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1.
Time spent in various behaviors by the rat was recorded in a defensive burying paradigm. Experiment 1 revealed that rats spent more time burying the shock prod than a control prod and that doubling the size of the test chamber did not have a significant effect on the time spent in any behavior. In Experiment 2, the location of bedding material in a two-compartment test chamber was found to affect the occurrence of burying (both the shock and control prods) and burrowing behavior. Burying did not occur when bedding was not available in the shock compartment but was located in the escape compartment. Burrowing was more likely to occur when bedding was in both compartments than when it was in only one compartment. Immobility and escape latencies were shorter than burying latencies in all subjects. Burying was viewed as belonging to a second stage of defensive behavior. 相似文献
2.
Natural sources of aversive stimuli are frequently well-defined material objects that are present both before and after the aversive event. In the present experiment, rats acquired information about such a source after the aversive event and used this information to guide their subsequent defensive reactions to it. The rats were shocked by one of two possible sources, either a black or a striped prod, mounted on opposite end walls of the test chamber. Immediately following the shock, the houselights were momentarily extinguished and the patterns on the two prods were automatically switched for subjects in the experimental condition or left unchanged for subjects in the control condition. The rats were left in the chamber for another 5 min with the patterns in their new positions before being removed for 2 min while the two prods were mounted on the side walls. During the ensuing test of conditioned defensive burying, the rats in the control condition directed the majority of their burying behavior at the prod exhibiting the pattern displayed by the shock source prior to and during the shock administration. In contrast, the rats in the experimental group buried the prod exhibiting the pattern displayed by the shock source during the postshock period more than they did the prod displaying the pattern present on the shock source prior to and during the shock administration. 相似文献
3.
Hooded rats and golden hamsters were shocked by one of two prods in a chamber with a sawdust-covered floor. Rats buried the prod through which they had been shocked, but hamsters displayed no burying behavior. Hamsters may not have buried the prod because they could not perform the required motor pattern. However, hamsters can carry and pile food pellets. Therefore, in a second experiment, rats and hamsters were shocked in a chamber with wooden blocks on the floor. Rats piled blocks around the prod through which they had been shocked, but hamsters did not. The third experiment established that, like rats, hamsters can associate a prod with shock in one trial, since they showed differential avoidance of a prod through which they had been shocked. Since hamsters are nonsocial and rats are social, these results are consistent with suggestions that burying sources of aversive stimulation evolved as an altruistic behavior. 相似文献
4.
Two strains of rats (albino Wistar and hooded PVG/c) were exposed to a conditioned defensive burying paradigm that consisted of placing rats in a test chamber with bedding material on the floor, shocking them with a shock prod, and recording the time each rat spent in burying responses toward the prod. Various behaviors other than burying (freezing, grooming/paw licking) were observed by a time-sampling procedure during the control, conditioning, and extinction sessions, each of which was 15 min in duration. Wistar rats generally showed behavioral inhibition, as evidenced by less burying, lower exploratory and ambulatory behavior, and higher freezing behavior. PVG/c rats spent significantly more time engaged in burying and accumulated more bedding material in the conditioning session than did the Wistar rats. No significant differences between the two strains of rats were observed during the extinction session in terms of these measurements. The results indicate that Wistar rats have a greater tendency to freeze when coping with the noxious stimulus in a conditioned defensive burying paradigm, whereas the dominant coping style for PVG/c rats is defensive burying. 相似文献
5.
The degree of spatial and temporal contiguity between contact with a prod and shock was varied in three experiments to see how these factors contribute to defensive burying. In Experiment 1, rats shocked once through a grid floor while touching a prod buried the prod just as much as did rats shocked through the prod. Experiment 2 showed that rats either shocked through the floor more than 1 min after touching the prod or shocked in the absence of a prod did not bury the prod. Thus, close temporal contiguity between grid shock and prod contact appears necessary for burying. Nevertheless, grid-shocked rats do learn something different from prod-shocked rats, since they bury the prod less and the walls more than do prod-shocked rats when the position of the prod is changed in the test chamber (Experiment 3). 相似文献
6.
