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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Psychopharmacology 84 (1984), S. 383-387 
    ISSN: 1432-2072
    Keywords: Naloxone ; Naltrexone ; Exploration ; Locomotor activity ; Rats
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Exploratory head-poke responses, locomotor activity, and rearing were studied in five groups of rats (n=8 per group) during two 30-min sessions. The opiate antagonists naloxone and naltrexone (0.5 and 2 mg/kg) were administered once, 30 min before the first session. Delayed drug effects were studied during the second session, 24 h after the first session. During the initial 10 min of the first session naloxone and naltrexone decreased the number of head-poke responses without reducing locomotor activity and rearing. Both drugs decreased the number of head-poke responses, locomotor activity, and rearing during the remainder of this session. Equivalent doses of naloxone and naltrexone produced similar effects. The duration of a head-poke response increased during the session. Drug effects on head-poke duration were not observed. Delayed drug effects on behavior during the second session were not obtained. The observation that both naloxone and naltrexone were effective in the present procedure suggests that the effects of naloxone and naltrexone reported here are a function of opiate antagonist properties of these drugs. The data suggest further that the extent to which opiate receptor blockade results in a specific reduction of exploratory behavior may be partly dependent upon the length of the test session.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-2072
    Keywords: Vigilance performance ; Electroencephalogram ; Event-related potentials ; Benzodiazepines ; Arousal ; Signal detection measures
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Eighteen males performed two vigilance tasks with static and dynamic stimuli under the influence of oxazepam (20 and 40 mg) in a placebo-controlled, double blind, crossover design. Oxazepam dose-dependently impaired overall level of performance and aggravated the decrement with time in measures of accuracy and sensitivity relative to placebo. The drug reduced the amplitudes of the P1, N1, P2N2, and P3 (dose-dependently) waves of event-related potentials (ERPs). Oxazepam aggravated the linear decline with time of the P3 amplitude only. Oxazepam impaired accuracy was related to deterioration of central processing involved in stimulus discrimination (P2N2). Impairment of response-related performance measures (RT and RI) was associated with processing manifest in the P1, N1, and P3 waves. Oxazepam effects on the amplitudes of N1 and P3 correlated with drug effects on power in alpha 1 (8–10 Hz). Drug effects on over-all performance and alpha were also related; the drug effect on response speed correlated only with the drug effect on beta 1 (12.5-21 Hz). Effects of time-on-task on performance and EEG were unrelated, but oxazepam induced performance declines with time may have been caused by declines in resource allocation, as manifest in the amplitude of P3. Time effects on EEG power bands and ERP amplitudes were not significantly related to the time course of oxazepam activity. A curious dissociation emerged: both oxazepam and time-on-task impaired performance, but the drug induced a decrease of theta and alpha 1 power, whereas time-on-task increased power. Various processes play a role in performance decrements with time, and various aspects of processing may be involved in signal-detection measures which makes terms such as sensitivity quite meaningless. So-called computational processing was indistinguishable from energetic processes, which questions the validity of the distinction between these two domains. Explanations of EEG activity in terms of a unidimensional theory of arousal are untenable.
    Type of Medium: Electronic Resource
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