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  • Aggression  (1)
  • Attentional mechanisms  (1)
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Psychopharmacology 79 (1983), S. 370-371 
    ISSN: 1432-2072
    Keywords: Aggression ; Opioids ; Naloxone ; Pain ; Mice
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Aggression and thermal pain thresholds were measured in separate groups of isolated male mice following 0.2–5.0 mg/kg SC injections of the opiate antagonist naloxone. The drug inhibited aggressive behaviors dose-dependently, but had no effect on pain. These results suggest that endogenous opioid systems may be activated during repeated intermale aggressive encounters.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-2072
    Keywords: Tachistoscopic discrimination ; Primate visual discrimination ; Sodium pentobarbital ; Chlorpromazine ; Attentional mechanisms ; Reticular formation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Sodium pentobarbital and chlorpromazine were evaluated for the degree to which they differentially reduce the speed or efficiency with which sensory information can be processed. Rhesus monkeys were tested under comparable doses of sodium pentobarbital and CPZ on a visual discrimination problem with varying durations of tachistoscopically presented stimulus information. When unlimited stimulus information was available, no effects of the two drugs were observed at the doses used, but as the duration of stimulus presentation was progressively decreased, the effects of sodium pentobarbital became more severe, whereas CPZ did not differ from the saline control at any presentation duration. While previously published literature indicates that CPZ impairs performance by intermittantly blocking sensory input or transmission, the present data provide the first direct behavioral confirmation that barbiturates impair performance by retarding the rate at which sensory stimuli can be processed and utilized.
    Type of Medium: Electronic Resource
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