2 edition of Intracerebroventricular chlordiazepoxide and the partial reinforcement extinction effect. found in the catalog.
Intracerebroventricular chlordiazepoxide and the partial reinforcement extinction effect.
Thesis (D. Phil.) - University of Ulster, 1996.
Pain and fear are different motivations - Volume 3 Issue 2 - Elzbieta Fonberg. Gray, J. A. ( a) Sodium amobarbital, the hippocampal theta rhythm and the partial reinforcement extinction effect. Effects of d-amphetamine and by: The effect of chlordiazepoxide on the stimulus-intensity phenomenon. Donald Ray Green University of Massachusetts Amherst Follow this and additional works at: This thesis is brought to you for free and open access by [email protected] Amherst. It has been accepted for inclusion in Masters Theses -Author: Donald Ray Green.
A perceptual-defensive-recuperative model of fear and pain - Volume 3 Issue 2 - Robert C. Bolles, Michael S. Fanselow the hippocampal theta rhythm and the partial reinforcement extinction effect. Effects of d-amphetamine and by: partial reinforcement extinction effect. Extinction Bursts and Your Baby’s Sleep. by Emily DeJeu in Now, don't run off on me. I know the term "extinction bursts" seems really clinical and cold, but don't worry: we're going to go over exactly what this term means, why it can derail even the best sleep training, and how you (the sleep.
Clonidine has been reported to exert anti-anxiety effects in animals and man similar to those of benzodiazepines. The present experiment examined the effects of clonidine administration on the partial reinforcement extinction effect (PREE) which is known to be sensitive to benzodiazepine by: 7. Feldon, J. & Gray, J. A. ( a) Effects of medial and lateral septal lesions on the partial reinforcement extinction effect at one trial a day. Quarterly Cited by:
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PHARMAC. BIOCHEM. BEHAV. 7(5)- Rats were trained to run in a straight alley under conditions of partial or continuous reinforcement. Extinction was slower after partial reinforcement. Chlordiazepoxide, administered during acquisition only, had no effect on acquisition but abolished the partial reinforcement extinction by: 9.
The partial reinforcement extinction effect after treatment with chlordiazepoxide. Feldon J, Gray JA. Two experiments are reported, in which rats were run in a straight alley for food reward with or without injections of the anti-anxiety drug, chlordiazepoxide (CDP).
Cited by: Willner PJ, Crowe R () Effect of chlordiazepoxide on the partial reinforcement extinction effect. Pharmacol Biochem Behav – Google Scholar Ziff DR, Capaldi EJ () Amytal and the small trial partial reinforcement effect: Stimulus properties of early trial by: They were tested in the straight alley with food reward on either continuous (CRF) or partial (PRF) reinforcement at one trial a day and were injected with either 5 mg/kg chlordiazepoxide HCl (CDP) or with saline before the daily trial throughout acquisition and extinction.
The effects of the drug on resistance to extinction interacted with those of the LS lesion in ways which were consistent with the hypothesis that CDP Cited by: The partial reinforcement extinction effect: influence of chlordiazepoxide in septal lesioned rats.
Feldon J, Gray JA. Rats sustained electrolytic lesions either in the medial septal (MS) or lateral septal (LS) area or they were by: The partial reinforcement extinction effect (PREE) was analyzed in humans using a quasi-multiple schedule of reinforcement with two discrete trial tasks.
The first task was a videogame analog of a shuttle box. Using a joystick, subjects were required to move a cue in one of four directions for rein. This study describes the relationship between the tranquilizing drug chlordiazepoxide HCL and different magnitudes of reward during acquisition and extinction of a partially reinforced runway response.
The results do not support predictions drawn directly from Amsel’s (, ) frustrative nonreward hypothesis. Animals exhibited the same magnitude of reward extinction effect whether Cited by: 5.
The PREE is defined as an increased resistance to extinction that is observed after training with partial reinforcement as compared to continuous reinforcement. This paradoxical learning effect constitutes an experimental example of response-outcome uncertainty during acquisition that results in an increased, rather than in a decreased, behavioural persistence during extinction Cited by: 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 Cited by: Effects of ethanol and partial reinforcement upon runway acquisition Article (PDF Available) in Psychonomic science 3() March with 11 Reads How we measure 'reads'.
Intracerebroventricular chlordiazepoxide and the partial reinforcement extinction effect. Author: McCullough, Trevor. ISNI: X Awarding Body: University of Ulster Current Institution: Ulster University Date of Award: The behavioral data indicated that subjects exposed to partial reinforcement were more persistent than subjects exposed to continuous reinforcement.
Significant increases in skin conductance were observed at the start of acquisition and extinction, but there were no differences between the two reinforcement Cited by: 4. The PREE was abolished when amphetamine was administered throughout the acquisition trials or on nonrewarded trials, irrespective of drug treatment on rewarded trials.
d-Amphetamine Continuous reinforcement Partial reinforcement Rewarded trials Resistance to extinction Rat IN the partial reinforcement extinction effect (PREE) paradigm animals are trained in the first (acquisition) stage Cited by: Extinction was slower after partial reinforcement.
Chlordiazepoxide, administered during acquisition only, had no effect on acquisition but abolished the partial reinforcement extinction effect. The partial reinforcement extinction effect in humans: effects of schizophrenia, schizotypy and low doses of amphetamineCited by: 5.
Paradoxical Effects: Partial Reinforcement Extinction Effect Frustration theory A theory of partial reinforcement extinction effect, according to which extinction is retarded after partial reinforcement because the instrumental response becomes conditioned to to the anticipation of frustrative non-reward.
Effects of Reinforcement Schedule on Facilitation of Operant Extinction by Chlordiazepoxide Article (PDF Available) in Journal of the Experimental Analysis of Behavior 84(3) December.
Under vehicle injections, extinction and re-extinction curves were indistinguishable, but drug treatments showed that there was less resistance to extinction in the re-extinction phase. Chlordiazepoxide facilitated extinction and re-extinction, with an earlier effect during by: 3.
Effects on the extinction of GABAergic drug, chlordiazepoxide (CDP), and glutamatergic drug, D: cycloserine (DCS), in C57BL/6 mice were compared. Following a palatability test (Experiment 1), Experiments involved food-reinforced lever press training followed by extinction sessions at 1.
Within the operant extinction experiment, the effects of chlordiazepoxide in comparison with saline were just as have been obtained previously with this benzodiazepine in this procedure (e.g. Shaw.
exTincTion-indUced VaRiaBiliTy in hUMan BehaVioR Jennifer M. Kinloch, t. Mary Foster, and James S. A. Mcewan University of Waikato Participants earned points by pressing a computer space bar (Experiment 1) or forming rectangles on the screen with the mouse (Experiment2) under differential-reinforcement-of-low-rate schedules, followed by extinction.A number of animal studies indicate a partial reinforcement extinction effect, whereby partial reinforcement leads to more durable responding than continuous reinforcement [23,25,27,35].
Thus, partial reinforcement may be one way to increase the longevity of placebo by: The effect of chlordiazepoxide on acquisition and extinction responding for rewarding brain stimulation.
Ronald. Gandelman University of Massachusetts Amherst Follow this and additional works at: This thesis is brought to you for free and open access by [email protected] : Ronald. Gandelman.