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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Psychopharmacology 87 (1985), S. 219-224 
    ISSN: 1432-2072
    Keywords: Propranolol ; Beta-adrenergic blocker ; Differential reinforcement of low rates of response (DRL) ; Differential punishment of high rates of response (DPH) ; Chlordiazepoxide ; Rat
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Ten rats were trained to lever press for food reward on a schedule of differential reinforcement of low rates of response with a 20-s criterion (DRL 20). Ten more were trained on a new schedule of punishment, designed to be comparable to DRL 20 — differential punishment of high rates of response (DPH 20). Under this schedule, responses with a latency of 20 s or more earned food rewards, while those of less than 20 s were followed by food reward and brief electric footshock. After 42 sessions, rats on each schedule showed temporal discrimination in the distribution of inter-response times. The effects on these baselines of the anxiolytic chlordiazepoxide (CDP; 1 mg/kg IP) and the beta-blocker propranolol (2, 5 and 10 mg/kg IP) were investigated. Both drugs reduced numbers of responses reaching criterion (criterion resonses) in DPH, CDP increasing total responses. CDP acted similarly under DRL, but propranolol only affected performance at the highest doese, which reduced criterion responses, probably because of changes in total responding. Each drug increased response bursts. It is concluded that propranolol can exert a disinhibitory action in these schedules, although with some differences from that of the benzodiazepine CDP.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-2072
    Keywords: 6-Hydroxydopamine ; Differential reinforcement of low rates of response (DRL) ; Sympathetic nervous system ; Noradrenaline ; Rat
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract First, it was confirmed that systemic injection of the neurotoxin 6-hydroxydopamine HBr (30 mg/kg IP) depleted noradrenaline levels in rat heart, but not centrally. Losses averaged 90% of control 1 day after injection, and 50% at 42 days. The same drug and dose was then administered to 50% of a group of rats which had been trained to lever-press for food reward on continuous reinforcement (CRF). After further CRF sessions, the rats were changed to a schedule of Differential Reinforcement of Low Rates of Response with a 20-s criterion (DRL 20). The drugged rats earned fewer reinforcements during DRL than did controls, and made fewer responses. Temporal discrimination (shown by the IRT/Opp distribution) was disrupted. It is concluded that peripheral noradrenergic systems may be involved in the control over responding by temporal cues associated with reward and non-reward.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1432-2072
    Keywords: GABAergic hypothesis of anxiolytic action ; Muscimol ; Baclofen ; Chlordiazepoxide ; Picrotoxin ; Bicuculline ; Spontaneous alternation ; Response to stimulus change ; Exploration ; Novelty ; Rat
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Two methods were used to test rats' responses to novelty in the T-maze: (1) a test of spontaneous alternation allowing separate measurement of place and body turn alternation; and (2) a test of entry into an arm of changed brightness (“response to stimulus change”). Chlordiazepoxide reduced spontaneous alternation by specifically weakening body turn alternation and eliminated the response to stimulus change. These findings are similar to those previously reported for the barbiturate sodium amylobarbitone. The same pattern of change in the two tests was seen after a low dose of the GABAA agonist muscimol (0.00125 mg/kg); when the dose of muscimol was raised (0.01 and 0.25 mg/kg), place alternation was also reduced. Picrotoxin but not bicuculline (both GABAA blockers) reversed the effects of muscimol and partially those of chlordiazepoxide on the response to stimulus change; in the spontaneous alternation test picrotoxin only marginally affected the response to 0.25 mg/kg muscimol and actually enhanced the effect of 0.000125 mg/kg. The GABAB agonist baclofen (1 mg/kg) acted in the test of response to stimulus change like chlordiazepoxide and muscimol; however, when baclofen was combined with muscimol, the two drugs tended to show mutual blocking. These results are generally consistent with the hypothesis that GABAergic mechanisms play a role in anxiolytic behavioural activity, but many details are difficult to explain.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1432-2072
    Keywords: Propranolol ; d-Propranolol ; l-Propranolol ; Punishment ; Conditioned suppression ; Non-reward ; Rat
