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At least 91 records · Page 5Linked to original sources
PubMed1986

Behavioral control of breathing in the cat.

Respiration depends upon brainstem neuronal circuits that produce the respiratory rhythm and relay it, via the ventrolateral columns, to motor neurons in the spinal cord. This brainstem system produces respiration automatically, i.e. without conscious effort, and is responsive to chemical and mechanical stimuli that signal imbalances in respiratory homeostasis. In addition to this automatic/metabolic respiratory system, there is a voluntary/behavioral system that controls the respiratory muscles during speaking, breath holding, and other voluntary respiratory acts. It has been proposed that this behavioral system involves corticofugal fibers that bypass the automatic system, course in the dorsolateral columns, and end at the level of the respiratory motor neurons. According to this scheme, the integration of behavioral control with automatic/metabolic control occurs at the level of the motor neurons and not within the automatic system. This proposed scheme has not been investigated experimentally. In the present study, we trained cats to control their respiration and recorded the activity of cells within the automatic system in the medulla during this behavioral control. We trained the animals to terminate inspiration and prolong expiration when a tone sounded. Microelectrode recordings from 40 medullary respiratory neurons showed that most cells, inspiratory and expiratory, became inactive during the behavioral apneic response. The exceptions were some expiratory cells that were activated during the task. These results suggest that the integration of behavioral influences occurs within the automatic system.

Aerosols↗
PubMed2002

Lead exposure and dorsomedial striatum mediation of fixed interval schedule-controlled behavior.

Prior studies demonstrate a critical role for mesolimbic dopamine systems, particularly nucleus accumbens, in the mediation of fixed interval (FI) schedule-controlled behavior and an enhancement of nucleus accumbens dopamine activity as a mechanism of chronic postweaning lead (Pb)-induced increases in Fl response rates. Since dorsomedial striatum, like nucleus accumbens, receives limbic input, it could also conceivably contribute to Pb-related effects on FI performance. Therefore, changes in FI schedule-controlled behavior were examined following administration of dopamine or the non-specific irreversible dopamine antagonist N-ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline (EEDQ) into dorsomedial striatum of rats exposed from weaning to 0, 50 or 500 ppm Pb acetate drinking solutions. The 500 ppm exposure increased baseline FI response rates relative to both 0 and 50 ppm. Intra-dorsomedial striatum EEDQ and dopamine had no effects when examined across all animals. However, both compounds produced rate-dependent effects, i.e. increases or decreases in rate in different subjects, depending upon baseline Fl overall rates. The rate-increasing effects of intra-dorsomedial striatum dopamine actually mimicked Pb effects, increasing Fl overall and run rates and shortening postreinforcement pause times. Further, Pb exposure modulated effects of dopamine and EEDQ in dorsomedial striatum. While these collective findings conceivably suggest dorsomedial striatum as another potential site through which postweaning Pb exposure influences FI performance, this possibility is not supported by other studies that show that chronic postweaning Pb alters dopamine binding sites and evoked dopamine release in nucleus accumbens but not in dorsomedial striatum even over a year exposure period. Thus, while both regions may play a role in mediating Fl performance under normal conditions, it appears that alterations in nucleus accumbens dopamine activity may be sufficient to induce chronic postweaning Pb-induced increases in FI response rates.

Animals↗
PubMed1980

Effects of acute and chronic administration of phenobarbital and d-amphetamine on schedule-controlled behavior.

The effects of acute and chronic administration of phenobarbital and d-amphetamine were determined in rats responding under a multiple fixed-interval five minute fixed-ratio 30 (mult FI 5 FR 30) schedule of food presentation. After determining the acute effects of each drug, the drugs were injected daily with one group of rats receiving the drugs before each behavioral session while another group received the drugs immediately after each daily session. After four to seven consecutive injections, tolerance developed to the effects of phenobarbital on the average rates of responding under FI and FR schedule components only if the drug was administered before each session. Tolerance was more pronounced for responding druing the terminal portions of the FI component than for responding during either the initial portions of the FI or the FR component. Evidence for a selective tolerance to the effects of the drug on responding during the final segments of the FI was also obtained in rats responding under an FI 5 schedule. In contrast, injection of d-amphetamine for seven to eight consecutive days failed to produce any tolerance to the effects of the drug on responding under mult FI 5 FR 30, FI 5, or FR 30 schedules. These results indicate that the development of tolerance to the effects of phenobarbital depended both upon the temporal relationship of the drug effects to the behavioral testing and upon the schedules controlling behavior. These findings are discussed in terms of theories of behavioral tolerance.

Animals↗
PubMed1980

The effects of cognitive and behavioral control on post-stress performance.

