Reduction of morphine abstinence in mice with a mutation in the gene encoding CREB

Science. 1996 Aug 2;273(5275):657-9. doi: 10.1126/science.273.5275.657.

Abstract

Chronic morphine administration induces an up-regulation of several components of the cyclic adenosine 5'-monophosphate (cAMP) signal transduction cascade. The behavioral and biochemical consequences of opiate withdrawal were investigated in mice with a genetic disruption of the alpha and Delta isoforms of the cAMP-responsive element-binding protein (CREB). In CREBalphadelta mutant mice the main symptoms of morphine withdrawal were strongly attenuated. No change in opioid binding sites or in morphine-induced analgesia was observed in these mutant mice, and the increase of adenylyl cyclase activity and immediate early gene expression after morphine withdrawal was normal. Thus, CREB-dependent gene transcription is a factor in the onset of behavioral manifestations of opiate dependence.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenylyl Cyclases / metabolism
  • Analgesia
  • Animals
  • Behavior, Animal
  • Cerebral Cortex / enzymology
  • Cyclic AMP Response Element-Binding Protein / genetics*
  • Cyclic AMP Response Element-Binding Protein / physiology*
  • Drug Tolerance
  • Gene Expression Regulation
  • Gene Targeting
  • Genes, Immediate-Early
  • Locus Coeruleus / metabolism
  • Mice
  • Morphine / administration & dosage*
  • Morphine / adverse effects
  • Morphine / pharmacology
  • Morphine Dependence / etiology*
  • Morphine Dependence / metabolism
  • Mutation
  • Naloxone / pharmacology
  • Receptors, Opioid / metabolism
  • Signal Transduction
  • Substance Withdrawal Syndrome / physiopathology*

Substances

  • Cyclic AMP Response Element-Binding Protein
  • Receptors, Opioid
  • Naloxone
  • Morphine
  • Adenylyl Cyclases