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1.
In a blocking procedure, conditioned stimulus (CS) A is paired with the unconditioned stimulus (US) in Phase 1, and a compound of CSs A and X is then paired with the US in Phase 2. The usual result of such a treatment is that X elicits less conditioned responding than if the A-US pairings of Phase 1 had not occurred. Obtaining blocking with human participants has proven difficult, especially if a behavioral task is used or if the control group experiences reinforcement of a CS different from the blocking CS in Phase 1. In the present series, in which human participants and a behavioral measure of learning were used, we provide evidence of blocking, using the above described control condition. Most important, we demonstrate that extinction of the blocking CS (A) following blocking treatment reverses the blocking deficit (i.e., increases responding to X). These results are at odds with traditional associative theories of learning, but they support current associative theories that predict that posttraining manipulations of the competing stimulus can result in a reversal of stimulus competition phenomena.  相似文献   

2.
Blocking of conditioned suppression in rats was studied in three experiments using serial and simultaneous compounds in Pavlovian trace conditioning procedures. Experimental groups were first given trace conditioning trials with a 2-sec stimulus (A) presented at least 60 sec before an electric grid shock US. Next, both experimental and control groups received reinforced trials with a compound stimulus (AB). Both A and B were 2 sec in duration and were presented at least 60 sec before the US. For some groups during AB training, the A stimulus preceded the B stimulus; for others, B preceded A; for still others, A and B occurred simultaneously. Conditioning was subsequently assessed separately to both A and B. The results were as follows: First, varying the interval between the onset of A and the US during A training appeared to produce significantly different levels of conditioning to A but did not detectably affect A’s ability to block conditioning to B. Second, blocking was observed in both simultaneous and serial procedures. Third, in the serial procedure, A blocked conditioning to B whether it preceded B or followed B in the AB compound. Fourth, in tests given after AB conditioning, the experimental and control groups suppressed similarly to A. The relevance of these results to the conditioning model of Rescorla and Wagner (1972) and to Mackintosh’s (1975b) theory of attention are discussed.  相似文献   

3.
In three experiments, groups of albino rats received one strictly simultaneous pairing of a 4-sec auditory conditioned stimulus (CS) and a 4-sec 1-mA shock unconditioned stimulus (US). Other groups received a backward pairing, in which the US began before the CS, or a forward pairing, in which the CS began before the US. Control groups received only the US or received both the CS and the US but widely separated in time. Later, the CS was presented while the rats licked a drinking tube for water, and CS-elicited suppression of licking was taken as an index of the Pavlovian conditioned response (CR). It was found that groups receiving a single forward or a single simultaneous pairing suppressed more than groups that had received a backward pairing; and the backward groups, in turn, suppressed more than the control groups. It appears, then, that excitatory fear conditioning, as reflected in conditioned suppression of licking in rats, can be produced in a single trial by both backward and simultaneous conditioning procedures.  相似文献   

4.
In a conditioned suppression paradigm, a partially overlapping compound stimulus signaled occurrences of electric shock. That compound CS consisted of 3 min of continuous illumination of the houselight with three discrete 5-see presentations of a tone superimposed. A .5-sec electric shock was coterminous with each tone presentation. Rats that received this treatment in early conditioning sessions showed considerable recovery from conditioned suppression to the houselight as the experiment progressed. However, the effect was not reversible, and it could not be demonstrated in rats that experienced extensive prior conditioning to the houselight alone. These results are discussed in relation to a hypothesis concerning the modulation of behavioral control exerted by elements of compound stimuli and as they relate to a recent theoretical model for Pavlovian fear conditioning.  相似文献   

