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[Learning and resistance to extinction in external-self dual reinforcement as compared with those in external reinforcement].

Learning and resistance to extinction in external-self dual reinforcement (ESR) were compared with those in external reinforcement (ER). delta ESR (delta: extinction process) was also compared with the corresponding process of other two conditions; 1) discontinuation of self reinforcement after external-self dual reinforcement (delta SR), 2) discontinuation of external reinforcement following the dual reinforcement (delta ER). Undergraduates (n = 58 in Experiment I, n = 74 in Experiment II) were randomly assigned to one of the four conditions. Subjects were given association learning in Exp. I and memory task in Exp. II, respectively. Those who responded successfully were then shifted to extinction session for testing. Effects of ESR on learning were same as those of ER in the two experiments. Resistance to extinction in Exp. I was significantly higher for delta SR and delta ESR as compared with delta ER and *ER (extinction switched from external reinforcement). Resistance for delta SR in Exp. II was significantly higher than for the remaining conditions. Based on these findings, high level of the resistance for delta ESR was discussed by attributing it to the internalization of ESR.

Adult↗

Different requirements for protein synthesis in acquisition and extinction of spatial preferences and context-evoked fear.

Many molecular accounts of long-term memory storage postulate that the synthesis of new proteins is necessary for long-term changes in neuronal function. These experiments generally have examined the learning that occurs as associations are acquired between neutral and biologically important stimuli. Little is known about the importance of protein synthesis in the establishment of memories for extinction, which occurs as the relations established during acquisition are severed. Extinction appears to be an active learning process that results in the formation of new memories rather than in the simple erasure or forgetting of memories from acquisition. Furthermore, under certain circumstances, extinction can result in long-term changes in behavior lasting for days to weeks. Here we show that although memories for the acquisition of spatial and contextual learning required protein synthesis, memories for extinction formed in the absence of protein synthesis. These results suggest that acquisition and extinction are mediated by distinct molecular mechanisms and that long-term memories can form in the absence of protein synthesis.

Animals↗

Mitogen-activated protein kinase cascade in the basolateral nucleus of amygdala is involved in extinction of fear-potentiated startle.

Previous results indicate that intra-amygdala infusions of NMDA receptor antagonists block the extinction of conditioned fear. Mitogen-activated protein kinase (MAPK) can be activated by NMDA receptor stimulation and is involved in excitatory fear conditioning. Here, we evaluate the role of MAPK within the basolateral amygdala in the extinction of conditioned fear. Rats received 10 light-shock pairings. After 24 hr, fear was assessed by eliciting the acoustic startle reflex in the presence of the conditioned stimulus (CS) (CS-noise trials) and also in its absence (noise-alone trials). Rats subsequently received an intra-amygdala or intrahippocampal infusion of either 20% DMSO or the MAPK inhibitor PD98059 (500 ng/side) followed 10 min later by 30 presentations of the light CS without shock (extinction training). After 24 hr, they were again tested for fear-potentiated startle. PD98059 infusions into the basolateral amygdala but not the hippocampus significantly reduced extinction, which was otherwise evident in DMSO-infused rats. Control experiments indicated that the effect of intra-amygdala PD98059 could not be attributed to lasting damage to the amygdala or to state dependency. These results suggest that a MAPK-dependent signaling cascade within or very near the basolateral amygdala plays an important role in the extinction of conditioned fear.

Amygdala↗

Treatment of infant sleep disturbance by trimeprazine in combination with extinction.

Chronic sleep disturbance is a common problem in preschool children. Prescription and non-prescription sedatives provide short-term palliative relief. Behavioral extinction by withdrawal of parental attention is enduringly effective but may be distressing short-term because of postextinction bursts of intense activity by the child. This study evaluated the effects of combining extinction and sedative medication (trimeprazine tartrate), prescribed in a reducing dose over the first 10 days of extinction. Control groups received either extinction alone or a placebo administered double-blind. After baseline, all subjects reduced their sleep disturbance to low levels, the extinction and placebo groups declining slowly, the medication group abruptly. These gains were maintained at follow-up. Measures of infant security and maternal anxiety showed improvements with treatment.

