Postnatal development of heart rate patterns elicited by an aversive CS and US in cats

Heart rate and motor responses were recorded in cats of different ages during classical conditioning. A deceleratory-acceleratory heart rate pattern observed during the CS-US interval in one and four-week-old kittens is an alpha conditioned response, a potentiated original response to the CS. At eight weeks of age two new distinct patterns of pure acceleration or pure deceleration are acquired during conditioning and in the absence of motor learning. At 12 weeks of age and in adult subjects, heart rate patterns during the CS-US interval become more complex and conditioned motor responses can be observed. A covariance of HR acceleration and motor responses during the CS-US interval is absent in eight-week-old subjects, but quite high in 12-week-old subjects and adult cats. The data are interpreted as suggesting separate elicitatory mechanisms of HR and motor responses which may show synchrony later in ontogeny.     

Blocking of inhibitory conditioning within a serial conditioned stimulus-conditioned inhibitor compound: Maintenance of acquired behavior without an unconditioned stimulus

Well-trained classically conditioned stimuli, presented unreinforced, were protected from extinction when they were followed by a signal of the omission of the reinforcer (conditioned inhibitor Konorskian type) in eight cats. An aversive classical conditioning paradigm with shock as the reinforcer was used. Of several behavioral (leg flexion, vocalization) and organismic arousal (heart rate, respiration rate, respiration amplitude) measures of conditioned responses, the respiration amplitude changes were found to be most informative for the continuous assessment of elicited arousal of low and medium intensity. In all subjects conditioned stimuli presented during extinction in serial compound with the conditioned inhibitor elicited larger responses than did conditioned stimuli presented alone during extinction. The mechanism of protection from extinction in a paradigm in which the elicitor of learned behavior occurs prior to the conditioned inhibitor provides the organism with the mechanism for the maintenance of learned behavior in the absence of a reinforcer.     

The effect of response force on avoidance rate

In a Sidman-avoidance schedule of counter losses for two human subjects, the loss-to-loss and response-to-loss intervals were 20 sec. The avoidance response was a vocal response that was louder than a minimum vocal requirement. This requirement was set at 80 db, 95 db, or 110 db. In addition to vocal responses meeting the minimum requirement, all responses exceeding a threshold of 75 db or louder were recorded. The rate of both above-threshold and avoidance responses decreased as the response-force requirement increased. Thus, high response-force requirements produced an effect on avoidance responding similar to its effect on positively reinforced responding.     

Differential conditional emotional and cardiovascular responses--a training technique for monkeys

A training technique has been developed which combines classical differential conditioning and conditional emotional response (CER) procedures. After monkeys were trained to lever-press on a variable-interval schedule, two stimulus lights were presented. One light (CS) was always followed, upon termination, by electrical shock; the other light (DS) was never followed by shock. The response to the CS was a decreased rate of lever-pressing and increased heart rate and blood-flow velocity. None of these responses occurred to the DS. This technique eliminates the possibility of pseudoconditioning and provides measurement of both somatic and autonomic responses in a CER situation.     

Operant control of vocal behavior in the cat

Evidence of operant control of vocal behavior in the cat is presented: (1) On mult FR 12 S^Δ schedule, cats miaowed rapidly during periods of S^D and much less or not at all during S^Δ. (2) This control was re-established following reversal of stimuli. (3) The frequency distribution of response durations was shifted to both shorter and longer values by the differential reinforcement of shorter or longer response durations respectively. Since both the frequency and duration of vocal responses were shown to be under the control of the schedule of reinforcement, it is concluded that at least some of the vocal behavior of the cat is susceptible to operant control.     

Classical aversive conditioning of catecholamine and corticosterone responses.

Some earlier work, not rigorously controlled, suggested that conditional increases in sympathoadrenal stress hormones could occur. The purpose of this experiment was to test this idea further using an appropriately controlled design. To do this, we subjected rats living in a tether-type apparatus to differential fear conditioning. Chronic catheterization allowed us to sample blood before and after conditional stimulus probes without having to touch the rats. No evidence for conditional changes in norepinephrine and corticosterone was found. In contrast, differential conditioning of epinephrine responses was found. The conditional response, however, was not a simple one in that conditional increases in epinephrine following CS+ probes were not always seen. These data support the idea that learned changes in hormonal stress respondents can occur. But they leave open the question of why clear cut conditional changes in these visceral systems are so difficult to obtain.     

