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  • OAG; L-α-1-oleoyl-2-acetoyl-sn-3-glycerol  (1)
  • Opioids enkephalins supraoptic  (1)
  • 1
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Biochemical and Biophysical Research Communications 163 (1989), S. 902-907 
    ISSN: 0006-291X
    Keywords: OAG; L-α-1-oleoyl-2-acetoyl-sn-3-glycerol ; RASM; rat aortic smooth muscle
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Experimental brain research 60 (1985), S. 192-196 
    ISSN: 1432-1106
    Keywords: Opioids enkephalins supraoptic ; Nucleus oxytocin
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary When electrical stimuli are applied to the neural stalk of the pituitary, oxytocin, vasopressin, and probably several opioid peptides also contained in nerve terminals in the gland are released: one action of the released opioids appears to be to inhibit oxytocin release by an action that has been likened to pre-synaptic inhibition. Thus, when Clarke et al. (1979) stimulated the neural stalk following intravenous injection of the opioid antagonist naloxone, they observed that the evoked oxytocin release was potentiated. In the present study we confirm this result and show that oxytocin release evoked by stimulation of the supraoptic nucleus is similarly potentiated by naloxone. This finding is consistent with the hypothesis that the opioid responsible for inhibition of oxytocin release coexists with either oxytocin or vasopressin. We further report that the specific δ-receptor antagonist ICI 174864 does not potentiate oxytocin release either in vivo or in vitro. Thus, it seems unlikely that the enkephalins, putative δ-receptor agonists present in neurohypophysial fibres, are the opioids responsible for the observed inhibition of oxytocin release.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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