Social reinforcement of somatic versus psychological description of depressive events

The cultural construction of illness model explains the clinical observation that psychological correlates of depression such as sadness and worthlessness are frequently reported in Western cultures, whereas somatic or vegetative complaints are often associated with depression in non-Western cultures. This study employed Portnoy and Salzinger's (J. Gen. Psychol. 70 (1964) 311) verbal conditioning paradigm to determine whether social contingencies, in the form of verbal and non-verbal reinforcement contingent upon verbal responses, affect the reporting of experiences related to depressive events. Using an ABA design, this experimental study (N=36) demonstrated that one's reporting of experiences of hypothetical depressive events, via psychological, somatic, or neutral verbal response classes, can be conditioned by verbal and non-verbal positive social reinforcement, and therefore socially constructed through environmental contingencies. This suggests one pathway by which culture can shape symptom presentation. Implications for clinical interviewing and behavioral assessment, especially in the cross-cultural context, are discussed.     

Classical fear conditioning in the anxiety disorders: a meta-analysis

Fear conditioning represents the process by which a neutral stimulus comes to evoke fear following its repeated pairing with an aversive stimulus. Although fear conditioning has long been considered a central pathogenic mechanism in anxiety disorders, studies employing lab-based conditioning paradigms provide inconsistent support for this idea. A quantitative review of 20 such studies, representing fear-learning scores for 453 anxiety patients and 455 healthy controls, was conducted to verify the aggregated result of this literature and to assess the moderating influences of study characteristics. Results point to modest increases in both acquisition of fear learning and conditioned responding during extinction among anxiety patients. Importantly, these patient-control differences are not apparent when looking at discrimination studies alone and primarily emerge from studies employing simple, single-cue paradigms where only danger cues are presented and no inhibition of fear to safety cues is required.     

Cannabinoid agonists and antagonists modulate lithium-induced conditioned gaping in rats

Considerable evidence indicates that conditioned gaping in rats reflects nausea in this species that does not vomit. A series of experiments evaluated the potential of psychoactive cannabinoid agonists, Δ-9-THC and HU-210, and non-psychoactive cannabinoids, Cannabidiol (CBD) and its dimethylheptyl homolog (CBD-dmh), to interfere with the establishment and the expression of conditioned gaping in rats. All agents attenuated both the establishment and the expression of conditioned gaping. Furthermore, the CB1 antagonist, SR-141716, reversed the suppressive effect of HU-210 on conditioned gaping. Finally, SR-141716 potentiated lithium-induced conditioned gaping, suggesting that the endogenous cannabinoid system plays a role in the control of nausea.     

Variable-ratio conditioning history produces high- and low-rate fixed-interval performance in rats

Four rats were exposed to an A-B-A-B series of 30 sessions each of variable-ratio 20 (A) and fixed-interval 30-s (B) schedules. Four other rats received 120 sessions of fixed-interval 30 s. The rats with a history of variable-ratio responding subsequently showed primarily high or low response-rate patterns on the fixed-interval schedule without evidence of classical scalloping (i.e., increased rates of responding throughout the interreinforcement interval), except infrequently in 1 rat. The rats exposed to only the fixed-interval 30-s schedule displayed the expected sequence of scalloping giving way to lower rate break-run or simply low-rate responding over time. This experiment shows that when naive rats are exposed to even a simple history of reinforcement (in this case, a variable-ratio 20), their subsequent fixed-interval performance is very different from comparable performance in naive rats, and might be said to be more similar to the responding of adult humans. The argument is made that care should be taken in comparing the fixed-interval performance of humans and nonhumans because humans have a complex history of reinforcement, whereas laboratory nonhumans are typically naive.     

Signaled avoidance in the eye withdrawal reflex of the green crab

Learning in a signaled avoidance procedure was studied in the eye withdrawal reflex of the green crab, Carcinus maenas. A puff of air to the eye, which causes eye retraction, was used as the unconditioned stimulus (US). A mild vibration on the carapace, which has no effect on untrained animals, was used as a warning (conditioned) stimulus (CS). Eye withdrawal during the CS led to the omission of the otherwise scheduled US. Acquisition was rapid, reaching about 75% avoidance after 30 trials. Extinction occurred slowly over the course of 40 CS-only trials. Yoked controls did not perform as well. The behavior of experimental animals in the avoidance procedure was found to be essentially identical to the performance of animals subjected to a classical conditioning paradigm in which CS responses had no effect on US presentation. Additional groups of animals were subjected to experiments in which (a) avoidance conditioning (60 trials) was followed by classical conditioning (40 trials) or (b) classical conditioning was followed by avoidance. The behavior of these groups was, again, essentially identical. The results suggest that there may be an underlying Pavlovian mechanism for the learned response, although the contribution of an operant process is not excluded. The results expand the range of invertebrate animals in which fundamental conditioning phenomena can be demonstrated, and may provide a neuronal model for learning in a signaled avoidance procedure.     

