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  • Articles: DFG German National Licenses  (2)
  • Electronic Resource  (2)
  • Dreaming  (1)
  • Key words Thyrotropin-releasing hormone  (1)
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  • Articles: DFG German National Licenses  (2)
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  • Electronic Resource  (2)
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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Psychopharmacology 37 (1974), S. 59-66 
    ISSN: 1432-2072
    Keywords: Cocaine ; Stimulants ; Depression ; Sleep ; Dreaming ; Electroencephalograph
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Cocaine was administered orally on a double-blind basis to depressed patients and effects on EEG-monitored sleep were assessed. In doses which did not produce consistent effects on vital signs or mood, cocaine significantly reduced total sleep and rapid eye movement (REM) sleep. The REM sleep supression with cocaine administration and rebound upon cocaine discontinuation was dose related; there was a greater effect at higher doses. Two properties of cocaine appear to closely correspond to those of many other drugs which suppress REM sleep in man—enhancement of functional catecholamines and/or high drug-abuse potential.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-2072
    Keywords: Key words Thyrotropin-releasing hormone ; Dopamine ; 5-Hydroxytryptamine ; Vagus nerve ; Locomotor activity ; Behavior ; Microdialysis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract  The systemic administration of thyrotropin-releasing hormone (TRH) to rats elicits locomotor activation, wet dog shakes, jaw movements, paw licking and tail rattle. Central dopamine (DA) and 5-hydroxytryptamine (5-HT) systems and peripheral vagal afferents have been implicated in these responses. To define this circuitry further, the effects of lesions of these pathways on the behavioral responses elicited by intraperitoneal (IP) injections of TRH were assessed in rats. Lesions of the DAergic innervation of the nucleus accumbens did not affect the locomotor activation, wet dog shakes, paw licking, jaw movements or tail rattle elicited by TRH. This is consistent with our in vivo microdialysis finding that TRH did not affect the release of DA in the nucleus accumbens at a dose that strongly increased locomotor activity. Depletion of spinal 5-HT significantly decreased the wet dog shakes induced by TRH, while depletion of forebrain 5-HT had no effect on any behavior. Bilateral vagotomy did not affect the locomotor response to TRH or any of the other behaviors measured. Taken together, these results suggest that the DAergic mesolimbic, the 5-HTergic projections to the forebrain and vagal afferent systems are not mediators of the behavioral responses to systemic TRH. In contrast, the raphe-spinal 5-HTergic projection system may serve to modulate the wet dog shakes elicited by this peptide.
    Type of Medium: Electronic Resource
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