Jon L. Williams 《Learning & behavior》1987,15(3):333-341
In Experiment 1, rats received a session of 80 inescapable tail shocks or no shocks while restrained in a tube. During tests of conditioned defensive burying 24 h later, the bedding of the chamber contained odors from either stressed or nonstressed conspecific donor rats. Following a single prod shock, subjects that had had prior shocks or that were tested with the stress odors spent significantly less time burying the prod, made smaller piles of bedding, and displayed more freezing behavior. The combination of prior shock and stress odors during later testing enhanced these effects. In Experiment 2, a yoked group of rats that was given inescapable shocks, in contrast to a group that had wheel-turn escape training and one that was restrained but not shocked, later showed significantly less burying and more freezing when tested for defensive burying with stress odors present. In both experiments the duration of burying and the heights of piles were positively correlated, and both of these measures were negatively correlated with freezing. The demonstrated capacity of unconditioned stress odors to mediate different degrees of fear, depending upon the controllability of prior shock, is related to other studies of learned helplessness, and the predominance of freezing over burying is discussed in terms of various types of defensive strategies, stimulus-control processes, and the author’s stress-coping-fear-defense (SCFD) theory. 相似文献
7.
Genotypically based within-species differences in defensive burying were examined in 180 mice representing 15 inbred strains. Each mouse was tested twice in a cylindrical test chamber containing two similar prods. In the first test, one of the prods was electrified, whereas in the second test (24 h later), neither prod was. Although most strains selectively buried the shock prod in the first test (as determined by bedding-height-at-prod and position-of-highest-bedding-pile criteria), some strains did not discriminate between the shock and dummy prods and still others displayed little prod-directed bedding displacement at all (thereby resembling a heterogeneous nonshocked control group). In general, burying tended to be somewhat reduced in the second test, but strain differences in retention were observed. Factors contributory to the observed differences among strains and the need for multiple measures of burying are discussed. Collectively, these findings indicate that intraspecific genetic variation, acting at multiple burying-relevant behavioral levels, can be an important determinant of the expression of the defensive-burying response in mice. 相似文献
8.
Rats shocked once by a stationary, wire-wrapped prod bury it if suitable materials are available. Does this conditioned defensive burying occur when rats have the opportunity to flee from the source of aversive stimulation, or is it limited to situations such as those in which it had previously been studied—those in which the relatively small test chamber confined each rat to the immediate vicinity of the prod? In the present experiments, the capacity of rats to flee from the shock prod was enhanced by increasing the floor dimensions of the test chamber up to 200X80 cm (Experiment 1) or by providing the rats with an opportunity to seek refuge in a separate, safe compartment (Experiment 2). Although both of these modifications to the usual conditioned-defensive-burying paradigm significantly reduced the duration of burying and the height of the accumulated mounds, burying remained well above control levels in all experimental conditions. 相似文献
9.
Genotypic and environmental contributions to the defensive burying response were examined by testing four sublines of two inbred strains of mice in test chambers of three different lengths. Burying was found to be dependent on both the particular subline tested and the length of the test chamber employed. For two sublines, specific increases in the length of the test chamber resulted in the complete abolition of defensive burying. A third subline never displayed defensive burying, and the fourth buried in all three chamber-length conditions. Sex differences in burying were never observed. Rather than being viewed as a species-specific defensive reaction, it was proposed that defensive burying should more appropriately be viewed as a genotypically dependent response, the expression of which is contingent on the specific environmental context in which an aversive stimulus is encountered. Apparent conflicts in the defensive-burying literature were reconciled in accordance with this interpretation. 相似文献
10.
