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  • 1
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Behavioral and Neural Biology 41 (1984), S. 180-189 
    ISSN: 0163-1047
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Psychology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Cellular and molecular life sciences 32 (1976), S. 371-372 
    ISSN: 1420-9071
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary In mice, pilocarpine — or oxotremorine — induced decrease in locomotor activity and increase of the reaction time to pain were antagonized by atropine and not by methylatropinium. Identical doses of atropine and methylatropinium suppressed the antagonism of the cholinergics towards reserpine-induced palpebral ptosis. Cholinergics-induced hypothermia was not clearly antagonized by atropine or methylatropinium.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 318 (1981), S. 94-99 
    ISSN: 1432-1912
    Keywords: Quaking mice ; Convulsions ; Alpha-adrenoceptors ; Catecholamine-liberating agents ; Noradrenaline-reuptake inhibitors
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Handling-induced convulsions in the quaking mouse can be blocked by: phenobarbital, pentobarbital or phenytoin; postsynaptic alpha-adrenoceptor agonists (noradrenaline, phenylephrine, CRL 40028); presynaptic alpha-adrenoceptor blockers (yohimbine, mianserine); catecholamine liberating agent (amphetamine); noradrenaline reuptake inhibitors (cocaine, imipramine, desipramine). Moreover, the protective effect of yohimbine was antagonized by clonidine, prazosin or alpha-methylparatyrosine, and the protective effect of CRL 40028 was antagonized by prazosin but not by alpha-methyltyrosine. Drugs acting by other mechanisms (pilocarpine, atropine, trihexyphenidyl, (−)-5-HTP, methysergide, pimozide, clonidine, alpha-methyl DOPA, prazosin, isoprenaline, salbutamol) did not protect against convulsions. A slight protection was obtained with high doses of apomorphine and also with (±)-propranolol. This effect is probably not related, to blockade of betaadrenoceptors because the same effect was obtained with (+)propranolol. In young quaking mice, where susceptibility to convulsions is low, both postsynaptic alpha-adrenoceptor blockers and presynaptic alpha-adrenoceptor antagonist lowered the convulsive threshold. Thus, this seems to constitute an interesting model for the in vivo study of substances which affect the central alpha-adrenoceptors either pre- or postsynaptically.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Psychopharmacology 92 (1987), S. 106-109 
    ISSN: 1432-2072
    Keywords: Staircase test ; Exploration ; Locomotion ; Anxiolytics ; Sedation ; Benzodiazepines ; Therapeutic index ; mice
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Eleven benzodiazepines were evaluated in the staircase test in mice. The behavioural parameters measured were the number of steps climbed and the number of rears during a 3-min test. Climbing and to a lesser extent rears were enhanced at low doses, whereas both parameters, particularly rearing, were reduced at higher doses. The differential effects of the drugs on the two parameters were used to determine indices of anxiolytic efficacy for each drug where increases in climbing were taken to indicate the onset of anxiolytic activity and decreases in rearing the onset of sedative activity. The compounds could be ranked according to these indices in a manner which appears to reflect their therapeutic profile in man.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1432-2072
    Keywords: Progressive ratio schedule ; Psychomotor stimulants ; Amphetamine ; Apomorphine ; Diazepam ; Imipramine ; Catecholamines ; Rats
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Male Wistar rats were trained to press a lever with food reinforcement according to a continuously reinforced schedule (CRF). Afterwards, rats were subjected to three experimental sessions (30 min each) during which responding was rewarded according to a progressive ratio schedule (following an initial 2-min CRF period, the number of presses necessary for the pellet delivery was doubled every second minute). Responding during the first half of each session, i.e., pressing for food, was maintained at a significant level, whereas it was almost suppressed during the second part of the session. As compared to controls (200±20 presses/30 min) animals given amfonelic acid (0.5, 1 mg/kg IP), methylphenidate (4, 8 mg/kg IP), caffeine (16 mg/kg IP), cocaine (4 mg/kg IP), oxolinic acid (32 mg/kg IP), nomifensine (4 mg/kg IP), DR 250 (2, 4 mg/kg IP) and d-amphetamine (0.25, 0.5, 1 mg/kg IP) showed an increased rate of responding ranging from 400 to 950 presses/30 min. In contrast, apomorphine, MK 486+l-dopa, trihexyphenidyl, imipramine, salbutamol and diazepam did not increase responding. These results suggested that this test is highly sensitive for psychomotor stimulants and perhaps for their ability to enhance the reinforcing value of the reward or stimuli associated with the reward. Such activity seemed related to a catecholaminergic substrate since the increase of responding induced by amphetamine was blocked by pimozide, d,l-propranolol and prazosin.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 1432-2072
    Keywords: Penbutolol ; Propranolol ; Alprenolol ; Practolol ; Psychopharmacological tests ; Beta blocking agents
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Common effects of four beta-adrenergic blocking drugs have been investigated in mice using classical and new psychopharmacological tests. Propranolol, alprenolol, practolol and penbutolol reduced the increase in locomotor activity produced by reserpine after MAO inhibition; they produce hypothermia when associated with amphetamine and they increase oxotremorine-induced hypothermia. Regarding these three tests the studied substances ranged themselves in the same order of potency: penbutolol 〉 propranolol 〉 alprenolol 〉 practolol. Propranolol and penbutolol decreased the toxicity provoked in crowded mice by amphetamine or by the association pargyline-reserpine; alprenolol and practolol did not. Propranolol, penbutolol and alprenolol antagonized the amphetamine-induced increase in motor activity; practolol did not. When used at doses for which d-l propranolol was active, the dextrogyre isomer of propranolol was without effect whatever the test studied. It is suggested that for the selection of a beta-blocking drug, regarding central effects in man, the tests described would deserve consideration.
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 1432-2072
    Keywords: Propranolol ; Prinodolol ; Practolol ; Beta-Adrenergic Blocking Agents ; Amphetamine ; Apomorphine ; Stereotyped Behavior ; Rats
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract The influence of three beta-adrenergic blocking agents was studied on the stereotyped behavior induced in rats by a range of doses of d-amphetamine or apomorphine. The stereotyped behavior was assessed either clinically (quotation from 0 to 3 at various times for each rat) or using the confinement motor activity test. From 8 mg/kg (i.p.) onwards, propranolol and prinodolol clearly potentiated the amphetamine-induced stereotyped behavior without any modification of the apomorphine-induced stereotyped behavior. Practolol, known for its poor passage through the blood-brain barrier had only a slight effect.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Psychopharmacology 45 (1975), S. 87-92 
    ISSN: 1432-2072
    Keywords: T.R.H. ; Psychotropic drugs ; Rodents
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract The following behavioral modifications were observed after a single i.p. administration of T.R.H. (thyreo-tropin-releasing hormone) in mice or rats at doses higher than 4mg · kg−1: I. an increased reactivity to stimuli, II. periods of excitation alternating with periods of aggressivity, III. unusual movements (“tail-rattling” and “wet-dog”), IV. the reserpine- or oxotremorine-induced hypothermia was antagonized in mice by T.R.H. in doses of 1 mg · kg−1 and higher, but only a few other symptoms were influenced. The prochlorperazine-induced catalepsy in rats was antagonized by T.R.H.; under the experimental conditions, sudden hyperkinetic episodes were observed. The toxicity of pargyline-l-Dopa association was slightly increased, amphetamine- or apomorphine-induced stereotyped behavior was unchanged. This spectrum of activity is different from other known psychotropic drugs.
    Type of Medium: Electronic Resource
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  • 9
    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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