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1.
Two groups of male Japanese quail (Coturnix japonica) to discriminate cocaine from saline in a conditioned approach procedure maintained by sexual reinforcement. For 1 group, cocaine (10 mg/kg ip) was administered prior to a conditioned stimulus (CS) that predicted copulation; saline followed by a CS predicted no copulation. A second group underwent the opposite training regimen. Results revealed apparent between-group differences in the rates of acquisition of the discrimination; however, during extinction trials, both groups responded more under the drug condition that predicted the female than to the condition that predicted no female. The results suggested that a drug discrimination may be maintained by sexual reinforcement. The findings are discussed with regard to interactions of cocaine and sexual reward, as well as to Pavlovian conditional stimulus control. (PsycINFO Database Record (c) 2010 APA, all rights reserved)  相似文献   

2.
P. Perruchet (1985b) showed a double dissociation of conditioned responses (CRs) and expectancy for an airpuff unconditioned stimulus (US) in a 50% partial reinforcement schedule in human eyeblink conditioning. In the Perruchet effect, participants show an increase in CRs and a concurrent decrease in expectancy for the airpuff across runs of reinforced trials; conversely, participants show a decrease in CRs and a concurrent increase in expectancy for the airpuff across runs of nonreinforced trials. Three eyeblink conditioning experiments investigated whether the linear trend in eyeblink CRs in the Perruchet effect is a result of changes in associative strength of the conditioned stimulus (CS), US sensitization, or learning the precise timing of the US. Experiments 1 and 2 demonstrated that the linear trend in eyeblink CRs is not the result of US sensitization. Experiment 3 showed that the linear trend in eyeblink CRs is present with both a fixed and a variable CS–US interval and so is not the result of learning the precise timing of the US. The results are difficult to reconcile with a single learning process model of associative learning in which expectancy mediates CRs. (PsycINFO Database Record (c) 2010 APA, all rights reserved)  相似文献   

3.
Four experiments with rats examined partial reinforcement in appetitive conditioning. In Experiment 1, adding nonreinforced trials to a continuous reinforcement schedule slowed acquisition, whereas deleting reinforcers did not. Trial massing suppressed performance and learning. In Experiment 2, conditioning with a short conditioned stimulus (CS) was rapid, and partial reinforcement with a short CS was as effective as continuous reinforcement with equal accumulated time in the CS. In Experiment 3, conditioning was nevertheless influenced by the probability of reinforcement. In Experiments 3 and 4, conditioning was especially disrupted when nonreinforced trials preceded reinforced trials closely in time. The results underscore the importance of temporal variables in conditioning but are more consistent with trial-based accounts than time-accumulation accounts of conditioning. (PsycINFO Database Record (c) 2010 APA, all rights reserved)  相似文献   

4.
Reports an error in the original article by J. R. Troisi, II and Chana Akins (Experimental and Clinical Psychopharmacology, 2004, Vol. 12, No. 4, pp. 237-242). The first sentence of the abstract, "Two groups of male Japanese quail (Coturnix japonica) to discriminate cocaine from saline in a conditioned approach procedure maintained by sexual reinforcement," was incomplete. The correct wording is "Two groups of male Japanese quail (Coturnix japonica) were trained to discriminate cocaine from saline in a conditioned approach procedure maintained by sexual reinforcement." (The following abstract of this article originally appeared in record 2004-20800-003.) Two groups of male Japanese quail (Coturnix japonica) to discriminate cocaine from saline in a conditioned approach procedure maintained by sexual reinforcement. For 1 group, cocaine (10 mg/kg ip) was administered prior to a conditioned stimulus (CS) that predicted copulation; saline followed by a CS predicted no copulation. A second group underwent the opposite training regimen. Results revealed apparent between-group differences in the rates of acquisition of the discrimination; however, during extinction trials, both groups responded more under the drug condition that predicted the female than to the condition that predicted no female. The results suggested that a drug discrimination may be maintained by sexual reinforcement. The findings are discussed with regard to interactions of cocaine and sexual reward, as well as to Pavlovian conditional stimulus control (PsycINFO Database Record (c) 2010 APA, all rights reserved)  相似文献   