Heidar A. Modaresi 《Learning & behavior》1982,10(1):97-102
Experiment 1 investigated the proposition that rats cover the source of aversive stimulation with the bedding material available to them and sought to determine whether familiarization with this material would affect burying. The results indicated that rats are no more likely to cover an aversive object than they are not to cover it, although they collect a considerable amount of bedding material in the area surrounding the aversive object. Experiment 2 demonstrated that the rat’s defensive “burying” toward an aversive object is affected by the subject’s predisposition to displace material toward the front side of the apparatus. Some theoretical complexities involved in considering the act of “burying” toward an aversive object as a defensive behavior are discussed. 相似文献
11.
In Experiment 1, male rats were exposed to either aggressive (i.e., alpha) or nonaggressive conspecific colonies and tested 24 h later, with or without alpha odors, for freezing behavior and burying of a wall prod that had been the source of a brief electric shock. The results indicated that prior defeat experience and the presence of alpha odors alone during testing had no significant effects, but the combination of prior defeat and alpha-odor testing significantly decreased burying and increased freezing behavior. In Experiment 2, we examined the effects of noncontact exposure to a cat, as a predatory Stressor, during subsequent prod-shock tests involving the presence or absence of cat odors. Exposure to a cat failed to disrupt later prod burying and did not produce freezing. However, the presence of cat odors during testing significantly reduced the amount of defensive burying,without resulting in an increment in freezing. In Experiment 3, rats were given 1, 5, or 30 inescapable preshocks in the presence of either cat odors or a hedonically neutral citronella odor and were tested 24 h later for prod burying and freezing with or without these odors. Both the cat and the citronella odors resulted in a significant reduction in burying and an increase in freezing for rats given 5 and 30 preshocks and tested in the presence of these respective conditioned odors. For the groups that were given 5 preshocks, preshock and later testing in the presence of cat odors resulted in significantly less prod burying and more freezing than for rats that were preshocked and tested in the presence of citronella. The findings of these three ethoexperimental studies are discussed in terms of the learned-helplessness theory, the stress-coping-fear-defense (SCFD) theory, and the concept of selective CS-US associability. 相似文献
12.
In Experiment 1, four groups of male rats were given a session as an intruder in either aggressive (i.e., alpha) or nonaggressive colonies of conspecifics and later received either a 2-h exposure to the odors of the alpha colonies or an exposure-control session with the odors of a nonalpha colony. Two additional groups of rats that had been attacked and defeated by alpha residents were later given a 12-h exposure session with alpha-colony odors or nonaipha-control odors. Twenty-four h after the colony-intruder session, all subjects were given a single 6.5-mA shock from a prod with alpha-colony odors present in the bedding of the test chamber. Attacked rats that had been given exposure-control sessions showed significantly less prod burying and greater freezing than nondefeated subjects. This implies that the alpha-colony odors elicited conditioned fear. In contrast, the attacked subjects that had been given a pretest exposure session with alpha-colony odors showed significantly more prod burying and significantly less freezing. This suggests that the alpha-odor exposure resulted in the extinction of fear to these odors. Furthermore, the 12-h exposure to alpha-colony odors was found to be more effective in reducing fear-mediated responses than was the 2-h exposure. In Experiment 2, three groups of rats were exposed to a cat while they were in a protective cage; later they were given a 12-h exposure session with cat odors, a 12-h exposure-control session with no cat odors, or no exposure treatment. Compared with the two control groups, the subjects that were exposed to cat odors showed less freezing during subsequent prod-shock tests in the presence of cat odors, but they did not show prod burying. The reported changes in fear-mediated reactions to the odors of conspecifics and a predator are discussed in terms of both associative and nonassociative processes. 相似文献
13.
Three experiments were conducted to determine whether a naive observer rat would avoid contact with a shock prod after watching a demonstrator rat contact, be shocked by, and defensively bury the prod. We found that observer rats took longer to contact prods that had delivered a shock to and been buried by a demonstrator rat than to contact prods that had not delivered shock and had not been buried. However, observer rats contacted prods buried by an unseen demonstrator rat or by an unseen experimenter with the same latencies as those for prods they had seen deliver shock to and be buried by a demonstrator rat. In large enclosures, subjects took 1–2 h longer to contact buried prods than to contact unburied prods. We conclude that alteration of the physical environment by individuals receiving noxious stimulation can significantly reduce the probability that conspecifics will contact the noxious stimulus. Observational learning per se, however, need not be involved. 相似文献
14.
