylhydrazine (NSD 1015)
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The O-methyl derivative methoxytyrosine accumulated rapidly in rat liver after an intraperitoneal injection of l-dopa (50 mg/kg) in combination with 3-hydroxybenzylhydrazine, an inhibitor of the aromatic amino acid decarboxylase. Methoxytyrosine levels reached a plateau 40–60 min after an i.p. injection of l-dopa, of which the tissue concentration declined monoexponentially. Injection of various doses of l-dopa revealed that methoxytyrosine formation was saturable and followed enzyme kinetics in rat liver. The catechol-O-methyltransferase inhibitors pyrogallol, tropolone and α-propyldopacetamide as well as the inhibitor of the aromatic amino acid decarboxylase benserazide inhibited the formation of methoxytyrosine dose-dependently and concomitantly increased the tissue concentration of dopa. The accumulation of methoxytyrosine from exogeneously applied l-dopa appears to be a reliable indicator of the in vivo activity of catechol-O-methyltransferase.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 284 (1974), S. 149-158 
    ISSN: 1432-1912
    Keywords: 3-Methoxytyramine ; Monoamine oxidase inhibitors ; Brain ; Dowex 50 W, X-4
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary A method for the chromatographic separation (Dowex 50 W, X-4) and fluorimetric determination of 3-methoxytyramine in brain tissue is described. The chromatographic procedure is an extension of the method for the separation of noradrenaline, dopamine and 5-hydroxytryptamine published by Atack and Magnusson (1970) and can be combined with that for monoamine precursors described by Kehr et al. (1972). 3-Methoxytyramine is eluted in N ethanolic (50%)-HCl and oxidized with potassium ferricyanide in ammonium hydroxide solution. Compared with previously published methods, the sensitivity is increased 2 to 5 fold. Reproducibility, recovery and specificity of the method are satisfactory. The level of 3-methoxytyramine found in normal rat brain is below the limit of sensitivity (10 ng/g). The amount of 3-methoxytyramine accumulating after inhibition of monoamine oxidase (MAO) differs depending on the inhibitor used. These differences in 3-methoxytyramine formation might be due to incomplete MAO inhibition, changes in dopamine synthesis, and releasing activity of the compounds investigated.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 284 (1974), S. 263-277 
    ISSN: 1432-1912
    Keywords: Diethyl Ether Anaesthesia ; Pentobarbitone Anaesthesia ; Monoamine Synthesis in Rat Brain ; Dopa ; 5-Hydroxytryptophan ; NSD 1015 (3-hydroxybenzylhydrazine HCl)
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Rats were injected i.p. with pentobarbitone sodium 40 mg/kg or were exposed to diethyl ether anaesthesia for 15 to 60 min. Monoamine synthesis in vivo was measured in various brain regions by determining the accumulation of dopa and 5-hydroxytryptophan (5-HTP) during 15 or 30 min after the i.p. injection of NSD 1015 (3-hydroxybenzylhydrazine HCl, 100 mg/kg), an inhibitor of the aromatic amino acid decarboxylase. Pentobarbitone retarded the formation of dopa and 5-HTP by about 25% in most brain regions but had no effect on striatal dopa formation. Ether accelerated the formation of dopa and 5-HTP in most brain regions, the action on striatal dopa being most pronounced (to 250% of control). The effect was generally somewhat less marked during the second than during the first half-hour of anaesthesia. A postanaesthetic inhibition of dopa formation was found in the striatum and of 5-HTP formation in whole brain. If hypothermia was allowed to develop, the stimulating action of ether on dopa and 5-HTP formation tended to be partly antagonized. A complex interaction between NSD 1015 and the hypothermic response to ether was observed.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 301 (1978), S. 163-169 
    ISSN: 1432-1912
