Spontaneous withdrawal from long-term treatment with morphine accelerates the turnover of alpha 2-adrenoceptors in the rat brain: up-regulation of receptors associated with increased receptor appearance

J Neurochem. 1995 Jun;64(6):2590-7. doi: 10.1046/j.1471-4159.1995.64062590.x.

Abstract

The aim of this study was to quantify and compare the turnover of brain alpha 2-adrenoceptors during chronic morphine treatment and after spontaneous morphine withdrawal in rats. The oral administration of increasing doses of morphine (10-90 mg/kg) for 20 days did not alter the specific binding of the agonist [3H]-clonidine in the cerebral cortex. However, spontaneous opiate withdrawal (24 h) significantly increased the density of cortical alpha 2-adrenoceptors (Bmax for [3H]clonidine was 21% greater). The recovery of [3H]clonidine binding after irreversible inactivation by N-ethoxycarbonyl-2-ethoxy-1,2- dihydroquinoline (1.6 mg/kg) was assessed in naive, morphine-dependent, and morphine-withdrawn rats to study the process of alpha 2-adrenoceptor repopulation and to calculate receptor turnover parameters. The simultaneous analysis of receptor recovery curves revealed that the turnover of brain alpha 2-adrenoceptors in morphine-withdrawn rats was accelerated [appearance rate constant (r) = 21 fmol/mg of protein/day; disappearance rate constant (k) = 0.25 day-1] compared with those in morphine-dependent (r = 13 fmol/mg of protein/day; k = 0.14 day-1) and naive (r = 15 fmol/mg of protein/day; k = 0.16 day-1) rats. Moreover, this analysis also indicated that the increased density of cortical alpha 2-adrenoceptors observed during morphine withdrawal was due to a significantly higher receptor appearance (delta r = 37-57%) and not to a decreased receptor disappearance, which in fact showed also an increase (delta k = 56-79%).(ABSTRACT TRUNCATED AT 250 WORDS)

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adrenergic alpha-Antagonists / pharmacology
  • Animals
  • Cerebral Cortex / metabolism*
  • Clonidine / metabolism
  • Male
  • Morphine / administration & dosage
  • Morphine / adverse effects*
  • Quinolines / pharmacology
  • Rats
  • Rats, Sprague-Dawley
  • Receptors, Adrenergic, alpha / metabolism*
  • Substance Withdrawal Syndrome / metabolism*
  • Time Factors
  • Up-Regulation*

Substances

  • Adrenergic alpha-Antagonists
  • Quinolines
  • Receptors, Adrenergic, alpha
  • EEDQ
  • Morphine
  • Clonidine