Stephen F. Davis Scott A. Moore Cynthia L. Cowen Debra K. Thurston John C. Maggio 《Learning & behavior》1982,10(4):516-520
Attempts to establish the generality of the defensive-burying response have proved quite successful with several strains of albino and hooded rats and with mice. However, three previous attempts to demonstrate this behavior in gerbils have been completely unsuccessful. Three additional defensive-burying experiments employing gerbils as subjects are reported. Defensive burying did not occur when testing took place in a rectangular chamber (Experiments 1 and 3), but did occur when a circular chamber was employed (Experiments 2 and 3). Hence, the geometric shape of the test chamber appears to be a crucial factor in determining the elicitation of this behavior in gerbils. Furthermore, the overall topography of the gerbil defensive-burying response was found to be different from that of previously examined species. 相似文献
15.
Rick Richardson Tania Q. Duffield Glynis K. Bailey R. Frederick Westbrook 《Learning & behavior》1999,27(4):399-415
Rats were shocked in the black but not the white compartment of a shuttlebox and then exposed to the black compartment in the absence of the shock unconditioned stimulus (US) to extinguish fear responses (passive avoidance). In five experiments, rats were then shocked in a reinstatement context (distinctively different from the shuttlebox) to determine the conditions that reinstate extinguished fear responding to the black compartment. Rats shocked immediately upon exposure to the reinstatement chamber failed to show either reinstatement of avoidance of the black compartment or fear responses (freezing) when tested in the reinstatement chamber. In contrast, rats shocked 30 sec after exposure to the reinstatement chamber exhibited both reinstatement of avoidance of the black compartment and freezing responses in the reinstatement chamber (Experiment 1). Rats shocked after 30 sec of exposure to the reinstatement chamber but then exposed to that chamber in the absence of shock failed to exhibit reinstatement of the avoidance response and did not freeze when tested in the reinstatement chamber (Experiment 2). Rats exposed to a signaled shock in the reinstatement chamber and then exposed to that chamber in the absence of shock also failed to exhibit reinstatement of the avoidance response (Experiment 5). These rats showed fear responses to the signal but not to the reinstatement chamber. Finally, rats exposed for some time (20 min) to the reinstatement chamber before shock exhibited reinstatement of the avoidance response but failed to freeze when tested in the reinstatement chamber (Experiments 3 and 4). These results are discussed in terms of the contextual conditioning (Bouton, 1994) and the US representation (Rescorla, 1979) accounts of postextinction reinstatement. 相似文献
16.
Robert J. Blanchard Charles F. Kleinschmidt Chantis Fukunaga-Stinson D. Caroline Blanchard 《Learning & behavior》1980,8(1):177-183
Male rats in a restraining tube bit and wounded the snout of an anesthetized male conspecific as a direct function of the intensity of tailshock, with bites declining systematically in the time interval after shock. Female rats’ bites on a male rat were also dependent on shock, but did not produce wounds. When an anesthetized cat was presented to rats in the same situation, females bit and wounded the cat before shock was given, while the males again bit only in response to shock. These data were interpreted as indicating that male bites on both a conspecific and a predator fit the same defensive biting pattern. In contrast, females’ bites on a male rat are actively inhibited, while females’ bites on a predator are neither inhibited nor shock dependent: this latter finding may reflect the adaptive value (protection of the young) of attacking a predator before it hurts the female rat. 相似文献
17.