Arousal↗

[Responses of the reticular nucleus neurons and dorsal thalamic nuclei neurons in the cat during extinction of a conditioned instrumental reflex].

Activity of 66 neurons of the reticular nucleus (R), 31 neurons of the ventroposterolateral nucleus and 14 neurons of the posterolateral nucleus-pulvinar complex of the thalamus was investigated during extinction of the conditioned instrumental alimentary reflex. The quantity of R neurons that show initial excitation in response to the conditional stimulus in the first 300 ms decreased during extinction. Conditioned placing reactions and late excitatory and inhibitory neuronal responses in the R and dorsal thalamic nuclei with latency above 300 ms disappeared during extinction simultaneously. The background unit activity decreased during extinction in the 2/3 of investigated neurons of R and dorsal thalamic nuclei. It is suggested that the efferent influence from the R decreased during extinction.

Animals↗

Visual neglect and extinction: a new test.

A new computerized test for visual neglect and extinction was developed and evaluated by testing twenty-five patients with right-hemisphere cerebrovascular accidents. The test consisted of a series of unilateral or bilateral lights on a semicircular array to which the subject responded by pushing a button. A computer controlled the sequence of stimuli and stored the responses. Results of the computer test were compared to conventional occupational therapy and beside clinical tests. Extinction was present in 16 subjects on the computerized test, and in 11 on the clinical test. Neglect was present in 13 subjects on the computerized test, in seven subjects on the occupational therapy test, and in five subjects on the clinical test. The computerized test was more sensitive than the other tests. On both computerized and clinical testing, all subjects with left-sided neglect also had left-sided extinction, but not all subjects with extinction had neglect. Neglect may represent a more severe manifestation of an underlying perceptual defect that produces both neglect and extinction.

Adolescent↗

Eyelid conditioning and intellectual level: effects of contextual change on extinction.

A repeated acquisition-extinction paradigm was used to investigate effects of auditory-verbal cues on the ordinarily slow extinction rate of conditioned eyelid responses of mentally retarded adults. Abrupt extinction occurred as a consequence of nearly filling extinction intertrial intervals with either relevant or irrelevant phrases, but the extinction rate was unaffected by a brief phrase in place of the absent unconditioned stimulus. Also, no evidence of transfer was found following reacquisition, when verbal cues were omitted entirely from reextinction. A contextual-change hypothesis, in terms of interference with memory of the unconditioned stimulus, was suggested to account for the data.

Acoustic Stimulation↗

Extinction of conditioned eyelid responses requires the anterior lobe of cerebellar cortex.

We test the hypothesis that the cerebellar cortex is required for the extinction of conditioned eyelid responses in rabbits trained using standard Pavlovian delay procedures. Following 10 daily training sessions during which rabbits achieved asymptotic performance, lesions of the ipsilateral hemisphere of the cerebellar cortex were made by aspiration. The target of these lesions was the anterior lobe, as suggested by previous observations that this region is necessary for the learning-dependent timing of conditioned eyelid responses (Perrett et al., 1993). We report that anterior lobe damage, as indicated by disrupted response timing and confirmed by tissue analysis, produces severe deficits in conditioned response extinction. Postlesion responses show no significant decline over ten training sessions, whereas response timing and extinction are unaffected by lesions that do not include the anterior lobe. These conditioned responses that do not extinguish display stimulus specificity, excluding the possibility that they are unlearned responses unmasked by cerebellar cortex lesions. These observations suggest that Pavlovian eyelid conditioning is mediated by synaptic plasticity in at least two sites and the anterior lobe of the cerebellar cortex influences one of these sites during extinction. Based on these and previous data, we propose the hypothesis that eyelid conditioning can involve plasticity in both the cerebellar cortex and interpositus nucleus and that plasticity in the nucleus is controlled by input from Purkinje cell activity in the cortex. This hypothesis is consistent with observations that the cerebellar cortex may not always be required for the expression of conditioned responses, but it is necessary for response timing and for extinction.

