Biomedical subjects

G D Gentry

Publications and source records attributed to G D Gentry.

8 recordsLinked to original sources

PubMed1988

Prenatal ethanol weakens the efficacy of reinforcers for adult mice.

Pregnant C57BL/6cr mice were fed a liquid diet containing 20% of the total calories from either ethanol (E) or sucrose (S) for gestation days 5-17. Adult male and female (six of each from both prenatal-treatment groups) offspring were tested under various schedules of food reinforcement. The first phase was a test of fixed-ratio (FR) acquisition in which the required number of responses per unit of reinforcement was increased from 1 to 20 to 100. Prenatal ethanol exposure interacted with other factors to produce an acquisition deficit. The second phase involved responding under extinction (Ext). Under standard Ext procedures there were no prenatal-ethanol effects; however, when a conditioned reinforcer was superimposed on an FR 5, the E males did not increase their rates as much as the S males. Finally, under a multiple FR 5 DRO 15-sec (differential-reinforcement-of-other-behavior) arrangement, prenatal-ethanol effects were found in each component. For the FR 5 component, prenatal ethanol eliminated the sex differences found in the S subjects. For the DRO 15-sec component, prenatal ethanol elevated response rates. The results indicate a general decreased efficacy of positive reinforcement in adult mice following prenatal ethanol exposure.

Age Factors↗

PubMed1986

Operant behavior in transition reflects neonatal exposure to cadmium.

Male Long-Evans rats were injected with 0, 1, 3, or 6 mg/kg of cadmium chloride on the first day of life. Animals free of morphological stigmata at weaning were selected for study. Tissue concentrations of cadmium and operant behavior under various fixed-ratio (FR) schedules of reinforcement were evaluated when these rats were adults. Dose-related increases in cadmium were present in the brains, livers, and kidneys. Dose-related differences in behavior were most evident during the transition from fixed ratio 25 (FR 25 or 25 responses/reinforcer) to FR 75. An inverted U describes the relationship between response output during the transition to FR 75 and cadmium chloride dose response output increased at 3 mg/kg and decreased at 6 mg/kg. The rate decreases were not correlated with weight loss that appeared after some of the animals exposed to 6 mg/kg reached 60 days of age. Challenge doses of d-amphetamine revealed no interaction between neonatal exposure to cadmium and d-amphetamine. The occurrence of alterations in operant behavior in animals that appeared normal on a number of preweaning evaluations suggests that operant behavior in transition was sensitive to subtle effects not observed with other commonly used tests. The data provide evidence for delayed effects in the adult that are due to neonatal exposure to cadmium.

Animals↗

PubMed1984

Graded differential reinforcement: Response-dependent reinforcer amount.

After key pecking had been autoshaped, six pigeons were exposed to a condition in which the duration of grain availability at the end of an 8-second trial depended on the number of responses emitted during the trial (0.25-second access to grain per response). This procedure, called correlated reinforcement, alternated across conditions with the automaintenance baseline in which the 8-second trial terminated with a constant 2.5-second access to grain. Two control procedures were run; in both, the reinforcer durations were yoked to those obtained in the last correlated session. In the yoked control no responses were required, but in the single-response yoked control at least one response was required to receive the yoked duration. The correlated condition maintained response rates above those produced by the two control conditions. These results may be accounted for by differential reinforcement.

Journal Article↗

PubMed1983

The microanalysis of fixed-interval responding.

The fixed-interval schedule of reinforcement is one of the more widely studied schedules in the experimental analysis of behavior and is also a common baseline for behavior pharmacology. Despite many intensive studies, the controlling variables and the pattern of behavior engendered are not well understood. The present study examined the microstructure and superstructure of the behavior engendered by a fixed-interval 5- and a fixed-interval 15-minute schedule of food reinforcement in the pigeon. Analysis of performance typical of fixed-interval responding indicated that the scalloped pattern does not result from smooth acceleration in responding, but, rather, from renewed pausing early in the interval. Individual interresponse-time (IRT) analyses provided no evidence of acceleration. There was a strong indication of alternation in shorter-longer IRTs, but these shorter-longer IRTs did not occur at random, reflecting instead a sequential dependency in successive IRTs. Furthermore, early in the interval there was a high relative frequency of short IRTs. Such a pattern of early pauses and short IRTs does not suggest behavior typical of reinforced responding as exemplified by the pattern found near the end of the interval. Thus, behavior from clearly scalloped performance can be classified into three states: postreinforcement pause, interim behavior, and terminal behavior.