Classical aversive conditioning of catecholamine and corticosterone responses

Some earlier work, not rigorously controlled, suggested that conditional increases in sympathoadrenal stress hormones could occur. The purpose of this experiment was to test this idea further using an appropriately controlled design. To do this, we subjected rats living in a tether-type apparatus to differential fear conditioning. Chronic catheterization allowed us to sample blood before and after conditional stimulus probes without having to touch the rats. No evidence for conditional changes in norepinephrine and corticosterone was found. In contrast, differential conditioning of epinephrine responses was found. The conditional response, however, was not a simple one in that conditional increases in epinephrine following CS+ probes were not always seen. These data support the idea that learned changes in hormonal stress respondents can occur. But they leave open the question of why clear cut conditional changes in these visceral systems are so difficult to obtain.     

Classically conditioned cardiac responses in "old" and "young" Fischer 344 rats

Male and female Fischer 344 rats, 12 or 26-28 months of age, received two sessions of Pavlovian heart rate conditioning, and were compared with same-sex and same-age controls receiving unpaired presentations of the tone conditional stimulus (CS) and the shock unconditional stimulus (US). Older rats of both sexes demonstrated slower acquisition of the heart rate (HR) conditioned response (CR), and smaller magnitude changes than did the younger animals. Control experiments in 6-, 12-, 24-, and 30-month-old animals indicated that these differences were not due to an impaired sensitivity to the CS or US in the older animals. Results are discussed in terms of their implications for use of this animal model in investigations of age-related deficits in associative learning.     

Attenuation of age-related conditioning deficits in humans by extension of the interstimulus interval

Young (17-22 years) and older (61-86 years) persons underwent classical conditioning of the eye-blink response to a tone conditioned stimulus (CS) and an airpuff unconditioned stimulus (UCS) at 1 of 3 interstimulus intervals (ISIs; 400, 650, and 900 ms). As in a previous study, older subjects conditioned more slowly and emitted fewer conditioned responses at the optimal 400-ms ISI. At longer ISIs, however, this age-related disruption of classical conditioning was attenuated. These differences in conditioning were not due to nonassociative factors, such as sensitivity to the tone CS or airpuff UCS or to differences in spontaneous blink rate, nor were they due to differences in general cognitive abilities. The results are discussed in terms of the role of temporal relationships between stimuli in conditioning across the life span.     

Ageing and attentional control

The research examines the structural bottleneck account and the resource account of the substantial dual-task deficits among older adults. Procedures from two common dual-task methodologies—the psychological refractory period and the relative-priority manipulation—were used to encourage maximization of the joint performance. Performance and time-sharing strategies from subjects between the ages of 20 and 70 years were examined. Age-related declines in time-sharing efficiency and in the precision of the executive control process were observed. The age-related effect was larger when two manual responses were required than when one manual and one vocal response were required, but no evidence for obligatory sequential processing was found. Except for the most demanding conditions, comparable practice effects were observed between the younger and older subjects, suggesting considerable cognitive plasticity in the older subjects. Implications for the two attentional accounts were discussed.     

Hippocampal regulation of context-dependent neuronal activity in the lateral amygdala

Pavlovian fear conditioning is a robust and enduring form of emotional learning that provides an ideal model system for studying contextual regulation of memory retrieval. After extinction the expression of fear conditional responses (CRs) is context-specific: A conditional stimulus (CS) elicits greater conditional responding outside compared with inside the extinction context. Dorsal hippocampal inactivation with muscimol attenuates context-specific CR expression. We have previously shown that CS-elicited spike firing in the lateral nucleus of the amygdala is context-specific after extinction. The present study examines whether dorsal hippocampal inactivation with muscimol disrupts context-specific firing in the lateral amygdala. We conditioned rats to two separate auditory CSs and then extinguished each CS in separate and distinct contexts. Thereafter, single-unit activity and conditional freezing were tested to one CS in both extinction contexts after saline or muscimol infusion into the dorsal hippocampus. After saline infusion, rats froze more to the CS when it was presented outside of its extinction context, but froze equally in both contexts after muscimol infusion. In parallel with the behavior, lateral nucleus neurons exhibited context-dependent firing to extinguished CSs, and hippocampal inactivation disrupted this activity pattern. These data reveal a novel role for the hippocampus in regulating the context-specific firing of lateral amygdala neurons after fear memory extinction.     