Animals↗

[The extinction of conditioned food reflexes acquired based on the dominant].

Extinction of alimentary conditioned responses, elaborated on the basis of the hunger dominant, when the animal, despite the realization of one-eye blinking reaction, did not receive food, took place in the course of 4-8 experiments. This process was of undulatory character. At the initial stage of extinction the manifestation of the swallowing and chewing reactions intensified, the amplitude of the blinking reaction of the trained eye increased and often acquired a tonic form, blinking of two eyes appeared, the general motor activity of the animal raised. At the end of extinction, when the goal-directed blinking reaction was absent, the number of the swallowing and chewing movements lowered, the general motor activity of the animal was decreased. It is suggested that at the first stage of extinction growing excitation takes place in the motivational "hunger centre". The process irradiates to other centres, as a result the behavioural reactions under study are realized. At the end of extinction the concentration of excitation takes place, leading to and absence of activation of the temporary connection between the "hunger centre" and the "blinking centre".

Acoustic Stimulation↗

Molecular extinction coefficients of lead sulfide and polymerized diaminobenzidine as final reaction products of histochemical phosphatase reactions.

Molar extinction coefficients of precipitated lead sulfide (PbS) and polymerized diaminobenzidine (polyDAB) have been determined at wavelengths of 450 nm and 480 nm, respectively, for quantitative histochemical analysis of phosphatase reactions. These values are essential for the conversion of cytophotometric (mean integrated) absorbance values to absolute units of substrate converted per unit time and volume of tissue. This conversion allows direct comparison of histochemical and biochemical data. The molar extinction coefficient of PbS at 450 nm was found to be 3,800 and therefore, per mole phosphate liberated, the molar extinction coefficient is 5,700 because 3 moles phosphate are captured by 2 moles lead at neutral or alkaline pH. Parallel experiments with the cerium-DAB method revealed that the molar extinction coefficient of polyDAB at 480 nm is 5,500 with respect to liberated phosphate. The molar extinction coefficients were applied for comparison of data from biochemical and histochemical assays of glucose-6-phosphatase activity in rat livers. A significant correlation was found between both sets of data. The values were in the same order of magnitude with histochemical values approximately 1.4 times higher than biochemical values.

3,3'-Diaminobenzidine↗

Extinction dynamics in mainland-island metapopulations: an N-patch stochastic model.

A generalization of the well-known Levins' model of metapopulations is studied. The generalization consists of (i) the introduction of immigration from a mainland, and (ii) assuming the dynamics is stochastic, rather than deterministic. A master equation, for the probability that n of the patches are occupied, is derived and the stationary probability Ps(n), together with the mean and higher moments in the stationary state, determined. The time-dependence of the probability distribution is also studied: through a Gaussian approximation for general n when the boundary at n = 0 has little effect, and by calculating P(0, t), the probability that no patches are occupied at time t, by using a linearization procedure. These analytic calculations are supplemented by carrying out numerical solutions of the master equation and simulations of the stochastic process. The various approaches are in very good agreement with each other. This allows us to use the forms for Ps(0) and P(0,t) in the linearization approximation as a basis for calculating the mean time for a metapopulation to become extinct. We give an analytical expression for the mean time to extinction derived within a mean field approach. We devise a simple method to apply our mean field approach even to complex patch networks in realistic model metapopulations. After studying two spatially extended versions of this nonspatial metapopulation model--a lattice metapopulation model and a spatially realistic model--we conclude that our analytical formula for the mean extinction time is generally applicable to those metapopulations which are really endangered, where extinction dynamics dominates over local colonization processes. The time evolution and, in particular, the scope of our analytical results, are studied by comparing these different models with the analytical approach for various values of the parameters: the rates of immigration from the mainland, the rates of colonization and extinction, and the number of patches making up the metapopulation.

Animals↗

Single-species models of the Allee effect: extinction boundaries, sex ratios and mate encounters.

