Uptake and efflux of 14-C-dopamine in platelets: evidence for a generalized defect in Parkinson's disease

Neurology. 1975 Jan;25(1):1-9. doi: 10.1212/wnl.25.1.1.

Abstract

Thirty-five parkinsonian patients (five untreated, six with levodopa only, seven with levodopa plus Ro 4-4602, nine with anticholinergic and/or antihistaminic medication, and eight with the anticholinergic/antihistaminic medication plus amantadine) and 35 age-matched control subjects were studied. Platelets isolated from each individual plasma were incubated with 14C-dopamine. Uptake was found to be decreased to a significant degree in all treated or untreated parkinsonian patients when compared with control subjects. Anticholinergic and/or antihistaminic medication, with or without amantadine, further decreased the dopamine uptake into platelets, while levodopa alone or with Ro 4-4602 returned uptake values to near normal. Dopamine efflux paralleled exactly the uptake values. The fact that parkinsonian platelets exhibit impaired dopamine uptake, while age-matched control platelets do not, constitutes the first direct evidence in favor of a generalized dopamine defect in Parkinson's disease.

Publication types

  • Comparative Study

MeSH terms

  • Adult
  • Aged
  • Amantadine / pharmacology
  • Aromatic Amino Acid Decarboxylase Inhibitors
  • Benserazide / therapeutic use
  • Blood Platelets / metabolism*
  • Carbon Radioisotopes
  • Depression, Chemical
  • Dopamine / metabolism*
  • Drug Synergism
  • Drug Therapy, Combination
  • Enzyme Inhibitors / administration & dosage
  • Enzyme Inhibitors / therapeutic use
  • Female
  • Histamine H1 Antagonists / therapeutic use
  • Humans
  • Levodopa / administration & dosage
  • Levodopa / therapeutic use
  • Male
  • Middle Aged
  • Parasympatholytics / therapeutic use
  • Parkinson Disease / drug therapy
  • Parkinson Disease / metabolism*
  • Time Factors
  • Trihexyphenidyl / pharmacology

Substances

  • Aromatic Amino Acid Decarboxylase Inhibitors
  • Carbon Radioisotopes
  • Enzyme Inhibitors
  • Histamine H1 Antagonists
  • Parasympatholytics
  • Levodopa
  • Trihexyphenidyl
  • Benserazide
  • Amantadine
  • Dopamine