Rats lived continuously in an operant chamber in which they were able to press a bar to obtain food on a chained FR50:CRF schedule that allowed them control of both the size and frequency of individual meals. Independent groups of animals were scheduled to receive 12, 24, 48, or 96 electric shocks per day, which were given randomly in time and independent of the subjects’ behavior. Rats could avoid shock by remaining in a safe area of the chamber, but they were always at risk while barpressing. The introduction of shock resulted in a number of changes in feeding patterns. In rats exposed to a possible 12 shocks/day, meal size increased whereas meal frequency changed very little. At 24 shocks/day, meal frequency decreased whereas meal size increased such that net intake remained stable relative to a preshock baseline period. As shock density was increased to 48 or 96 shocks/day, total intake was suppressed. At 96 shocks/day, both meal frequency and meal size decreased dramatically. Shock-related changes were also observed in rates of operant responding and in the amount of time the animals engaged in feeding-related behavior. All of the animals were able to achieve a greater than 50% reduction in the total number of shocks received relative to equivalent random samples of their position in the apparatus taken during baseline. These results support the position that the nature of defensive changes in feeding behavior that are seen when an aversive stimulus is introduced: into a simulated foraging situation varies as a function of risk. 相似文献
18.
Nigel W. Bond 《Learning & behavior》1984,12(3):323-331
Rats of the Australian High Avoider (AHA) and Australian Low Avoider (ALA) strains and their reciprocal crosses were exposed to 50 trials of one of three shuttlebox procedures. The avoidance group received pairings of a tone and shock. If the animals shuttled during the tone, they avoided the shock. If they waited until the shock came on, they could then escape it. The classical group received pairings of the tone and a brief inescapable shock. If they shuttled during the tone, the tone ceased and they immediately received the shock. If they did not shuttle, they received the brief shock at the termination of the tone. The pseudoconditioning group received the tone and the shock explicitly unpaired. If they shuttled during either the tone or the shock, the stimulus was terminated. There was no acquisition of anticipatory responding under the pseudoconditioning procedure. All groups evidenced an increase in anticipatory responding over trials under the classical procedure. The AHAs acquired the response faster and reached a higher asymptote than did the ALAs. Performance of the two reciprocal crosses fell in between. A similar pattern was observed under the avoidance procedure, albeit at slightly higher response levels. Subsequent studies established that the AHAs acquired a one-way avoidance response quickly, but were impaired on a passive avoidance task, whereas the reverse was the case for the ALAs. The reciprocal crosses were proficient at both tasks. These results suggest that shuttlebox avoidance is largely accounted for by classical conditioning of the predominant defensive response. When that response is compatible with performance on the task, acquisition is rapid (AHAs), and when it is not, acquisition is slow (ALAs). 相似文献
19.
John E. Kelsey 《Learning & behavior》1977,5(1):83-92
Male rats which had received approximately 21 min of pulsed, inescapable tail shock during a 6-h session in a wheel-turn chamber were markedly deficient in acquisition of an FR 2 crossing escape response in a shuttlebox when first tested 22 or 70 h later (Experiments 1 and 2). Rats which had received identical amounts and patterns of escapable/avoidable shock, however, were not deficient (Experiment 1). Preventing wheel-turn responses during the inescapable shocks prevented the occurrence of the subsequent escape deficit, whereas reducing the feedback provided for the first crossing response of the FR 2 requirement enhanced the deficit (Experiment 3). These data can be best explained by the learned helplessness hypothesis and indicate that the types of responses available and made during the inescapable shocks are more important than previously indicated. 相似文献
20.
Douglas A. Williams 《Learning & behavior》1994,22(2):203-213
Extinction of rats’ conditioned defensive freezing responses in a context associated with two bouts of massed shock (3 sec) separated by a long unreinforced interbout interval was slower than that in a context associated with distributed shock (60 sec). Resistance to extinction following two bouts of massed shock depended on the rats’ remaining undisturbed in the conditioning context during the long unreinforced interbout interval. Slow extinction of freezing was attributed to either the summation of temporal conditioning at the early and late session times or the formation of an association between the early and late bouts of shock. Importantly, the effects of the two bouts of massed shock could not be explained by what is known about the reinforcing effectiveness of massed shock. 相似文献