We critically review and classify models of single-species population dynamics subject to the demographic Allee effect with emphasis on non-spatial, deterministic approach. Inclusion of spatial movement and stochastic phenomena does not substantially change the behaviour; stochasticity only "blurs" step-like character of the Allee effect into a sigmoidal form. The outcome of all non-spatial, deterministic models is either unconditional extinction, extinction-survival scenario (ES), or unconditional survival. Three major model classes are recognized: (1) one-dimensional heuristic models, (2) one-dimensional models with mating probability and fixed sex ratio, and (3) two-sex models with variable adult sex ratio. Each class is characterized by the shape of extinction boundary which separates extinction from survival in the ES scenario. The latter two classes may give better predictions of extinction thresholds than heuristic models but require specific information and are data intensive. In one-dimensional models with fixed sex ratio, population cannot survive if density/number of males decreases below some threshold while there is no such restriction on females. Individual-based models seem to be most capable of explaining mechanisms leading to the Allee effect.

Animals↗

Conditioned Inhibition Produced by Extinction of a Conditioned Stimulus

Four experiments used a conditioned taste aversion procedure to examine the potential for CS-alone extinction treatment to produce a conditioned stimulus that possesses inhibitory properties. In Experiment 1, saccharin was paired with LiCl, and then saccharin was presented alone for several trials to produce extensive behavioral extinction. Animals receiving this treatment were retarded in reacquiring conditioned responding to saccharin relative to control subjects receiving conditioning to the flavor for the first time. In Experiment 2, the extinguished saccharin stimulus was shown to decrease conditioned responding to a known excitor when the two stimuli were presented in compound as a summation test. Experiments 3A and 3B replicated the findings of Experiments 1 and 2 while providing evidence that the effects were not due to the differential effects of neophobia during testing. These three experiments revealed that an extinguished conditioned excitor passes retardation and summation tests for conditioned inhibition. Experiment 4 found that extinction of a known excitor was slowed when the excitor was extinguished in compound with a previously extinguished conditioned stimulus. That is, an extinguished CS provided protection from extinction to another CS, a finding also consistent with the view that extinction produces conditioned inhibition.

Journal Article↗

Extinction risk in a temporally correlated fluctuating environment.

Usually extinction risk due to environmental stochasticity is estimated under the assumption of white environmental noise. This holds for a sufficiently short correlation time tauc of the fluctuations compared to the internal time scale of population growth r-1 (tauc/r-1<<1). Using a time-discrete simulation model we investigate when the white noise approximation is misleading. Environmental fluctuations are related to fluctuations of the birth and death rates of the species and the temporal correlation of these fluctuations (coloured noise) is described by a first-order autoregressive process. We found that extinction risk increases rapidly with correlation time tauc if the strength of noise is large. In this case the white noise approximation underestimates extinction risk essentially unless temporal correlation is very small (tauc/r-1<<0.1). Extinction risk increases only slowly with correlation time if the strength of noise is small. Then the white noise approximation may be used even for stronger temporal correlations (tauc/r-1>/=0.1). Thus, the estimation of extinction risk on the basis of white or coloured noise must be justified by time scale and strength of the fluctuations. Especially for species that are sensitive to environmental fluctuations the applicability of the white noise approximation should be carefully checked.

Animals↗

The relationship between species detection probability and local extinction probability.

In community-level ecological studies, generally not all species present in sampled areas are detected. Many authors have proposed the use of estimation methods that allow detection probabilities that are <1 and that are heterogeneous among species. These methods can also be used to estimate community-dynamic parameters such as species local extinction probability and turnover rates (Nichols et al. Ecol Appl 8:1213-1225; Conserv Biol 12:1390-1398). Here, we present an ad hoc approach to estimating community-level vital rates in the presence of joint heterogeneity of detection probabilities and vital rates. The method consists of partitioning the number of species into two groups using the detection frequencies and then estimating vital rates (e.g., local extinction probabilities) for each group. Estimators from each group are combined in a weighted estimator of vital rates that accounts for the effect of heterogeneity. Using data from the North American Breeding Bird Survey, we computed such estimates and tested the hypothesis that detection probabilities and local extinction probabilities were negatively related. Our analyses support the hypothesis that species detection probability covaries negatively with local probability of extinction and turnover rates. A simulation study was conducted to assess the performance of vital parameter estimators as well as other estimators relevant to questions about heterogeneity, such as coefficient of variation of detection probabilities and proportion of species in each group. Both the weighted estimator suggested in this paper and the original unweighted estimator for local extinction probability performed fairly well and provided no basis for preferring one to the other.