Domain-specific responses to power-based interaction

Variations in power-relevant information-processing (response latency on a lexical-decision making task), acoustical responses (vocal amplitude and pitch), and affective responses were measured as a function of a power-relevant priming manipulation, and gender. When participants were primed for a power challenge (as opposed to other challenges), males (but not females) manifested exceptionally fast processing of power-relevant adjectives - suggesting the greater accessibility of power cues for males. Regardless of gender, participants primed for a power challenge manifested lower vocal amplitude (consistent with a de-escalating strategy). However, only women manifested an elevated pitch level and self-reported apprehension - indicating that women, even more than men show a de-escalating response to a power challenge.     

The beginning of conversation: Early patterns of mother-infant vocal responsiveness

Microanalytic techniques were used to characterize the structure of the prespeech communication of 4-month-old infants and their mothers. Two observers continuously recorded the interactive behavior of mothers and their infants during hour-long observations in the homes of 25 families. Loglinear models were used to examine the extent to which the vocal behavior of one person was conditional upon the vocal behavior of the partner. Within the limits of this microanalytic approach, analyses indicated that patterns of mother-infant vocal exchange were structurally similar to patterns of adult conversation. Initial vocal responses were followed by suppression of vocalization, allowing the partner to join the conversation. The comparative effectiveness of vocal behavior as an elicitor of vocalization and as a response to vocalization was shown for mothers and infants relative to the other behaviors observed. Vocalization served as a modulator of visual attentiveness: When the partner was not visually attentive, vocalization elicited visual attention.     

An apparatus for behavioral and physiological study of aversive conditioning in cats and kittens

An apparatus for aversive conditioning of adult cats and kittens is described. Animals are held by a cloth harness and head restraint device in a metal frame with a movable treadmill floor. They are supported in a natural standing position, with freedom to flex and move each leg and to walk or run on the treadmill. Various transducers record respiration, EKG, vocalization, leg flexion, and locomotion on the treadmill.     

Similarity of cardiac CR forms in the rhesus monkey during several experimental procedures

Cardiac rates of rhesus monkeys were observed in a variety of different conditioning procedures, each of which involved a visual stimulus (CS) followed by an electric shock (US). With a 30-sec CS, cardiac rate accelerated rapidly after CS onset, reached a maximum in the middle of CS, and decelerated thereafter, with a terminal CS rate often at the level of, or below, pre-CS levels. A similar biphasic cardiac rate response in CS was also observed under subsequent exposure to intermittent pairings of CS and US, avoidance of US, response-produced termination of US, and when CS-US pairings were superimposed upon an avoidance baseline, even when CS duration was varied from 12 to 60 seconds. The unusual regularity of cardiac rate responses in several different procedures may result from one or more of these factors: (a) characteristics of the rhesus monkey, (b) initial exposure to Pavlovian conditioning, or (c) the uniformity of measurement of cardiac rate employed in this study.     

Imitation of mother’s inappropriate food preference in weanling kittens

Experiments were performed on four mother cats and their 22 kittens from 7 litters. Each mother was trained to eat banana or mashed potato in the presence of meat pellets in order to get a hypothalamic stimulation reward. Eighteen of twenty-two weanling kittens which accompanied the mother during the session imitated the mother in eating banana or potato and ignored meat pellets. The imitation of the mother started not earlier than at 35 days of age and in most kittens (10 of 18) began between 49 and 56 days of age. The kittens which ate banana or potato with the mother also ate that food when tested alone after weaning at 9 to 27 weeks of age, either during 10 min sessions in the experimental compartment or during 24 hr tests in the home compartment. When banana was offered to 9 control 13–23 week old kittens (of three other mothers) who never before had eaten that food or had seen their mother eat it, 8 of them did not consume banana during three 24 hr tests. Some consumption, however, occurred in the ninth kitten during the third of these tests. It has been concluded that weanling kittens in the period of transition from maternal to independent feeding tend to imitate the mother in food preferences, even if the food chosen by the mother is unusual for their species. The food preferences acquired through the imitation of the mother may influence the food preferences at the later stages of life.     

