L-dopa competes with tyrosine and tryptophan for human brain uptake

Nutr Metab. 1980;24(6):417-23. doi: 10.1159/000176359.

Abstract

Tyrosine and tryptophan have been assayed spectrofluorometrically in postmortem human brain areas of patients with Parkinson's disease treated orally with or without 3,4-dihydroxyphenylalanine (L-dopa) plus the peripherally acting decarboxylase inhibitor benserazide. Tyrosine as well as tryptophan decrease significantly after treatment with L-dopa, thus showing a competitive action of L-dopa to other aromatic amino acids on human brain uptake. It is suggested that some of the side effects of L-dopa treatment in Parkinson's disease are due to a disturbance in the brain and neural uptake of other, specially aromatic and branched-chain amino acids. An influence of L-dopa administration on protein synthesis also cannot be excluded.

MeSH terms

  • Aged
  • Benserazide / therapeutic use
  • Blood-Brain Barrier
  • Brain / metabolism*
  • Female
  • Humans
  • Levodopa / therapeutic use*
  • Male
  • Parkinson Disease / drug therapy
  • Parkinson Disease / metabolism*
  • Tryptophan / metabolism*
  • Tyrosine / metabolism*

Substances

  • Tyrosine
  • Levodopa
  • Benserazide
  • Tryptophan