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  • Electronic Resource  (4)
  • Anxiety  (2)
  • Monoamine Synthesis in Rat Brain  (2)
  • Ataxia  (1)
  • 1
    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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  • 2
    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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  • 3
    ISSN: 1432-2072
    Keywords: Benzodiazepine receptors ; β-Carboline-3-carboxylates ; Anxiety ; Epilepsy ; Ataxia ; Rat ; Mouse
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract ZK 91296 (ethyl 5-benzyloxy-4-methoxymethyl-β-carboline-3-carboxylate) is a potent and selective ligand for benzodiazepine (BZ) receptors. Biochemical investigations indicate that ZK 91296 may be a partial agonist at BZ receptors. Such partial agonism may explain to some extent why ZK 91296 needs higher BZ receptor occupancy than diazepam for the same effect against chemical convulsants and for behavioural effects. The lack of sedatiye effects, and the very potent inhibition of reflex epilepsy, spontaneous epilepsy and DMCM-induced seizures suggest, furthermore, that ZK 91296 may possess pharmacological selectivity for a particular type of BZ receptor interaction, perhaps including topographic as well as receptor subtype differentiation.
    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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