5.
Five experiments examined the effects of altering the duration of a conditioned stimulus (CS) for extinction. For the first 3 experiments, rats received conditioning with a 10-s CS before different groups received extinction with a CS that was either the same duration or longer than that used for conditioning. For the remaining 2 experiments, conditioning was conducted with a 60-s CS before different groups received extinction with a CS of either the same duration or a shorter duration than that used for conditioning. In all experiments, extinction progressed more readily when the CS duration was different for the 2 stages than when it was constant. The results are discussed in terms of rate expectancy theory and associative learning theory. (PsycINFO Database Record (c) 2010 APA, all rights reserved)  相似文献   

6.
Six experiments studied the role of conditioned stimulus (CS) familiarity in determining the effects of the N-methyl-d-aspartate (NMDA) receptor antagonist MK-801 on fear extinction. Systemic administration of MK-801 (0.1 mg/kg) impaired initial extinction but not reextinction learning. MK-801 impaired reextinction learning when the CS was relatively novel during reextinction training but not initial extinction learning when the CS was relatively familiar during initial extinction training. A context change failed to reinstate the sensitivity of initial fear extinction learning about a relatively familiar CS to MK-801. These experiments show that CS familiarity is an important determinant of effects of MK-801 on fear extinction learning: MK-801 impaired extinction learning about novel stimuli but spared extinction learning about familiar stimuli. (PsycINFO Database Record (c) 2010 APA, all rights reserved)  相似文献   

7.
Three experiments investigated the effects of varying the conditioned stimulus (CS) duration between training and extinction. Ring doves (Streptopelia risoria) were autoshaped on a fixed CS-unconditioned stimulus (US) interval and extinguished with CS presentations that were longer, shorter, or the same as the training duration. During a subsequent test session, the training CS duration was reintroduced. Results suggest that the cessation of responding during an extinction session is controlled by generalization of excitation between the training and extinction CSs and by the number of nonreinforced CS presentations. Transfer of extinction to the training CS is controlled by the similarity between the extinction and training CSs. Extinction learning is temporally specific. (PsycINFO Database Record (c) 2010 APA, all rights reserved)  相似文献   

8.
Domesticated quail (Coturnix japonica) received a discrete conditioned stimulus (CS) at one end of the experimental chamber paired with the opportunity to copulate with a female quail (the unconditioned stimulus) in a goal box located 112 cm away. Approach to the CS (sign tracking) and approach to the goal area (goal tracking) were measured. The duration of exposure to the experimental context (C) was varied in Experiment 1, and the duration of the conditioning trials (T) was varied in Experiment 2 for independent groups, creating C/T ratios of 1.0, 1.5, 4.5, 45, and 180. Contrary to previous reports of a direct relation between the C/T ratio and conditioned responding, in the present experiments, a shift in the topography and stimulus control of conditioned behavior occurred. Low C/T ratios (1.0–4.5) produced goal tracking controlled by contextual cues, whereas high C/T ratios (45 and 180) produced sign tracking controlled by the discrete CS. (PsycINFO Database Record (c) 2010 APA, all rights reserved)  相似文献   

9.
Three experiments used delay conditioning of magazine approach in rats to examine the summation of responding when two conditioned stimuli (CSs) are presented together as a compound. The duration of each CS varied randomly from trial-to-trial around a mean that differed between the CSs. This meant that the rats' response rate to each CS was systematically related to the reinforcement rate of that CS, but remained steady as time elapsed during the CS (Harris & Carpenter, 2011; Harris, Gharaei, & Pincham, 2011). When the rats were presented with a compound of two CSs that had been conditioned separately, they responded more during the compound than during either of the CSs individually. More significantly, however, in all three experiments, the rats responded to the compound at the same rate as they responded to a third CS that had been reinforced at a rate equal to the sum of the reinforcement rates of the two CSs in compound. We discuss the implications of this finding for associative models (e.g., Rescorla & Wagner, 1972) and rate-based models (Gallistel & Gibbon, 2000) of conditioning. (PsycINFO Database Record (c) 2011 APA, all rights reserved)  相似文献   

10.
The present experiments demonstrated that, in the rabbit nictitating membrane preparation, a conditioned response (CR) can be selectively eliminated in one portion of a conditioned stimulus (CS) while it is still paired with the unconditioned stimulus (US). Rabbits were initially trained with two stimuli (tone, light). Each was paired with the US by using a mixture of two CS-US interstimulus intervals (ISIs): 200 ms and 1,200 ms in Experiment 1; 150 ms and 500 ms in Experiment 2. The CRs showed double peaks, one for each ISI. Subsequently, one CS (A) was trained with only the longer ISI, whereas the other CS (B) continued to be trained with both ISIs. Consequently, the CR peak based on the shorter ISI disappeared for CSA but not for CSB. The later CR peaks during both CSA and CSB were maintained. These results support time-based models of conditioning. Implications for proposed mechanisms of extinction are discussed. (PsycINFO Database Record (c) 2010 APA, all rights reserved)  相似文献   