5.
Twenty-eight male albino rats were given a single 4-sec 1-mA electric-grid-shock unconditioned stimulus (US). In the same session they received two 12-sec conditioned stimuli (CSs). One CS (explicitly unpaired) terminated 180 sec before the US began; the other (backward paired) began immediately after the US terminated. The CSs used were a 1000-Hz 85-dB tone and an 84-dB click; their roles were counterbalanced. Over the next 2 days, each CS was presented for 2 min while the rats drank from a water bottle. The backward-paired CS was found to suppress licking more than the explicitly unpaired CS. This suppression was accompanied by an increase in defensive behavior (freezing and freeze/nod) and by a decrease in other activity. The suppression did not seem to be due to a maintained or enhanced CS-orienting response reflex, nor could it be attributed to an adventitiously reinforced interfering operant. The results support the presumption made in previous reports that the lick suppression evoked by a backward CS reflected one-trial backward excitatory fear conditioning.  相似文献   

6.
In a typical conditional discrimination, a target stimulus (X) is reinforced during one feature cue (A→X+), but not during another feature cue (B→X−). The present experiments used only a single “feature” cue (a 66-sec tone). On half of the trials, the target stimulus (a 400-msec light) was paired with the reinforcer when the feature-target interval was one duration (e.g., 5 sec). On the remaining trials, the interval was different (e.g., 45 sec), and the target stimulus was presented without the reinforcer. All the animals acquired this temporal discrimination, and subsequent testing with other feature-target intervals yielded generalization-like gradients. These results provide solid evidence that each portion of a feature cue is encoded in a distinctive fashion. Had temporal encoding not occurred, the feature cue would have been just as ambiguous a predictor of the reinforcer as was the target stimulus, and discrimination would not have been possible. The integration of real-time temporal encoding mechanisms into models of conditional discrimination is discussed.  相似文献   

7.
Conditioned lick suppression in rats was used to explore the role of timing in trace conditioning. In Experiment 1, two groups of rats were exposed to pairings of a CS (CS1) with a US, under conditions in which the interstimulus interval (ISI) that separated CS1 offset and US onset was either 0 or 5 sec. Two additional groups were also exposed to the same CS1→US pairings with either a 0 or a 5-sec ISI, and then received “backward” second-order conditioning in which CS1 was immediately followed by a novel CS2 (i.e., CS1→CS2). A trace conditioning deficit was observed in that the CS1 conditioned with the 5-sec gap supported less excitatory responding than the CS1 conditioned with the 0-sec gap. However, CS2 elicited more conditioned responding in the group trained with the 5-sec CS1-US gap than in the group trained with the 0-sec CS1-US gap. Thus, the CS1-US interval had inverse effects on first- and second-order conditioned responding. Experiment 2 was conducted as a sensory preconditioning analogue to Experiment 1. In Experiment 2, rats received the CS1?CS2 pairings prior to the CS1→US pairings (in which CS1 was again conditioned with either a 0 or a 5-sec ISI). Experiment 2 showed a dissociation between first- and second-order conditioned responding similar to that observed in Experiment 1. These outcomes are not compatible with the view that differences in responding to CSs conditioned with different ISIs are mediated exclusively by differences in associative value. The results are discussed in the framework of the temporal coding hypothesis, according to which temporal relationships between events are encoded in elementary associations.  相似文献   

8.
The efficacy of conditioned inhibition in a novel conditioned stimulus/conditioned inhibitor (CS/CI) compound was tested in 6-, 10-, and 14-week-old kittens. The conditioned response was suppression of respiration elicited by a 5.1-sec CS paired with a brief, mild footshock. During original inhibitory training, a CI was presented 2 sec after the onset of the CS, and the stimuli coterminated 3 sec later without the shock. As previously reported, the CI trained in this paradigm is more potent in older kittens but passes a summation test in all age groups (Dess & Soltysik, 1989). In the transfer test, the order of the CS and CI was reversed, so that the CI preceded the CS with no stimulus overlap. Transfer of inhibition to this new compound was virtually absent in the 6-week-old kittens and nearly perfect in the 14-week-old kittens. The CI alone (before CS onset) elicited a strong fear response in the youngest kittens, moderate fear in the 10-week-old group, and very little fear in the oldest group. The transferability of inhibitory training to a different temporal configuration of the CS and CI is absent at 6 weeks of age and fully developed 8 weeks later.  相似文献   