A study was designed to investigate the effects of behavioral and cognitive control on post-stress performance. Half of the subjects exposed to loud unpredictable noise bursts were given "behavioral" control (a button which would terminate the noise), while the other half had no behavioral control. In addition, subjects were provided with one of three levels of feedback (success, failure, or no feedback) regarding their performance during the noise. It was expected that information about performance would provide subjects with an increased sense of "cognitive" control which would affect their appraisal of stressful events and their later performance. The results indicated that subjected that subjects given feedback performed better on subsequent tasks than those given no feedback. Perceived behavioral control had little effect on performance. The causal attributions made by subjects were used to interpret these effects. These findings were viewed as supportive of Averill's notion than various types of control are related to stress in a complex fashion. The data may also support Abramson, Seligman, and Teasdale's reformulation of learned helplessness theory.

Adult↗
PubMed1986

Effective and reliable behavioral control technology.

The fiberglass-reinforced plastics industry and the literature on controlling exposures to toxic substances were surveyed to select work practices and housekeeping conditions that might be useful in reducing workers' exposures to styrene. A training program was developed to teach the selected behaviors to workers, and a behavior maintenance program was developed to encourage their continued use after training. These behavioral controls were introduced to appropriate workers in three different plants and were effective in changing all selected behaviors and conditions. Statistically reliable reductions in workers' exposures to styrene accompanied the changes in behaviors. All improvements were maintained throughout the course of data collection. The research provides a clear demonstration that behavioral controls can be used reliably to reduce workers' exposures to toxic substances.

Behavior Therapy↗
PubMed2003

Dissociating valence of outcome from behavioral control in human orbital and ventral prefrontal cortices.

The precise role of orbitofrontal cortex (OFC) in affective processing is still debated. One view suggests OFC represents stimulus reward value and supports learning and relearning of stimulus-reward associations. An alternate view implicates OFC in behavioral control after rewarding or punishing feedback. To discriminate between these possibilities, we used event-related functional magnetic resonance imaging in subjects performing a reversal task in which, on each trial, selection of the correct stimulus led to a 70% probability of receiving a monetary reward and a 30% probability of obtaining a monetary punishment. The incorrect stimulus had the reverse contingency. In one condition (choice), subjects had to choose which stimulus to select and switch their response to the other stimulus once contingencies had changed. In another condition (imperative), subjects had simply to track the currently rewarded stimulus. In some regions of OFC and medial prefrontal cortex, activity was related to valence of outcome, whereas in adjacent areas activity was associated with behavioral choice, signaling maintenance of the current response strategy on a subsequent trial. Caudolateral OFC-anterior insula was activated by punishing feedback preceding a switch in stimulus in both the choice and imperative conditions, indicating a possible role for this region in signaling a change in reward contingencies. These results suggest functional heterogeneity within the OFC, with a role for this region in representing stimulus-reward values, signaling changes in reinforcement contingencies and in behavioral control.

Behavior↗
PubMed1988

Similarities and differences between behavioral control by drug-produced stimuli and by sensory stimuli.

Drug-induced state-dependent learning and drug discriminations may be based on sensory stimuli induced by drug actions, or at least on events in the brain that have properties analogous to those of sensory stimuli. A variety of comparisons between behavioral control by drug-induced stimuli and by classically defined interoceptive and exteroceptive stimuli are possible. These allow inferences to be made about the nature of drug stimuli, the properties of behavioral paradigms that we use to investigate them, and the mechanisms by which drugs achieve behavioral control in drug discrimination and state-dependent learning paradigms. Each of these topics is selectively reviewed in this paper.

Animals↗
PubMed1995

The relationship between stress and weight-control behavior in African-American women.

Obesity is a problem for African-American women across all socioeconomic strata. Age-adjusted prevalence of overweight is 48.5% among African-American women compared with 21% among white women. An exploratory field was designed to examine selected psychosocial factors that influence the weight-control behavior of middle-income African-American women. A triangulation methodology was used in which both qualitative and quantitative data were collected. First, semistructured interviews were held with 36 African-American women between the ages of 25 and 75. Second, a Global Stress Scale was administered to measure perceived stress. Statistical analysis of the data revealed a positive correlation between body weight and stress in that women who were more overweight were experiencing more stress. Ethnographic analysis of the data showed that more than 50% of the women thought that stress negatively affected their weight-control behavior. Additionally, occupational stressors related to racism, sexism, and workload were major stressors for this group of women. Recognition of factors that influence weight-control health practices will enable health professionals to assist African-American women to manage their weight.

Adult↗
PubMed1975

Stimuli associated with drug injections as events that control behavior.

