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J B Appel

Publications and source records attributed to J B Appel.

87 records · Page 5Linked to original sources
PubMed1968

Fixed-interval punishment.

The average rate of bar-pressing maintained by a variable-interval schedule of milk reinforcement in 33 rats was found to be a decreasing function of intensity of concurrent punishment and, over a wide range of shock intensities, was inversely related to punishment frequency. Cumulative records were, however, negatively accelerated during 30-min punishment sessions with complete suppression occurring earlier and earlier (after fewer and fewer shocks) as intensity increased. In addition, acceleration was often observed between successive fixed-interval shock presentations and, at low and moderate intensities, bursts of responding occurred after each shock. The time to recover between punishment sessions (post-punishment recovery) was an increasing monotonic function of punishment intensity.

Journal Article↗
PubMed1966

Variable-interval punishment during variable-interval reinforcement.

Variable-interval punishment was superimposed on a variable-interval food reinforcement baseline for three groups of rats. The value for the variable-interval punishment schedule was the same as that for the variable-interval food reinforcement schedule, although the two schedules were programmed independently. The three groups were Variable Intervals 0.5, 1, and 3 min. Little or no suppression occurred in the three groups at mild (0.2 and 0.4 ma) intensities of punishment, but at 0.6 ma, complete suppression occurred almost uniformly. During continued punishment, there was no consistent recovery toward the pre-punishment baseline at suppressing intensities of punishment. After punishment was discontinued, recovery from suppression was more rapid the lower the punishment intensity, and the lower the value of the variable-interval schedules of reinforcement and punishment.

Animals↗
PubMedDate not supplied

Para-chlorophenylalanine, serotonin and killing behavior.

Both p-chlorophenylalanine (PCPA) and PCPA methyl ester were found to reliably induce mouse-killing in non-killer rats only when unusually large doses were used (three successive daily injections of 300 mg/kg) and brain serotonin (5-HT) concentration was drastically reduced (about 90 percent). Neither three doses of 100 mg/kg of PCPA nor p-chloroamphetamine (3 times 3.5 mg/kg) caused similar effects in spite of the fact that these compounds depleted brain 5-HT by 85 percent and 60 percent, respectively. PCPA-induced mouse killing was reversed by 5-HTP (100 mg/kg) only when this serotonin precursor completely restored levels of 5-HT. The topography of PCPA-induced killing did not resemble normal interspecies aggression and was also directed toward fat pups. These findings suggest that 5-HT depletion might facilitate nonspecific killing reactions, but is not a sufficient condition to induce the species-specific predatory behavior in rats.

5-Hydroxytryptophan↗
PubMedDate not supplied

Comparison of the discriminative stimulus properties of delta9-THC and psilocybin in rats.

Male albino rats were trained to respond differentially on the left or right lever in a 2-lever chamber on the basis of which drug had been given intra-peritoneally (IP) 30 min before experimentation. In 1 group 1.9 mg/kg of delta9-THC and control injections (vehicle) served as the discriminative stimuli associated with each lever and in another group the drug stimuli were 1.0 mg/kg of delta9-THC and 1.0 mg/kg of psilocybin. The results confirmed those of other experiments using different procedures; that delta9-THC can acquire discriminative control over responding. The fact that delta9-THC and psilocybin were also found to differentially control lever choice demonstrates that these 2 drugs probably produce discriminably different states in rats.

Animals↗
PubMedDate not supplied

LSD and fixed-internal responding in the rat.

A series of 6 doses of lysergic acid diethylamide-25 (LSD) altered the bar-pressing behavior of 6 rats maintained on a fixed-interval, 5 min (FI 5) schedule of reinforcement. High doses of LSD (0.16, 0.32 mg/kg) depressed overall rates of responding. Low response rates, which occurred during the first half of the interval between successive reinforcements, were increased by low (0.01, 0.02 mg/kg), moderate (0.04, 0.08 mg/kg), and high doses of LSD; high rates of responding which occurred during the final half of the interval were decreased only by high doses of LSD. All doses (except the lowest) decreased the Index of Curvature, a statistic describing the temporal distribution of responses. The results were discussed in terms of baseline rate of responding and the presence or absence of timing behavior.

Animals↗
PubMedDate not supplied

Signal detection theory and the psychophysics of pain: an introduction and review.

A brief explanation of signal detection theory is presented, followed by a review of the literature in which differences in pain report were analyzed to determine if changes were in sensitivity (physiological processes) or in response bias (a subject's willingness to report that a signal occurred). Three kinds of studies are reviewed: modification, procedural, and comparative and normative. The advantages of using a signal detection approach in pain research are emphasized. It is concluded that experimenters applying signal detection analysis to pain research should give greater consideration to methodological procedures and be cognizant of all possibilities for shifts in sensitivity (d)'.

Acupuncture Therapy↗