11.
Five conditioned suppression experiments, with 160 Wistar rats, explored the role of the conditioning history of the conditioned stimulus (CS) in determining the effects of contextual fear on performance to the CS. Contextual fear was produced by postconditioning exposure to unconditioned stimulus/stimuli (UCS) alone in the context of conditioning; it was independently assessed with context-preference tests. When the number of reinforced and nonreinforced trials was equated across extinction, partial reinforcement, and latent inhibition procedures, only the extinction procedure produced a CS whose performance was subsequently affected (i.e., augmented) by contextual fear. Contextual fear's relatively unique augmenting effect on fear of an extinguished CS was abolished by extensive, but not by less extensive, reacquisition training. Results indicate that, depending on the CS's conditioning history, contextual fear either augments or has little effect on fear of the CS. It is suggested that augmentation by context should be viewed as the restoration of fear that is otherwise depressed by extinction. (28 ref) (PsycINFO Database Record (c) 2010 APA, all rights reserved)  相似文献   

12.
In this experiment, the observing-response procedure was adapted for use with drug self-administration. Rats' responding for oral ethanol was sometimes reinforced on a random-ratio schedule, whereas at other times it had no effect (i.e., extinction). Behavior producing stimuli associated with the otherwise unsignaled random-ratio and extinction periods (i.e., observing behavior) was acquired and maintained. In a vehicle control condition, both self-administration and observing behavior decreased, but observing decreased less rapidly proportionally to baseline than vehicle consumption. Thus, conditioned reinforcers may have persistent effects that are relatively independent of the current status of the primary reinforcer. The procedure allows long-term study of drug-associated conditioned reinforcement and provides independent indexes of the conditioned reinforcing and discriminative stimulus effects of drug stimuli. (PsycINFO Database Record (c) 2010 APA, all rights reserved)  相似文献   

13.
Male albino Wistar rats (N = 96) served as Ss in 2 within-S partial reinforcement experiments, designed to lessen generalization in acquisition as a means of eliminating the generalized partial reinforcement effect in extinction. When the use of a separate-phase mode of training alone proved to be unsuccessful for this purpose, a phase of extinction was interpolated between the continuously and partially reinforced acquisition phases. This manipulation was successful and Ss receiving the training sequence of partial reinforcement-extinction followed by continuous reinforcement-extinction did not show the generalized partial reinforcement effect in the final extinction phase. It is suggested that during the phase of interpolated extinction avoidance responses were counterconditioned to the stimulus complex which included nonreward. (French summary) (25 ref) (PsycINFO Database Record (c) 2010 APA, all rights reserved)  相似文献   

14.
Rats received a single pairing of an auditory conditioned stimulus (CS) with a footshock unconditioned stimulus (US). The fear (freezing) that had accrued to the CS was then extinguished. Injection of naloxone prior to this extinction significantly impaired the development of extinction. This impairment was mediated by opioid receptors in the brain and was not observed when naloxone was injected after extinction training. Finally, an injection of naloxone on test failed to reinstate extinguished responding that had already accrued to the CS. These experiments show that opioid receptors regulate the development, but not the expression, of fear extinction and are discussed with reference to the roles of opioid receptors in US processing, memory, and appetitive motivation. (PsycINFO Database Record (c) 2010 APA, all rights reserved)  相似文献   

15.
Reports an error in the original article by Perry S. Kinkaide (Journal of Comparative and Physiological Psychology, 1974[Jun], 86[6], 1132-1140). The lower portion of Figure 3 on page 1138 should have represented the last two conditions for Group T as Test AV and reTest AV. The last sentence of the caption should have been deleted. (The following abstract of this article originally appeared in record 1979-05368-001) Conducted 2 experiments, using a total of 24 female New Zealand white rabbits, in which a "visual" stimulus (V), either flashes or electrical stimulation of the optic chiasma, was reinforced in compound with a differentially reinforced (CS+) or nonreinforced (CS-) nonvisual stimulus. Visual stimulus control of conditioned eyeblink activity was acquired if V was reinforced in compound with CS- but was "blocked" when reinforced in compound with CS+. Both effects were demonstrable within Ss and were independent of the method of visual stimulation. Extinction and backward conditioning of chiasmic stimulation preceded retraining of 6 Ss. The establishment and blocking of visual stimulus control were again evident within Ss. The data are interpretable in terms of either attentional or associative theory. (PsycINFO Database Record (c) 2010 APA, all rights reserved)  相似文献   