In this paper, some of the ways were briefly reviewed in which environmental stimuli that have been associated with injections of morphine or narcotic antagonists can come to modify and control behavior. Many of the effects described have also been demonstrated with drugs from other pharmacological classes. Environmental stimuli that occur in association with human drug-seeking and drug-taking behavior play an important role in the development, control, and perpetuation of this behavior. A variety of approaches to the experimental analysis of the control of behavior by such stimuli have been illustrated. Studies with these approaches promise to expand our understanding of the dynamic processes involved in drug use by human addicts.

Animals↗
PubMedDate not supplied

A method for adjusting exposure levels of volatile solvents based on effects on schedule-controlled behavior.

A novel adjusting procedure was employed to assess the acute behavioral effects of inhaled 1,1,1-trichloroethane (TCE) and m-xylene. Mice were trained to lever press under a fixed ratio 20 schedule of milk reinforcement. During 30-min test sessions, TCE concentrations were altered every 5 min dependent upon rates of responding in the preceding 5-min segment of the session. When response rates during a 5-min interval were not decreased by greater than 30% from control rates, the TCE concentration for the next interval was increased. Reduction in response rates of more than 30% from the previous interval resulted in a lowering of the TCE concentration in the subsequent 5-min interval. TCE produced concentration-dependent decreases in response rates similar to what has been shown previously and many mice adjusted their exposure levels such that there were alternating intervals of increasing and decreasing concentration exposures. This provided a means of determining, in a single test session, no effect (subthreshold) and minimal effect concentrations of TCE for effects on schedule controlled behavior. Alteration of the starting TCE concentration from 1000 to 6000 ppm increased the TCE threshold for effects. When the response rate contingency was removed and TCE concentrations were "played back" from an earlier adjustment session, concentration-effect curves were similar to what were obtained under adjusting conditions. Using the adjusting procedure, we were also able to rapidly obtain a concentration-effect curve and threshold concentrations for m-xylene that are consistent with published results. This procedure for response rate adjusting exposure concentrations should be useful for rapid assessment of inhalant effects on schedule-controlled behavior and for focusing attention on near threshold levels of exposure.

Animals↗
PubMed1984

Chemical and behavioral control of breathing in adult twins.

Whether genetic influence on chemical and behavioral control of breathing is still present in adulthood was examined in 28 pairs of monozygotic (mean age, 40 +/- SD 9.9 yr) and 10 dizygotic (35 +/- 9.3 yr) twins. Mean values for hypoxic and hypercapnic ventilatory responses, threshold for perceiving added inspiratory resistance, and respiratory patterns were not different between monozygotic and dizygotic twins. However, within-pair variance ratios (those in monozygotic twins being denominators) for hypoxic response (4.08, p less than 0.005), hypercapnic response (4.89, p less than 0.005), respiratory frequency during air breathing (3.96, p less than 0.005), inspiratory time during air breathing (5.47, p less than 0.005), and inspiratory time during hypoxia (9.08, p less than 0.005) were significantly larger than 1. Within-pair variances for threshold for resistive load perception and respiratory pattern during hypercapnia were equivalent between the 2 groups. These results indicate that ventilatory responses to hypoxia and hypercapnia and respiratory patterns while breathing air include genetically determined factors, whereas perception threshold for added resistance and respiratory patterns during hypercapnia are influenced predominantly by environmental force in adulthood.

Adult↗
PubMed1980

"Out of control" behavior in adolescents.

The physician should approach a problem of "out of control" behavior in an adolescent as a family issue rather than an individual issue, for not only the behavior itself bu the parental response to the behavior are key factors in understanding and coping with it. Areas of commonly encountered misbehavior are explored.

Adolescent↗
PubMed2002

Familial correlates of extreme weight control behaviors among adolescents.

OBJECTIVE: To identify familial factors associated with extreme weight control among adolescents. METHOD: Analysis of a comprehensive 1996 health survey of Connecticut students. Familial factors among extreme dieters who deliberately vomited, took diet pills, laxatives, or diuretics were compared with youth reporting none of these behaviors, using logistic regression controlling for age and body mass index. RESULTS: Nearly 7% of adolescents reported engaging in extreme weight control behaviors. Boys' risk factors included high parental supervision/monitoring and sexual abuse history. Protective factors included high parental expectations, maternal presence, and connectedness with friends and other adults. The only significant risk factor for girls was sexual abuse history. Protective factors included family connectedness, positive family communication, parental supervision/monitoring, and maternal presence. CONCLUSIONS: Extreme dieting appears to be less an expression of body composition than of psychosocial issues. That connectedness to family, other adults, and friends is protective further demonstrates interrelationships of extreme weight control behaviors with family/social issues.