Journal Article↗

PubMed1982

Intractable properties of responding under a fixed-interval schedule.

The behavior engendered by the fixed-interval schedule is characterized by its variability within and across intervals. The present experiment was designed to assess further the magnitude of interval-to-interval dynamics and to explore conditions which might enhance control by response number for subsequent output. Pigeons were exposed to three experimental manipulations after responding had stabilized under a fixed-interval five-minute schedule. First, a discrete five-stimulus counter was added so that the key color changed after a fixed number of responses. Then additional grain presentations were made at the end of the interval so that high response output was differentially reinforced in the presence of the counter stimuli. Finally, the counter stimuli were presented as an irregular clock (i.e., independently of responding), but the durations were yoked to performance under the counter condition. The data show that response number can exert influence from one interval to the next, but this source of control is weak and not influenced by the experimental manipulations. Results from the clock arrangement indicate that behavior is controlled largely by the stimulus conditions prevailing at the time of interval onset.

Journal Article↗

PubMed1980

Choice and reinforcement delay.

Previous studies of choice between two delayed reinforcers have indicated that the relative immediacy of the reinforcer is a major determinant of the relative frequency of responding. Parallel studies of choice between two interresponse times have found exceptions to this generality. The present study looked at the choice by pigeons between two delays, one of which was always four times longer than the other, but whose absolute durations were varied across conditions. The results indicated that choice is not uniquely determined by the relative immediacy of reinforcement, but that absolute delays are also involved. Models for concurrent chained schedules appear to be more applicable to the present data than the matching relation; however, these too failed to predict choice for long delays.

Journal Article↗

PubMedDate not supplied

Prenatal ethanol effects on reward efficacy for adult mice are gestation stage specific.

We previously reported that adult mice exposed to ethanol throughout gestation (G5-17) responded slower than controls on reinforcement schedules which required large numbers of responses per unit of food, i.e., high fixed ratio (FR) schedules. The primary finding of the present study was that ethanol exposure during the last 5 days of gestation (G12-17) is sufficient to produce this effect whereas a similar exposure early in gestation (G5-10) is not. Both male and female mice exposed to ethanol late in gestation responded slower than either lab chow or pair-fed controls, and the effect was similar to that of mice exposed to ethanol throughout gestation (G5-17) in our earlier study. Thus, developmental events occurring late in gestation are important for the reduced reinforcing efficacy of food for prenatal-ethanol-exposed mice. In addition, the present experiment established the comparability of the sucrose and lab chow controls on this task. The results of the present study and our previous report are compatible with the hypothesis that the reduced responding on high FR schedules exhibited by prenatal-ethanol-exposed mice reflects a reduction in the efficacy of food reward. It is possible that the reduction in reward efficacy is due to altered development of neuronal systems functionally related to reward which develop late in gestation.

Animals↗

PubMedDate not supplied

Effects of prenatal maternal ethanol on male offspring progressive-ratio performance and response to amphetamine.

This study was designed to further explore the nature of our previously reported reduction in the efficacy of food reinforces for prenatal ethanol-exposed mice. We determined the effect of prenatal ethanol exposure on responding for food delivered on a progressive-ratio (PR) reinforcement schedule, which has been shown to be sensitive to changes in motivation and/or value of reinforcers, and we assessed the effects of amphetamine on responding maintained by the PR schedule. Subjects were adult (12 months old) male offspring of C57BL/6J mice fed liquid diets containing either ethanol (25% ethanol-derived calories, N = 12) or sucrose (25% sucrose-derived calories, N = 9) during gestation days 5-17. Prenatal ethanol-exposed mice differed from controls by having lower response rates and a greater disruption of responding following amphetamine injections. The reduced responding for food reward on the PR schedule supports our previously advanced hypothesis that prenatal ethanol reduces the efficacy of food reinforcers. The enhanced effects of amphetamine found in these adult mice is in agreement with previous reports on young rats. Although either of the effects of prenatal ethanol exposure observed in the present study are suggestive of altered DA systems, current neurochemical studies on either rats or mice provide no support for the hypothesis.

Amphetamine↗