Animals↗

Auditory cortex lesions prevent the extinction of Pavlovian differential heart rate conditioning to tonal stimuli in rabbits.

The present study examined the role of the auditory cortex in the extinction of differentially conditioned heart rate (HR) responses in rabbits. Lesions were placed bilaterally in either the auditory cortex or the visual cortex. Three days after recovery from surgery, the auditory cortex lesion group and the visual cortex lesion control group were habituated to the tonal conditioned stimuli (CSs), and then given 2 days of Pavlovian differential conditioning (60 trials per day) in which one tone (CS+) was always paired with the unconditioned stimulus and another tone (CS-) was never paired with the unconditioned stimulus. Animals that had demonstrated reliable differential conditioning (CS+ response at least 5 beats greater than the CS- response) were placed on an extinction schedule for 7 days. The extinction schedule was identical to the differential conditioning schedule with the exception that shock never followed the CS+. The results of the study indicate that auditory cortex lesions prevent the extinction of differential bradycardia conditioned responses (CRs) to tonal CSs. Whereas the bradycardia responses to the CS+ quickly extinguished in the group that had control lesions in the visual cortex, the auditory cortex lesion group continued to exhibit significantly larger bradycardiac HR CRs to the CS+ relative to the CS- during all 7 days of extinction. These results suggest that the animals in the auditory cortex lesioned group did not inhibit responses to a previously reinforced stimulus (i.e., CS+) as well as animals with control lesions in the visual cortex.

Acoustic Stimulation↗

Modulation of long-term memory and extinction responses induced by growth hormone (GH) and growth hormone releasing hormone (GHRH) in rats.

The purpose of this work is to study the participation of growth hormone (GH) and growth hormone releasing hormone (GHRH) in the modulation of long-term memory and the extinction response of a passive avoidance task in rats. However, the effect on memory vary according to the age of the animals due to plasma levels of either hormone being modified during the aging process. Male Wistar rats were divided according to age into two experimental blocks (young rats 3 months old and aged rats 24 months old at the start of the experiment) where each block received the same treatment. Each experimental block was then divided randomly into three groups where two were experimental and the other served as control. The animals were then submitted to a one-trial passive avoidance conditioning and tested for memory retention 24 hrs after as well as twice a week until the extinction response occurred. The control group received an isotonic saline solution and the other two groups received 0.8 U.I. of GH or 4 mcg of GHRH respectively. All substances were in a 0.08 ml volume and applied 24 hrs before training as well as 24 hrs before each retention session. The results indicate that GH and GHRH modulate long-term memory as well as the extinction response and in either case the response seems to vary with age. GH and GHRH facilitates long-term memory in young rats but not in aged rats. Finally, whereas GH delays the extinction response in both groups, GHRH retards the extinction only in aged rats.

Aging↗

Effects of receptor blockers on ACTH-induced changes in extinction of active avoidance reflex in rat.

The actions of blockers of dopaminergic receptors (haloperidol), alpha-receptors (phenoxybenzamine), beta-receptors (propranolol) and muscarinic cholinergic receptor (atropine) on the ACTH-induced delay of the extinction of active avoidance behavior were studied in rats. In the doses used, none of the receptor blockers modified the extinction of active avoidance behavior. ACTH delayed the extinction. However, the dopamine receptor blocker (haloperidol) and the muscarinic cholinergic receptor blocker (atropine) did prevent the action of ACTH in delaying the extinction of active avoidance behavior, whereas the alpha-(phenoxybenzamine) and beta- (propranolol) receptor blockers were ineffective. The results suggest that mainly dopaminergic and cholinergic mediations are involved in the delaying action of ACTH on the extinction of active avoidance behavior.

Adrenocorticotropic Hormone↗