Nor-binaltorphimine decreases deprivation and opioid-induced feeding

Brain Res. 1990 Nov 26;534(1-2):60-4. doi: 10.1016/0006-8993(90)90112-o.

Abstract

We evaluated the effect of the kappa antagonist, nor-binaltorphimine (nor-BNI) on deprivation and opioid-induced feeding in rats. Intracerebroventricular administration of nor-BNI (100 nmol) decreased deprivation-induced feeding for as long as 24 h, albeit in a fairly weak manner (maximum decrease of approximately 28%). Nor-BNI (1, 10 and 100 nmol) decreased feeding induced by the kappa ligand U-50,488H by as much as 85% during the first hour of the study. This kappa antagonist also decreased feeding induced by the delta agonist DSLET and the mu agonist DAMGO. Based on previous studies indicating that nor-BNI is a selective kappa antagonist, we conclude that not only U-50,488H (kappa), but also DSLET (delta) and DAMGO (mu)-induced feeding are dependent upon an active kappa receptor.

Publication types

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

MeSH terms

  • 3,4-Dichloro-N-methyl-N-(2-(1-pyrrolidinyl)-cyclohexyl)-benzeneacetamide, (trans)-Isomer
  • Analgesics / pharmacology*
  • Animals
  • Enkephalin, Ala(2)-MePhe(4)-Gly(5)-
  • Enkephalin, Leucine* / analogs & derivatives*
  • Enkephalins / pharmacology*
  • Feeding Behavior / drug effects*
  • Food Deprivation*
  • Male
  • Naltrexone / analogs & derivatives*
  • Naltrexone / pharmacology
  • Oligopeptides / pharmacology*
  • Pyrrolidines / pharmacology*
  • Rats
  • Rats, Inbred Strains
  • Receptors, Opioid / drug effects
  • Receptors, Opioid / physiology
  • Reference Values

Substances

  • Analgesics
  • Enkephalins
  • Oligopeptides
  • Pyrrolidines
  • Receptors, Opioid
  • Enkephalin, Ala(2)-MePhe(4)-Gly(5)-
  • norbinaltorphimine
  • Enkephalin, Leucine
  • Naltrexone
  • 3,4-Dichloro-N-methyl-N-(2-(1-pyrrolidinyl)-cyclohexyl)-benzeneacetamide, (trans)-Isomer
  • enkephalin, Ser(2), Leu(5), Thr(6)-