Monoamine oxidase inhibition dramatically prolongs the duration of nicotine withdrawal-induced place aversion

Biol Psychiatry. 2008 Jan 15;63(2):158-63. doi: 10.1016/j.biopsych.2007.04.029. Epub 2007 Jul 23.

Abstract

Background: Long-lasting effects of withdrawal from nicotine are hypothesized to contribute to relapse and persistence of tobacco habits, and significant evidence supports a role of monoamine oxidase inhibitors (MAOI) contained in cigarette smoke as potent modulators of the rewarding effects of tobacco.

Methods: With quantification of somatic signs of withdrawal and the place aversion conditioning paradigm, we assessed the effects of MAOI pretreatment on both somatic and aversive motivational components of mecamylamine-induced nicotine withdrawal in rats rendered dependent on nicotine by the subcutaneous implantation of osmotic minipumps (vehicle or nicotine tartrate 9 mg/kg/day).

Results: In nicotine-infused rats, mecamylamine induced a place aversion that lasted 6 weeks. When nicotine-infused rats were also treated with a MAOI, mecamylamine-induced conditioned place aversion persisted for at least 8 months of abstinence. The MAOI treatment slightly decreased ratings of somatic signs induced by mecamylamine administration but had no effect on the threshold or the magnitude of mecamylamine-induced conditioned place aversion.

Conclusions: These results show that MAOI pretreatment induces a long-lasting conditioned placed aversion associated with nicotine withdrawal, possibly through a potentiation of learning and memory process, and provides some indications on protracted abstinence that might be useful for delineating the neurobiological substrate of relapse.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Analysis of Variance
  • Animals
  • Avoidance Learning / drug effects
  • Avoidance Learning / physiology*
  • Behavior, Animal / drug effects
  • Conditioning, Psychological / drug effects
  • Conditioning, Psychological / physiology*
  • Dose-Response Relationship, Drug
  • Drug Administration Routes
  • Drug Interactions
  • Male
  • Mecamylamine / pharmacology
  • Monoamine Oxidase / metabolism*
  • Monoamine Oxidase Inhibitors / pharmacology
  • Nicotine / adverse effects
  • Nicotinic Agonists / adverse effects
  • Nicotinic Antagonists / pharmacology
  • Rats
  • Rats, Sprague-Dawley
  • Substance Withdrawal Syndrome / etiology
  • Substance Withdrawal Syndrome / physiopathology
  • Substance Withdrawal Syndrome / psychology*

Substances

  • Monoamine Oxidase Inhibitors
  • Nicotinic Agonists
  • Nicotinic Antagonists
  • Mecamylamine
  • Nicotine
  • Monoamine Oxidase