9.
In two experiments with rats, we examined the developmental emergence of conditioned freezing following trace and short-delay conditioning and also included a long-delay comparison group. In the short-delay and trace groups, a 10-sec conditioned stimulus (CS) was paired with shock; for the trace rats, a 10-sec trace interval followed CS termination. The long-delay groups received a 20-sec CS paired with shock, to equate for the longer interstimulus interval (ISI) in the trace group. Trace conditioning emerged later in development than did short-delay conditioning (see Moye & Rudy, 1987). Importantly, long-delay conditioning emerged in parallel with trace conditioning, at a similar time, and with similar strength. These findings suggest a role for the longer ISI, as opposed to the unfilled gap per se, in the late emergence of trace conditioning. The role of the hippocampus in trace conditioning and the possibility that young rats encode the temporal relationship between CSs and unconditioned stimuli are also considered.  相似文献   

10.
A variant of the taste aversion procedure for sensory preconditioning, as used by Rescorla and Cunningham (1978), was employed in a study of the context dependency of within-event learning. In two experiments, rats received Phase 1 exposure to a simultaneous flavor compound, AX; flavor X was paired with illness during Phase 2, and any tendency for the resulting aversion to be elicited by A was measured. It was found that subjects were less likely to shun flavor A as a consequence of this training if the Phase 1 and test episodes were conducted in distinctively different contexts. This effect was evident both when the change of context occurred just before the test with flavor A (Experiment 1) and when it occurred before Phase 2 (Experiment 2). These results were taken to imply that, as is often found with serial associations, the retrieval of within-event associations is subject to contextual control. The implications of these findings for the interpretation of perceptual learning effects are discussed.  相似文献   

11.
Most associative theories have assumed that stimulus competition occurs only between conditioned stimuli (CSs) that are trained in compound. The present research investigated the possibility of competition between two CSs that were individually paired to the same unconditioned stimulus (US). We used human subjects in an anticipatory suppression analogue to Pavlovian conditioning. Experiment 1 showed that X+ training followed by A+ training resulted in impaired responding to X. This did not occur when A+ training preceded X+ training. Experiment 2 replicated the basic effect and showed that it did not occur when the Phase 2 training consisted of A? instead of A+ nor when the A+ pairings occurred in a second context. Experiment 3 showed that A+ pairings occurring in a second context could still produce the effect when X was tested in the context in which the A+ pairings had occurred, but not when X was tested in a context different from that used for A+ training. Collectively, these results suggest that individually trained CSs may compete with each other when one of those CSs is more strongly activated by the test context than the other one.  相似文献   

12.
Weanling rats were tested for retention of an aversion to a novel flavor (chocolate milk) that had been conditioned as a single-element conditioned stimulus (CS) or in compound with a novel ambient odor (banana). The presence of the ambient odor during conditioning had no effect on flavor aversion shortly thereafter, confirming previous results. The flavor aversion observed 21 days after conditioning, however, was significantly stronger for pups conditioned with the single-element CS than for those given the flavor-odor compound as the CS. This retention effect was due to a surprisingincrease in the conditioned aversion observed 21 days after conditioning with the single-element CS. A second experiment confirmed this paradoxical increase in retention of the aversion to chocolate milk. This experiment also verified that no such increase occurred in retention of the conditioned aversion to a different flavor (saccharin), whether the initial aversion was strong or weak. The results may be explained in terms of generalized latent inhibition from consumption of mother’s milk.  相似文献   

13.
Three experiments with rat subjects sought to enhance one-trial excitatory simultaneous and backward fear conditioning by using a two-element compound conditioned stimulus (CS) instead of only a single element. During conditioning, experimental groups received a 4-sec CS either coextensively with a 1-mA grid-shock unconditioned stimulus (US) or immediately after US termination. In subsequent tests, CSs evoked more lick suppression and freezing in these groups than in various controls. Compound CSs evoked more lick suppression and freezing than did CS elements, but did so equally for experimental and control groups. Therefore, the use of compounds did not enhance conditioning. Unexpectedly, an explicitly unpaired control in which CS followed US termination by 3 min tended to show more CS-evoked suppression and freezing than did a control in which CS preceded US onset by 3 min. This result raises the possibility that associations between the CS and the training context might engender responding to backward-paired CSs.  相似文献   

