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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Psychopharmacology 17 (1970), S. 151-159 
    ISSN: 1432-2072
    Keywords: Amphetamine ; Conditioning ; Neuroleptics ; Rats
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The inhibitory effects of four neuroleptic drugs on amphetamineinduced stimulation in a discriminated Sidman avoidance procedure in rats were measured. Amphetamine 0.63 mg/kg s.c. increased R (responses) and decreased W (warning stimuli), WR (warning responses) and S (shocks). Relatively low doses of all four neuroleptics antagonized the amphetamineinduced changes. The order of potency was haloperidol 〉 pimozide 〉 chlorpromazine 〉 pipamperone. The duration of action was pimozide 〉 haloperidol 〉 pipamperone 〉 chlorpromazine. Haloperidol, pimozide and pipamperone restored the amphetamine-induced changes to the initial control levels in the order: S, W, WR and R. With chlorpromazine this order was reversed, except for R. The different pharmacological profiles of haloperidol, pimozide and pipamperone are discussed.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Psychopharmacology 18 (1970), S. 249-259 
    ISSN: 1432-2072
    Keywords: Neuroleptics ; Rats ; Trained ; Noise Escape ; Shuttle Box
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract The effects of twenty neuroleptic drugs on noise escape behavior were studied in rats trained to interrupt an aversive noise (95 decibels recycling every 20 sec) by jumping, in a shuttle box, from one compartment into the other. All twenty drugs prolonged the latency (T) and reduced the frequency (F) of the noise escape response rate. Under the described experimental conditions, the order of potency of the 20 neuroleptics studied was: spiroperidol 〉 spirilene ⩾ trifluperidol 〉 benperidol 〉 droperidol 〉 spiramide 〉 clofluperol ⩾ moperone 〉 perphenazine 〉 haloperidol ⩾ fluphenazine 〉 amiperone 〉 trifluperazine 〉 pimozide 〉 thioperazine 〉 triflupromazine ⩾ fluanisone 〉 chlorpromazine 〉 pipamperone 〉 thioridazine. For all compounds tested, T was more sensitive to drug effect than F. Using the F 45/T 900 ratio, the order of specificity of the compounds studied was: pimozide 〉 benperidol ⩾ spirilene ⩾ clofluperol 〉 trifluperidol ⩾ haloperidol ⩾ fluphenazine ⩾ spiroperidol = perphenazine ⩾ moperone = trifluperazine = thioperazine ⩾ spiramide 〉 amiperone ⩾ droperidol 〉 triflupromazine ⩾ chlorpromazine ⩾ fluanisone 〉 thioridazine ⩾ pipamperone. As far as potency was concerned, there was a good correlation (r=0.974) between the F 900-values of the noise escape test and the ED50-values in the nondiscriminated Sidman avoidance test in rats and, as far as sedative properties were concerned, between the F 45/T 900 ratio and the palpebral ptosis/catalepsy ratio (r = −0.960) of the observation test in rats.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1432-2072
    Keywords: Haloperidol ; Amphetamine ; Rats ; Noise-Escape ; Shuttle Box ; Skinner Box
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract The learning process of two different noise-escape responses—lever pressing and jumping—was studied in the same rats using a shuttle box automatically transformable during the experimental sessions into two Skinner boxes. The effects of different doses of haloperidol and amphetamine were studied in rats overtrained in the two situations. The learning process was slower in the Skinner box than in the shuttle box. To reach the maximum response level in 50% of the rats 13 to 18 training sessions of 5 min were necessary in the shuttle box versus 31 to 36 in the Skinner box. Haloperidol prolonged the latency (T) and reduced the frequency (F and F′) of both lever pressing (L) and jumping responses (J) to about the same extent at the same dose levels (lowest effective dose 0.04 mg/kg s.c.). At 0.005 mg/kg haloperidol slightly increased F′L. At doses lower than 2.5 mg/kg, amphetamine decreased T in both the Skinner and the shuttle box and the ineffective responses (F′) were increased up to 4 to 5 times their control values. The lowest effective dose was 0.16 mg/kg in the shuttle box (F′J) and 0.31 mg/kg in the Skinner box (F′L). At 2.5 mg/kg amphetamine increased T and reduced F.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Psychopharmacology 16 (1969), S. 161-174 
    ISSN: 1432-2072
    Keywords: Drugs ; Neuroleptics ; Behaviour ; Conditioning ; Rats
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The effect of twenty neuroleptic drugs on conditioned behaviour was studied in rats by means of a lever-press shock-avoidance procedure (shock-shock 20 sec, response-shock 20 sec). All twenty drugs inhibited lever-press response and reduced the shock-avoidance rate at very low dose levels. The order of potency was: benperidol=spiroperidol 〉 trifluperidol 〉 droperidol=spiramide 〉 clofluperol=fluphenazine=haloperidol=spirilene 〉 moperone 〉 perphenazine 〉 amiperone 〉 fluanisone=trifluperazine 〉 pimozide 〉 thioperazine 〉 chlorpromazine 〉 pipamperone=thioridazine 〉 promazine.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Psychopharmacology 16 (1969), S. 175-182 
    ISSN: 1432-2072
    Keywords: Neuroleptics ; Conditioning ; Extinction ; IRT's ; Rats
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The effects of seven neuroleptic drugs on conditioned behaviour were studied in rats by means of a lever-press shock-avoidance procedure (shock-shock 20 sec; response-shock 20 sec) with alternate reinforcement and extinction periods. All seven drugs inhibited the lever-press response and the shock-avoidance rate; their order of potency was trifluperidol 〉 droperidol 〉 haloperidol 〉 pimozide 〉 fluanisone 〉 chlorpromazine 〉 pipamperone. For all seven drugs, the response rate during the extinction periods was a more sensitive indicator of drug effect than the response rate during the reinforcement periods. Analysis of the temporal distribution of the IRT's shows that IRT's of 0–5″ and of 6–15″ were more sensitive to drug effects than IRT's of 16–20″ and of 〉 20″. The introduction of extinction periods together with the analysis of IRT's rendered the Sidman avoidance procedure the most sensitive test available for the quantitative evaluation of the potency of neuroleptic drugs in rats. The qualitative differences between the neuroleptics studied were less pronounced. There is some indication, however, that specific neuroleptics (e.g. pimozide) inhibit the response rate to about the same extent during both reinforcement and extinction periods, while aspecific neuroleptics (e.g. pipamperone) are more active inhibitors of the responses during extinction than during the corresponding reinforcement periods.
    Type of Medium: Electronic Resource
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