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Psychopharmacology (Berl) ; 137(4): 326-32, 1998 Jun.
Article in English | MEDLINE | ID: mdl-9676891

ABSTRACT

The objectives of the current study were to determine 1) the effects of various doses of dynorphin A (1-13) on opiate withdrawal in humans and 2) the safety of dynorphin at these doses. Opiate dependent subjects who had been stabilized on morphine received a single IV dose of placebo, 150, 500 or 1000 microg/kg dynorphin after exhibiting spontaneous withdrawal using a randomized, double-blinded, between-subjects study design. Observer Withdrawal Scores were lower in the 150 and 1000 microg/kg groups as compared to placebo (P < 0.05) but no significant differences were observed on the observer-rated Wang or Sickness Scales. Significant decreases were also found for self-reported symptoms of nervousness, runny nose, sneezing, and painful joints in the 500 microg/kg group. Significant increases in serum prolactin levels were seen after all dynorphin doses; however, these were not dose-related. Dynorphin A (1-13) was well tolerated and safe, with no changes in physiologic parameters. We conclude that dynorphin A (1-13) has a modest effect in reducing mild opiate withdrawal in humans and is well tolerated at doses up to 1000 microg/kg.


Subject(s)
Dynorphins/therapeutic use , Narcotics/adverse effects , Narcotics/therapeutic use , Peptide Fragments/therapeutic use , Substance Withdrawal Syndrome/drug therapy , Adult , Biomarkers , Dose-Response Relationship, Drug , Double-Blind Method , Dynorphins/adverse effects , Evoked Potentials/drug effects , Female , Humans , Male , Middle Aged , Morphine/adverse effects , Peptide Fragments/adverse effects , Prolactin/blood , Substance Withdrawal Syndrome/physiopathology , Substance Withdrawal Syndrome/psychology , Treatment Outcome
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