Literature DB >> 4029302

Resistance to extinction after schedules of partial delay or partial reinforcement in rats with hippocampal lesions.

J N Rawlins, J Feldon, H Ursin, J A Gray.   

Abstract

Two experimental procedures were employed to establish the reason why hippocampal lesions apparently block the development of tolerance for aversive events in partial reinforcement experiments, but do not do so in partial punishment experiments. Rats were trained to run in a straight alley following hippocampal lesions (HC), cortical control lesions (CC) or sham operations (SO), and resistance to extinction was assessed following differing acquisition conditions. In Experiment 1 a 4-8 min inter-trial interval (ITI) was used. Either every acquisition trial was rewarded immediately (Continuous Reinforcement, CR), or only a randomly selected half of the trials were immediately rewarded, the reward being delayed for thirty seconds on the other trials (Partial Delay, PD). This delay procedure produced increased resistance to extinction in rats in all lesion groups. In Experiment 2 the ITI was reduced to a few seconds, and rats were trained either on a CR schedule, or on a schedule in which only half the trials were rewarded (Partial Reinforcement, PR). This form of partial reinforcement procedure also produced increased resistance to extinction in rats in all lesion groups. It thus appears that hippocampal lesions only prevent the development of resistance to aversive events when the interval between aversive and subsequent appetitive events exceeds some minimum value.

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Year:  1985        PMID: 4029302     DOI: 10.1007/bf00230907

Source DB:  PubMed          Journal:  Exp Brain Res        ISSN: 0014-4819            Impact factor:   1.972


  24 in total

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3.  Persistence of runway performance after septal lesions in rats.

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9.  Fornix-fimbria section and the partial reinforcement extinction effect.

Authors:  J Feldon; J N Rawlins; J A Gray
Journal:  Exp Brain Res       Date:  1985       Impact factor: 1.972

10.  The partial reinforcement extinction effect after treatment with chlordiazepoxide.

Authors:  J Feldon; J A Gray
Journal:  Psychopharmacology (Berl)       Date:  1981       Impact factor: 4.530

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  4 in total

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Journal:  Exp Brain Res       Date:  1986       Impact factor: 1.972

2.  Fornix-fimbria section and the partial reinforcement extinction effect.

Authors:  J Feldon; J N Rawlins; J A Gray
Journal:  Exp Brain Res       Date:  1985       Impact factor: 1.972

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