Behavioral determinants of drug action. The contributions of Peter B. Dews

Peter B. Dews played a significant role in shaping the distinctive characteristics and defining the underlying principles of the discipline of behavioral pharmacology. His early and sophisticated use of schedules of reinforcement in the 1950s, incorporated from research in the experimental analysis of behavior and integrated into the discipline of pharmacology, provided tremendous insight, inspiration, and impetus to the newly emerging field of behavioral pharmacology. The experimental findings generated by Dews' research, blending the sophisticated use of behavior and pharmacological principles together with the elegant manner of their presentation and far-reaching implications, provided the force and momentum to establish and direct behavioral pharmacology for several decades. This article attempts to capture some of Dews' research that integrated and inspired the blending of sophisticated behavioral work with that of pharmacology.     

Inhibitory priming effects in auditory word recognition: when the target's competitors conflict with the prime word

Several studies indicate that the number of similar sounding words that are activated during recognition is a powerful predictor of performance on auditory targets. Words with few competitors are processed more quickly and accurately than words with many competitors. In the present study, we examined the contribution of the competitor set size in determining the magnitude of the inhibitory priming effect. The data show that the priming effect is stronger when word targets have few competitors. This result supports the view of direct competition between lexical candidates.     

A procedure for generating differential "sample" responding without different exteroceptive stimuli

Sidman (1994, 2000) suggested that responses as well as stimuli can join equivalence classes, a hypothesis difficult to test because differential responding typically requires different stimuli. The present experiments describe a procedure with pigeons that avoids this potential confounding effect. In Experiment 1, spacing two responses 3 s apart (a differential-reinforcement-of-low-rate [DRL] schedule) to a white stimulus on some trials produced food or the comparison stimuli in a matching task, whereas pecking 10 or more times with no temporal restrictions (a fixed-ratio [FR] schedule) produced the same effect on other trials. Completing the alternative (unscheduled) requirement terminated the white stimulus and repeated the trial. Following such errors, pigeons learned to switch to the alternative response pattern on the repeat trials. In addition, the correct response pattern functioned as a conditional cue for comparison choice. In Experiment 2, mixed DRL-FR training was preceded by two-sample/two-alternative matching-to-sample with DRL and FR sample-response requirements. In a subsequent transfer test in which the correct response pattern to white served as the sample, pigeons preferentially chose the comparison previously reinforced following that pattern in the baseline task. This "unsignaled response" procedure may be useful for assessing whether differential responses can be members of acquired equivalence classes.     

Effects of differences in interreinforcer intervals between past and current schedules on fixed-interval responding

Undergraduates were exposed to a mixed fixed-ratio differential-reinforcement-of-low-rate schedule. Values of the schedule components were adjusted so that interreinforcer intervals in one component were longer than those in another component. Following this, a mixed fixed-interval 5-s fixed-interval 20-s schedule (Experiment 1) or six fixed-interval schedules in which the values ranged from 5 to 40 s (Experiment 2) were in effect. In both experiments, response rates under the fixed-interval schedules were higher when the interreinforcer intervals approximated those produced under the fixed-ratio schedule, whereas the rates were lower when the interreinforcer intervals approximated those produced under the different-reinforcement-of-low-rate schedule. The present results demonstrate that the effects of behavioral history were under control of the interreinforcer intervals as discriminative stimuli.     

Relative reinforcing effects of different oral ethanol doses in rhesus monkeys

The relative reinforcing effects of different doses of orally delivered ethanol were evaluated. Mouth-contact responding by rhesus monkeys was measured under concurrent fixed-ratio fixed-ratio schedules of liquid delivery (0.67 ml/delivery) from each of two spouts during daily 3-hr sessions. Experiment 1 examined persistence of responding with ethanol (2%, 8%, and 32% wt/vol) and water available. When fixed-ratio values from 8 to 128 were tested, the number of ethanol deliveries obtained per session decreased as the response requirement increased. The decrease in deliveries was less at higher than at lower ethanol concentrations, however. Experiment 2 examined choice between two ethanol concentrations under concurrent fixed-ratio 16 schedules (4% vs. 8%, 4% vs. 16%, 8% vs. 16%, 2% vs. 8%, 2% vs. 32%, 8% vs. 32%). Higher concentrations (16%, 32%) generally maintained more responding than concurrently available concentrations of 8% or less. An exception was the observation of a preference for 8% over 32% ethanol. When the fixed-ratio value was increased, however, the relative preference for these two doses was reversed so that 32% ethanol maintained more responding than 8% ethanol. Thus, the direction of the preference depended on the size of the response requirement. These results indicate that the reinforcing effects of ethanol increase with dose.     

