3H-xylamine binds to presynaptic rat striatal membranes

Life Sci. 1986 May 12;38(19):1715-21. doi: 10.1016/0024-3205(86)90121-9.

Abstract

3H-xylamine (3H-XYL), an irreversible catecholamine uptake inhibitor, was incubated with rat striatal synaptosomes, and the membrane fraction was examined by fluorography of a sodium dodecyl sulfate-polyacrylamide gel. A number of peptides were labeled. To determine their location, the striatal dopaminergic presynaptic nerve terminals were destroyed by unilateral electrolytic lesions through the nigrostriatal fibers prior to 3H-XYL exposure. The 3H-XYL bound to membranes from lesioned striata was about 29% of that bound to control membranes, which is consistent with the 83% reduction in dopamine (DA) uptake and the 68% reduction in DA content in the lesioned tissue. The decrease in peptide-bound 3H-XYL paralleled the decrease in DA content, with the exception of a 45% decrease in binding to a 45K peptide. These data show that 3H-XYL binding is predominantly localized in the dopaminergic presynaptic nerve terminals of the striatum.

MeSH terms

  • Animals
  • Binding Sites
  • Corpus Striatum / metabolism*
  • Denervation
  • Dopamine / physiology*
  • Membrane Proteins / analysis
  • Nerve Tissue Proteins / analysis
  • Nitrogen Mustard Compounds / metabolism*
  • Rats
  • Synaptic Membranes / analysis
  • Synaptic Membranes / metabolism*
  • Synaptosomes / metabolism

Substances

  • Membrane Proteins
  • Nerve Tissue Proteins
  • Nitrogen Mustard Compounds
  • xylamine
  • Dopamine