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  • Articles: DFG German National Licenses  (3)
  • Locomotor activity  (3)
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  • Articles: DFG German National Licenses  (3)
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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Psychopharmacology 68 (1980), S. 15-23 
    ISSN: 1432-2072
    Keywords: RU 24213 ; Dopaminergic agonists ; Locomotor activity ; Stereotypies ; Chcling ; Anorexia ; Emesis ; Core temperature
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract The psychopharmacological properties of RU 24213 were compared to those of other dopaminergic agonists (apomorphine, dexamphetamine, bromocriptine and l-dopa) in various behavioural tests. In naive mice the drug reduced the locomotor hyperactivity in the primary exploratory phase and produced stimulation in the subsequent stabilized activity period. In rats it provoked dose-related stereotypies, specially gnawing and sniffing. It delayed the cataleptic state induced by prochlorperazine without affecting its intensity. In animals unilaterally lesioned with 6-OHDA in the nigro-striatal pathway, RU 24213 caused contralateral turning. It exhibited relatively weak emetic and anorexic effects in dogs. Core temperature recordings in rats revealed a biphasic hypo- and hyperthermic activity. In drug interaction studies it was observed that stereotypies and rotations induced by RU 24213 were blocked by haloperidol and decreased by αMT. Reserpine respectively decreased stereotypies and increased ipsilateral rotations in rats with unilateral electrolytical striatal lesion. The results obtained suggest that RU 24213 stimulates dopamine receptors both directly and indirectly. In this respect it could be compared to bromocriptine but unlike this latter compound it has an immediate effect which is of shorter duration.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Psychopharmacology 45 (1975), S. 197-201 
    ISSN: 1432-2072
    Keywords: Locomotor activity ; Diazepam ; Benzodiazepines ; Dexamphetamine ; Anticholinergics ; Mice
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Experiments were carried out in mice to investigate the influence of diazepam (DZP) on dexamphetamine, para-chloro-N-methylamphetamine (pCMA), cocaine, morphine, trihexyphenidyl or (in MAOIs pretreated) reserpine induced motor hyperactivity. The interaction of DZP with these hyperactivities in which probably different biochemical central mechanisms are involved allows to construct a profile of action of DZP and to approach its mechanism of action. The locomotor hyperactivities induced by dexamphetamine, pCMA, morphine, cocaine were not reduced by DZP even by doses which decrease spontaneous locomotor activity; low doses of DZP enhance the hyperactivity induced by these compounds. Those induced by trihexyphenidyle or by reserpine (after MAOI) were reduced by DZP at doses which produce no decrease in spontaneous motor activity. Inasmuch as DZP at low doses potentiates the effects of 4 different substances, the results can hardly be satisfactorily explained neither by an interference of the benzodiazepine on the metabolism of the drugs or by a depression of the anxiogenic action of dexamphetamine. Even though it may be difficult to relate the antagonism of DZP on trihexyphenidyl- or on reserpine- (after MAOI) induced motor hyperactivity to the suggested anticholinergic and dopaminergic actions of DZP, these effects may partly be involved in the increase in locomotor hyperactivity induced by dexamphetamine, morphine or cocaine. The observed effect of DZP on pCMA induced locomotor hyperactivity does not support a possible antiserotonine action often suggested to explain the effects of benzodiazepines in conflict situations.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1432-2072
    Keywords: Rearing conditions ; Overcrowding ; Locomotor activity ; Emotionality ; Amphetamine ; Pentobarbital ; Rats
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Behavioral and pharmacological tests were performed on rats (males Wistar A.F.) maintained either during 6 weeks at 20 or 5 in a cage (40×40×17 cm) or during 6 weeks at 20 and during 8 days at 5 in cage. When compared to 5/cage-reared rats, overcrowded rats (20/cage) exhibit a lessened locomotor activity in the open field, staircase test, and Y maze; rearings, intrasession habituation, and spontaneous alternation were not altered. It seems difficult to relate this lessened locomotor activity to an enhanced emotionality level. Although overcrowded rats showed heavier adrenals, their susceptibility to restraint-induced gastric ulcers, their ‘neophobic’ responses to new food, and their sensitivity to the stimulating effect of oxazepam in the Y maze were not modified. Sensitivity to amphetamine-induced stereotyped behavior and to pentobarbital-induced hypnosis was found to be increased in overcrowded rats. Apomorphine-induced stereotypy and barbital sleeping time were not modified. All these data (except the fact that barbital onset of hypnosis was delayed in overcrowded rats) may suggest an altered hepatic metabolism in rats reared at 20 in a cage. In overcrowded rats an enhanced amphetamine-induced stereotyped behavior was associated with a lessened locomotor activity. Moreover, after 8 days at 5 in a cage, this increased sensitivity to amphetamine (and to pentobarbital) completely disappeared, whereas locomotor activity was not fully restored. This suggests that amphetamine sensitivity is not related to the predrug activity level of the animals.
    Type of Medium: Electronic Resource
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