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  • 1
    ISSN: 1432-2072
    Keywords: Latent inhibition ; Dopamine ; Ondansetron ; 5HT3 antagonists ; Amphetamine
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Latent inhibition (LI) is a behavioural phenomenon whereby preexposure to a stimulus without reinforcement interferes with the formation of subsequent associations to that stimulus. Using preexposure to a tone stimulus which subsequently serves as a conditioned stimulus for suppression of licking, we have confirmed that LI is disrupted by a low dose of amphetamine. Haloperidol was able to prevent this effect of amphetamine. Ondansetron, a selective and potent 5HT3 receptor antagonist, was also shown to be effective at blocking the amphetamine-induced disruption of LI at a dose of 0.01 mg/kg, but not at 0.1 mg/kg. In addition, it was demonstrated that ondansetron could enhance LI; using only ten preexposures, no LI was obtained in the saline group, but was apparent in animals given ondansetron, an effect which has been previously shown with haloperidol. Haloperidol, at the higher dose used, reduced suppression of licking, however, ondansetron at the effective dose had no such effect. It is concluded that ondansetron is able to attenuate increases in dopamine activity, produced pharmacologically with amphetamine without affecting baseline dopamine activity. The implications of these findings for a possible antipsychotic action of ondansetron are discussed.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-2072
    Keywords: Mixture, Amphetamine-Amylobarbitone ; Resistance to Extinction ; Frustration
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract 32 male rats were trained to run in an alley for food reward on continuons reinforcement. During extinction they were divided into 4 equal groups and injected with either 0.75 mg/kg amphetamine sulphate, 17.5 mg/kg amylobarbitone sodium, both of these two drugs, or saline. Amylobarbitone significantly retarded extinction and amphetamine on its own had no effect on resistance to extinction. Amphetamine in combination with amylobarbitone, however, potentiated the effects of the latter. These results confirm previous findings of a more-than-additive effect on behaviour of amphetamine and amylobarbitone in combination. It is suggested that, in conjunction with earlier reports, they add weight to the hypothesis that the psychological states of ‘fear’ and ‘frustration’ share a common physiological substrate.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1432-2072
    Keywords: Amylobarbitone ; Resistance to Extinction ; Medial Septal Lesion
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract 32 male rats, of which half had sustained small electrolytic lesions in the medial septal area and half had received sham operations, were trained on continuous reinforcement to run an alley for water reward and then given four days of extinction testing. Half of both the lesioned and sham-operated groups were given sodium amylobarbitone on Days 1 and 2 of extinction and the other half on Days 3 and 4, saline being administered on non-drug days. The drug, unusually, decreased resistance to extinction. This effect was probably due to the subjects having taken part in a previous experiment in which they had received, without drugs, training and extinction under the same conditions as in this experiment. In the goal section of the alley, the drug effect was greater in lesioned than shamoperated rats. The lesions retarded extinction, and this effect was reduced by the drug. A model for the neural loci at which amylobarbitone acts to affect resistance to extinction, based on these and other results, is proposed.
    Type of Medium: Electronic Resource
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