14.
The present research examined the temporal distribution of responding in a lick suppression paradigm. In Experiment 1, rats were trained with either a 30- or a 120-s conditioned stimulus (CS), which was followed either by a footshock (unconditioned stimulus [US]) or nothing. Licking during the CS was suppressed only in the former condition. Suppression was more pronounced early in the CS. In Experiment 2, rats were exposed to two 30-s or two 120-s CSs, with delivery of the shock being contingent on CS1 for half of the animals and on CS2 for the other half. For both the paired and the unpaired conditions, suppression at the beginning of CS1 was observed for all the groups. By discounting the possibility of generalization between CS1 and CS2, it appears that this initial suppression was not a conditioned response to the CS, but an unconditioned one due to mere exposure to the shock US.  相似文献   

15.
Adult rats were injected with lithium chloride (LiCl) after consumption of a novel flavor (chocolate milk) that either was or was not presented together with a novel ambient odor (banana) as a compound conditioned stimulus (CS). In Experiment 1, the adults’ consumption of the flavor 24 h after conditioning was compared with that of weanling rats given the same conditioning treatment on Postnatal Day 21. The results confirmed previous indications that the reduction in aversion observed for adults conditioned with the compound CS (overshadowing) was weak or nonexistent in weanlings. After a longer retention interval (21 days), there was no evidence of overshadowing in adults despite maintained retention of the basic conditioned aversion. In Experiment 2 this decrease in overshadowing after a long retention interval was replicated with adult animals and extended to a different method of testing. The form of the effect was the same as in Experiment 1: The decrease in overshadowing occurred over the retention interval without loss in retention of the basic taste aversion; the decrease in overshadowing was a consequence of anincrease in the flavor aversion displayed by animals conditioned with the compound CS. The impaired flavor aversion (i.e., the overshadowing) observed shortly after conditioning apparently was due to factors associated with memory retrieval, rather than to reduced attentional or associative strength.  相似文献   

16.
In seven experiments, an effect of the intertriai interval (ITI) duration on barpressing by rats was studied. A stimulus signaled a 15-sec variable-interval trial. The first response after the interval elapsed turned the stimulus off and was rewarded with food. Trials were separated by long (about 300 sec) or short (about 10 sec) ITIs. A within-subjects design established that response rate on trials after long ITIs was lower than that after short ITIs (Experiments 1 and 3–7). The effect was not cumulative (the effect of one and five consecutive short ITIs was the same). Response rate after short and long ITIs was the same when a between-subjects design was used (Experiment 2). Response rate was higher after 160-sec ITIs than after 300-sec ITIs, suggesting that the ITI duration at which all longer ITIs are treated the same (i.e., the upper limit) is greater than 160 sec (Experiment 3). When food, the trial stimulus, a novel stimulus, or a familiar stimulus never paired with food, was presented 10 sec before the next trial during some of the long ITIs, response rate on the next trial was similar to that found after 10-sec ITIs (Experiments 4–6). This similarity suggested that these events could mark the start of the ITI. However, the familiar stimulus did so only when it reliably predicted that the next trial would occur after a short interval. The effect of ITI duration on responding was apparently attributable to response latency. Response latency was greater after long ITIs, but once responding began, it was similar after long and short ITIs (Experiment 7).  相似文献   

17.
Three experiments examined the effect of systemic administration of the benzodiazepine midazolam on extinction and re-extinction of conditioned fear. Experiment 1 demonstrated that midazolam administration prior to extinction of a conditioned stimulus (CS) impaired that extinction when rats were subsequently tested drug free; however, extinction was spared if rats were extinguished, reconditioned, and re-extinguished under midazolam. Experiment 2 provided a replication of this effect within-subjects; rats were conditioned to two CSs (A and B), extinguished to one (A-), reconditioned to both, and then extinguished/re-extinguished to both stimuli in compound (AB-), under either vehicle or midazolam. On the drug-free test, rats given midazolam froze more to the CS that had been extinguished (B) than the one that been re-extinguished (A). The final experiment examined whether extinction under midazolam was regulated by prediction error. Rats were trained with three CSs (A, B, C) and extinguished to two (A-, C-). These stimuli then underwent additional extinction under midazolam or vehicle, with one CS now presented in compound with the non-extinguished CS (AB-, C-). Rats were then tested for fear of A relative to C. Rats given vehicle showed a deepening of extinction to A relative to C, as is predicted from error-correction models; however, rats given midazolam failed to show any such discrepancy in responding. The results are interpreted to indicate that the drug reduced prediction error during extinction by reducing fear, and rats were able to re-extinguish fear via a retrieval mechanism that is independent of prediction error.  相似文献   