16.
During Pavlovian fear conditioning a conditioned stimulus (CS) is repeatedly paired with an aversive unconditioned stimulus (UCS). In many studies the CS and UCS are paired on every trial, whereas in others the CS and UCS are paired intermittently. To better understand the influence of the CS-UCS pairing rate on brain activity, the experimenters presented continuously, intermittently, and non-paired CSs during fear conditioning. Amygdala, anterior cingulate, and fusiform gyrus activity increased linearly with the CS-UCS pairing rate. In contrast, insula and left dorsolateral prefrontal cortex responses were larger during intermittently paired CS presentations relative to continuously and non-paired CSs. These results demonstrate two distinct patterns of activity in disparate brain regions. Amygdala, anterior cingulate, and fusiform gyrus activity paralleled the CS-UCS pairing rate, whereas the insula and dorsolateral prefrontal cortex appeared to respond to the uncertainty inherent in intermittent CS-UCS pairing procedures. These findings may further clarify the role of these brain regions in Pavlovian fear conditioning. (PsycINFO Database Record (c) 2010 APA, all rights reserved)  相似文献   

17.
The effects of altering the contingency between the conditioned stimulus (CS) and the unconditioned stimulus (US) on the acquisition of autoshaped responding was investigated by changing the frequency of unsignaled USs during the intertrial interval. The addition of the unsignaled USs had an effect on acquisition speed comparable with that of massing trials. The effects of these manipulations can be understood in terms of their effect on the amount of information (number of bits) that the average CS conveys to the subject about the timing of the next US. The number of reinforced CSs prior to acquisition is inversely related to the information content of the CS. (PsycINFO Database Record (c) 2010 APA, all rights reserved)  相似文献   

18.
Autoshaped key pecking in pigeons was eliminated by presenting reinforcers only during non-CS periods (negatively contingent reinforcement) or in both non-CS and CS periods (noncontingent reinforcement). In either case, when all reinforcers were subsequently removed (simple extinction), responding recovered strongly (Experiment 1). Recovery in extinction occurred only if the CS was in a conditioned state when non-CS reinforcers were introduced (Experiment 2). Recovery from noncontingent reinforcement was virtually complete, since total responding in extinction after response elimination was not less than in control groups extinguished without an intervening response-elimination phase (Experiment 3). Recovery also occurred for nonautoshapable, instrumentally reinforced key pecking (Experiment 4). The hypothesis that recovery is due to reinstatement of the non-CS stimulus conditions of acquisition (absence of food) was not supported (Experiments 5 and 6). Other accounts of recovery are considered.  相似文献   

19.
The authors studied the role of context in reinstatement. Freezing was reinstated when the conditioned stimulus (CS) was extinguished in 1 context and rats moved to another context for reexposure to the shock unconditioned stimulus (US) and test. It was also reinstated (rather than renewed) when rats were shocked in the extinction context and moved to another context for test. This reinstatement was CS specific and reduced by nonreinforced exposures to the extinction context. Rats shocked in the context in which a stimulus had been preexposed froze when tested in another context. These findings suggest 2 roles for context in reinstatement: conditioning of the test context (M. E. Bouton, 1993) and mediated conditioning by the extinction context (P. C. Holland, 1990). (PsycINFO Database Record (c) 2010 APA, all rights reserved)  相似文献   

20.
Extinguishing a conditioned response (CR) has entailed separating the conditioned stimulus (CS) from the unconditioned stimulus (US). This research reveals that elimination of the rabbit (Oryctolagus cuniculus) nictitating membrane response occurred during continuous CS-US pairings. Initial training contained a mixture of 2 CS-US interstimulus intervals (ISIs): 200 ms and 1,200 ms. The CRs showed double peaks, one for each ISI. When 1 ISI was removed, its CR peak showed the hallmarks of extinction: a decline across sessions, spontaneous recovery between sessions, and rapid reacquisition when the absent ISI was reintroduced. These results support real-time models of conditioning that segment the CS into microstimuli while challenging theories that rely on contextual control, US representations, CS processing, and response inhibition. (PsycINFO Database Record (c) 2010 APA, all rights reserved)  相似文献   

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