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract In Experiment I, two groups of rats were rewarded for lever-pressing under RI 64. During signalled 3-min intrusion periods shocks were delivered response-contingently (on RI 64) for the Punishment group and non-contingently (on RT 64) for the Conditioned Suppression group.d,l-Propranolol (2, 5 mg/kg) released intrusion responding to a similar extent in the two groups. Experiment II comprised two distinct experiments: two groups of rats were trained in parallel on signalled multiple schedules in which responding during the baseline component was rewarded on RI 20. For the second component responding was extinguished in Experiment IIa; it continued to be rewarded but was also punished by electric shock in Experiment IIb. Shock levels were adjusted individually so as to produce similar levels of response suppression in these two groups.d,l-Propranolol released non-rewarded responding (2–5 mg/kg; Expt IIa) but had no effect on punishment (2–10 mg/kg; Expt IIb).l-Propranolol (2.5 mg/kg) but notd-propranolol (2.5 mg/kg) also released non-rewarded responding in Expt IIa. In a further triald,l-propranolol (5 mg/kg) released punished responding in Expt IIb in a group of animals in which response suppression had been partially relieved by reducing shock intensity. It is hypothesized that beta-adrenergic stimuli may influence response suppression to the extent that the unconditioned aversive event causing suppression is not salient.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1432-2072
    Keywords: Key wordsd-Amphetamine ; Haloperidol ; Procedural learning ; Automatic processing ; Dopamine ; Neuroleptic medication
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract The effects of an indirect dopamine-agonist, d-amphetamine, and a non-selective dopamine receptor antagonist, haloperidol, were investigated in normal male volunteers using a between-subjects double-blind design in a procedural learning task, thought mainly to involve unconscious/automatic learning. The results showed: (1) d-amphetamine facilitated response speed, whereas haloperidol inhibited it, in comparison to placebo; (2) the linear increase in procedural learning corresponded with pharmacological manipulation of degree of dopaminergic activity, i.e. subjects given haloperidol showed the least, and subjects given d-amphetamine the greatest, procedural learning. The implications of these findings are discussed in relation to investigation of abnormalities of procedural learning processes in schizophrenia.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 1432-2072
    Keywords: Nicotine ; Latent inhibition ; Dopamine ; N. accumbens ; Haloperidol
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Latent inhibition (LI) is a cognitive process whereby repeated exposure of a stimulus without consequence impedes the formation of subsequent associations with that stimulus. A number of studies in the rat have reported that LI is impaired by moderate systemic doses of amphetamine, an effect believed to be mediated via dopamine (DA) release in the nucleus accumbens. We and others have reported that nicotine has a selective effect in releasing DA in the accumbens rather than the caudate nucleus. We have therefore examined the ability of nicotine to disrupt LI, using a conditioned emotional response paradigm. Pre-exposure of a tone stimulus impaired subsequent conditioning between that stimulus and mild footshock, as indexed by suppression of licking by the tone subsequently presented alone. This LI effect was prevented, by an effect confined to the pre-exposed group, by doses of 0.4 or 0.6 mg/kg nicotine SC, which are accumbens selective, given before pre-exposure and before conditioning. The effect of nicotine in disrupting LI was prevented by prior administration of haloperidol at a dose (0.5 mg/kg) reported to reverse the disruptive effect of amphetamine on LI. Although the amphetamine effect requires two administrations, the effect of two administrations of nicotine was reproduced by a single dose of nicotine given before conditioning, but not by a single dose before pre-exposure. The results are discussed in relation to studies in human control and schizophrenic subjects, which suggest that increased DA activity in humans is also associated with impaired LI. The results indicate that nicotine does indeed increase functional DA activity in the rat accumbens; the consequent disruption of LI critically depends upon an action at the time of conditioning, and is independent of processes which occur during pre-exposure. In more general terms, this indicates the potential of drug experiments to complement behavioural studies on the mechanism of latent inhibition.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Psychopharmacology 86 (1985), S. 480-486 
    ISSN: 1432-2072
    Keywords: Propranolol ; Beta-adrenergic blocker ; Differential reinforcement of low rates of response (DRL) ; Anxiety ; Antianxiety drugs ; Rat
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Rats were trained over 40 days to lever-press for food reward under a schedule of differential reinforcement of low rates of response with a 20-s criterion (DRL 20), following seven sessions of continuous reinforcement. The effect of injecting a beta-adrenergic blocker, propranolol (5 mg/kg IP), before and at two different delays after each daily session of DRL were investigated. In Experiment I, rats drugged 5–8 min before every session earned fewer reinforcements compared to controls, and showed impaired temporal discrimination. In Experiment II, this result was not replicated, but similar effects were clear in animals drugged pre-session from the 15th day of acquisition. By contrast, an improved temporal discrimination, and increased number of reinforcements were seen in rats drugged 5–8 min after every session. In Experiment III, the postsession effects were replicated and found also in rats drugged 4–5.5 h after each session. These results suggest that propranolol has an acute effect on DRL responding which resembles that of anxiolytics, and a chronic effect which opposes the acute one.
    Type of Medium: Electronic Resource
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