Disruption of temporally organized behavior by morphine

Four pigeons pecked keys in two different procedures commonly used in the study of timing, or temporal discrimination. Sessions consisted of 40 trials. During half of the trials, two keys were presented for 50 s. Left-key pecks were reinforced according to a variable-interval 67.86-s schedule during the first 25 s of the trial, and right-key pecks were not reinforced. During the second 25 s of the trial, right-key pecks were reinforced according to the same schedule, and left-key pecks were not reinforced. In the other half of the 40-trial session, the center key was presented. The majority of these trials arranged fixed-interval 2.5-s schedules. Occasionally a probe, or peak-interval, trial was presented. These trials were 100 s in duration and terminated without reinforcement. These two procedures were used to examine the effects of morphine on indexes of timing and on patterns of responding. Morphine altered behavior in a race-dependent manner in both procedures. Low baseline (saline) response rates were increased following morphine administration, and high baseline rates were either unaffected or decreased slightly. Rate-dependent effects appeared as leftward shifts in the timing index for two-key trials and decreases in the index of curvature for fixed-interval trials. Despite large changes in response rates, no consistent shift of the peak time was observed during peak-interval trials. These results are discussed primarily in terms of rate dependency; that is, rates of responding following drug administration tend to be determined in large part by rates of responding under baseline conditions.     

Against Blameless Wrongdoing

I argue against the standard view that it is possible to describe extensionally different consequentialist theories by describing different evaluative focal points. I argue that for consequentialist purposes, the important sense of the word act must include all motives and side effects, and thus these things cannot be separated.     

Effects of cocaine on fixed-interval responding reinforced by the opportunity to run

Rate-dependent drug effects have been observed for operant responding maintained by food, water, heat, light onset, electrical brain stimulation, shock-stimulus termination, and shock presentation. The present study sought to determine if the effects of cocaine on lever pressing maintained by the opportunity to run could also be described as rate dependent. Seven male Wistar rats were trained to respond on levers for the opportunity to run in a wheel. The schedule of reinforcement was fixed-interval 60 s, and the reinforcing consequence was the opportunity to run for 60 s. On this schedule, overall rates of responding were low, usually below six presses per minute, and pauses frequently exceeded the 60-s interval. Despite these differences, an overall scalloped pattern of lever pressing was evident for each rat. Doses of 1, 2, 4, 8, and 16 mg/kg cocaine were administered 10 min prior to a session. Only at the 16 mg/kg dose did the responding of the majority of rats change in a manner suggestive of a rate-dependent drug effect. Specifically, lower response rates at the beginning of the intervals increased and higher rates at the end of the intervals decreased, as indicated by the fact that slopes from the regression of drug rates on control rates decreased. These data provide tentative support for the generalization of rate-dependent effects to operant responding maintained by wheel running. Differences in the baseline performance maintained by wheel running compared to those for food and water point to the need for further experimentation before this effect can be firmly established.     

Many-body potential for nitrogen in α-iron

N atom is one of the most frequent foreign interstitial atoms in α-iron along with C atoms. The Fe–C potential has been well-developed and can reproduce many significant interactions of C with point defects present in α-iron. However, there exists no satisfactory Fe–N potential to describe the interactions of N with point defects. Here, we develop a many-body potential for N in α-iron. The potential parameters are determined by fitting to ab initio data, which includes energetics, configurations, and relaxations of Fe atoms close to N atom. This potential successfully describes the interactions of Fe–N across a wide range of defect environments. The potential employs the embedded atom method form and hence is appropriate for large-scale molecular dynamics simulation.