Suppression by dynorphin A-(1-13) of the expression of opiate withdrawal and tolerance in mice

Eur J Pharmacol. 1992 Oct 20;221(2-3):223-6. doi: 10.1016/0014-2999(92)90705-9.

Abstract

Dynorphin A-(1-13) has been shown to suppress the expression of opiate withdrawal and tolerance dose dependently in morphine-dependent mice when administered i.v. The ED50 of naloxone to precipitate withdrawal jumping was increased by 1.5- and 7-fold when morphine-dependent mice were pretreated with 2.5 and 5.0 mumol/kg of dynorphin A-(1-13), respectively. When dynorphin A-(1-13) (5.0 mumol/kg, i.v.) was administered after the precipitation of withdrawal with naloxone, the ED50 of naloxone was still increased by over 2-fold. Also, the expression of tolerance which was estimated by noting the antinociceptive ED50 of morphine, was inhibited by over 70% with a dynorphin A-(1-13) dose of 2.5 mumol/kg and completely suppressed by pretreatment with 5.0 mumol/kg of dynorphin A-(1-13) i.v. The mechanism by which dynorphin A-(1-13) produces these effects when given i.v. remains to be elucidated.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Drug Tolerance
  • Dynorphins / pharmacology*
  • Male
  • Mice
  • Morphine / adverse effects
  • Naloxone / pharmacology
  • Opioid-Related Disorders / drug therapy
  • Peptide Fragments / pharmacology*
  • Substance Withdrawal Syndrome / prevention & control*

Substances

  • Peptide Fragments
  • Naloxone
  • dynorphin (1-13)
  • Dynorphins
  • Morphine