Cerebral monoamine oxidase A inhibition in tobacco smokers confirmed with PET and [11C]befloxatone

J Clin Psychopharmacol. 2009 Feb;29(1):86-8. doi: 10.1097/JCP.0b013e31819e98f.

Abstract

The inhibition of cerebral monoamine oxidases (MAOs) by cigarette smoke components could participate to the tobacco addiction. However, the actual extent of this inhibition in vivo in smokers is still poorly known. We investigated cerebral MAO-A availability in 7 tobacco-dependent subjects and 6 healthy nonsmokers, using positron emission tomography (PET) and the MAO-A selective radioligand [C]befloxatone. In comparison to nonsmokers, smokers showed a significant overall reduction of [C]befloxatone binding potential (BP) in cortical areas (average reduction, -60%) and a similar trend in caudate and thalamus (-40%). Our findings confirm a widespread inhibition of cerebral MAO-A in smokers. This mechanism may contribute to tobacco addiction and for a possible mood-modulating effect of tobacco.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Carbon Radioisotopes
  • Cerebral Cortex / diagnostic imaging*
  • Cerebral Cortex / enzymology*
  • Humans
  • Male
  • Monoamine Oxidase / metabolism*
  • Monoamine Oxidase Inhibitors / metabolism
  • Monoamine Oxidase Inhibitors / pharmacology*
  • Nicotine / administration & dosage
  • Nicotine / pharmacology
  • Nicotinic Agonists / administration & dosage
  • Nicotinic Agonists / pharmacology
  • Oxazoles / pharmacokinetics*
  • Positron-Emission Tomography
  • Radiopharmaceuticals / pharmacokinetics*
  • Smoking / physiopathology
  • Tissue Distribution

Substances

  • Carbon Radioisotopes
  • Monoamine Oxidase Inhibitors
  • Nicotinic Agonists
  • Oxazoles
  • Radiopharmaceuticals
  • befloxatone
  • Nicotine
  • Monoamine Oxidase