(-)-Deprenyl treatment of patients with Parkinson's disease does not affect erythrocyte catechol-O-methyl transferase activity

J Neural Transm Park Dis Dement Sect. 1991;3(3):215-23. doi: 10.1007/BF02259539.

Abstract

(-)-Deprenyl has been increasingly used in recent years as an adjuvant with levodopa and a decarboxylase inhibitor in the treatment of Parkinson's disease. The inhibition of dopa decarboxylase and monoamine oxidase B resulting from this combination suggests that there may be a counter-regulatory increase in the activity of the third main enzyme in the catabolism of levodopa, i.e. catecholamine-O-methyl transferase (COMT). The current study on 36 patients with Parkinson's disease under long-term treatment with levodopa/dopadecarboxylase inhibitor showed, however, that the erythrocyte-COMT was unaffected by additional (-)-deprenyl medication. The patients in this study received levodopa and benserazide either with (-)-deprenyl (n = 21) or without (-)-deprenyl (n = 15). When allowance was made for the different genotypes, COMTLL, COMTLH, and COMTHH, there were no differences in the enzyme activities between the two treatment groups and the untreated controls (n = 26). On the basis of these results, consideration is given to the conditions in which COMT inhibitors are likely to be of value in the treatment of Parkinson's disease.

MeSH terms

  • Aged
  • Benserazide / pharmacology
  • Catechol O-Methyltransferase / blood
  • Catechol O-Methyltransferase / drug effects*
  • Erythrocytes / drug effects
  • Erythrocytes / enzymology*
  • Female
  • Humans
  • Kinetics
  • Levodopa / pharmacology
  • Male
  • Middle Aged
  • Monoamine Oxidase / blood
  • Monoamine Oxidase / drug effects
  • Parkinson Disease / drug therapy
  • Parkinson Disease / enzymology*
  • Selegiline / pharmacology*
  • Selegiline / therapeutic use

Substances

  • Selegiline
  • Levodopa
  • Benserazide
  • Monoamine Oxidase
  • Catechol O-Methyltransferase