[18F]fluoro-L-dopa for the in vivo study of intracerebral dopamine

Int J Rad Appl Instrum A. 1986;37(8):669-75. doi: 10.1016/0883-2889(86)90260-1.

Abstract

6-[18F]Fluoro-L-dopa was designed to trace the dopamine metabolism in the brain with positron tomography. 6-[18F]Fluoro-L-dopa resembles natural L-dopa biochemically, it crosses the blood-brain barrier with the similar kinetics, it is decarboxylated by dopa decarboxylase and is stored intraneuronally in vesicles. In addition the rate of O-methylation of 6-[18F]fluoro-L-dopa by catechol-O-methyl transferase is only 1/4 of that of natural L-dopa. The low rate of O-methylation, especially in the periphery, is particularly beneficial for PT investigations of the brain. The radiotracer has been synthesized using a variety of electrophilic fluorinating agents.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Brain / diagnostic imaging
  • Brain / metabolism*
  • Dihydroxyphenylalanine / analogs & derivatives*
  • Dihydroxyphenylalanine / chemical synthesis
  • Dihydroxyphenylalanine / metabolism
  • Dopamine / metabolism*
  • Humans
  • Methylation
  • Radiochemistry
  • Radioisotopes
  • Safety
  • Tomography, Emission-Computed

Substances

  • Radioisotopes
  • fluorodopa F 18
  • Dihydroxyphenylalanine
  • Dopamine