Electrodermal conditioning to stimuli of evolutionary significance: Failure to replicate the preparedness effect

In the present study, an attempt was made to replicate the preparedness effect reported by Öhman, Fredrickson, Hugdahl, & Rimmö (1976). Following Öhman et al. (1976) as closely as possible, a differential conditioning procedure was carried out in which subjects'skin conductance responses (SCRs) were conditioned either to stimuli of evolutionary significance (slides of snakes and spiders) or to evolutionally neutral stimuli (slides of mushrooms and flowers). The experiment consisted of 8 habituation, 12 acquisition, and 20 extinction trials. Electric shock served as an unconditioned stimulus during the acquisition phase. Although SCRs showed significant decreases during habituation and were significantly influenced by the conditioning procedure during acquisition, they were not found to extinguish significantly more slowly in the group that saw slides of snakes and spiders. This result contradicts the earlier results reported by Öman and colleagues. Possible explanations for this failure to replicate their results are discussed.     

Conditioned orienting and defensive responses in the developing rat

Infant rats (16, 21, and 26 days old) received 3 days of classical conditioning training to Tone/Shock pairings using heart rate as the index of conditioning. The youngest group (16 days old) showed no evidence of conditioning at any stage of acquisition. In the 21- and 26-day-olds, response to the conditioned stimulus (CS) was a deceleration in heart rate during the first day of training. By day 3, the conditioned response (CR) shifted to cardioacceleration. The data were interpreted as offering strong support for a two-stage model of information processing in the infant rat, comprised of a conditioned orienting response in the first stage and a conditioned defensive response in the second.     

Emotional modulation of attention orienting: A classical conditioning study

Emotional modulation of attention shifting was investigated in Posner's (1980) spatial orienting task by conditioning the attention cue to an aversive white noise. Prior to the attention task, the Conditioning group received a 90dB white noise unconditioned stimulus (UCS) contingent upon the frame-lit rectangle attention cue, while the Control group received non-contingent presentations. The Conditioning group evidenced greater skin conductance responses to the frame-lit rectangle in the conditioning phase, reflecting an electrodermal conditioned response. In the attention phase, the frame-lit rectangle served as the attention cue in the spatial orienting task. The Conditioning group showed equally fast reaction times (RTs) to targets presented outside the location of the cue as to targets at the same location as the cue, reflecting elimination of the cognitive cost usually involved in shifting attention. The Control group evidenced the regular cost of shifting attention away from the location of the cue. The Conditioning group also evidenced a larger N1-component with a parietal distribution of the event-related brain potentials to the cue and a larger N1-component at the frontal regions to targets presented outside the cued location. This suggests that both visual orienting to the cue and attention shifting from cue to target on invalid trials were amplified by the emotional salience attached to the cue through the classical conditioning procedure.     

Contribution of Ventrolateral Prefrontal Cortex to the Acquisition and Extinction of Conditioned Fear in Rats

The ventrolateral, agranular insular portion of prefrontal cortex (PFC) in rats is involved in visceral functions and has been shown to be involved in emotional processes. However, its contribution to aversive learning has not been well defined. Classical fear conditioning has been a powerful tool for illuminating some of the primary neural structures involved in aversive emotional learning. We measured both the acquisition and the extinction of conditioned fear following lesions of the ventrolateral PFC of rats. Lesions reduced fear reactivity to contextual stimuli associated with conditioning without affecting CS acquisition, and had no effect on response extinction. Ventrolateral PFC may normally be involved in the processing of contextual information while not being directly involved in extinction processes within the aversive domain.     

Mechanics of the animate.

Behavior is treated as basic physics. Dimensions are identified and their transformations from physical specification to axes in behavioral space are suggested. Responses are treated as action patterns arrayed along a continuum of activation energy. Behavior is seen as movement along a trajectory through this behavior space. Incentives or reinforcers are attractors in behavior space, at the centers of basins of lowered potential. Trajectories impinging on such basins may be captured; repeated capture will warp the trajectory toward a geodesic, a process called conditioning. Conditioning is enhanced by contiguity, the proximity between the measured behavior and the incentive at the end of the trajectory, and by contingency, the depth of the trajectory below the average level of the potential energy landscape. Motivation is seen as the potential of an organism for motion under the forces impinging on it. Degree of motivation is characterized by the depth of the potential field, with low motivation corresponding to a flat field and a flat gradient of activation energy. Drives are the forces of incentives propagated through behavior space. Different laws for the attenuation of drive with behavioral distance are discussed, as is the dynamics of action. The basic postulate of behavior mechanics is incentive-tracking in behavior space, the energy for which is provided by decreases in potential. The relation of temporal gradients to response differentiation and temporal discrimination is analyzed. Various two-body problems are sketched to illustrate the application of these ideas to association, choice, scalar timing, self-control, and freedom.