In vivo voltammetric characterization of low affinity striatal dopamine uptake: drug inhibition profile and relation to dopaminergic innervation density

Brain Res. 1986 May 14;373(1-2):85-91. doi: 10.1016/0006-8993(86)90318-5.

Abstract

Electrical stimulation of the median forebrain bundle evoked dopamine release in the ipsilateral striatum which was monitored with high-speed cyclic voltammetry. After stimulation, the extracellular concentration of dopamine fell due to uptake in a biphasic manner, showing zero-order and first-order components. The zero-order phase corresponded to a Vmax of 42.8 +/- 1.8 nmol/min/g tissue. The uptake system could be blocked by D-amphetamine, methylphenidate and nomifensine, but not by benztropine, amfonelic acid or mazindol. The density of uptake sites showed a correlation with the density of striatal dopamine innervation.

Publication types

  • Comparative Study

MeSH terms

  • Animals
  • Benztropine / pharmacology
  • Corpus Striatum / metabolism*
  • Dextroamphetamine / pharmacology
  • Dopamine / metabolism*
  • Electric Stimulation
  • Male
  • Mazindol / pharmacology
  • Medial Forebrain Bundle / physiology*
  • Methylphenidate / pharmacology
  • Nalidixic Acid / analogs & derivatives
  • Naphthyridines / pharmacology
  • Neural Pathways / physiology*
  • Nomifensine / pharmacology
  • Rats
  • Rats, Inbred Strains

Substances

  • Naphthyridines
  • Nomifensine
  • Benztropine
  • Methylphenidate
  • Nalidixic Acid
  • Mazindol
  • amfonelic acid
  • Dextroamphetamine
  • Dopamine