Effect of selective and reversible MAO inhibitors on dopamine outflow in rat striatum: a microdialysis study

J Neural Transm Suppl. 1990:32:79-84. doi: 10.1007/978-3-7091-9113-2_9.

Abstract

The effect of reversible inhibitors of the monoamine oxidase type A (MAO-A), moclobemide (Aurorix) and Ro 41-1049 (20 mg/kg i.p. each), as well as of reversible inhibitors of the MAO type B (MAO-B), Ro 19-6327 (1 mg/kg i.p.), on the outflow of dopamine (DA), 3,4-dihydroxyphenylacetic acid (DOPAC) and homovanillic acid (HVA) was studied in the rat by transstriatal microdialysis. Reversible MAO-A inhibitors markedly increased the output of DA and concomitantly decreased the output of DOPAC and HVA. These effects were absent with the highly selective MAO-B inhibitor Ro 19-6327.

MeSH terms

  • 3,4-Dihydroxyphenylacetic Acid / metabolism
  • Animals
  • Benzamides
  • Corpus Striatum / drug effects
  • Corpus Striatum / metabolism*
  • Deamination
  • Dialysis
  • Dopamine / metabolism*
  • Homovanillic Acid / metabolism
  • Male
  • Moclobemide
  • Monoamine Oxidase Inhibitors / pharmacology*
  • Picolinic Acids
  • Rats
  • Rats, Inbred Strains
  • Thiazoles

Substances

  • Benzamides
  • Monoamine Oxidase Inhibitors
  • Picolinic Acids
  • Thiazoles
  • 3,4-Dihydroxyphenylacetic Acid
  • Ro 41-1049
  • lazabemide
  • Moclobemide
  • Dopamine
  • Homovanillic Acid