Adolescent↗
PubMed2005

Alcohol-induced impairment of behavioral control: differential effects on engaging vs. disengaging responses.

RATIONALE: Model-based assessments of behavioral control have been used to study the acute effects of alcohol on the ability to execute and inhibit behavioral responses. Response inhibition appears more vulnerable to the impairing effects of alcohol than response execution. Current information processing models have yet to account for this observation. OBJECTIVES: The present study used a reductionist approach to determine if the particular vulnerability of response inhibition to the effects of alcohol occurs at the level of the action (motor program). The study examined the effects of alcohol on the ability to execute and inhibit behavior in a context in which preliminary information signaled the likelihood that a response should be executed or suppressed. The engagement and disengagement of responses were directly compared under alcohol. METHODS: Adults (N = 24) performed a cued go/no-go task that required quick responses to go targets and suppression of responses to no-go targets. Response requirements were manipulated by varying the nature of the action required whereby half of the participants made key press responses (response engagement) and the other half released ongoing key presses (response disengagement). Performance was tested under three doses of alcohol: 0.00, 0.45, and 0.65 g/kg. RESULTS: Dose-dependent increases in commission errors were only observed with response engagement and not with response disengagement. Reaction times were faster for response engagement than response disengagement. CONCLUSIONS: Response disengagement affords some protection against alcohol-induced impairment of inhibition, indicating that not all aspects of motor processing requiring inhibition are equally impaired by alcohol.

Adult↗
PubMed1978

Effects of repeated administration of cocaine on schedule-controlled behavior of rats.

The effects of cocaine (4.0--32 mg/kg) on schedule-controlled behavior of rats were determined before and during a period of repeated administration of cocaine. In rats trained to lever press on a fixed ratio 40 schedule for food delivery, cocaine (8.0--32 mg/kg) initially decreased response rate in a dose-related manner. During the period of repeated administration, the effects of cocaine on response rate and running rate were attenuated in 2 rats and did not change in 2 others. When dose-effect functions of cocaine were redetermined, a shift to the right was observed in several measures indicating the development of tolerance to these effects of cocaine on performance. In rats trained to lever press on a DRL 20" schedule for food delivery, cocaine (4.0--32 mg/kg) increased response rates, decreased number of reinforcements per session and shifted interresponse time distributions to the left (shorter IRT's in all rats). During the period of repeated administration, the effects of the daily dose of cocaine (16 mg/kg) on all these measures were attenuated. Tolerance to cocaine was further indicated by a shift in the dose effect function of cocaine to the right during the redetermination.

Animals↗
PubMed1997

Effects of chronic caffeine administration on respiration and schedule-controlled behavior in rhesus monkeys.

The effects of chronic caffeine administration on ventilation and schedule-controlled behavior were studied in 12 adult rhesus monkeys. In seated subjects prepared with a head plethysmograph, ventilation was measured during exposure to air (normocapnia) and to elevated levels of CO2 (3%, 4% and 5%) mixed in air (hypercapnia). Acute administration of caffeine (10.0-30.0 mg/kg i.m.) produced marked, dose-dependent increases in ventilation during conditions of normocapnia and hypercapnia. However, daily administration of caffeine (10.0 mg/kg i.m.) for 8 consecutive days resulted in tolerance to its respiratory-stimulant effects that was surmountable with higher doses. Caffeine-tolerant subjects also were cross-tolerant to theophylline, an active metabolite of caffeine, and to rolipram and Ro 20-1724, selective phosphodiesterase inhibitors. When chronic administration was terminated and the acute effects of caffeine were redetermined, sensitivity returned to levels obtained before chronic administration within 9 days. Drug effects on behavior were studied in monkeys trained to respond under a fixed-interval schedule of stimulus termination. Acute administration of caffeine (1.0-30.0 mg/kg i.m.) produced significant rate-increasing effects on fixed-interval responding, but chronic administration resulted in tolerance that was insurmountable, such that no dose increased responding above control rates. Although the time course for development and loss of tolerance to the behavioral effects of caffeine corresponded closely with respiration, cross-tolerance did not extend to the behavioral effects of rolipram. Chronic caffeine administration had little effect on caffeine metabolism or clearance, which indicated that caffeine tolerance was pharmacodynamic. The results suggest that different neurochemical mechanisms mediate the effects of caffeine on respiration and behavior, and that inhibition of type IV phosphodiesterase plays a prominent role in caffeine-induced respiratory stimulation.

4-(3-Butoxy-4-methoxybenzyl)-2-imidazolidinone↗