    Keywords: Dopamine receptors ; Striatum ; LSD ; Lisuride ; Reserpine ; Monoamine synthesis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The effect of d-lysergic acid diethylamide (LSD) and lisuride on the synthesis of monoamines was evaluated in rat brain regions using an in vivo method in which the accumulation of dopa and 5-hydroxytryptophan (5-HTP) is measured after inhibition of the aromatic amino acid decarboxylase by means of 3-hydroxybenzylhydrazine. LSD (50–1000 μg/kg i.p.) caused a dose-dependent increase in dopa formation and a slight elevation of tyrosine and tryptophan concentrations in the intact rat forebrain; moreover, it reduced the accumulation of 5-HTP. The increase in dopa formation in the terminal system of the rat forebrain following an axotomy of the ascending monoaminergic fiber system was antagonized by LSD at a dose of 0.5 mg/kg i.p. Haloperidol (2 mg/kg i.p.) counteracted the effect of LSD. The increase in dopa formation in c. striatum and the dopamine-rich part of the limbic system following treatment with reserpine was antagonized by lisuride as well as by LSD. However, lisuride was at least 10 times as potent as LSD. In reserpinized animals LSD counteracted the inhibitory effect on dopa accumulation of the direct dopamine receptor stimulant apomorphine while lisuride did not. The data suggest that LSD is a weak agonist at dopamine receptors in vivo with partial receptor blocking properties at higher doses, while the action of lisuride on dopamine receptors is a potent, purely agonistic one.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 293 (1976), S. 209-215 
    ISSN: 1432-1912
    Keywords: 3-Methoxytyramine ; Dopamine release in rat brain ; Monoamine oxidase inhibition ; Apomorphine ; Haloperidol ; γ-Butyrolactone
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary 3-Methoxytyramine and dopamine accumulated in vivo in rat brain after monoamine oxidase inhibition with pargyline HCl. A dose of 100 mg/kg i.p. appeared to inhibit monoamine oxidase completely and led to a linear accumulation of 3-methoxytyramine for the first 90 min. Axotomy of the ascending dopaminergic fiber tract by means of a complete transverse cerebral hemisection almost completely blocked 3-methoxytyramine formation provided that catecholamine synthesis was inhibited with H 44/68 (methylester of α-methyl-p-tyrosine). The dopamine receptor agonist apomorphine, 0.5 mg/kg i.p., decreased, while the dopamine receptor antagonist haloperidol, 2 mg/kg i.p., accelerated 3-methoxytyramine formation. γ-Butyrolactone, 750 mg/kg i.p., not only decreased 3-methoxytyramine formation per se but also effectively antagonized the haloperidol-induced increase in 3-methoxytyramine accumulation. 3-Methoxytyramine formation after inhibition of monoamine oxidase appears to be a reliable indicator of impulse-induced dopamine release and metabolism.
    Type of Medium: Electronic Resource
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  • 10
    ISSN: 1432-2072
    Keywords: β-Carbolines ; Drug discrimination ; Benzodiazepine ; Diazepam ; Chlordiazepoxide ; Pentylenetetrazol ; Anxiety ; FG 7142 ; ZK 93423 ; ZK 91 296 ; Rat
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract The discriminative stimulus properties of three β-carboline derivatives were studied in three groups of rats trained, respectively, to discriminate diazepam (2.5 mg/kg IP), chlordiazepoxide (CDP, 5 mg/kg IP) or pentylenetetrazol (PTZ, 15 mg/kg IP) from saline in standard procedures employing two-lever operant chambers. Two β-carbolines, ZK 91296 and ZK 93423, substituted for the benzodiazepines in both CDP- and diazepam-trained rats. The neutral benzodiazepine antagonist Ro 15-1788 blocked the diazepam discriminative stimulus and the ability of ZK 91296 to substitute for diazepam. A third β-carboline, FG 7142, was not identified as benzodiazepine-like in generalization tests in either diazepam- or CDP-trained rats, but when administered together with CDP antagonized the benzodiazepine discriminative stimulus. In rats trained to discriminate PTZ from saline (a discrimination which is thought to depend on the anxiogenic properties of PTZ) the PTZ cue was antagonized by diazepam and ZK 93423, and partially antagonized by ZK 91296. The PTZ cue generalized to FG 7142 and this generalization was partially antagonized by Ro 15-1788. These results suggest that the three β-carbolines provide more than one kind of discriminative stimulus, consistent with the classification of ZK 93423 as an agonist at central benzodiazepine receptors, with ZK 91 296 as a partial agonist, and with FG 7142 as an inverse agonist. Pharmacologically, ZK 93 423 and ZK 91 296 may exhibit anxiolytic qualities, whereas FG 7142 produces anxiogenic effects.
    Type of Medium: Electronic Resource
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