18.
The serial presentation of two different CSs, with each stimulus having an 8-sec duration (S18/S28), consistently has resulted in most of the shuttlebox avoidance responses being recorded to the S2 component. Experiment 1 attempted to attenuate this serial CS, delayed-response effect by conditioning the separate components of a serial CS prior to ordering them sequentially. Ten component-training trials were administered, with subjects receiving CS-US pairing to S1 only, S2 only, or to both S1 and S2 presented on separate trials. Two CS durations (8 or 16 sec) during this phase also were compared. Subjects were then given 100 avoidance test trials using the standard serial procedure. The 10 best avoidance responders in each group were selected for analysis. Shorter avoidance latencies were obtained only for subjects receiving component conditioning to S1. CS duration was not a factor in establishing the shorter latencies. Component conditioning to S2 resulted in increasing the total avoidances. Experiment 2 increased the number of component-training trials and the generality of the findings by using a different strain of rats and by extending the testing phase of the study so that all subjects could be included in the analysis. Comparable results were obtained. The theoretical implications of these data were discussed.  相似文献   

19.
Two experiments examined the effects of differences in the parameters of a clocked interfood interval on the obtained distribution of responding to the stimuli in that interval. In the first experiment, a 3×3 factorial design assessed the effects of the number of components and the durations of those components. Food was presented irrespective of behavior following 5, 10, or 20 discrete stimuli across durations of 3, 6, or 12 sec each. Responding began at the approximate midpoint of the interval. More responding occurred in earlier portions of the last half of the interval as the number and the durations of individual stimuli decreased or as the overall interfood interval decreased. The second experiment, also a 3×3 factorial design, manipulated the probability and duration of food presentation following a 60-sec trial containing 10 discrete stimuli. A 2.0-, 3.5-, or 5.0-sec food presentation followed 100%, 25%, or 10% of the trials. Responding again began at the approximate midpoint of the interval. More responding occurred in earlier portions of the last half of the interval only when both food duration and the proportion of reinforced trials increased. Both experiments therefore showed that the onset of responding occurs at the approximate midpoint of clocked interfood intervals in spite of a wide variety of CS and US manipulations.  相似文献   

20.
Higher order occasion setting with serially presented stimuli was investigated in an appetitively motivated, discrete-trial operant study with rats. Reinforcement of barpressing during an occasion-setting light (a discriminative stimulus) was contingent on immediately preceding second-order occasion setters (i.e., a click train or a buzzer served as a conditional discriminative stimulus). Moreover, the meanings of the clicks and buzzer were themselves indicated by a third-order occasion setter that preceded them (i.e., a white noise acted as a second-order conditional discriminative stimulus). Subjects responded more frequently and had shorter latencies to the first response in the presence of the light on trials during which barpressing was reinforced than on trials during which barpressing was not reinforced. The likelihood that the subjects solved the problem by responding to unique compound stimuli was minimized by the insertion of a 5-sec gap between the different controlling stimuli presented on each trial. Thus, these subjects appear to have mastered a second-order conditional discrimination, which is equivalent to third-order occasion setting if the discriminative stimulus (light) is viewed as a first-order occasion setter. Although the subjects learned to respond appropriately to each of the compound stimuli, differences in responding to specific stimuli were consistent with a higher order feature-positive effect. Some implications of higher order occasion setting are discussed, including the issue of independence between the different levels of occasion setting signaled by a single stimulus.  相似文献   

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