The problem of switching in conditional behavior

This article reviews studies of various authors on the phenomenon of “switching,” which is observed in both classical and instrumental conditioning and consists in elicitation of different responses to the same conditional stimulus (CS) when it is applied in an environment different than the original one. The different responses include a decrease or an absence of the previously trained conditional response (CR), elicitation of an appetitive response instead a defensive one, or vice versa, as well as elicitation of two different instrumental CRs in the same trial. The studies suggest that, due to the repeated occurrence of CS in the same environment (E), also called “situation” or “context,” associations are formed between CS and E. Consequently, the CR is elicited to a compound CS+E rather than to CS alone. When the CS is applied alone in a different E than the original one, the previously formed associations are inactive and the CR cannot be elicited; this leads to switching. Studies also suggest that E plays a dominant role in conditioning compared with that of CS alone, which often appears to be only a trigger for eliciting the response. However, CS tested in a different E may still produce some components of the previously acquired CR, such as a general fear behavior to an originally defensive CS or an approach behavior to an originally alimentary CS. The environmental stimuli can be considered the “determining” stimuli that determine the kind of reaction to be elicited, or “tonic” stimuli that increase the tonus in the brain but do not elicit the CR. The “determining” or “tonic” stimuli do not seem to be a special class of stimuli. Instead, they are stimuli that initially can produce the CR (e.g., intertrial CRs), but by being not reinforced they become partly inhibited; nevertheless, due to associations with the reinforcement, they still can produce some excitement related to it, thus facilitating the CR.     

Reinforcement strength in classical conditioning of leg flexion,freezing, and heart rate in cats

Stable leg-flexion CRs were successfully elaborated in cats receiving tone-strong shock pairings, but not in cats receiving tone-weak shock pairings. Both shock USs elicited reliable flexion URs in the presence of the CS, thus satisfying the contiguity requirement basic to the Pavlovian paradigm. Elaboration of the flexion CRs required a large number of trials relative to the conditioned freezing and decelerative heart rate responses which appeared after only a very few trials in the strong-US cats. As with flexion CRs, freezing and heart-rate responses never developed with the weak-shock US. When the weak-US cats were later switched to the strong US, freezing and heart-rate CRs quickly appeared and flexion CRs appeared after fewer strong-US trials than in cats receiving the strong shock originally. The results were interpreted as supporting a reinforcement conception of classical defense conditioning and as indicating the importance of using a US capable of eliciting emotional responses.     

The role of muscle tension in “repression”

Using an active partial avoidance conditioning paradigm, muscle tension was conditioned to a verbal conditional stimulus (CS), and recall of words semantically unrelated and related to the CS was tested under conditions of three levels of induced muscle tension with 20 subjects (Ss). Results showed the expected decrease in latency of response with moderate tension for all stimuli during the pretreatment period and for the unrelated words during the posttreatment period and a significant increase in latency of response for the related words during the posttreatment period. It is suggested that if the level of muscle tension associated with the conditional response (CR) is induced in Ss, then recall of CS-related material will be inhibited or “repressed.”     

Autonomic nervous control of heart rate orienting and alpha responses in dog

The object of this experiment is to study the autonomic nervous control of alpha responses elicited in classical conditioning. Twenty-two mongrel dogs were trained in classical discriminative conditioning. Typical two-phase tachycardic responses were observed in positive (CS+) trials while only the earliest, phase 1, response was observed in negative (CS-) trials. The phase 1 response, which was identical in CS+ and CS-trials, was compared in dogs before and after selective SA-nodal parasympathectomy (N=7) and beta-adrenergic blockade (N=11). The phase 1 tachycardic response was eliminated by selective SA-nodal parasympathectomy but not by beta-adrenergic blockade. We conclude that the phase 1 response observed in both CS+ and CS-trials with similar time sequence and magnitude is an alpha response. The heart rate orienting response results from a withdrawal of parasympathetic activity with little or no change in sympathetic tone.